geneid | 23511 |
---|---|
ensemblid | ENSG00000095319.14 |
hgncid | 17859 |
symbol | NUP188 |
name | nucleoporin 188 |
refseq_nuc | NM_015354.3 |
refseq_prot | NP_056169.1 |
ensembl_nuc | ENST00000372577.2 |
ensembl_prot | ENSP00000361658.2 |
mane_status | MANE Select |
chr | chr9 |
start | 128947699 |
end | 129007096 |
strand | + |
ver | v1.2 |
region | chr9:128947699-129007096 |
region5000 | chr9:128942699-129012096 |
regionname0 | NUP188_chr9_128947699_129007096 |
regionname5000 | NUP188_chr9_128942699_129012096 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 1749 | 275 | 66 | 56 | 108 | 12 | 31 | 81 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
a0002 | 0/0 | 1749 | 6 | 5 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
a0003 | 0/0 | 1749 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
a0004 | 0/0 | 1749 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
a0005 | 0/0 | 1749 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
a0006 | 0/0 | 1749 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
a0007 | 0/0 | 1749 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
a0008 | 0/0 | 1749 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
a0009 | 0/0 | 1749 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
a0010 | 0/0 | 1749 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
a0011 | 0/0 | 1749 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
a0012 | 0/0 | 1749 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
a0013 | 0/0 | 1749 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 5250 | 137 | 32 | 24 | 54 | 6 | 20 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
c0002 | 0/1 | 5250 | 98 | 17 | 27 | 38 | 6 | 9 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
c0003 | 0/0 | 5250 | 14 | 0 | 0 | 12 | 0 | 2 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
c0004 | 0/0 | 5250 | 10 | 9 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
c0005 | 0/0 | 5250 | 5 | 5 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
c0006 | 0/0 | 5250 | 4 | 4 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
c0007 | 0/0 | 5250 | 2 | 2 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
c0008 | 0/0 | 5250 | 2 | 2 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
c0009 | 0/0 | 5250 | 2 | 2 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
c0010 | 0/0 | 5250 | 2 | 0 | 2 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
c0011 | 0/0 | 5250 | 1 | 0 | 0 | 0 | 1 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
c0012 | 0/0 | 5250 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
c0013 | 0/0 | 5250 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
c0014 | 0/0 | 5250 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
c0015 | 0/0 | 5250 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
c0016 | 0/0 | 5250 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
c0017 | 0/0 | 5250 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
c0018 | 0/0 | 5250 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
c0019 | 0/0 | 5250 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
c0020 | 0/0 | 5250 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
c0021 | 0/0 | 5250 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
c0022 | 0/0 | 5250 | 1 | 0 | 0 | 0 | 1 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
c0023 | 0/0 | 5250 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
c0024 | 0/0 | 5250 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
c0025 | 0/0 | 5250 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
c0026 | 0/0 | 5250 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
c0027 | 0/0 | 5250 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
c0028 | 0/0 | 5250 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
c0029 | 0/0 | 5250 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
c0030 | 0/0 | 5250 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 440 | 273 | 73 | 60 | 97 | 14 | 27 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
t0002 | 0/0 | 440 | 13 | 0 | 0 | 12 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
t0003 | 0/0 | 440 | 3 | 0 | 0 | 0 | 0 | 3 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
t0004 | 0/0 | 440 | 2 | 2 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
t0005 | 0/0 | 440 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
t0006 | 0/0 | 440 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
t0007 | 0/0 | 440 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
t0008 | 0/0 | 440 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
t0009 | 0/0 | 440 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0061 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0231 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 5250 | 137 | 32 | 24 | 54 | 6 | 20 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
a0001c0002 | 0/1 | 5250 | 98 | 17 | 27 | 38 | 6 | 9 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
a0001c0003 | 0/0 | 5250 | 14 | 0 | 0 | 12 | 0 | 2 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
a0001c0004 | 0/0 | 5250 | 10 | 9 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
a0001c0007 | 0/0 | 5250 | 2 | 2 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
a0001c0008 | 0/0 | 5250 | 2 | 2 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
a0001c0009 | 0/0 | 5250 | 2 | 2 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
a0001c0013 | 0/0 | 5250 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
a0001c0014 | 0/0 | 5250 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
a0001c0017 | 0/0 | 5250 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
a0001c0020 | 0/0 | 5250 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
a0001c0021 | 0/0 | 5250 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
a0001c0023 | 0/0 | 5250 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
a0001c0025 | 0/0 | 5250 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
a0001c0027 | 0/0 | 5250 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
a0001c0028 | 0/0 | 5250 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
a0001c0029 | 0/0 | 5250 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
a0002c0005 | 0/0 | 5250 | 5 | 5 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
a0002c0012 | 0/0 | 5250 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
a0003c0006 | 0/0 | 5250 | 4 | 4 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
a0004c0010 | 0/0 | 5250 | 2 | 0 | 2 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
a0005c0011 | 0/0 | 5250 | 1 | 0 | 0 | 0 | 1 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
a0006c0030 | 0/0 | 5250 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
a0007c0016 | 0/0 | 5250 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
a0008c0018 | 0/0 | 5250 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
a0009c0019 | 0/0 | 5250 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
a0010c0022 | 0/0 | 5250 | 1 | 0 | 0 | 0 | 1 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
a0011c0024 | 0/0 | 5250 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
a0012c0015 | 0/0 | 5250 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
a0013c0026 | 0/0 | 5250 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 5689 | 129 | 30 | 24 | 53 | 6 | 15 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
a0001c0001t0003 | 0/0 | 5689 | 3 | 0 | 0 | 0 | 0 | 3 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
a0001c0001t0004 | 0/0 | 5689 | 2 | 2 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
a0001c0001t0005 | 0/0 | 5689 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
a0001c0001t0006 | 0/0 | 5689 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
a0001c0001t0007 | 0/0 | 5689 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
a0001c0002t0001 | 0/1 | 5689 | 98 | 17 | 27 | 38 | 6 | 9 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
a0001c0003t0002 | 0/0 | 5689 | 13 | 0 | 0 | 12 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
a0001c0003t0009 | 0/0 | 5689 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
a0001c0004t0001 | 0/0 | 5689 | 9 | 8 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
a0001c0004t0008 | 0/0 | 5689 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
a0001c0007t0001 | 0/0 | 5689 | 2 | 2 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
a0001c0008t0001 | 0/0 | 5689 | 2 | 2 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
a0001c0009t0001 | 0/0 | 5689 | 2 | 2 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
a0001c0013t0001 | 0/0 | 5689 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
a0001c0014t0001 | 0/0 | 5689 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
a0001c0017t0001 | 0/0 | 5689 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
a0001c0020t0001 | 0/0 | 5689 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
a0001c0021t0001 | 0/0 | 5689 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
a0001c0023t0001 | 0/0 | 5689 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
a0001c0025t0001 | 0/0 | 5689 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
a0001c0027t0001 | 0/0 | 5689 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
a0001c0028t0001 | 0/0 | 5689 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
a0001c0029t0001 | 0/0 | 5689 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
a0002c0005t0001 | 0/0 | 5689 | 5 | 5 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
a0002c0012t0001 | 0/0 | 5689 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
a0003c0006t0001 | 0/0 | 5689 | 4 | 4 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
a0004c0010t0001 | 0/0 | 5689 | 2 | 0 | 2 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
a0005c0011t0001 | 0/0 | 5689 | 1 | 0 | 0 | 0 | 1 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
a0006c0030t0001 | 0/0 | 5689 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
a0007c0016t0001 | 0/0 | 5689 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
a0008c0018t0001 | 0/0 | 5689 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
a0009c0019t0001 | 0/0 | 5689 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
a0010c0022t0001 | 0/0 | 5689 | 1 | 0 | 0 | 0 | 1 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
a0011c0024t0001 | 0/0 | 5689 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
a0012c0015t0001 | 0/0 | 5689 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
a0013c0026t0001 | 0/0 | 5689 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | copy fasta | chr9 | 128942699 | 129012096 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0061 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0003g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0003g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0003g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0004g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0004g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0005g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0006g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0001t0007g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0002t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0002t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0002t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0002t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0002t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0002t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0002t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0002t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0002t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0002t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0002t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0002t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0002t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0002t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0002t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0002t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0002t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0002t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0002t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0002t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0002t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0002t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0002t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0002t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0002t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0002t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0002t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0002t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0002t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0002t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0002t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0002t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0002t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0002t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0002t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0002t0001g0231 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0002t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0002t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0002t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0002t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0002t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0002t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0002t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0002t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0002t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0002t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0002t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0002t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0002t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0002t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0002t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0002t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0003t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0003t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0003t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0003t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0003t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0003t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0003t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0003t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0003t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0003t0002g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0003t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0003t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0003t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0003t0009g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0004t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0004t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0004t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0004t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0004t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0004t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0004t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0004t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0004t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0004t0008g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0007t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0007t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0008t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0008t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0009t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0009t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0013t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0014t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0017t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0020t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0021t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0023t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0025t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0027t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0028t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0001c0029t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0002c0005t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0002c0005t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0002c0005t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0002c0005t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0002c0005t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0002c0012t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0003c0006t0001g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0003c0006t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0003c0006t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0004c0010t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0004c0010t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0005c0011t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0006c0030t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0007c0016t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0008c0018t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0009c0019t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0010c0022t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0011c0024t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0012c0015t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
a0013c0026t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0002 | t0001 | g0226 | EUR | GBR | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0126 | EUR | GBR | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG00140 | hp1 | a0001 | c0002 | t0001 | g0235 | EUR | GBR | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG00140 | hp2 | a0005 | c0011 | t0001 | g0152 | EUR | GBR | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0111 | EUR | FIN | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG00280 | hp2 | a0001 | c0002 | t0001 | g0033 | EUR | FIN | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | CHS | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | CHS | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG00438 | hp1 | a0001 | c0002 | t0001 | g0220 | EAS | CHS | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG00438 | hp2 | a0001 | c0002 | t0001 | g0237 | EAS | CHS | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | CHS | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | CHS | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG00597 | hp1 | a0013 | c0026 | t0001 | g0117 | EAS | CHS | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | CHS | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG00642 | hp2 | a0004 | c0010 | t0001 | g0234 | AMR | PUR | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | CHS | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | CHS | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG00735 | hp1 | a0001 | c0013 | t0001 | g0200 | AMR | PUR | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG00738 | hp1 | a0001 | c0002 | t0001 | g0048 | AMR | PUR | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG00738 | hp2 | a0001 | c0002 | t0001 | g0219 | AMR | PUR | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG00741 | hp1 | a0001 | c0002 | t0001 | g0242 | AMR | PUR | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG00741 | hp2 | a0001 | c0002 | t0001 | g0067 | AMR | PUR | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG01069 | hp1 | a0001 | c0002 | t0001 | g0244 | AMR | PUR | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG01074 | hp1 | a0001 | c0002 | t0001 | g0099 | AMR | PUR | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG01099 | hp1 | a0001 | c0004 | t0001 | g0257 | AMR | PUR | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG01109 | hp1 | a0001 | c0002 | t0001 | g0240 | AMR | PUR | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG01167 | hp1 | a0002 | c0012 | t0001 | g0291 | AMR | PUR | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG01167 | hp2 | a0001 | c0002 | t0001 | g0177 | AMR | PUR | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG01169 | hp1 | a0001 | c0002 | t0001 | g0188 | AMR | PUR | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG01175 | hp1 | a0001 | c0002 | t0001 | g0216 | AMR | PUR | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG01243 | hp1 | a0001 | c0002 | t0001 | g0243 | AMR | PUR | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG01243 | hp2 | a0001 | c0021 | t0001 | g0133 | AMR | PUR | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG01255 | hp1 | a0001 | c0002 | t0001 | g0193 | AMR | CLM | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG01255 | hp2 | a0001 | c0002 | t0001 | g0027 | AMR | CLM | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | CLM | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG01256 | hp2 | a0004 | c0010 | t0001 | g0169 | AMR | CLM | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG01257 | hp1 | a0001 | c0002 | t0001 | g0024 | AMR | CLM | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG01257 | hp2 | a0001 | c0002 | t0001 | g0186 | AMR | CLM | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG01261 | hp1 | a0001 | c0002 | t0001 | g0209 | AMR | CLM | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | CLM | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG01346 | hp1 | a0012 | c0015 | t0001 | g0165 | AMR | CLM | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG01346 | hp2 | a0001 | c0002 | t0001 | g0224 | AMR | CLM | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | CLM | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | CLM | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG01433 | hp1 | a0001 | c0002 | t0001 | g0080 | AMR | CLM | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG01433 | hp2 | a0001 | c0020 | t0001 | g0084 | AMR | CLM | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0262 | AMR | CLM | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | CLM | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0113 | EUR | IBS | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0118 | EUR | IBS | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG01516 | hp1 | a0001 | c0002 | t0001 | g0189 | EUR | IBS | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG01516 | hp2 | a0010 | c0022 | t0001 | g0156 | EUR | IBS | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG01517 | hp1 | a0001 | c0002 | t0001 | g0191 | EUR | IBS | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0114 | EUR | IBS | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | ACB | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG01928 | hp1 | a0001 | c0002 | t0001 | g0215 | AMR | PEL | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PEL | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG01934 | hp1 | a0001 | c0002 | t0001 | g0236 | AMR | PEL | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | PEL | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG01952 | hp1 | a0001 | c0002 | t0001 | g0225 | AMR | PEL | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | PEL | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PEL | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | PEL | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | PEL | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG01993 | hp2 | a0001 | c0002 | t0001 | g0206 | AMR | PEL | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG02015 | hp1 | a0001 | c0002 | t0001 | g0175 | EAS | KHV | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | KHV | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG02027 | hp1 | a0001 | c0003 | t0002 | g0280 | EAS | KHV | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | KHV | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG02040 | hp1 | a0001 | c0002 | t0001 | g0020 | EAS | KHV | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG02040 | hp2 | a0001 | c0002 | t0001 | g0011 | EAS | KHV | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | ACB | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | KHV | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG02056 | hp2 | a0001 | c0002 | t0001 | g0196 | EAS | KHV | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | KHV | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | KHV | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG02132 | hp1 | a0001 | c0002 | t0001 | g0198 | EAS | KHV | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | KHV | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG02145 | hp1 | a0001 | c0002 | t0001 | g0246 | AFR | ACB | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | ACB | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | CDX | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG02165 | hp2 | a0001 | c0002 | t0001 | g0182 | EAS | CDX | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG02257 | hp1 | a0001 | c0002 | t0001 | g0223 | AFR | ACB | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | ACB | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG02258 | hp1 | a0001 | c0002 | t0001 | g0176 | AFR | ACB | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG02258 | hp2 | a0001 | c0004 | t0001 | g0255 | AFR | ACB | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG02273 | hp1 | a0001 | c0002 | t0001 | g0217 | AMR | PEL | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG02273 | hp2 | a0001 | c0002 | t0001 | g0261 | AMR | PEL | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | ACB | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG02280 | hp2 | a0001 | c0004 | t0008 | g0256 | AFR | ACB | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG02293 | hp1 | a0001 | c0002 | t0001 | g0171 | AMR | PEL | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG02293 | hp2 | a0001 | c0002 | t0001 | g0260 | AMR | PEL | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG02300 | hp1 | a0001 | c0025 | t0001 | g0197 | AMR | PEL | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | PEL | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG02451 | hp1 | a0001 | c0009 | t0001 | g0267 | AFR | ACB | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG02451 | hp2 | a0002 | c0005 | t0001 | g0294 | AFR | ACB | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG02523 | hp1 | a0001 | c0002 | t0001 | g0021 | EAS | KHV | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG02523 | hp2 | a0001 | c0002 | t0001 | g0174 | EAS | KHV | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0047 | SAS | PJL | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG02602 | hp2 | a0008 | c0018 | t0001 | g0089 | SAS | PJL | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG02615 | hp1 | a0002 | c0005 | t0001 | g0295 | AFR | GWD | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | GWD | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG02622 | hp1 | a0001 | c0002 | t0001 | g0233 | AFR | GWD | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | GWD | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG02630 | hp1 | a0001 | c0007 | t0001 | g0263 | AFR | GWD | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | GWD | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | GWD | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG02647 | hp2 | a0001 | c0002 | t0001 | g0271 | AFR | GWD | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG02683 | hp1 | a0001 | c0002 | t0001 | g0208 | SAS | PJL | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG02683 | hp2 | a0001 | c0001 | t0005 | g0065 | SAS | PJL | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0151 | SAS | PJL | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0062 | SAS | PJL | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG02717 | hp2 | a0001 | c0008 | t0001 | g0161 | AFR | GWD | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0125 | SAS | PJL | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | GWD | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG02886 | hp2 | a0001 | c0004 | t0001 | g0250 | AFR | GWD | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG02895 | hp2 | a0001 | c0002 | t0001 | g0266 | AFR | GWD | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG02896 | hp1 | a0001 | c0002 | t0001 | g0218 | AFR | GWD | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG02896 | hp2 | a0001 | c0001 | t0004 | g0288 | AFR | GWD | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG02897 | hp2 | a0001 | c0001 | t0004 | g0287 | AFR | GWD | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG02965 | hp2 | a0001 | c0004 | t0001 | g0247 | AFR | ESN | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG02970 | hp1 | a0001 | c0002 | t0001 | g0241 | AFR | ESN | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG02970 | hp2 | a0001 | c0002 | t0001 | g0269 | AFR | ESN | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | ESN | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG02976 | hp2 | a0001 | c0004 | t0001 | g0258 | AFR | ESN | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG03017 | hp1 | a0001 | c0001 | t0007 | g0088 | SAS | PJL | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG03017 | hp2 | a0001 | c0002 | t0001 | g0190 | SAS | PJL | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG03041 | hp1 | a0011 | c0024 | t0001 | g0252 | AFR | GWD | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG03041 | hp2 | a0002 | c0005 | t0001 | g0293 | AFR | GWD | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG03098 | hp1 | a0001 | c0007 | t0001 | g0123 | AFR | MSL | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | MSL | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG03130 | hp1 | a0001 | c0009 | t0001 | g0268 | AFR | ESN | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG03139 | hp1 | a0001 | c0008 | t0001 | g0135 | AFR | ESN | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG03139 | hp2 | a0001 | c0002 | t0001 | g0254 | AFR | ESN | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | ESN | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG03195 | hp2 | a0001 | c0004 | t0001 | g0253 | AFR | ESN | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | MSL | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG03209 | hp2 | a0001 | c0002 | t0001 | g0213 | AFR | MSL | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | MSL | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG03225 | hp2 | a0002 | c0005 | t0001 | g0290 | AFR | MSL | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG03453 | hp1 | a0003 | c0006 | t0001 | g0071 | AFR | MSL | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG03453 | hp2 | a0001 | c0002 | t0001 | g0228 | AFR | MSL | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG03486 | hp1 | a0001 | c0004 | t0001 | g0249 | AFR | MSL | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG03486 | hp2 | a0003 | c0006 | t0001 | g0001 | AFR | MSL | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0144 | SAS | PJL | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG03491 | hp2 | a0001 | c0002 | t0001 | g0170 | SAS | PJL | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0046 | SAS | PJL | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG03492 | hp2 | a0001 | c0002 | t0001 | g0207 | SAS | PJL | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | GWD | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | GWD | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG03579 | hp1 | a0001 | c0002 | t0001 | g0265 | AFR | MSL | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG03579 | hp2 | a0003 | c0006 | t0001 | g0160 | AFR | MSL | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0090 | SAS | PJL | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG03654 | hp2 | a0006 | c0030 | t0001 | g0150 | SAS | PJL | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG03688 | hp1 | a0007 | c0016 | t0001 | g0230 | SAS | STU | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0042 | SAS | STU | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG03710 | hp1 | a0001 | c0002 | t0001 | g0205 | SAS | PJL | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG03710 | hp2 | a0001 | c0001 | t0003 | g0032 | SAS | PJL | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG03834 | hp1 | a0001 | c0001 | t0003 | g0128 | SAS | BEB | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG03834 | hp2 | a0001 | c0003 | t0002 | g0283 | SAS | BEB | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG03942 | hp1 | a0001 | c0002 | t0001 | g0179 | SAS | BEB | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG03942 | hp2 | a0001 | c0001 | t0003 | g0132 | SAS | BEB | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG04115 | hp1 | a0001 | c0003 | t0009 | g0281 | SAS | STU | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG04115 | hp2 | a0001 | c0002 | t0001 | g0212 | SAS | STU | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0063 | SAS | STU | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG04199 | hp2 | a0001 | c0002 | t0001 | g0239 | SAS | STU | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG04228 | hp1 | a0001 | c0002 | t0001 | g0238 | SAS | STU | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | STU | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | CHB | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | CHB | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
NA18941 | hp2 | a0001 | c0003 | t0002 | g0275 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
NA18943 | hp1 | a0001 | c0002 | t0001 | g0184 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
NA18943 | hp2 | a0001 | c0002 | t0001 | g0162 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
NA18946 | hp2 | a0001 | c0002 | t0001 | g0229 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
NA18951 | hp2 | a0001 | c0003 | t0002 | g0278 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
NA18954 | hp1 | a0001 | c0001 | t0006 | g0022 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
NA18954 | hp2 | a0001 | c0002 | t0001 | g0023 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
NA18962 | hp2 | a0001 | c0023 | t0001 | g0168 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
NA18964 | hp1 | a0001 | c0002 | t0001 | g0081 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
NA18966 | hp1 | a0001 | c0002 | t0001 | g0040 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
NA18968 | hp2 | a0001 | c0017 | t0001 | g0211 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
NA18975 | hp1 | a0001 | c0003 | t0002 | g0276 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
NA18975 | hp2 | a0001 | c0002 | t0001 | g0025 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
NA18979 | hp1 | a0001 | c0002 | t0001 | g0096 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
NA18982 | hp1 | a0001 | c0002 | t0001 | g0187 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
NA18983 | hp2 | a0001 | c0002 | t0001 | g0201 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
NA18984 | hp1 | a0001 | c0002 | t0001 | g0183 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
NA18984 | hp2 | a0001 | c0002 | t0001 | g0034 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
NA18985 | hp2 | a0001 | c0003 | t0002 | g0282 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
NA18986 | hp1 | a0001 | c0003 | t0002 | g0277 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
NA18987 | hp1 | a0001 | c0029 | t0001 | g0185 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
NA18999 | hp1 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
NA18999 | hp2 | a0001 | c0002 | t0001 | g0203 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
NA19000 | hp2 | a0001 | c0002 | t0001 | g0085 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
NA19004 | hp1 | a0001 | c0002 | t0001 | g0026 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
NA19004 | hp2 | a0001 | c0003 | t0002 | g0284 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
NA19009 | hp1 | a0001 | c0002 | t0001 | g0202 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
NA19043 | hp1 | a0001 | c0002 | t0001 | g0210 | AFR | LWK | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
NA19043 | hp2 | a0001 | c0028 | t0001 | g0259 | AFR | LWK | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
NA19055 | hp1 | a0001 | c0002 | t0001 | g0222 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
NA19056 | hp1 | a0009 | c0019 | t0001 | g0092 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
NA19056 | hp2 | a0001 | c0002 | t0001 | g0178 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
NA19057 | hp1 | a0001 | c0002 | t0001 | g0172 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
NA19062 | hp1 | a0001 | c0003 | t0002 | g0274 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
NA19064 | hp2 | a0001 | c0002 | t0001 | g0192 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
NA19065 | hp1 | a0001 | c0003 | t0002 | g0273 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
NA19065 | hp2 | a0001 | c0002 | t0001 | g0195 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
NA19066 | hp2 | a0001 | c0002 | t0001 | g0245 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
NA19067 | hp2 | a0001 | c0002 | t0001 | g0232 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
NA19074 | hp2 | a0001 | c0003 | t0002 | g0279 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
NA19078 | hp2 | a0001 | c0014 | t0001 | g0180 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
NA19081 | hp1 | a0001 | c0003 | t0002 | g0286 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
NA19082 | hp1 | a0001 | c0003 | t0002 | g0285 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
NA19084 | hp2 | a0001 | c0002 | t0001 | g0227 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
NA19085 | hp1 | a0001 | c0002 | t0001 | g0181 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
NA19088 | hp2 | a0001 | c0002 | t0001 | g0214 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
NA19240 | hp1 | a0003 | c0006 | t0001 | g0001 | AFR | YRI | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
NA19240 | hp2 | a0001 | c0002 | t0001 | g0006 | AFR | YRI | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | ASW | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
NA20129 | hp2 | a0001 | c0002 | t0001 | g0194 | AFR | ASW | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0120 | EUR | TSI | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
NA20805 | hp2 | a0001 | c0002 | t0001 | g0204 | EUR | TSI | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0053 | SAS | GIH | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0049 | SAS | GIH | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG01123 | hp1 | a0001 | c0002 | t0001 | g0199 | AMR | CLM | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | CLM | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | ACB | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG02109 | hp2 | a0001 | c0004 | t0001 | g0251 | AFR | ACB | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0264 | AFR | ACB | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG02559 | hp2 | a0002 | c0005 | t0001 | g0292 | AFR | ACB | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | MSL | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | MSL | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG06807 | hp1 | a0001 | c0002 | t0001 | g0270 | AFR | USA | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
HG06807 | hp2 | a0001 | c0027 | t0001 | g0289 | AFR | USA | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
NA18955 | hp2 | a0001 | c0002 | t0001 | g0173 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
NA21309 | hp1 | a0001 | c0004 | t0001 | g0248 | AFR | LWK | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0272 | AFR | LWK | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0001 | g0231 | REF | REF | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0061 | REF | REF | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:128947736
|
G | C | 1 | a0005 | 1 | HG00140.hp2 | missense_variant | MODERATE | c.17G>C | p.Gly6Ala | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 1/44 | 38/5689 | 17/5250 | 6/1749 | chr9 | 128947736 | ||
chr9:128947738
|
G | A | 1 | a0002 | 6 | HG01167.hp1 HG02451.hp2 HG02559.hp2 others(3): Show |
missense_variant | MODERATE | c.19G>A | p.Gly7Arg | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 1/44 | 40/5689 | 19/5250 | 7/1749 | chr9 | 128947738 | ||
chr9:128956378
|
A | G | 1 | a0006 | 1 | HG03654.hp2 | missense_variant | MODERATE | c.190A>G | p.Asn64Asp | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 4/44 | 211/5689 | 190/5250 | 64/1749 | chr9 | 128956378 | ||
chr9:128979263
|
A | G | 1 | a0013 | 1 | HG00597.hp1 | missense_variant&splice_region_variant | MODERATE | c.1205A>G | p.Asp402Gly | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 13/44 | 1226/5689 | 1205/5250 | 402/1749 | chr9 | 128979263 | ||
chr9:128993282
|
T | C | 1 | a0012 | 1 | HG01346.hp1 | missense_variant | MODERATE | c.2726T>C | p.Ile909Thr | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 26/44 | 2747/5689 | 2726/5250 | 909/1749 | chr9 | 128993282 | ||
chr9:128993643
|
A | G | 1 | a0011 | 1 | HG03041.hp1 | missense_variant | MODERATE | c.2966A>G | p.His989Arg | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 27/44 | 2987/5689 | 2966/5250 | 989/1749 | chr9 | 128993643 | ||
chr9:128998185
|
G | A | 1 | a0007 | 1 | HG03688.hp1 | missense_variant | MODERATE | c.3386G>A | p.Arg1129His | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 31/44 | 3407/5689 | 3386/5250 | 1129/1749 | chr9 | 128998185 | ||
chr9:128999742
|
G | T | 1 | a0004 | 2 | HG00642.hp2 HG01256.hp2 |
missense_variant | MODERATE | c.3780G>T | p.Glu1260Asp | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 34/44 | 3801/5689 | 3780/5250 | 1260/1749 | chr9 | 128999742 | ||
chr9:128999801
|
A | G | 1 | a0003 | 4 | HG03453.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
missense_variant | MODERATE | c.3839A>G | p.Asp1280Gly | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 34/44 | 3860/5689 | 3839/5250 | 1280/1749 | chr9 | 128999801 | ||
chr9:129001595
|
C | G | 1 | a0010 | 1 | HG01516.hp2 | missense_variant | MODERATE | c.3910C>G | p.Leu1304Val | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 35/44 | 3931/5689 | 3910/5250 | 1304/1749 | chr9 | 129001595 | ||
chr9:129001659
|
G | A | 1 | a0008 | 1 | HG02602.hp2 | missense_variant | MODERATE | c.3974G>A | p.Arg1325His | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 35/44 | 3995/5689 | 3974/5250 | 1325/1749 | chr9 | 129001659 | ||
chr9:129002931
|
G | A | 1 | a0009 | 1 | NA19056.hp1 | missense_variant | MODERATE | c.4252G>A | p.Glu1418Lys | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 37/44 | 4273/5689 | 4252/5250 | 1418/1749 | chr9 | 129002931 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:128958885
|
C | T | 2 | a0001c0029a0002c0012 | 2 | HG01167.hp1 NA18987.hp1 |
synonymous_variant | LOW | c.456C>T | p.His152His | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 7/44 | 477/5689 | 456/5250 | 152/1749 | chr9 | 128958885 | ||
chr9:128968607
|
C | T | 1 | a0001c0028 | 1 | NA19043.hp2 | synonymous_variant | LOW | c.687C>T | p.Pro229Pro | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 9/44 | 708/5689 | 687/5250 | 229/1749 | chr9 | 128968607 | ||
chr9:128969439
|
C | T | 2 | a0001c0003a0001c0027 | 15 | HG02027.hp1 HG03834.hp2 HG04115.hp1 others(12): Show |
synonymous_variant | LOW | c.837C>T | p.Ile279Ile | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 10/44 | 858/5689 | 837/5250 | 279/1749 | chr9 | 128969439 | ||
chr9:128984936
|
C | A | 1 | a0001c0013 | 1 | HG00735.hp1 | synonymous_variant | LOW | c.1998C>A | p.Leu666Leu | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 20/44 | 2019/5689 | 1998/5250 | 666/1749 | chr9 | 128984936 | ||
chr9:128986834
|
T | C | 2 | a0001c0007a0001c0008 | 4 | HG02630.hp1 HG02717.hp2 HG03098.hp1 others(1): Show |
synonymous_variant | LOW | c.2223T>C | p.His741His | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 22/44 | 2244/5689 | 2223/5250 | 741/1749 | chr9 | 128986834 | ||
chr9:128990166
|
C | T | 1 | a0001c0025 | 1 | HG02300.hp1 | synonymous_variant | LOW | c.2580C>T | p.Tyr860Tyr | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 25/44 | 2601/5689 | 2580/5250 | 860/1749 | chr9 | 128990166 | ||
chr9:128993262
|
G | A | 1 | a0001c0014 | 1 | NA19078.hp2 | synonymous_variant | LOW | c.2706G>A | p.Leu902Leu | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 26/44 | 2727/5689 | 2706/5250 | 902/1749 | chr9 | 128993262 | ||
chr9:128993391
|
T | C | 1 | a0001c0027 | 1 | HG06807.hp2 | synonymous_variant | LOW | c.2835T>C | p.Ser945Ser | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 26/44 | 2856/5689 | 2835/5250 | 945/1749 | chr9 | 128993391 | ||
chr9:128993612
|
C | T | 3 | a0001c0004a0001c0028a0011c0024 | 12 | HG01099.hp1 HG02109.hp2 HG02258.hp2 others(9): Show |
synonymous_variant | LOW | c.2935C>T | p.Leu979Leu | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 27/44 | 2956/5689 | 2935/5250 | 979/1749 | chr9 | 128993612 | ||
chr9:128995418
|
C | T | 2 | a0001c0008a0001c0023 | 3 | HG02717.hp2 HG03139.hp1 NA18962.hp2 |
synonymous_variant | LOW | c.3255C>T | p.His1085His | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 30/44 | 3276/5689 | 3255/5250 | 1085/1749 | chr9 | 128995418 | ||
chr9:129001612
|
G | A | 1 | a0001c0017 | 1 | NA18968.hp2 | synonymous_variant | LOW | c.3927G>A | p.Arg1309Arg | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 35/44 | 3948/5689 | 3927/5250 | 1309/1749 | chr9 | 129001612 | ||
chr9:129005389
|
A | C | 19 | a0001c0002a0001c0003a0001c0004others(16): Show | 146 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(143): Show |
synonymous_variant | LOW | c.4596A>C | p.Ser1532Ser | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 40/44 | 4617/5689 | 4596/5250 | 1532/1749 | chr9 | 129005389 | ||
chr9:129006094
|
C | T | 1 | a0001c0021 | 1 | HG01243.hp2 | synonymous_variant | LOW | c.4914C>T | p.Ser1638Ser | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 42/44 | 4935/5689 | 4914/5250 | 1638/1749 | chr9 | 129006094 | ||
chr9:129006507
|
G | A | 1 | a0001c0020 | 1 | HG01433.hp2 | synonymous_variant | LOW | c.5079G>A | p.Thr1693Thr | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 44/44 | 5100/5689 | 5079/5250 | 1693/1749 | chr9 | 129006507 | ||
chr9:129006643
|
T | C | 1 | a0001c0009 | 2 | HG02451.hp1 HG03130.hp1 |
synonymous_variant | LOW | c.5215T>C | p.Leu1739Leu | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 44/44 | 5236/5689 | 5215/5250 | 1739/1749 | chr9 | 129006643 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:128947706
|
G | A | 1 | a0001c0001t0005 | 1 | HG02683.hp2 | 5_prime_UTR_variant | MODIFIER | c.-14G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 1/44 | 14 | chr9 | 128947706 | |||||
chr9:128947707
|
C | T | 2 | a0001c0003t0002a0001c0003t0009 | 14 | HG02027.hp1 HG03834.hp2 HG04115.hp1 others(11): Show |
5_prime_UTR_variant | MODIFIER | c.-13C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 1/44 | 13 | chr9 | 128947707 | |||||
chr9:129006761
|
C | T | 1 | a0001c0004t0008 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*83C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 44/44 | 83 | chr9 | 129006761 | |||||
chr9:129006769
|
A | G | 1 | a0001c0001t0007 | 1 | HG03017.hp1 | 3_prime_UTR_variant | MODIFIER | c.*91A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 44/44 | 91 | chr9 | 129006769 | |||||
chr9:129006798
|
C | T | 1 | a0001c0001t0006 | 1 | NA18954.hp1 | 3_prime_UTR_variant | MODIFIER | c.*120C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 44/44 | 120 | chr9 | 129006798 | |||||
chr9:129006832
|
C | T | 2 | a0001c0003t0002a0001c0003t0009 | 14 | HG02027.hp1 HG03834.hp2 HG04115.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*154C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 44/44 | 154 | chr9 | 129006832 | |||||
chr9:129006881
|
A | G | 1 | a0001c0001t0004 | 2 | HG02896.hp2 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*203A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 44/44 | 203 | chr9 | 129006881 | |||||
chr9:129006964
|
G | A | 1 | a0001c0001t0003 | 3 | HG03710.hp2 HG03834.hp1 HG03942.hp2 |
3_prime_UTR_variant | MODIFIER | c.*286G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 44/44 | 286 | chr9 | 129006964 | |||||
chr9:129006972
|
G | T | 1 | a0001c0003t0009 | 1 | HG04115.hp1 | 3_prime_UTR_variant | MODIFIER | c.*294G>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 44/44 | 294 | chr9 | 129006972 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:128947846
|
A | G | 31 | a0001c0001t0001g0272a0001c0001t0004g0287a0001c0001t0004g0288others(28): Show | 31 | HG01167.hp1 HG02027.hp1 HG02451.hp1 others(28): Show |
intron_variant | MODIFIER | c.32+95A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 1/43 | chr9 | 128947846 | ||||||
chr9:128947888
|
G | A | 6 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(3): Show | 6 | HG01891.hp2 HG02055.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.32+137G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 1/43 | chr9 | 128947888 | ||||||
chr9:128947907
|
A | G | 3 | a0001c0001t0001g0262a0001c0001t0001g0264a0001c0007t0001g0263 | 3 | HG01496.hp1 HG02559.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.32+156A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 1/43 | chr9 | 128947907 | ||||||
chr9:128948062
|
C | T | 6 | a0002c0005t0001g0290a0002c0005t0001g0292a0002c0005t0001g0293others(3): Show | 6 | HG01167.hp1 HG02451.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.32+311C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 1/43 | chr9 | 128948062 | ||||||
chr9:128948127
|
C | A | 13 | a0001c0002t0001g0265a0001c0002t0001g0266a0001c0002t0001g0269others(10): Show | 13 | HG01167.hp1 HG02451.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.32+376C>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 1/43 | chr9 | 128948127 | ||||||
chr9:128948272
|
C | G | 2 | a0001c0002t0001g0260a0001c0002t0001g0261 | 2 | HG02273.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.32+521C>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 1/43 | chr9 | 128948272 | ||||||
chr9:128948530
|
C | G | 1 | a0001c0027t0001g0289 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.33-659C>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 1/43 | chr9 | 128948530 | ||||||
chr9:128948553
|
A | G | 2 | a0001c0001t0004g0287a0001c0001t0004g0288 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.33-636A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 1/43 | chr9 | 128948553 | ||||||
chr9:128948555
|
C | T | 13 | a0001c0002t0001g0254a0001c0004t0001g0247a0001c0004t0001g0248others(10): Show | 13 | HG01099.hp1 HG02109.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.33-634C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 1/43 | chr9 | 128948555 | ||||||
chr9:128948568
|
A | G | 122 | a0001c0001t0001g0221a0001c0001t0004g0287a0001c0001t0004g0288others(119): Show | 122 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.33-621A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 1/43 | chr9 | 128948568 | ||||||
chr9:128948630
|
T | C | 14 | a0001c0003t0002g0273a0001c0003t0002g0274a0001c0003t0002g0275others(11): Show | 14 | HG02027.hp1 HG03834.hp2 HG04115.hp1 others(11): Show |
intron_variant | MODIFIER | c.33-559T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 1/43 | chr9 | 128948630 | ||||||
chr9:128948673
|
G | T | 1 | a0001c0027t0001g0289 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.33-516G>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 1/43 | chr9 | 128948673 | ||||||
chr9:128948711
|
C | CT | 74 | a0001c0001t0001g0007a0001c0001t0001g0094a0001c0001t0001g0095others(71): Show | 74 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(71): Show |
intron_variant | MODIFIER | c.33-446dupT | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 1/43 | INFO_REALIGN_3_PRIME | chr9 | 128948711 | |||||
chr9:128948711
|
C | CTT | 23 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0155others(20): Show | 24 | HG00423.hp2 HG00642.hp1 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.33-447_33-446dupTT | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 1/43 | INFO_REALIGN_3_PRIME | chr9 | 128948711 | |||||
chr9:128948711
|
CT | C | 74 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(71): Show | 74 | HG00280.hp2 HG00558.hp2 HG00735.hp1 others(71): Show |
intron_variant | MODIFIER | c.33-446delT | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 1/43 | INFO_REALIGN_3_PRIME | chr9 | 128948711 | |||||
chr9:128948711
|
CTT | C | 9 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0012others(6): Show | 9 | HG01256.hp2 HG02040.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.33-447_33-446delTT | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 1/43 | INFO_REALIGN_3_PRIME | chr9 | 128948711 | |||||
chr9:128948711
|
CTTTTTT | C | 8 | a0001c0002t0001g0254a0001c0004t0001g0247a0001c0004t0001g0248others(5): Show | 8 | HG02109.hp2 HG02886.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.33-451_33-446delTT others(4): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 1/43 | INFO_REALIGN_3_PRIME | chr9 | 128948711 | |||||
