geneid | 23225 |
---|---|
ensemblid | ENSG00000132182.13 |
hgncid | 30052 |
symbol | NUP210 |
name | nucleoporin 210 |
refseq_nuc | NM_024923.4 |
refseq_prot | NP_079199.2 |
ensembl_nuc | ENST00000254508.7 |
ensembl_prot | ENSP00000254508.5 |
mane_status | MANE Select |
chr | chr3 |
start | 13316235 |
end | 13420322 |
strand | - |
ver | v1.2 |
region | chr3:13316235-13420322 |
region5000 | chr3:13311235-13425322 |
regionname0 | NUP210_chr3_13316235_13420322 |
regionname5000 | NUP210_chr3_13311235_13425322 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 1887 | 105 | 9 | 21 | 56 | 6 | 12 | 48 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
a0002 | 0/0 | 1887 | 86 | 16 | 16 | 45 | 3 | 6 | 38 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
a0003 | 0/0 | 1887 | 33 | 28 | 2 | 1 | 0 | 2 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
a0004 | 0/0 | 1887 | 29 | 9 | 1 | 14 | 2 | 3 | 11 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
a0005 | 0/0 | 1887 | 29 | 4 | 10 | 4 | 1 | 10 | 4 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
a0006 | 0/0 | 1887 | 16 | 8 | 7 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
a0007 | 0/0 | 1887 | 4 | 0 | 1 | 3 | 0 | 0 | 2 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
a0008 | 0/0 | 1887 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
a0009 | 0/0 | 1887 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
a0010 | 0/0 | 1887 | 2 | 0 | 0 | 2 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
a0011 | 0/0 | 1887 | 2 | 1 | 0 | 0 | 0 | 1 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
a0012 | 0/0 | 1887 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
a0013 | 0/0 | 1887 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
a0014 | 1/0 | 1887 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
a0015 | 0/0 | 1887 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
a0016 | 0/0 | 1887 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
a0017 | 0/0 | 1887 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
a0018 | 0/0 | 1887 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
a0019 | 0/0 | 1887 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
a0020 | 0/0 | 1887 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
a0021 | 0/0 | 1887 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
a0022 | 0/0 | 1887 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
a0023 | 0/0 | 1887 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
a0024 | 0/0 | 1887 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 5664 | 101 | 9 | 19 | 55 | 6 | 11 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
c0002 | 0/0 | 5664 | 83 | 16 | 16 | 43 | 3 | 5 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
c0003 | 0/0 | 5664 | 29 | 4 | 10 | 4 | 1 | 10 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
c0004 | 0/0 | 5664 | 26 | 7 | 1 | 13 | 2 | 3 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
c0005 | 0/0 | 5664 | 16 | 15 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
c0006 | 0/0 | 5664 | 14 | 10 | 1 | 1 | 0 | 2 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
c0007 | 0/0 | 5664 | 14 | 6 | 7 | 0 | 1 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
c0008 | 0/0 | 5664 | 4 | 0 | 1 | 3 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
c0009 | 0/0 | 5664 | 3 | 3 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
c0010 | 0/0 | 5664 | 2 | 2 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
c0011 | 0/0 | 5664 | 2 | 2 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
c0012 | 0/0 | 5664 | 2 | 0 | 2 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
c0013 | 0/0 | 5664 | 2 | 0 | 0 | 2 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
c0014 | 0/0 | 5664 | 2 | 0 | 0 | 2 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
c0015 | 0/0 | 5664 | 2 | 1 | 0 | 0 | 0 | 1 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
c0016 | 0/0 | 5664 | 2 | 2 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
c0017 | 0/0 | 5664 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
c0018 | 0/0 | 5664 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
c0019 | 0/0 | 5664 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
c0020 | 0/0 | 5664 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
c0021 | 0/0 | 5664 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
c0022 | 0/0 | 5664 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
c0023 | 0/0 | 5664 | 1 | 0 | 0 | 0 | 0 | 1 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
c0024 | 0/0 | 5664 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
c0025 | 0/0 | 5664 | 1 | 0 | 0 | 0 | 0 | 1 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
c0026 | 0/0 | 5664 | 1 | 0 | 0 | 0 | 1 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
c0027 | 0/0 | 5664 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
c0028 | 0/0 | 5664 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
c0029 | 0/0 | 5664 | 1 | 0 | 0 | 0 | 0 | 1 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
c0030 | 0/0 | 5664 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
c0031 | 0/0 | 5664 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
c0032 | 0/0 | 5664 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
c0033 | 0/0 | 5664 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
c0034 | 1/0 | 5664 | 1 | 0 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
c0035 | 0/0 | 5664 | 1 | 0 | 0 | 0 | 0 | 1 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
c0036 | 0/0 | 5664 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
c0037 | 0/0 | 5664 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
c0038 | 0/0 | 5664 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/0 | 1543 | 115 | 35 | 31 | 24 | 5 | 19 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
t0002 | 0/1 | 1543 | 110 | 6 | 22 | 63 | 6 | 12 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
t0003 | 0/0 | 1543 | 26 | 9 | 1 | 11 | 2 | 3 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
t0004 | 0/0 | 1543 | 26 | 0 | 3 | 23 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
t0005 | 0/0 | 1543 | 24 | 19 | 2 | 1 | 0 | 2 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
t0006 | 0/0 | 1543 | 8 | 8 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
t0007 | 0/0 | 1543 | 5 | 0 | 0 | 5 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
t0008 | 0/0 | 1543 | 3 | 3 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
t0009 | 0/0 | 1543 | 3 | 3 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
t0010 | 0/0 | 1543 | 3 | 0 | 0 | 3 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
t0011 | 0/0 | 1543 | 1 | 0 | 0 | 0 | 1 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
t0012 | 0/0 | 1543 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
t0013 | 0/0 | 1543 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0002 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0047 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0074 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0293 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0311 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 5664 | 101 | 9 | 19 | 55 | 6 | 11 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
a0001c0032 | 0/0 | 5664 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
a0001c0033 | 0/0 | 5664 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
a0001c0035 | 0/0 | 5664 | 1 | 0 | 0 | 0 | 0 | 1 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
a0001c0037 | 0/0 | 5664 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
a0002c0002 | 0/0 | 5664 | 83 | 16 | 16 | 43 | 3 | 5 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
a0002c0013 | 0/0 | 5664 | 2 | 0 | 0 | 2 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
a0002c0029 | 0/0 | 5664 | 1 | 0 | 0 | 0 | 0 | 1 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
a0003c0005 | 0/0 | 5664 | 16 | 15 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
a0003c0006 | 0/0 | 5664 | 14 | 10 | 1 | 1 | 0 | 2 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
a0003c0011 | 0/0 | 5664 | 2 | 2 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
a0003c0019 | 0/0 | 5664 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
a0004c0004 | 0/0 | 5664 | 26 | 7 | 1 | 13 | 2 | 3 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
a0004c0016 | 0/0 | 5664 | 2 | 2 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
a0004c0036 | 0/0 | 5664 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
a0005c0003 | 0/0 | 5664 | 29 | 4 | 10 | 4 | 1 | 10 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
a0006c0007 | 0/0 | 5664 | 14 | 6 | 7 | 0 | 1 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
a0006c0010 | 0/0 | 5664 | 2 | 2 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
a0007c0008 | 0/0 | 5664 | 4 | 0 | 1 | 3 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
a0008c0009 | 0/0 | 5664 | 3 | 3 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
a0009c0027 | 0/0 | 5664 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
a0009c0028 | 0/0 | 5664 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
a0009c0030 | 0/0 | 5664 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
a0010c0014 | 0/0 | 5664 | 2 | 0 | 0 | 2 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
a0011c0015 | 0/0 | 5664 | 2 | 1 | 0 | 0 | 0 | 1 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
a0012c0012 | 0/0 | 5664 | 2 | 0 | 2 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
a0013c0031 | 0/0 | 5664 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
a0014c0034 | 1/0 | 5664 | 1 | 0 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
a0015c0021 | 0/0 | 5664 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
a0016c0025 | 0/0 | 5664 | 1 | 0 | 0 | 0 | 0 | 1 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
a0017c0024 | 0/0 | 5664 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
a0018c0023 | 0/0 | 5664 | 1 | 0 | 0 | 0 | 0 | 1 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
a0019c0022 | 0/0 | 5664 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
a0020c0020 | 0/0 | 5664 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
a0021c0018 | 0/0 | 5664 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
a0022c0017 | 0/0 | 5664 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
a0023c0026 | 0/0 | 5664 | 1 | 0 | 0 | 0 | 1 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
a0024c0038 | 0/0 | 5664 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002 | 0/1 | 7206 | 98 | 6 | 19 | 55 | 6 | 11 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
a0001c0001t0009 | 0/0 | 7206 | 3 | 3 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
a0001c0032t0002 | 0/0 | 7206 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
a0001c0033t0002 | 0/0 | 7206 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
a0001c0035t0002 | 0/0 | 7206 | 1 | 0 | 0 | 0 | 0 | 1 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
a0001c0037t0002 | 0/0 | 7206 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
a0002c0002t0001 | 0/0 | 7206 | 56 | 16 | 14 | 18 | 3 | 5 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
a0002c0002t0004 | 0/0 | 7206 | 21 | 0 | 1 | 20 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
a0002c0002t0007 | 0/0 | 7206 | 5 | 0 | 0 | 5 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
a0002c0002t0012 | 0/0 | 7206 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
a0002c0013t0004 | 0/0 | 7206 | 2 | 0 | 0 | 2 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
a0002c0029t0001 | 0/0 | 7206 | 1 | 0 | 0 | 0 | 0 | 1 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
a0003c0005t0005 | 0/0 | 7206 | 16 | 15 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
a0003c0006t0005 | 0/0 | 7206 | 4 | 0 | 1 | 1 | 0 | 2 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
a0003c0006t0006 | 0/0 | 7206 | 7 | 7 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
a0003c0006t0008 | 0/0 | 7206 | 3 | 3 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
a0003c0011t0001 | 0/0 | 7206 | 2 | 2 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
a0003c0019t0013 | 0/0 | 7206 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
a0004c0004t0003 | 0/0 | 7206 | 23 | 7 | 1 | 10 | 2 | 3 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
a0004c0004t0010 | 0/0 | 7206 | 3 | 0 | 0 | 3 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
a0004c0016t0005 | 0/0 | 7206 | 2 | 2 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
a0004c0036t0003 | 0/0 | 7206 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
a0005c0003t0001 | 0/0 | 7206 | 29 | 4 | 10 | 4 | 1 | 10 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
a0006c0007t0001 | 0/0 | 7206 | 14 | 6 | 7 | 0 | 1 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
a0006c0010t0001 | 0/0 | 7206 | 2 | 2 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
a0007c0008t0002 | 0/0 | 7206 | 4 | 0 | 1 | 3 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
a0008c0009t0001 | 0/0 | 7206 | 3 | 3 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
a0009c0027t0003 | 0/0 | 7206 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
a0009c0028t0003 | 0/0 | 7206 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
a0009c0030t0005 | 0/0 | 7206 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
a0010c0014t0002 | 0/0 | 7206 | 2 | 0 | 0 | 2 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
a0011c0015t0001 | 0/0 | 7206 | 2 | 1 | 0 | 0 | 0 | 1 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
a0012c0012t0004 | 0/0 | 7206 | 2 | 0 | 2 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
a0013c0031t0001 | 0/0 | 7206 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
a0014c0034t0001 | 1/0 | 7206 | 1 | 0 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
a0015c0021t0001 | 0/0 | 7206 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
a0016c0025t0001 | 0/0 | 7206 | 1 | 0 | 0 | 0 | 0 | 1 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
a0017c0024t0002 | 0/0 | 7206 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
a0018c0023t0001 | 0/0 | 7206 | 1 | 0 | 0 | 0 | 0 | 1 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
a0019c0022t0004 | 0/0 | 7206 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
a0020c0020t0001 | 0/0 | 7206 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
a0021c0018t0006 | 0/0 | 7206 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
a0022c0017t0005 | 0/0 | 7206 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
a0023c0026t0011 | 0/0 | 7206 | 1 | 0 | 0 | 0 | 1 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
a0024c0038t0002 | 0/0 | 7206 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | copy fasta | chr3 | 13311235 | 13425322 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0001c0001t0002g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0001c0001t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0001c0001t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0001c0001t0002g0047 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0001c0001t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0001c0001t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0001c0001t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0001c0001t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0001c0001t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0001c0001t0002g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0001c0001t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0001c0001t0002g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0001c0001t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0001c0001t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0001c0001t0002g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0001c0001t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0001c0001t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0001c0001t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0001c0001t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0001c0001t0002g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0001c0001t0002g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0001c0001t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0001c0001t0009g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0001c0001t0009g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0001c0001t0009g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0001c0032t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0001c0033t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0001c0035t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0001c0037t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0002c0002t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0002c0002t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0002c0002t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0002c0002t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0002c0002t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0002c0002t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0002c0002t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0002c0002t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0002c0002t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0002c0002t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0002c0002t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0002c0002t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0002c0002t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0002c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0002c0002t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0002c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0002c0002t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0002c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0002c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0002c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0002c0002t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0002c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0002c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0002c0002t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0002c0002t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0002c0002t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0002c0002t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0002c0002t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0002c0002t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0002c0002t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0002c0002t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0002c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0002c0002t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0002c0002t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0002c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0002c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0002c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0002c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0002c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0002c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0002c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0002c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0002c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0002c0002t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0002c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0002c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0002c0002t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0002c0002t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0002c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0002c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0002c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0002c0002t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0002c0002t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0002c0002t0001g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0002c0002t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0002c0002t0001g0311 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0002c0002t0004g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0002c0002t0004g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0002c0002t0004g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0002c0002t0004g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0002c0002t0004g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0002c0002t0004g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0002c0002t0004g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0002c0002t0004g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0002c0002t0004g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0002c0002t0004g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0002c0002t0004g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0002c0002t0004g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0002c0002t0004g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0002c0002t0004g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0002c0002t0004g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0002c0002t0004g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0002c0002t0004g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0002c0002t0004g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0002c0002t0004g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0002c0002t0004g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0002c0002t0004g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0002c0002t0007g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0002c0002t0007g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0002c0002t0007g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0002c0002t0007g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0002c0002t0007g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0002c0002t0012g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0002c0013t0004g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0002c0013t0004g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0002c0029t0001g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0003c0005t0005g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0003c0005t0005g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0003c0005t0005g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0003c0005t0005g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0003c0005t0005g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0003c0005t0005g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0003c0005t0005g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0003c0005t0005g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0003c0005t0005g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0003c0005t0005g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0003c0005t0005g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0003c0005t0005g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0003c0005t0005g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0003c0005t0005g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0003c0005t0005g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0003c0005t0005g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0003c0006t0005g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0003c0006t0005g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0003c0006t0005g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0003c0006t0005g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0003c0006t0006g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0003c0006t0006g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0003c0006t0006g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0003c0006t0006g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0003c0006t0006g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0003c0006t0006g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0003c0006t0006g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0003c0006t0008g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0003c0006t0008g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0003c0006t0008g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0003c0011t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0003c0011t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0003c0019t0013g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0004c0004t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0004c0004t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0004c0004t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0004c0004t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0004c0004t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0004c0004t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0004c0004t0003g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0004c0004t0003g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0004c0004t0003g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0004c0004t0003g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0004c0004t0003g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0004c0004t0003g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0004c0004t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0004c0004t0003g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0004c0004t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0004c0004t0003g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0004c0004t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0004c0004t0003g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0004c0004t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0004c0004t0003g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0004c0004t0003g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0004c0004t0003g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0004c0004t0003g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0004c0004t0010g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0004c0004t0010g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0004c0004t0010g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0004c0016t0005g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0004c0016t0005g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0004c0036t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0005c0003t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0005c0003t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0005c0003t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0005c0003t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0005c0003t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0005c0003t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0005c0003t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0005c0003t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0005c0003t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0005c0003t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0005c0003t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0005c0003t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0005c0003t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0005c0003t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0005c0003t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0005c0003t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0005c0003t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0005c0003t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0005c0003t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0005c0003t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0005c0003t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0005c0003t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0005c0003t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0005c0003t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0005c0003t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0005c0003t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0005c0003t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0005c0003t0001g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0005c0003t0001g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0006c0007t0001g0002 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0006c0007t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0006c0007t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0006c0007t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0006c0007t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0006c0007t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0006c0007t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0006c0007t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0006c0007t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0006c0007t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0006c0007t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0006c0007t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0006c0007t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0006c0010t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0006c0010t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0007c0008t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0007c0008t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0007c0008t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0007c0008t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0008c0009t0001g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0008c0009t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0009c0027t0003g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0009c0028t0003g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0009c0030t0005g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0010c0014t0002g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0011c0015t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0011c0015t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0012c0012t0004g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0012c0012t0004g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0013c0031t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0014c0034t0001g0074 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0015c0021t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0016c0025t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0017c0024t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0018c0023t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0019c0022t0004g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0020c0020t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0021c0018t0006g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0022c0017t0005g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0023c0026t0011g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
a0024c0038t0002g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0002 | t0001 | g0311 | EUR | GBR | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0082 | EUR | GBR | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG00140 | hp1 | a0023 | c0026 | t0011 | g0290 | EUR | GBR | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG00140 | hp2 | a0006 | c0007 | t0001 | g0002 | EUR | GBR | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG00280 | hp1 | a0001 | c0001 | t0002 | g0099 | EUR | FIN | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG00280 | hp2 | a0002 | c0002 | t0001 | g0220 | EUR | FIN | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0062 | EUR | FIN | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG00323 | hp2 | a0002 | c0002 | t0001 | g0217 | EUR | FIN | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG00438 | hp1 | a0002 | c0002 | t0004 | g0205 | EAS | CHS | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0129 | EAS | CHS | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG00544 | hp1 | a0004 | c0004 | t0003 | g0182 | EAS | CHS | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG00544 | hp2 | a0002 | c0002 | t0001 | g0258 | EAS | CHS | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG00558 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | CHS | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG00558 | hp2 | a0002 | c0002 | t0004 | g0156 | EAS | CHS | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG00597 | hp1 | a0017 | c0024 | t0002 | g0275 | EAS | CHS | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0151 | EAS | CHS | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG00621 | hp1 | a0002 | c0002 | t0001 | g0249 | EAS | CHS | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG00621 | hp2 | a0007 | c0008 | t0002 | g0136 | EAS | CHS | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG00639 | hp1 | a0001 | c0032 | t0002 | g0109 | AMR | PUR | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG00639 | hp2 | a0006 | c0007 | t0001 | g0012 | AMR | PUR | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG00642 | hp1 | a0002 | c0002 | t0001 | g0226 | AMR | PUR | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG00642 | hp2 | a0005 | c0003 | t0001 | g0319 | AMR | PUR | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG00733 | hp1 | a0006 | c0007 | t0001 | g0002 | AMR | PUR | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG00733 | hp2 | a0002 | c0002 | t0001 | g0224 | AMR | PUR | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG00735 | hp1 | a0006 | c0007 | t0001 | g0014 | AMR | PUR | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG00735 | hp2 | a0005 | c0003 | t0001 | g0304 | AMR | PUR | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0111 | AMR | PUR | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG00741 | hp2 | a0002 | c0002 | t0001 | g0228 | AMR | PUR | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG01070 | hp1 | a0005 | c0003 | t0001 | g0301 | AMR | PUR | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG01070 | hp2 | a0001 | c0001 | t0002 | g0084 | AMR | PUR | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0083 | AMR | PUR | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG01071 | hp2 | a0005 | c0003 | t0001 | g0297 | AMR | PUR | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG01074 | hp1 | a0002 | c0002 | t0001 | g0225 | AMR | PUR | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG01074 | hp2 | a0005 | c0003 | t0001 | g0215 | AMR | PUR | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG01081 | hp1 | a0004 | c0004 | t0003 | g0192 | AMR | PUR | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG01081 | hp2 | a0005 | c0003 | t0001 | g0295 | AMR | PUR | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG01099 | hp1 | a0006 | c0007 | t0001 | g0013 | AMR | PUR | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG01099 | hp2 | a0002 | c0002 | t0001 | g0199 | AMR | PUR | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG01109 | hp1 | a0003 | c0005 | t0005 | g0029 | AMR | PUR | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG01109 | hp2 | a0002 | c0002 | t0001 | g0273 | AMR | PUR | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG01167 | hp1 | a0002 | c0002 | t0001 | g0222 | AMR | PUR | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG01167 | hp2 | a0001 | c0001 | t0002 | g0130 | AMR | PUR | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG01168 | hp1 | a0006 | c0007 | t0001 | g0010 | AMR | PUR | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG01168 | hp2 | a0001 | c0001 | t0002 | g0133 | AMR | PUR | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG01169 | hp1 | a0001 | c0001 | t0002 | g0086 | AMR | PUR | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG01169 | hp2 | a0002 | c0002 | t0001 | g0221 | AMR | PUR | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG01175 | hp1 | a0006 | c0007 | t0001 | g0011 | AMR | PUR | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG01175 | hp2 | a0006 | c0007 | t0001 | g0015 | AMR | PUR | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0135 | AMR | PUR | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG01243 | hp2 | a0003 | c0006 | t0005 | g0049 | AMR | PUR | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG01257 | hp1 | a0002 | c0002 | t0001 | g0223 | AMR | CLM | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG01257 | hp2 | a0005 | c0003 | t0001 | g0292 | AMR | CLM | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG01258 | hp1 | a0002 | c0002 | t0001 | g0227 | AMR | CLM | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0103 | AMR | CLM | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG01261 | hp1 | a0001 | c0037 | t0002 | g0112 | AMR | CLM | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG01261 | hp2 | a0005 | c0003 | t0001 | g0296 | AMR | CLM | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG01346 | hp1 | a0001 | c0001 | t0002 | g0042 | AMR | CLM | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0131 | AMR | CLM | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG01358 | hp1 | a0001 | c0001 | t0002 | g0146 | AMR | CLM | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG01358 | hp2 | a0005 | c0003 | t0001 | g0300 | AMR | CLM | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG01361 | hp1 | a0002 | c0002 | t0012 | g0307 | AMR | CLM | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG01361 | hp2 | a0001 | c0001 | t0002 | g0137 | AMR | CLM | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG01433 | hp1 | a0002 | c0002 | t0001 | g0310 | AMR | CLM | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG01433 | hp2 | a0002 | c0002 | t0001 | g0218 | AMR | CLM | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0110 | AMR | CLM | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG01496 | hp2 | a0007 | c0008 | t0002 | g0089 | AMR | CLM | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG01516 | hp1 | a0001 | c0001 | t0002 | g0067 | EUR | IBS | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG01516 | hp2 | a0004 | c0004 | t0003 | g0178 | EUR | IBS | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG01517 | hp1 | a0004 | c0004 | t0003 | g0180 | EUR | IBS | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG01517 | hp2 | a0005 | c0003 | t0001 | g0293 | EUR | IBS | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG01884 | hp1 | a0003 | c0005 | t0005 | g0026 | AFR | ACB | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG01884 | hp2 | a0001 | c0001 | t0009 | g0198 | AFR | ACB | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG01891 | hp1 | a0006 | c0007 | t0001 | g0040 | AFR | ACB | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG01891 | hp2 | a0002 | c0002 | t0001 | g0206 | AFR | ACB | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG01934 | hp1 | a0002 | c0002 | t0001 | g0230 | AMR | PEL | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG01934 | hp2 | a0001 | c0001 | t0002 | g0142 | AMR | PEL | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG01975 | hp1 | a0001 | c0001 | t0002 | g0087 | AMR | PEL | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG01975 | hp2 | a0012 | c0012 | t0004 | g0272 | AMR | PEL | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG01978 | hp1 | a0012 | c0012 | t0004 | g0318 | AMR | PEL | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0045 | AMR | PEL | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG01981 | hp1 | a0001 | c0001 | t0002 | g0094 | AMR | PEL | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG01981 | hp2 | a0002 | c0002 | t0001 | g0231 | AMR | PEL | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG01993 | hp1 | a0005 | c0003 | t0001 | g0216 | AMR | PEL | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG01993 | hp2 | a0001 | c0001 | t0002 | g0100 | AMR | PEL | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG02004 | hp1 | a0002 | c0002 | t0004 | g0320 | AMR | PEL | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG02004 | hp2 | a0001 | c0001 | t0002 | g0077 | AMR | PEL | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG02015 | hp1 | a0002 | c0002 | t0004 | g0289 | EAS | KHV | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG02015 | hp2 | a0001 | c0001 | t0002 | g0127 | EAS | KHV | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG02071 | hp1 | a0004 | c0004 | t0003 | g0107 | EAS | KHV | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG02071 | hp2 | a0004 | c0036 | t0003 | g0176 | EAS | KHV | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG02129 | hp1 | a0024 | c0038 | t0002 | g0321 | EAS | KHV | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG02129 | hp2 | a0001 | c0001 | t0002 | g0073 | EAS | KHV | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0070 | EAS | KHV | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG02132 | hp2 | a0001 | c0001 | t0002 | g0065 | EAS | KHV | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG02135 | hp1 | a0010 | c0014 | t0002 | g0003 | EAS | KHV | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG02135 | hp2 | a0003 | c0006 | t0005 | g0044 | EAS | KHV | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG02145 | hp1 | a0002 | c0002 | t0001 | g0162 | AFR | ACB | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG02145 | hp2 | a0006 | c0007 | t0001 | g0018 | AFR | ACB | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG02258 | hp1 | a0004 | c0004 | t0003 | g0170 | AFR | ACB | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG02258 | hp2 | a0001 | c0001 | t0009 | g0195 | AFR | ACB | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG02280 | hp1 | a0002 | c0002 | t0001 | g0201 | AFR | ACB | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG02280 | hp2 | a0003 | c0005 | t0005 | g0061 | AFR | ACB | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG02451 | hp1 | a0001 | c0001 | t0002 | g0141 | AFR | ACB | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG02451 | hp2 | a0005 | c0003 | t0001 | g0291 | AFR | ACB | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG02523 | hp1 | a0010 | c0014 | t0002 | g0003 | EAS | KHV | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG02523 | hp2 | a0002 | c0002 | t0004 | g0253 | EAS | KHV | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG02572 | hp1 | a0001 | c0001 | t0002 | g0157 | AFR | GWD | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG02572 | hp2 | a0003 | c0005 | t0005 | g0039 | AFR | GWD | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG02602 | hp1 | a0005 | c0003 | t0001 | g0298 | SAS | PJL | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0152 | SAS | PJL | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG02615 | hp1 | a0002 | c0002 | t0001 | g0203 | AFR | GWD | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG02615 | hp2 | a0008 | c0009 | t0001 | g0004 | AFR | GWD | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG02622 | hp1 | a0004 | c0016 | t0005 | g0191 | AFR | GWD | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG02622 | hp2 | a0003 | c0006 | t0006 | g0051 | AFR | GWD | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG02630 | hp1 | a0003 | c0005 | t0005 | g0025 | AFR | GWD | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG02630 | hp2 | a0004 | c0004 | t0003 | g0172 | AFR | GWD | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG02683 | hp1 | a0002 | c0002 | t0001 | g0229 | SAS | PJL | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG02683 | hp2 | a0001 | c0001 | t0002 | g0095 | SAS | PJL | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG02717 | hp1 | a0011 | c0015 | t0001 | g0197 | AFR | GWD | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG02717 | hp2 | a0003 | c0006 | t0006 | g0055 | AFR | GWD | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG02723 | hp1 | a0002 | c0002 | t0001 | g0269 | AFR | GWD | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG02723 | hp2 | a0009 | c0030 | t0005 | g0009 | AFR | GWD | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0154 | SAS | PJL | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG02738 | hp2 | a0001 | c0001 | t0002 | g0148 | SAS | PJL | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG02809 | hp1 | a0006 | c0010 | t0001 | g0016 | AFR | GWD | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG02809 | hp2 | a0001 | c0001 | t0002 | g0132 | AFR | GWD | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG02818 | hp1 | a0005 | c0003 | t0001 | g0302 | AFR | GWD | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG02818 | hp2 | a0004 | c0004 | t0003 | g0169 | AFR | GWD | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG02895 | hp1 | a0004 | c0004 | t0003 | g0187 | AFR | GWD | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG02895 | hp2 | a0003 | c0005 | t0005 | g0032 | AFR | GWD | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG02896 | hp1 | a0005 | c0003 | t0001 | g0306 | AFR | GWD | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG02896 | hp2 | a0003 | c0005 | t0005 | g0024 | AFR | GWD | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG02922 | hp1 | a0003 | c0011 | t0001 | g0036 | AFR | ESN | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG02922 | hp2 | a0004 | c0004 | t0003 | g0173 | AFR | ESN | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG02965 | hp1 | a0003 | c0006 | t0008 | g0005 | AFR | ESN | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG02965 | hp2 | a0006 | c0007 | t0001 | g0017 | AFR | ESN | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG02970 | hp1 | a0003 | c0005 | t0005 | g0030 | AFR | ESN | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG02970 | hp2 | a0008 | c0009 | t0001 | g0194 | AFR | ESN | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG02976 | hp1 | a0003 | c0006 | t0006 | g0058 | AFR | ESN | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG02976 | hp2 | a0003 | c0005 | t0005 | g0278 | AFR | ESN | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG03017 | hp1 | a0005 | c0003 | t0001 | g0281 | SAS | PJL | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG03017 | hp2 | a0002 | c0002 | t0001 | g0286 | SAS | PJL | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG03041 | hp1 | a0003 | c0005 | t0005 | g0028 | AFR | GWD | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG03041 | hp2 | a0002 | c0002 | t0001 | g0163 | AFR | GWD | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG03098 | hp1 | a0003 | c0019 | t0013 | g0164 | AFR | MSL | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG03098 | hp2 | a0003 | c0006 | t0006 | g0053 | AFR | MSL | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG03130 | hp1 | a0003 | c0005 | t0005 | g0060 | AFR | ESN | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG03130 | hp2 | a0003 | c0006 | t0008 | g0006 | AFR | ESN | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG03139 | hp1 | a0004 | c0004 | t0003 | g0174 | AFR | ESN | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG03139 | hp2 | a0008 | c0009 | t0001 | g0004 | AFR | ESN | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG03195 | hp1 | a0022 | c0017 | t0005 | g0057 | AFR | ESN | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG03195 | hp2 | a0002 | c0002 | t0001 | g0207 | AFR | ESN | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG03209 | hp1 | a0002 | c0002 | t0001 | g0257 | AFR | MSL | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG03209 | hp2 | a0003 | c0006 | t0008 | g0007 | AFR | MSL | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG03225 | hp1 | a0006 | c0007 | t0001 | g0305 | AFR | MSL | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG03225 | hp2 | a0002 | c0002 | t0001 | g0212 | AFR | MSL | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG03239 | hp1 | a0005 | c0003 | t0001 | g0241 | SAS | PJL | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG03239 | hp2 | a0001 | c0035 | t0002 | g0075 | SAS | PJL | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG03453 | hp1 | a0006 | c0010 | t0001 | g0020 | AFR | MSL | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG03453 | hp2 | a0003 | c0005 | t0005 | g0023 | AFR | MSL | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG03486 | hp1 | a0002 | c0002 | t0001 | g0161 | AFR | MSL | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG03486 | hp2 | a0003 | c0006 | t0006 | g0052 | AFR | MSL | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG03491 | hp1 | a0004 | c0004 | t0003 | g0188 | SAS | PJL | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG03491 | hp2 | a0005 | c0003 | t0001 | g0247 | SAS | PJL | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0069 | SAS | PJL | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG03492 | hp2 | a0004 | c0004 | t0003 | g0189 | SAS | PJL | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG03516 | hp1 | a0001 | c0001 | t0002 | g0116 | AFR | ESN | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG03516 | hp2 | a0003 | c0005 | t0005 | g0033 | AFR | ESN | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG03540 | hp1 | a0001 | c0001 | t0002 | g0043 | AFR | GWD | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG03540 | hp2 | a0003 | c0005 | t0005 | g0037 | AFR | GWD | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG03579 | hp1 | a0001 | c0001 | t0002 | g0106 | AFR | MSL | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG03579 | hp2 | a0002 | c0002 | t0001 | g0200 | AFR | MSL | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG03654 | hp1 | a0005 | c0003 | t0001 | g0299 | SAS | PJL | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG03654 | hp2 | a0002 | c0002 | t0001 | g0213 | SAS | PJL | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG03688 | hp1 | a0011 | c0015 | t0001 | g0098 | SAS | STU | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG03688 | hp2 | a0005 | c0003 | t0001 | g0256 | SAS | STU | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG03710 | hp1 | a0005 | c0003 | t0001 | g0245 | SAS | PJL | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0064 | SAS | PJL | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG03831 | hp1 | a0003 | c0006 | t0005 | g0046 | SAS | BEB | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG03831 | hp2 | a0005 | c0003 | t0001 | g0317 | SAS | BEB | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG03834 | hp1 | a0016 | c0025 | t0001 | g0232 | SAS | BEB | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0153 | SAS | BEB | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG03927 | hp1 | a0018 | c0023 | t0001 | g0177 | SAS | BEB | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG03927 | hp2 | a0003 | c0006 | t0005 | g0008 | SAS | BEB | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0113 | SAS | STU | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG04115 | hp2 | a0002 | c0002 | t0001 | g0308 | SAS | STU | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0080 | SAS | STU | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG04199 | hp2 | a0002 | c0029 | t0001 | g0315 | SAS | STU | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG04204 | hp1 | a0005 | c0003 | t0001 | g0234 | SAS | STU | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0041 | SAS | STU | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG04228 | hp1 | a0005 | c0003 | t0001 | g0294 | SAS | STU | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0101 | SAS | STU | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA18522 | hp1 | a0002 | c0002 | t0001 | g0160 | AFR | YRI | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA18522 | hp2 | a0004 | c0004 | t0003 | g0171 | AFR | YRI | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHB | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA18747 | hp2 | a0002 | c0002 | t0004 | g0252 | EAS | CHB | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA18906 | hp1 | a0002 | c0002 | t0001 | g0204 | AFR | YRI | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA18906 | hp2 | a0002 | c0002 | t0001 | g0210 | AFR | YRI | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA18939 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA18939 | hp2 | a0005 | c0003 | t0001 | g0242 | EAS | JPT | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA18942 | hp1 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA18942 | hp2 | a0002 | c0002 | t0004 | g0285 | EAS | JPT | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA18944 | hp1 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA18944 | hp2 | a0002 | c0002 | t0001 | g0235 | EAS | JPT | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA18945 | hp2 | a0001 | c0001 | t0002 | g0288 | EAS | JPT | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA18946 | hp1 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA18946 | hp2 | a0005 | c0003 | t0001 | g0238 | EAS | JPT | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA18950 | hp1 | a0007 | c0008 | t0002 | g0115 | EAS | JPT | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA18950 | hp2 | a0002 | c0002 | t0007 | g0264 | EAS | JPT | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA18953 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA18953 | hp2 | a0002 | c0002 | t0004 | g0254 | EAS | JPT | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA18954 | hp1 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA18954 | hp2 | a0002 | c0002 | t0001 | g0246 | EAS | JPT | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA18956 | hp1 | a0005 | c0003 | t0001 | g0268 | EAS | JPT | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA18956 | hp2 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA18959 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA18959 | hp2 | a0002 | c0002 | t0001 | g0244 | EAS | JPT | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA18961 | hp1 | a0013 | c0031 | t0001 | g0093 | EAS | JPT | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA18961 | hp2 | a0002 | c0002 | t0004 | g0260 | EAS | JPT | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA18962 | hp1 | a0005 | c0003 | t0001 | g0313 | EAS | JPT | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA18962 | hp2 | a0004 | c0004 | t0003 | g0165 | EAS | JPT | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA18964 | hp1 | a0002 | c0002 | t0001 | g0219 | EAS | JPT | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA18965 | hp1 | a0002 | c0002 | t0001 | g0243 | EAS | JPT | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA18965 | hp2 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA18966 | hp1 | a0002 | c0002 | t0004 | g0279 | EAS | JPT | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA18966 | hp2 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA18967 | hp1 | a0002 | c0002 | t0001 | g0237 | EAS | JPT | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA18967 | hp2 | a0004 | c0004 | t0003 | g0168 | EAS | JPT | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA18969 | hp1 | a0004 | c0004 | t0003 | g0175 | EAS | JPT | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA18969 | hp2 | a0002 | c0002 | t0007 | g0209 | EAS | JPT | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA18970 | hp1 | a0004 | c0004 | t0003 | g0179 | EAS | JPT | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA18970 | hp2 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA18973 | hp1 | a0002 | c0002 | t0001 | g0255 | EAS | JPT | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA18973 | hp2 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA18978 | hp1 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA18978 | hp2 | a0002 | c0002 | t0001 | g0211 | EAS | JPT | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA18981 | hp1 | a0001 | c0001 | t0002 | g0144 | EAS | JPT | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA18981 | hp2 | a0002 | c0002 | t0004 | g0312 | EAS | JPT | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA18983 | hp1 | a0004 | c0004 | t0003 | g0108 | EAS | JPT | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA18983 | hp2 | a0001 | c0033 | t0002 | g0266 | EAS | JPT | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA18984 | hp1 | a0004 | c0004 | t0003 | g0166 | EAS | JPT | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA18984 | hp2 | a0002 | c0002 | t0001 | g0208 | EAS | JPT | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA18988 | hp1 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA18988 | hp2 | a0004 | c0004 | t0003 | g0185 | EAS | JPT | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA18992 | hp1 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA18992 | hp2 | a0002 | c0002 | t0007 | g0309 | EAS | JPT | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA18993 | hp1 | a0002 | c0002 | t0004 | g0250 | EAS | JPT | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA18993 | hp2 | a0004 | c0004 | t0010 | g0186 | EAS | JPT | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA18994 | hp1 | a0002 | c0002 | t0001 | g0282 | EAS | JPT | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA18994 | hp2 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA18995 | hp1 | a0004 | c0004 | t0003 | g0167 | EAS | JPT | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA18995 | hp2 | a0002 | c0002 | t0004 | g0038 | EAS | JPT | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA18998 | hp1 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA18998 | hp2 | a0001 | c0001 | t0002 | g0274 | EAS | JPT | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA18999 | hp1 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA18999 | hp2 | a0002 | c0002 | t0004 | g0251 | EAS | JPT | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA19000 | hp1 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA19000 | hp2 | a0002 | c0002 | t0001 | g0239 | EAS | JPT | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA19002 | hp1 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA19002 | hp2 | a0001 | c0001 | t0002 | g0276 | EAS | JPT | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA19004 | hp1 | a0002 | c0002 | t0001 | g0277 | EAS | JPT | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA19004 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA19005 | hp1 | a0002 | c0002 | t0004 | g0316 | EAS | JPT | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA19005 | hp2 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA19009 | hp2 | a0004 | c0004 | t0010 | g0184 | EAS | JPT | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA19010 | hp1 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA19010 | hp2 | a0002 | c0002 | t0004 | g0259 | EAS | JPT | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA19012 | hp1 | a0002 | c0002 | t0007 | g0314 | EAS | JPT | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA19012 | hp2 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA19030 | hp1 | a0003 | c0005 | t0005 | g0031 | AFR | LWK | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA19030 | hp2 | a0003 | c0011 | t0001 | g0035 | AFR | LWK | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA19043 | hp1 | a0006 | c0007 | t0001 | g0021 | AFR | LWK | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA19043 | hp2 | a0009 | c0028 | t0003 | g0034 | AFR | LWK | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA19056 | hp1 | a0002 | c0002 | t0004 | g0261 | EAS | JPT | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA19056 | hp2 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA19058 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA19058 | hp2 | a0004 | c0004 | t0010 | g0181 | EAS | JPT | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA19060 | hp1 | a0002 | c0013 | t0004 | g0233 | EAS | JPT | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA19060 | hp2 | a0007 | c0008 | t0002 | g0091 | EAS | JPT | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA19062 | hp1 | a0002 | c0002 | t0004 | g0270 | EAS | JPT | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA19062 | hp2 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA19064 | hp1 | a0019 | c0022 | t0004 | g0271 | EAS | JPT | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA19064 | hp2 | a0001 | c0001 | t0002 | g0138 | EAS | JPT | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA19066 | hp1 | a0002 | c0002 | t0004 | g0262 | EAS | JPT | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA19066 | hp2 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA19067 | hp1 | a0002 | c0002 | t0001 | g0263 | EAS | JPT | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA19067 | hp2 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA19070 | hp1 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA19070 | hp2 | a0001 | c0001 | t0002 | g0265 | EAS | JPT | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA19074 | hp1 | a0002 | c0002 | t0001 | g0248 | EAS | JPT | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA19074 | hp2 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA19077 | hp1 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA19077 | hp2 | a0002 | c0013 | t0004 | g0240 | EAS | JPT | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA19079 | hp1 | a0002 | c0002 | t0001 | g0280 | EAS | JPT | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA19079 | hp2 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA19081 | hp1 | a0002 | c0002 | t0004 | g0287 | EAS | JPT | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA19081 | hp2 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA19082 | hp1 | a0015 | c0021 | t0001 | g0267 | EAS | JPT | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA19082 | hp2 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA19084 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA19084 | hp2 | a0002 | c0002 | t0004 | g0283 | EAS | JPT | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA19090 | hp1 | a0002 | c0002 | t0007 | g0236 | EAS | JPT | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA19090 | hp2 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA19091 | hp1 | a0002 | c0002 | t0001 | g0284 | EAS | JPT | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA19091 | hp2 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA19240 | hp1 | a0006 | c0007 | t0001 | g0022 | AFR | YRI | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA19240 | hp2 | a0004 | c0016 | t0005 | g0190 | AFR | YRI | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0048 | EUR | TSI | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0159 | EUR | TSI | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA20905 | hp1 | a0002 | c0002 | t0001 | g0214 | SAS | GIH | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA20905 | hp2 | a0004 | c0004 | t0003 | g0183 | SAS | GIH | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG02486 | hp1 | a0003 | c0006 | t0006 | g0059 | AFR | ACB | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG02486 | hp2 | a0005 | c0003 | t0001 | g0303 | AFR | ACB | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG02559 | hp1 | a0003 | c0006 | t0006 | g0056 | AFR | ACB | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG02559 | hp2 | a0009 | c0027 | t0003 | g0019 | AFR | ACB | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG03471 | hp1 | a0002 | c0002 | t0001 | g0050 | AFR | MSL | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG03471 | hp2 | a0020 | c0020 | t0001 | g0193 | AFR | MSL | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG06807 | hp1 | a0021 | c0018 | t0006 | g0054 | AFR | USA | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
HG06807 | hp2 | a0001 | c0001 | t0009 | g0196 | AFR | USA | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA20300 | hp1 | a0003 | c0005 | t0005 | g0027 | AFR | USA | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
NA20300 | hp2 | a0002 | c0002 | t0001 | g0202 | AFR | USA | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0047 | REF | REF | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
homoSapiens_grch38 | hp1 | a0014 | c0034 | t0001 | g0074 | REF | REF | NUP210_chr3_13311235_13425322 | NUP210 | chr3 | 13311235 | 13425322 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:13319787
|
C | T | 12 | a0001a0003a0004others(9): Show | 184 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(181): Show |
missense_variant | MODERATE | c.5359G>A | p.Val1787Met | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 37/40 | 5455/7206 | 5359/5664 | 1787/1887 | chr3 | 13319787 | ||
chr3:13319891
|
A | G | 19 | a0001a0002a0003others(16): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(290): Show |
missense_variant | MODERATE | c.5255T>C | p.Leu1752Ser | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 37/40 | 5351/7206 | 5255/5664 | 1752/1887 | chr3 | 13319891 | ||
chr3:13319903
|
G | A | 1 | a0015 | 1 | NA19082.hp1 | missense_variant | MODERATE | c.5243C>T | p.Thr1748Met | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 37/40 | 5339/7206 | 5243/5664 | 1748/1887 | chr3 | 13319903 | ||
chr3:13321602
|
C | T | 1 | a0022 | 1 | HG03195.hp1 | missense_variant | MODERATE | c.5149G>A | p.Val1717Ile | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 36/40 | 5245/7206 | 5149/5664 | 1717/1887 | chr3 | 13321602 | ||
chr3:13323410
|
C | A | 1 | a0021 | 1 | HG06807.hp1 | missense_variant | MODERATE | c.4667G>T | p.Arg1556Met | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 34/40 | 4763/7206 | 4667/5664 | 1556/1887 | chr3 | 13323410 | ||
chr3:13325857
|
G | A | 1 | a0012 | 2 | HG01975.hp2 HG01978.hp1 |
missense_variant | MODERATE | c.4582C>T | p.Arg1528Trp | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 33/40 | 4678/7206 | 4582/5664 | 1528/1887 | chr3 | 13325857 | ||
chr3:13325902
|
T | C | 1 | a0010 | 2 | HG02135.hp1 HG02523.hp1 |
missense_variant | MODERATE | c.4537A>G | p.Asn1513Asp | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 33/40 | 4633/7206 | 4537/5664 | 1513/1887 | chr3 | 13325902 | ||
chr3:13330470
|
A | G | 1 | a0020 | 1 | HG03471.hp2 | missense_variant | MODERATE | c.4100T>C | p.Val1367Ala | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 30/40 | 4196/7206 | 4100/5664 | 1367/1887 | chr3 | 13330470 | ||
chr3:13330531
|
C | T | 1 | a0018 | 1 | HG03927.hp1 | missense_variant | MODERATE | c.4039G>A | p.Gly1347Arg | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 30/40 | 4135/7206 | 4039/5664 | 1347/1887 | chr3 | 13330531 | ||
chr3:13339919
|
C | T | 1 | a0023 | 1 | HG00140.hp1 | missense_variant | MODERATE | c.3406G>A | p.Gly1136Ser | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 25/40 | 3502/7206 | 3406/5664 | 1136/1887 | chr3 | 13339919 | ||
chr3:13340018
|
C | T | 1 | a0019 | 1 | NA19064.hp1 | missense_variant | MODERATE | c.3307G>A | p.Gly1103Ser | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 25/40 | 3403/7206 | 3307/5664 | 1103/1887 | chr3 | 13340018 | ||
chr3:13340239
|
C | T | 1 | a0015 | 1 | NA19082.hp1 | missense_variant | MODERATE | c.3288G>A | p.Met1096Ile | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 24/40 | 3384/7206 | 3288/5664 | 1096/1887 | chr3 | 13340239 | ||
chr3:13342096
|
A | G | 1 | a0008 | 3 | HG02615.hp2 HG02970.hp2 HG03139.hp2 |
missense_variant | MODERATE | c.2992T>C | p.Tyr998His | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 22/40 | 3088/7206 | 2992/5664 | 998/1887 | chr3 | 13342096 | ||
chr3:13343248
|
A | G | 2 | a0007a0013 | 5 | HG00621.hp2 HG01496.hp2 NA18950.hp1 others(2): Show |
missense_variant | MODERATE | c.2891T>C | p.Val964Ala | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 21/40 | 2987/7206 | 2891/5664 | 964/1887 | chr3 | 13343248 | ||
chr3:13353975
|
G | C | 7 | a0002a0012a0015others(4): Show | 93 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(90): Show |
missense_variant | MODERATE | c.2461C>G | p.Pro821Ala | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 17/40 | 2557/7206 | 2461/5664 | 821/1887 | chr3 | 13353975 | ||
chr3:13354079
|
C | A | 17 | a0002a0003a0004others(14): Show | 210 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(207): Show |
missense_variant | MODERATE | c.2357G>T | p.Arg786Leu | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 17/40 | 2453/7206 | 2357/5664 | 786/1887 | chr3 | 13354079 | ||
chr3:13358286
|
G | A | 4 | a0005a0006a0009others(1): Show | 49 | HG00140.hp1 HG00140.hp2 HG00639.hp2 others(46): Show |
missense_variant | MODERATE | c.2264C>T | p.Ala755Val | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 16/40 | 2360/7206 | 2264/5664 | 755/1887 | chr3 | 13358286 | ||
chr3:13366056
|
T | C | 17 | a0002a0003a0004others(14): Show | 210 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(207): Show |
missense_variant | MODERATE | c.1822A>G | p.Ile608Val | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 14/40 | 1918/7206 | 1822/5664 | 608/1887 | chr3 | 13366056 | ||
chr3:13379650
|
C | T | 15 | a0002a0003a0005others(12): Show | 178 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(175): Show |
missense_variant | MODERATE | c.889G>A | p.Ala297Thr | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 7/40 | 985/7206 | 889/5664 | 297/1887 | chr3 | 13379650 | ||
chr3:13420145
|
G | C | 1 | a0024 | 1 | HG02129.hp1 | missense_variant | MODERATE | c.82C>G | p.Leu28Val | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/40 | 178/7206 | 82/5664 | 28/1887 | chr3 | 13420145 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:13319091
|
G | A | 1 | a0001c0033 | 1 | NA18983.hp2 | synonymous_variant | LOW | c.5544C>T | p.Ser1848Ser | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 39/40 | 5640/7206 | 5544/5664 | 1848/1887 | chr3 | 13319091 | ||
chr3:13321714
|
C | T | 1 | a0008c0009 | 3 | HG02615.hp2 HG02970.hp2 HG03139.hp2 |
synonymous_variant | LOW | c.5037G>A | p.Glu1679Glu | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 36/40 | 5133/7206 | 5037/5664 | 1679/1887 | chr3 | 13321714 | ||
chr3:13323376
|
G | T | 19 | a0001c0001a0001c0032a0001c0033others(16): Show | 164 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(161): Show |
synonymous_variant | LOW | c.4701C>A | p.Thr1567Thr | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 34/40 | 4797/7206 | 4701/5664 | 1567/1887 | chr3 | 13323376 | ||
chr3:13325906
|
C | T | 13 | a0001c0001a0001c0032a0001c0033others(10): Show | 142 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(139): Show |
synonymous_variant | LOW | c.4533G>A | p.Ser1511Ser | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 33/40 | 4629/7206 | 4533/5664 | 1511/1887 | chr3 | 13325906 | ||
chr3:13327221
|
C | T | 1 | a0001c0032 | 1 | HG00639.hp1 | synonymous_variant | LOW | c.4503G>A | p.Leu1501Leu | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 32/40 | 4599/7206 | 4503/5664 | 1501/1887 | chr3 | 13327221 | ||
chr3:13327224
|
G | A | 1 | a0008c0009 | 3 | HG02615.hp2 HG02970.hp2 HG03139.hp2 |
synonymous_variant | LOW | c.4500C>T | p.Ser1500Ser | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 32/40 | 4596/7206 | 4500/5664 | 1500/1887 | chr3 | 13327224 | ||
chr3:13327323
|
C | T | 1 | a0003c0011 | 2 | HG02922.hp1 NA19030.hp2 |
synonymous_variant | LOW | c.4401G>A | p.Ser1467Ser | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 32/40 | 4497/7206 | 4401/5664 | 1467/1887 | chr3 | 13327323 | ||
chr3:13327392
|
G | A | 17 | a0002c0002a0002c0013a0002c0029others(14): Show | 145 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(142): Show |
synonymous_variant | LOW | c.4332C>T | p.Cys1444Cys | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 32/40 | 4428/7206 | 4332/5664 | 1444/1887 | chr3 | 13327392 | ||
chr3:13337900
|
C | T | 22 | a0002c0002a0002c0013a0002c0029others(19): Show | 176 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(173): Show |
synonymous_variant | LOW | c.3489G>A | p.Glu1163Glu | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 26/40 | 3585/7206 | 3489/5664 | 1163/1887 | chr3 | 13337900 | ||
chr3:13339926
|
G | A | 1 | a0004c0036 | 1 | HG02071.hp2 | synonymous_variant | LOW | c.3399C>T | p.Ile1133Ile | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 25/40 | 3495/7206 | 3399/5664 | 1133/1887 | chr3 | 13339926 | ||
chr3:13342040
|
A | G | 27 | a0002c0002a0002c0013a0002c0029others(24): Show | 210 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(207): Show |
synonymous_variant | LOW | c.3048T>C | p.Phe1016Phe | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 22/40 | 3144/7206 | 3048/5664 | 1016/1887 | chr3 | 13342040 | ||
chr3:13352131
|
G | A | 1 | a0002c0013 | 2 | NA19060.hp1 NA19077.hp2 |
synonymous_variant | LOW | c.2682C>T | p.Asp894Asp | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 19/40 | 2778/7206 | 2682/5664 | 894/1887 | chr3 | 13352131 | ||
chr3:13354039
|
G | A | 1 | a0001c0035 | 1 | HG03239.hp2 | synonymous_variant | LOW | c.2397C>T | p.Phe799Phe | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 17/40 | 2493/7206 | 2397/5664 | 799/1887 | chr3 | 13354039 | ||
chr3:13371871
|
G | A | 1 | a0001c0037 | 1 | HG01261.hp1 | synonymous_variant | LOW | c.1749C>T | p.Val583Val | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 13/40 | 1845/7206 | 1749/5664 | 583/1887 | chr3 | 13371871 | ||
chr3:13371892
|
G | A | 1 | a0009c0028 | 1 | NA19043.hp2 | synonymous_variant | LOW | c.1728C>T | p.Cys576Cys | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 13/40 | 1824/7206 | 1728/5664 | 576/1887 | chr3 | 13371892 | ||
chr3:13376318
|
G | A | 1 | a0008c0009 | 3 | HG02615.hp2 HG02970.hp2 HG03139.hp2 |
synonymous_variant | LOW | c.1266C>T | p.Asp422Asp | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 10/40 | 1362/7206 | 1266/5664 | 422/1887 | chr3 | 13376318 | ||
chr3:13377498
|
G | A | 1 | a0008c0009 | 3 | HG02615.hp2 HG02970.hp2 HG03139.hp2 |
synonymous_variant | LOW | c.1110C>T | p.Ile370Ile | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 9/40 | 1206/7206 | 1110/5664 | 370/1887 | chr3 | 13377498 | ||
chr3:13377522
|
G | A | 2 | a0002c0029a0009c0030 | 2 | HG02723.hp2 HG04199.hp2 |
synonymous_variant | LOW | c.1086C>T | p.Thr362Thr | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 9/40 | 1182/7206 | 1086/5664 | 362/1887 | chr3 | 13377522 | ||
chr3:13388345
|
C | T | 1 | a0006c0010 | 2 | HG02809.hp1 HG03453.hp1 |
synonymous_variant | LOW | c.642G>A | p.Gly214Gly | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 5/40 | 738/7206 | 642/5664 | 214/1887 | chr3 | 13388345 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:13316403
|
C | T | 1 | a0002c0002t0012 | 1 | HG01361.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1278G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 40/40 | 1278 | chr3 | 13316403 | |||||
chr3:13316441
|
C | A | 1 | a0003c0019t0013 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1240G>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 40/40 | 1240 | chr3 | 13316441 | |||||
chr3:13316444
|
A | G | 1 | a0023c0026t0011 | 1 | HG00140.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1237T>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 40/40 | 1237 | chr3 | 13316444 | |||||
chr3:13316486
|
A | G | 23 | a0001c0001t0002a0001c0001t0009a0001c0032t0002others(20): Show | 177 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(174): Show |
3_prime_UTR_variant | MODIFIER | c.*1195T>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 40/40 | 1195 | chr3 | 13316486 | |||||
chr3:13316505
|
G | A | 1 | a0003c0019t0013 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1176C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 40/40 | 1176 | chr3 | 13316505 | |||||
chr3:13316630
|
C | T | 17 | a0001c0001t0002a0001c0001t0009a0001c0032t0002others(14): Show | 150 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(147): Show |
3_prime_UTR_variant | MODIFIER | c.*1051G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 40/40 | 1051 | chr3 | 13316630 | |||||
chr3:13316671
|
T | G | 15 | a0001c0001t0002a0001c0001t0009a0001c0032t0002others(12): Show | 142 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(139): Show |
3_prime_UTR_variant | MODIFIER | c.*1010A>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 40/40 | 1010 | chr3 | 13316671 | |||||
chr3:13316704
|
G | A | 10 | a0001c0001t0002a0001c0001t0009a0001c0032t0002others(7): Show | 113 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(110): Show |
3_prime_UTR_variant | MODIFIER | c.*977C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 40/40 | 977 | chr3 | 13316704 | |||||
chr3:13316934
|
C | T | 1 | a0004c0004t0010 | 3 | NA18993.hp2 NA19009.hp2 NA19058.hp2 |
3_prime_UTR_variant | MODIFIER | c.*747G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 40/40 | 747 | chr3 | 13316934 | |||||
chr3:13316937
|
G | A | 1 | a0002c0002t0007 | 5 | NA18950.hp2 NA18969.hp2 NA18992.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*744C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 40/40 | 744 | chr3 | 13316937 | |||||
chr3:13317272
|
C | T | 1 | a0001c0001t0009 | 3 | HG01884.hp2 HG02258.hp2 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*409G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 40/40 | 409 | chr3 | 13317272 | |||||
chr3:13317316
|
T | A | 4 | a0002c0002t0004a0002c0013t0004a0012c0012t0004others(1): Show | 26 | HG00438.hp1 HG00558.hp2 HG01975.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*365A>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 40/40 | 365 | chr3 | 13317316 | |||||
chr3:13420316
|
A | G | 1 | a0003c0006t0008 | 3 | HG02965.hp1 HG03130.hp2 HG03209.hp2 |
5_prime_UTR_variant | MODIFIER | c.-90T>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/40 | 90 | chr3 | 13420316 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:13317789
|
G | A | 10 | a0003c0006t0006g0051a0003c0006t0006g0052a0003c0006t0006g0053others(7): Show | 11 | HG02486.hp1 HG02559.hp1 HG02615.hp2 others(8): Show |
splice_region_variant&intron_variant | LOW | c.5564-8C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 39/39 | chr3 | 13317789 | ||||||
chr3:13317827
|
C | T | 3 | a0006c0007t0001g0018a0006c0010t0001g0016a0006c0010t0001g0020 | 3 | HG02145.hp2 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.5564-46G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 39/39 | chr3 | 13317827 | ||||||
chr3:13317933
|
G | A | 139 | a0001c0001t0002g0001a0001c0001t0002g0041a0001c0001t0002g0042others(136): Show | 142 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.5564-152C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 39/39 | chr3 | 13317933 | ||||||
chr3:13317971
|
C | T | 1 | a0012c0012t0004g0272 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.5564-190G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 39/39 | chr3 | 13317971 | ||||||
chr3:13318105
|
C | T | 1 | a0009c0028t0003g0034 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.5564-324G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 39/39 | chr3 | 13318105 | ||||||
chr3:13318120
|
C | T | 1 | a0022c0017t0005g0057 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.5564-339G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 39/39 | chr3 | 13318120 | ||||||
chr3:13318163
|
C | T | 1 | a0003c0005t0005g0031 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.5564-382G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 39/39 | chr3 | 13318163 | ||||||
chr3:13318215
|
G | A | 1 | a0001c0001t0002g0144 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.5564-434C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 39/39 | chr3 | 13318215 | ||||||
chr3:13318299
|
C | T | 1 | a0001c0001t0002g0148 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.5564-518G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 39/39 | chr3 | 13318299 | ||||||
chr3:13318436
|
C | T | 2 | a0008c0009t0001g0004a0008c0009t0001g0194 | 3 | HG02615.hp2 HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.5563+636G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 39/39 | chr3 | 13318436 | ||||||
chr3:13318498
|
G | C | 4 | a0003c0006t0005g0008a0003c0006t0005g0044a0003c0006t0005g0046others(1): Show | 4 | HG01243.hp2 HG02135.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.5563+574C>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 39/39 | chr3 | 13318498 | ||||||
chr3:13318636
|
G | A | 1 | a0004c0036t0003g0176 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.5563+436C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 39/39 | chr3 | 13318636 | ||||||
chr3:13318735
|
G | T | 3 | a0005c0003t0001g0234a0005c0003t0001g0241a0005c0003t0001g0256 | 3 | HG03239.hp1 HG03688.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.5563+337C>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 39/39 | chr3 | 13318735 | ||||||
chr3:13318788
|
T | G | 273 | a0001c0001t0002g0001a0001c0001t0002g0041a0001c0001t0002g0042others(270): Show | 277 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.5563+284A>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 39/39 | chr3 | 13318788 | ||||||
chr3:13319013
|
C | T | 110 | a0001c0001t0002g0001a0001c0001t0002g0041a0001c0001t0002g0042others(107): Show | 113 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.5563+59G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 39/39 | chr3 | 13319013 | ||||||
chr3:13319063
|
G | C | 1 | a0001c0001t0002g0148 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.5563+9C>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 39/39 | chr3 | 13319063 | ||||||
chr3:13319199
|
A | G | 1 | a0002c0002t0004g0316 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.5479+31T>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 38/39 | chr3 | 13319199 | ||||||
chr3:13319214
|
C | T | 8 | a0003c0006t0006g0051a0003c0006t0006g0052a0003c0006t0006g0053others(5): Show | 8 | HG02486.hp1 HG02559.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.5479+16G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 38/39 | chr3 | 13319214 | ||||||
chr3:13319517
|
T | C | 1 | a0002c0002t0001g0226 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.5384-192A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 37/39 | chr3 | 13319517 | ||||||
chr3:13319540
|
A | AGAG | 180 | a0001c0001t0002g0001a0001c0001t0002g0041a0001c0001t0002g0042others(177): Show | 184 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.5384-218_5384-216d others(5): Show |
NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 37/39 | chr3 | 13319540 | ||||||
chr3:13319667
|
T | C | 1 | a0005c0003t0001g0296 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.5383+96A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 37/39 | chr3 | 13319667 | ||||||
chr3:13319680
|
A | G | 1 | a0005c0003t0001g0292 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.5383+83T>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 37/39 | chr3 | 13319680 | ||||||
chr3:13319738
|
C | T | 176 | a0001c0001t0002g0001a0001c0001t0002g0041a0001c0001t0002g0042others(173): Show | 180 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.5383+25G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 37/39 | chr3 | 13319738 | ||||||