chr9:128948711
|
CTTTTTTT others(2): Show |
C | 13 | a0001c0002t0001g0265a0001c0002t0001g0266a0001c0002t0001g0269others(10): Show | 13 | HG01167.hp1 HG02451.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.33-454_33-446delTT others(7): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 1/43 | INFO_REALIGN_3_PRIME | chr9 | 128948711 | |||||
chr9:128948711
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0027t0001g0289 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.33-455_33-446delTT others(8): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 1/43 | INFO_REALIGN_3_PRIME | chr9 | 128948711 | |||||
chr9:128948711
|
CTTTTTTT others(8): Show |
C | 2 | a0001c0001t0004g0287a0001c0001t0004g0288 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.33-460_33-446delTT others(13): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 1/43 | INFO_REALIGN_3_PRIME | chr9 | 128948711 | |||||
chr9:128948800
|
A | T | 1 | a0001c0001t0001g0035 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.33-389A>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 1/43 | chr9 | 128948800 | ||||||
chr9:128949039
|
A | G | 1 | a0001c0001t0001g0093 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.33-150A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 1/43 | chr9 | 128949039 | ||||||
chr9:128949098
|
C | T | 1 | a0005c0011t0001g0152 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.33-91C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 1/43 | chr9 | 128949098 | ||||||
chr9:128949257
|
T | G | 14 | a0001c0003t0002g0273a0001c0003t0002g0274a0001c0003t0002g0275others(11): Show | 14 | HG02027.hp1 HG03834.hp2 HG04115.hp1 others(11): Show |
intron_variant | MODIFIER | c.87+14T>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 2/43 | chr9 | 128949257 | ||||||
chr9:128949300
|
C | CA | 5 | a0001c0001t0001g0036a0001c0001t0001g0094a0001c0001t0001g0153others(2): Show | 5 | HG02293.hp1 HG03225.hp1 NA18985.hp1 others(2): Show |
intron_variant | MODIFIER | c.87+65dupA | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 2/43 | INFO_REALIGN_3_PRIME | chr9 | 128949300 | |||||
chr9:128949519
|
A | G | 1 | a0001c0002t0001g0240 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.87+276A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 2/43 | chr9 | 128949519 | ||||||
chr9:128949900
|
A | G | 14 | a0001c0003t0002g0273a0001c0003t0002g0274a0001c0003t0002g0275others(11): Show | 14 | HG02027.hp1 HG03834.hp2 HG04115.hp1 others(11): Show |
intron_variant | MODIFIER | c.87+657A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 2/43 | chr9 | 128949900 | ||||||
chr9:128949919
|
C | CT | 14 | a0001c0001t0001g0036a0001c0001t0001g0090a0001c0001t0001g0091others(11): Show | 14 | HG01175.hp2 HG01346.hp1 HG01952.hp2 others(11): Show |
intron_variant | MODIFIER | c.87+701dupT | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 2/43 | INFO_REALIGN_3_PRIME | chr9 | 128949919 | |||||
chr9:128949919
|
CT | C | 140 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(137): Show | 140 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(137): Show |
intron_variant | MODIFIER | c.87+701delT | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 2/43 | INFO_REALIGN_3_PRIME | chr9 | 128949919 | |||||
chr9:128950085
|
G | A | 1 | a0001c0001t0001g0057 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.87+842G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 2/43 | chr9 | 128950085 | ||||||
chr9:128950684
|
T | A | 2 | a0001c0001t0001g0037a0001c0001t0001g0095 | 2 | HG00673.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.87+1441T>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 2/43 | chr9 | 128950684 | ||||||
chr9:128950689
|
T | A | 13 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0015others(10): Show | 13 | HG00558.hp2 HG00673.hp1 HG02080.hp1 others(10): Show |
intron_variant | MODIFIER | c.87+1446T>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 2/43 | chr9 | 128950689 | ||||||
chr9:128950812
|
C | T | 1 | a0001c0002t0001g0218 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.87+1569C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 2/43 | chr9 | 128950812 | ||||||
chr9:128950822
|
G | A | 1 | a0001c0002t0001g0271 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.87+1579G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 2/43 | chr9 | 128950822 | ||||||
chr9:128950988
|
G | C | 2 | a0001c0001t0004g0287a0001c0001t0004g0288 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.87+1745G>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 2/43 | chr9 | 128950988 | ||||||
chr9:128951028
|
T | C | 2 | a0001c0001t0004g0287a0001c0001t0004g0288 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.88-1745T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 2/43 | chr9 | 128951028 | ||||||
chr9:128951200
|
C | T | 6 | a0001c0001t0001g0147a0002c0005t0001g0292a0002c0005t0001g0293others(3): Show | 6 | HG01167.hp1 HG02451.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.88-1573C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 2/43 | chr9 | 128951200 | ||||||
chr9:128951306
|
C | CA | 6 | a0001c0001t0001g0059a0001c0001t0001g0262a0001c0001t0001g0264others(3): Show | 6 | HG01496.hp1 HG02040.hp1 HG02080.hp2 others(3): Show |
intron_variant | MODIFIER | c.88-1447dupA | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 2/43 | INFO_REALIGN_3_PRIME | chr9 | 128951306 | |||||
chr9:128951306
|
CA | C | 109 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0056others(106): Show | 109 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.88-1447delA | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 2/43 | INFO_REALIGN_3_PRIME | chr9 | 128951306 | |||||
chr9:128951306
|
CAA | C | 16 | a0001c0003t0002g0273a0001c0003t0002g0274a0001c0003t0002g0275others(13): Show | 16 | HG02027.hp1 HG03195.hp2 HG03834.hp2 others(13): Show |
intron_variant | MODIFIER | c.88-1448_88-1447del others(2): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 2/43 | INFO_REALIGN_3_PRIME | chr9 | 128951306 | |||||
chr9:128951439
|
A | G | 1 | a0001c0027t0001g0289 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.88-1334A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 2/43 | chr9 | 128951439 | ||||||
chr9:128951477
|
T | C | 3 | a0001c0004t0001g0255a0001c0004t0001g0257a0001c0004t0008g0256 | 3 | HG01099.hp1 HG02258.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.88-1296T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 2/43 | chr9 | 128951477 | ||||||
chr9:128951517
|
T | A | 2 | a0001c0001t0001g0060a0008c0018t0001g0089 | 2 | HG01496.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.88-1256T>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 2/43 | chr9 | 128951517 | ||||||
chr9:128951597
|
A | G | 3 | a0001c0001t0001g0060a0001c0001t0001g0087a0008c0018t0001g0089 | 3 | HG01069.hp2 HG01496.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.88-1176A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 2/43 | chr9 | 128951597 | ||||||
chr9:128951670
|
T | C | 1 | a0001c0002t0001g0021 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.88-1103T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 2/43 | chr9 | 128951670 | ||||||
chr9:128951683
|
A | G | 2 | a0001c0001t0004g0287a0001c0001t0004g0288 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.88-1090A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 2/43 | chr9 | 128951683 | ||||||
chr9:128951789
|
T | G | 1 | a0001c0002t0001g0254 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.88-984T>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 2/43 | chr9 | 128951789 | ||||||
chr9:128951791
|
AT | A | 35 | a0001c0001t0001g0029a0001c0001t0001g0104a0001c0001t0001g0105others(32): Show | 35 | HG01167.hp1 HG02027.hp1 HG02451.hp1 others(32): Show |
intron_variant | MODIFIER | c.88-964delT | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 2/43 | INFO_REALIGN_3_PRIME | chr9 | 128951791 | |||||
chr9:128951793
|
T | C | 2 | a0001c0001t0004g0287a0001c0001t0004g0288 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.88-980T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 2/43 | chr9 | 128951793 | ||||||
chr9:128951814
|
C | T | 1 | a0001c0001t0001g0146 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.88-959C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 2/43 | chr9 | 128951814 | ||||||
chr9:128951841
|
A | G | 294 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(291): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.88-932A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 2/43 | chr9 | 128951841 | ||||||
chr9:128951917
|
C | T | 1 | a0001c0001t0001g0102 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.88-856C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 2/43 | chr9 | 128951917 | ||||||
chr9:128952044
|
C | T | 1 | a0001c0001t0001g0086 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.88-729C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 2/43 | chr9 | 128952044 | ||||||
chr9:128952073
|
C | G | 16 | a0001c0001t0004g0287a0001c0001t0004g0288a0001c0003t0002g0273others(13): Show | 16 | HG02027.hp1 HG02896.hp2 HG02897.hp2 others(13): Show |
intron_variant | MODIFIER | c.88-700C>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 2/43 | chr9 | 128952073 | ||||||
chr9:128952084
|
T | C | 2 | a0001c0001t0001g0062a0001c0001t0001g0086 | 2 | HG02698.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.88-689T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 2/43 | chr9 | 128952084 | ||||||
chr9:128952085
|
G | T | 2 | a0001c0001t0004g0287a0001c0001t0004g0288 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.88-688G>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 2/43 | chr9 | 128952085 | ||||||
chr9:128952184
|
T | G | 2 | a0001c0001t0004g0287a0001c0001t0004g0288 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.88-589T>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 2/43 | chr9 | 128952184 | ||||||
chr9:128952242
|
C | CA | 21 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0015others(18): Show | 21 | HG00558.hp2 HG00673.hp1 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.88-523dupA | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 2/43 | INFO_REALIGN_3_PRIME | chr9 | 128952242 | |||||
chr9:128952393
|
C | T | 13 | a0001c0002t0001g0265a0001c0002t0001g0266a0001c0002t0001g0269others(10): Show | 13 | HG01167.hp1 HG02451.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.88-380C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 2/43 | chr9 | 128952393 | ||||||
chr9:128952398
|
CA | C | 11 | a0001c0001t0001g0013a0001c0001t0001g0140a0001c0001t0001g0272others(8): Show | 11 | HG01167.hp1 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.88-357delA | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 2/43 | INFO_REALIGN_3_PRIME | chr9 | 128952398 | |||||
chr9:128952461
|
G | A | 12 | a0001c0004t0001g0247a0001c0004t0001g0248a0001c0004t0001g0249others(9): Show | 12 | HG01099.hp1 HG02109.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.88-312G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 2/43 | chr9 | 128952461 | ||||||
chr9:128952469
|
T | C | 3 | a0001c0002t0001g0241a0001c0002t0001g0244a0001c0002t0001g0246 | 3 | HG01069.hp1 HG02145.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.88-304T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 2/43 | chr9 | 128952469 | ||||||
chr9:128952496
|
G | T | 1 | a0001c0004t0001g0257 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.88-277G>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 2/43 | chr9 | 128952496 | ||||||
chr9:128952722
|
C | CA | 7 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0004g0287others(4): Show | 7 | HG02015.hp1 HG02055.hp1 HG02523.hp2 others(4): Show |
intron_variant | MODIFIER | c.88-36dupA | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 2/43 | INFO_REALIGN_3_PRIME | chr9 | 128952722 | |||||
chr9:128953108
|
A | G | 1 | a0001c0002t0001g0020 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.161+262A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 3/43 | chr9 | 128953108 | ||||||
chr9:128953393
|
G | A | 3 | a0001c0001t0001g0262a0001c0001t0001g0264a0001c0007t0001g0263 | 3 | HG01496.hp1 HG02559.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.161+547G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 3/43 | chr9 | 128953393 | ||||||
chr9:128953395
|
G | T | 3 | a0001c0001t0001g0262a0001c0001t0001g0264a0001c0007t0001g0263 | 3 | HG01496.hp1 HG02559.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.161+549G>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 3/43 | chr9 | 128953395 | ||||||
chr9:128953564
|
C | A | 14 | a0001c0003t0002g0273a0001c0003t0002g0274a0001c0003t0002g0275others(11): Show | 14 | HG02027.hp1 HG03834.hp2 HG04115.hp1 others(11): Show |
intron_variant | MODIFIER | c.161+718C>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 3/43 | chr9 | 128953564 | ||||||
chr9:128953894
|
A | G | 13 | a0001c0002t0001g0265a0001c0002t0001g0266a0001c0002t0001g0269others(10): Show | 13 | HG01167.hp1 HG02451.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.161+1048A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 3/43 | chr9 | 128953894 | ||||||
chr9:128953922
|
C | T | 1 | a0001c0002t0001g0210 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.161+1076C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 3/43 | chr9 | 128953922 | ||||||
chr9:128953986
|
C | T | 77 | a0001c0001t0001g0221a0001c0002t0001g0170a0001c0002t0001g0171others(74): Show | 77 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.161+1140C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 3/43 | chr9 | 128953986 | ||||||
chr9:128954249
|
TTGTGGCC others(163): Show |
T | 3 | a0001c0002t0001g0096a0001c0002t0001g0265a0001c0002t0001g0266 | 3 | HG02895.hp2 HG03579.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.161+1501_161+1670d others(2): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 3/43 | INFO_REALIGN_3_PRIME | chr9 | 128954249 | |||||
chr9:128954362
|
C | T | 1 | a0001c0001t0001g0139 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.161+1516C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 3/43 | chr9 | 128954362 | ||||||
chr9:128954383
|
C | CT | 11 | a0001c0001t0001g0014a0001c0001t0001g0058a0001c0001t0001g0138others(8): Show | 11 | HG01261.hp1 HG02280.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.161+1556dupT | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 3/43 | INFO_REALIGN_3_PRIME | chr9 | 128954383 | |||||
chr9:128954383
|
CT | C | 7 | a0001c0001t0001g0109a0001c0002t0001g0172a0001c0002t0001g0213others(4): Show | 7 | HG01069.hp1 HG02145.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.161+1556delT | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 3/43 | INFO_REALIGN_3_PRIME | chr9 | 128954383 | |||||
chr9:128954406
|
A | G | 2 | a0001c0001t0004g0287a0001c0001t0004g0288 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.161+1560A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 3/43 | chr9 | 128954406 | ||||||
chr9:128954474
|
T | A | 1 | a0001c0001t0001g0041 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.161+1628T>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 3/43 | chr9 | 128954474 | ||||||
chr9:128954517
|
A | G | 5 | a0002c0005t0001g0292a0002c0005t0001g0293a0002c0005t0001g0294others(2): Show | 5 | HG01167.hp1 HG02451.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.161+1671A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 3/43 | chr9 | 128954517 | ||||||
chr9:128954528
|
G | T | 1 | a0001c0002t0001g0240 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.161+1682G>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 3/43 | chr9 | 128954528 | ||||||
chr9:128954576
|
G | C | 1 | a0001c0001t0001g0110 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.161+1730G>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 3/43 | chr9 | 128954576 | ||||||
chr9:128954650
|
C | T | 1 | a0001c0002t0001g0209 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.162-1700C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 3/43 | chr9 | 128954650 | ||||||
chr9:128954662
|
G | A | 13 | a0001c0002t0001g0265a0001c0002t0001g0266a0001c0002t0001g0269others(10): Show | 13 | HG01167.hp1 HG02451.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.162-1688G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 3/43 | chr9 | 128954662 | ||||||
chr9:128954902
|
C | T | 3 | a0001c0001t0001g0137a0001c0001t0001g0146a0001c0001t0001g0163 | 3 | HG02145.hp2 HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.162-1448C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 3/43 | chr9 | 128954902 | ||||||
chr9:128954905
|
G | A | 2 | a0001c0009t0001g0267a0001c0009t0001g0268 | 2 | HG02451.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.162-1445G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 3/43 | chr9 | 128954905 | ||||||
chr9:128954910
|
A | G | 122 | a0001c0001t0001g0221a0001c0001t0004g0287a0001c0001t0004g0288others(119): Show | 122 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.162-1440A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 3/43 | chr9 | 128954910 | ||||||
chr9:128954913
|
G | GTGCGATT others(9): Show |
1 | a0001c0002t0001g0027 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.162-1433_162-1418d others(18): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 3/43 | INFO_REALIGN_3_PRIME | chr9 | 128954913 | |||||
chr9:128954938
|
T | C | 122 | a0001c0001t0001g0221a0001c0001t0004g0287a0001c0001t0004g0288others(119): Show | 122 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.162-1412T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 3/43 | chr9 | 128954938 | ||||||
chr9:128954950
|
T | C | 14 | a0001c0003t0002g0273a0001c0003t0002g0274a0001c0003t0002g0275others(11): Show | 14 | HG02027.hp1 HG03834.hp2 HG04115.hp1 others(11): Show |
intron_variant | MODIFIER | c.162-1400T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 3/43 | chr9 | 128954950 | ||||||
chr9:128955097
|
C | T | 14 | a0001c0003t0002g0273a0001c0003t0002g0274a0001c0003t0002g0275others(11): Show | 14 | HG02027.hp1 HG03834.hp2 HG04115.hp1 others(11): Show |
intron_variant | MODIFIER | c.162-1253C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 3/43 | chr9 | 128955097 | ||||||
chr9:128955125
|
A | G | 1 | a0001c0002t0001g0266 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.162-1225A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 3/43 | chr9 | 128955125 | ||||||
chr9:128955158
|
C | G | 1 | a0001c0027t0001g0289 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.162-1192C>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 3/43 | chr9 | 128955158 | ||||||
chr9:128955251
|
A | G | 13 | a0001c0002t0001g0265a0001c0002t0001g0266a0001c0002t0001g0269others(10): Show | 13 | HG01167.hp1 HG02451.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.162-1099A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 3/43 | chr9 | 128955251 | ||||||
chr9:128955437
|
G | A | 2 | a0001c0009t0001g0267a0001c0009t0001g0268 | 2 | HG02451.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.162-913G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 3/43 | chr9 | 128955437 | ||||||
chr9:128955614
|
G | A | 14 | a0001c0003t0002g0273a0001c0003t0002g0274a0001c0003t0002g0275others(11): Show | 14 | HG02027.hp1 HG03834.hp2 HG04115.hp1 others(11): Show |
intron_variant | MODIFIER | c.162-736G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 3/43 | chr9 | 128955614 | ||||||
chr9:128955752
|
C | T | 1 | a0001c0001t0001g0091 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.162-598C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 3/43 | chr9 | 128955752 | ||||||
chr9:128955987
|
C | CCTTT | 249 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(246): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.162-361_162-360ins others(4): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 3/43 | INFO_REALIGN_3_PRIME | chr9 | 128955987 | |||||
chr9:128956017
|
G | A | 1 | a0001c0002t0001g0220 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.162-333G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 3/43 | chr9 | 128956017 | ||||||
chr9:128956075
|
A | G | 1 | a0001c0001t0001g0036 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.162-275A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 3/43 | chr9 | 128956075 | ||||||
chr9:128956121
|
T | G | 1 | a0001c0002t0001g0220 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.162-229T>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 3/43 | chr9 | 128956121 | ||||||
chr9:128956182
|
G | GGT | 69 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(66): Show | 69 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(66): Show |
intron_variant | MODIFIER | c.162-140_162-139dup others(2): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 3/43 | INFO_REALIGN_3_PRIME | chr9 | 128956182 | |||||
chr9:128956182
|
G | GGTGT | 7 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(4): Show | 7 | HG01891.hp2 HG02040.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.162-142_162-139dup others(4): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 3/43 | INFO_REALIGN_3_PRIME | chr9 | 128956182 | |||||
chr9:128956182
|
GGT | G | 20 | a0001c0001t0001g0029a0001c0001t0001g0035a0001c0001t0001g0054others(17): Show | 20 | HG01099.hp1 HG01109.hp2 HG01261.hp2 others(17): Show |
intron_variant | MODIFIER | c.162-140_162-139del others(2): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 3/43 | INFO_REALIGN_3_PRIME | chr9 | 128956182 | |||||
chr9:128956182
|
GGTGT | G | 3 | a0001c0001t0001g0069a0001c0002t0001g0240a0002c0005t0001g0295 | 3 | HG01109.hp1 HG02615.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.162-142_162-139del others(4): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 3/43 | INFO_REALIGN_3_PRIME | chr9 | 128956182 | |||||
chr9:128956182
|
GGTGTGT | G | 12 | a0001c0002t0001g0265a0001c0002t0001g0266a0001c0002t0001g0269others(9): Show | 12 | HG01167.hp1 HG02451.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.162-144_162-139del others(6): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 3/43 | INFO_REALIGN_3_PRIME | chr9 | 128956182 | |||||
chr9:128956186
|
T | G | 1 | a0001c0028t0001g0259 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.162-164T>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 3/43 | chr9 | 128956186 | ||||||
chr9:128956208
|
T | C | 3 | a0001c0001t0001g0111a0001c0001t0004g0287a0001c0001t0004g0288 | 3 | HG00280.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.162-142T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 3/43 | chr9 | 128956208 | ||||||
chr9:128956210
|
T | TGC | 67 | a0001c0001t0001g0221a0001c0002t0001g0171a0001c0002t0001g0172others(64): Show | 67 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(64): Show |
intron_variant | MODIFIER | c.162-138_162-137dup others(2): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 3/43 | INFO_REALIGN_3_PRIME | chr9 | 128956210 | |||||
chr9:128956210
|
T | TGTGC | 9 | a0001c0002t0001g0170a0001c0002t0001g0204a0001c0002t0001g0205others(6): Show | 9 | HG00738.hp2 HG01243.hp1 HG01993.hp2 others(6): Show |
intron_variant | MODIFIER | c.162-139_162-138ins others(4): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 3/43 | INFO_REALIGN_3_PRIME | chr9 | 128956210 | |||||
chr9:128956214
|
T | G | 1 | a0001c0002t0001g0027 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.162-136T>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 3/43 | chr9 | 128956214 | ||||||
chr9:128956216
|
T | C | 1 | a0001c0002t0001g0240 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.162-134T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 3/43 | chr9 | 128956216 | ||||||
chr9:128956449
|
G | A | 2 | a0001c0001t0001g0062a0001c0001t0001g0086 | 2 | HG02698.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.246+15G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 4/43 | chr9 | 128956449 | ||||||
chr9:128956500
|
A | C | 1 | a0001c0002t0001g0176 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.246+66A>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 4/43 | chr9 | 128956500 | ||||||
chr9:128956665
|
C | T | 1 | a0001c0001t0001g0097 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.246+231C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 4/43 | chr9 | 128956665 | ||||||
chr9:128956819
|
T | C | 2 | a0001c0001t0004g0287a0001c0001t0004g0288 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.247-133T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 4/43 | chr9 | 128956819 | ||||||
chr9:128957398
|
T | G | 1 | a0001c0001t0001g0030 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.327+366T>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 5/43 | chr9 | 128957398 | ||||||
chr9:128957527
|
T | C | 2 | a0001c0001t0004g0287a0001c0001t0004g0288 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.328-483T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 5/43 | chr9 | 128957527 | ||||||
chr9:128957706
|
C | T | 1 | a0006c0030t0001g0150 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.328-304C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 5/43 | chr9 | 128957706 | ||||||
chr9:128958115
|
C | T | 2 | a0001c0001t0004g0287a0001c0001t0004g0288 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.372+61C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 6/43 | chr9 | 128958115 | ||||||
chr9:128958196
|
A | G | 17 | a0001c0001t0004g0287a0001c0001t0004g0288a0001c0003t0002g0273others(14): Show | 17 | HG02027.hp1 HG02896.hp2 HG02897.hp2 others(14): Show |
intron_variant | MODIFIER | c.372+142A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 6/43 | chr9 | 128958196 | ||||||
chr9:128958406
|
T | G | 2 | a0001c0001t0004g0287a0001c0001t0004g0288 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.372+352T>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 6/43 | chr9 | 128958406 | ||||||
chr9:128958758
|
A | G | 3 | a0001c0001t0001g0137a0001c0001t0001g0146a0001c0001t0001g0163 | 3 | HG02145.hp2 HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.373-44A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 6/43 | chr9 | 128958758 | ||||||
chr9:128959294
|
G | A | 2 | a0001c0001t0001g0029a0001c0001t0001g0105 | 2 | NA18969.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.585+160G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128959294 | ||||||
chr9:128959384
|
C | T | 18 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0015others(15): Show | 18 | HG00558.hp2 HG00673.hp1 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.585+250C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128959384 | ||||||
chr9:128959427
|
C | T | 2 | a0001c0001t0004g0287a0001c0001t0004g0288 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.585+293C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128959427 | ||||||
chr9:128959439
|
G | A | 1 | a0001c0002t0001g0219 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.585+305G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128959439 | ||||||
chr9:128959527
|
C | CT | 16 | a0001c0001t0001g0014a0001c0001t0001g0052a0001c0001t0001g0053others(13): Show | 16 | HG01099.hp1 HG01109.hp1 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.585+413dupT | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128959527 | |||||
chr9:128959527
|
C | CTTTT | 13 | a0001c0003t0002g0273a0001c0003t0002g0274a0001c0003t0002g0276others(10): Show | 13 | HG02027.hp1 HG03834.hp2 HG04115.hp1 others(10): Show |
intron_variant | MODIFIER | c.585+410_585+413dup others(4): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128959527 | |||||
chr9:128959527
|
C | CTTTTTTT others(7): Show |
1 | a0001c0027t0001g0289 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.585+400_585+413dup others(14): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128959527 | |||||
chr9:128959527
|
C | CTTTTTTT others(8): Show |
1 | a0001c0001t0004g0287 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.585+399_585+413dup others(15): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128959527 | |||||
chr9:128959527
|
C | CTTTTTTT others(9): Show |
1 | a0001c0001t0004g0288 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.585+398_585+413dup others(16): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128959527 | |||||
chr9:128959625
|
C | T | 1 | a0001c0001t0001g0066 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.585+491C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128959625 | ||||||
chr9:128959748
|
C | T | 1 | a0001c0001t0001g0066 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.585+614C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128959748 | ||||||
chr9:128959759
|
C | T | 92 | a0001c0001t0001g0221a0001c0002t0001g0170a0001c0002t0001g0171others(89): Show | 92 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.585+625C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128959759 | ||||||
chr9:128959803
|
G | A | 1 | a0001c0001t0001g0090 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.585+669G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128959803 | ||||||
chr9:128959864
|
A | G | 3 | a0001c0001t0001g0051a0001c0001t0001g0101a0001c0001t0001g0134 | 3 | HG02647.hp1 HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.585+730A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128959864 | ||||||
chr9:128960059
|
C | CT | 27 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0010others(24): Show | 27 | HG00438.hp1 HG00558.hp1 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.585+947dupT | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128960059 | |||||
chr9:128960059
|
C | CTT | 13 | a0001c0001t0001g0100a0001c0002t0001g0040a0001c0002t0001g0096others(10): Show | 13 | HG01167.hp1 HG02451.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.585+946_585+947dup others(2): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128960059 | |||||
chr9:128960059
|
CT | C | 6 | a0001c0001t0001g0121a0001c0002t0001g0172a0001c0002t0001g0176others(3): Show | 6 | HG01167.hp2 HG02258.hp1 NA18941.hp1 others(3): Show |
intron_variant | MODIFIER | c.585+947delT | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128960059 | |||||
chr9:128960230
|
AT | A | 15 | a0001c0003t0002g0273a0001c0003t0002g0274a0001c0003t0002g0275others(12): Show | 15 | HG02027.hp1 HG03834.hp2 HG04115.hp1 others(12): Show |
intron_variant | MODIFIER | c.585+1102delT | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128960230 | |||||
chr9:128960259
|
G | GT | 12 | a0001c0004t0001g0247a0001c0004t0001g0248a0001c0004t0001g0249others(9): Show | 12 | HG01099.hp1 HG02109.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.585+1134dupT | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128960259 | |||||
chr9:128960270
|
G | A | 13 | a0001c0002t0001g0265a0001c0002t0001g0266a0001c0002t0001g0269others(10): Show | 13 | HG01167.hp1 HG02451.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.585+1136G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128960270 | ||||||
chr9:128960310
|
A | G | 8 | a0001c0001t0001g0030a0001c0001t0001g0076a0001c0001t0001g0077others(5): Show | 8 | HG00597.hp2 HG01099.hp2 HG01975.hp1 others(5): Show |
intron_variant | MODIFIER | c.585+1176A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128960310 | ||||||
chr9:128960363
|
G | A | 77 | a0001c0001t0001g0221a0001c0002t0001g0170a0001c0002t0001g0171others(74): Show | 77 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.585+1229G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128960363 | ||||||
chr9:128960376
|
A | T | 2 | a0001c0004t0001g0255a0001c0004t0008g0256 | 2 | HG02258.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.585+1242A>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128960376 | ||||||
chr9:128960453
|
A | C | 1 | a0001c0027t0001g0289 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.585+1319A>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128960453 | ||||||
chr9:128960616
|
G | A | 2 | a0001c0001t0004g0287a0001c0001t0004g0288 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.585+1482G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128960616 | ||||||
chr9:128960646
|
G | C | 3 | a0001c0001t0001g0149a0001c0001t0001g0166a0012c0015t0001g0165 | 3 | HG01175.hp2 HG01346.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.585+1512G>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128960646 | ||||||
chr9:128960882
|
C | G | 1 | a0001c0027t0001g0289 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.585+1748C>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128960882 | ||||||
chr9:128960888
|
C | T | 2 | a0001c0001t0001g0118a0001c0001t0001g0151 | 2 | HG01515.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.585+1754C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128960888 | ||||||
chr9:128960912
|
T | C | 122 | a0001c0001t0001g0221a0001c0001t0004g0287a0001c0001t0004g0288others(119): Show | 122 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.585+1778T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128960912 | ||||||
chr9:128960913
|
C | T | 14 | a0001c0003t0002g0273a0001c0003t0002g0274a0001c0003t0002g0275others(11): Show | 14 | HG02027.hp1 HG03834.hp2 HG04115.hp1 others(11): Show |
intron_variant | MODIFIER | c.585+1779C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128960913 | ||||||
chr9:128960914
|
G | A | 2 | a0001c0001t0004g0287a0001c0001t0004g0288 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.585+1780G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128960914 | ||||||
chr9:128961054
|
C | T | 3 | a0001c0001t0001g0149a0001c0001t0001g0166a0012c0015t0001g0165 | 3 | HG01175.hp2 HG01346.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.585+1920C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128961054 | ||||||
chr9:128961081
|
G | T | 1 | a0001c0001t0001g0053 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.585+1947G>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128961081 | ||||||
chr9:128961085
|
C | CA | 50 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0036others(47): Show | 50 | HG00140.hp2 HG00423.hp1 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.585+1969dupA | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128961085 | |||||
chr9:128961109
|
A | G | 1 | a0001c0027t0001g0289 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.585+1975A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128961109 | ||||||
chr9:128961169
|
CA | C | 17 | a0001c0001t0004g0287a0001c0001t0004g0288a0001c0003t0002g0273others(14): Show | 17 | HG02027.hp1 HG02896.hp2 HG02897.hp2 others(14): Show |
intron_variant | MODIFIER | c.585+2046delA | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128961169 | |||||
chr9:128961273
|
T | G | 2 | a0001c0001t0001g0056a0001c0001t0001g0103 | 2 | NA18955.hp1 NA18987.hp2 |
intron_variant | MODIFIER | c.585+2139T>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128961273 | ||||||
chr9:128961389
|
G | A | 1 | a0001c0008t0001g0135 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.585+2255G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128961389 | ||||||
chr9:128961512
|
AAAAT | A | 14 | a0001c0003t0002g0273a0001c0003t0002g0274a0001c0003t0002g0275others(11): Show | 14 | HG02027.hp1 HG03834.hp2 HG04115.hp1 others(11): Show |
intron_variant | MODIFIER | c.585+2401_585+2404d others(6): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128961512 | |||||
chr9:128961572
|
C | T | 1 | a0001c0001t0001g0130 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.585+2438C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128961572 | ||||||
chr9:128961582
|
C | CTAGATAG others(5): Show |
2 | a0001c0001t0004g0287a0001c0001t0004g0288 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.585+2450_585+2451i others(14): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128961582 | |||||
chr9:128961585
|
T | G | 5 | a0001c0001t0004g0287a0001c0001t0004g0288a0001c0002t0001g0269others(2): Show | 5 | HG02647.hp2 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.585+2451T>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128961585 | ||||||
chr9:128961586
|
C | A | 5 | a0001c0001t0004g0287a0001c0001t0004g0288a0001c0002t0001g0269others(2): Show | 5 | HG02647.hp2 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.585+2452C>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128961586 | ||||||
chr9:128961586
|
C | CTAGATAG others(1): Show |
3 | a0001c0001t0001g0003a0001c0002t0001g0009a0002c0005t0001g0292 | 3 | HG02559.hp2 HG02717.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.585+2454_585+2455i others(10): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128961586 | |||||
chr9:128961586
|
C | CTAGATAG others(5): Show |
2 | a0001c0027t0001g0289a0002c0005t0001g0290 | 2 | HG03225.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.585+2454_585+2455i others(14): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128961586 | |||||
chr9:128961589
|
T | G | 18 | a0001c0001t0001g0003a0001c0001t0001g0064a0001c0001t0001g0113others(15): Show | 18 | HG00639.hp2 HG01109.hp1 HG01361.hp1 others(15): Show |
intron_variant | MODIFIER | c.585+2455T>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128961589 | ||||||
chr9:128961590
|
C | A | 18 | a0001c0001t0001g0003a0001c0001t0001g0064a0001c0001t0001g0113others(15): Show | 18 | HG00639.hp2 HG01109.hp1 HG01361.hp1 others(15): Show |
intron_variant | MODIFIER | c.585+2456C>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128961590 | ||||||
chr9:128961590
|
C | CTAGA | 24 | a0001c0001t0001g0031a0001c0001t0001g0058a0001c0001t0001g0072others(21): Show | 24 | HG01123.hp2 HG01261.hp2 HG01928.hp2 others(21): Show |
intron_variant | MODIFIER | c.585+2486_585+2489d others(6): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128961590 | |||||
chr9:128961590
|
C | CTAGATAG others(1): Show |
43 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0014others(40): Show | 43 | HG00738.hp1 HG01109.hp2 HG01167.hp1 others(40): Show |
intron_variant | MODIFIER | c.585+2482_585+2489d others(10): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128961590 | |||||
chr9:128961590
|
C | CTAGATAG others(5): Show |
28 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(25): Show | 29 | HG00558.hp2 HG00673.hp1 HG01433.hp1 others(26): Show |
intron_variant | MODIFIER | c.585+2478_585+2489d others(14): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128961590 | |||||
chr9:128961590
|
C | CTAGATAG others(9): Show |
6 | a0001c0001t0001g0005a0001c0001t0001g0043a0001c0001t0001g0130others(3): Show | 6 | HG00280.hp2 HG00639.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.585+2474_585+2489d others(18): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128961590 | |||||
chr9:128961590
|
C | CTATCTAG others(5): Show |
9 | a0001c0004t0001g0248a0001c0004t0001g0249a0001c0004t0001g0250others(6): Show | 9 | HG01099.hp1 HG02109.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.585+2458_585+2459i others(14): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128961590 | |||||
chr9:128961590
|
C | CTATCTAG others(9): Show |
4 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0004t0001g0255others(1): Show | 4 | HG02258.hp2 HG02280.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.585+2458_585+2459i others(18): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128961590 | |||||
chr9:128961590
|
C | CTATCTAG others(13): Show |
1 | a0001c0004t0001g0247 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.585+2458_585+2459i others(22): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128961590 | |||||
chr9:128961590
|
CTAGATAG others(1): Show |
C | 4 | a0001c0001t0001g0138a0001c0001t0001g0262a0001c0001t0001g0264others(1): Show | 4 | HG01496.hp1 HG02280.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.585+2482_585+2489d others(10): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128961590 | |||||
chr9:128961622
|
A | AT | 79 | a0001c0001t0001g0166a0001c0001t0001g0221a0001c0002t0001g0170others(76): Show | 79 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.585+2504dupT | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128961622 | |||||
chr9:128961622
|
A | ATAGAT | 10 | a0001c0002t0001g0172a0001c0002t0001g0174a0001c0002t0001g0181others(7): Show | 10 | HG01109.hp1 HG02165.hp2 HG02523.hp2 others(7): Show |
intron_variant | MODIFIER | c.585+2489_585+2490i others(7): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128961622 | |||||
chr9:128961623
|
T | TAGATAGA | 3 | a0001c0001t0006g0022a0001c0002t0001g0023a0001c0002t0001g0099 | 3 | HG01074.hp1 NA18954.hp1 NA18954.hp2 |
intron_variant | MODIFIER | c.585+2489_585+2490i others(9): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128961623 | ||||||
chr9:128961661
|
G | C | 14 | a0001c0003t0002g0273a0001c0003t0002g0274a0001c0003t0002g0275others(11): Show | 14 | HG02027.hp1 HG03834.hp2 HG04115.hp1 others(11): Show |
intron_variant | MODIFIER | c.585+2527G>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128961661 | ||||||
chr9:128961676
|
C | T | 1 | a0001c0027t0001g0289 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.585+2542C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128961676 | ||||||
chr9:128961755
|
G | A | 2 | a0001c0001t0001g0062a0001c0001t0001g0086 | 2 | HG02698.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.585+2621G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128961755 | ||||||
chr9:128961940
|
C | CT | 15 | a0001c0001t0001g0063a0001c0003t0002g0273a0001c0003t0002g0274others(12): Show | 15 | HG02027.hp1 HG03834.hp2 HG04115.hp1 others(12): Show |
intron_variant | MODIFIER | c.585+2820dupT | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128961940 | |||||
chr9:128961958
|
C | T | 2 | a0001c0002t0001g0228a0001c0002t0001g0233 | 2 | HG02622.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.585+2824C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128961958 | ||||||
chr9:128961959
|
G | A | 1 | a0001c0001t0001g0044 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.585+2825G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128961959 | ||||||
chr9:128961993
|
A | G | 2 | a0001c0002t0001g0265a0001c0002t0001g0266 | 2 | HG02895.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.585+2859A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128961993 | ||||||
chr9:128962001
|
A | G | 2 | a0001c0001t0004g0287a0001c0001t0004g0288 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.585+2867A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128962001 | ||||||
chr9:128962163
|
G | C | 3 | a0001c0001t0001g0064a0001c0001t0001g0113a0001c0001t0001g0114 | 3 | HG01515.hp1 HG01517.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.585+3029G>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128962163 | ||||||
chr9:128962248
|
C | CT | 24 | a0001c0001t0001g0014a0001c0001t0001g0131a0001c0001t0001g0137others(21): Show | 24 | HG00738.hp1 HG01069.hp1 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.585+3132dupT | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128962248 | |||||
chr9:128962248
|
C | CTT | 14 | a0001c0003t0002g0273a0001c0003t0002g0274a0001c0003t0002g0275others(11): Show | 14 | HG02027.hp1 HG03130.hp1 HG03834.hp2 others(11): Show |
intron_variant | MODIFIER | c.585+3131_585+3132d others(4): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128962248 | |||||
chr9:128962251
|
T | G | 1 | a0001c0001t0001g0262 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.585+3117T>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128962251 | ||||||
chr9:128962274
|
A | G | 2 | a0001c0001t0004g0287a0001c0001t0004g0288 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.585+3140A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128962274 | ||||||
chr9:128962289
|
C | G | 1 | a0001c0001t0001g0090 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.585+3155C>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128962289 | ||||||
chr9:128962318
|
G | T | 1 | a0001c0001t0001g0050 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.585+3184G>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128962318 | ||||||
chr9:128962341
|
C | A | 13 | a0001c0002t0001g0254a0001c0004t0001g0247a0001c0004t0001g0248others(10): Show | 13 | HG01099.hp1 HG02109.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.585+3207C>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128962341 | ||||||
chr9:128962405
|
C | A | 1 | a0001c0001t0005g0065 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.585+3271C>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128962405 | ||||||
chr9:128962476
|
C | T | 1 | a0001c0001t0001g0138 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.585+3342C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128962476 | ||||||
chr9:128962485
|
C | G | 122 | a0001c0001t0001g0221a0001c0001t0004g0287a0001c0001t0004g0288others(119): Show | 122 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.585+3351C>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128962485 | ||||||
chr9:128962492
|
A | C | 15 | a0001c0003t0002g0273a0001c0003t0002g0274a0001c0003t0002g0275others(12): Show | 15 | HG02027.hp1 HG03834.hp2 HG04115.hp1 others(12): Show |
intron_variant | MODIFIER | c.585+3358A>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128962492 | ||||||
chr9:128962493
|
C | T | 2 | a0001c0001t0004g0287a0001c0001t0004g0288 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.585+3359C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128962493 | ||||||
chr9:128962524
|
C | T | 1 | a0001c0001t0001g0086 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.585+3390C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128962524 | ||||||
chr9:128962805
|
T | C | 14 | a0001c0003t0002g0273a0001c0003t0002g0274a0001c0003t0002g0275others(11): Show | 14 | HG02027.hp1 HG03834.hp2 HG04115.hp1 others(11): Show |
intron_variant | MODIFIER | c.585+3671T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128962805 | ||||||
chr9:128963282
|
A | AT | 8 | a0001c0001t0001g0090a0001c0001t0001g0129a0001c0001t0001g0143others(5): Show | 8 | HG01169.hp2 HG01175.hp1 HG01928.hp2 others(5): Show |
intron_variant | MODIFIER | c.585+4169dupT | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128963282 | |||||
chr9:128963282
|
A | ATT | 10 | a0001c0003t0002g0273a0001c0003t0002g0276a0001c0003t0002g0277others(7): Show | 10 | HG02027.hp1 HG03834.hp2 NA18951.hp2 others(7): Show |
intron_variant | MODIFIER | c.585+4168_585+4169d others(4): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128963282 | |||||
chr9:128963282
|
A | G | 1 | a0001c0002t0001g0237 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.585+4148A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128963282 | ||||||
chr9:128963282
|
AT | A | 10 | a0001c0001t0001g0012a0001c0001t0001g0052a0001c0001t0001g0130others(7): Show | 10 | HG00639.hp1 HG00642.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.585+4169delT | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128963282 | |||||
chr9:128963282
|
ATT | A | 13 | a0001c0001t0004g0288a0001c0002t0001g0265a0001c0002t0001g0269others(10): Show | 13 | HG01167.hp1 HG02451.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.585+4168_585+4169d others(4): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128963282 | |||||
chr9:128963294
|
T | C | 2 | a0001c0009t0001g0267a0001c0009t0001g0268 | 2 | HG02451.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.585+4160T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128963294 | ||||||
chr9:128963328
|
C | T | 3 | a0001c0002t0001g0269a0001c0002t0001g0270a0001c0002t0001g0271 | 3 | HG02647.hp2 HG02970.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.585+4194C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128963328 | ||||||
chr9:128963348
|
C | T | 1 | a0003c0006t0001g0160 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.585+4214C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128963348 | ||||||
chr9:128963509
|
T | TG | 123 | a0001c0001t0001g0221a0001c0001t0004g0287a0001c0001t0004g0288others(120): Show | 123 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.585+4376dupG | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128963509 | |||||
chr9:128963526
|
A | T | 15 | a0001c0003t0002g0273a0001c0003t0002g0274a0001c0003t0002g0275others(12): Show | 15 | HG02027.hp1 HG03834.hp2 HG04115.hp1 others(12): Show |
intron_variant | MODIFIER | c.585+4392A>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128963526 | ||||||
chr9:128963814
|
GT | G | 32 | a0001c0001t0001g0122a0001c0001t0001g0142a0001c0001t0004g0287others(29): Show | 32 | HG00639.hp2 HG01167.hp1 HG01256.hp1 others(29): Show |
intron_variant | MODIFIER | c.586-4678delT | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128963814 | |||||
chr9:128963840
|
G | A | 2 | a0001c0001t0001g0069a0001c0001t0001g0109 | 2 | NA19009.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.586-4666G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128963840 | ||||||
chr9:128964049
|
T | C | 1 | a0001c0027t0001g0289 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.586-4457T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128964049 | ||||||
chr9:128964171
|
C | T | 2 | a0001c0001t0004g0287a0001c0001t0004g0288 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.586-4335C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128964171 | ||||||
chr9:128964252
|
T | C | 1 | a0001c0027t0001g0289 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.586-4254T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128964252 | ||||||
chr9:128964364
|
CT | C | 18 | a0001c0001t0001g0140a0001c0001t0004g0287a0001c0001t0004g0288others(15): Show | 18 | HG01099.hp1 HG02109.hp2 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.586-4127delT | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128964364 | |||||
chr9:128964404
|
C | G | 9 | a0001c0001t0001g0063a0001c0001t0001g0112a0001c0001t0001g0143others(6): Show | 9 | HG00642.hp1 HG01123.hp2 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.586-4102C>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128964404 | ||||||
chr9:128964424
|
G | A | 7 | a0001c0002t0001g0177a0001c0002t0001g0188a0001c0002t0001g0209others(4): Show | 7 | HG00741.hp1 HG01167.hp2 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.586-4082G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128964424 | ||||||
chr9:128964536
|
A | ATT | 13 | a0001c0003t0002g0273a0001c0003t0002g0274a0001c0003t0002g0276others(10): Show | 13 | HG02027.hp1 HG03834.hp2 HG06807.hp2 others(10): Show |
intron_variant | MODIFIER | c.586-3954_586-3953d others(4): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128964536 | |||||
chr9:128964536
|
AT | A | 91 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0140others(88): Show | 91 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.586-3953delT | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128964536 | |||||
chr9:128964706
|
A | AT | 7 | a0001c0001t0001g0079a0001c0001t0004g0288a0001c0002t0001g0048others(4): Show | 7 | HG00738.hp1 HG02300.hp2 HG02602.hp2 others(4): Show |
intron_variant | MODIFIER | c.586-3781dupT | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128964706 | |||||
chr9:128964706
|
AT | A | 41 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0031others(38): Show | 41 | HG01099.hp1 HG01109.hp1 HG01257.hp1 others(38): Show |
intron_variant | MODIFIER | c.586-3781delT | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128964706 | |||||
chr9:128964706
|
ATT | A | 75 | a0001c0001t0001g0221a0001c0002t0001g0009a0001c0002t0001g0170others(72): Show | 75 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.586-3782_586-3781d others(4): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128964706 | |||||
chr9:128964801
|
G | A | 1 | a0001c0002t0001g0217 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.586-3705G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128964801 | ||||||
chr9:128964828
|
T | C | 1 | a0001c0002t0001g0025 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.586-3678T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128964828 | ||||||
chr9:128964916
|
C | T | 1 | a0001c0027t0001g0289 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.586-3590C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128964916 | ||||||
chr9:128964953
|
G | A | 2 | a0001c0001t0004g0287a0001c0001t0004g0288 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.586-3553G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128964953 | ||||||
chr9:128965022
|
A | G | 1 | a0002c0005t0001g0290 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.586-3484A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128965022 | ||||||
chr9:128965063
|
T | G | 1 | a0001c0027t0001g0289 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.586-3443T>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128965063 | ||||||
chr9:128965272
|
A | G | 1 | a0001c0027t0001g0289 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.586-3234A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128965272 | ||||||
chr9:128965681
|
G | T | 1 | a0001c0001t0001g0042 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.586-2825G>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128965681 | ||||||
chr9:128965804
|
A | AT | 11 | a0001c0002t0001g0265a0001c0002t0001g0269a0001c0002t0001g0270others(8): Show | 11 | HG01167.hp1 HG02451.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.586-2687dupT | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128965804 | |||||