chr3:13320063
|
G | A | 10 | a0002c0002t0004g0156a0002c0002t0004g0250a0002c0002t0004g0251others(7): Show | 10 | HG00558.hp2 NA18747.hp2 NA18942.hp2 others(7): Show |
intron_variant | MODIFIER | c.5167-84C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 36/39 | chr3 | 13320063 | ||||||
chr3:13320220
|
C | G | 274 | a0001c0001t0002g0001a0001c0001t0002g0041a0001c0001t0002g0042others(271): Show | 278 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.5167-241G>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 36/39 | chr3 | 13320220 | ||||||
chr3:13320359
|
C | A | 1 | a0020c0020t0001g0193 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.5167-380G>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 36/39 | chr3 | 13320359 | ||||||
chr3:13320359
|
C | T | 2 | a0008c0009t0001g0004a0008c0009t0001g0194 | 3 | HG02615.hp2 HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.5167-380G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 36/39 | chr3 | 13320359 | ||||||
chr3:13320429
|
C | T | 8 | a0001c0001t0002g0062a0001c0001t0002g0064a0001c0001t0002g0086others(5): Show | 8 | HG00323.hp1 HG01167.hp2 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.5167-450G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 36/39 | chr3 | 13320429 | ||||||
chr3:13320584
|
G | C | 8 | a0003c0006t0006g0051a0003c0006t0006g0052a0003c0006t0006g0053others(5): Show | 8 | HG02486.hp1 HG02559.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.5167-605C>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 36/39 | chr3 | 13320584 | ||||||
chr3:13320632
|
C | CA | 149 | a0001c0001t0002g0001a0001c0001t0002g0041a0001c0001t0002g0042others(146): Show | 152 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.5167-654dupT | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 36/39 | chr3 | 13320632 | ||||||
chr3:13320632
|
C | CAA | 7 | a0001c0001t0002g0092a0001c0001t0002g0095a0001c0001t0002g0116others(4): Show | 7 | HG02071.hp2 HG02559.hp2 HG02683.hp2 others(4): Show |
intron_variant | MODIFIER | c.5167-655_5167-654d others(4): Show |
NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 36/39 | chr3 | 13320632 | ||||||
chr3:13320632
|
CA | C | 12 | a0002c0002t0001g0207a0002c0002t0001g0223a0003c0006t0005g0008others(9): Show | 12 | HG01243.hp2 HG01257.hp1 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.5167-654delT | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 36/39 | chr3 | 13320632 | ||||||
chr3:13320891
|
C | CA | 169 | a0001c0001t0002g0001a0001c0001t0002g0041a0001c0001t0002g0042others(166): Show | 173 | HG00099.hp2 HG00280.hp1 HG00438.hp2 others(170): Show |
intron_variant | MODIFIER | c.5166+693dupT | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 36/39 | chr3 | 13320891 | ||||||
chr3:13320891
|
C | CAA | 6 | a0001c0001t0002g0148a0001c0032t0002g0109a0003c0006t0005g0044others(3): Show | 6 | HG00639.hp1 HG02135.hp2 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.5166+692_5166+693d others(4): Show |
NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 36/39 | chr3 | 13320891 | ||||||
chr3:13320956
|
G | T | 11 | a0003c0006t0005g0008a0003c0006t0005g0044a0003c0006t0005g0046others(8): Show | 11 | HG01243.hp2 HG02135.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.5166+629C>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 36/39 | chr3 | 13320956 | ||||||
chr3:13320974
|
C | T | 2 | a0003c0011t0001g0035a0003c0011t0001g0036 | 2 | HG02922.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.5166+611G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 36/39 | chr3 | 13320974 | ||||||
chr3:13320979
|
A | C | 11 | a0003c0006t0005g0008a0003c0006t0005g0044a0003c0006t0005g0046others(8): Show | 11 | HG01243.hp2 HG02135.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.5166+606T>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 36/39 | chr3 | 13320979 | ||||||
chr3:13320989
|
C | T | 1 | a0022c0017t0005g0057 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.5166+596G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 36/39 | chr3 | 13320989 | ||||||
chr3:13321007
|
G | C | 2 | a0008c0009t0001g0004a0008c0009t0001g0194 | 3 | HG02615.hp2 HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.5166+578C>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 36/39 | chr3 | 13321007 | ||||||
chr3:13321047
|
G | A | 2 | a0008c0009t0001g0004a0008c0009t0001g0194 | 3 | HG02615.hp2 HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.5166+538C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 36/39 | chr3 | 13321047 | ||||||
chr3:13321110
|
C | T | 2 | a0008c0009t0001g0004a0008c0009t0001g0194 | 3 | HG02615.hp2 HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.5166+475G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 36/39 | chr3 | 13321110 | ||||||
chr3:13321243
|
C | T | 1 | a0002c0002t0001g0206 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.5166+342G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 36/39 | chr3 | 13321243 | ||||||
chr3:13321291
|
G | A | 2 | a0003c0006t0008g0006a0003c0006t0008g0007 | 2 | HG03130.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.5166+294C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 36/39 | chr3 | 13321291 | ||||||
chr3:13321375
|
G | A | 3 | a0002c0002t0001g0204a0002c0002t0001g0231a0002c0002t0001g0257 | 3 | HG01981.hp2 HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.5166+210C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 36/39 | chr3 | 13321375 | ||||||
chr3:13321399
|
G | A | 20 | a0002c0002t0001g0208a0002c0002t0001g0235a0002c0002t0001g0237others(17): Show | 20 | HG00099.hp1 HG00544.hp2 HG00621.hp1 others(17): Show |
intron_variant | MODIFIER | c.5166+186C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 36/39 | chr3 | 13321399 | ||||||
chr3:13321513
|
T | C | 2 | a0003c0011t0001g0035a0003c0011t0001g0036 | 2 | HG02922.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.5166+72A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 36/39 | chr3 | 13321513 | ||||||
chr3:13321840
|
G | A | 2 | a0008c0009t0001g0004a0008c0009t0001g0194 | 3 | HG02615.hp2 HG02970.hp2 HG03139.hp2 |
splice_region_variant&intron_variant | LOW | c.4916-5C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 35/39 | chr3 | 13321840 | ||||||
chr3:13321883
|
C | G | 1 | a0003c0005t0005g0029 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.4916-48G>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 35/39 | chr3 | 13321883 | ||||||
chr3:13321908
|
C | T | 1 | a0001c0001t0002g0113 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.4916-73G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 35/39 | chr3 | 13321908 | ||||||
chr3:13321987
|
C | T | 1 | a0005c0003t0001g0242 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.4916-152G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 35/39 | chr3 | 13321987 | ||||||
chr3:13322027
|
A | T | 2 | a0003c0011t0001g0035a0003c0011t0001g0036 | 2 | HG02922.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.4915+166T>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 35/39 | chr3 | 13322027 | ||||||
chr3:13322122
|
G | A | 1 | a0003c0005t0005g0031 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.4915+71C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 35/39 | chr3 | 13322122 | ||||||
chr3:13322357
|
G | A | 4 | a0002c0002t0001g0160a0002c0002t0001g0161a0002c0002t0001g0162others(1): Show | 4 | HG02145.hp1 HG03041.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.4769-18C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 34/39 | chr3 | 13322357 | ||||||
chr3:13322628
|
A | G | 1 | a0005c0003t0001g0313 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.4769-289T>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 34/39 | chr3 | 13322628 | ||||||
chr3:13322751
|
C | T | 1 | a0004c0036t0003g0176 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.4769-412G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 34/39 | chr3 | 13322751 | ||||||
chr3:13322785
|
C | G | 15 | a0003c0005t0005g0023a0003c0005t0005g0024a0003c0005t0005g0025others(12): Show | 15 | HG01109.hp1 HG01884.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.4769-446G>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 34/39 | chr3 | 13322785 | ||||||
chr3:13322832
|
C | T | 2 | a0008c0009t0001g0004a0008c0009t0001g0194 | 3 | HG02615.hp2 HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.4768+477G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 34/39 | chr3 | 13322832 | ||||||
chr3:13322903
|
T | C | 1 | a0002c0002t0004g0261 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.4768+406A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 34/39 | chr3 | 13322903 | ||||||
chr3:13322941
|
G | A | 1 | a0003c0019t0013g0164 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.4768+368C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 34/39 | chr3 | 13322941 | ||||||
chr3:13322971
|
T | C | 176 | a0001c0001t0002g0001a0001c0001t0002g0041a0001c0001t0002g0042others(173): Show | 180 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.4768+338A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 34/39 | chr3 | 13322971 | ||||||
chr3:13322974
|
C | T | 1 | a0005c0003t0001g0238 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.4768+335G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 34/39 | chr3 | 13322974 | ||||||
chr3:13323001
|
G | C | 1 | a0001c0001t0002g0148 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.4768+308C>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 34/39 | chr3 | 13323001 | ||||||
chr3:13323067
|
T | G | 15 | a0003c0005t0005g0023a0003c0005t0005g0024a0003c0005t0005g0025others(12): Show | 15 | HG01109.hp1 HG01884.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.4768+242A>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 34/39 | chr3 | 13323067 | ||||||
chr3:13323154
|
C | T | 10 | a0002c0002t0001g0211a0002c0002t0001g0213a0002c0002t0001g0214others(7): Show | 10 | HG03654.hp2 HG03688.hp1 HG03927.hp1 others(7): Show |
intron_variant | MODIFIER | c.4768+155G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 34/39 | chr3 | 13323154 | ||||||
chr3:13323479
|
G | A | 2 | a0003c0011t0001g0035a0003c0011t0001g0036 | 2 | HG02922.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.4645-47C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 33/39 | chr3 | 13323479 | ||||||
chr3:13323536
|
G | A | 1 | a0002c0002t0007g0309 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.4645-104C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 33/39 | chr3 | 13323536 | ||||||
chr3:13323540
|
C | T | 16 | a0003c0005t0005g0023a0003c0005t0005g0024a0003c0005t0005g0025others(13): Show | 16 | HG01109.hp1 HG01884.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.4645-108G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 33/39 | chr3 | 13323540 | ||||||
chr3:13323685
|
C | A | 1 | a0002c0002t0001g0208 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.4645-253G>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 33/39 | chr3 | 13323685 | ||||||
chr3:13323794
|
T | C | 1 | a0006c0007t0001g0040 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.4645-362A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 33/39 | chr3 | 13323794 | ||||||
chr3:13323989
|
A | C | 1 | a0004c0004t0003g0175 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.4645-557T>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 33/39 | chr3 | 13323989 | ||||||
chr3:13324057
|
C | T | 1 | a0001c0001t0002g0095 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.4645-625G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 33/39 | chr3 | 13324057 | ||||||
chr3:13324153
|
T | C | 176 | a0001c0001t0002g0001a0001c0001t0002g0041a0001c0001t0002g0042others(173): Show | 180 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.4645-721A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 33/39 | chr3 | 13324153 | ||||||
chr3:13324209
|
A | AC | 137 | a0001c0001t0002g0001a0001c0001t0002g0041a0001c0001t0002g0042others(134): Show | 140 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.4645-778dupG | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 33/39 | chr3 | 13324209 | ||||||
chr3:13324209
|
A | C | 1 | a0001c0001t0002g0081 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.4645-777T>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 33/39 | chr3 | 13324209 | ||||||
chr3:13324319
|
C | T | 2 | a0004c0016t0005g0190a0004c0016t0005g0191 | 2 | HG02622.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.4645-887G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 33/39 | chr3 | 13324319 | ||||||
chr3:13324494
|
C | T | 1 | a0020c0020t0001g0193 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.4645-1062G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 33/39 | chr3 | 13324494 | ||||||
chr3:13324648
|
G | A | 1 | a0004c0004t0010g0186 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.4644+1147C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 33/39 | chr3 | 13324648 | ||||||
chr3:13324756
|
C | G | 1 | a0001c0001t0002g0067 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.4644+1039G>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 33/39 | chr3 | 13324756 | ||||||
chr3:13324759
|
T | C | 1 | a0002c0002t0001g0237 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.4644+1036A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 33/39 | chr3 | 13324759 | ||||||
chr3:13325021
|
G | A | 2 | a0004c0016t0005g0190a0004c0016t0005g0191 | 2 | HG02622.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.4644+774C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 33/39 | chr3 | 13325021 | ||||||
chr3:13325045
|
C | T | 93 | a0002c0002t0001g0050a0002c0002t0001g0160a0002c0002t0001g0161others(90): Show | 93 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(90): Show |
intron_variant | MODIFIER | c.4644+750G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 33/39 | chr3 | 13325045 | ||||||
chr3:13325164
|
C | A | 1 | a0001c0001t0002g0158 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.4644+631G>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 33/39 | chr3 | 13325164 | ||||||
chr3:13325201
|
C | T | 1 | a0006c0007t0001g0040 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.4644+594G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 33/39 | chr3 | 13325201 | ||||||
chr3:13325294
|
A | T | 273 | a0001c0001t0002g0001a0001c0001t0002g0041a0001c0001t0002g0042others(270): Show | 277 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.4644+501T>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 33/39 | chr3 | 13325294 | ||||||
chr3:13325373
|
C | G | 175 | a0001c0001t0002g0001a0001c0001t0002g0041a0001c0001t0002g0042others(172): Show | 179 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.4644+422G>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 33/39 | chr3 | 13325373 | ||||||
chr3:13325374
|
C | G | 1 | a0001c0001t0002g0081 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.4644+421G>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 33/39 | chr3 | 13325374 | ||||||
chr3:13325454
|
C | T | 1 | a0003c0005t0005g0031 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.4644+341G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 33/39 | chr3 | 13325454 | ||||||
chr3:13325514
|
G | A | 5 | a0001c0001t0002g0265a0001c0001t0002g0274a0001c0001t0002g0276others(2): Show | 5 | NA18945.hp2 NA18983.hp2 NA18998.hp2 others(2): Show |
intron_variant | MODIFIER | c.4644+281C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 33/39 | chr3 | 13325514 | ||||||
chr3:13325550
|
C | T | 2 | a0002c0002t0001g0263a0002c0002t0001g0282 | 2 | NA18994.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.4644+245G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 33/39 | chr3 | 13325550 | ||||||
chr3:13325612
|
A | C | 2 | a0002c0002t0001g0239a0015c0021t0001g0267 | 2 | NA19000.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.4644+183T>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 33/39 | chr3 | 13325612 | ||||||
chr3:13325716
|
T | C | 1 | a0006c0007t0001g0305 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.4644+79A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 33/39 | chr3 | 13325716 | ||||||
chr3:13326035
|
A | AC | 13 | a0001c0001t0002g0068a0001c0001t0002g0081a0001c0001t0002g0100others(10): Show | 13 | HG00438.hp1 HG01099.hp2 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.4508-105dupG | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 32/39 | chr3 | 13326035 | ||||||
chr3:13326040
|
C | G | 1 | a0002c0002t0004g0253 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.4508-109G>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 32/39 | chr3 | 13326040 | ||||||
chr3:13326344
|
A | G | 14 | a0005c0003t0001g0234a0005c0003t0001g0238a0005c0003t0001g0241others(11): Show | 14 | HG02602.hp1 HG03017.hp1 HG03239.hp1 others(11): Show |
intron_variant | MODIFIER | c.4508-413T>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 32/39 | chr3 | 13326344 | ||||||
chr3:13326360
|
C | CA | 320 | a0001c0001t0002g0001a0001c0001t0002g0041a0001c0001t0002g0042others(317): Show | 325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.4508-430dupT | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 32/39 | chr3 | 13326360 | ||||||
chr3:13326394
|
C | T | 1 | a0020c0020t0001g0193 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.4508-463G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 32/39 | chr3 | 13326394 | ||||||
chr3:13326539
|
T | TA | 137 | a0001c0001t0002g0001a0001c0001t0002g0041a0001c0001t0002g0042others(134): Show | 140 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.4508-609dupT | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 32/39 | chr3 | 13326539 | ||||||
chr3:13326585
|
A | G | 2 | a0006c0007t0001g0010a0006c0007t0001g0015 | 2 | HG01168.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.4507+632T>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 32/39 | chr3 | 13326585 | ||||||
chr3:13326770
|
G | A | 1 | a0001c0001t0002g0141 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.4507+447C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 32/39 | chr3 | 13326770 | ||||||
chr3:13326901
|
G | A | 1 | a0003c0019t0013g0164 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.4507+316C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 32/39 | chr3 | 13326901 | ||||||
chr3:13326911
|
A | G | 1 | a0001c0001t0002g0081 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.4507+306T>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 32/39 | chr3 | 13326911 | ||||||
chr3:13326954
|
A | G | 1 | a0005c0003t0001g0215 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.4507+263T>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 32/39 | chr3 | 13326954 | ||||||
chr3:13326992
|
C | T | 146 | a0002c0002t0001g0050a0002c0002t0001g0160a0002c0002t0001g0161others(143): Show | 148 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(145): Show |
intron_variant | MODIFIER | c.4507+225G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 32/39 | chr3 | 13326992 | ||||||
chr3:13327136
|
G | A | 1 | a0001c0001t0002g0134 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.4507+81C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 32/39 | chr3 | 13327136 | ||||||
chr3:13327178
|
C | T | 8 | a0003c0006t0006g0051a0003c0006t0006g0052a0003c0006t0006g0053others(5): Show | 8 | HG02486.hp1 HG02559.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.4507+39G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 32/39 | chr3 | 13327178 | ||||||
chr3:13327545
|
C | T | 1 | a0001c0001t0002g0146 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.4287-108G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 31/39 | chr3 | 13327545 | ||||||
chr3:13327591
|
C | T | 47 | a0005c0003t0001g0215a0005c0003t0001g0216a0005c0003t0001g0234others(44): Show | 48 | HG00140.hp1 HG00140.hp2 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.4287-154G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 31/39 | chr3 | 13327591 | ||||||
chr3:13327748
|
G | A | 1 | a0002c0002t0001g0208 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.4287-311C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 31/39 | chr3 | 13327748 | ||||||
chr3:13327872
|
C | T | 2 | a0002c0002t0001g0308a0022c0017t0005g0057 | 2 | HG03195.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.4287-435G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 31/39 | chr3 | 13327872 | ||||||
chr3:13327982
|
A | G | 1 | a0003c0005t0005g0031 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.4287-545T>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 31/39 | chr3 | 13327982 | ||||||
chr3:13328117
|
C | T | 1 | a0002c0002t0001g0210 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.4286+654G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 31/39 | chr3 | 13328117 | ||||||
chr3:13328202
|
C | T | 46 | a0005c0003t0001g0215a0005c0003t0001g0216a0005c0003t0001g0234others(43): Show | 47 | HG00140.hp1 HG00140.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.4286+569G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 31/39 | chr3 | 13328202 | ||||||
chr3:13328340
|
G | A | 6 | a0001c0001t0002g0072a0001c0001t0002g0143a0001c0001t0002g0144others(3): Show | 6 | HG02922.hp1 NA18954.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.4286+431C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 31/39 | chr3 | 13328340 | ||||||
chr3:13328413
|
A | G | 1 | a0001c0001t0002g0067 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.4286+358T>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 31/39 | chr3 | 13328413 | ||||||
chr3:13328569
|
T | C | 1 | a0001c0001t0002g0122 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.4286+202A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 31/39 | chr3 | 13328569 | ||||||
chr3:13328637
|
G | A | 1 | a0009c0028t0003g0034 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.4286+134C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 31/39 | chr3 | 13328637 | ||||||
chr3:13328640
|
C | A | 3 | a0004c0004t0003g0169a0004c0004t0003g0170a0004c0004t0003g0187 | 3 | HG02258.hp1 HG02818.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.4286+131G>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 31/39 | chr3 | 13328640 | ||||||
chr3:13328667
|
A | G | 3 | a0006c0007t0001g0040a0009c0028t0003g0034a0009c0030t0005g0009 | 3 | HG01891.hp1 HG02723.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.4286+104T>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 31/39 | chr3 | 13328667 | ||||||
chr3:13329174
|
A | T | 23 | a0002c0002t0001g0208a0002c0002t0001g0235a0002c0002t0001g0237others(20): Show | 23 | HG00099.hp1 HG00544.hp2 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.4111-228T>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 30/39 | chr3 | 13329174 | ||||||
chr3:13329217
|
A | G | 16 | a0004c0004t0003g0107a0004c0004t0003g0108a0004c0004t0003g0166others(13): Show | 16 | HG00544.hp1 HG01516.hp2 HG01517.hp1 others(13): Show |
intron_variant | MODIFIER | c.4111-271T>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 30/39 | chr3 | 13329217 | ||||||
chr3:13329305
|
C | T | 10 | a0002c0002t0001g0160a0002c0002t0001g0161a0002c0002t0001g0162others(7): Show | 10 | HG02145.hp1 HG03041.hp2 HG03486.hp1 others(7): Show |
intron_variant | MODIFIER | c.4111-359G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 30/39 | chr3 | 13329305 | ||||||
chr3:13329463
|
C | G | 210 | a0002c0002t0001g0050a0002c0002t0001g0160a0002c0002t0001g0161others(207): Show | 212 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.4111-517G>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 30/39 | chr3 | 13329463 | ||||||
chr3:13329562
|
T | C | 1 | a0020c0020t0001g0193 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.4111-616A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 30/39 | chr3 | 13329562 | ||||||
chr3:13329735
|
T | A | 45 | a0005c0003t0001g0215a0005c0003t0001g0216a0005c0003t0001g0234others(42): Show | 46 | HG00140.hp1 HG00140.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.4110+725A>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 30/39 | chr3 | 13329735 | ||||||
chr3:13329755
|
A | C | 28 | a0004c0004t0003g0107a0004c0004t0003g0108a0004c0004t0003g0165others(25): Show | 28 | HG00544.hp1 HG01081.hp1 HG01516.hp2 others(25): Show |
intron_variant | MODIFIER | c.4110+705T>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 30/39 | chr3 | 13329755 | ||||||
chr3:13329799
|
G | A | 14 | a0002c0002t0001g0217a0002c0002t0001g0218a0002c0002t0001g0220others(11): Show | 14 | HG00280.hp2 HG00323.hp2 HG00642.hp1 others(11): Show |
intron_variant | MODIFIER | c.4110+661C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 30/39 | chr3 | 13329799 | ||||||
chr3:13329869
|
C | T | 1 | a0001c0001t0002g0111 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.4110+591G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 30/39 | chr3 | 13329869 | ||||||
chr3:13329997
|
C | T | 46 | a0003c0005t0005g0023a0003c0005t0005g0024a0003c0005t0005g0025others(43): Show | 47 | HG00544.hp1 HG01081.hp1 HG01109.hp1 others(44): Show |
intron_variant | MODIFIER | c.4110+463G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 30/39 | chr3 | 13329997 | ||||||
chr3:13330035
|
A | T | 1 | a0002c0002t0001g0207 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.4110+425T>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 30/39 | chr3 | 13330035 | ||||||
chr3:13330136
|
A | G | 209 | a0002c0002t0001g0050a0002c0002t0001g0160a0002c0002t0001g0161others(206): Show | 211 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.4110+324T>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 30/39 | chr3 | 13330136 | ||||||
chr3:13330200
|
C | T | 1 | a0005c0003t0001g0241 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.4110+260G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 30/39 | chr3 | 13330200 | ||||||
chr3:13330269
|
T | G | 41 | a0002c0002t0001g0199a0002c0002t0001g0200a0002c0002t0001g0201others(38): Show | 41 | HG00099.hp1 HG00544.hp2 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.4110+191A>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 30/39 | chr3 | 13330269 | ||||||
chr3:13330284
|
A | G | 1 | a0005c0003t0001g0295 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.4110+176T>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 30/39 | chr3 | 13330284 | ||||||
chr3:13330310
|
T | G | 1 | a0009c0028t0003g0034 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.4110+150A>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 30/39 | chr3 | 13330310 | ||||||
chr3:13330330
|
G | A | 1 | a0001c0001t0002g0080 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.4110+130C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 30/39 | chr3 | 13330330 | ||||||
chr3:13330706
|
G | A | 1 | a0004c0004t0003g0168 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.3936-72C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 29/39 | chr3 | 13330706 | ||||||
chr3:13330768
|
G | A | 2 | a0008c0009t0001g0004a0008c0009t0001g0194 | 3 | HG02615.hp2 HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.3936-134C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 29/39 | chr3 | 13330768 | ||||||
chr3:13330826
|
G | A | 1 | a0005c0003t0001g0304 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.3936-192C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 29/39 | chr3 | 13330826 | ||||||
chr3:13330829
|
A | G | 1 | a0020c0020t0001g0193 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3936-195T>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 29/39 | chr3 | 13330829 | ||||||
chr3:13331029
|
G | A | 3 | a0006c0007t0001g0002a0006c0007t0001g0012a0006c0007t0001g0013 | 4 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(1): Show |
intron_variant | MODIFIER | c.3936-395C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 29/39 | chr3 | 13331029 | ||||||
chr3:13331116
|
C | A | 1 | a0001c0001t0002g0129 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.3936-482G>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 29/39 | chr3 | 13331116 | ||||||
chr3:13331232
|
T | C | 1 | a0024c0038t0002g0321 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.3936-598A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 29/39 | chr3 | 13331232 | ||||||
chr3:13331690
|
T | C | 2 | a0002c0002t0001g0239a0015c0021t0001g0267 | 2 | NA19000.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.3935+603A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 29/39 | chr3 | 13331690 | ||||||
chr3:13331735
|
C | T | 2 | a0002c0002t0001g0243a0002c0002t0001g0244 | 2 | NA18959.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.3935+558G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 29/39 | chr3 | 13331735 | ||||||
chr3:13331774
|
G | A | 3 | a0004c0004t0010g0181a0004c0004t0010g0184a0004c0004t0010g0186 | 3 | NA18993.hp2 NA19009.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.3935+519C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 29/39 | chr3 | 13331774 | ||||||
chr3:13331845
|
G | A | 1 | a0001c0001t0002g0138 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.3935+448C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 29/39 | chr3 | 13331845 | ||||||
chr3:13331942
|
G | A | 46 | a0003c0005t0005g0023a0003c0005t0005g0024a0003c0005t0005g0025others(43): Show | 47 | HG00544.hp1 HG01081.hp1 HG01109.hp1 others(44): Show |
intron_variant | MODIFIER | c.3935+351C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 29/39 | chr3 | 13331942 | ||||||
chr3:13331955
|
C | T | 28 | a0004c0004t0003g0107a0004c0004t0003g0108a0004c0004t0003g0165others(25): Show | 28 | HG00544.hp1 HG01081.hp1 HG01516.hp2 others(25): Show |
intron_variant | MODIFIER | c.3935+338G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 29/39 | chr3 | 13331955 | ||||||
chr3:13332016
|
T | TG | 2 | a0008c0009t0001g0004a0008c0009t0001g0194 | 3 | HG02615.hp2 HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.3935+276dupC | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 29/39 | chr3 | 13332016 | ||||||
chr3:13332393
|
G | C | 61 | a0003c0005t0005g0023a0003c0005t0005g0024a0003c0005t0005g0025others(58): Show | 61 | HG00544.hp1 HG01081.hp1 HG01109.hp1 others(58): Show |
intron_variant | MODIFIER | c.3844-9C>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 28/39 | chr3 | 13332393 | ||||||
chr3:13332498
|
G | A | 2 | a0003c0011t0001g0035a0003c0011t0001g0036 | 2 | HG02922.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.3844-114C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 28/39 | chr3 | 13332498 | ||||||
chr3:13332722
|
A | C | 4 | a0002c0002t0001g0160a0002c0002t0001g0161a0002c0002t0001g0162others(1): Show | 4 | HG02145.hp1 HG03041.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.3844-338T>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 28/39 | chr3 | 13332722 | ||||||
chr3:13332727
|
A | T | 1 | a0005c0003t0001g0298 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.3844-343T>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 28/39 | chr3 | 13332727 | ||||||
chr3:13332742
|
CAT | C | 158 | a0002c0002t0001g0050a0002c0002t0001g0160a0002c0002t0001g0161others(155): Show | 159 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.3844-360_3844-359d others(4): Show |
NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 28/39 | chr3 | 13332742 | ||||||
chr3:13332744
|
T | C | 28 | a0004c0004t0003g0107a0004c0004t0003g0108a0004c0004t0003g0165others(25): Show | 28 | HG00544.hp1 HG01081.hp1 HG01516.hp2 others(25): Show |
intron_variant | MODIFIER | c.3844-360A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 28/39 | chr3 | 13332744 | ||||||
chr3:13332793
|
C | G | 2 | a0008c0009t0001g0004a0008c0009t0001g0194 | 3 | HG02615.hp2 HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.3844-409G>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 28/39 | chr3 | 13332793 | ||||||
chr3:13332990
|
T | C | 158 | a0002c0002t0001g0050a0002c0002t0001g0160a0002c0002t0001g0161others(155): Show | 159 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.3844-606A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 28/39 | chr3 | 13332990 | ||||||
chr3:13333091
|
C | T | 1 | a0020c0020t0001g0193 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3844-707G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 28/39 | chr3 | 13333091 | ||||||
chr3:13333119
|
G | A | 3 | a0002c0002t0001g0224a0002c0002t0001g0228a0002c0002t0001g0229 | 3 | HG00733.hp2 HG00741.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.3844-735C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 28/39 | chr3 | 13333119 | ||||||
chr3:13333144
|
G | A | 4 | a0002c0002t0001g0160a0002c0002t0001g0161a0002c0002t0001g0162others(1): Show | 4 | HG02145.hp1 HG03041.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.3844-760C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 28/39 | chr3 | 13333144 | ||||||
chr3:13333148
|
C | A | 87 | a0002c0002t0001g0199a0002c0002t0001g0200a0002c0002t0001g0201others(84): Show | 87 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.3844-764G>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 28/39 | chr3 | 13333148 | ||||||
chr3:13333232
|
A | G | 162 | a0001c0001t0002g0265a0001c0001t0002g0274a0001c0001t0002g0288others(159): Show | 163 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.3844-848T>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 28/39 | chr3 | 13333232 | ||||||
chr3:13333316
|
G | A | 1 | a0009c0027t0003g0019 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.3844-932C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 28/39 | chr3 | 13333316 | ||||||
chr3:13333446
|
C | T | 2 | a0001c0001t0002g0102a0001c0001t0002g0158 | 2 | NA18944.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.3844-1062G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 28/39 | chr3 | 13333446 | ||||||
chr3:13333455
|
C | T | 1 | a0020c0020t0001g0193 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3844-1071G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 28/39 | chr3 | 13333455 | ||||||
chr3:13333490
|
A | G | 1 | a0001c0001t0002g0153 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.3844-1106T>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 28/39 | chr3 | 13333490 | ||||||
chr3:13333540
|
T | G | 1 | a0001c0001t0002g0274 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.3844-1156A>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 28/39 | chr3 | 13333540 | ||||||
chr3:13333674
|
G | A | 26 | a0001c0001t0002g0001a0001c0001t0002g0088a0001c0001t0002g0092others(23): Show | 28 | HG00099.hp1 HG00544.hp2 HG00621.hp1 others(25): Show |
intron_variant | MODIFIER | c.3844-1290C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 28/39 | chr3 | 13333674 | ||||||
chr3:13333837
|
T | A | 14 | a0001c0001t0002g0066a0001c0001t0002g0070a0001c0001t0002g0097others(11): Show | 14 | HG00597.hp2 HG02132.hp1 NA18945.hp1 others(11): Show |
intron_variant | MODIFIER | c.3844-1453A>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 28/39 | chr3 | 13333837 | ||||||
chr3:13333931
|
A | C | 208 | a0002c0002t0001g0050a0002c0002t0001g0160a0002c0002t0001g0161others(205): Show | 210 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.3843+1523T>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 28/39 | chr3 | 13333931 | ||||||
chr3:13334201
|
G | T | 2 | a0001c0001t0002g0094a0001c0001t0002g0142 | 2 | HG01934.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.3843+1253C>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 28/39 | chr3 | 13334201 | ||||||
chr3:13334227
|
A | G | 1 | a0001c0001t0002g0042 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.3843+1227T>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 28/39 | chr3 | 13334227 | ||||||
chr3:13334380
|
G | C | 2 | a0003c0011t0001g0035a0003c0011t0001g0036 | 2 | HG02922.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.3843+1074C>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 28/39 | chr3 | 13334380 | ||||||
chr3:13334415
|
T | A | 1 | a0001c0001t0002g0138 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.3843+1039A>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 28/39 | chr3 | 13334415 | ||||||
chr3:13334423
|
G | A | 40 | a0001c0001t0002g0001a0001c0001t0002g0065a0001c0001t0002g0068others(37): Show | 43 | HG00621.hp2 HG01496.hp2 HG01934.hp2 others(40): Show |
intron_variant | MODIFIER | c.3843+1031C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 28/39 | chr3 | 13334423 | ||||||
chr3:13334467
|
G | A | 3 | a0002c0002t0001g0050a0008c0009t0001g0004a0008c0009t0001g0194 | 4 | HG02615.hp2 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.3843+987C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 28/39 | chr3 | 13334467 | ||||||
chr3:13334507
|
T | C | 1 | a0003c0019t0013g0164 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3843+947A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 28/39 | chr3 | 13334507 | ||||||
chr3:13334562
|
T | C | 1 | a0001c0001t0002g0088 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.3843+892A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 28/39 | chr3 | 13334562 | ||||||
chr3:13334966
|
C | T | 1 | a0001c0001t0002g0062 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.3843+488G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 28/39 | chr3 | 13334966 | ||||||
chr3:13335160
|
T | TTTGCTCT others(11): Show |
1 | a0002c0002t0001g0211 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.3843+276_3843+293d others(20): Show |
NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 28/39 | chr3 | 13335160 | ||||||
chr3:13335193
|
C | G | 3 | a0002c0002t0001g0237a0002c0002t0001g0243a0002c0002t0001g0244 | 3 | NA18959.hp2 NA18965.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.3843+261G>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 28/39 | chr3 | 13335193 | ||||||
chr3:13335221
|
A | C | 1 | a0001c0001t0002g0095 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.3843+233T>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 28/39 | chr3 | 13335221 | ||||||
chr3:13335295
|
G | A | 141 | a0002c0002t0001g0050a0002c0002t0001g0160a0002c0002t0001g0161others(138): Show | 142 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.3843+159C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 28/39 | chr3 | 13335295 | ||||||
chr3:13335312
|
C | T | 2 | a0008c0009t0001g0004a0008c0009t0001g0194 | 3 | HG02615.hp2 HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.3843+142G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 28/39 | chr3 | 13335312 | ||||||
chr3:13335313
|
G | A | 9 | a0003c0006t0006g0051a0003c0006t0006g0052a0003c0006t0006g0053others(6): Show | 9 | HG02486.hp1 HG02559.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.3843+141C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 28/39 | chr3 | 13335313 | ||||||
chr3:13335334
|
C | T | 18 | a0001c0001t0002g0106a0001c0001t0002g0116a0001c0001t0002g0135others(15): Show | 18 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.3843+120G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 28/39 | chr3 | 13335334 | ||||||
chr3:13335335
|
G | A | 1 | a0009c0028t0003g0034 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3843+119C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 28/39 | chr3 | 13335335 | ||||||
chr3:13335433
|
G | C | 1 | a0001c0033t0002g0266 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.3843+21C>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 28/39 | chr3 | 13335433 | ||||||
chr3:13335642
|
G | A | 1 | a0006c0007t0001g0040 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3685-30C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 27/39 | chr3 | 13335642 | ||||||
chr3:13335837
|
C | T | 1 | a0001c0001t0002g0077 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.3685-225G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 27/39 | chr3 | 13335837 | ||||||
chr3:13335846
|
T | C | 4 | a0002c0002t0001g0160a0002c0002t0001g0161a0002c0002t0001g0162others(1): Show | 4 | HG02145.hp1 HG03041.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.3685-234A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 27/39 | chr3 | 13335846 | ||||||
chr3:13336279
|
G | C | 1 | a0002c0002t0001g0280 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.3684+508C>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 27/39 | chr3 | 13336279 | ||||||
chr3:13336300
|
T | A | 1 | a0002c0029t0001g0315 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.3684+487A>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 27/39 | chr3 | 13336300 | ||||||
chr3:13336311
|
T | A | 1 | a0002c0029t0001g0315 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.3684+476A>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 27/39 | chr3 | 13336311 | ||||||
chr3:13336366
|
C | G | 3 | a0004c0004t0003g0192a0004c0016t0005g0190a0004c0016t0005g0191 | 3 | HG01081.hp1 HG02622.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.3684+421G>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 27/39 | chr3 | 13336366 | ||||||
chr3:13336488
|
C | A | 1 | a0009c0030t0005g0009 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.3684+299G>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 27/39 | chr3 | 13336488 | ||||||