chr9:128965804
|
AT | A | 9 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0100others(6): Show | 9 | HG02896.hp2 HG02897.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.586-2687delT | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128965804 | |||||
chr9:128965820
|
A | T | 13 | a0001c0002t0001g0265a0001c0002t0001g0266a0001c0002t0001g0269others(10): Show | 13 | HG01167.hp1 HG02451.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.586-2686A>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128965820 | ||||||
chr9:128966046
|
C | T | 6 | a0002c0005t0001g0290a0002c0005t0001g0292a0002c0005t0001g0293others(3): Show | 6 | HG01167.hp1 HG02451.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.586-2460C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128966046 | ||||||
chr9:128966128
|
C | CGT | 10 | a0001c0001t0001g0007a0001c0001t0001g0049a0001c0001t0001g0113others(7): Show | 10 | HG01515.hp1 HG01517.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.586-2338_586-2337d others(4): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128966128 | |||||
chr9:128966128
|
CGT | C | 102 | a0001c0001t0001g0003a0001c0001t0001g0029a0001c0001t0001g0031others(99): Show | 103 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.586-2338_586-2337d others(4): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128966128 | |||||
chr9:128966128
|
CGTGT | C | 86 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0015others(83): Show | 86 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.586-2340_586-2337d others(6): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128966128 | |||||
chr9:128966128
|
CGTGTGT | C | 21 | a0001c0001t0001g0093a0001c0001t0001g0102a0001c0001t0001g0107others(18): Show | 21 | HG00423.hp1 HG01109.hp2 HG01167.hp1 others(18): Show |
intron_variant | MODIFIER | c.586-2342_586-2337d others(8): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128966128 | |||||
chr9:128966128
|
CGTGTGTG others(1): Show |
C | 14 | a0001c0001t0001g0116a0001c0001t0001g0120a0001c0001t0001g0142others(11): Show | 14 | HG00140.hp2 HG00741.hp2 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.586-2344_586-2337d others(10): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128966128 | |||||
chr9:128966128
|
CGTGTGTG others(3): Show |
C | 3 | a0001c0002t0001g0254a0001c0004t0001g0248a0001c0027t0001g0289 | 3 | HG03139.hp2 HG06807.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.586-2346_586-2337d others(12): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128966128 | |||||
chr9:128966128
|
CGTGTGTG others(5): Show |
C | 8 | a0001c0003t0002g0275a0001c0003t0002g0277a0001c0003t0002g0278others(5): Show | 8 | HG02027.hp1 NA18941.hp2 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.586-2348_586-2337d others(14): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128966128 | |||||
chr9:128966128
|
CGTGTGTG others(7): Show |
C | 6 | a0001c0003t0002g0273a0001c0003t0002g0274a0001c0003t0002g0276others(3): Show | 6 | HG03834.hp2 HG04115.hp1 NA18975.hp1 others(3): Show |
intron_variant | MODIFIER | c.586-2350_586-2337d others(16): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128966128 | |||||
chr9:128966168
|
T | C | 1 | a0001c0001t0001g0003 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.586-2338T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128966168 | ||||||
chr9:128966260
|
C | CTG | 22 | a0001c0001t0001g0010a0001c0001t0001g0043a0001c0001t0001g0044others(19): Show | 22 | HG00099.hp2 HG01099.hp1 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.586-2220_586-2219d others(4): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128966260 | |||||
chr9:128966260
|
CTG | C | 79 | a0001c0001t0001g0072a0001c0001t0001g0221a0001c0002t0001g0170others(76): Show | 79 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.586-2220_586-2219d others(4): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128966260 | |||||
chr9:128966260
|
CTGTG | C | 8 | a0001c0002t0001g0176a0001c0002t0001g0177a0001c0002t0001g0188others(5): Show | 8 | HG00741.hp1 HG01167.hp2 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.586-2222_586-2219d others(6): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128966260 | |||||
chr9:128966260
|
CTGTGTG | C | 13 | a0001c0002t0001g0265a0001c0002t0001g0266a0001c0002t0001g0269others(10): Show | 13 | HG02027.hp1 HG02647.hp2 HG02895.hp2 others(10): Show |
intron_variant | MODIFIER | c.586-2224_586-2219d others(8): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128966260 | |||||
chr9:128966262
|
GTGTGTGT others(19): Show |
G | 1 | a0001c0001t0001g0097 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.586-2232_586-2207d others(28): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128966262 | |||||
chr9:128966286
|
GT | G | 3 | a0001c0002t0001g0009a0001c0002t0001g0172a0001c0002t0001g0244 | 3 | HG01069.hp1 NA18999.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.586-2217delT | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128966286 | |||||
chr9:128966287
|
T | TG | 4 | a0001c0001t0001g0115a0001c0001t0001g0125a0001c0001t0006g0022others(1): Show | 4 | HG01361.hp1 HG02735.hp1 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.586-2219_586-2218i others(3): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128966287 | ||||||
chr9:128966379
|
T | C | 14 | a0001c0003t0002g0273a0001c0003t0002g0274a0001c0003t0002g0275others(11): Show | 14 | HG02027.hp1 HG03834.hp2 HG04115.hp1 others(11): Show |
intron_variant | MODIFIER | c.586-2127T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128966379 | ||||||
chr9:128966385
|
T | G | 2 | a0001c0001t0004g0287a0001c0001t0004g0288 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.586-2121T>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128966385 | ||||||
chr9:128966504
|
C | T | 1 | a0001c0002t0001g0238 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.586-2002C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128966504 | ||||||
chr9:128966516
|
A | T | 14 | a0001c0003t0002g0273a0001c0003t0002g0274a0001c0003t0002g0275others(11): Show | 14 | HG02027.hp1 HG03834.hp2 HG04115.hp1 others(11): Show |
intron_variant | MODIFIER | c.586-1990A>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128966516 | ||||||
chr9:128966565
|
C | T | 1 | a0001c0001t0001g0148 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.586-1941C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128966565 | ||||||
chr9:128966603
|
G | A | 2 | a0001c0001t0001g0100a0001c0001t0001g0141 | 2 | NA19055.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.586-1903G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128966603 | ||||||
chr9:128967061
|
A | T | 2 | a0004c0010t0001g0169a0004c0010t0001g0234 | 2 | HG00642.hp2 HG01256.hp2 |
intron_variant | MODIFIER | c.586-1445A>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128967061 | ||||||
chr9:128967190
|
T | C | 2 | a0001c0001t0004g0287a0001c0001t0004g0288 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.586-1316T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128967190 | ||||||
chr9:128967285
|
T | C | 1 | a0001c0002t0001g0240 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.586-1221T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128967285 | ||||||
chr9:128967335
|
C | T | 1 | a0001c0001t0001g0008 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.586-1171C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128967335 | ||||||
chr9:128967350
|
A | G | 15 | a0001c0003t0002g0273a0001c0003t0002g0274a0001c0003t0002g0275others(12): Show | 15 | HG02027.hp1 HG03834.hp2 HG04115.hp1 others(12): Show |
intron_variant | MODIFIER | c.586-1156A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128967350 | ||||||
chr9:128967504
|
A | T | 2 | a0001c0001t0001g0057a0001c0001t0001g0070 | 2 | NA18942.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.586-1002A>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128967504 | ||||||
chr9:128967558
|
G | A | 2 | a0001c0001t0004g0287a0001c0001t0004g0288 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.586-948G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128967558 | ||||||
chr9:128967646
|
C | T | 6 | a0002c0005t0001g0290a0002c0005t0001g0292a0002c0005t0001g0293others(3): Show | 6 | HG01167.hp1 HG02451.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.586-860C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128967646 | ||||||
chr9:128967721
|
C | T | 2 | a0001c0001t0004g0287a0001c0001t0004g0288 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.586-785C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128967721 | ||||||
chr9:128967747
|
G | T | 1 | a0001c0001t0001g0052 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.586-759G>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128967747 | ||||||
chr9:128967785
|
C | T | 1 | a0001c0002t0001g0240 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.586-721C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128967785 | ||||||
chr9:128967790
|
CA | C | 7 | a0001c0002t0001g0190a0001c0002t0001g0191a0001c0002t0001g0269others(4): Show | 7 | HG01517.hp1 HG02451.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.586-701delA | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128967790 | |||||
chr9:128967790
|
CAA | C | 6 | a0002c0005t0001g0290a0002c0005t0001g0292a0002c0005t0001g0293others(3): Show | 6 | HG01167.hp1 HG02451.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.586-702_586-701del others(2): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128967790 | |||||
chr9:128967832
|
T | C | 1 | a0001c0002t0001g0242 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.586-674T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128967832 | ||||||
chr9:128967908
|
C | T | 1 | a0001c0001t0001g0105 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.586-598C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128967908 | ||||||
chr9:128968037
|
G | A | 1 | a0001c0001t0001g0086 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.586-469G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128968037 | ||||||
chr9:128968225
|
A | G | 1 | a0001c0002t0001g0176 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.586-281A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128968225 | ||||||
chr9:128968273
|
T | TA | 13 | a0001c0002t0001g0265a0001c0002t0001g0266a0001c0002t0001g0269others(10): Show | 13 | HG01167.hp1 HG02451.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.586-222dupA | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128968273 | |||||
chr9:128968361
|
C | G | 1 | a0001c0001t0007g0088 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.586-145C>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128968361 | ||||||
chr9:128968844
|
C | T | 4 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(1): Show | 4 | HG01891.hp2 HG02055.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.797+127C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 9/43 | chr9 | 128968844 | ||||||
chr9:128968858
|
C | G | 1 | a0001c0027t0001g0289 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.797+141C>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 9/43 | chr9 | 128968858 | ||||||
chr9:128968859
|
A | G | 1 | a0001c0001t0001g0047 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.797+142A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 9/43 | chr9 | 128968859 | ||||||
chr9:128969201
|
G | A | 13 | a0001c0002t0001g0265a0001c0002t0001g0266a0001c0002t0001g0269others(10): Show | 13 | HG01167.hp1 HG02451.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.798-199G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 9/43 | chr9 | 128969201 | ||||||
chr9:128969236
|
T | C | 13 | a0001c0002t0001g0254a0001c0004t0001g0247a0001c0004t0001g0248others(10): Show | 13 | HG01099.hp1 HG02109.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.798-164T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 9/43 | chr9 | 128969236 | ||||||
chr9:128969318
|
C | T | 1 | a0001c0001t0001g0126 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.798-82C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 9/43 | chr9 | 128969318 | ||||||
chr9:128969331
|
A | T | 1 | a0001c0002t0001g0176 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.798-69A>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 9/43 | chr9 | 128969331 | ||||||
chr9:128969572
|
A | G | 2 | a0001c0002t0001g0265a0001c0002t0001g0266 | 2 | HG02895.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.912+58A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 10/43 | chr9 | 128969572 | ||||||
chr9:128969734
|
A | G | 1 | a0001c0027t0001g0289 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.912+220A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 10/43 | chr9 | 128969734 | ||||||
chr9:128969744
|
C | G | 1 | a0001c0027t0001g0289 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.912+230C>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 10/43 | chr9 | 128969744 | ||||||
chr9:128969904
|
T | A | 6 | a0002c0005t0001g0290a0002c0005t0001g0292a0002c0005t0001g0293others(3): Show | 6 | HG01167.hp1 HG02451.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.912+390T>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 10/43 | chr9 | 128969904 | ||||||
chr9:128970085
|
G | A | 1 | a0001c0002t0001g0269 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.912+571G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 10/43 | chr9 | 128970085 | ||||||
chr9:128970225
|
G | A | 2 | a0001c0009t0001g0267a0001c0009t0001g0268 | 2 | HG02451.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.913-533G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 10/43 | chr9 | 128970225 | ||||||
chr9:128970326
|
A | G | 13 | a0001c0002t0001g0254a0001c0004t0001g0247a0001c0004t0001g0248others(10): Show | 13 | HG01099.hp1 HG02109.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.913-432A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 10/43 | chr9 | 128970326 | ||||||
chr9:128970392
|
G | A | 1 | a0001c0001t0001g0086 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.913-366G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 10/43 | chr9 | 128970392 | ||||||
chr9:128970585
|
G | A | 2 | a0001c0001t0001g0137a0001c0001t0001g0163 | 2 | HG02145.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.913-173G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 10/43 | chr9 | 128970585 | ||||||
chr9:128970725
|
C | T | 3 | a0001c0001t0001g0137a0001c0001t0001g0146a0001c0001t0001g0163 | 3 | HG02145.hp2 HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.913-33C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 10/43 | chr9 | 128970725 | ||||||
chr9:128971174
|
T | G | 14 | a0001c0003t0002g0273a0001c0003t0002g0274a0001c0003t0002g0275others(11): Show | 14 | HG02027.hp1 HG03834.hp2 HG04115.hp1 others(11): Show |
intron_variant | MODIFIER | c.1113+216T>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 11/43 | chr9 | 128971174 | ||||||
chr9:128971268
|
A | G | 1 | a0001c0002t0001g0198 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1113+310A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 11/43 | chr9 | 128971268 | ||||||
chr9:128971408
|
CTTGT | C | 15 | a0001c0002t0001g0254a0001c0003t0002g0273a0001c0003t0002g0274others(12): Show | 15 | HG02027.hp1 HG03139.hp2 HG03834.hp2 others(12): Show |
intron_variant | MODIFIER | c.1113+473_1113+476d others(6): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 11/43 | INFO_REALIGN_3_PRIME | chr9 | 128971408 | |||||
chr9:128971637
|
C | A | 13 | a0001c0002t0001g0265a0001c0002t0001g0266a0001c0002t0001g0269others(10): Show | 13 | HG01167.hp1 HG02451.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.1113+679C>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 11/43 | chr9 | 128971637 | ||||||
chr9:128971879
|
C | G | 1 | a0001c0001t0001g0141 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1113+921C>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 11/43 | chr9 | 128971879 | ||||||
chr9:128971914
|
G | A | 1 | a0001c0001t0001g0073 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1113+956G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 11/43 | chr9 | 128971914 | ||||||
chr9:128972051
|
T | C | 1 | a0001c0027t0001g0289 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1113+1093T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 11/43 | chr9 | 128972051 | ||||||
chr9:128972462
|
ACACAGAG others(5): Show |
A | 28 | a0001c0002t0001g0265a0001c0002t0001g0266a0001c0002t0001g0269others(25): Show | 28 | HG01167.hp1 HG02027.hp1 HG02451.hp1 others(25): Show |
intron_variant | MODIFIER | c.1114-685_1114-674d others(14): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 11/43 | INFO_REALIGN_3_PRIME | chr9 | 128972462 | |||||
chr9:128972764
|
A | G | 1 | a0001c0001t0001g0042 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1114-396A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 11/43 | chr9 | 128972764 | ||||||
chr9:128972922
|
G | A | 4 | a0001c0002t0001g0187a0001c0002t0001g0192a0001c0002t0001g0214others(1): Show | 4 | NA18968.hp2 NA18982.hp1 NA19064.hp2 others(1): Show |
intron_variant | MODIFIER | c.1114-238G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 11/43 | chr9 | 128972922 | ||||||
chr9:128973280
|
T | C | 77 | a0001c0001t0001g0221a0001c0002t0001g0170a0001c0002t0001g0171others(74): Show | 77 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.1203+31T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 12/43 | chr9 | 128973280 | ||||||
chr9:128973371
|
A | AT | 13 | a0001c0002t0001g0265a0001c0002t0001g0266a0001c0002t0001g0269others(10): Show | 13 | HG01167.hp1 HG02451.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.1203+129dupT | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 12/43 | INFO_REALIGN_3_PRIME | chr9 | 128973371 | |||||
chr9:128974094
|
A | G | 15 | a0001c0003t0002g0273a0001c0003t0002g0274a0001c0003t0002g0275others(12): Show | 15 | HG02027.hp1 HG03834.hp2 HG04115.hp1 others(12): Show |
intron_variant | MODIFIER | c.1203+845A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 12/43 | chr9 | 128974094 | ||||||
chr9:128974262
|
C | G | 2 | a0001c0001t0001g0012a0001c0001t0001g0013 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1203+1013C>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 12/43 | chr9 | 128974262 | ||||||
chr9:128974294
|
A | C | 2 | a0001c0001t0001g0012a0001c0001t0001g0013 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1203+1045A>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 12/43 | chr9 | 128974294 | ||||||
chr9:128974303
|
C | T | 1 | a0001c0001t0001g0087 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1203+1054C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 12/43 | chr9 | 128974303 | ||||||
chr9:128974389
|
G | GT | 54 | a0001c0001t0001g0014a0001c0001t0001g0050a0001c0001t0001g0054others(51): Show | 54 | HG00423.hp2 HG00639.hp2 HG00735.hp2 others(51): Show |
intron_variant | MODIFIER | c.1203+1160dupT | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 12/43 | INFO_REALIGN_3_PRIME | chr9 | 128974389 | |||||
chr9:128974389
|
G | GTTT | 11 | a0001c0003t0002g0273a0001c0003t0002g0274a0001c0003t0002g0275others(8): Show | 11 | HG02027.hp1 HG03834.hp2 NA18941.hp2 others(8): Show |
intron_variant | MODIFIER | c.1203+1158_1203+116 others(7): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 12/43 | INFO_REALIGN_3_PRIME | chr9 | 128974389 | |||||
chr9:128974389
|
G | T | 2 | a0001c0001t0001g0042a0001c0003t0002g0282 | 2 | HG03688.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.1203+1140G>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 12/43 | chr9 | 128974389 | ||||||
chr9:128974392
|
T | G | 3 | a0001c0001t0001g0060a0001c0001t0001g0087a0008c0018t0001g0089 | 3 | HG01069.hp2 HG01496.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.1203+1143T>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 12/43 | chr9 | 128974392 | ||||||
chr9:128974432
|
C | T | 2 | a0001c0001t0001g0012a0001c0001t0001g0013 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1203+1183C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 12/43 | chr9 | 128974432 | ||||||
chr9:128974622
|
A | T | 1 | a0001c0028t0001g0259 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1203+1373A>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 12/43 | chr9 | 128974622 | ||||||
chr9:128974624
|
C | G | 19 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0015others(16): Show | 19 | HG00558.hp2 HG00673.hp1 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.1203+1375C>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 12/43 | chr9 | 128974624 | ||||||
chr9:128974680
|
T | C | 13 | a0001c0002t0001g0265a0001c0002t0001g0266a0001c0002t0001g0269others(10): Show | 13 | HG01167.hp1 HG02451.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.1203+1431T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 12/43 | chr9 | 128974680 | ||||||
chr9:128974773
|
C | CT | 34 | a0001c0001t0001g0029a0001c0001t0001g0031a0001c0001t0001g0036others(31): Show | 35 | HG00639.hp1 HG00673.hp2 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.1203+1539dupT | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 12/43 | INFO_REALIGN_3_PRIME | chr9 | 128974773 | |||||
chr9:128974828
|
G | A | 1 | a0001c0002t0001g0176 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1203+1579G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 12/43 | chr9 | 128974828 | ||||||
chr9:128974898
|
A | G | 14 | a0001c0003t0002g0273a0001c0003t0002g0274a0001c0003t0002g0275others(11): Show | 14 | HG02027.hp1 HG03834.hp2 HG04115.hp1 others(11): Show |
intron_variant | MODIFIER | c.1203+1649A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 12/43 | chr9 | 128974898 | ||||||
chr9:128975060
|
T | C | 247 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(244): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.1203+1811T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 12/43 | chr9 | 128975060 | ||||||
chr9:128975159
|
T | G | 14 | a0001c0003t0002g0273a0001c0003t0002g0274a0001c0003t0002g0275others(11): Show | 14 | HG02027.hp1 HG03834.hp2 HG04115.hp1 others(11): Show |
intron_variant | MODIFIER | c.1203+1910T>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 12/43 | chr9 | 128975159 | ||||||
chr9:128975163
|
G | T | 28 | a0001c0002t0001g0265a0001c0002t0001g0266a0001c0002t0001g0269others(25): Show | 28 | HG01167.hp1 HG02027.hp1 HG02451.hp1 others(25): Show |
intron_variant | MODIFIER | c.1203+1914G>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 12/43 | chr9 | 128975163 | ||||||
chr9:128975226
|
C | CTTTTT | 12 | a0001c0003t0002g0273a0001c0003t0002g0274a0001c0003t0002g0275others(9): Show | 12 | HG02027.hp1 HG03834.hp2 NA18941.hp2 others(9): Show |
intron_variant | MODIFIER | c.1203+1990_1203+199 others(9): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 12/43 | INFO_REALIGN_3_PRIME | chr9 | 128975226 | |||||
chr9:128975235
|
T | C | 1 | a0011c0024t0001g0252 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1203+1986T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 12/43 | chr9 | 128975235 | ||||||
chr9:128975238
|
T | C | 1 | a0001c0002t0001g0220 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1203+1989T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 12/43 | chr9 | 128975238 | ||||||
chr9:128975323
|
A | G | 15 | a0001c0002t0001g0176a0001c0002t0001g0240a0001c0002t0001g0254others(12): Show | 15 | HG01099.hp1 HG01109.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1203+2074A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 12/43 | chr9 | 128975323 | ||||||
chr9:128975362
|
A | T | 28 | a0001c0002t0001g0265a0001c0002t0001g0266a0001c0002t0001g0269others(25): Show | 28 | HG01167.hp1 HG02027.hp1 HG02451.hp1 others(25): Show |
intron_variant | MODIFIER | c.1203+2113A>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 12/43 | chr9 | 128975362 | ||||||
chr9:128975405
|
G | A | 2 | a0001c0002t0001g0265a0001c0002t0001g0266 | 2 | HG02895.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1203+2156G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 12/43 | chr9 | 128975405 | ||||||
chr9:128975468
|
C | T | 76 | a0001c0001t0001g0221a0001c0002t0001g0170a0001c0002t0001g0171others(73): Show | 76 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.1203+2219C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 12/43 | chr9 | 128975468 | ||||||
chr9:128975511
|
C | T | 1 | a0001c0001t0001g0145 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1203+2262C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 12/43 | chr9 | 128975511 | ||||||
chr9:128975682
|
G | A | 1 | a0001c0008t0001g0135 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1203+2433G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 12/43 | chr9 | 128975682 | ||||||
chr9:128975896
|
G | A | 1 | a0001c0001t0001g0157 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1203+2647G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 12/43 | chr9 | 128975896 | ||||||
chr9:128975932
|
C | T | 15 | a0001c0003t0002g0273a0001c0003t0002g0274a0001c0003t0002g0275others(12): Show | 15 | HG02027.hp1 HG03834.hp2 HG04115.hp1 others(12): Show |
intron_variant | MODIFIER | c.1203+2683C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 12/43 | chr9 | 128975932 | ||||||
chr9:128976012
|
A | G | 1 | a0001c0001t0001g0046 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1203+2763A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 12/43 | chr9 | 128976012 | ||||||
chr9:128976048
|
A | C | 294 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(291): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.1203+2799A>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 12/43 | chr9 | 128976048 | ||||||
chr9:128976069
|
T | C | 1 | a0001c0001t0001g0052 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1203+2820T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 12/43 | chr9 | 128976069 | ||||||
chr9:128976250
|
A | T | 13 | a0001c0002t0001g0265a0001c0002t0001g0266a0001c0002t0001g0269others(10): Show | 13 | HG01167.hp1 HG02451.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.1203+3001A>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 12/43 | chr9 | 128976250 | ||||||
chr9:128976359
|
T | G | 1 | a0001c0027t0001g0289 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1204-2903T>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 12/43 | chr9 | 128976359 | ||||||
chr9:128976950
|
C | T | 1 | a0001c0001t0007g0088 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1204-2312C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 12/43 | chr9 | 128976950 | ||||||
chr9:128976952