chr3:13336524
|
A | C | 1 | a0020c0020t0001g0193 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3684+263T>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 27/39 | chr3 | 13336524 | ||||||
chr3:13336574
|
G | A | 34 | a0003c0011t0001g0035a0003c0011t0001g0036a0004c0004t0003g0107others(31): Show | 35 | HG00544.hp1 HG01081.hp1 HG01516.hp2 others(32): Show |
intron_variant | MODIFIER | c.3684+213C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 27/39 | chr3 | 13336574 | ||||||
chr3:13336611
|
A | G | 1 | a0003c0005t0005g0031 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3684+176T>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 27/39 | chr3 | 13336611 | ||||||
chr3:13336662
|
G | A | 1 | a0001c0001t0002g0103 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.3684+125C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 27/39 | chr3 | 13336662 | ||||||
chr3:13337227
|
C | T | 2 | a0003c0011t0001g0035a0003c0011t0001g0036 | 2 | HG02922.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.3553-309G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 26/39 | chr3 | 13337227 | ||||||
chr3:13337246
|
G | A | 1 | a0001c0001t0002g0146 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.3553-328C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 26/39 | chr3 | 13337246 | ||||||
chr3:13337291
|
C | T | 209 | a0002c0002t0001g0050a0002c0002t0001g0160a0002c0002t0001g0161others(206): Show | 211 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.3553-373G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 26/39 | chr3 | 13337291 | ||||||
chr3:13337365
|
G | A | 1 | a0003c0006t0005g0046 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.3553-447C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 26/39 | chr3 | 13337365 | ||||||
chr3:13337414
|
C | G | 34 | a0003c0011t0001g0035a0003c0011t0001g0036a0004c0004t0003g0107others(31): Show | 35 | HG00544.hp1 HG01081.hp1 HG01516.hp2 others(32): Show |
intron_variant | MODIFIER | c.3552+423G>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 26/39 | chr3 | 13337414 | ||||||
chr3:13337430
|
G | A | 175 | a0002c0002t0001g0050a0002c0002t0001g0160a0002c0002t0001g0161others(172): Show | 176 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.3552+407C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 26/39 | chr3 | 13337430 | ||||||
chr3:13337450
|
G | A | 2 | a0006c0007t0001g0040a0009c0030t0005g0009 | 2 | HG01891.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.3552+387C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 26/39 | chr3 | 13337450 | ||||||
chr3:13337539
|
T | A | 4 | a0005c0003t0001g0245a0005c0003t0001g0247a0005c0003t0001g0281others(1): Show | 4 | HG03017.hp1 HG03491.hp2 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.3552+298A>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 26/39 | chr3 | 13337539 | ||||||
chr3:13337923
|
G | A | 1 | a0002c0002t0001g0208 | 1 | NA18984.hp2 | splice_region_variant&intron_variant | LOW | c.3472-6C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 25/39 | chr3 | 13337923 | ||||||
chr3:13337952
|
G | A | 89 | a0002c0002t0001g0050a0002c0002t0001g0199a0002c0002t0001g0200others(86): Show | 89 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.3472-35C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 25/39 | chr3 | 13337952 | ||||||
chr3:13338178
|
T | G | 1 | a0001c0001t0002g0123 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.3472-261A>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 25/39 | chr3 | 13338178 | ||||||
chr3:13338185
|
G | A | 5 | a0006c0007t0001g0002a0006c0007t0001g0011a0006c0007t0001g0012others(2): Show | 6 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(3): Show |
intron_variant | MODIFIER | c.3472-268C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 25/39 | chr3 | 13338185 | ||||||
chr3:13338273
|
C | A | 1 | a0003c0005t0005g0023 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3472-356G>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 25/39 | chr3 | 13338273 | ||||||
chr3:13338334
|
C | T | 1 | a0001c0001t0002g0125 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.3472-417G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 25/39 | chr3 | 13338334 | ||||||
chr3:13338336
|
T | A | 1 | a0002c0002t0001g0208 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.3472-419A>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 25/39 | chr3 | 13338336 | ||||||
chr3:13338382
|
C | T | 1 | a0020c0020t0001g0193 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3472-465G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 25/39 | chr3 | 13338382 | ||||||
chr3:13338515
|
C | G | 1 | a0001c0001t0002g0106 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3472-598G>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 25/39 | chr3 | 13338515 | ||||||
chr3:13338550
|
A | T | 32 | a0003c0011t0001g0035a0003c0011t0001g0036a0004c0004t0003g0107others(29): Show | 32 | HG00544.hp1 HG01081.hp1 HG01516.hp2 others(29): Show |
intron_variant | MODIFIER | c.3472-633T>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 25/39 | chr3 | 13338550 | ||||||
chr3:13338595
|
T | C | 208 | a0002c0002t0001g0050a0002c0002t0001g0160a0002c0002t0001g0161others(205): Show | 210 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.3472-678A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 25/39 | chr3 | 13338595 | ||||||
chr3:13338620
|
C | T | 1 | a0002c0002t0007g0309 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.3472-703G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 25/39 | chr3 | 13338620 | ||||||
chr3:13338621
|
G | A | 4 | a0002c0002t0001g0160a0002c0002t0001g0161a0002c0002t0001g0162others(1): Show | 4 | HG02145.hp1 HG03041.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.3472-704C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 25/39 | chr3 | 13338621 | ||||||
chr3:13338703
|
C | A | 3 | a0003c0011t0001g0035a0003c0011t0001g0036a0020c0020t0001g0193 | 3 | HG02922.hp1 HG03471.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.3472-786G>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 25/39 | chr3 | 13338703 | ||||||
chr3:13338951
|
G | A | 4 | a0003c0006t0005g0008a0003c0006t0005g0044a0003c0006t0005g0046others(1): Show | 4 | HG01243.hp2 HG02135.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.3471+903C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 25/39 | chr3 | 13338951 | ||||||
chr3:13339021
|
T | C | 2 | a0008c0009t0001g0004a0008c0009t0001g0194 | 3 | HG02615.hp2 HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.3471+833A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 25/39 | chr3 | 13339021 | ||||||
chr3:13339053
|
A | C | 93 | a0002c0002t0001g0050a0002c0002t0001g0160a0002c0002t0001g0161others(90): Show | 93 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(90): Show |
intron_variant | MODIFIER | c.3471+801T>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 25/39 | chr3 | 13339053 | ||||||
chr3:13339096
|
T | C | 29 | a0004c0004t0003g0107a0004c0004t0003g0108a0004c0004t0003g0165others(26): Show | 29 | HG00544.hp1 HG01081.hp1 HG01516.hp2 others(26): Show |
intron_variant | MODIFIER | c.3471+758A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 25/39 | chr3 | 13339096 | ||||||
chr3:13339113
|
A | G | 16 | a0003c0006t0005g0008a0003c0006t0005g0044a0003c0006t0005g0046others(13): Show | 16 | HG01243.hp2 HG02135.hp2 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.3471+741T>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 25/39 | chr3 | 13339113 | ||||||
chr3:13339115
|
T | G | 1 | a0004c0016t0005g0190 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3471+739A>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 25/39 | chr3 | 13339115 | ||||||
chr3:13339158
|
C | T | 1 | a0003c0005t0005g0031 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3471+696G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 25/39 | chr3 | 13339158 | ||||||
chr3:13339185
|
G | C | 1 | a0006c0007t0001g0017 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.3471+669C>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 25/39 | chr3 | 13339185 | ||||||
chr3:13339205
|
T | C | 1 | a0002c0002t0004g0279 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.3471+649A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 25/39 | chr3 | 13339205 | ||||||
chr3:13339259
|
A | C | 1 | a0001c0001t0002g0123 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.3471+595T>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 25/39 | chr3 | 13339259 | ||||||
chr3:13339274
|
G | C | 1 | a0005c0003t0001g0238 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.3471+580C>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 25/39 | chr3 | 13339274 | ||||||
chr3:13339389
|
G | A | 29 | a0004c0004t0003g0107a0004c0004t0003g0108a0004c0004t0003g0165others(26): Show | 29 | HG00544.hp1 HG01081.hp1 HG01516.hp2 others(26): Show |
intron_variant | MODIFIER | c.3471+465C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 25/39 | chr3 | 13339389 | ||||||
chr3:13339475
|
C | T | 6 | a0002c0002t0004g0250a0002c0002t0004g0251a0002c0002t0004g0254others(3): Show | 6 | NA18942.hp2 NA18953.hp2 NA18961.hp2 others(3): Show |
intron_variant | MODIFIER | c.3471+379G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 25/39 | chr3 | 13339475 | ||||||
chr3:13339556
|
T | C | 2 | a0003c0006t0005g0008a0003c0006t0005g0049 | 2 | HG01243.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.3471+298A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 25/39 | chr3 | 13339556 | ||||||
chr3:13339651
|
T | C | 34 | a0003c0011t0001g0035a0003c0011t0001g0036a0004c0004t0003g0107others(31): Show | 35 | HG00544.hp1 HG01081.hp1 HG01516.hp2 others(32): Show |
intron_variant | MODIFIER | c.3471+203A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 25/39 | chr3 | 13339651 | ||||||
chr3:13339705
|
C | T | 1 | a0001c0001t0002g0072 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.3471+149G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 25/39 | chr3 | 13339705 | ||||||
chr3:13339765
|
G | A | 1 | a0002c0002t0001g0286 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.3471+89C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 25/39 | chr3 | 13339765 | ||||||
chr3:13339841
|
G | C | 1 | a0003c0005t0005g0278 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.3471+13C>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 25/39 | chr3 | 13339841 | ||||||
chr3:13340039
|
C | T | 33 | a0001c0001t0002g0001a0001c0001t0002g0065a0001c0001t0002g0068others(30): Show | 35 | HG00621.hp2 HG01496.hp2 HG01934.hp2 others(32): Show |
splice_region_variant&intron_variant | LOW | c.3292-6G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 24/39 | chr3 | 13340039 | ||||||
chr3:13340068
|
C | T | 4 | a0005c0003t0001g0245a0005c0003t0001g0247a0005c0003t0001g0281others(1): Show | 4 | HG03017.hp1 HG03491.hp2 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.3292-35G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 24/39 | chr3 | 13340068 | ||||||
chr3:13340123
|
C | T | 15 | a0003c0005t0005g0023a0003c0005t0005g0024a0003c0005t0005g0025others(12): Show | 15 | HG01109.hp1 HG01884.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.3292-90G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 24/39 | chr3 | 13340123 | ||||||
chr3:13340702
|
T | C | 1 | a0020c0020t0001g0193 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3229-404A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 23/39 | chr3 | 13340702 | ||||||
chr3:13340816
|
G | A | 15 | a0003c0005t0005g0023a0003c0005t0005g0024a0003c0005t0005g0025others(12): Show | 15 | HG01109.hp1 HG01884.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.3229-518C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 23/39 | chr3 | 13340816 | ||||||
chr3:13340974
|
G | A | 1 | a0005c0003t0001g0238 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.3229-676C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 23/39 | chr3 | 13340974 | ||||||
chr3:13341085
|
C | T | 3 | a0001c0001t0002g0099a0008c0009t0001g0004a0008c0009t0001g0194 | 4 | HG00280.hp1 HG02615.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.3228+663G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 23/39 | chr3 | 13341085 | ||||||
chr3:13341138
|
A | T | 1 | a0004c0004t0003g0192 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.3228+610T>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 23/39 | chr3 | 13341138 | ||||||
chr3:13341174
|
T | C | 5 | a0004c0004t0003g0169a0004c0004t0003g0170a0004c0004t0003g0171others(2): Show | 5 | HG02258.hp1 HG02630.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.3228+574A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 23/39 | chr3 | 13341174 | ||||||
chr3:13341528
|
G | T | 2 | a0006c0007t0001g0010a0006c0007t0001g0015 | 2 | HG01168.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.3228+220C>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 23/39 | chr3 | 13341528 | ||||||
chr3:13341592
|
T | A | 1 | a0004c0036t0003g0176 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.3228+156A>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 23/39 | chr3 | 13341592 | ||||||
chr3:13341600
|
G | A | 8 | a0001c0001t0002g0062a0001c0001t0002g0064a0001c0001t0002g0086others(5): Show | 8 | HG00323.hp1 HG01167.hp2 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.3228+148C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 23/39 | chr3 | 13341600 | ||||||
chr3:13341650
|
T | C | 1 | a0006c0007t0001g0040 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3228+98A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 23/39 | chr3 | 13341650 | ||||||
chr3:13341696
|
C | G | 1 | a0002c0002t0012g0307 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.3228+52G>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 23/39 | chr3 | 13341696 | ||||||
chr3:13341721
|
A | T | 1 | a0005c0003t0001g0238 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.3228+27T>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 23/39 | chr3 | 13341721 | ||||||
chr3:13342146
|
C | T | 2 | a0003c0011t0001g0035a0003c0011t0001g0036 | 2 | HG02922.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2965-23G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 21/39 | chr3 | 13342146 | ||||||
chr3:13342149
|
G | A | 11 | a0002c0002t0001g0217a0002c0002t0001g0218a0002c0002t0001g0220others(8): Show | 11 | HG00280.hp2 HG00323.hp2 HG00642.hp1 others(8): Show |
intron_variant | MODIFIER | c.2965-26C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 21/39 | chr3 | 13342149 | ||||||
chr3:13342150
|
G | T | 1 | a0023c0026t0011g0290 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2965-27C>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 21/39 | chr3 | 13342150 | ||||||
chr3:13342151
|
G | A | 2 | a0008c0009t0001g0004a0008c0009t0001g0194 | 3 | HG02615.hp2 HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2965-28C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 21/39 | chr3 | 13342151 | ||||||
chr3:13342398
|
G | C | 1 | a0001c0001t0002g0111 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2965-275C>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 21/39 | chr3 | 13342398 | ||||||
chr3:13342421
|
T | C | 1 | a0001c0001t0002g0105 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.2965-298A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 21/39 | chr3 | 13342421 | ||||||
chr3:13342482
|
A | G | 317 | a0001c0001t0002g0001a0001c0001t0002g0041a0001c0001t0002g0042others(314): Show | 322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.2965-359T>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 21/39 | chr3 | 13342482 | ||||||
chr3:13342544
|
T | C | 5 | a0002c0002t0001g0199a0002c0002t0001g0200a0002c0002t0001g0201others(2): Show | 5 | HG01099.hp2 HG02280.hp1 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.2965-421A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 21/39 | chr3 | 13342544 | ||||||
chr3:13342767
|
G | A | 1 | a0005c0003t0001g0238 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2964+408C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 21/39 | chr3 | 13342767 | ||||||
chr3:13342935
|
G | C | 1 | a0009c0030t0005g0009 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2964+240C>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 21/39 | chr3 | 13342935 | ||||||
chr3:13343019
|
G | A | 2 | a0001c0001t0002g0073a0001c0001t0002g0126 | 2 | HG02129.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2964+156C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 21/39 | chr3 | 13343019 | ||||||
chr3:13343032
|
G | A | 5 | a0006c0007t0001g0002a0006c0007t0001g0011a0006c0007t0001g0012others(2): Show | 6 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(3): Show |
intron_variant | MODIFIER | c.2964+143C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 21/39 | chr3 | 13343032 | ||||||
chr3:13343609
|
G | T | 1 | a0020c0020t0001g0193 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2836-306C>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 20/39 | chr3 | 13343609 | ||||||
chr3:13343777
|
G | A | 2 | a0008c0009t0001g0004a0008c0009t0001g0194 | 3 | HG02615.hp2 HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2836-474C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 20/39 | chr3 | 13343777 | ||||||
chr3:13343780
|
A | C | 1 | a0005c0003t0001g0295 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2836-477T>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 20/39 | chr3 | 13343780 | ||||||
chr3:13344195
|
G | T | 1 | a0002c0002t0001g0213 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2836-892C>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 20/39 | chr3 | 13344195 | ||||||
chr3:13344304
|
T | C | 317 | a0001c0001t0002g0001a0001c0001t0002g0041a0001c0001t0002g0042others(314): Show | 322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.2836-1001A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 20/39 | chr3 | 13344304 | ||||||
chr3:13344458
|
G | T | 3 | a0003c0011t0001g0035a0003c0011t0001g0036a0020c0020t0001g0193 | 3 | HG02922.hp1 HG03471.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2836-1155C>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 20/39 | chr3 | 13344458 | ||||||
chr3:13344763
|
G | A | 2 | a0007c0008t0002g0115a0013c0031t0001g0093 | 2 | NA18950.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.2836-1460C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 20/39 | chr3 | 13344763 | ||||||
chr3:13344887
|
C | T | 1 | a0001c0001t0002g0123 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.2836-1584G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 20/39 | chr3 | 13344887 | ||||||
chr3:13344922
|
T | C | 34 | a0003c0011t0001g0035a0003c0011t0001g0036a0004c0004t0003g0107others(31): Show | 35 | HG00544.hp1 HG01081.hp1 HG01516.hp2 others(32): Show |
intron_variant | MODIFIER | c.2836-1619A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 20/39 | chr3 | 13344922 | ||||||
chr3:13344964
|
T | C | 2 | a0003c0011t0001g0035a0003c0011t0001g0036 | 2 | HG02922.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2836-1661A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 20/39 | chr3 | 13344964 | ||||||
chr3:13345024
|
C | T | 1 | a0004c0004t0003g0170 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2836-1721G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 20/39 | chr3 | 13345024 | ||||||
chr3:13345104
|
A | G | 1 | a0003c0005t0005g0031 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2836-1801T>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 20/39 | chr3 | 13345104 | ||||||
chr3:13345315
|
C | T | 1 | a0003c0006t0005g0044 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.2836-2012G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 20/39 | chr3 | 13345315 | ||||||
chr3:13345409
|
C | T | 7 | a0002c0002t0001g0212a0002c0002t0001g0269a0004c0004t0003g0169others(4): Show | 7 | HG02258.hp1 HG02630.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.2836-2106G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 20/39 | chr3 | 13345409 | ||||||
chr3:13345661
|
A | T | 4 | a0005c0003t0001g0303a0005c0003t0001g0304a0005c0003t0001g0306others(1): Show | 4 | HG00735.hp2 HG02486.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.2836-2358T>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 20/39 | chr3 | 13345661 | ||||||
chr3:13345689
|
C | T | 308 | a0001c0001t0002g0001a0001c0001t0002g0041a0001c0001t0002g0062others(305): Show | 313 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(310): Show |
intron_variant | MODIFIER | c.2836-2386G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 20/39 | chr3 | 13345689 | ||||||
chr3:13345773
|
C | G | 1 | a0005c0003t0001g0241 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2836-2470G>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 20/39 | chr3 | 13345773 | ||||||
chr3:13345979
|
C | T | 1 | a0002c0002t0001g0160 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2836-2676G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 20/39 | chr3 | 13345979 | ||||||
chr3:13346118
|
G | A | 4 | a0002c0002t0001g0160a0002c0002t0001g0161a0002c0002t0001g0162others(1): Show | 4 | HG02145.hp1 HG03041.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2836-2815C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 20/39 | chr3 | 13346118 | ||||||
chr3:13346193
|
C | T | 29 | a0004c0004t0003g0107a0004c0004t0003g0108a0004c0004t0003g0165others(26): Show | 29 | HG00544.hp1 HG01081.hp1 HG01516.hp2 others(26): Show |
intron_variant | MODIFIER | c.2836-2890G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 20/39 | chr3 | 13346193 | ||||||
chr3:13346377
|
G | A | 29 | a0004c0004t0003g0107a0004c0004t0003g0108a0004c0004t0003g0165others(26): Show | 29 | HG00544.hp1 HG01081.hp1 HG01516.hp2 others(26): Show |
intron_variant | MODIFIER | c.2836-3074C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 20/39 | chr3 | 13346377 | ||||||
chr3:13346386
|
T | C | 1 | a0003c0006t0005g0044 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.2836-3083A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 20/39 | chr3 | 13346386 | ||||||
chr3:13346392
|
C | A | 2 | a0006c0007t0001g0010a0006c0007t0001g0015 | 2 | HG01168.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.2836-3089G>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 20/39 | chr3 | 13346392 | ||||||
chr3:13346584
|
T | C | 208 | a0002c0002t0001g0050a0002c0002t0001g0160a0002c0002t0001g0161others(205): Show | 210 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.2836-3281A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 20/39 | chr3 | 13346584 | ||||||
chr3:13346699
|
G | A | 11 | a0005c0003t0001g0234a0005c0003t0001g0238a0005c0003t0001g0241others(8): Show | 11 | HG03017.hp1 HG03239.hp1 HG03491.hp2 others(8): Show |
intron_variant | MODIFIER | c.2836-3396C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 20/39 | chr3 | 13346699 | ||||||
chr3:13346703
|
G | C | 1 | a0001c0001t0002g0148 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2836-3400C>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 20/39 | chr3 | 13346703 | ||||||
chr3:13346823
|
G | A | 2 | a0008c0009t0001g0004a0008c0009t0001g0194 | 3 | HG02615.hp2 HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2836-3520C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 20/39 | chr3 | 13346823 | ||||||
chr3:13346917
|
G | A | 1 | a0006c0007t0001g0040 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2836-3614C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 20/39 | chr3 | 13346917 | ||||||
chr3:13346966
|
A | G | 1 | a0003c0005t0005g0023 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2836-3663T>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 20/39 | chr3 | 13346966 | ||||||
chr3:13346970
|
C | T | 1 | a0009c0030t0005g0009 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2836-3667G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 20/39 | chr3 | 13346970 | ||||||
chr3:13347214
|
G | A | 1 | a0002c0002t0001g0206 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2836-3911C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 20/39 | chr3 | 13347214 | ||||||
chr3:13347440
|
G | C | 1 | a0004c0004t0003g0179 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.2836-4137C>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 20/39 | chr3 | 13347440 | ||||||
chr3:13347478
|
C | T | 1 | a0005c0003t0001g0238 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2836-4175G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 20/39 | chr3 | 13347478 | ||||||
chr3:13347572
|
G | A | 2 | a0008c0009t0001g0004a0008c0009t0001g0194 | 3 | HG02615.hp2 HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2836-4269C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 20/39 | chr3 | 13347572 | ||||||
chr3:13347608
|
A | G | 29 | a0004c0004t0003g0107a0004c0004t0003g0108a0004c0004t0003g0165others(26): Show | 29 | HG00544.hp1 HG01081.hp1 HG01516.hp2 others(26): Show |
intron_variant | MODIFIER | c.2835+4271T>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 20/39 | chr3 | 13347608 | ||||||
chr3:13347672
|
C | G | 2 | a0002c0002t0001g0221a0002c0002t0001g0222 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.2835+4207G>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 20/39 | chr3 | 13347672 | ||||||
chr3:13347678
|
G | A | 29 | a0004c0004t0003g0107a0004c0004t0003g0108a0004c0004t0003g0165others(26): Show | 29 | HG00544.hp1 HG01081.hp1 HG01516.hp2 others(26): Show |
intron_variant | MODIFIER | c.2835+4201C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 20/39 | chr3 | 13347678 | ||||||
chr3:13347921
|
G | A | 1 | a0002c0002t0001g0230 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.2835+3958C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 20/39 | chr3 | 13347921 | ||||||
chr3:13347927
|
A | G | 3 | a0003c0011t0001g0035a0003c0011t0001g0036a0020c0020t0001g0193 | 3 | HG02922.hp1 HG03471.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2835+3952T>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 20/39 | chr3 | 13347927 | ||||||
chr3:13348033
|
G | A | 5 | a0001c0001t0002g0042a0001c0001t0002g0043a0001c0001t0002g0045others(2): Show | 5 | HG01346.hp1 HG01978.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.2835+3846C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 20/39 | chr3 | 13348033 | ||||||
chr3:13348061
|
C | A | 29 | a0004c0004t0003g0107a0004c0004t0003g0108a0004c0004t0003g0165others(26): Show | 29 | HG00544.hp1 HG01081.hp1 HG01516.hp2 others(26): Show |
intron_variant | MODIFIER | c.2835+3818G>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 20/39 | chr3 | 13348061 | ||||||
chr3:13348338
|
C | A | 3 | a0004c0004t0003g0165a0004c0004t0003g0175a0004c0036t0003g0176 | 3 | HG02071.hp2 NA18962.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.2835+3541G>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 20/39 | chr3 | 13348338 | ||||||
chr3:13348650
|
C | T | 1 | a0001c0001t0002g0155 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2835+3229G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 20/39 | chr3 | 13348650 | ||||||
chr3:13348791
|
G | A | 2 | a0008c0009t0001g0004a0008c0009t0001g0194 | 3 | HG02615.hp2 HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2835+3088C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 20/39 | chr3 | 13348791 | ||||||
chr3:13348979
|
C | T | 1 | a0003c0005t0005g0031 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2835+2900G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 20/39 | chr3 | 13348979 | ||||||
chr3:13349055
|
C | T | 1 | a0002c0002t0001g0237 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.2835+2824G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 20/39 | chr3 | 13349055 | ||||||
chr3:13349129
|
A | G | 208 | a0002c0002t0001g0050a0002c0002t0001g0160a0002c0002t0001g0161others(205): Show | 210 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.2835+2750T>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 20/39 | chr3 | 13349129 | ||||||
chr3:13349240
|
T | G | 208 | a0002c0002t0001g0050a0002c0002t0001g0160a0002c0002t0001g0161others(205): Show | 210 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.2835+2639A>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 20/39 | chr3 | 13349240 | ||||||
chr3:13349453
|
C | T | 1 | a0001c0001t0002g0082 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2835+2426G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 20/39 | chr3 | 13349453 | ||||||
chr3:13349655
|
A | T | 2 | a0003c0006t0005g0008a0003c0006t0005g0049 | 2 | HG01243.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.2835+2224T>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 20/39 | chr3 | 13349655 | ||||||
chr3:13349669
|
C | T | 1 | a0002c0029t0001g0315 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2835+2210G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 20/39 | chr3 | 13349669 | ||||||
chr3:13349921
|
C | A | 1 | a0018c0023t0001g0177 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2835+1958G>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 20/39 | chr3 | 13349921 | ||||||
chr3:13350191
|
CGTGTGTG others(27): Show |
C | 18 | a0003c0005t0005g0031a0003c0006t0005g0008a0003c0006t0005g0044others(15): Show | 18 | HG01243.hp2 HG02135.hp2 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.2835+1654_2835+168 others(38): Show |
NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 20/39 | chr3 | 13350191 | ||||||
chr3:13350437
|
A | AAAAAC | 49 | a0001c0001t0002g0042a0001c0001t0002g0043a0001c0001t0002g0045others(46): Show | 49 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(46): Show |
intron_variant | MODIFIER | c.2835+1437_2835+144 others(9): Show |
NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 20/39 | chr3 | 13350437 | ||||||
chr3:13350437
|
A | AAAAACAA others(3): Show |
7 | a0001c0001t0002g0071a0001c0001t0002g0076a0001c0001t0002g0077others(4): Show | 7 | HG00558.hp1 HG00639.hp1 HG01496.hp1 others(4): Show |
intron_variant | MODIFIER | c.2835+1432_2835+144 others(14): Show |
NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 20/39 | chr3 | 13350437 | ||||||
chr3:13350437
|
AAAAAC | A | 120 | a0001c0001t0002g0116a0001c0001t0002g0147a0001c0001t0002g0152others(117): Show | 120 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(117): Show |
intron_variant | MODIFIER | c.2835+1437_2835+144 others(9): Show |
NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 20/39 | chr3 | 13350437 | ||||||
chr3:13350437
|
AAAAACAA others(3): Show |
A | 22 | a0001c0001t0002g0113a0002c0002t0004g0259a0003c0005t0005g0023others(19): Show | 22 | HG01109.hp1 HG01884.hp1 HG02280.hp2 others(19): Show |
intron_variant | MODIFIER | c.2835+1432_2835+144 others(14): Show |
NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 20/39 | chr3 | 13350437 | ||||||
chr3:13350437
|
AAAAACAA others(8): Show |
A | 3 | a0002c0002t0001g0277a0008c0009t0001g0004a0008c0009t0001g0194 | 4 | HG02615.hp2 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.2835+1427_2835+144 others(19): Show |
NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 20/39 | chr3 | 13350437 | ||||||
chr3:13350457
|
CAAAACAA others(15): Show |
C | 46 | a0005c0003t0001g0215a0005c0003t0001g0216a0005c0003t0001g0234others(43): Show | 47 | HG00140.hp1 HG00140.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.2835+1400_2835+142 others(26): Show |
NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 20/39 | chr3 | 13350457 | ||||||
chr3:13350462
|
CAAAACAA others(10): Show |
C | 1 | a0002c0002t0004g0289 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.2835+1400_2835+141 others(21): Show |
NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 20/39 | chr3 | 13350462 | ||||||
chr3:13350543
|
T | A | 1 | a0001c0001t0002g0139 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.2835+1336A>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 20/39 | chr3 | 13350543 | ||||||
chr3:13350692
|
C | CT | 10 | a0001c0001t0002g0129a0001c0001t0002g0134a0001c0001t0002g0140others(7): Show | 10 | HG00438.hp2 HG00621.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.2835+1186dupA | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 20/39 | chr3 | 13350692 | ||||||
chr3:13350692
|
CT | C | 39 | a0001c0001t0002g0100a0001c0001t0002g0101a0001c0001t0002g0131others(36): Show | 40 | HG00544.hp1 HG01081.hp1 HG01243.hp1 others(37): Show |
intron_variant | MODIFIER | c.2835+1186delA | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 20/39 | chr3 | 13350692 | ||||||
chr3:13350730
|
G | A | 29 | a0004c0004t0003g0107a0004c0004t0003g0108a0004c0004t0003g0165others(26): Show | 29 | HG00544.hp1 HG01081.hp1 HG01516.hp2 others(26): Show |
intron_variant | MODIFIER | c.2835+1149C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 20/39 | chr3 | 13350730 | ||||||
chr3:13351129
|
C | T | 2 | a0003c0011t0001g0035a0003c0011t0001g0036 | 2 | HG02922.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2835+750G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 20/39 | chr3 | 13351129 | ||||||
chr3:13351404
|
G | A | 1 | a0020c0020t0001g0193 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2835+475C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 20/39 | chr3 | 13351404 | ||||||
chr3:13351420
|
C | T | 20 | a0002c0002t0001g0208a0002c0002t0001g0235a0002c0002t0001g0237others(17): Show | 20 | HG00099.hp1 HG00544.hp2 HG00621.hp1 others(17): Show |
intron_variant | MODIFIER | c.2835+459G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 20/39 | chr3 | 13351420 | ||||||
chr3:13351579
|
G | A | 1 | a0006c0007t0001g0022 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2835+300C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 20/39 | chr3 | 13351579 | ||||||
chr3:13351632
|
C | T | 1 | a0001c0001t0002g0131 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2835+247G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 20/39 | chr3 | 13351632 | ||||||
chr3:13351666
|
CT | C | 158 | a0002c0002t0001g0050a0002c0002t0001g0160a0002c0002t0001g0161others(155): Show | 159 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.2835+212delA | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 20/39 | chr3 | 13351666 | ||||||
chr3:13351666
|
CTT | C | 11 | a0003c0005t0005g0278a0003c0006t0006g0051a0003c0006t0006g0052others(8): Show | 11 | HG02486.hp1 HG02559.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.2835+211_2835+212d others(4): Show |
NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 20/39 | chr3 | 13351666 | ||||||
chr3:13351793
|
G | C | 1 | a0020c0020t0001g0193 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2835+86C>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 20/39 | chr3 | 13351793 | ||||||
chr3:13351861
|
C | A | 1 | a0002c0002t0004g0262 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.2835+18G>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 20/39 | chr3 | 13351861 | ||||||
chr3:13352224
|
T | C | 1 | a0002c0002t0007g0209 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.2629-40A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 18/39 | chr3 | 13352224 | ||||||
chr3:13352240
|
C | T | 2 | a0008c0009t0001g0004a0008c0009t0001g0194 | 3 | HG02615.hp2 HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2629-56G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 18/39 | chr3 | 13352240 | ||||||
chr3:13352516
|
A | G | 1 | a0003c0006t0005g0049 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2629-332T>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 18/39 | chr3 | 13352516 | ||||||
chr3:13352635
|
A | C | 2 | a0008c0009t0001g0004a0008c0009t0001g0194 | 3 | HG02615.hp2 HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2629-451T>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 18/39 | chr3 | 13352635 | ||||||
chr3:13352638
|
T | C | 1 | a0002c0029t0001g0315 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2629-454A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 18/39 | chr3 | 13352638 | ||||||
chr3:13352759
|
G | C | 320 | a0001c0001t0002g0001a0001c0001t0002g0041a0001c0001t0002g0042others(317): Show | 325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.2629-575C>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 18/39 | chr3 | 13352759 | ||||||
chr3:13352857
|
G | T | 11 | a0004c0004t0003g0166a0004c0004t0003g0167a0004c0004t0003g0168others(8): Show | 11 | HG00544.hp1 HG01516.hp2 HG01517.hp1 others(8): Show |
intron_variant | MODIFIER | c.2629-673C>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 18/39 | chr3 | 13352857 | ||||||
chr3:13352949
|
G | C | 1 | a0001c0001t0002g0042 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2628+605C>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 18/39 | chr3 | 13352949 | ||||||
chr3:13352999
|
G | A | 1 | a0009c0028t0003g0034 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2628+555C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 18/39 | chr3 | 13352999 | ||||||
chr3:13353062
|
C | G | 1 | a0001c0001t0002g0105 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.2628+492G>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 18/39 | chr3 | 13353062 | ||||||
chr3:13353184
|
G | A | 2 | a0002c0002t0001g0223a0002c0002t0001g0227 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.2628+370C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 18/39 | chr3 | 13353184 | ||||||
chr3:13353188
|
C | T | 30 | a0002c0002t0001g0239a0002c0002t0004g0038a0002c0002t0004g0156others(27): Show | 30 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(27): Show |
intron_variant | MODIFIER | c.2628+366G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 18/39 | chr3 | 13353188 | ||||||
chr3:13353360
|
A | C | 3 | a0001c0001t0002g0072a0001c0001t0002g0143a0001c0001t0002g0145 | 3 | NA18954.hp1 NA18994.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.2628+194T>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 18/39 | chr3 | 13353360 | ||||||
chr3:13353432
|
G | T | 30 | a0002c0002t0001g0239a0002c0002t0004g0038a0002c0002t0004g0156others(27): Show | 30 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(27): Show |
intron_variant | MODIFIER | c.2628+122C>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 18/39 | chr3 | 13353432 | ||||||
chr3:13353680
|
A | T | 1 | a0004c0004t0003g0172 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2522-20T>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 17/39 | chr3 | 13353680 | ||||||
chr3:13353893
|
A | G | 1 | a0002c0002t0004g0320 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.2521+22T>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 17/39 | chr3 | 13353893 | ||||||
chr3:13354453
|
G | A | 1 | a0001c0001t0002g0153 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2329-346C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 16/39 | chr3 | 13354453 | ||||||
chr3:13354495
|
C | G | 3 | a0003c0011t0001g0035a0003c0011t0001g0036a0020c0020t0001g0193 | 3 | HG02922.hp1 HG03471.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2329-388G>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 16/39 | chr3 | 13354495 | ||||||
chr3:13354496
|
G | A | 1 | a0003c0006t0006g0051 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2329-389C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 16/39 | chr3 | 13354496 | ||||||
chr3:13354787
|
C | T | 2 | a0008c0009t0001g0004a0008c0009t0001g0194 | 3 | HG02615.hp2 HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2329-680G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 16/39 | chr3 | 13354787 | ||||||
chr3:13355183
|
G | A | 1 | a0001c0001t0002g0102 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.2329-1076C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 16/39 | chr3 | 13355183 | ||||||
chr3:13355201
|
C | G | 31 | a0003c0005t0005g0023a0003c0005t0005g0024a0003c0005t0005g0025others(28): Show | 31 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.2329-1094G>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 16/39 | chr3 | 13355201 | ||||||
chr3:13355212
|
A | G | 1 | a0004c0004t0003g0168 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.2329-1105T>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 16/39 | chr3 | 13355212 | ||||||
chr3:13355242
|
A | T | 1 | a0003c0006t0006g0059 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2329-1135T>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 16/39 | chr3 | 13355242 | ||||||
chr3:13355274
|
T | G | 3 | a0004c0004t0003g0165a0004c0004t0003g0175a0004c0036t0003g0176 | 3 | HG02071.hp2 NA18962.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.2329-1167A>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 16/39 | chr3 | 13355274 | ||||||
chr3:13355602
|
C | T | 1 | a0003c0005t0005g0028 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2329-1495G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 16/39 | chr3 | 13355602 | ||||||
chr3:13355722
|
C | A | 1 | a0004c0036t0003g0176 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.2329-1615G>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 16/39 | chr3 | 13355722 | ||||||
chr3:13355848
|
C | A | 4 | a0003c0006t0005g0008a0003c0006t0005g0044a0003c0006t0005g0046others(1): Show | 4 | HG01243.hp2 HG02135.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.2329-1741G>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 16/39 | chr3 | 13355848 | ||||||
chr3:13355860
|
T | C | 1 | a0002c0002t0001g0208 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.2329-1753A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 16/39 | chr3 | 13355860 | ||||||
chr3:13355913
|
A | G | 2 | a0003c0011t0001g0035a0003c0011t0001g0036 | 2 | HG02922.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2329-1806T>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 16/39 | chr3 | 13355913 | ||||||
chr3:13355935
|
G | A | 3 | a0005c0003t0001g0234a0005c0003t0001g0241a0005c0003t0001g0256 | 3 | HG03239.hp1 HG03688.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.2329-1828C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 16/39 | chr3 | 13355935 | ||||||
chr3:13356109
|
C | T | 4 | a0001c0001t0002g0265a0001c0001t0002g0274a0001c0001t0002g0288others(1): Show | 4 | NA18945.hp2 NA18983.hp2 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.2329-2002G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 16/39 | chr3 | 13356109 | ||||||
chr3:13356143
|
A | G | 2 | a0008c0009t0001g0004a0008c0009t0001g0194 | 3 | HG02615.hp2 HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2329-2036T>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 16/39 | chr3 | 13356143 | ||||||
chr3:13356146
|
C | T | 2 | a0001c0001t0002g0087a0001c0001t0002g0140 | 2 | HG01975.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.2329-2039G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 16/39 | chr3 | 13356146 | ||||||
chr3:13356382
|
C | T | 1 | a0001c0001t0002g0080 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2328+1840G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 16/39 | chr3 | 13356382 | ||||||
chr3:13356512
|
G | A | 1 | a0007c0008t0002g0136 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.2328+1710C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 16/39 | chr3 | 13356512 | ||||||
chr3:13356600
|
G | A | 29 | a0004c0004t0003g0107a0004c0004t0003g0108a0004c0004t0003g0165others(26): Show | 29 | HG00544.hp1 HG01081.hp1 HG01516.hp2 others(26): Show |
intron_variant | MODIFIER | c.2328+1622C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 16/39 | chr3 | 13356600 | ||||||
chr3:13356954
|
T | C | 1 | a0001c0001t0002g0139 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.2328+1268A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 16/39 | chr3 | 13356954 | ||||||
chr3:13357353
|
G | A | 1 | a0002c0002t0001g0203 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2328+869C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 16/39 | chr3 | 13357353 | ||||||
chr3:13357463
|
T | C | 174 | a0001c0001t0002g0130a0002c0002t0001g0050a0002c0002t0001g0160others(171): Show | 175 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.2328+759A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 16/39 | chr3 | 13357463 | ||||||
chr3:13357644
|
C | T | 2 | a0012c0012t0004g0272a0012c0012t0004g0318 | 2 | HG01975.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.2328+578G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 16/39 | chr3 | 13357644 | ||||||
chr3:13357685
|
A | G | 1 | a0001c0001t0002g0149 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.2328+537T>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 16/39 | chr3 | 13357685 | ||||||
chr3:13357696
|
G | A | 2 | a0001c0001t0002g0106a0001c0001t0002g0116 | 2 | HG03516.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2328+526C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 16/39 | chr3 | 13357696 | ||||||
chr3:13357837
|
C | T | 1 | a0001c0001t0002g0158 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.2328+385G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 16/39 | chr3 | 13357837 | ||||||
chr3:13357971
|
C | T | 2 | a0006c0007t0001g0010a0006c0007t0001g0015 | 2 | HG01168.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.2328+251G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 16/39 | chr3 | 13357971 | ||||||
chr3:13358147
|
T | G | 1 | a0011c0015t0001g0098 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2328+75A>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 16/39 | chr3 | 13358147 | ||||||
chr3:13358148
|
G | A | 1 | a0001c0001t0002g0063 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.2328+74C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 16/39 | chr3 | 13358148 | ||||||
chr3:13358182
|
G | A | 29 | a0004c0004t0003g0107a0004c0004t0003g0108a0004c0004t0003g0165others(26): Show | 29 | HG00544.hp1 HG01081.hp1 HG01516.hp2 others(26): Show |
intron_variant | MODIFIER | c.2328+40C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 16/39 | chr3 | 13358182 | ||||||
chr3:13358448
|
T | C | 48 | a0005c0003t0001g0215a0005c0003t0001g0216a0005c0003t0001g0234others(45): Show | 49 | HG00140.hp1 HG00140.hp2 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.2155-53A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 15/39 | chr3 | 13358448 | ||||||
chr3:13358496
|
C | G | 14 | a0001c0001t0002g0066a0001c0001t0002g0070a0001c0001t0002g0097others(11): Show | 14 | HG00597.hp2 HG02132.hp1 NA18945.hp1 others(11): Show |
intron_variant | MODIFIER | c.2155-101G>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 15/39 | chr3 | 13358496 | ||||||
chr3:13358571
|
A | G | 1 | a0020c0020t0001g0193 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2155-176T>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 15/39 | chr3 | 13358571 | ||||||
chr3:13358606
|
G | C | 2 | a0004c0004t0003g0178a0004c0004t0003g0180 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.2155-211C>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 15/39 | chr3 | 13358606 | ||||||
chr3:13358656
|
C | T | 2 | a0002c0002t0001g0310a0002c0002t0001g0311 | 2 | HG00099.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.2155-261G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 15/39 | chr3 | 13358656 | ||||||
chr3:13358717
|
A | G | 1 | a0005c0003t0001g0295 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2155-322T>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 15/39 | chr3 | 13358717 | ||||||
chr3:13358775
|
G | A | 29 | a0004c0004t0003g0107a0004c0004t0003g0108a0004c0004t0003g0165others(26): Show | 29 | HG00544.hp1 HG01081.hp1 HG01516.hp2 others(26): Show |
intron_variant | MODIFIER | c.2155-380C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 15/39 | chr3 | 13358775 | ||||||
chr3:13359116
|
C | A | 2 | a0003c0011t0001g0035a0003c0011t0001g0036 | 2 | HG02922.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2155-721G>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 15/39 | chr3 | 13359116 | ||||||
chr3:13359221
|
C | G | 174 | a0002c0002t0001g0050a0002c0002t0001g0160a0002c0002t0001g0161others(171): Show | 175 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.2155-826G>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 15/39 | chr3 | 13359221 | ||||||
chr3:13359226
|
A | G | 2 | a0008c0009t0001g0004a0008c0009t0001g0194 | 3 | HG02615.hp2 HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2155-831T>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 15/39 | chr3 | 13359226 | ||||||
chr3:13359364
|
C | T | 1 | a0003c0005t0005g0031 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2154+906G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 15/39 | chr3 | 13359364 | ||||||
chr3:13359716
|
C | T | 1 | a0001c0001t0002g0094 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.2154+554G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 15/39 | chr3 | 13359716 | ||||||
chr3:13359720
|
A | T | 2 | a0008c0009t0001g0004a0008c0009t0001g0194 | 3 | HG02615.hp2 HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2154+550T>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 15/39 | chr3 | 13359720 | ||||||
chr3:13359723
|
C | T | 2 | a0008c0009t0001g0004a0008c0009t0001g0194 | 3 | HG02615.hp2 HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2154+547G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 15/39 | chr3 | 13359723 | ||||||
chr3:13359933
|
C | T | 1 | a0002c0002t0004g0253 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2154+337G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 15/39 | chr3 | 13359933 | ||||||
chr3:13360141
|
T | C | 2 | a0002c0002t0001g0231a0002c0002t0001g0257 | 2 | HG01981.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.2154+129A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 15/39 | chr3 | 13360141 | ||||||
chr3:13360229
|
T | C | 2 | a0003c0011t0001g0035a0003c0011t0001g0036 | 2 | HG02922.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2154+41A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 15/39 | chr3 | 13360229 | ||||||
chr3:13360508
|
C | A | 1 | a0003c0019t0013g0164 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1933-17G>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 14/39 | chr3 | 13360508 | ||||||
chr3:13360650
|
C | T | 208 | a0002c0002t0001g0050a0002c0002t0001g0160a0002c0002t0001g0161others(205): Show | 210 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.1933-159G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 14/39 | chr3 | 13360650 | ||||||
chr3:13360689
|
T | C | 1 | a0020c0020t0001g0193 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1933-198A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 14/39 | chr3 | 13360689 | ||||||
chr3:13360891
|
C | T | 3 | a0003c0011t0001g0035a0003c0011t0001g0036a0020c0020t0001g0193 | 3 | HG02922.hp1 HG03471.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1933-400G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 14/39 | chr3 | 13360891 | ||||||
chr3:13360967
|
G | A | 1 | a0003c0019t0013g0164 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1933-476C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 14/39 | chr3 | 13360967 | ||||||
chr3:13361051
|
G | A | 1 | a0001c0001t0002g0088 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1933-560C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 14/39 | chr3 | 13361051 | ||||||
chr3:13361118
|
T | C | 1 | a0002c0002t0007g0309 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1933-627A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 14/39 | chr3 | 13361118 | ||||||
chr3:13361165
|
G | A | 1 | a0001c0001t0002g0073 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1933-674C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 14/39 | chr3 | 13361165 | ||||||
chr3:13361311
|
A | AAAG | 3 | a0003c0011t0001g0035a0003c0011t0001g0036a0020c0020t0001g0193 | 3 | HG02922.hp1 HG03471.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1933-823_1933-821d others(5): Show |
NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 14/39 | chr3 | 13361311 | ||||||
chr3:13361359
|
G | A | 2 | a0008c0009t0001g0004a0008c0009t0001g0194 | 3 | HG02615.hp2 HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1933-868C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 14/39 | chr3 | 13361359 | ||||||
chr3:13361375
|
T | C | 32 | a0003c0011t0001g0035a0003c0011t0001g0036a0004c0004t0003g0107others(29): Show | 32 | HG00544.hp1 HG01081.hp1 HG01516.hp2 others(29): Show |
intron_variant | MODIFIER | c.1933-884A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 14/39 | chr3 | 13361375 | ||||||
chr3:13361391
|
G | A | 34 | a0003c0011t0001g0035a0003c0011t0001g0036a0004c0004t0003g0107others(31): Show | 35 | HG00544.hp1 HG01081.hp1 HG01516.hp2 others(32): Show |
intron_variant | MODIFIER | c.1933-900C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 14/39 | chr3 | 13361391 | ||||||
chr3:13361669
|
T | C | 208 | a0002c0002t0001g0050a0002c0002t0001g0160a0002c0002t0001g0161others(205): Show | 210 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.1933-1178A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 14/39 | chr3 | 13361669 | ||||||
chr3:13361881
|
T | G | 29 | a0004c0004t0003g0107a0004c0004t0003g0108a0004c0004t0003g0165others(26): Show | 29 | HG00544.hp1 HG01081.hp1 HG01516.hp2 others(26): Show |
intron_variant | MODIFIER | c.1933-1390A>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 14/39 | chr3 | 13361881 | ||||||
chr3:13361937
|
C | T | 1 | a0002c0002t0001g0284 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1933-1446G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 14/39 | chr3 | 13361937 | ||||||
chr3:13362140
|
C | G | 34 | a0003c0011t0001g0035a0003c0011t0001g0036a0004c0004t0003g0107others(31): Show | 35 | HG00544.hp1 HG01081.hp1 HG01516.hp2 others(32): Show |
intron_variant | MODIFIER | c.1933-1649G>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 14/39 | chr3 | 13362140 | ||||||
chr3:13362170
|
G | A | 1 | a0002c0002t0001g0230 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1933-1679C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 14/39 | chr3 | 13362170 | ||||||
chr3:13362344
|
C | T | 2 | a0003c0011t0001g0035a0003c0011t0001g0036 | 2 | HG02922.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1933-1853G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 14/39 | chr3 | 13362344 | ||||||
chr3:13362426
|
A | G | 1 | a0002c0002t0001g0235 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1933-1935T>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 14/39 | chr3 | 13362426 | ||||||
chr3:13362861
|
G | A | 2 | a0001c0001t0002g0086a0001c0001t0002g0133 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1933-2370C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 14/39 | chr3 | 13362861 | ||||||
chr3:13362987
|
T | C | 1 | a0009c0030t0005g0009 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1933-2496A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 14/39 | chr3 | 13362987 | ||||||
chr3:13363095
|
C | A | 2 | a0003c0011t0001g0035a0003c0011t0001g0036 | 2 | HG02922.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1933-2604G>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 14/39 | chr3 | 13363095 | ||||||
chr3:13363217
|
T | C | 174 | a0002c0002t0001g0050a0002c0002t0001g0160a0002c0002t0001g0161others(171): Show | 175 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.1933-2726A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 14/39 | chr3 | 13363217 | ||||||
chr3:13363261
|
G | A | 174 | a0002c0002t0001g0050a0002c0002t0001g0160a0002c0002t0001g0161others(171): Show | 175 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.1932+2685C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 14/39 | chr3 | 13363261 | ||||||
chr3:13363307
|
T | G | 2 | a0002c0002t0001g0249a0002c0002t0001g0258 | 2 | HG00544.hp2 HG00621.hp1 |
intron_variant | MODIFIER | c.1932+2639A>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 14/39 | chr3 | 13363307 | ||||||
chr3:13363419
|
G | A | 1 | a0005c0003t0001g0215 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1932+2527C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 14/39 | chr3 | 13363419 | ||||||
chr3:13363567
|
T | C | 2 | a0003c0011t0001g0035a0003c0011t0001g0036 | 2 | HG02922.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1932+2379A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 14/39 | chr3 | 13363567 | ||||||
chr3:13363720
|
G | A | 15 | a0003c0005t0005g0023a0003c0005t0005g0024a0003c0005t0005g0025others(12): Show | 15 | HG01109.hp1 HG01884.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.1932+2226C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 14/39 | chr3 | 13363720 | ||||||
chr3:13363800
|
C | T | 1 | a0020c0020t0001g0193 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1932+2146G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 14/39 | chr3 | 13363800 | ||||||
chr3:13363982
|
C | A | 5 | a0001c0001t0002g0265a0001c0001t0002g0274a0001c0001t0002g0276others(2): Show | 5 | NA18945.hp2 NA18983.hp2 NA18998.hp2 others(2): Show |
intron_variant | MODIFIER | c.1932+1964G>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 14/39 | chr3 | 13363982 | ||||||
chr3:13364203
|
G | A | 32 | a0003c0011t0001g0035a0003c0011t0001g0036a0004c0004t0003g0107others(29): Show | 32 | HG00544.hp1 HG01081.hp1 HG01516.hp2 others(29): Show |
intron_variant | MODIFIER | c.1932+1743C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 14/39 | chr3 | 13364203 | ||||||
chr3:13364228
|
G | A | 4 | a0005c0003t0001g0238a0005c0003t0001g0242a0005c0003t0001g0268others(1): Show | 4 | NA18939.hp2 NA18946.hp2 NA18956.hp1 others(1): Show |
intron_variant | MODIFIER | c.1932+1718C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 14/39 | chr3 | 13364228 | ||||||
chr3:13364269
|
A | T | 1 | a0004c0004t0003g0168 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1932+1677T>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 14/39 | chr3 | 13364269 | ||||||
chr3:13364279
|
T | C | 1 | a0002c0002t0001g0218 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1932+1667A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 14/39 | chr3 | 13364279 | ||||||
chr3:13364388
|
C | T | 1 | a0001c0001t0002g0274 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1932+1558G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 14/39 | chr3 | 13364388 | ||||||
chr3:13364392
|
G | A | 1 | a0002c0002t0004g0287 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1932+1554C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 14/39 | chr3 | 13364392 | ||||||
chr3:13364557
|
G | A | 2 | a0003c0011t0001g0035a0003c0011t0001g0036 | 2 | HG02922.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1932+1389C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 14/39 | chr3 | 13364557 | ||||||
chr3:13364557
|
G | T | 1 | a0020c0020t0001g0193 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1932+1389C>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 14/39 | chr3 | 13364557 | ||||||
chr3:13365173
|
C | T | 1 | a0004c0004t0003g0165 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1932+773G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 14/39 | chr3 | 13365173 | ||||||
chr3:13365239
|
C | T | 15 | a0003c0005t0005g0023a0003c0005t0005g0024a0003c0005t0005g0025others(12): Show | 15 | HG01109.hp1 HG01884.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.1932+707G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 14/39 | chr3 | 13365239 | ||||||
chr3:13365325
|
C | T | 2 | a0003c0006t0008g0006a0003c0006t0008g0007 | 2 | HG03130.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1932+621G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 14/39 | chr3 | 13365325 | ||||||
chr3:13365326
|
C | A | 2 | a0003c0006t0008g0006a0003c0006t0008g0007 | 2 | HG03130.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1932+620G>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 14/39 | chr3 | 13365326 | ||||||
chr3:13365433
|
G | A | 1 | a0003c0019t0013g0164 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1932+513C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 14/39 | chr3 | 13365433 | ||||||
chr3:13365539
|
C | T | 7 | a0006c0007t0001g0002a0006c0007t0001g0010a0006c0007t0001g0011others(4): Show | 8 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(5): Show |
intron_variant | MODIFIER | c.1932+407G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 14/39 | chr3 | 13365539 | ||||||
chr3:13365546
|
G | A | 1 | a0009c0027t0003g0019 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1932+400C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 14/39 | chr3 | 13365546 | ||||||
chr3:13365564
|
C | T | 3 | a0002c0002t0007g0209a0002c0002t0007g0264a0002c0002t0007g0314 | 3 | NA18950.hp2 NA18969.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.1932+382G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 14/39 | chr3 | 13365564 | ||||||
chr3:13365647
|
C | G | 205 | a0002c0002t0001g0050a0002c0002t0001g0160a0002c0002t0001g0161others(202): Show | 207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.1932+299G>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 14/39 | chr3 | 13365647 | ||||||
chr3:13365674
|
T | C | 1 | a0001c0001t0002g0043 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1932+272A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 14/39 | chr3 | 13365674 | ||||||
chr3:13365718
|
G | A | 1 | a0001c0001t0002g0127 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1932+228C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 14/39 | chr3 | 13365718 | ||||||
chr3:13366144
|
T | G | 1 | a0004c0004t0003g0174 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1787-53A>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 13/39 | chr3 | 13366144 | ||||||
chr3:13366257
|
T | C | 16 | a0003c0006t0005g0008a0003c0006t0005g0044a0003c0006t0005g0046others(13): Show | 16 | HG01243.hp2 HG02135.hp2 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.1787-166A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 13/39 | chr3 | 13366257 | ||||||
chr3:13366314
|
T | C | 1 | a0020c0020t0001g0193 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1787-223A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 13/39 | chr3 | 13366314 | ||||||
chr3:13366516
|
C | CT | 11 | a0001c0001t0002g0062a0001c0001t0002g0064a0001c0001t0002g0130others(8): Show | 12 | HG00323.hp1 HG01167.hp2 HG01517.hp1 others(9): Show |
intron_variant | MODIFIER | c.1787-426dupA | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 13/39 | chr3 | 13366516 | ||||||
chr3:13366516
|
C | CTT | 26 | a0004c0004t0003g0107a0004c0004t0003g0108a0004c0004t0003g0165others(23): Show | 26 | HG00544.hp1 HG01081.hp1 HG01516.hp2 others(23): Show |
intron_variant | MODIFIER | c.1787-427_1787-426d others(4): Show |
NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 13/39 | chr3 | 13366516 | ||||||
chr3:13366516
|
CT | C | 155 | a0001c0001t0002g0084a0001c0001t0002g0128a0002c0002t0001g0050others(152): Show | 156 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.1787-426delA | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 13/39 | chr3 | 13366516 | ||||||
chr3:13366520
|
T | C | 2 | a0001c0001t0002g0106a0001c0001t0002g0116 | 2 | HG03516.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1787-429A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 13/39 | chr3 | 13366520 | ||||||
chr3:13366596
|
C | A | 1 | a0002c0002t0004g0316 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1787-505G>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 13/39 | chr3 | 13366596 | ||||||
chr3:13366640
|
C | T | 1 | a0003c0019t0013g0164 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1787-549G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 13/39 | chr3 | 13366640 | ||||||
chr3:13366643
|
G | A | 1 | a0020c0020t0001g0193 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1787-552C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 13/39 | chr3 | 13366643 | ||||||
chr3:13366675
|
G | A | 1 | a0002c0002t0007g0236 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1787-584C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 13/39 | chr3 | 13366675 | ||||||
chr3:13366807
|
G | A | 29 | a0004c0004t0003g0107a0004c0004t0003g0108a0004c0004t0003g0165others(26): Show | 29 | HG00544.hp1 HG01081.hp1 HG01516.hp2 others(26): Show |
intron_variant | MODIFIER | c.1787-716C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 13/39 | chr3 | 13366807 | ||||||
chr3:13366847
|
A | G | 179 | a0002c0002t0001g0050a0002c0002t0001g0160a0002c0002t0001g0161others(176): Show | 181 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(178): Show |
intron_variant | MODIFIER | c.1787-756T>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 13/39 | chr3 | 13366847 | ||||||
chr3:13366852
|
C | T | 9 | a0003c0006t0006g0051a0003c0006t0006g0052a0003c0006t0006g0053others(6): Show | 9 | HG02486.hp1 HG02559.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.1787-761G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 13/39 | chr3 | 13366852 | ||||||
chr3:13366900
|
G | A | 2 | a0001c0001t0002g0140a0004c0004t0003g0107 | 2 | HG02071.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.1787-809C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 13/39 | chr3 | 13366900 | ||||||
chr3:13366958
|
C | T | 1 | a0006c0007t0001g0011 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1787-867G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 13/39 | chr3 | 13366958 | ||||||
chr3:13367018
|
C | T | 1 | a0005c0003t0001g0293 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.1787-927G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 13/39 | chr3 | 13367018 | ||||||
chr3:13367224
|
G | C | 30 | a0004c0004t0003g0107a0004c0004t0003g0108a0004c0004t0003g0165others(27): Show | 30 | HG00544.hp1 HG01081.hp1 HG01516.hp2 others(27): Show |
intron_variant | MODIFIER | c.1787-1133C>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 13/39 | chr3 | 13367224 | ||||||
chr3:13367337
|
A | C | 1 | a0001c0001t0002g0080 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1787-1246T>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 13/39 | chr3 | 13367337 | ||||||
chr3:13367407
|
C | T | 1 | a0002c0002t0004g0312 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1787-1316G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 13/39 | chr3 | 13367407 | ||||||
chr3:13367408
|
G | A | 1 | a0003c0005t0005g0023 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1787-1317C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 13/39 | chr3 | 13367408 | ||||||
chr3:13367607
|
G | A | 176 | a0002c0002t0001g0050a0002c0002t0001g0160a0002c0002t0001g0161others(173): Show | 177 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.1787-1516C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 13/39 | chr3 | 13367607 | ||||||
chr3:13367617
|
C | T | 1 | a0002c0002t0004g0287 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1787-1526G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 13/39 | chr3 | 13367617 | ||||||
chr3:13367740
|
G | A | 176 | a0002c0002t0001g0050a0002c0002t0001g0160a0002c0002t0001g0161others(173): Show | 177 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.1787-1649C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 13/39 | chr3 | 13367740 | ||||||
chr3:13367756
|
C | T | 29 | a0004c0004t0003g0107a0004c0004t0003g0108a0004c0004t0003g0165others(26): Show | 29 | HG00544.hp1 HG01081.hp1 HG01516.hp2 others(26): Show |
intron_variant | MODIFIER | c.1787-1665G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 13/39 | chr3 | 13367756 | ||||||
chr3:13367856
|
G | A | 4 | a0002c0002t0001g0160a0002c0002t0001g0161a0002c0002t0001g0162others(1): Show | 4 | HG02145.hp1 HG03041.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1787-1765C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 13/39 | chr3 | 13367856 | ||||||
chr3:13367921
|
C | T | 1 | a0020c0020t0001g0193 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1787-1830G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 13/39 | chr3 | 13367921 | ||||||
chr3:13367954
|
C | T | 1 | a0001c0001t0002g0043 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1787-1863G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 13/39 | chr3 | 13367954 | ||||||
chr3:13367984
|
G | A | 177 | a0002c0002t0001g0050a0002c0002t0001g0160a0002c0002t0001g0161others(174): Show | 178 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.1787-1893C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 13/39 | chr3 | 13367984 | ||||||
chr3:13368028
|
C | T | 177 | a0002c0002t0001g0050a0002c0002t0001g0160a0002c0002t0001g0161others(174): Show | 178 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.1787-1937G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 13/39 | chr3 | 13368028 | ||||||
chr3:13368055
|
C | T | 29 | a0004c0004t0003g0107a0004c0004t0003g0108a0004c0004t0003g0165others(26): Show | 29 | HG00544.hp1 HG01081.hp1 HG01516.hp2 others(26): Show |
intron_variant | MODIFIER | c.1787-1964G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 13/39 | chr3 | 13368055 | ||||||
chr3:13368083
|
AT | A | 177 | a0002c0002t0001g0050a0002c0002t0001g0160a0002c0002t0001g0161others(174): Show | 178 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.1787-1993delA | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 13/39 | chr3 | 13368083 | ||||||
chr3:13368147
|
C | T | 1 | a0002c0002t0001g0208 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1787-2056G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 13/39 | chr3 | 13368147 | ||||||
chr3:13368475
|
G | A | 1 | a0017c0024t0002g0275 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1787-2384C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 13/39 | chr3 | 13368475 | ||||||
chr3:13368584
|
A | G | 166 | a0002c0002t0001g0050a0002c0002t0001g0160a0002c0002t0001g0161others(163): Show | 167 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.1787-2493T>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 13/39 | chr3 | 13368584 | ||||||
chr3:13368663
|
C | T | 1 | a0020c0020t0001g0193 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1787-2572G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 13/39 | chr3 | 13368663 | ||||||
chr3:13368740
|
G | A | 1 | a0001c0001t0002g0138 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1787-2649C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 13/39 | chr3 | 13368740 | ||||||
chr3:13368754
|
C | T | 1 | a0020c0020t0001g0193 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1787-2663G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 13/39 | chr3 | 13368754 | ||||||
chr3:13368815
|
T | C | 1 | a0001c0001t0002g0155 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1787-2724A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 13/39 | chr3 | 13368815 | ||||||
chr3:13368891
|
T | C | 1 | a0009c0027t0003g0019 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1787-2800A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 13/39 | chr3 | 13368891 | ||||||
chr3:13369202
|
G | A | 6 | a0001c0001t0002g0110a0001c0032t0002g0109a0002c0002t0001g0160others(3): Show | 6 | HG00639.hp1 HG01496.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.1786+2632C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 13/39 | chr3 | 13369202 | ||||||
chr3:13369206
|
G | C | 1 | a0009c0028t0003g0034 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1786+2628C>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 13/39 | chr3 | 13369206 | ||||||
chr3:13369263
|
T | A | 1 | a0001c0001t0002g0154 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1786+2571A>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 13/39 | chr3 | 13369263 | ||||||
chr3:13369561
|
T | C | 1 | a0006c0007t0001g0040 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1786+2273A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 13/39 | chr3 | 13369561 | ||||||
chr3:13369624
|
A | T | 5 | a0001c0001t0002g0042a0001c0001t0002g0043a0001c0001t0002g0045others(2): Show | 5 | HG01346.hp1 HG01978.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1786+2210T>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 13/39 | chr3 | 13369624 | ||||||
chr3:13369633
|
G | A | 1 | a0020c0020t0001g0193 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1786+2201C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 13/39 | chr3 | 13369633 | ||||||
chr3:13369701
|
C | G | 1 | a0001c0001t0002g0116 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1786+2133G>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 13/39 | chr3 | 13369701 | ||||||
chr3:13369894
|
G | A | 2 | a0001c0001t0002g0132a0001c0001t0002g0157 | 2 | HG02572.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1786+1940C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 13/39 | chr3 | 13369894 | ||||||
chr3:13369946
|
C | T | 1 | a0001c0001t0002g0077 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1786+1888G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 13/39 | chr3 | 13369946 | ||||||
chr3:13370006
|
T | A | 2 | a0001c0001t0009g0196a0011c0015t0001g0197 | 2 | HG02717.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1786+1828A>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 13/39 | chr3 | 13370006 | ||||||
chr3:13370184
|
GCCCTACA others(5): Show |
G | 3 | a0004c0004t0003g0165a0004c0004t0003g0175a0004c0036t0003g0176 | 3 | HG02071.hp2 NA18962.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.1786+1638_1786+164 others(16): Show |
NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 13/39 | chr3 | 13370184 | ||||||
chr3:13370204
|
C | T | 1 | a0003c0005t0005g0031 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1786+1630G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 13/39 | chr3 | 13370204 | ||||||
chr3:13370323
|
T | C | 177 | a0002c0002t0001g0050a0002c0002t0001g0160a0002c0002t0001g0161others(174): Show | 178 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.1786+1511A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 13/39 | chr3 | 13370323 | ||||||
chr3:13370329
|
G | A | 1 | a0002c0029t0001g0315 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1786+1505C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 13/39 | chr3 | 13370329 | ||||||
chr3:13370436
|
A | G | 1 | a0002c0002t0001g0239 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1786+1398T>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 13/39 | chr3 | 13370436 | ||||||
chr3:13370573
|
G | A | 177 | a0002c0002t0001g0050a0002c0002t0001g0160a0002c0002t0001g0161others(174): Show | 178 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.1786+1261C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 13/39 | chr3 | 13370573 | ||||||
chr3:13370610
|
C | T | 1 | a0001c0001t0002g0041 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1786+1224G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 13/39 | chr3 | 13370610 | ||||||
chr3:13370766
|
C | T | 1 | a0001c0001t0002g0113 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1786+1068G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 13/39 | chr3 | 13370766 | ||||||
chr3:13370861
|
T | C | 2 | a0008c0009t0001g0004a0008c0009t0001g0194 | 3 | HG02615.hp2 HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1786+973A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 13/39 | chr3 | 13370861 | ||||||
chr3:13370902
|
C | T | 1 | a0005c0003t0001g0268 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1786+932G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 13/39 | chr3 | 13370902 | ||||||
chr3:13370916
|
G | A | 5 | a0002c0002t0004g0250a0002c0002t0004g0251a0002c0002t0004g0254others(2): Show | 5 | NA18942.hp2 NA18953.hp2 NA18993.hp1 others(2): Show |
intron_variant | MODIFIER | c.1786+918C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 13/39 | chr3 | 13370916 | ||||||
chr3:13370990
|
G | C | 1 | a0006c0007t0001g0017 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1786+844C>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 13/39 | chr3 | 13370990 | ||||||
chr3:13371157
|
A | G | 208 | a0002c0002t0001g0050a0002c0002t0001g0160a0002c0002t0001g0161others(205): Show | 210 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.1786+677T>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 13/39 | chr3 | 13371157 | ||||||
chr3:13371169
|
C | T | 1 | a0004c0004t0003g0170 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1786+665G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 13/39 | chr3 | 13371169 | ||||||
chr3:13371198
|
A | C | 5 | a0002c0002t0007g0209a0002c0002t0007g0236a0002c0002t0007g0264others(2): Show | 5 | NA18950.hp2 NA18969.hp2 NA18992.hp2 others(2): Show |
intron_variant | MODIFIER | c.1786+636T>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 13/39 | chr3 | 13371198 | ||||||
chr3:13371264
|
C | T | 29 | a0004c0004t0003g0107a0004c0004t0003g0108a0004c0004t0003g0165others(26): Show | 29 | HG00544.hp1 HG01081.hp1 HG01516.hp2 others(26): Show |
intron_variant | MODIFIER | c.1786+570G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 13/39 | chr3 | 13371264 | ||||||
chr3:13371359
|
C | T | 2 | a0008c0009t0001g0004a0008c0009t0001g0194 | 3 | HG02615.hp2 HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1786+475G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 13/39 | chr3 | 13371359 | ||||||
chr3:13371374
|
C | T | 2 | a0008c0009t0001g0004a0008c0009t0001g0194 | 3 | HG02615.hp2 HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1786+460G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 13/39 | chr3 | 13371374 | ||||||
chr3:13371425
|
T | A | 1 | a0002c0002t0004g0316 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1786+409A>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 13/39 | chr3 | 13371425 | ||||||
chr3:13371428
|
A | T | 31 | a0003c0005t0005g0023a0003c0005t0005g0024a0003c0005t0005g0025others(28): Show | 31 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.1786+406T>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 13/39 | chr3 | 13371428 | ||||||
chr3:13371445
|
C | A | 1 | a0003c0005t0005g0028 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1786+389G>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 13/39 | chr3 | 13371445 | ||||||
chr3:13371740
|
C | T | 2 | a0008c0009t0001g0004a0008c0009t0001g0194 | 3 | HG02615.hp2 HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1786+94G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 13/39 | chr3 | 13371740 | ||||||
chr3:13371798
|
C | T | 1 | a0004c0004t0003g0107 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1786+36G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 13/39 | chr3 | 13371798 | ||||||
chr3:13372052
|
C | T | 3 | a0003c0011t0001g0035a0003c0011t0001g0036a0020c0020t0001g0193 | 3 | HG02922.hp1 HG03471.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1588-20G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 12/39 | chr3 | 13372052 | ||||||
chr3:13372166
|
G | A | 4 | a0003c0006t0005g0008a0003c0006t0005g0044a0003c0006t0005g0046others(1): Show | 4 | HG01243.hp2 HG02135.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.1588-134C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 12/39 | chr3 | 13372166 | ||||||
chr3:13372173
|
C | G | 1 | a0001c0001t0002g0043 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1588-141G>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 12/39 | chr3 | 13372173 | ||||||
chr3:13372175
|
G | A | 3 | a0004c0004t0010g0181a0004c0004t0010g0184a0004c0004t0010g0186 | 3 | NA18993.hp2 NA19009.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.1588-143C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 12/39 | chr3 | 13372175 | ||||||
chr3:13372390
|
G | A | 2 | a0003c0011t0001g0035a0003c0011t0001g0036 | 2 | HG02922.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1588-358C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 12/39 | chr3 | 13372390 | ||||||
chr3:13372404
|
T | C | 1 | a0002c0002t0001g0050 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1588-372A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 12/39 | chr3 | 13372404 | ||||||
chr3:13372539
|
C | T | 2 | a0001c0001t0002g0086a0001c0001t0002g0133 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1588-507G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 12/39 | chr3 | 13372539 | ||||||
chr3:13372631
|
T | C | 29 | a0004c0004t0003g0107a0004c0004t0003g0108a0004c0004t0003g0165others(26): Show | 29 | HG00544.hp1 HG01081.hp1 HG01516.hp2 others(26): Show |
intron_variant | MODIFIER | c.1588-599A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 12/39 | chr3 | 13372631 | ||||||
chr3:13372666
|
C | T | 5 | a0003c0011t0001g0035a0003c0011t0001g0036a0008c0009t0001g0004others(2): Show | 6 | HG02615.hp2 HG02922.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1588-634G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 12/39 | chr3 | 13372666 | ||||||
chr3:13372693
|
T | A | 1 | a0001c0001t0002g0105 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1588-661A>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 12/39 | chr3 | 13372693 | ||||||
chr3:13372824
|
A | G | 16 | a0004c0004t0003g0107a0004c0004t0003g0108a0004c0004t0003g0166others(13): Show | 16 | HG00544.hp1 HG01516.hp2 HG01517.hp1 others(13): Show |
intron_variant | MODIFIER | c.1588-792T>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 12/39 | chr3 | 13372824 | ||||||
chr3:13372851
|
G | A | 3 | a0003c0011t0001g0035a0003c0011t0001g0036a0020c0020t0001g0193 | 3 | HG02922.hp1 HG03471.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1588-819C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 12/39 | chr3 | 13372851 | ||||||
chr3:13372937
|
C | T | 1 | a0020c0020t0001g0193 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1587+781G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 12/39 | chr3 | 13372937 | ||||||
chr3:13372996
|
G | T | 1 | a0005c0003t0001g0291 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1587+722C>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 12/39 | chr3 | 13372996 | ||||||
chr3:13373102
|
G | C | 1 | a0002c0002t0001g0050 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1587+616C>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 12/39 | chr3 | 13373102 | ||||||
chr3:13373109
|
C | T | 31 | a0005c0003t0001g0215a0005c0003t0001g0216a0005c0003t0001g0234others(28): Show | 31 | HG00140.hp1 HG00642.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.1587+609G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 12/39 | chr3 | 13373109 | ||||||
chr3:13373111
|
T | C | 2 | a0008c0009t0001g0004a0008c0009t0001g0194 | 3 | HG02615.hp2 HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1587+607A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 12/39 | chr3 | 13373111 | ||||||