|
C | T | 13 | a0001c0002t0001g0254a0001c0004t0001g0247a0001c0004t0001g0248others(10): Show | 13 | HG01099.hp1 HG02109.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.1204-2310C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 12/43 | chr9 | 128976952 | ||||||
chr9:128977117
|
A | AT | 23 | a0001c0001t0001g0005a0001c0001t0001g0037a0001c0001t0001g0045others(20): Show | 23 | HG00642.hp1 HG00673.hp1 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.1204-2124dupT | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 12/43 | INFO_REALIGN_3_PRIME | chr9 | 128977117 | |||||
chr9:128977117
|
AT | A | 96 | a0001c0001t0001g0221a0001c0002t0001g0170a0001c0002t0001g0171others(93): Show | 96 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.1204-2124delT | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 12/43 | INFO_REALIGN_3_PRIME | chr9 | 128977117 | |||||
chr9:128977198
|
C | T | 15 | a0001c0002t0001g0176a0001c0002t0001g0240a0001c0002t0001g0254others(12): Show | 15 | HG01099.hp1 HG01109.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1204-2064C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 12/43 | chr9 | 128977198 | ||||||
chr9:128977239
|
C | A | 77 | a0001c0001t0001g0221a0001c0002t0001g0170a0001c0002t0001g0171others(74): Show | 77 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.1204-2023C>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 12/43 | chr9 | 128977239 | ||||||
chr9:128977306
|
G | T | 1 | a0001c0001t0001g0103 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1204-1956G>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 12/43 | chr9 | 128977306 | ||||||
chr9:128977773
|
T | C | 1 | a0001c0001t0001g0042 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1204-1489T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 12/43 | chr9 | 128977773 | ||||||
chr9:128978141
|
C | A | 14 | a0001c0003t0002g0273a0001c0003t0002g0274a0001c0003t0002g0275others(11): Show | 14 | HG02027.hp1 HG03834.hp2 HG04115.hp1 others(11): Show |
intron_variant | MODIFIER | c.1204-1121C>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 12/43 | chr9 | 128978141 | ||||||
chr9:128978435
|
C | T | 1 | a0001c0001t0001g0082 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1204-827C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 12/43 | chr9 | 128978435 | ||||||
chr9:128978550
|
G | A | 1 | a0001c0003t0002g0280 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1204-712G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 12/43 | chr9 | 128978550 | ||||||
chr9:128978556
|
C | CA | 51 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0063others(48): Show | 51 | HG00597.hp2 HG00639.hp1 HG01099.hp1 others(48): Show |
intron_variant | MODIFIER | c.1204-683dupA | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 12/43 | INFO_REALIGN_3_PRIME | chr9 | 128978556 | |||||
chr9:128978556
|
C | CAA | 7 | a0001c0001t0001g0103a0001c0003t0002g0274a0001c0003t0002g0276others(4): Show | 8 | HG03098.hp1 HG03453.hp1 HG03486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1204-684_1204-683d others(4): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 12/43 | INFO_REALIGN_3_PRIME | chr9 | 128978556 | |||||
chr9:128978556
|
CAAAA | C | 64 | a0001c0002t0001g0170a0001c0002t0001g0171a0001c0002t0001g0173others(61): Show | 64 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.1204-686_1204-683d others(6): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 12/43 | INFO_REALIGN_3_PRIME | chr9 | 128978556 | |||||
chr9:128978556
|
CAAAAA | C | 8 | a0001c0001t0001g0221a0001c0002t0001g0172a0001c0002t0001g0181others(5): Show | 8 | HG00423.hp1 HG06807.hp2 NA18943.hp1 others(5): Show |
intron_variant | MODIFIER | c.1204-687_1204-683d others(7): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 12/43 | INFO_REALIGN_3_PRIME | chr9 | 128978556 | |||||
chr9:128978556
|
CAAAAAAA others(8): Show |
C | 2 | a0001c0002t0001g0195a0001c0029t0001g0185 | 2 | NA18987.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.1204-697_1204-683d others(17): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 12/43 | INFO_REALIGN_3_PRIME | chr9 | 128978556 | |||||
chr9:128978584
|
A | C | 13 | a0001c0002t0001g0265a0001c0002t0001g0266a0001c0002t0001g0269others(10): Show | 13 | HG01167.hp1 HG02451.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.1204-678A>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 12/43 | chr9 | 128978584 | ||||||
chr9:128978865
|
C | T | 1 | a0001c0001t0001g0154 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1204-397C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 12/43 | chr9 | 128978865 | ||||||
chr9:128978883
|
G | A | 1 | a0001c0028t0001g0259 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1204-379G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 12/43 | chr9 | 128978883 | ||||||
chr9:128979155
|
T | C | 14 | a0001c0003t0002g0273a0001c0003t0002g0274a0001c0003t0002g0275others(11): Show | 14 | HG02027.hp1 HG03834.hp2 HG04115.hp1 others(11): Show |
intron_variant | MODIFIER | c.1204-107T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 12/43 | chr9 | 128979155 | ||||||
chr9:128979180
|
T | C | 2 | a0001c0003t0002g0284a0001c0003t0002g0285 | 2 | NA19004.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.1204-82T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 12/43 | chr9 | 128979180 | ||||||
chr9:128979188
|
A | G | 1 | a0001c0014t0001g0180 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1204-74A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 12/43 | chr9 | 128979188 | ||||||
chr9:128979354
|
A | G | 8 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0083others(5): Show | 8 | HG02109.hp1 HG02622.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1269+27A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 13/43 | chr9 | 128979354 | ||||||
chr9:128979587
|
T | C | 1 | a0001c0002t0001g0204 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1269+260T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 13/43 | chr9 | 128979587 | ||||||
chr9:128979616
|
GT | G | 120 | a0001c0001t0001g0221a0001c0002t0001g0026a0001c0002t0001g0170others(117): Show | 120 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.1269+300delT | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 13/43 | INFO_REALIGN_3_PRIME | chr9 | 128979616 | |||||
chr9:128979736
|
A | G | 1 | a0001c0001t0001g0050 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1269+409A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 13/43 | chr9 | 128979736 | ||||||
chr9:128979764
|
C | G | 2 | a0001c0001t0004g0287a0001c0001t0004g0288 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1269+437C>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 13/43 | chr9 | 128979764 | ||||||
chr9:128979782
|
G | A | 2 | a0001c0002t0001g0265a0001c0002t0001g0266 | 2 | HG02895.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1269+455G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 13/43 | chr9 | 128979782 | ||||||
chr9:128979867
|
C | T | 2 | a0001c0002t0001g0011a0001c0002t0001g0021 | 2 | HG02040.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.1269+540C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 13/43 | chr9 | 128979867 | ||||||
chr9:128979868
|
G | A | 1 | a0001c0001t0001g0018 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1269+541G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 13/43 | chr9 | 128979868 | ||||||
chr9:128979901
|
G | C | 1 | a0002c0005t0001g0290 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1269+574G>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 13/43 | chr9 | 128979901 | ||||||
chr9:128980146
|
A | G | 1 | a0001c0004t0008g0256 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1270-460A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 13/43 | chr9 | 128980146 | ||||||
chr9:128980238
|
G | A | 1 | a0001c0001t0001g0060 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1270-368G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 13/43 | chr9 | 128980238 | ||||||
chr9:128980367
|
A | G | 1 | a0001c0002t0001g0238 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1270-239A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 13/43 | chr9 | 128980367 | ||||||
chr9:128980390
|
G | A | 2 | a0001c0002t0001g0178a0001c0002t0001g0203 | 2 | NA18999.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.1270-216G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 13/43 | chr9 | 128980390 | ||||||
chr9:128980421
|
C | T | 14 | a0001c0003t0002g0273a0001c0003t0002g0274a0001c0003t0002g0275others(11): Show | 14 | HG02027.hp1 HG03834.hp2 HG04115.hp1 others(11): Show |
intron_variant | MODIFIER | c.1270-185C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 13/43 | chr9 | 128980421 | ||||||
chr9:128980545
|
T | C | 10 | a0001c0001t0001g0098a0001c0001t0001g0130a0001c0001t0001g0147others(7): Show | 11 | HG00639.hp1 HG02615.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.1270-61T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 13/43 | chr9 | 128980545 | ||||||
chr9:128980592
|
C | T | 1 | a0001c0001t0001g0130 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1270-14C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 13/43 | chr9 | 128980592 | ||||||
chr9:128980835
|
T | C | 15 | a0001c0003t0002g0273a0001c0003t0002g0274a0001c0003t0002g0275others(12): Show | 15 | HG02027.hp1 HG03834.hp2 HG04115.hp1 others(12): Show |
intron_variant | MODIFIER | c.1389+110T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 14/43 | chr9 | 128980835 | ||||||
chr9:128980880
|
A | G | 1 | a0001c0001t0001g0042 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1389+155A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 14/43 | chr9 | 128980880 | ||||||
chr9:128981619
|
A | G | 1 | a0001c0001t0001g0264 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1516+229A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 15/43 | chr9 | 128981619 | ||||||
chr9:128981678
|
C | T | 5 | a0002c0005t0001g0292a0002c0005t0001g0293a0002c0005t0001g0294others(2): Show | 5 | HG01167.hp1 HG02451.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.1516+288C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 15/43 | chr9 | 128981678 | ||||||
chr9:128981693
|
C | T | 1 | a0001c0001t0001g0136 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1516+303C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 15/43 | chr9 | 128981693 | ||||||
chr9:128981853
|
G | A | 2 | a0001c0001t0001g0042a0001c0001t0001g0119 | 2 | HG00597.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.1516+463G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 15/43 | chr9 | 128981853 | ||||||
chr9:128981906
|
C | T | 6 | a0002c0005t0001g0290a0002c0005t0001g0292a0002c0005t0001g0293others(3): Show | 6 | HG01167.hp1 HG02451.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1516+516C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 15/43 | chr9 | 128981906 | ||||||
chr9:128981907
|
G | A | 77 | a0001c0001t0001g0221a0001c0002t0001g0170a0001c0002t0001g0171others(74): Show | 77 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.1516+517G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 15/43 | chr9 | 128981907 | ||||||
chr9:128982034
|
G | A | 13 | a0001c0002t0001g0265a0001c0002t0001g0266a0001c0002t0001g0269others(10): Show | 13 | HG01167.hp1 HG02451.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.1517-515G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 15/43 | chr9 | 128982034 | ||||||
chr9:128982039
|
T | C | 1 | a0001c0027t0001g0289 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1517-510T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 15/43 | chr9 | 128982039 | ||||||
chr9:128982120
|
T | G | 294 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(291): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.1517-429T>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 15/43 | chr9 | 128982120 | ||||||
chr9:128982189
|
G | A | 13 | a0001c0002t0001g0265a0001c0002t0001g0266a0001c0002t0001g0269others(10): Show | 13 | HG01167.hp1 HG02451.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.1517-360G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 15/43 | chr9 | 128982189 | ||||||
chr9:128982716
|
C | T | 1 | a0001c0002t0001g0085 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1669+15C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 16/43 | chr9 | 128982716 | ||||||
chr9:128982731
|
C | T | 2 | a0001c0001t0007g0088a0001c0027t0001g0289 | 2 | HG03017.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1669+30C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 16/43 | chr9 | 128982731 | ||||||
chr9:128982823
|
T | C | 13 | a0001c0003t0002g0273a0001c0003t0002g0274a0001c0003t0002g0276others(10): Show | 13 | HG02027.hp1 HG03834.hp2 HG04115.hp1 others(10): Show |
intron_variant | MODIFIER | c.1670-79T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 16/43 | chr9 | 128982823 | ||||||
chr9:128982872
|
C | T | 1 | a0001c0001t0001g0106 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1670-30C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 16/43 | chr9 | 128982872 | ||||||
chr9:128982883
|
A | T | 1 | a0001c0001t0001g0120 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1670-19A>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 16/43 | chr9 | 128982883 | ||||||
chr9:128983081
|
T | C | 1 | a0001c0001t0001g0015 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1796+53T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 17/43 | chr9 | 128983081 | ||||||
chr9:128983115
|
A | C | 1 | a0001c0002t0001g0235 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1796+87A>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 17/43 | chr9 | 128983115 | ||||||
chr9:128983130
|
G | A | 2 | a0001c0001t0001g0056a0001c0001t0001g0103 | 2 | NA18955.hp1 NA18987.hp2 |
intron_variant | MODIFIER | c.1796+102G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 17/43 | chr9 | 128983130 | ||||||
chr9:128983269
|
T | C | 85 | a0001c0001t0001g0031a0001c0001t0001g0057a0001c0001t0001g0069others(82): Show | 85 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.1797-24T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 17/43 | chr9 | 128983269 | ||||||
chr9:128983392
|
G | C | 1 | a0001c0001t0001g0146 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1884+12G>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 18/43 | chr9 | 128983392 | ||||||
chr9:128983573
|
G | A | 1 | a0001c0001t0001g0072 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1961+23G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 19/43 | chr9 | 128983573 | ||||||
chr9:128983599
|
A | G | 1 | a0001c0002t0001g0096 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1961+49A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 19/43 | chr9 | 128983599 | ||||||
chr9:128983686
|
C | T | 5 | a0001c0002t0001g0241a0001c0002t0001g0244a0001c0002t0001g0246others(2): Show | 5 | HG01069.hp1 HG02145.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.1961+136C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 19/43 | chr9 | 128983686 | ||||||
chr9:128983777
|
G | A | 1 | a0001c0001t0001g0035 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1961+227G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 19/43 | chr9 | 128983777 | ||||||
chr9:128983862
|
C | T | 1 | a0001c0027t0001g0289 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1961+312C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 19/43 | chr9 | 128983862 | ||||||
chr9:128983870
|
G | T | 1 | a0001c0002t0001g0178 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1961+320G>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 19/43 | chr9 | 128983870 | ||||||
chr9:128983936
|
T | C | 1 | a0001c0002t0001g0237 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1961+386T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 19/43 | chr9 | 128983936 | ||||||
chr9:128984037
|
G | C | 1 | a0001c0027t0001g0289 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1961+487G>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 19/43 | chr9 | 128984037 | ||||||
chr9:128984102
|
G | A | 1 | a0001c0002t0001g0254 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1961+552G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 19/43 | chr9 | 128984102 | ||||||
chr9:128984124
|
A | AT | 24 | a0001c0001t0001g0050a0001c0001t0001g0059a0001c0001t0001g0078others(21): Show | 24 | HG00438.hp2 HG00558.hp1 HG02027.hp1 others(21): Show |
intron_variant | MODIFIER | c.1961+593dupT | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 19/43 | INFO_REALIGN_3_PRIME | chr9 | 128984124 | |||||
chr9:128984124
|
A | ATTTTTTT others(4): Show |
1 | a0001c0002t0001g0026 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1961+583_1961+593d others(13): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 19/43 | INFO_REALIGN_3_PRIME | chr9 | 128984124 | |||||
chr9:128984124
|
A | ATTTTTTT others(5): Show |
1 | a0001c0027t0001g0289 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1961+582_1961+593d others(14): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 19/43 | INFO_REALIGN_3_PRIME | chr9 | 128984124 | |||||
chr9:128984124
|
A | ATTTTTTT others(6): Show |
2 | a0002c0005t0001g0293a0002c0005t0001g0295 | 2 | HG02615.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1961+581_1961+593d others(15): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 19/43 | INFO_REALIGN_3_PRIME | chr9 | 128984124 | |||||
chr9:128984124
|
A | ATTTTTTT others(7): Show |
3 | a0002c0005t0001g0290a0002c0005t0001g0294a0002c0012t0001g0291 | 3 | HG01167.hp1 HG02451.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1961+580_1961+593d others(16): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 19/43 | INFO_REALIGN_3_PRIME | chr9 | 128984124 | |||||
chr9:128984124
|
A | ATTTTTTT others(8): Show |
2 | a0001c0001t0001g0038a0001c0002t0001g0020 | 2 | HG02040.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.1961+579_1961+593d others(17): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 19/43 | INFO_REALIGN_3_PRIME | chr9 | 128984124 | |||||
chr9:128984124
|
A | ATTTTTTT others(10): Show |
3 | a0001c0002t0001g0265a0001c0002t0001g0266a0001c0002t0001g0270 | 3 | HG02895.hp2 HG03579.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1961+577_1961+593d others(19): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 19/43 | INFO_REALIGN_3_PRIME | chr9 | 128984124 | |||||
chr9:128984124
|
A | ATTTTTTT others(11): Show |
2 | a0001c0002t0001g0269a0001c0002t0001g0271 | 2 | HG02647.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1961+576_1961+593d others(20): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 19/43 | INFO_REALIGN_3_PRIME | chr9 | 128984124 | |||||
chr9:128984124
|
A | ATTTTTTT others(13): Show |
9 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0051others(6): Show | 9 | HG01074.hp1 HG02559.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.1961+593_1961+594i others(22): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 19/43 | INFO_REALIGN_3_PRIME | chr9 | 128984124 | |||||
chr9:128984124
|
A | ATTTTTTT others(14): Show |
12 | a0001c0001t0001g0010a0001c0001t0001g0035a0001c0001t0001g0041others(9): Show | 12 | HG00738.hp1 HG01891.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.1961+593_1961+594i others(23): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 19/43 | INFO_REALIGN_3_PRIME | chr9 | 128984124 | |||||
chr9:128984124
|
A | ATTTTTTT others(15): Show |
9 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(6): Show | 9 | HG00673.hp1 HG01496.hp1 HG02080.hp1 others(6): Show |
intron_variant | MODIFIER | c.1961+593_1961+594i others(24): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 19/43 | INFO_REALIGN_3_PRIME | chr9 | 128984124 | |||||
chr9:128984124
|
A | ATTTTTTT others(16): Show |
1 | a0001c0001t0001g0052 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1961+593_1961+594i others(25): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 19/43 | INFO_REALIGN_3_PRIME | chr9 | 128984124 | |||||
chr9:128984124
|
A | ATTTTTTT others(17): Show |
4 | a0001c0001t0001g0003a0001c0001t0001g0124a0001c0002t0001g0011others(1): Show | 4 | HG02040.hp2 HG02451.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1961+593_1961+594i others(26): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 19/43 | INFO_REALIGN_3_PRIME | chr9 | 128984124 | |||||
chr9:128984124
|
A | ATTTTTTT others(18): Show |
3 | a0001c0002t0001g0009a0001c0002t0001g0021a0001c0002t0001g0027 | 3 | HG01255.hp2 HG02523.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.1961+593_1961+594i others(27): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 19/43 | INFO_REALIGN_3_PRIME | chr9 | 128984124 | |||||
chr9:128984124
|
A | ATTTTTTT others(19): Show |
4 | a0001c0001t0001g0045a0001c0002t0001g0024a0001c0002t0001g0034others(1): Show | 4 | HG01257.hp1 HG02886.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1961+593_1961+594i others(28): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 19/43 | INFO_REALIGN_3_PRIME | chr9 | 128984124 | |||||
chr9:128984124
|
A | ATTTTTTT others(20): Show |
3 | a0001c0001t0001g0008a0001c0001t0001g0019a0001c0001t0001g0028 | 3 | NA18966.hp2 NA18969.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.1961+593_1961+594i others(29): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 19/43 | INFO_REALIGN_3_PRIME | chr9 | 128984124 | |||||
chr9:128984124
|
A | ATTTTTTT others(21): Show |
5 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0016others(2): Show | 5 | HG00558.hp2 HG02293.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1961+593_1961+594i others(30): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 19/43 | INFO_REALIGN_3_PRIME | chr9 | 128984124 | |||||
chr9:128984124
|
A | ATTTTTTT others(22): Show |
3 | a0001c0001t0001g0058a0001c0001t0001g0108a0001c0002t0001g0006 | 3 | HG03540.hp1 NA19000.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1961+593_1961+594i others(31): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 19/43 | INFO_REALIGN_3_PRIME | chr9 | 128984124 | |||||
chr9:128984124
|
A | ATTTTTTT others(23): Show |
5 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0002t0001g0025others(2): Show | 5 | HG01433.hp1 HG01891.hp2 HG02273.hp2 others(2): Show |
intron_variant | MODIFIER | c.1961+593_1961+594i others(32): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 19/43 | INFO_REALIGN_3_PRIME | chr9 | 128984124 | |||||
chr9:128984124
|
A | ATTTTTTT others(24): Show |
1 | a0001c0002t0001g0033 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1961+593_1961+594i others(33): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 19/43 | INFO_REALIGN_3_PRIME | chr9 | 128984124 | |||||
chr9:128984124
|
A | ATTTTTTT others(25): Show |
1 | a0001c0002t0001g0085 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1961+593_1961+594i others(34): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 19/43 | INFO_REALIGN_3_PRIME | chr9 | 128984124 | |||||
chr9:128984124
|
A | ATTTTTTT others(26): Show |
2 | a0001c0001t0001g0018a0001c0002t0001g0096 | 2 | NA18747.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.1961+593_1961+594i others(35): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 19/43 | INFO_REALIGN_3_PRIME | chr9 | 128984124 | |||||
chr9:128984124
|
A | ATTTTTTT others(31): Show |
1 | a0001c0001t0001g0107 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1961+593_1961+594i others(40): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 19/43 | INFO_REALIGN_3_PRIME | chr9 | 128984124 | |||||
chr9:128984124
|
A | ATTTTTTT others(33): Show |
1 | a0001c0001t0001g0005 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1961+593_1961+594i others(42): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 19/43 | INFO_REALIGN_3_PRIME | chr9 | 128984124 | |||||
chr9:128984124
|
A | ATTTTTTT others(40): Show |
1 | a0001c0002t0001g0023 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1961+593_1961+594i others(49): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 19/43 | INFO_REALIGN_3_PRIME | chr9 | 128984124 | |||||
chr9:128984124
|
AT | A | 17 | a0001c0001t0001g0029a0001c0001t0001g0129a0001c0001t0001g0140others(14): Show | 17 | HG01099.hp1 HG01169.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.1961+593delT | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 19/43 | INFO_REALIGN_3_PRIME | chr9 | 128984124 | |||||
chr9:128984157
|
G | A | 2 | a0001c0002t0001g0213a0001c0002t0001g0218 | 2 | HG02896.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1961+607G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 19/43 | chr9 | 128984157 | ||||||
chr9:128984207
|
A | G | 68 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(65): Show | 68 | HG00280.hp2 HG00558.hp2 HG00673.hp1 others(65): Show |
intron_variant | MODIFIER | c.1961+657A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 19/43 | chr9 | 128984207 | ||||||
chr9:128984228
|
G | A | 1 | a0013c0026t0001g0117 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1962-672G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 19/43 | chr9 | 128984228 | ||||||
chr9:128984280
|
C | G | 83 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(80): Show | 83 | HG00280.hp2 HG00558.hp2 HG00673.hp1 others(80): Show |
intron_variant | MODIFIER | c.1962-620C>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 19/43 | chr9 | 128984280 | ||||||
chr9:128984468
|
A | G | 2 | a0001c0002t0001g0178a0001c0002t0001g0203 | 2 | NA18999.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.1962-432A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 19/43 | chr9 | 128984468 | ||||||
chr9:128984617
|
C | T | 1 | a0001c0001t0001g0131 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1962-283C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 19/43 | chr9 | 128984617 | ||||||
chr9:128984651
|
G | C | 28 | a0001c0002t0001g0265a0001c0002t0001g0266a0001c0002t0001g0269others(25): Show | 28 | HG01167.hp1 HG02027.hp1 HG02451.hp1 others(25): Show |
intron_variant | MODIFIER | c.1962-249G>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 19/43 | chr9 | 128984651 | ||||||
chr9:128985340
|
T | C | 1 | a0001c0003t0009g0281 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2076+326T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 20/43 | chr9 | 128985340 | ||||||
chr9:128985432
|
A | G | 97 | a0001c0001t0001g0221a0001c0002t0001g0067a0001c0002t0001g0170others(94): Show | 97 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.2076+418A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 20/43 | chr9 | 128985432 | ||||||
chr9:128985710
|
C | T | 1 | a0001c0002t0001g0176 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2076+696C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 20/43 | chr9 | 128985710 | ||||||