chr3:13373250
|
C | T | 1 | a0016c0025t0001g0232 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1587+468G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 12/39 | chr3 | 13373250 | ||||||
chr3:13373364
|
G | A | 174 | a0002c0002t0001g0050a0002c0002t0001g0160a0002c0002t0001g0161others(171): Show | 175 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.1587+354C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 12/39 | chr3 | 13373364 | ||||||
chr3:13373380
|
G | T | 2 | a0008c0009t0001g0004a0008c0009t0001g0194 | 3 | HG02615.hp2 HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1587+338C>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 12/39 | chr3 | 13373380 | ||||||
chr3:13373429
|
T | C | 31 | a0003c0005t0005g0023a0003c0005t0005g0024a0003c0005t0005g0025others(28): Show | 31 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.1587+289A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 12/39 | chr3 | 13373429 | ||||||
chr3:13373492
|
T | C | 179 | a0002c0002t0001g0050a0002c0002t0001g0160a0002c0002t0001g0161others(176): Show | 181 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(178): Show |
intron_variant | MODIFIER | c.1587+226A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 12/39 | chr3 | 13373492 | ||||||
chr3:13373610
|
G | A | 1 | a0020c0020t0001g0193 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1587+108C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 12/39 | chr3 | 13373610 | ||||||
chr3:13373646
|
G | T | 177 | a0002c0002t0001g0050a0002c0002t0001g0160a0002c0002t0001g0161others(174): Show | 178 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.1587+72C>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 12/39 | chr3 | 13373646 | ||||||
chr3:13373663
|
G | A | 2 | a0003c0011t0001g0035a0003c0011t0001g0036 | 2 | HG02922.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1587+55C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 12/39 | chr3 | 13373663 | ||||||
chr3:13373964
|
G | A | 1 | a0002c0002t0004g0285 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1432-91C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 11/39 | chr3 | 13373964 | ||||||
chr3:13374010
|
A | G | 3 | a0002c0002t0001g0237a0002c0002t0001g0243a0002c0002t0001g0244 | 3 | NA18959.hp2 NA18965.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.1432-137T>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 11/39 | chr3 | 13374010 | ||||||
chr3:13374352
|
G | A | 5 | a0003c0011t0001g0035a0003c0011t0001g0036a0008c0009t0001g0004others(2): Show | 6 | HG02615.hp2 HG02922.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1432-479C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 11/39 | chr3 | 13374352 | ||||||
chr3:13374751
|
G | A | 1 | a0002c0002t0004g0279 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1431+753C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 11/39 | chr3 | 13374751 | ||||||
chr3:13374904
|
C | A | 2 | a0002c0002t0001g0223a0002c0002t0001g0227 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1431+600G>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 11/39 | chr3 | 13374904 | ||||||
chr3:13375138
|
T | TTC | 8 | a0003c0006t0006g0051a0003c0006t0006g0053a0003c0006t0006g0055others(5): Show | 8 | HG02486.hp1 HG02559.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.1431+364_1431+365d others(4): Show |
NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 11/39 | chr3 | 13375138 | ||||||
chr3:13375142
|
C | CT | 146 | a0001c0001t0002g0045a0001c0001t0002g0081a0001c0001t0002g0116others(143): Show | 148 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(145): Show |
intron_variant | MODIFIER | c.1431+361dupA | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 11/39 | chr3 | 13375142 | ||||||
chr3:13375142
|
C | CTT | 8 | a0002c0002t0004g0205a0003c0006t0005g0008a0003c0006t0005g0044others(5): Show | 8 | HG00438.hp1 HG01243.hp2 HG02135.hp2 others(5): Show |
intron_variant | MODIFIER | c.1431+360_1431+361d others(4): Show |
NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 11/39 | chr3 | 13375142 | ||||||
chr3:13375159
|
C | T | 1 | a0020c0020t0001g0193 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1431+345G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 11/39 | chr3 | 13375159 | ||||||
chr3:13375307
|
T | C | 2 | a0003c0011t0001g0035a0003c0011t0001g0036 | 2 | HG02922.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1431+197A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 11/39 | chr3 | 13375307 | ||||||
chr3:13375729
|
G | C | 1 | a0002c0013t0004g0240 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1294-88C>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 10/39 | chr3 | 13375729 | ||||||
chr3:13375807
|
C | T | 5 | a0004c0004t0003g0169a0004c0004t0003g0170a0004c0004t0003g0171others(2): Show | 5 | HG02258.hp1 HG02630.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1294-166G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 10/39 | chr3 | 13375807 | ||||||
chr3:13375887
|
T | TC | 142 | a0002c0002t0001g0050a0002c0002t0001g0160a0002c0002t0001g0161others(139): Show | 143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.1294-247dupG | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 10/39 | chr3 | 13375887 | ||||||
chr3:13375968
|
C | G | 2 | a0008c0009t0001g0004a0008c0009t0001g0194 | 3 | HG02615.hp2 HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1293+323G>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 10/39 | chr3 | 13375968 | ||||||
chr3:13375988
|
G | A | 1 | a0001c0001t0002g0131 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1293+303C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 10/39 | chr3 | 13375988 | ||||||
chr3:13376087
|
C | T | 1 | a0001c0001t0002g0065 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1293+204G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 10/39 | chr3 | 13376087 | ||||||
chr3:13376164
|
C | T | 1 | a0020c0020t0001g0193 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1293+127G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 10/39 | chr3 | 13376164 | ||||||
chr3:13376235
|
C | T | 3 | a0006c0007t0001g0018a0006c0010t0001g0016a0006c0010t0001g0020 | 3 | HG02145.hp2 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1293+56G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 10/39 | chr3 | 13376235 | ||||||
chr3:13376462
|
G | A | 1 | a0002c0002t0001g0214 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1153-31C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 9/39 | chr3 | 13376462 | ||||||
chr3:13376586
|
C | A | 174 | a0002c0002t0001g0050a0002c0002t0001g0160a0002c0002t0001g0161others(171): Show | 175 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.1153-155G>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 9/39 | chr3 | 13376586 | ||||||
chr3:13376643
|
T | G | 29 | a0004c0004t0003g0107a0004c0004t0003g0108a0004c0004t0003g0165others(26): Show | 29 | HG00544.hp1 HG01081.hp1 HG01516.hp2 others(26): Show |
intron_variant | MODIFIER | c.1153-212A>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 9/39 | chr3 | 13376643 | ||||||
chr3:13376761
|
C | T | 1 | a0002c0002t0001g0258 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1153-330G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 9/39 | chr3 | 13376761 | ||||||
chr3:13376827
|
C | T | 177 | a0002c0002t0001g0050a0002c0002t0001g0160a0002c0002t0001g0161others(174): Show | 178 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.1153-396G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 9/39 | chr3 | 13376827 | ||||||
chr3:13376831
|
A | T | 208 | a0002c0002t0001g0050a0002c0002t0001g0160a0002c0002t0001g0161others(205): Show | 210 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.1153-400T>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 9/39 | chr3 | 13376831 | ||||||
chr3:13376846
|
G | A | 1 | a0005c0003t0001g0281 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1153-415C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 9/39 | chr3 | 13376846 | ||||||
chr3:13376867
|
T | G | 1 | a0004c0004t0010g0181 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1153-436A>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 9/39 | chr3 | 13376867 | ||||||
chr3:13376882
|
C | T | 1 | a0020c0020t0001g0193 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1153-451G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 9/39 | chr3 | 13376882 | ||||||
chr3:13376883
|
G | A | 89 | a0002c0002t0001g0050a0002c0002t0001g0199a0002c0002t0001g0200others(86): Show | 89 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.1153-452C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 9/39 | chr3 | 13376883 | ||||||
chr3:13376985
|
C | A | 1 | a0001c0001t0002g0146 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1152+471G>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 9/39 | chr3 | 13376985 | ||||||
chr3:13377047
|
T | C | 4 | a0002c0002t0001g0160a0002c0002t0001g0161a0002c0002t0001g0162others(1): Show | 4 | HG02145.hp1 HG03041.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1152+409A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 9/39 | chr3 | 13377047 | ||||||
chr3:13377051
|
G | C | 2 | a0001c0001t0002g0094a0001c0001t0002g0142 | 2 | HG01934.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.1152+405C>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 9/39 | chr3 | 13377051 | ||||||
chr3:13377585
|
G | A | 2 | a0008c0009t0001g0004a0008c0009t0001g0194 | 3 | HG02615.hp2 HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1046-23C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 8/39 | chr3 | 13377585 | ||||||
chr3:13377599
|
C | T | 1 | a0001c0001t0002g0139 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1046-37G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 8/39 | chr3 | 13377599 | ||||||
chr3:13377623
|
T | TG | 48 | a0005c0003t0001g0215a0005c0003t0001g0216a0005c0003t0001g0234others(45): Show | 49 | HG00140.hp1 HG00140.hp2 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.1046-62dupC | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 8/39 | chr3 | 13377623 | ||||||
chr3:13377665
|
G | A | 31 | a0003c0005t0005g0023a0003c0005t0005g0024a0003c0005t0005g0025others(28): Show | 31 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.1046-103C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 8/39 | chr3 | 13377665 | ||||||
chr3:13377699
|
ACCACCCA others(37): Show |
A | 3 | a0001c0001t0002g0066a0001c0001t0002g0077a0004c0036t0003g0176 | 3 | HG02004.hp2 HG02071.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.1046-181_1046-138d others(46): Show |
NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 8/39 | chr3 | 13377699 | ||||||
chr3:13377787
|
T | TCCACCCA others(59): Show |
26 | a0002c0002t0004g0156a0002c0002t0004g0205a0002c0002t0004g0250others(23): Show | 26 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(23): Show |
intron_variant | MODIFIER | c.1046-291_1046-226d others(68): Show |
NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 8/39 | chr3 | 13377787 | ||||||
chr3:13377787
|
TCCACCCA others(59): Show |
T | 1 | a0003c0005t0005g0278 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1046-291_1046-226d others(68): Show |
NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 8/39 | chr3 | 13377787 | ||||||
chr3:13377799
|
CAGGCCCC others(37): Show |
C | 1 | a0002c0002t0001g0213 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1046-281_1046-238d others(46): Show |
NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 8/39 | chr3 | 13377799 | ||||||
chr3:13377821
|
G | GAGGCCCC others(15): Show |
1 | a0004c0004t0003g0167 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1046-281_1046-260d others(24): Show |
NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 8/39 | chr3 | 13377821 | ||||||
chr3:13377853
|
A | ACCACCCA others(37): Show |
1 | a0020c0020t0001g0193 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1046-292_1046-291i others(46): Show |
NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 8/39 | chr3 | 13377853 | ||||||
chr3:13377923
|
C | T | 1 | a0002c0002t0001g0282 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1046-361G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 8/39 | chr3 | 13377923 | ||||||
chr3:13377931
|
CAGGCCCT others(15): Show |
C | 1 | a0002c0002t0001g0050 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1046-391_1046-370d others(24): Show |
NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 8/39 | chr3 | 13377931 | ||||||
chr3:13378071
|
T | G | 1 | a0001c0001t0002g0105 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1046-509A>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 8/39 | chr3 | 13378071 | ||||||
chr3:13378189
|
C | T | 15 | a0003c0005t0005g0023a0003c0005t0005g0024a0003c0005t0005g0025others(12): Show | 15 | HG01109.hp1 HG01884.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.1046-627G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 8/39 | chr3 | 13378189 | ||||||
chr3:13378202
|
C | A | 1 | a0020c0020t0001g0193 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1046-640G>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 8/39 | chr3 | 13378202 | ||||||
chr3:13378232
|
T | C | 2 | a0008c0009t0001g0004a0008c0009t0001g0194 | 3 | HG02615.hp2 HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1046-670A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 8/39 | chr3 | 13378232 | ||||||
chr3:13378505
|
A | C | 174 | a0002c0002t0001g0050a0002c0002t0001g0160a0002c0002t0001g0161others(171): Show | 175 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.1045+407T>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 8/39 | chr3 | 13378505 | ||||||
chr3:13378553
|
T | C | 2 | a0004c0004t0003g0188a0004c0004t0003g0189 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1045+359A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 8/39 | chr3 | 13378553 | ||||||
chr3:13378581
|
T | C | 1 | a0001c0001t0002g0095 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1045+331A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 8/39 | chr3 | 13378581 | ||||||
chr3:13378584
|
G | C | 1 | a0001c0001t0002g0095 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1045+328C>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 8/39 | chr3 | 13378584 | ||||||
chr3:13378605
|
T | C | 1 | a0005c0003t0001g0295 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1045+307A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 8/39 | chr3 | 13378605 | ||||||
chr3:13378631
|
C | A | 1 | a0020c0020t0001g0193 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1045+281G>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 8/39 | chr3 | 13378631 | ||||||
chr3:13378631
|
C | T | 11 | a0003c0006t0006g0051a0003c0006t0006g0052a0003c0006t0006g0053others(8): Show | 11 | HG02486.hp1 HG02559.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.1045+281G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 8/39 | chr3 | 13378631 | ||||||
chr3:13378787
|
T | A | 38 | a0001c0001t0002g0001a0001c0001t0002g0065a0001c0001t0002g0068others(35): Show | 41 | HG00621.hp2 HG01496.hp2 HG01934.hp2 others(38): Show |
intron_variant | MODIFIER | c.1045+125A>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 8/39 | chr3 | 13378787 | ||||||
chr3:13379124
|
G | A | 177 | a0002c0002t0001g0050a0002c0002t0001g0160a0002c0002t0001g0161others(174): Show | 178 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.977-144C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 7/39 | chr3 | 13379124 | ||||||
chr3:13379416
|
A | T | 3 | a0004c0004t0010g0181a0004c0004t0010g0184a0004c0004t0010g0186 | 3 | NA18993.hp2 NA19009.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.976+147T>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 7/39 | chr3 | 13379416 | ||||||
chr3:13379449
|
G | A | 1 | a0001c0001t0002g0113 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.976+114C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 7/39 | chr3 | 13379449 | ||||||
chr3:13379490
|
G | T | 2 | a0008c0009t0001g0004a0008c0009t0001g0194 | 3 | HG02615.hp2 HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.976+73C>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 7/39 | chr3 | 13379490 | ||||||
chr3:13379511
|
C | T | 1 | a0006c0007t0001g0013 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.976+52G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 7/39 | chr3 | 13379511 | ||||||
chr3:13379524
|
C | T | 11 | a0002c0002t0001g0217a0002c0002t0001g0218a0002c0002t0001g0220others(8): Show | 11 | HG00280.hp2 HG00323.hp2 HG00642.hp1 others(8): Show |
intron_variant | MODIFIER | c.976+39G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 7/39 | chr3 | 13379524 | ||||||
chr3:13379820
|
T | C | 179 | a0002c0002t0001g0050a0002c0002t0001g0160a0002c0002t0001g0161others(176): Show | 181 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(178): Show |
intron_variant | MODIFIER | c.818-99A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 6/39 | chr3 | 13379820 | ||||||
chr3:13379841
|
G | A | 1 | a0001c0001t0002g0045 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.818-120C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 6/39 | chr3 | 13379841 | ||||||
chr3:13379956
|
T | TA | 29 | a0004c0004t0003g0107a0004c0004t0003g0108a0004c0004t0003g0165others(26): Show | 29 | HG00544.hp1 HG01081.hp1 HG01516.hp2 others(26): Show |
intron_variant | MODIFIER | c.818-236dupT | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 6/39 | chr3 | 13379956 | ||||||
chr3:13379956
|
TA | T | 174 | a0002c0002t0001g0050a0002c0002t0001g0160a0002c0002t0001g0161others(171): Show | 175 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.818-236delT | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 6/39 | chr3 | 13379956 | ||||||
chr3:13380059
|
G | C | 3 | a0005c0003t0001g0234a0005c0003t0001g0241a0005c0003t0001g0256 | 3 | HG03239.hp1 HG03688.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.818-338C>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 6/39 | chr3 | 13380059 | ||||||
chr3:13380137
|
G | T | 29 | a0004c0004t0003g0107a0004c0004t0003g0108a0004c0004t0003g0165others(26): Show | 29 | HG00544.hp1 HG01081.hp1 HG01516.hp2 others(26): Show |
intron_variant | MODIFIER | c.818-416C>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 6/39 | chr3 | 13380137 | ||||||
chr3:13380169
|
A | T | 1 | a0001c0001t0002g0141 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.818-448T>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 6/39 | chr3 | 13380169 | ||||||
chr3:13380269
|
T | G | 3 | a0004c0004t0010g0181a0004c0004t0010g0184a0004c0004t0010g0186 | 3 | NA18993.hp2 NA19009.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.818-548A>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 6/39 | chr3 | 13380269 | ||||||
chr3:13380407
|
C | T | 177 | a0002c0002t0001g0050a0002c0002t0001g0160a0002c0002t0001g0161others(174): Show | 178 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.818-686G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 6/39 | chr3 | 13380407 | ||||||
chr3:13380442
|
G | A | 208 | a0002c0002t0001g0050a0002c0002t0001g0160a0002c0002t0001g0161others(205): Show | 210 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.818-721C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 6/39 | chr3 | 13380442 | ||||||
chr3:13380481
|
T | C | 179 | a0002c0002t0001g0050a0002c0002t0001g0160a0002c0002t0001g0161others(176): Show | 181 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(178): Show |
intron_variant | MODIFIER | c.818-760A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 6/39 | chr3 | 13380481 | ||||||
chr3:13380555
|
G | A | 2 | a0008c0009t0001g0004a0008c0009t0001g0194 | 3 | HG02615.hp2 HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.818-834C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 6/39 | chr3 | 13380555 | ||||||
chr3:13380599
|
C | A | 1 | a0017c0024t0002g0275 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.818-878G>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 6/39 | chr3 | 13380599 | ||||||
chr3:13380711
|
G | T | 4 | a0005c0003t0001g0303a0005c0003t0001g0304a0005c0003t0001g0306others(1): Show | 4 | HG00735.hp2 HG02486.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.818-990C>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 6/39 | chr3 | 13380711 | ||||||
chr3:13380771
|
C | T | 177 | a0002c0002t0001g0050a0002c0002t0001g0160a0002c0002t0001g0161others(174): Show | 178 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.818-1050G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 6/39 | chr3 | 13380771 | ||||||
chr3:13380913
|
A | G | 1 | a0005c0003t0001g0299 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.818-1192T>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 6/39 | chr3 | 13380913 | ||||||
chr3:13380987
|
A | T | 2 | a0001c0001t0002g0118a0001c0001t0002g0119 | 2 | NA18964.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.818-1266T>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 6/39 | chr3 | 13380987 | ||||||
chr3:13381178
|
T | C | 1 | a0009c0027t0003g0019 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.818-1457A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 6/39 | chr3 | 13381178 | ||||||
chr3:13381183
|
T | C | 179 | a0002c0002t0001g0050a0002c0002t0001g0160a0002c0002t0001g0161others(176): Show | 181 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(178): Show |
intron_variant | MODIFIER | c.818-1462A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 6/39 | chr3 | 13381183 | ||||||
chr3:13381292
|
C | A | 176 | a0002c0002t0001g0050a0002c0002t0001g0160a0002c0002t0001g0161others(173): Show | 177 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.818-1571G>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 6/39 | chr3 | 13381292 | ||||||
chr3:13381420
|
C | CT | 72 | a0002c0002t0004g0252a0002c0002t0004g0287a0002c0002t0007g0209others(69): Show | 72 | HG00544.hp1 HG01081.hp1 HG01109.hp1 others(69): Show |
intron_variant | MODIFIER | c.818-1700dupA | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 6/39 | chr3 | 13381420 | ||||||
chr3:13381420
|
C | CTT | 133 | a0002c0002t0001g0050a0002c0002t0001g0160a0002c0002t0001g0161others(130): Show | 135 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.818-1701_818-1700d others(4): Show |
NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 6/39 | chr3 | 13381420 | ||||||
chr3:13381489
|
T | G | 177 | a0002c0002t0001g0050a0002c0002t0001g0160a0002c0002t0001g0161others(174): Show | 178 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.818-1768A>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 6/39 | chr3 | 13381489 | ||||||
chr3:13381610
|
G | A | 208 | a0002c0002t0001g0050a0002c0002t0001g0160a0002c0002t0001g0161others(205): Show | 210 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.818-1889C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 6/39 | chr3 | 13381610 | ||||||
chr3:13381700
|
G | A | 1 | a0020c0020t0001g0193 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.818-1979C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 6/39 | chr3 | 13381700 | ||||||
chr3:13381908
|
C | G | 1 | a0024c0038t0002g0321 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.818-2187G>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 6/39 | chr3 | 13381908 | ||||||
chr3:13382079
|
C | T | 2 | a0003c0006t0008g0006a0003c0006t0008g0007 | 2 | HG03130.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.818-2358G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 6/39 | chr3 | 13382079 | ||||||
chr3:13382156
|
T | C | 174 | a0002c0002t0001g0050a0002c0002t0001g0160a0002c0002t0001g0161others(171): Show | 175 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.818-2435A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 6/39 | chr3 | 13382156 | ||||||
chr3:13382327
|
T | G | 1 | a0001c0001t0002g0096 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.818-2606A>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 6/39 | chr3 | 13382327 | ||||||
chr3:13382450
|
C | T | 2 | a0008c0009t0001g0004a0008c0009t0001g0194 | 3 | HG02615.hp2 HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.818-2729G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 6/39 | chr3 | 13382450 | ||||||
chr3:13382638
|
T | C | 1 | a0003c0006t0005g0044 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.818-2917A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 6/39 | chr3 | 13382638 | ||||||
chr3:13382892
|
T | C | 208 | a0002c0002t0001g0050a0002c0002t0001g0160a0002c0002t0001g0161others(205): Show | 210 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.818-3171A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 6/39 | chr3 | 13382892 | ||||||
chr3:13382918
|
G | A | 1 | a0003c0019t0013g0164 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.818-3197C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 6/39 | chr3 | 13382918 | ||||||
chr3:13382991
|
A | C | 1 | a0024c0038t0002g0321 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.818-3270T>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 6/39 | chr3 | 13382991 | ||||||
chr3:13383227
|
G | A | 1 | a0003c0006t0005g0044 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.817+3048C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 6/39 | chr3 | 13383227 | ||||||
chr3:13383266
|
A | G | 9 | a0003c0006t0006g0051a0003c0006t0006g0052a0003c0006t0006g0053others(6): Show | 9 | HG02486.hp1 HG02559.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.817+3009T>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 6/39 | chr3 | 13383266 | ||||||
chr3:13383516
|
C | CT | 10 | a0001c0001t0002g0041a0001c0001t0002g0090a0001c0001t0002g0118others(7): Show | 11 | HG00597.hp2 HG02451.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.817+2758dupA | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 6/39 | chr3 | 13383516 | ||||||
chr3:13383516
|
C | CTT | 6 | a0002c0002t0001g0163a0003c0005t0005g0026a0003c0005t0005g0031others(3): Show | 6 | HG01168.hp1 HG01884.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.817+2757_817+2758d others(4): Show |
NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 6/39 | chr3 | 13383516 | ||||||
chr3:13383516
|
C | CTTT | 122 | a0002c0002t0001g0050a0002c0002t0001g0160a0002c0002t0001g0161others(119): Show | 123 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.817+2756_817+2758d others(5): Show |
NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 6/39 | chr3 | 13383516 | ||||||
chr3:13383516
|
C | CTTTT | 42 | a0002c0002t0001g0162a0002c0002t0001g0199a0002c0002t0001g0200others(39): Show | 42 | HG00140.hp1 HG00597.hp1 HG00621.hp1 others(39): Show |
intron_variant | MODIFIER | c.817+2755_817+2758d others(6): Show |
NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 6/39 | chr3 | 13383516 | ||||||
chr3:13383551
|
C | A | 1 | a0002c0002t0004g0312 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.817+2724G>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 6/39 | chr3 | 13383551 | ||||||
chr3:13383606
|
C | A | 1 | a0009c0030t0005g0009 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.817+2669G>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 6/39 | chr3 | 13383606 | ||||||
chr3:13383669
|
T | C | 3 | a0002c0002t0007g0209a0002c0002t0007g0264a0002c0002t0007g0314 | 3 | NA18950.hp2 NA18969.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.817+2606A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 6/39 | chr3 | 13383669 | ||||||
chr3:13383790
|
A | G | 1 | a0002c0002t0001g0217 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.817+2485T>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 6/39 | chr3 | 13383790 | ||||||
chr3:13383916
|
C | T | 31 | a0005c0003t0001g0215a0005c0003t0001g0216a0005c0003t0001g0234others(28): Show | 31 | HG00140.hp1 HG00642.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.817+2359G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 6/39 | chr3 | 13383916 | ||||||
chr3:13384016
|
G | C | 1 | a0001c0001t0002g0124 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.817+2259C>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 6/39 | chr3 | 13384016 | ||||||
chr3:13384038
|
C | T | 1 | a0002c0002t0001g0286 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.817+2237G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 6/39 | chr3 | 13384038 | ||||||
chr3:13384120
|
A | G | 2 | a0003c0011t0001g0035a0003c0011t0001g0036 | 2 | HG02922.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.817+2155T>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 6/39 | chr3 | 13384120 | ||||||
chr3:13384151
|
C | T | 4 | a0002c0002t0001g0160a0002c0002t0001g0161a0002c0002t0001g0162others(1): Show | 4 | HG02145.hp1 HG03041.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.817+2124G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 6/39 | chr3 | 13384151 | ||||||
chr3:13384240
|
C | T | 1 | a0007c0008t0002g0089 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.817+2035G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 6/39 | chr3 | 13384240 | ||||||
chr3:13384315
|
G | C | 1 | a0002c0002t0007g0314 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.817+1960C>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 6/39 | chr3 | 13384315 | ||||||
chr3:13384340
|
G | A | 1 | a0001c0001t0002g0153 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.817+1935C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 6/39 | chr3 | 13384340 | ||||||
chr3:13384374
|
T | G | 1 | a0001c0001t0002g0071 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.817+1901A>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 6/39 | chr3 | 13384374 | ||||||
chr3:13384403
|
T | C | 2 | a0008c0009t0001g0004a0008c0009t0001g0194 | 3 | HG02615.hp2 HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.817+1872A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 6/39 | chr3 | 13384403 | ||||||
chr3:13384499
|
A | C | 208 | a0002c0002t0001g0050a0002c0002t0001g0160a0002c0002t0001g0161others(205): Show | 210 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.817+1776T>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 6/39 | chr3 | 13384499 | ||||||
chr3:13384515
|
G | A | 1 | a0002c0002t0001g0208 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.817+1760C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 6/39 | chr3 | 13384515 | ||||||
chr3:13384546
|
T | G | 179 | a0002c0002t0001g0050a0002c0002t0001g0160a0002c0002t0001g0161others(176): Show | 181 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(178): Show |
intron_variant | MODIFIER | c.817+1729A>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 6/39 | chr3 | 13384546 | ||||||
chr3:13384550
|
C | T | 1 | a0011c0015t0001g0098 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.817+1725G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 6/39 | chr3 | 13384550 | ||||||
chr3:13384650
|
T | C | 3 | a0002c0002t0007g0209a0002c0002t0007g0264a0002c0002t0007g0314 | 3 | NA18950.hp2 NA18969.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.817+1625A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 6/39 | chr3 | 13384650 | ||||||
chr3:13384694
|
C | T | 1 | a0001c0001t0002g0120 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.817+1581G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 6/39 | chr3 | 13384694 | ||||||
chr3:13384839
|
C | T | 2 | a0003c0011t0001g0035a0003c0011t0001g0036 | 2 | HG02922.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.817+1436G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 6/39 | chr3 | 13384839 | ||||||
chr3:13384852
|
C | T | 1 | a0009c0030t0005g0009 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.817+1423G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 6/39 | chr3 | 13384852 | ||||||
chr3:13385096
|
C | T | 1 | a0003c0006t0006g0058 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.817+1179G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 6/39 | chr3 | 13385096 | ||||||
chr3:13385108
|
T | A | 14 | a0001c0001t0002g0066a0001c0001t0002g0070a0001c0001t0002g0097others(11): Show | 14 | HG00597.hp2 HG02132.hp1 NA18945.hp1 others(11): Show |
intron_variant | MODIFIER | c.817+1167A>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 6/39 | chr3 | 13385108 | ||||||
chr3:13385110
|
T | C | 179 | a0001c0001t0002g0103a0002c0002t0001g0050a0002c0002t0001g0160others(176): Show | 181 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(178): Show |
intron_variant | MODIFIER | c.817+1165A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 6/39 | chr3 | 13385110 | ||||||
chr3:13385334
|
C | T | 4 | a0003c0006t0005g0008a0003c0006t0005g0044a0003c0006t0005g0046others(1): Show | 4 | HG01243.hp2 HG02135.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.817+941G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 6/39 | chr3 | 13385334 | ||||||
chr3:13385348
|
C | T | 14 | a0001c0001t0002g0066a0001c0001t0002g0070a0001c0001t0002g0097others(11): Show | 14 | HG00597.hp2 HG02132.hp1 NA18945.hp1 others(11): Show |
intron_variant | MODIFIER | c.817+927G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 6/39 | chr3 | 13385348 | ||||||
chr3:13385368
|
G | T | 28 | a0004c0004t0003g0107a0004c0004t0003g0108a0004c0004t0003g0165others(25): Show | 28 | HG01081.hp1 HG01516.hp2 HG01517.hp1 others(25): Show |
intron_variant | MODIFIER | c.817+907C>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 6/39 | chr3 | 13385368 | ||||||
chr3:13385447
|
G | A | 206 | a0002c0002t0001g0050a0002c0002t0001g0160a0002c0002t0001g0161others(203): Show | 208 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(205): Show |
intron_variant | MODIFIER | c.817+828C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 6/39 | chr3 | 13385447 | ||||||
chr3:13385510
|
C | G | 1 | a0002c0002t0001g0282 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.817+765G>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 6/39 | chr3 | 13385510 | ||||||
chr3:13385541
|
C | T | 1 | a0002c0002t0001g0280 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.817+734G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 6/39 | chr3 | 13385541 | ||||||
chr3:13385788
|
GGATGAAT others(5): Show |
G | 176 | a0002c0002t0001g0050a0002c0002t0001g0160a0002c0002t0001g0161others(173): Show | 177 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.817+475_817+486del others(12): Show |
NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 6/39 | chr3 | 13385788 | ||||||
chr3:13385833
|
T | C | 29 | a0004c0004t0003g0107a0004c0004t0003g0108a0004c0004t0003g0165others(26): Show | 29 | HG00544.hp1 HG01081.hp1 HG01516.hp2 others(26): Show |
intron_variant | MODIFIER | c.817+442A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 6/39 | chr3 | 13385833 | ||||||
chr3:13385974
|
C | T | 1 | a0001c0001t0002g0144 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.817+301G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 6/39 | chr3 | 13385974 | ||||||
chr3:13385986
|
A | T | 1 | a0001c0001t0002g0066 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.817+289T>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 6/39 | chr3 | 13385986 | ||||||
chr3:13386026
|
A | C | 2 | a0003c0011t0001g0035a0003c0011t0001g0036 | 2 | HG02922.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.817+249T>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 6/39 | chr3 | 13386026 | ||||||
chr3:13386426
|
C | T | 4 | a0002c0002t0001g0160a0002c0002t0001g0161a0002c0002t0001g0162others(1): Show | 4 | HG02145.hp1 HG03041.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.685-19G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 5/39 | chr3 | 13386426 | ||||||
chr3:13386441
|
G | A | 2 | a0006c0007t0001g0040a0009c0030t0005g0009 | 2 | HG01891.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.685-34C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 5/39 | chr3 | 13386441 | ||||||
chr3:13386468
|
G | A | 1 | a0002c0002t0001g0207 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.685-61C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 5/39 | chr3 | 13386468 | ||||||
chr3:13386487
|
G | C | 1 | a0002c0002t0001g0229 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.685-80C>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 5/39 | chr3 | 13386487 | ||||||
chr3:13386498
|
G | T | 172 | a0002c0002t0001g0050a0002c0002t0001g0160a0002c0002t0001g0161others(169): Show | 173 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.685-91C>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 5/39 | chr3 | 13386498 | ||||||
chr3:13386534
|
C | A | 1 | a0001c0001t0002g0070 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.685-127G>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 5/39 | chr3 | 13386534 | ||||||
chr3:13386534
|
C | T | 87 | a0002c0002t0001g0050a0002c0002t0001g0199a0002c0002t0001g0200others(84): Show | 87 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.685-127G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 5/39 | chr3 | 13386534 | ||||||
chr3:13386642
|
C | T | 2 | a0001c0001t0002g0118a0001c0001t0002g0119 | 2 | NA18964.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.685-235G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 5/39 | chr3 | 13386642 | ||||||
chr3:13386666
|
T | C | 3 | a0005c0003t0001g0234a0005c0003t0001g0241a0005c0003t0001g0256 | 3 | HG03239.hp1 HG03688.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.685-259A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 5/39 | chr3 | 13386666 | ||||||
chr3:13386673
|
C | A | 1 | a0004c0004t0003g0192 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.685-266G>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 5/39 | chr3 | 13386673 | ||||||
chr3:13386735
|
G | A | 175 | a0002c0002t0001g0050a0002c0002t0001g0160a0002c0002t0001g0161others(172): Show | 176 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.685-328C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 5/39 | chr3 | 13386735 | ||||||
chr3:13386878
|
C | T | 2 | a0008c0009t0001g0004a0008c0009t0001g0194 | 3 | HG02615.hp2 HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.685-471G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 5/39 | chr3 | 13386878 | ||||||
chr3:13386879
|
C | T | 13 | a0003c0005t0005g0023a0003c0005t0005g0024a0003c0005t0005g0025others(10): Show | 13 | HG01109.hp1 HG01884.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.685-472G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 5/39 | chr3 | 13386879 | ||||||
chr3:13386898
|
C | A | 1 | a0002c0029t0001g0315 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.685-491G>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 5/39 | chr3 | 13386898 | ||||||
chr3:13386913
|
C | T | 176 | a0002c0002t0001g0050a0002c0002t0001g0160a0002c0002t0001g0161others(173): Show | 178 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.685-506G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 5/39 | chr3 | 13386913 | ||||||
chr3:13387081
|
A | G | 207 | a0002c0002t0001g0050a0002c0002t0001g0160a0002c0002t0001g0161others(204): Show | 209 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(206): Show |
intron_variant | MODIFIER | c.685-674T>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 5/39 | chr3 | 13387081 | ||||||
chr3:13387133
|
G | A | 1 | a0004c0016t0005g0191 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.685-726C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 5/39 | chr3 | 13387133 | ||||||
chr3:13387252
|
A | T | 1 | a0005c0003t0001g0268 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.685-845T>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 5/39 | chr3 | 13387252 | ||||||
chr3:13387298
|
T | G | 2 | a0005c0003t0001g0245a0005c0003t0001g0317 | 2 | HG03710.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.685-891A>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 5/39 | chr3 | 13387298 | ||||||
chr3:13387315
|
C | T | 1 | a0020c0020t0001g0193 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.685-908G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 5/39 | chr3 | 13387315 | ||||||
chr3:13387470
|
A | G | 6 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(3): Show | 6 | HG01346.hp1 HG01978.hp2 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.684+833T>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 5/39 | chr3 | 13387470 | ||||||
chr3:13387536
|
A | G | 1 | a0002c0002t0001g0255 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.684+767T>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 5/39 | chr3 | 13387536 | ||||||
chr3:13387539
|
A | T | 1 | a0005c0003t0001g0268 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.684+764T>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 5/39 | chr3 | 13387539 | ||||||
chr3:13387577
|
C | T | 1 | a0001c0001t0002g0082 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.684+726G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 5/39 | chr3 | 13387577 | ||||||
chr3:13387670
|
T | C | 1 | a0003c0005t0005g0031 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.684+633A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 5/39 | chr3 | 13387670 | ||||||
chr3:13387790
|
A | G | 207 | a0002c0002t0001g0050a0002c0002t0001g0160a0002c0002t0001g0161others(204): Show | 209 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(206): Show |