chr9:128985805
|
C | T | 1 | a0001c0001t0001g0091 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.2077-753C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 20/43 | chr9 | 128985805 | ||||||
chr9:128986041
|
G | A | 18 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0015others(15): Show | 18 | HG00558.hp2 HG00673.hp1 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.2077-517G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 20/43 | chr9 | 128986041 | ||||||
chr9:128986218
|
C | T | 1 | a0003c0006t0001g0160 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2077-340C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 20/43 | chr9 | 128986218 | ||||||
chr9:128986224
|
A | G | 1 | a0001c0001t0001g0010 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.2077-334A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 20/43 | chr9 | 128986224 | ||||||
chr9:128986265
|
C | G | 1 | a0001c0028t0001g0259 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2077-293C>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 20/43 | chr9 | 128986265 | ||||||
chr9:128986405
|
A | C | 1 | a0001c0027t0001g0289 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2077-153A>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 20/43 | chr9 | 128986405 | ||||||
chr9:128986424
|
C | G | 1 | a0001c0001t0001g0124 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2077-134C>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 20/43 | chr9 | 128986424 | ||||||
chr9:128986433
|
C | A | 2 | a0001c0001t0001g0012a0001c0001t0001g0013 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2077-125C>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 20/43 | chr9 | 128986433 | ||||||
chr9:128986934
|
C | A | 12 | a0001c0004t0001g0247a0001c0004t0001g0248a0001c0004t0001g0249others(9): Show | 12 | HG01099.hp1 HG02109.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.2264+59C>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 22/43 | chr9 | 128986934 | ||||||
chr9:128987064
|
T | TGA | 46 | a0001c0001t0001g0029a0001c0001t0001g0041a0001c0001t0001g0045others(43): Show | 46 | HG00140.hp1 HG00438.hp1 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.2264+213_2264+214d others(4): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 22/43 | INFO_REALIGN_3_PRIME | chr9 | 128987064 | |||||
chr9:128987064
|
T | TGAGA | 15 | a0001c0001t0001g0124a0001c0001t0001g0262a0001c0001t0001g0264others(12): Show | 15 | HG01069.hp1 HG01496.hp1 HG01934.hp1 others(12): Show |
intron_variant | MODIFIER | c.2264+211_2264+214d others(6): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 22/43 | INFO_REALIGN_3_PRIME | chr9 | 128987064 | |||||
chr9:128987064
|
T | TGAGAGA | 3 | a0001c0002t0001g0204a0001c0002t0001g0205a0001c0014t0001g0180 | 3 | HG03710.hp1 NA19078.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.2264+209_2264+214d others(8): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 22/43 | INFO_REALIGN_3_PRIME | chr9 | 128987064 | |||||
chr9:128987064
|
TGA | T | 32 | a0001c0001t0001g0003a0001c0001t0001g0049a0001c0001t0001g0056others(29): Show | 32 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(29): Show |
intron_variant | MODIFIER | c.2264+213_2264+214d others(4): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 22/43 | INFO_REALIGN_3_PRIME | chr9 | 128987064 | |||||
chr9:128987084
|
AGAGAGTG others(5): Show |
A | 5 | a0001c0002t0001g0265a0001c0002t0001g0266a0001c0002t0001g0271others(2): Show | 5 | HG02451.hp1 HG02647.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.2264+211_2264+222d others(14): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 22/43 | INFO_REALIGN_3_PRIME | chr9 | 128987084 | |||||
chr9:128987084
|
AGAGAGTG others(7): Show |
A | 3 | a0001c0002t0001g0269a0001c0002t0001g0270a0001c0027t0001g0289 | 3 | HG02970.hp2 HG06807.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2264+211_2264+224d others(16): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 22/43 | INFO_REALIGN_3_PRIME | chr9 | 128987084 | |||||
chr9:128987086
|
A | AGT | 18 | a0001c0001t0001g0031a0001c0001t0001g0059a0001c0001t0001g0069others(15): Show | 19 | HG00639.hp1 HG00673.hp2 HG01433.hp1 others(16): Show |
intron_variant | MODIFIER | c.2264+212_2264+213i others(4): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 22/43 | INFO_REALIGN_3_PRIME | chr9 | 128987086 | |||||
chr9:128987086
|
A | AGTGT | 7 | a0001c0001t0001g0036a0001c0001t0001g0060a0001c0001t0001g0086others(4): Show | 7 | HG01069.hp2 HG01496.hp2 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.2264+212_2264+213i others(6): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 22/43 | INFO_REALIGN_3_PRIME | chr9 | 128987086 | |||||
chr9:128987086
|
A | T | 2 | a0001c0001t0001g0075a0001c0001t0001g0159 | 2 | HG00423.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.2264+211A>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 22/43 | chr9 | 128987086 | ||||||
chr9:128987086
|
AGAGT | A | 3 | a0001c0001t0001g0148a0001c0001t0001g0166a0001c0001t0003g0132 | 3 | HG01175.hp2 HG02257.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.2264+213_2264+216d others(6): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 22/43 | INFO_REALIGN_3_PRIME | chr9 | 128987086 | |||||
chr9:128987086
|
AGAGTGT | A | 3 | a0001c0001t0001g0115a0001c0001t0001g0122a0001c0001t0001g0151 | 3 | HG00639.hp2 HG01361.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.2264+213_2264+218d others(8): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 22/43 | INFO_REALIGN_3_PRIME | chr9 | 128987086 | |||||
chr9:128987088
|
A | AGAGAGAG others(1): Show |
4 | a0001c0007t0001g0123a0001c0007t0001g0263a0001c0008t0001g0135others(1): Show | 4 | HG02630.hp1 HG02717.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.2264+214_2264+215i others(10): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 22/43 | INFO_REALIGN_3_PRIME | chr9 | 128987088 | |||||
chr9:128987088
|
A | AGAGAGAG others(3): Show |
1 | a0001c0001t0001g0047 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2264+214_2264+215i others(12): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 22/43 | INFO_REALIGN_3_PRIME | chr9 | 128987088 | |||||
chr9:128987088
|
A | AGAGAGTG others(3): Show |
1 | a0001c0001t0001g0042 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2264+214_2264+215i others(12): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 22/43 | INFO_REALIGN_3_PRIME | chr9 | 128987088 | |||||
chr9:128987088
|
A | AGAGAGTG others(5): Show |
1 | a0001c0002t0001g0048 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2264+214_2264+215i others(14): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 22/43 | INFO_REALIGN_3_PRIME | chr9 | 128987088 | |||||
chr9:128987088
|
A | AGAGT | 6 | a0001c0001t0001g0035a0001c0001t0001g0044a0001c0001t0001g0052others(3): Show | 6 | HG01891.hp1 HG02015.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.2264+214_2264+215i others(6): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 22/43 | INFO_REALIGN_3_PRIME | chr9 | 128987088 | |||||
chr9:128987088
|
A | AGAGTGTG others(9): Show |
1 | a0001c0002t0001g0099 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2264+214_2264+215i others(18): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 22/43 | INFO_REALIGN_3_PRIME | chr9 | 128987088 | |||||
chr9:128987088
|
A | AGT | 16 | a0001c0001t0001g0017a0001c0001t0001g0028a0001c0001t0001g0038others(13): Show | 16 | HG01109.hp2 HG02735.hp2 HG02886.hp2 others(13): Show |
intron_variant | MODIFIER | c.2264+256_2264+257d others(4): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 22/43 | INFO_REALIGN_3_PRIME | chr9 | 128987088 | |||||
chr9:128987088
|
A | AGTGT | 3 | a0001c0001t0001g0015a0001c0004t0001g0253a0001c0020t0001g0084 | 3 | HG01433.hp2 HG03195.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.2264+254_2264+257d others(6): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 22/43 | INFO_REALIGN_3_PRIME | chr9 | 128987088 | |||||
chr9:128987088
|
A | T | 46 | a0001c0001t0001g0031a0001c0001t0001g0036a0001c0001t0001g0050others(43): Show | 47 | HG00280.hp2 HG00423.hp2 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.2264+213A>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 22/43 | chr9 | 128987088 | ||||||
chr9:128987088
|
AGT | A | 32 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(29): Show | 32 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.2264+256_2264+257d others(4): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 22/43 | INFO_REALIGN_3_PRIME | chr9 | 128987088 | |||||
chr9:128987088
|
AGTGT | A | 5 | a0001c0001t0001g0112a0001c0001t0001g0272a0001c0002t0001g0218others(2): Show | 5 | HG01109.hp1 HG01261.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.2264+254_2264+257d others(6): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 22/43 | INFO_REALIGN_3_PRIME | chr9 | 128987088 | |||||
chr9:128987088
|
AGTGTGTG others(3): Show |
A | 6 | a0002c0005t0001g0290a0002c0005t0001g0292a0002c0005t0001g0293others(3): Show | 6 | HG01167.hp1 HG02451.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.2264+248_2264+257d others(12): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 22/43 | INFO_REALIGN_3_PRIME | chr9 | 128987088 | |||||
chr9:128987088
|
AGTGTGTG others(5): Show |
A | 13 | a0001c0003t0002g0273a0001c0003t0002g0274a0001c0003t0002g0275others(10): Show | 13 | HG02027.hp1 HG04115.hp1 NA18941.hp2 others(10): Show |
intron_variant | MODIFIER | c.2264+246_2264+257d others(14): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 22/43 | INFO_REALIGN_3_PRIME | chr9 | 128987088 | |||||
chr9:128987090
|
T | A | 72 | a0001c0001t0001g0010a0001c0001t0001g0037a0001c0001t0001g0041others(69): Show | 72 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.2264+215T>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 22/43 | chr9 | 128987090 | ||||||
chr9:128987092
|
T | A | 75 | a0001c0001t0001g0010a0001c0001t0001g0221a0001c0002t0001g0006others(72): Show | 75 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.2264+217T>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 22/43 | chr9 | 128987092 | ||||||
chr9:128987094
|
T | A | 70 | a0001c0001t0001g0221a0001c0002t0001g0067a0001c0002t0001g0170others(67): Show | 70 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.2264+219T>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 22/43 | chr9 | 128987094 | ||||||
chr9:128987096
|
T | A | 11 | a0001c0002t0001g0183a0001c0002t0001g0189a0001c0002t0001g0191others(8): Show | 11 | HG00438.hp1 HG00642.hp2 HG01123.hp1 others(8): Show |
intron_variant | MODIFIER | c.2264+221T>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 22/43 | chr9 | 128987096 | ||||||
chr9:128987098
|
T | A | 2 | a0001c0002t0001g0218a0004c0010t0001g0234 | 2 | HG00642.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.2264+223T>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 22/43 | chr9 | 128987098 | ||||||
chr9:128987100
|
T | A | 1 | a0001c0002t0001g0218 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2264+225T>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 22/43 | chr9 | 128987100 | ||||||
chr9:128987102
|
T | A | 3 | a0001c0002t0001g0218a0001c0003t0002g0285a0001c0003t0009g0281 | 3 | HG02896.hp1 HG04115.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.2264+227T>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 22/43 | chr9 | 128987102 | ||||||
chr9:128987119
|
GTGTGTGT others(7): Show |
G | 1 | a0001c0003t0002g0283 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2264+250_2264+263d others(16): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 22/43 | INFO_REALIGN_3_PRIME | chr9 | 128987119 | |||||
chr9:128987127
|
G | A | 1 | a0001c0001t0001g0049 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2264+252G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 22/43 | chr9 | 128987127 | ||||||
chr9:128987296
|
T | A | 14 | a0001c0003t0002g0273a0001c0003t0002g0274a0001c0003t0002g0275others(11): Show | 14 | HG02027.hp1 HG03834.hp2 HG04115.hp1 others(11): Show |
intron_variant | MODIFIER | c.2265-293T>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 22/43 | chr9 | 128987296 | ||||||
chr9:128987297
|
G | T | 14 | a0001c0003t0002g0273a0001c0003t0002g0274a0001c0003t0002g0275others(11): Show | 14 | HG02027.hp1 HG03834.hp2 HG04115.hp1 others(11): Show |
intron_variant | MODIFIER | c.2265-292G>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 22/43 | chr9 | 128987297 | ||||||
chr9:128987331
|
T | G | 1 | a0002c0005t0001g0290 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2265-258T>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 22/43 | chr9 | 128987331 | ||||||
chr9:128987432
|
G | A | 15 | a0001c0003t0002g0273a0001c0003t0002g0274a0001c0003t0002g0275others(12): Show | 15 | HG02027.hp1 HG03834.hp2 HG04115.hp1 others(12): Show |
intron_variant | MODIFIER | c.2265-157G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 22/43 | chr9 | 128987432 | ||||||
chr9:128987454
|
G | T | 1 | a0001c0002t0001g0206 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.2265-135G>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 22/43 | chr9 | 128987454 | ||||||
chr9:128987935
|
C | T | 12 | a0001c0004t0001g0247a0001c0004t0001g0248a0001c0004t0001g0249others(9): Show | 12 | HG01099.hp1 HG02109.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.2394-112C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 23/43 | chr9 | 128987935 | ||||||
chr9:128988394
|
A | G | 15 | a0001c0003t0002g0273a0001c0003t0002g0274a0001c0003t0002g0275others(12): Show | 15 | HG02027.hp1 HG03834.hp2 HG04115.hp1 others(12): Show |
intron_variant | MODIFIER | c.2533+208A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 24/43 | chr9 | 128988394 | ||||||
chr9:128988719
|
A | AT | 32 | a0001c0001t0001g0005a0001c0001t0001g0042a0001c0001t0001g0051others(29): Show | 32 | HG00140.hp2 HG00280.hp2 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.2533+560dupT | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 24/43 | INFO_REALIGN_3_PRIME | chr9 | 128988719 | |||||
chr9:128988719
|
AT | A | 143 | a0001c0001t0001g0013a0001c0001t0001g0018a0001c0001t0001g0030others(140): Show | 144 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(141): Show |
intron_variant | MODIFIER | c.2533+560delT | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 24/43 | INFO_REALIGN_3_PRIME | chr9 | 128988719 | |||||
chr9:128988719
|
ATT | A | 20 | a0001c0001t0001g0029a0001c0001t0001g0031a0001c0001t0001g0068others(17): Show | 20 | HG00423.hp2 HG00558.hp1 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.2533+559_2533+560d others(4): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 24/43 | INFO_REALIGN_3_PRIME | chr9 | 128988719 | |||||
chr9:128988719
|
ATTTTTTT others(5): Show |
A | 2 | a0001c0004t0001g0255a0001c0004t0008g0256 | 2 | HG02258.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.2533+549_2533+560d others(14): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 24/43 | INFO_REALIGN_3_PRIME | chr9 | 128988719 | |||||
chr9:128988719
|
ATTTTTTT others(6): Show |
A | 13 | a0001c0002t0001g0176a0001c0002t0001g0240a0001c0002t0001g0254others(10): Show | 13 | HG01099.hp1 HG01109.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.2533+548_2533+560d others(15): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 24/43 | INFO_REALIGN_3_PRIME | chr9 | 128988719 | |||||
chr9:128988764
|
T | C | 1 | a0001c0027t0001g0289 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2533+578T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 24/43 | chr9 | 128988764 | ||||||
chr9:128988796
|
G | C | 13 | a0001c0002t0001g0265a0001c0002t0001g0266a0001c0002t0001g0269others(10): Show | 13 | HG01167.hp1 HG02451.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.2533+610G>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 24/43 | chr9 | 128988796 | ||||||
chr9:128989285
|
C | A | 1 | a0001c0007t0001g0123 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2534-835C>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 24/43 | chr9 | 128989285 | ||||||
chr9:128989726
|
A | G | 124 | a0001c0001t0001g0221a0001c0002t0001g0170a0001c0002t0001g0171others(121): Show | 124 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.2534-394A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 24/43 | chr9 | 128989726 | ||||||
chr9:128989774
|
G | A | 12 | a0001c0004t0001g0247a0001c0004t0001g0248a0001c0004t0001g0249others(9): Show | 12 | HG01099.hp1 HG02109.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.2534-346G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 24/43 | chr9 | 128989774 | ||||||
chr9:128989786
|
C | T | 1 | a0001c0002t0001g0220 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.2534-334C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 24/43 | chr9 | 128989786 | ||||||
chr9:128989787
|
G | A | 3 | a0001c0001t0001g0115a0001c0001t0001g0122a0001c0001t0001g0148 | 3 | HG00639.hp2 HG01361.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.2534-333G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 24/43 | chr9 | 128989787 | ||||||
chr9:128990244
|
G | GCA | 14 | a0001c0003t0002g0273a0001c0003t0002g0274a0001c0003t0002g0275others(11): Show | 14 | HG02027.hp1 HG03834.hp2 HG04115.hp1 others(11): Show |
intron_variant | MODIFIER | c.2640+26_2640+27dup others(2): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 25/43 | INFO_REALIGN_3_PRIME | chr9 | 128990244 | |||||
chr9:128990316
|
G | A | 1 | a0001c0002t0001g0190 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2640+90G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 25/43 | chr9 | 128990316 | ||||||
chr9:128990541
|
G | A | 13 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0015others(10): Show | 13 | HG00558.hp2 HG00673.hp1 HG02080.hp1 others(10): Show |
intron_variant | MODIFIER | c.2640+315G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 25/43 | chr9 | 128990541 | ||||||
chr9:128990602
|
C | T | 2 | a0001c0001t0001g0062a0001c0001t0001g0086 | 2 | HG02698.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.2640+376C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 25/43 | chr9 | 128990602 | ||||||
chr9:128990603
|
G | A | 1 | a0001c0002t0001g0220 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.2640+377G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 25/43 | chr9 | 128990603 | ||||||
chr9:128990613
|
C | G | 1 | a0001c0029t0001g0185 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.2640+387C>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 25/43 | chr9 | 128990613 | ||||||
chr9:128990662
|
A | C | 1 | a0001c0001t0001g0053 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2640+436A>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 25/43 | chr9 | 128990662 | ||||||
chr9:128990692
|
T | A | 15 | a0001c0003t0002g0273a0001c0003t0002g0274a0001c0003t0002g0275others(12): Show | 15 | HG02027.hp1 HG03834.hp2 HG04115.hp1 others(12): Show |
intron_variant | MODIFIER | c.2640+466T>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 25/43 | chr9 | 128990692 | ||||||
chr9:128990788
|
T | C | 292 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(289): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.2640+562T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 25/43 | chr9 | 128990788 | ||||||
chr9:128990820
|
G | A | 8 | a0001c0003t0002g0275a0001c0003t0002g0277a0001c0003t0002g0278others(5): Show | 8 | HG02027.hp1 NA18941.hp2 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.2640+594G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 25/43 | chr9 | 128990820 | ||||||
chr9:128990821
|
C | T | 14 | a0001c0003t0002g0273a0001c0003t0002g0274a0001c0003t0002g0275others(11): Show | 14 | HG02027.hp1 HG03834.hp2 HG04115.hp1 others(11): Show |
intron_variant | MODIFIER | c.2640+595C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 25/43 | chr9 | 128990821 | ||||||
chr9:128990822
|
G | A | 1 | a0001c0002t0001g0196 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2640+596G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 25/43 | chr9 | 128990822 | ||||||
chr9:128990991
|
C | G | 1 | a0001c0001t0001g0049 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2640+765C>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 25/43 | chr9 | 128990991 | ||||||
chr9:128991012
|
C | T | 6 | a0002c0005t0001g0290a0002c0005t0001g0292a0002c0005t0001g0293others(3): Show | 6 | HG01167.hp1 HG02451.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.2640+786C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 25/43 | chr9 | 128991012 | ||||||
chr9:128991162
|
CT | C | 118 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0018others(115): Show | 118 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.2640+956delT | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 25/43 | INFO_REALIGN_3_PRIME | chr9 | 128991162 | |||||
chr9:128991162
|
CTT | C | 9 | a0001c0002t0001g0177a0001c0002t0001g0178a0001c0002t0001g0191others(6): Show | 9 | HG00642.hp2 HG01069.hp1 HG01167.hp2 others(6): Show |
intron_variant | MODIFIER | c.2640+955_2640+956d others(4): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 25/43 | INFO_REALIGN_3_PRIME | chr9 | 128991162 | |||||
chr9:128991253
|
G | A | 15 | a0001c0003t0002g0273a0001c0003t0002g0274a0001c0003t0002g0275others(12): Show | 15 | HG02027.hp1 HG03834.hp2 HG04115.hp1 others(12): Show |
intron_variant | MODIFIER | c.2640+1027G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 25/43 | chr9 | 128991253 | ||||||
chr9:128991298
|
G | T | 1 | a0001c0002t0001g0212 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2640+1072G>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 25/43 | chr9 | 128991298 | ||||||
chr9:128991568
|
G | A | 13 | a0001c0002t0001g0254a0001c0004t0001g0247a0001c0004t0001g0248others(10): Show | 13 | HG01099.hp1 HG02109.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.2640+1342G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 25/43 | chr9 | 128991568 | ||||||
chr9:128991611
|
G | T | 14 | a0001c0003t0002g0273a0001c0003t0002g0274a0001c0003t0002g0275others(11): Show | 14 | HG02027.hp1 HG03834.hp2 HG04115.hp1 others(11): Show |
intron_variant | MODIFIER | c.2640+1385G>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 25/43 | chr9 | 128991611 | ||||||
chr9:128991700
|
G | A | 1 | a0001c0027t0001g0289 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2640+1474G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 25/43 | chr9 | 128991700 | ||||||
chr9:128991707
|
G | T | 1 | a0001c0002t0001g0176 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2640+1481G>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 25/43 | chr9 | 128991707 | ||||||
chr9:128991830
|
C | CA | 18 | a0001c0001t0001g0087a0001c0001t0001g0094a0001c0002t0001g0212others(15): Show | 18 | HG00597.hp1 HG01069.hp2 HG01175.hp1 others(15): Show |
intron_variant | MODIFIER | c.2641-1351dupA | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 25/43 | INFO_REALIGN_3_PRIME | chr9 | 128991830 | |||||
chr9:128991907
|
C | CT | 7 | a0001c0001t0001g0041a0001c0001t0001g0044a0001c0001t0001g0059others(4): Show | 7 | HG01361.hp2 HG02027.hp2 HG02080.hp2 others(4): Show |
intron_variant | MODIFIER | c.2641-1272dupT | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 25/43 | INFO_REALIGN_3_PRIME | chr9 | 128991907 | |||||
chr9:128991907
|
CT | C | 91 | a0001c0001t0001g0086a0001c0001t0001g0106a0001c0001t0001g0221others(88): Show | 91 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.2641-1272delT | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 25/43 | INFO_REALIGN_3_PRIME | chr9 | 128991907 | |||||
chr9:128992032
|
G | A | 1 | a0001c0002t0001g0240 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2641-1165G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 25/43 | chr9 | 128992032 | ||||||
chr9:128992035
|
T | G | 1 | a0001c0001t0001g0149 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.2641-1162T>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 25/43 | chr9 | 128992035 | ||||||
chr9:128992157
|
A | G | 2 | a0001c0002t0001g0204a0001c0002t0001g0205 | 2 | HG03710.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.2641-1040A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 25/43 | chr9 | 128992157 | ||||||
chr9:128992356
|
C | A | 2 | a0001c0002t0001g0265a0001c0002t0001g0266 | 2 | HG02895.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2641-841C>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 25/43 | chr9 | 128992356 | ||||||
chr9:128992873
|
C | T | 1 | a0001c0001t0001g0141 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.2641-324C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 25/43 | chr9 | 128992873 | ||||||
chr9:128992886
|
G | C | 123 | a0001c0001t0001g0221a0001c0002t0001g0170a0001c0002t0001g0171others(120): Show | 123 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.2641-311G>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 25/43 | chr9 | 128992886 | ||||||
chr9:128993001
|
C | G | 1 | a0001c0001t0001g0110 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.2641-196C>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 25/43 | chr9 | 128993001 | ||||||
chr9:128993146
|
A | G | 14 | a0001c0003t0002g0273a0001c0003t0002g0274a0001c0003t0002g0275others(11): Show | 14 | HG02027.hp1 HG03834.hp2 HG04115.hp1 others(11): Show |
intron_variant | MODIFIER | c.2641-51A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 25/43 | chr9 | 128993146 | ||||||
chr9:128993767
|
A | G | 1 | a0001c0001t0001g0045 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3017+73A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 27/43 | chr9 | 128993767 | ||||||
chr9:128993790
|
G | A | 1 | a0001c0001t0001g0130 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.3017+96G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 27/43 | chr9 | 128993790 | ||||||
chr9:128993834
|
A | G | 1 | a0001c0001t0001g0044 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.3017+140A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 27/43 | chr9 | 128993834 | ||||||
chr9:128993848
|
T | C | 4 | a0001c0007t0001g0123a0001c0007t0001g0263a0001c0008t0001g0135others(1): Show | 4 | HG02630.hp1 HG02717.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.3017+154T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 27/43 | chr9 | 128993848 | ||||||
chr9:128994019
|
C | T | 1 | a0001c0001t0001g0139 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.3017+325C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 27/43 | chr9 | 128994019 | ||||||
chr9:128994136
|
G | A | 15 | a0001c0003t0002g0273a0001c0003t0002g0274a0001c0003t0002g0275others(12): Show | 15 | HG02027.hp1 HG03834.hp2 HG04115.hp1 others(12): Show |
intron_variant | MODIFIER | c.3018-237G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 27/43 | chr9 | 128994136 | ||||||
chr9:128994358
|
T | G | 1 | a0001c0002t0001g0182 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.3018-15T>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 27/43 | chr9 | 128994358 | ||||||
chr9:128994607
|
T | C | 1 | a0001c0002t0001g0219 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.3087+165T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 28/43 | chr9 | 128994607 | ||||||
chr9:128994687
|
C | T | 1 | a0001c0001t0001g0047 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.3088-169C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 28/43 | chr9 | 128994687 | ||||||
chr9:128994846
|
A | G | 28 | a0001c0002t0001g0265a0001c0002t0001g0266a0001c0002t0001g0269others(25): Show | 28 | HG01167.hp1 HG02027.hp1 HG02451.hp1 others(25): Show |
intron_variant | MODIFIER | c.3088-10A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 28/43 | chr9 | 128994846 | ||||||
chr9:128995158
|
C | T | 1 | a0001c0027t0001g0289 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3156-161C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 29/43 | chr9 | 128995158 | ||||||
chr9:128995239
|
C | T | 1 | a0001c0001t0001g0102 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3156-80C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 29/43 | chr9 | 128995239 | ||||||
chr9:128995720
|
GA | G | 14 | a0001c0003t0002g0273a0001c0003t0002g0274a0001c0003t0002g0275others(11): Show | 14 | HG02027.hp1 HG03834.hp2 HG04115.hp1 others(11): Show |
intron_variant | MODIFIER | c.3351+208delA | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 30/43 | INFO_REALIGN_3_PRIME | chr9 | 128995720 | |||||
chr9:128996089
|
C | T | 1 | a0001c0028t0001g0259 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3351+575C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 30/43 | chr9 | 128996089 | ||||||
chr9:128996095
|
G | A | 1 | a0001c0002t0001g0174 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.3351+581G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 30/43 | chr9 | 128996095 | ||||||
chr9:128996134
|
G | A | 2 | a0001c0001t0001g0062a0001c0001t0001g0086 | 2 | HG02698.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.3351+620G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 30/43 | chr9 | 128996134 | ||||||
chr9:128996149
|
AT | A | 13 | a0001c0002t0001g0177a0001c0002t0001g0254a0001c0004t0001g0247others(10): Show | 13 | HG01099.hp1 HG01167.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.3351+650delT | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 30/43 | INFO_REALIGN_3_PRIME | chr9 | 128996149 | |||||
chr9:128996240
|
T | C | 122 | a0001c0002t0001g0048a0001c0002t0001g0067a0001c0002t0001g0099others(119): Show | 122 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.3351+726T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 30/43 | chr9 | 128996240 | ||||||
chr9:128996267
|
A | G | 2 | a0001c0001t0001g0110a0001c0001t0001g0131 | 2 | NA18968.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.3351+753A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 30/43 | chr9 | 128996267 | ||||||
chr9:128996517
|
T | G | 1 | a0001c0027t0001g0289 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3351+1003T>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 30/43 | chr9 | 128996517 | ||||||
chr9:128996800
|
T | A | 13 | a0001c0002t0001g0265a0001c0002t0001g0266a0001c0002t0001g0269others(10): Show | 13 | HG01167.hp1 HG02451.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.3351+1286T>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 30/43 | chr9 | 128996800 | ||||||
chr9:128996969
|
C | T | 77 | a0001c0001t0001g0221a0001c0002t0001g0170a0001c0002t0001g0171others(74): Show | 77 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.3352-1182C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 30/43 | chr9 | 128996969 | ||||||
chr9:128997189
|
G | T | 1 | a0001c0002t0001g0237 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.3352-962G>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 30/43 | chr9 | 128997189 | ||||||
chr9:128997292
|
A | C | 2 | a0001c0002t0001g0213a0001c0002t0001g0218 | 2 | HG02896.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.3352-859A>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 30/43 | chr9 | 128997292 | ||||||
chr9:128997470
|
A | C | 3 | a0001c0001t0001g0064a0001c0001t0001g0114a0001c0001t0001g0118 | 3 | HG01515.hp2 HG01517.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.3352-681A>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 30/43 | chr9 | 128997470 | ||||||
chr9:128997477
|
C | A | 2 | a0001c0001t0001g0012a0001c0001t0001g0013 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.3352-674C>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 30/43 | chr9 | 128997477 | ||||||
chr9:128997502
|
T | C | 1 | a0001c0027t0001g0289 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3352-649T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 30/43 | chr9 | 128997502 | ||||||
chr9:128997590
|
C | T | 1 | a0001c0001t0001g0073 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.3352-561C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 30/43 | chr9 | 128997590 | ||||||
chr9:128997887
|
AT | A | 6 | a0002c0005t0001g0290a0002c0005t0001g0292a0002c0005t0001g0293others(3): Show | 6 | HG01167.hp1 HG02451.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.3352-259delT | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 30/43 | INFO_REALIGN_3_PRIME | chr9 | 128997887 | |||||
chr9:128997919
|
C | T | 1 | a0001c0001t0001g0078 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.3352-232C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 30/43 | chr9 | 128997919 | ||||||
chr9:128998261
|
C | T | 1 | a0001c0001t0001g0015 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.3429+33C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 31/43 | chr9 | 128998261 | ||||||
chr9:128998337
|
G | A | 1 | a0001c0002t0001g0245 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.3429+109G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 31/43 | chr9 | 128998337 | ||||||
chr9:128998338
|
G | C | 1 | a0001c0002t0001g0245 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.3429+110G>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 31/43 | chr9 | 128998338 | ||||||
chr9:128998361
|
G | A | 1 | a0001c0001t0001g0008 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.3429+133G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 31/43 | chr9 | 128998361 | ||||||
chr9:128998388
|
G | C | 1 | a0001c0027t0001g0289 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3430-150G>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 31/43 | chr9 | 128998388 | ||||||
chr9:128998419
|
C | T | 4 | a0001c0007t0001g0123a0001c0007t0001g0263a0001c0008t0001g0135others(1): Show | 4 | HG02630.hp1 HG02717.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.3430-119C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 31/43 | chr9 | 128998419 | ||||||
chr9:128998494
|
G | A | 1 | a0001c0002t0001g0261 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.3430-44G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 31/43 | chr9 | 128998494 | ||||||
chr9:128998497
|
T | C | 1 | a0001c0002t0001g0020 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.3430-41T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 31/43 | chr9 | 128998497 | ||||||
chr9:128998711
|
G | A | 2 | a0001c0001t0001g0012a0001c0001t0001g0013 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.3515+88G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 32/43 | chr9 | 128998711 | ||||||
chr9:128998856
|
C | CT | 79 | a0001c0001t0001g0036a0001c0001t0001g0098a0001c0001t0001g0130others(76): Show | 80 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.3515+251dupT | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 32/43 | INFO_REALIGN_3_PRIME | chr9 | 128998856 | |||||
chr9:128998896
|
G | A | 1 | a0001c0001t0001g0130 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.3515+273G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 32/43 | chr9 | 128998896 | ||||||
chr9:128998918
|
G | A | 4 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0107others(1): Show | 4 | HG01109.hp2 HG02055.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.3516-254G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 32/43 | chr9 | 128998918 | ||||||
chr9:128998998
|
G | A | 43 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(40): Show | 43 | HG00280.hp2 HG00558.hp2 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.3516-174G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 32/43 | chr9 | 128998998 | ||||||
chr9:128999041
|
CAG | C | 14 | a0001c0003t0002g0273a0001c0003t0002g0274a0001c0003t0002g0275others(11): Show | 14 | HG02027.hp1 HG03834.hp2 HG04115.hp1 others(11): Show |
intron_variant | MODIFIER | c.3516-130_3516-129d others(4): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 32/43 | chr9 | 128999041 | ||||||
chr9:128999145
|
G | A | 1 | a0001c0001t0001g0093 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.3516-27G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 32/43 | chr9 | 128999145 | ||||||
chr9:128999158
|
A | G | 79 | a0001c0001t0001g0221a0001c0002t0001g0048a0001c0002t0001g0099others(76): Show | 79 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.3516-14A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 32/43 | chr9 | 128999158 | ||||||
chr9:128999325
|
G | C | 1 | a0001c0027t0001g0289 | 1 | HG06807.hp2 | splice_region_variant&intron_variant | LOW | c.3661+8G>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 33/43 | chr9 | 128999325 | ||||||
chr9:128999380
|
A | G | 79 | a0001c0002t0001g0048a0001c0002t0001g0099a0001c0002t0001g0170others(76): Show | 79 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.3661+63A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 33/43 | chr9 | 128999380 | ||||||
chr9:128999437
|
A | T | 94 | a0001c0001t0001g0221a0001c0002t0001g0048a0001c0002t0001g0099others(91): Show | 94 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.3661+120A>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 33/43 | chr9 | 128999437 | ||||||
chr9:128999438
|
T | C | 1 | a0001c0001t0001g0141 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.3661+121T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 33/43 | chr9 | 128999438 | ||||||
chr9:128999523
|
G | A | 1 | a0007c0016t0001g0230 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.3662-101G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 33/43 | chr9 | 128999523 | ||||||
chr9:128999620
|
A | G | 94 | a0001c0001t0001g0221a0001c0002t0001g0048a0001c0002t0001g0099others(91): Show | 94 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(91): Show |
splice_region_variant&intron_variant | LOW | c.3662-4A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 33/43 | chr9 | 128999620 | ||||||
chr9:128999878
|
G | C | 1 | a0001c0027t0001g0289 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3843+73G>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 34/43 | chr9 | 128999878 | ||||||
chr9:129000101
|
T | C | 79 | a0001c0001t0001g0221a0001c0002t0001g0048a0001c0002t0001g0099others(76): Show | 79 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.3843+296T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 34/43 | chr9 | 129000101 | ||||||
chr9:129000169
|
C | G | 1 | a0001c0027t0001g0289 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3843+364C>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 34/43 | chr9 | 129000169 | ||||||
chr9:129000231
|
A | ACAGGCG | 79 | a0001c0001t0001g0221a0001c0002t0001g0048a0001c0002t0001g0099others(76): Show | 79 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.3843+427_3843+432d others(8): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 34/43 | INFO_REALIGN_3_PRIME | chr9 | 129000231 | |||||
chr9:129000237
|
G | A | 14 | a0001c0003t0002g0273a0001c0003t0002g0274a0001c0003t0002g0275others(11): Show | 14 | HG02027.hp1 HG03834.hp2 HG04115.hp1 others(11): Show |
intron_variant | MODIFIER | c.3843+432G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 34/43 | chr9 | 129000237 | ||||||
chr9:129000341
|
A | G | 4 | a0001c0002t0001g0187a0001c0002t0001g0192a0001c0002t0001g0214others(1): Show | 4 | NA18968.hp2 NA18982.hp1 NA19064.hp2 others(1): Show |
intron_variant | MODIFIER | c.3843+536A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 34/43 | chr9 | 129000341 | ||||||
chr9:129000341
|
A | T | 1 | a0001c0027t0001g0289 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3843+536A>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 34/43 | chr9 | 129000341 | ||||||
chr9:129000431
|
A | G | 81 | a0001c0001t0001g0047a0001c0001t0001g0221a0001c0002t0001g0048others(78): Show | 81 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.3843+626A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 34/43 | chr9 | 129000431 | ||||||
chr9:129000444
|
G | A | 77 | a0001c0001t0001g0221a0001c0002t0001g0170a0001c0002t0001g0171others(74): Show | 77 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.3843+639G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 34/43 | chr9 | 129000444 | ||||||
chr9:129000479
|
C | T | 1 | a0001c0002t0001g0213 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3843+674C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 34/43 | chr9 | 129000479 | ||||||
chr9:129000576
|
C | T | 2 | a0001c0001t0001g0090a0001c0001t0005g0065 | 2 | HG02683.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.3843+771C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 34/43 | chr9 | 129000576 | ||||||
chr9:129000634
|
T | A | 3 | a0001c0002t0001g0170a0001c0002t0001g0195a0001c0002t0001g0207 | 3 | HG03491.hp2 HG03492.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.3843+829T>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 34/43 | chr9 | 129000634 | ||||||
chr9:129000774
|
A | C | 28 | a0001c0002t0001g0176a0001c0002t0001g0240a0001c0002t0001g0254others(25): Show | 28 | HG01099.hp1 HG01109.hp1 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.3844-755A>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 34/43 | chr9 | 129000774 | ||||||
chr9:129000776
|
C | T | 1 | a0002c0005t0001g0290 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.3844-753C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 34/43 | chr9 | 129000776 | ||||||
chr9:129000991
|
C | T | 1 | a0001c0021t0001g0133 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.3844-538C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 34/43 | chr9 | 129000991 | ||||||
chr9:129001145
|
G | C | 2 | a0001c0002t0001g0189a0001c0002t0001g0191 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.3844-384G>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 34/43 | chr9 | 129001145 | ||||||
chr9:129001159
|
G | A | 110 | a0001c0001t0001g0221a0001c0002t0001g0048a0001c0002t0001g0099others(107): Show | 110 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.3844-370G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 34/43 | chr9 | 129001159 | ||||||
chr9:129001239
|
G | A | 1 | a0001c0002t0001g0254 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.3844-290G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 34/43 | chr9 | 129001239 | ||||||
chr9:129001266
|
G | A | 1 | a0008c0018t0001g0089 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.3844-263G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 34/43 | chr9 | 129001266 | ||||||
chr9:129001735
|
A | C | 68 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(65): Show | 68 | HG00280.hp2 HG00558.hp2 HG00673.hp1 others(65): Show |
splice_region_variant&intron_variant | LOW | c.4044+6A>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 35/43 | chr9 | 129001735 | ||||||
chr9:129001745
|
G | A | 1 | a0001c0002t0001g0048 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.4044+16G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 35/43 | chr9 | 129001745 | ||||||
chr9:129001836
|
A | G | 6 | a0002c0005t0001g0290a0002c0005t0001g0292a0002c0005t0001g0293others(3): Show | 6 | HG01167.hp1 HG02451.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.4045-48A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 35/43 | chr9 | 129001836 | ||||||
chr9:129002099
|
G | A | 1 | a0001c0002t0001g0245 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.4137+123G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 36/43 | chr9 | 129002099 | ||||||
chr9:129002347
|
G | A | 1 | a0001c0001t0001g0147 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.4137+371G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 36/43 | chr9 | 129002347 | ||||||
chr9:129002541
|
G | T | 1 | a0001c0002t0001g0162 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.4138-276G>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 36/43 | chr9 | 129002541 | ||||||
chr9:129002578
|
G | A | 79 | a0001c0001t0001g0221a0001c0002t0001g0048a0001c0002t0001g0099others(76): Show | 79 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.4138-239G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 36/43 | chr9 | 129002578 | ||||||
chr9:129002579
|
C | T | 2 | a0001c0001t0001g0100a0001c0001t0001g0141 | 2 | NA19055.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.4138-238C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 36/43 | chr9 | 129002579 | ||||||
chr9:129002644
|
T | C | 14 | a0001c0003t0002g0273a0001c0003t0002g0274a0001c0003t0002g0275others(11): Show | 14 | HG02027.hp1 HG03834.hp2 HG04115.hp1 others(11): Show |
intron_variant | MODIFIER | c.4138-173T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 36/43 | chr9 | 129002644 | ||||||
chr9:129002690
|
A | G | 81 | a0001c0001t0001g0221a0001c0002t0001g0048a0001c0002t0001g0067others(78): Show | 81 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.4138-127A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 36/43 | chr9 | 129002690 | ||||||
chr9:129002705
|
A | G | 4 | a0001c0002t0001g0170a0001c0002t0001g0207a0001c0002t0001g0219others(1): Show | 4 | HG00738.hp2 HG01243.hp1 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.4138-112A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 36/43 | chr9 | 129002705 | ||||||
chr9:129003051
|
G | A | 6 | a0001c0002t0001g0172a0001c0002t0001g0173a0001c0002t0001g0181others(3): Show | 6 | NA18943.hp1 NA18955.hp2 NA18962.hp2 others(3): Show |
intron_variant | MODIFIER | c.4296+76G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 37/43 | chr9 | 129003051 | ||||||
chr9:129003070
|
G | A | 2 | a0001c0001t0001g0077a0001c0001t0001g0094 | 2 | NA18962.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.4296+95G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 37/43 | chr9 | 129003070 | ||||||
chr9:129003099
|
T | C | 80 | a0001c0001t0001g0221a0001c0002t0001g0048a0001c0002t0001g0099others(77): Show | 80 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.4296+124T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 37/43 | chr9 | 129003099 | ||||||
chr9:129003154
|
G | A | 1 | a0001c0002t0001g0240 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.4297-163G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 37/43 | chr9 | 129003154 | ||||||
chr9:129003269
|
G | A | 1 | a0001c0027t0001g0289 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.4297-48G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 37/43 | chr9 | 129003269 | ||||||
chr9:129003517
|
G | T | 1 | a0001c0001t0001g0119 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.4434+63G>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 38/43 | chr9 | 129003517 | ||||||
chr9:129003521
|
C | T | 1 | a0001c0002t0001g0199 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.4434+67C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 38/43 | chr9 | 129003521 | ||||||
chr9:129003532
|
T | C | 1 | a0001c0027t0001g0289 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.4434+78T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 38/43 | chr9 | 129003532 | ||||||
chr9:129003648
|
T | C | 14 | a0001c0003t0002g0273a0001c0003t0002g0274a0001c0003t0002g0275others(11): Show | 14 | HG02027.hp1 HG03834.hp2 HG04115.hp1 others(11): Show |
intron_variant | MODIFIER | c.4434+194T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 38/43 | chr9 | 129003648 | ||||||
chr9:129003708
|
T | C | 143 | a0001c0002t0001g0009a0001c0002t0001g0011a0001c0002t0001g0020others(140): Show | 143 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.4434+254T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 38/43 | chr9 | 129003708 | ||||||
chr9:129003978
|
GA | G | 11 | a0001c0001t0001g0004a0001c0001t0004g0287a0001c0001t0004g0288others(8): Show | 11 | HG02622.hp1 HG02630.hp1 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.4434+539delA | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 38/43 | INFO_REALIGN_3_PRIME | chr9 | 129003978 | |||||
chr9:129004073
|
C | T | 76 | a0001c0002t0001g0170a0001c0002t0001g0171a0001c0002t0001g0172others(73): Show | 76 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.4434+619C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 38/43 | chr9 | 129004073 | ||||||
chr9:129004148
|
A | G | 92 | a0001c0002t0001g0067a0001c0002t0001g0170a0001c0002t0001g0171others(89): Show | 92 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.4434+694A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 38/43 | chr9 | 129004148 | ||||||
chr9:129004281
|
C | CA | 8 | a0001c0001t0001g0014a0001c0001t0001g0031a0001c0001t0001g0060others(5): Show | 8 | HG01496.hp2 HG02056.hp1 NA18946.hp1 others(5): Show |
intron_variant | MODIFIER | c.4434+845dupA | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 38/43 | INFO_REALIGN_3_PRIME | chr9 | 129004281 | |||||
chr9:129004281
|
CA | C | 20 | a0001c0001t0001g0059a0001c0001t0001g0087a0001c0002t0001g0034others(17): Show | 20 | HG00738.hp2 HG01069.hp2 HG02027.hp1 others(17): Show |
intron_variant | MODIFIER | c.4434+845delA | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 38/43 | INFO_REALIGN_3_PRIME | chr9 | 129004281 | |||||
chr9:129004281
|
CAA | C | 74 | a0001c0002t0001g0170a0001c0002t0001g0171a0001c0002t0001g0172others(71): Show | 74 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.4434+844_4434+845d others(4): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 38/43 | INFO_REALIGN_3_PRIME | chr9 | 129004281 | |||||
chr9:129004290
|
A | G | 2 | a0001c0009t0001g0267a0001c0009t0001g0268 | 2 | HG02451.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.4434+836A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 38/43 | chr9 | 129004290 | ||||||
chr9:129004501
|
A | G | 1 | a0001c0009t0001g0268 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.4435-646A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 38/43 | chr9 | 129004501 | ||||||
chr9:129004661
|
C | T | 5 | a0002c0005t0001g0292a0002c0005t0001g0293a0002c0005t0001g0294others(2): Show | 5 | HG01167.hp1 HG02451.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.4435-486C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 38/43 | chr9 | 129004661 | ||||||
chr9:129004696
|
G | A | 1 | a0001c0002t0001g0219 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.4435-451G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 38/43 | chr9 | 129004696 | ||||||
chr9:129004791
|
C | T | 1 | a0001c0001t0006g0022 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.4435-356C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 38/43 | chr9 | 129004791 | ||||||
chr9:129004828
|
C | G | 14 | a0001c0003t0002g0273a0001c0003t0002g0274a0001c0003t0002g0275others(11): Show | 14 | HG02027.hp1 HG03834.hp2 HG04115.hp1 others(11): Show |
intron_variant | MODIFIER | c.4435-319C>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 38/43 | chr9 | 129004828 | ||||||
chr9:129004945
|
C | CAGGGGAG others(21): Show |
5 | a0001c0002t0001g0193a0001c0002t0001g0215a0001c0002t0001g0224others(2): Show | 5 | HG01255.hp1 HG01346.hp2 HG01928.hp1 others(2): Show |
intron_variant | MODIFIER | c.4435-143_4435-116d others(30): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 38/43 | INFO_REALIGN_3_PRIME | chr9 | 129004945 | |||||
chr9:129004945
|
C | CAGGGGAG others(49): Show |
3 | a0001c0002t0001g0181a0001c0002t0001g0183a0001c0023t0001g0168 | 3 | NA18962.hp2 NA18984.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.4435-171_4435-116d others(58): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 38/43 | INFO_REALIGN_3_PRIME | chr9 | 129004945 | |||||
chr9:129004945
|
CAGGGGAG others(21): Show |
C | 4 | a0001c0002t0001g0187a0001c0002t0001g0192a0001c0002t0001g0214others(1): Show | 4 | NA18968.hp2 NA18982.hp1 NA19064.hp2 others(1): Show |
intron_variant | MODIFIER | c.4435-143_4435-116d others(30): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 38/43 | INFO_REALIGN_3_PRIME | chr9 | 129004945 | |||||
chr9:129004947
|
G | A | 1 | a0001c0001t0001g0050 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.4435-200G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 38/43 | chr9 | 129004947 | ||||||
chr9:129005566
|
A | G | 1 | a0001c0027t0001g0289 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.4737+36A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 40/43 | chr9 | 129005566 | ||||||
chr9:129005781
|
G | A | 1 | a0001c0027t0001g0289 | 1 | HG06807.hp2 | splice_region_variant&intron_variant | LOW | c.4869+5G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 41/43 | chr9 | 129005781 | ||||||
chr9:129005823
|
C | T | 14 | a0001c0003t0002g0273a0001c0003t0002g0274a0001c0003t0002g0275others(11): Show | 14 | HG02027.hp1 HG03834.hp2 HG04115.hp1 others(11): Show |
intron_variant | MODIFIER | c.4869+47C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 41/43 | chr9 | 129005823 | ||||||
chr9:129005912
|
A | G | 28 | a0001c0001t0001g0010a0001c0001t0001g0041a0001c0001t0001g0042others(25): Show | 28 | HG00423.hp1 HG00738.hp1 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.4869+136A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 41/43 | chr9 | 129005912 | ||||||
chr9:129005983
|
G | A | 4 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(1): Show | 4 | HG01891.hp2 HG02055.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.4870-67G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 41/43 | chr9 | 129005983 | ||||||
chr9:129006461
|
C | G | 2 | a0001c0002t0001g0213a0001c0002t0001g0218 | 2 | HG02896.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.5074-41C>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 43/43 | chr9 | 129006461 | ||||||
chr9:129006497
|
T | C | 14 | a0001c0003t0002g0273a0001c0003t0002g0274a0001c0003t0002g0275others(11): Show | 14 | HG02027.hp1 HG03834.hp2 HG04115.hp1 others(11): Show |
splice_region_variant&intron_variant | LOW | c.5074-5T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 43/43 | chr9 | 129006497 |