intron_variant | MODIFIER | c.684+513T>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 5/39 | chr3 | 13387790 | ||||||
chr3:13388006
|
A | C | 38 | a0001c0001t0002g0001a0001c0001t0002g0065a0001c0001t0002g0068others(35): Show | 41 | HG00621.hp2 HG01496.hp2 HG01934.hp2 others(38): Show |
intron_variant | MODIFIER | c.684+297T>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 5/39 | chr3 | 13388006 | ||||||
chr3:13388050
|
A | G | 1 | a0005c0003t0001g0292 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.684+253T>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 5/39 | chr3 | 13388050 | ||||||
chr3:13388223
|
G | A | 1 | a0020c0020t0001g0193 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.684+80C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 5/39 | chr3 | 13388223 | ||||||
chr3:13388255
|
T | C | 1 | a0003c0011t0001g0036 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.684+48A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 5/39 | chr3 | 13388255 | ||||||
chr3:13388494
|
C | T | 1 | a0001c0001t0002g0071 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.534-41G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 4/39 | chr3 | 13388494 | ||||||
chr3:13388642
|
G | A | 1 | a0001c0001t0002g0043 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.534-189C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 4/39 | chr3 | 13388642 | ||||||
chr3:13388707
|
C | G | 1 | a0001c0001t0002g0088 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.534-254G>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 4/39 | chr3 | 13388707 | ||||||
chr3:13388734
|
C | T | 172 | a0002c0002t0001g0050a0002c0002t0001g0160a0002c0002t0001g0161others(169): Show | 173 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.534-281G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 4/39 | chr3 | 13388734 | ||||||
chr3:13388908
|
G | C | 1 | a0009c0028t0003g0034 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.534-455C>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 4/39 | chr3 | 13388908 | ||||||
chr3:13388951
|
C | T | 1 | a0005c0003t0001g0299 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.534-498G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 4/39 | chr3 | 13388951 | ||||||
chr3:13388997
|
G | A | 6 | a0001c0001t0002g0076a0001c0001t0002g0077a0001c0001t0002g0078others(3): Show | 6 | HG00558.hp1 HG00639.hp1 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.534-544C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 4/39 | chr3 | 13388997 | ||||||
chr3:13389000
|
G | A | 1 | a0001c0001t0002g0081 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.534-547C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 4/39 | chr3 | 13389000 | ||||||
chr3:13389019
|
T | C | 2 | a0002c0002t0001g0206a0002c0002t0001g0210 | 2 | HG01891.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.534-566A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 4/39 | chr3 | 13389019 | ||||||
chr3:13389138
|
G | A | 30 | a0004c0004t0003g0107a0004c0004t0003g0108a0004c0004t0003g0165others(27): Show | 30 | HG00544.hp1 HG01081.hp1 HG01516.hp2 others(27): Show |
intron_variant | MODIFIER | c.534-685C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 4/39 | chr3 | 13389138 | ||||||
chr3:13389188
|
T | C | 2 | a0002c0002t0001g0211a0002c0002t0001g0248 | 2 | NA18978.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.534-735A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 4/39 | chr3 | 13389188 | ||||||
chr3:13389225
|
G | C | 1 | a0009c0030t0005g0009 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.534-772C>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 4/39 | chr3 | 13389225 | ||||||
chr3:13389455
|
G | C | 172 | a0002c0002t0001g0050a0002c0002t0001g0160a0002c0002t0001g0161others(169): Show | 173 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.534-1002C>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 4/39 | chr3 | 13389455 | ||||||
chr3:13389477
|
G | A | 1 | a0004c0004t0003g0165 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.534-1024C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 4/39 | chr3 | 13389477 | ||||||
chr3:13389512
|
A | G | 1 | a0001c0001t0002g0067 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.534-1059T>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 4/39 | chr3 | 13389512 | ||||||
chr3:13389721
|
C | A | 2 | a0003c0011t0001g0035a0003c0011t0001g0036 | 2 | HG02922.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.534-1268G>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 4/39 | chr3 | 13389721 | ||||||
chr3:13389930
|
T | C | 172 | a0002c0002t0001g0050a0002c0002t0001g0160a0002c0002t0001g0161others(169): Show | 173 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.533+1281A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 4/39 | chr3 | 13389930 | ||||||
chr3:13390034
|
G | A | 5 | a0003c0005t0005g0031a0003c0005t0005g0032a0003c0005t0005g0033others(2): Show | 5 | HG02895.hp2 HG03098.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.533+1177C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 4/39 | chr3 | 13390034 | ||||||
chr3:13390062
|
T | C | 1 | a0003c0005t0005g0031 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.533+1149A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 4/39 | chr3 | 13390062 | ||||||
chr3:13390157
|
G | A | 1 | a0002c0002t0004g0279 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.533+1054C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 4/39 | chr3 | 13390157 | ||||||
chr3:13390221
|
G | A | 16 | a0003c0006t0005g0008a0003c0006t0005g0044a0003c0006t0005g0046others(13): Show | 16 | HG01243.hp2 HG02135.hp2 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.533+990C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 4/39 | chr3 | 13390221 | ||||||
chr3:13390238
|
G | C | 2 | a0008c0009t0001g0004a0008c0009t0001g0194 | 3 | HG02615.hp2 HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.533+973C>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 4/39 | chr3 | 13390238 | ||||||
chr3:13390240
|
C | T | 2 | a0003c0011t0001g0035a0003c0011t0001g0036 | 2 | HG02922.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.533+971G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 4/39 | chr3 | 13390240 | ||||||
chr3:13390337
|
A | C | 2 | a0003c0011t0001g0035a0003c0011t0001g0036 | 2 | HG02922.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.533+874T>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 4/39 | chr3 | 13390337 | ||||||
chr3:13390382
|
A | C | 1 | a0002c0002t0001g0219 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.533+829T>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 4/39 | chr3 | 13390382 | ||||||
chr3:13390388
|
G | T | 207 | a0002c0002t0001g0050a0002c0002t0001g0160a0002c0002t0001g0161others(204): Show | 209 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(206): Show |
intron_variant | MODIFIER | c.533+823C>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 4/39 | chr3 | 13390388 | ||||||
chr3:13390444
|
C | T | 2 | a0008c0009t0001g0004a0008c0009t0001g0194 | 3 | HG02615.hp2 HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.533+767G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 4/39 | chr3 | 13390444 | ||||||
chr3:13390535
|
T | G | 1 | a0022c0017t0005g0057 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.533+676A>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 4/39 | chr3 | 13390535 | ||||||
chr3:13390641
|
G | A | 45 | a0005c0003t0001g0215a0005c0003t0001g0216a0005c0003t0001g0234others(42): Show | 46 | HG00140.hp1 HG00140.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.533+570C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 4/39 | chr3 | 13390641 | ||||||
chr3:13390655
|
C | T | 1 | a0003c0006t0006g0055 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.533+556G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 4/39 | chr3 | 13390655 | ||||||
chr3:13390713
|
C | T | 175 | a0002c0002t0001g0050a0002c0002t0001g0160a0002c0002t0001g0161others(172): Show | 176 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.533+498G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 4/39 | chr3 | 13390713 | ||||||
chr3:13390722
|
A | G | 176 | a0002c0002t0001g0050a0002c0002t0001g0160a0002c0002t0001g0161others(173): Show | 178 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.533+489T>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 4/39 | chr3 | 13390722 | ||||||
chr3:13390763
|
G | A | 1 | a0005c0003t0001g0300 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.533+448C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 4/39 | chr3 | 13390763 | ||||||
chr3:13390798
|
T | C | 1 | a0002c0002t0001g0050 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.533+413A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 4/39 | chr3 | 13390798 | ||||||
chr3:13390817
|
T | C | 1 | a0003c0005t0005g0031 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.533+394A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 4/39 | chr3 | 13390817 | ||||||
chr3:13390834
|
G | A | 14 | a0001c0001t0002g0104a0002c0002t0001g0235a0002c0002t0001g0246others(11): Show | 14 | HG00544.hp2 HG00621.hp1 NA18944.hp2 others(11): Show |
intron_variant | MODIFIER | c.533+377C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 4/39 | chr3 | 13390834 | ||||||
chr3:13390859
|
G | A | 1 | a0005c0003t0001g0297 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.533+352C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 4/39 | chr3 | 13390859 | ||||||
chr3:13391030
|
C | T | 1 | a0001c0001t0002g0141 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.533+181G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 4/39 | chr3 | 13391030 | ||||||
chr3:13391081
|
A | G | 207 | a0002c0002t0001g0050a0002c0002t0001g0160a0002c0002t0001g0161others(204): Show | 209 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(206): Show |
intron_variant | MODIFIER | c.533+130T>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 4/39 | chr3 | 13391081 | ||||||
chr3:13391404
|
C | A | 2 | a0003c0011t0001g0035a0003c0011t0001g0036 | 2 | HG02922.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.437-97G>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 3/39 | chr3 | 13391404 | ||||||
chr3:13391451
|
A | G | 1 | a0004c0036t0003g0176 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.437-144T>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 3/39 | chr3 | 13391451 | ||||||
chr3:13391620
|
C | T | 175 | a0002c0002t0001g0050a0002c0002t0001g0160a0002c0002t0001g0161others(172): Show | 176 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.437-313G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 3/39 | chr3 | 13391620 | ||||||
chr3:13391658
|
T | G | 177 | a0002c0002t0001g0050a0002c0002t0001g0160a0002c0002t0001g0161others(174): Show | 179 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.437-351A>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 3/39 | chr3 | 13391658 | ||||||
chr3:13391734
|
G | A | 1 | a0001c0001t0002g0063 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.437-427C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 3/39 | chr3 | 13391734 | ||||||
chr3:13391735
|
A | G | 1 | a0001c0001t0002g0063 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.437-428T>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 3/39 | chr3 | 13391735 | ||||||
chr3:13391997
|
A | C | 1 | a0003c0005t0005g0032 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.437-690T>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 3/39 | chr3 | 13391997 | ||||||
chr3:13392413
|
A | G | 44 | a0002c0002t0001g0199a0002c0002t0001g0200a0002c0002t0001g0201others(41): Show | 44 | HG00099.hp1 HG00544.hp2 HG00621.hp1 others(41): Show |
intron_variant | MODIFIER | c.437-1106T>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 3/39 | chr3 | 13392413 | ||||||
chr3:13392599
|
T | C | 207 | a0002c0002t0001g0050a0002c0002t0001g0160a0002c0002t0001g0161others(204): Show | 209 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(206): Show |
intron_variant | MODIFIER | c.437-1292A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 3/39 | chr3 | 13392599 | ||||||
chr3:13392669
|
C | T | 1 | a0006c0007t0001g0015 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.437-1362G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 3/39 | chr3 | 13392669 | ||||||
chr3:13392684
|
A | G | 1 | a0003c0006t0008g0005 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.437-1377T>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 3/39 | chr3 | 13392684 | ||||||
chr3:13392685
|
T | G | 5 | a0006c0007t0001g0002a0006c0007t0001g0012a0006c0007t0001g0013others(2): Show | 6 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(3): Show |
intron_variant | MODIFIER | c.437-1378A>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 3/39 | chr3 | 13392685 | ||||||
chr3:13392719
|
T | C | 2 | a0003c0011t0001g0035a0003c0011t0001g0036 | 2 | HG02922.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.437-1412A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 3/39 | chr3 | 13392719 | ||||||
chr3:13392764
|
G | A | 172 | a0002c0002t0001g0050a0002c0002t0001g0160a0002c0002t0001g0161others(169): Show | 173 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.437-1457C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 3/39 | chr3 | 13392764 | ||||||
chr3:13392993
|
A | G | 1 | a0020c0020t0001g0193 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.437-1686T>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 3/39 | chr3 | 13392993 | ||||||
chr3:13393043
|
A | G | 175 | a0002c0002t0001g0050a0002c0002t0001g0160a0002c0002t0001g0161others(172): Show | 176 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.437-1736T>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 3/39 | chr3 | 13393043 | ||||||
chr3:13393118
|
T | C | 18 | a0004c0004t0003g0107a0004c0004t0003g0108a0004c0004t0003g0166others(15): Show | 18 | HG00544.hp1 HG01516.hp2 HG01517.hp1 others(15): Show |
intron_variant | MODIFIER | c.437-1811A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 3/39 | chr3 | 13393118 | ||||||
chr3:13393396
|
C | T | 2 | a0004c0004t0003g0173a0004c0004t0003g0174 | 2 | HG02922.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.437-2089G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 3/39 | chr3 | 13393396 | ||||||
chr3:13393478
|
G | A | 1 | a0006c0007t0001g0015 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.437-2171C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 3/39 | chr3 | 13393478 | ||||||
chr3:13393493
|
C | T | 2 | a0008c0009t0001g0004a0008c0009t0001g0194 | 3 | HG02615.hp2 HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.437-2186G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 3/39 | chr3 | 13393493 | ||||||
chr3:13393508
|
G | C | 1 | a0001c0001t0002g0105 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.437-2201C>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 3/39 | chr3 | 13393508 | ||||||
chr3:13393595
|
G | A | 175 | a0002c0002t0001g0050a0002c0002t0001g0160a0002c0002t0001g0161others(172): Show | 176 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.437-2288C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 3/39 | chr3 | 13393595 | ||||||
chr3:13393622
|
C | A | 1 | a0005c0003t0001g0245 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.437-2315G>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 3/39 | chr3 | 13393622 | ||||||
chr3:13393641
|
G | T | 1 | a0003c0019t0013g0164 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.437-2334C>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 3/39 | chr3 | 13393641 | ||||||
chr3:13393852
|
A | G | 177 | a0002c0002t0001g0050a0002c0002t0001g0160a0002c0002t0001g0161others(174): Show | 179 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.437-2545T>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 3/39 | chr3 | 13393852 | ||||||
chr3:13393862
|
C | T | 13 | a0003c0005t0005g0023a0003c0005t0005g0024a0003c0005t0005g0025others(10): Show | 13 | HG01109.hp1 HG01884.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.437-2555G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 3/39 | chr3 | 13393862 | ||||||
chr3:13393892
|
C | G | 177 | a0002c0002t0001g0050a0002c0002t0001g0160a0002c0002t0001g0161others(174): Show | 179 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.437-2585G>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 3/39 | chr3 | 13393892 | ||||||
chr3:13393913
|
C | T | 30 | a0004c0004t0003g0107a0004c0004t0003g0108a0004c0004t0003g0165others(27): Show | 30 | HG00544.hp1 HG01081.hp1 HG01516.hp2 others(27): Show |
intron_variant | MODIFIER | c.437-2606G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 3/39 | chr3 | 13393913 | ||||||
chr3:13393916
|
T | C | 45 | a0005c0003t0001g0215a0005c0003t0001g0216a0005c0003t0001g0234others(42): Show | 46 | HG00140.hp1 HG00140.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.437-2609A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 3/39 | chr3 | 13393916 | ||||||
chr3:13394004
|
G | A | 13 | a0003c0005t0005g0023a0003c0005t0005g0024a0003c0005t0005g0025others(10): Show | 13 | HG01109.hp1 HG01884.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.437-2697C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 3/39 | chr3 | 13394004 | ||||||
chr3:13394050
|
T | C | 177 | a0002c0002t0001g0050a0002c0002t0001g0160a0002c0002t0001g0161others(174): Show | 179 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.437-2743A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 3/39 | chr3 | 13394050 | ||||||
chr3:13394360
|
G | T | 175 | a0002c0002t0001g0050a0002c0002t0001g0160a0002c0002t0001g0161others(172): Show | 176 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.436+2997C>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 3/39 | chr3 | 13394360 | ||||||
chr3:13394417
|
G | A | 175 | a0002c0002t0001g0050a0002c0002t0001g0160a0002c0002t0001g0161others(172): Show | 176 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.436+2940C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 3/39 | chr3 | 13394417 | ||||||
chr3:13394429
|
G | A | 1 | a0003c0005t0005g0061 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.436+2928C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 3/39 | chr3 | 13394429 | ||||||
chr3:13394647
|
T | C | 1 | a0004c0004t0003g0192 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.436+2710A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 3/39 | chr3 | 13394647 | ||||||
chr3:13394666
|
T | C | 1 | a0002c0002t0001g0163 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.436+2691A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 3/39 | chr3 | 13394666 | ||||||
chr3:13394747
|
G | A | 1 | a0005c0003t0001g0300 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.436+2610C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 3/39 | chr3 | 13394747 | ||||||
chr3:13394836
|
A | C | 172 | a0002c0002t0001g0050a0002c0002t0001g0160a0002c0002t0001g0161others(169): Show | 173 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.436+2521T>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 3/39 | chr3 | 13394836 | ||||||
chr3:13394839
|
T | C | 12 | a0003c0006t0006g0051a0003c0006t0006g0052a0003c0006t0006g0053others(9): Show | 12 | HG02486.hp1 HG02559.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.436+2518A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 3/39 | chr3 | 13394839 | ||||||
chr3:13394870
|
T | A | 2 | a0008c0009t0001g0004a0008c0009t0001g0194 | 3 | HG02615.hp2 HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.436+2487A>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 3/39 | chr3 | 13394870 | ||||||
chr3:13394889
|
G | GGCAAAAG others(4): Show |
2 | a0002c0002t0001g0263a0002c0002t0001g0282 | 2 | NA18994.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.436+2457_436+2467d others(13): Show |
NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 3/39 | chr3 | 13394889 | ||||||
chr3:13395092
|
A | T | 1 | a0001c0001t0002g0150 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.436+2265T>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 3/39 | chr3 | 13395092 | ||||||
chr3:13395120
|
G | A | 30 | a0004c0004t0003g0107a0004c0004t0003g0108a0004c0004t0003g0165others(27): Show | 30 | HG00544.hp1 HG01081.hp1 HG01516.hp2 others(27): Show |
intron_variant | MODIFIER | c.436+2237C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 3/39 | chr3 | 13395120 | ||||||
chr3:13395217
|
C | T | 1 | a0002c0002t0001g0230 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.436+2140G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 3/39 | chr3 | 13395217 | ||||||
chr3:13395474
|
C | T | 90 | a0002c0002t0001g0160a0002c0002t0001g0161a0002c0002t0001g0162others(87): Show | 90 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.436+1883G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 3/39 | chr3 | 13395474 | ||||||
chr3:13395552
|
G | A | 175 | a0002c0002t0001g0050a0002c0002t0001g0160a0002c0002t0001g0161others(172): Show | 176 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.436+1805C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 3/39 | chr3 | 13395552 | ||||||
chr3:13395665
|
G | A | 1 | a0002c0002t0001g0273 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.436+1692C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 3/39 | chr3 | 13395665 | ||||||
chr3:13395775
|
T | C | 177 | a0002c0002t0001g0050a0002c0002t0001g0160a0002c0002t0001g0161others(174): Show | 179 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.436+1582A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 3/39 | chr3 | 13395775 | ||||||
chr3:13396174
|
T | C | 1 | a0002c0002t0001g0284 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.436+1183A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 3/39 | chr3 | 13396174 | ||||||
chr3:13396268
|
A | G | 2 | a0008c0009t0001g0004a0008c0009t0001g0194 | 3 | HG02615.hp2 HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.436+1089T>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 3/39 | chr3 | 13396268 | ||||||
chr3:13396272
|
A | G | 5 | a0004c0004t0003g0169a0004c0004t0003g0170a0004c0004t0003g0171others(2): Show | 5 | HG02258.hp1 HG02630.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.436+1085T>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 3/39 | chr3 | 13396272 | ||||||
chr3:13396383
|
G | T | 177 | a0002c0002t0001g0050a0002c0002t0001g0160a0002c0002t0001g0161others(174): Show | 179 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.436+974C>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 3/39 | chr3 | 13396383 | ||||||
chr3:13396397
|
T | A | 30 | a0004c0004t0003g0107a0004c0004t0003g0108a0004c0004t0003g0165others(27): Show | 30 | HG00544.hp1 HG01081.hp1 HG01516.hp2 others(27): Show |
intron_variant | MODIFIER | c.436+960A>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 3/39 | chr3 | 13396397 | ||||||
chr3:13396450
|
C | T | 172 | a0002c0002t0001g0050a0002c0002t0001g0160a0002c0002t0001g0161others(169): Show | 173 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.436+907G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 3/39 | chr3 | 13396450 | ||||||
chr3:13396519
|
G | A | 4 | a0003c0006t0005g0008a0003c0006t0005g0044a0003c0006t0005g0046others(1): Show | 4 | HG01243.hp2 HG02135.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.436+838C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 3/39 | chr3 | 13396519 | ||||||
chr3:13396593
|
C | CA | 12 | a0001c0001t0002g0106a0001c0001t0002g0116a0001c0001t0002g0154others(9): Show | 13 | HG02135.hp2 HG02615.hp2 HG02683.hp1 others(10): Show |
intron_variant | MODIFIER | c.436+763dupT | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 3/39 | chr3 | 13396593 | ||||||
chr3:13396593
|
CA | C | 52 | a0001c0001t0002g0087a0001c0001t0002g0148a0002c0002t0001g0050others(49): Show | 53 | HG00140.hp2 HG00544.hp1 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.436+763delT | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 3/39 | chr3 | 13396593 | ||||||
chr3:13396629
|
A | G | 1 | a0003c0006t0006g0055 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.436+728T>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 3/39 | chr3 | 13396629 | ||||||
chr3:13396657
|
G | C | 2 | a0001c0001t0002g0132a0001c0001t0002g0157 | 2 | HG02572.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.436+700C>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 3/39 | chr3 | 13396657 | ||||||
chr3:13396696
|
G | A | 1 | a0003c0005t0005g0028 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.436+661C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 3/39 | chr3 | 13396696 | ||||||
chr3:13396734
|
T | C | 208 | a0001c0001t0002g0072a0002c0002t0001g0050a0002c0002t0001g0160others(205): Show | 210 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.436+623A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 3/39 | chr3 | 13396734 | ||||||
chr3:13396760
|
C | CA | 117 | a0001c0001t0002g0001a0001c0001t0002g0041a0001c0001t0002g0042others(114): Show | 120 | HG00280.hp1 HG00438.hp2 HG00558.hp1 others(117): Show |
intron_variant | MODIFIER | c.436+596dupT | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 3/39 | chr3 | 13396760 | ||||||
chr3:13396760
|
C | CAA | 170 | a0001c0001t0002g0071a0001c0001t0002g0078a0001c0001t0002g0082others(167): Show | 171 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(168): Show |
intron_variant | MODIFIER | c.436+595_436+596dup others(2): Show |
NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 3/39 | chr3 | 13396760 | ||||||
chr3:13396760
|
C | CAAA | 22 | a0001c0001t0009g0198a0002c0002t0001g0263a0002c0002t0004g0254others(19): Show | 22 | HG00544.hp1 HG01517.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.436+594_436+596dup others(3): Show |
NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 3/39 | chr3 | 13396760 | ||||||
chr3:13396791
|
T | C | 7 | a0001c0001t0002g0071a0001c0001t0002g0076a0001c0001t0002g0077others(4): Show | 7 | HG00558.hp1 HG00639.hp1 HG01496.hp1 others(4): Show |
intron_variant | MODIFIER | c.436+566A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 3/39 | chr3 | 13396791 | ||||||
chr3:13396819
|
G | A | 179 | a0001c0001t0002g0132a0001c0001t0002g0157a0002c0002t0001g0050others(176): Show | 181 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(178): Show |
intron_variant | MODIFIER | c.436+538C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 3/39 | chr3 | 13396819 | ||||||
chr3:13396920
|
G | T | 45 | a0005c0003t0001g0215a0005c0003t0001g0216a0005c0003t0001g0234others(42): Show | 46 | HG00140.hp1 HG00140.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.436+437C>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 3/39 | chr3 | 13396920 | ||||||
chr3:13397330
|
A | G | 177 | a0001c0001t0002g0111a0002c0002t0001g0050a0002c0002t0001g0160others(174): Show | 179 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.436+27T>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 3/39 | chr3 | 13397330 | ||||||
chr3:13397505
|
A | G | 66 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(63): Show | 68 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(65): Show |
intron_variant | MODIFIER | c.305-17T>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 2/39 | chr3 | 13397505 | ||||||
chr3:13397658
|
A | G | 1 | a0023c0026t0011g0290 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.305-170T>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 2/39 | chr3 | 13397658 | ||||||
chr3:13397712
|
C | G | 1 | a0009c0030t0005g0009 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.305-224G>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 2/39 | chr3 | 13397712 | ||||||
chr3:13398012
|
C | T | 1 | a0005c0003t0001g0215 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.305-524G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 2/39 | chr3 | 13398012 | ||||||
chr3:13398042
|
A | G | 1 | a0004c0004t0010g0184 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.305-554T>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 2/39 | chr3 | 13398042 | ||||||
chr3:13398138
|
C | T | 1 | a0023c0026t0011g0290 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.305-650G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 2/39 | chr3 | 13398138 | ||||||
chr3:13398321
|
C | T | 11 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(8): Show | 11 | HG01243.hp2 HG01346.hp1 HG01978.hp2 others(8): Show |
intron_variant | MODIFIER | c.305-833G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 2/39 | chr3 | 13398321 | ||||||
chr3:13398338
|
G | A | 1 | a0006c0007t0001g0015 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.305-850C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 2/39 | chr3 | 13398338 | ||||||
chr3:13398356
|
T | C | 2 | a0008c0009t0001g0004a0008c0009t0001g0194 | 3 | HG02615.hp2 HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.305-868A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 2/39 | chr3 | 13398356 | ||||||
chr3:13398366
|
C | A | 1 | a0001c0001t0002g0144 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.305-878G>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 2/39 | chr3 | 13398366 | ||||||
chr3:13398485
|
A | C | 1 | a0007c0008t0002g0136 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.305-997T>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 2/39 | chr3 | 13398485 | ||||||
chr3:13398534
|
C | T | 2 | a0008c0009t0001g0004a0008c0009t0001g0194 | 3 | HG02615.hp2 HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.305-1046G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 2/39 | chr3 | 13398534 | ||||||
chr3:13398621
|
G | A | 1 | a0009c0027t0003g0019 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.304+1104C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 2/39 | chr3 | 13398621 | ||||||
chr3:13398803
|
G | T | 62 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(59): Show | 64 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(61): Show |
intron_variant | MODIFIER | c.304+922C>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 2/39 | chr3 | 13398803 | ||||||
chr3:13398999
|
T | C | 28 | a0004c0004t0003g0165a0004c0004t0003g0166a0004c0004t0003g0167others(25): Show | 28 | HG00544.hp1 HG01081.hp1 HG01516.hp2 others(25): Show |
intron_variant | MODIFIER | c.304+726A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 2/39 | chr3 | 13398999 | ||||||
chr3:13399035
|
G | A | 1 | a0001c0001t0002g0113 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.304+690C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 2/39 | chr3 | 13399035 | ||||||
chr3:13399122
|
C | A | 2 | a0006c0007t0001g0040a0009c0030t0005g0009 | 2 | HG01891.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.304+603G>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 2/39 | chr3 | 13399122 | ||||||
chr3:13399195
|
G | C | 2 | a0008c0009t0001g0004a0008c0009t0001g0194 | 3 | HG02615.hp2 HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.304+530C>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 2/39 | chr3 | 13399195 | ||||||
chr3:13399222
|
C | T | 9 | a0003c0006t0006g0051a0003c0006t0006g0052a0003c0006t0006g0053others(6): Show | 9 | HG02486.hp1 HG02559.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.304+503G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 2/39 | chr3 | 13399222 | ||||||
chr3:13399265
|
C | CA | 63 | a0001c0001t0002g0063a0001c0001t0002g0071a0001c0001t0002g0111others(60): Show | 63 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.304+459dupT | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 2/39 | chr3 | 13399265 | ||||||
chr3:13399265
|
C | CAA | 22 | a0002c0002t0001g0206a0002c0013t0004g0240a0003c0005t0005g0032others(19): Show | 23 | HG00140.hp2 HG00733.hp1 HG00735.hp1 others(20): Show |
intron_variant | MODIFIER | c.304+458_304+459dup others(2): Show |
NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 2/39 | chr3 | 13399265 | ||||||
chr3:13399265
|
CA | C | 25 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(22): Show | 25 | HG01243.hp2 HG01346.hp1 HG01978.hp2 others(22): Show |
intron_variant | MODIFIER | c.304+459delT | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 2/39 | chr3 | 13399265 | ||||||
chr3:13399476
|
T | G | 1 | a0003c0019t0013g0164 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.304+249A>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 2/39 | chr3 | 13399476 | ||||||
chr3:13399520
|
C | G | 60 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(57): Show | 61 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(58): Show |
intron_variant | MODIFIER | c.304+205G>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 2/39 | chr3 | 13399520 | ||||||
chr3:13399565
|
G | A | 1 | a0001c0001t0002g0141 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.304+160C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 2/39 | chr3 | 13399565 | ||||||
chr3:13400108
|
A | G | 3 | a0003c0006t0008g0005a0003c0006t0008g0006a0003c0006t0008g0007 | 3 | HG02965.hp1 HG03130.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.168-247T>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13400108 | ||||||
chr3:13400172
|
G | A | 1 | a0005c0003t0001g0242 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.168-311C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13400172 | ||||||
chr3:13400187
|
G | A | 1 | a0001c0001t0002g0144 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.168-326C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13400187 | ||||||
chr3:13400248
|
G | A | 1 | a0002c0002t0001g0308 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.168-387C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13400248 | ||||||
chr3:13400290
|
A | G | 59 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(56): Show | 60 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(57): Show |
intron_variant | MODIFIER | c.168-429T>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13400290 | ||||||
chr3:13400298
|
C | T | 1 | a0004c0004t0003g0165 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.168-437G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13400298 | ||||||
chr3:13400352
|
C | T | 1 | a0020c0020t0001g0193 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.168-491G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13400352 | ||||||
chr3:13400456
|
C | T | 12 | a0003c0006t0006g0051a0003c0006t0006g0052a0003c0006t0006g0053others(9): Show | 12 | HG02486.hp1 HG02559.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.168-595G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13400456 | ||||||
chr3:13400790
|
C | G | 1 | a0015c0021t0001g0267 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.168-929G>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13400790 | ||||||
chr3:13400820
|
G | C | 1 | a0022c0017t0005g0057 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.168-959C>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13400820 | ||||||
chr3:13400929
|
AAGG | A | 59 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(56): Show | 60 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(57): Show |
intron_variant | MODIFIER | c.168-1071_168-1069d others(5): Show |
NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13400929 | ||||||
chr3:13400995
|
T | A | 1 | a0003c0006t0008g0007 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.168-1134A>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13400995 | ||||||
chr3:13401128
|
A | G | 217 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(214): Show | 219 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.168-1267T>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13401128 | ||||||
chr3:13401152
|
G | A | 4 | a0001c0001t0002g0072a0001c0001t0002g0143a0001c0001t0002g0144others(1): Show | 4 | NA18954.hp1 NA18981.hp1 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.168-1291C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13401152 | ||||||
chr3:13401173
|
C | T | 1 | a0002c0002t0001g0231 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.168-1312G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13401173 | ||||||
chr3:13401183
|
C | T | 2 | a0003c0011t0001g0035a0003c0011t0001g0036 | 2 | HG02922.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.168-1322G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13401183 | ||||||
chr3:13401186
|
C | G | 320 | a0001c0001t0002g0001a0001c0001t0002g0041a0001c0001t0002g0042others(317): Show | 325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.168-1325G>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13401186 | ||||||
chr3:13401195
|
GC | G | 320 | a0001c0001t0002g0001a0001c0001t0002g0041a0001c0001t0002g0042others(317): Show | 325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.168-1335delG | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13401195 | ||||||
chr3:13401259
|
C | CA | 8 | a0001c0001t0002g0080a0001c0001t0002g0114a0001c0001t0002g0116others(5): Show | 8 | HG02738.hp1 HG02738.hp2 HG03516.hp1 others(5): Show |
intron_variant | MODIFIER | c.168-1399dupT | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13401259 | ||||||
chr3:13401259
|
C | CAAAAAA | 41 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(38): Show | 42 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.168-1404_168-1399d others(8): Show |
NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13401259 | ||||||
chr3:13401259
|
C | CAAAAAAA | 17 | a0001c0001t0002g0045a0003c0005t0005g0028a0003c0005t0005g0029others(14): Show | 17 | HG01109.hp1 HG01175.hp1 HG01978.hp2 others(14): Show |
intron_variant | MODIFIER | c.168-1405_168-1399d others(9): Show |
NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13401259 | ||||||
chr3:13401259
|
C | CAAAAAAA others(3): Show |
15 | a0002c0002t0001g0160a0002c0002t0001g0161a0004c0004t0003g0165others(12): Show | 16 | HG00544.hp1 HG01516.hp2 HG01517.hp1 others(13): Show |
intron_variant | MODIFIER | c.168-1408_168-1399d others(12): Show |
NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13401259 | ||||||
chr3:13401259
|
C | CAAAAAAA others(4): Show |
16 | a0002c0002t0001g0162a0002c0002t0001g0163a0004c0004t0003g0166others(13): Show | 16 | HG01081.hp1 HG02145.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.168-1409_168-1399d others(13): Show |
NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13401259 | ||||||
chr3:13401259
|
C | CAAAAAAA others(5): Show |
3 | a0004c0004t0003g0172a0004c0004t0010g0186a0004c0016t0005g0191 | 3 | HG02622.hp1 HG02630.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.168-1410_168-1399d others(14): Show |
NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13401259 | ||||||
chr3:13401259
|
C | CAAAAAAA others(7): Show |
2 | a0002c0002t0001g0218a0002c0002t0001g0229 | 2 | HG01433.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.168-1412_168-1399d others(16): Show |
NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13401259 | ||||||
chr3:13401259
|
C | CAAAAAAA others(8): Show |
46 | a0002c0002t0001g0207a0002c0002t0001g0208a0002c0002t0001g0214others(43): Show | 46 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(43): Show |
intron_variant | MODIFIER | c.168-1413_168-1399d others(17): Show |
NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13401259 | ||||||
chr3:13401259
|
C | CAAAAAAA others(9): Show |
45 | a0001c0001t0002g0265a0001c0033t0002g0266a0002c0002t0001g0199others(42): Show | 45 | HG00544.hp2 HG00558.hp2 HG00733.hp2 others(42): Show |
intron_variant | MODIFIER | c.168-1414_168-1399d others(18): Show |
NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13401259 | ||||||
chr3:13401259
|
C | CAAAAAAA others(10): Show |
23 | a0001c0001t0002g0274a0001c0001t0002g0288a0002c0002t0001g0200others(20): Show | 23 | HG00642.hp1 HG00642.hp2 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.168-1415_168-1399d others(19): Show |
NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13401259 | ||||||
chr3:13401259
|
C | CAAAAAAA others(11): Show |
5 | a0001c0001t0002g0276a0002c0002t0004g0279a0005c0003t0001g0238others(2): Show | 5 | HG00597.hp1 HG01978.hp1 NA18946.hp2 others(2): Show |
intron_variant | MODIFIER | c.168-1416_168-1399d others(20): Show |
NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13401259 | ||||||
chr3:13401259
|
C | CAAAAAAA others(12): Show |
1 | a0002c0002t0001g0237 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.168-1417_168-1399d others(21): Show |
NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13401259 | ||||||
chr3:13401259
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0002g0117 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.168-1409_168-1399d others(13): Show |
NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13401259 | ||||||
chr3:13401292
|
G | A | 1 | a0006c0007t0001g0040 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.168-1431C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13401292 | ||||||
chr3:13401383
|
G | C | 32 | a0002c0002t0001g0160a0002c0002t0001g0161a0002c0002t0001g0162others(29): Show | 32 | HG00544.hp1 HG01081.hp1 HG01516.hp2 others(29): Show |
intron_variant | MODIFIER | c.168-1522C>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13401383 | ||||||
chr3:13401392
|
G | C | 3 | a0003c0005t0005g0032a0003c0005t0005g0033a0009c0028t0003g0034 | 3 | HG02895.hp2 HG03516.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.168-1531C>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13401392 | ||||||
chr3:13401400
|
C | T | 59 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(56): Show | 60 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(57): Show |
intron_variant | MODIFIER | c.168-1539G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13401400 | ||||||
chr3:13401426
|
C | T | 2 | a0008c0009t0001g0004a0008c0009t0001g0194 | 3 | HG02615.hp2 HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.168-1565G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13401426 | ||||||
chr3:13401460
|
A | G | 1 | a0002c0002t0001g0246 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.168-1599T>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13401460 | ||||||
chr3:13401495
|
C | A | 1 | a0020c0020t0001g0193 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.168-1634G>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13401495 | ||||||
chr3:13401541
|
C | T | 1 | a0005c0003t0001g0245 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.168-1680G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13401541 | ||||||
chr3:13401709
|
G | A | 2 | a0008c0009t0001g0004a0008c0009t0001g0194 | 3 | HG02615.hp2 HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.168-1848C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13401709 | ||||||
chr3:13401741
|
A | T | 1 | a0024c0038t0002g0321 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.168-1880T>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13401741 | ||||||
chr3:13401819
|
C | T | 5 | a0004c0004t0003g0169a0004c0004t0003g0170a0004c0004t0003g0171others(2): Show | 5 | HG02258.hp1 HG02630.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.168-1958G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13401819 | ||||||
chr3:13401827
|
G | A | 60 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(57): Show | 61 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(58): Show |
intron_variant | MODIFIER | c.168-1966C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13401827 | ||||||
chr3:13401892
|
T | TA | 51 | a0001c0001t0002g0066a0001c0001t0002g0070a0001c0001t0002g0073others(48): Show | 51 | HG00438.hp2 HG00544.hp1 HG00558.hp2 others(48): Show |
intron_variant | MODIFIER | c.168-2032dupT | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13401892 | ||||||
chr3:13401893
|
A | T | 59 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(56): Show | 60 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(57): Show |
intron_variant | MODIFIER | c.168-2032T>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13401893 | ||||||
chr3:13401935
|
C | T | 2 | a0006c0007t0001g0010a0006c0007t0001g0011 | 2 | HG01168.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.168-2074G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13401935 | ||||||
chr3:13402016
|
G | A | 28 | a0004c0004t0003g0165a0004c0004t0003g0166a0004c0004t0003g0167others(25): Show | 28 | HG00544.hp1 HG01081.hp1 HG01516.hp2 others(25): Show |
intron_variant | MODIFIER | c.168-2155C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13402016 | ||||||
chr3:13402040
|
A | T | 2 | a0003c0011t0001g0035a0003c0011t0001g0036 | 2 | HG02922.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.168-2179T>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13402040 | ||||||
chr3:13402286
|
C | T | 5 | a0002c0002t0001g0237a0002c0002t0001g0243a0002c0002t0001g0244others(2): Show | 5 | HG00438.hp1 NA18959.hp2 NA18965.hp1 others(2): Show |
intron_variant | MODIFIER | c.168-2425G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13402286 | ||||||
chr3:13402323
|
C | T | 1 | a0020c0020t0001g0193 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.168-2462G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13402323 | ||||||
chr3:13402415
|
T | G | 1 | a0001c0001t0002g0130 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.168-2554A>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13402415 | ||||||
chr3:13402581
|
G | A | 1 | a0002c0002t0001g0228 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.168-2720C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13402581 | ||||||
chr3:13402707
|
CA | C | 62 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(59): Show | 64 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(61): Show |
intron_variant | MODIFIER | c.168-2847delT | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13402707 | ||||||
chr3:13402733
|
A | G | 2 | a0003c0011t0001g0035a0003c0011t0001g0036 | 2 | HG02922.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.168-2872T>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13402733 | ||||||
chr3:13402960
|
TA | T | 121 | a0001c0001t0002g0265a0001c0001t0002g0274a0001c0001t0002g0276others(118): Show | 121 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.168-3100delT | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13402960 | ||||||
chr3:13402973
|
A | G | 32 | a0002c0002t0001g0160a0002c0002t0001g0161a0002c0002t0001g0162others(29): Show | 32 | HG00544.hp1 HG01081.hp1 HG01516.hp2 others(29): Show |
intron_variant | MODIFIER | c.168-3112T>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13402973 | ||||||
chr3:13403010
|
C | T | 1 | a0003c0006t0008g0005 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.168-3149G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13403010 | ||||||
chr3:13403011
|
G | A | 1 | a0002c0002t0001g0229 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.168-3150C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13403011 | ||||||
chr3:13403113
|
C | T | 1 | a0001c0001t0002g0067 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.168-3252G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13403113 | ||||||
chr3:13403220
|
A | G | 1 | a0002c0002t0001g0280 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.168-3359T>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13403220 | ||||||
chr3:13403368
|
C | A | 1 | a0006c0010t0001g0020 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.168-3507G>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13403368 | ||||||
chr3:13403413
|
C | A | 28 | a0004c0004t0003g0165a0004c0004t0003g0166a0004c0004t0003g0167others(25): Show | 28 | HG00544.hp1 HG01081.hp1 HG01516.hp2 others(25): Show |
intron_variant | MODIFIER | c.168-3552G>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13403413 | ||||||
chr3:13403882
|
C | G | 32 | a0002c0002t0001g0160a0002c0002t0001g0161a0002c0002t0001g0162others(29): Show | 32 | HG00544.hp1 HG01081.hp1 HG01516.hp2 others(29): Show |
intron_variant | MODIFIER | c.168-4021G>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13403882 | ||||||
chr3:13403987
|
C | G | 1 | a0005c0003t0001g0242 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.168-4126G>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13403987 | ||||||
chr3:13404130
|
C | G | 2 | a0002c0002t0001g0310a0002c0002t0001g0311 | 2 | HG00099.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.168-4269G>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13404130 | ||||||
chr3:13404134
|
T | C | 34 | a0002c0002t0001g0160a0002c0002t0001g0161a0002c0002t0001g0162others(31): Show | 35 | HG00544.hp1 HG01081.hp1 HG01516.hp2 others(32): Show |
intron_variant | MODIFIER | c.168-4273A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13404134 | ||||||
chr3:13404498
|
A | G | 1 | a0004c0004t0003g0169 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.168-4637T>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13404498 | ||||||
chr3:13404576
|
G | A | 36 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(33): Show | 36 | HG01109.hp1 HG01243.hp2 HG01346.hp1 others(33): Show |
intron_variant | MODIFIER | c.168-4715C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13404576 | ||||||
chr3:13404617
|
C | A | 59 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(56): Show | 60 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(57): Show |
intron_variant | MODIFIER | c.168-4756G>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13404617 | ||||||
chr3:13404741
|
G | A | 1 | a0001c0001t0002g0047 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.168-4880C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13404741 | ||||||
chr3:13404784
|
C | G | 2 | a0001c0001t0002g0132a0001c0001t0002g0157 | 2 | HG02572.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.168-4923G>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13404784 | ||||||
chr3:13404832
|
G | A | 1 | a0001c0001t0002g0079 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.168-4971C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13404832 | ||||||
chr3:13404982
|
A | G | 34 | a0002c0002t0001g0160a0002c0002t0001g0161a0002c0002t0001g0162others(31): Show | 35 | HG00544.hp1 HG01081.hp1 HG01516.hp2 others(32): Show |
intron_variant | MODIFIER | c.168-5121T>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13404982 | ||||||
chr3:13405233
|
T | C | 122 | a0001c0001t0002g0265a0001c0001t0002g0274a0001c0001t0002g0276others(119): Show | 122 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.168-5372A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13405233 | ||||||
chr3:13405271
|
T | G | 5 | a0002c0002t0001g0199a0002c0002t0001g0200a0002c0002t0001g0201others(2): Show | 5 | HG01099.hp2 HG02280.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.168-5410A>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13405271 | ||||||
chr3:13405287
|
C | T | 1 | a0005c0003t0001g0241 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.168-5426G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13405287 | ||||||
chr3:13405455
|
T | C | 1 | a0018c0023t0001g0177 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.168-5594A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13405455 | ||||||
chr3:13405558
|
T | C | 2 | a0008c0009t0001g0004a0008c0009t0001g0194 | 3 | HG02615.hp2 HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.168-5697A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13405558 | ||||||
chr3:13405802
|
G | A | 1 | a0002c0002t0004g0287 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.168-5941C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13405802 | ||||||
chr3:13406125
|
G | A | 317 | a0001c0001t0002g0001a0001c0001t0002g0041a0001c0001t0002g0042others(314): Show | 322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.168-6264C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13406125 | ||||||
chr3:13406166
|
C | G | 1 | a0006c0007t0001g0040 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.168-6305G>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13406166 | ||||||
chr3:13406181
|
G | T | 1 | a0003c0019t0013g0164 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.168-6320C>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13406181 | ||||||
chr3:13406291
|
T | C | 94 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(91): Show | 96 | HG00140.hp2 HG00544.hp1 HG00639.hp2 others(93): Show |
intron_variant | MODIFIER | c.168-6430A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13406291 | ||||||
chr3:13406330
|
T | C | 60 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(57): Show | 61 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(58): Show |
intron_variant | MODIFIER | c.168-6469A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13406330 | ||||||
chr3:13406493
|
A | G | 1 | a0001c0001t0002g0063 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.168-6632T>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13406493 | ||||||
chr3:13406593
|
C | T | 1 | a0004c0004t0003g0168 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.168-6732G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13406593 | ||||||
chr3:13406594
|
G | A | 60 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(57): Show | 61 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(58): Show |
intron_variant | MODIFIER | c.168-6733C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13406594 | ||||||
chr3:13406707
|
T | C | 1 | a0022c0017t0005g0057 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.168-6846A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13406707 | ||||||
chr3:13406848
|
C | A | 2 | a0008c0009t0001g0004a0008c0009t0001g0194 | 3 | HG02615.hp2 HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.168-6987G>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13406848 | ||||||
chr3:13406857
|
C | T | 1 | a0002c0002t0004g0289 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.168-6996G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13406857 | ||||||
chr3:13406860
|
C | A | 12 | a0003c0006t0006g0051a0003c0006t0006g0052a0003c0006t0006g0053others(9): Show | 12 | HG02486.hp1 HG02559.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.168-6999G>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13406860 | ||||||
chr3:13406892
|
G | A | 53 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(50): Show | 55 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.168-7031C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13406892 | ||||||
chr3:13406941
|
G | A | 1 | a0001c0001t0002g0131 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.168-7080C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13406941 | ||||||
chr3:13406965
|
G | A | 94 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(91): Show | 96 | HG00140.hp2 HG00544.hp1 HG00639.hp2 others(93): Show |
intron_variant | MODIFIER | c.168-7104C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13406965 | ||||||
chr3:13406986
|
T | C | 1 | a0002c0002t0001g0277 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.168-7125A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13406986 | ||||||
chr3:13407276
|
G | A | 4 | a0004c0004t0003g0165a0004c0004t0003g0175a0004c0036t0003g0176others(1): Show | 4 | HG02071.hp2 HG03927.hp1 NA18962.hp2 others(1): Show |
intron_variant | MODIFIER | c.168-7415C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13407276 | ||||||
chr3:13407433
|
T | C | 1 | a0003c0005t0005g0278 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.168-7572A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13407433 | ||||||
chr3:13407442
|
C | T | 60 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(57): Show | 61 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(58): Show |
intron_variant | MODIFIER | c.168-7581G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13407442 | ||||||
chr3:13407547
|
C | T | 5 | a0006c0007t0001g0017a0006c0007t0001g0018a0006c0010t0001g0016others(2): Show | 5 | HG02145.hp2 HG02559.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.168-7686G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13407547 | ||||||
chr3:13407557
|
A | G | 47 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(44): Show | 48 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(45): Show |
intron_variant | MODIFIER | c.168-7696T>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13407557 | ||||||
chr3:13407690
|
C | T | 60 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(57): Show | 61 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(58): Show |
intron_variant | MODIFIER | c.168-7829G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13407690 | ||||||
chr3:13407691
|
A | G | 60 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(57): Show | 61 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(58): Show |
intron_variant | MODIFIER | c.168-7830T>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13407691 | ||||||
chr3:13407798
|
T | C | 122 | a0001c0001t0002g0265a0001c0001t0002g0274a0001c0001t0002g0276others(119): Show | 122 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.168-7937A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13407798 | ||||||
chr3:13407804
|
C | T | 1 | a0001c0001t0002g0082 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.168-7943G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13407804 | ||||||
chr3:13407830
|
T | G | 2 | a0008c0009t0001g0004a0008c0009t0001g0194 | 3 | HG02615.hp2 HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.168-7969A>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13407830 | ||||||
chr3:13407995
|
G | A | 2 | a0001c0001t0002g0132a0001c0001t0002g0157 | 2 | HG02572.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.168-8134C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13407995 | ||||||
chr3:13407995
|
G | T | 1 | a0002c0002t0004g0289 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.168-8134C>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13407995 | ||||||
chr3:13408017
|
T | C | 60 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(57): Show | 61 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(58): Show |
intron_variant | MODIFIER | c.168-8156A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13408017 | ||||||
chr3:13408182
|
T | A | 15 | a0001c0001t0002g0048a0004c0004t0003g0166a0004c0004t0003g0167others(12): Show | 15 | HG00544.hp1 HG01516.hp2 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.168-8321A>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13408182 | ||||||
chr3:13408331
|
C | T | 216 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(213): Show | 218 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.168-8470G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13408331 | ||||||
chr3:13408385
|
A | G | 1 | a0002c0002t0004g0287 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.168-8524T>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13408385 | ||||||
chr3:13408519
|
A | G | 60 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(57): Show | 61 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(58): Show |
intron_variant | MODIFIER | c.168-8658T>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13408519 | ||||||
chr3:13408527
|
T | C | 1 | a0001c0001t0002g0159 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.168-8666A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13408527 | ||||||
chr3:13408536
|
T | C | 13 | a0002c0002t0001g0050a0003c0005t0005g0023a0003c0005t0005g0024others(10): Show | 13 | HG01109.hp1 HG01884.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.168-8675A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13408536 | ||||||
chr3:13408657
|
G | A | 59 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(56): Show | 60 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(57): Show |
intron_variant | MODIFIER | c.168-8796C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13408657 | ||||||
chr3:13408766
|
T | C | 13 | a0002c0002t0001g0050a0003c0005t0005g0023a0003c0005t0005g0024others(10): Show | 13 | HG01109.hp1 HG01884.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.168-8905A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13408766 | ||||||
chr3:13408787
|
C | CA | 50 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(47): Show | 51 | HG01109.hp1 HG01168.hp2 HG01243.hp2 others(48): Show |
intron_variant | MODIFIER | c.168-8927dupT | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13408787 | ||||||
chr3:13408787
|
C | CAA | 14 | a0006c0007t0001g0002a0006c0007t0001g0010a0006c0007t0001g0011others(11): Show | 15 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(12): Show |
intron_variant | MODIFIER | c.168-8928_168-8927d others(4): Show |
NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13408787 | ||||||
chr3:13408787
|
CA | C | 9 | a0001c0001t0002g0066a0001c0001t0002g0151a0002c0002t0001g0207others(6): Show | 9 | HG00323.hp2 HG00597.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.168-8927delT | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13408787 | ||||||
chr3:13409022
|
C | T | 1 | a0004c0004t0003g0167 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.168-9161G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13409022 | ||||||
chr3:13409155
|
G | A | 60 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(57): Show | 61 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(58): Show |
intron_variant | MODIFIER | c.168-9294C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13409155 | ||||||
chr3:13409243
|
T | C | 60 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(57): Show | 61 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(58): Show |
intron_variant | MODIFIER | c.168-9382A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13409243 | ||||||
chr3:13409354
|
C | T | 1 | a0001c0001t0002g0065 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.168-9493G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13409354 | ||||||
chr3:13409355
|
G | A | 1 | a0002c0002t0001g0280 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.168-9494C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13409355 | ||||||
chr3:13409501
|
T | G | 1 | a0005c0003t0001g0281 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.168-9640A>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13409501 | ||||||
chr3:13409803
|
G | A | 1 | a0001c0001t0002g0135 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.168-9942C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13409803 | ||||||
chr3:13409839
|
A | AT | 58 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(55): Show | 59 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(56): Show |
intron_variant | MODIFIER | c.168-9979_168-9978i others(3): Show |
NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13409839 | ||||||
chr3:13409840
|
A | AT | 152 | a0001c0001t0002g0265a0001c0001t0002g0274a0001c0001t0002g0276others(149): Show | 153 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.168-9980dupA | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13409840 | ||||||
chr3:13409840
|
A | T | 60 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(57): Show | 61 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(58): Show |
intron_variant | MODIFIER | c.168-9979T>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13409840 | ||||||
chr3:13409961
|
C | T | 60 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(57): Show | 61 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(58): Show |
intron_variant | MODIFIER | c.167+10099G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13409961 | ||||||
chr3:13409986
|
G | C | 60 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(57): Show | 61 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(58): Show |
intron_variant | MODIFIER | c.167+10074C>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13409986 | ||||||
chr3:13410019
|
A | AT | 8 | a0001c0001t0002g0064a0001c0001t0002g0081a0001c0001t0002g0150others(5): Show | 8 | HG01433.hp1 HG03491.hp1 HG03492.hp2 others(5): Show |
intron_variant | MODIFIER | c.167+10040dupA | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13410019 | ||||||
chr3:13410019
|
ATT | A | 59 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(56): Show | 60 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(57): Show |
intron_variant | MODIFIER | c.167+10039_167+1004 others(6): Show |
NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13410019 | ||||||
chr3:13410258
|
G | A | 1 | a0020c0020t0001g0193 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.167+9802C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13410258 | ||||||
chr3:13410309
|
G | T | 94 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(91): Show | 96 | HG00140.hp2 HG00544.hp1 HG00639.hp2 others(93): Show |
intron_variant | MODIFIER | c.167+9751C>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13410309 | ||||||
chr3:13410315
|
G | A | 2 | a0008c0009t0001g0004a0008c0009t0001g0194 | 3 | HG02615.hp2 HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.167+9745C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13410315 | ||||||
chr3:13410360
|
C | T | 60 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(57): Show | 61 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(58): Show |
intron_variant | MODIFIER | c.167+9700G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13410360 | ||||||
chr3:13410369
|
G | A | 2 | a0005c0003t0001g0301a0005c0003t0001g0302 | 2 | HG01070.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.167+9691C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13410369 | ||||||
chr3:13410640
|
G | A | 60 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(57): Show | 61 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(58): Show |
intron_variant | MODIFIER | c.167+9420C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13410640 | ||||||
chr3:13410714
|
G | C | 2 | a0008c0009t0001g0004a0008c0009t0001g0194 | 3 | HG02615.hp2 HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.167+9346C>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13410714 | ||||||
chr3:13410725
|
G | A | 61 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(58): Show | 62 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(59): Show |
intron_variant | MODIFIER | c.167+9335C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13410725 | ||||||
chr3:13410744
|
C | T | 2 | a0003c0005t0005g0031a0006c0007t0001g0040 | 2 | HG01891.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.167+9316G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13410744 | ||||||
chr3:13410762
|
C | CA | 60 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(57): Show | 61 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(58): Show |
intron_variant | MODIFIER | c.167+9297dupT | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13410762 | ||||||
chr3:13410866
|
T | C | 62 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(59): Show | 64 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(61): Show |
intron_variant | MODIFIER | c.167+9194A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13410866 | ||||||
chr3:13410875
|
A | G | 60 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(57): Show | 61 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(58): Show |
intron_variant | MODIFIER | c.167+9185T>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13410875 | ||||||
chr3:13410909
|
C | T | 1 | a0002c0002t0001g0230 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.167+9151G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13410909 | ||||||
chr3:13410917
|
C | CA | 10 | a0001c0001t0002g0080a0001c0001t0002g0137a0001c0001t0002g0138others(7): Show | 10 | HG00140.hp1 HG00621.hp2 HG01361.hp2 others(7): Show |
intron_variant | MODIFIER | c.167+9142dupT | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13410917 | ||||||
chr3:13410917
|
C | CAA | 120 | a0001c0001t0002g0158a0001c0001t0002g0265a0001c0001t0002g0274others(117): Show | 121 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(118): Show |
intron_variant | MODIFIER | c.167+9141_167+9142d others(4): Show |
NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13410917 | ||||||
chr3:13410921
|
A | AAAT | 23 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(20): Show | 23 | HG01243.hp2 HG01346.hp1 HG01978.hp2 others(20): Show |
intron_variant | MODIFIER | c.167+9138_167+9139i others(5): Show |
NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13410921 | ||||||
chr3:13410927
|
A | AAAT | 37 | a0002c0002t0001g0050a0003c0005t0005g0023a0003c0005t0005g0024others(34): Show | 38 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.167+9132_167+9133i others(5): Show |
NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13410927 | ||||||
chr3:13410927
|
A | T | 23 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(20): Show | 23 | HG01243.hp2 HG01346.hp1 HG01978.hp2 others(20): Show |
intron_variant | MODIFIER | c.167+9133T>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13410927 | ||||||
chr3:13410959
|
C | A | 5 | a0006c0007t0001g0017a0006c0007t0001g0018a0006c0010t0001g0016others(2): Show | 5 | HG02145.hp2 HG02559.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.167+9101G>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13410959 | ||||||
chr3:13411241
|
A | G | 60 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(57): Show | 61 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(58): Show |
intron_variant | MODIFIER | c.167+8819T>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13411241 | ||||||
chr3:13411300
|
T | G | 2 | a0006c0007t0001g0021a0006c0007t0001g0022 | 2 | NA19043.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.167+8760A>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13411300 | ||||||
chr3:13411443
|
C | T | 4 | a0002c0002t0001g0199a0002c0002t0001g0200a0002c0002t0001g0201others(1): Show | 4 | HG01099.hp2 HG02280.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.167+8617G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13411443 | ||||||
chr3:13411932
|
G | A | 1 | a0002c0002t0001g0204 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.167+8128C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13411932 | ||||||
chr3:13411950
|
C | T | 60 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(57): Show | 61 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(58): Show |
intron_variant | MODIFIER | c.167+8110G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13411950 | ||||||
chr3:13411970
|
T | A | 1 | a0002c0002t0001g0284 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.167+8090A>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13411970 | ||||||
chr3:13411995
|
G | A | 60 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(57): Show | 61 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(58): Show |
intron_variant | MODIFIER | c.167+8065C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13411995 | ||||||
chr3:13412080
|
C | A | 62 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(59): Show | 64 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(61): Show |
intron_variant | MODIFIER | c.167+7980G>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13412080 | ||||||
chr3:13412108
|
G | C | 1 | a0002c0002t0001g0214 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.167+7952C>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13412108 | ||||||
chr3:13412221
|
T | C | 1 | a0001c0001t0002g0141 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.167+7839A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13412221 | ||||||
chr3:13412231
|
C | CTTTTTT | 112 | a0001c0001t0002g0265a0001c0001t0002g0274a0001c0001t0002g0276others(109): Show | 112 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.167+7823_167+7828d others(8): Show |
NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13412231 | ||||||
chr3:13412231
|
C | CTTTTTTC others(1): Show |
31 | a0002c0002t0001g0160a0002c0002t0001g0161a0002c0002t0001g0162others(28): Show | 31 | HG00544.hp1 HG01081.hp1 HG01516.hp2 others(28): Show |
intron_variant | MODIFIER | c.167+7828_167+7829i others(10): Show |
NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13412231 | ||||||
chr3:13412231
|
C | CTTTTTTT | 8 | a0002c0002t0001g0200a0002c0002t0001g0217a0002c0002t0001g0235others(5): Show | 8 | HG00323.hp2 HG02486.hp2 HG03579.hp2 others(5): Show |
intron_variant | MODIFIER | c.167+7822_167+7828d others(9): Show |
NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13412231 | ||||||
chr3:13412231
|
C | CTTTTTTT others(10): Show |
1 | a0008c0009t0001g0004 | 2 | HG02615.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.167+7828_167+7829i others(19): Show |
NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13412231 | ||||||
chr3:13412231
|
C | CTTTTTTT others(11): Show |
1 | a0008c0009t0001g0194 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.167+7828_167+7829i others(20): Show |
NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13412231 | ||||||
chr3:13412247
|
T | TTTTTTTT others(2): Show |
41 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(38): Show | 42 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.167+7812_167+7813i others(11): Show |
NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13412247 | ||||||
chr3:13412247
|
T | TTTTTTTT others(3): Show |
12 | a0003c0006t0005g0008a0003c0006t0005g0049a0003c0006t0006g0052others(9): Show | 12 | HG01243.hp2 HG02486.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.167+7812_167+7813i others(12): Show |
NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13412247 | ||||||
chr3:13412247
|
T | TTTTTTTT others(4): Show |
3 | a0003c0006t0006g0051a0009c0028t0003g0034a0020c0020t0001g0193 | 3 | HG02622.hp2 HG03471.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.167+7812_167+7813i others(13): Show |
NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13412247 | ||||||
chr3:13412252
|
G | C | 1 | a0003c0006t0005g0049 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.167+7808C>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13412252 | ||||||
chr3:13412343
|
T | C | 29 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(26): Show | 29 | HG01243.hp2 HG01346.hp1 HG01891.hp1 others(26): Show |
intron_variant | MODIFIER | c.167+7717A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13412343 | ||||||
chr3:13412411
|
A | G | 1 | a0001c0001t0002g0080 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.167+7649T>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13412411 | ||||||
chr3:13412511
|
C | T | 1 | a0016c0025t0001g0232 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.167+7549G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13412511 | ||||||
chr3:13412535
|
G | A | 1 | a0001c0001t0002g0142 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.167+7525C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13412535 | ||||||
chr3:13412542
|
C | T | 122 | a0001c0001t0002g0265a0001c0001t0002g0274a0001c0001t0002g0276others(119): Show | 122 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.167+7518G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13412542 | ||||||
chr3:13412571
|
G | A | 1 | a0020c0020t0001g0193 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.167+7489C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13412571 | ||||||
chr3:13412766
|
G | T | 61 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(58): Show | 63 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(60): Show |
intron_variant | MODIFIER | c.167+7294C>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13412766 | ||||||
chr3:13412815
|
C | T | 1 | a0003c0005t0005g0031 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.167+7245G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13412815 | ||||||
chr3:13412839
|
C | T | 2 | a0004c0004t0003g0188a0004c0004t0003g0189 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.167+7221G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13412839 | ||||||
chr3:13412888
|
G | A | 36 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(33): Show | 36 | HG01109.hp1 HG01243.hp2 HG01346.hp1 others(33): Show |
intron_variant | MODIFIER | c.167+7172C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13412888 | ||||||
chr3:13412919
|
C | T | 59 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(56): Show | 60 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(57): Show |
intron_variant | MODIFIER | c.167+7141G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13412919 | ||||||
chr3:13412926
|
A | G | 2 | a0003c0011t0001g0035a0003c0011t0001g0036 | 2 | HG02922.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.167+7134T>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13412926 | ||||||
chr3:13412958
|
AAG | A | 2 | a0008c0009t0001g0004a0008c0009t0001g0194 | 3 | HG02615.hp2 HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.167+7100_167+7101d others(4): Show |
NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13412958 | ||||||
chr3:13413048
|
C | T | 59 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(56): Show | 60 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(57): Show |
intron_variant | MODIFIER | c.167+7012G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13413048 | ||||||
chr3:13413093
|
C | T | 4 | a0001c0001t0002g0076a0001c0001t0002g0077a0001c0001t0002g0078others(1): Show | 4 | HG00558.hp1 HG02004.hp2 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.167+6967G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13413093 | ||||||
chr3:13413146
|
C | T | 94 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(91): Show | 96 | HG00140.hp2 HG00544.hp1 HG00639.hp2 others(93): Show |
intron_variant | MODIFIER | c.167+6914G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13413146 | ||||||
chr3:13413194
|
G | A | 1 | a0003c0005t0005g0023 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.167+6866C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13413194 | ||||||
chr3:13413196
|
G | A | 1 | a0001c0001t0002g0062 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.167+6864C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13413196 | ||||||
chr3:13413205
|
C | T | 2 | a0008c0009t0001g0004a0008c0009t0001g0194 | 3 | HG02615.hp2 HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.167+6855G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13413205 | ||||||
chr3:13413264
|
G | A | 1 | a0002c0002t0004g0287 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.167+6796C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13413264 | ||||||
chr3:13413309
|
T | C | 1 | a0001c0001t0002g0288 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.167+6751A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13413309 | ||||||
chr3:13413326
|
C | T | 59 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(56): Show | 60 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(57): Show |
intron_variant | MODIFIER | c.167+6734G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13413326 | ||||||
chr3:13413469
|
C | CA | 57 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(54): Show | 58 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(55): Show |
intron_variant | MODIFIER | c.167+6590dupT | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13413469 | ||||||
chr3:13413841
|
G | A | 2 | a0008c0009t0001g0004a0008c0009t0001g0194 | 3 | HG02615.hp2 HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.167+6219C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13413841 | ||||||
chr3:13413901
|
A | G | 94 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(91): Show | 96 | HG00140.hp2 HG00544.hp1 HG00639.hp2 others(93): Show |
intron_variant | MODIFIER | c.167+6159T>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13413901 | ||||||
chr3:13413965
|
T | C | 1 | a0020c0020t0001g0193 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.167+6095A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13413965 | ||||||
chr3:13413992
|
T | C | 14 | a0006c0007t0001g0002a0006c0007t0001g0010a0006c0007t0001g0011others(11): Show | 15 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(12): Show |
intron_variant | MODIFIER | c.167+6068A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13413992 | ||||||
chr3:13414102
|
A | T | 1 | a0002c0002t0001g0206 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.167+5958T>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13414102 | ||||||
chr3:13414268
|
G | A | 5 | a0003c0005t0005g0031a0003c0005t0005g0032a0003c0005t0005g0033others(2): Show | 5 | HG01891.hp1 HG02895.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.167+5792C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13414268 | ||||||
chr3:13414275
|
C | T | 4 | a0002c0002t0001g0160a0002c0002t0001g0161a0002c0002t0001g0162others(1): Show | 4 | HG02145.hp1 HG03041.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.167+5785G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13414275 | ||||||
chr3:13414394
|
G | A | 2 | a0002c0002t0004g0289a0020c0020t0001g0193 | 2 | HG02015.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.167+5666C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13414394 | ||||||
chr3:13414416
|
C | T | 59 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(56): Show | 60 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(57): Show |
intron_variant | MODIFIER | c.167+5644G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13414416 | ||||||
chr3:13414460
|
C | T | 1 | a0001c0035t0002g0075 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.167+5600G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13414460 | ||||||
chr3:13414478
|
C | T | 2 | a0005c0003t0001g0303a0005c0003t0001g0304 | 2 | HG00735.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.167+5582G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13414478 | ||||||
chr3:13414507
|
C | A | 4 | a0001c0001t0002g0072a0001c0001t0002g0143a0001c0001t0002g0144others(1): Show | 4 | NA18954.hp1 NA18981.hp1 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.167+5553G>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13414507 | ||||||
chr3:13414513
|
C | CA | 320 | a0001c0001t0002g0001a0001c0001t0002g0041a0001c0001t0002g0042others(317): Show | 325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.167+5546dupT | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13414513 | ||||||
chr3:13414559
|
C | A | 1 | a0006c0007t0001g0040 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.167+5501G>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13414559 | ||||||
chr3:13414628
|
C | T | 2 | a0003c0011t0001g0035a0003c0011t0001g0036 | 2 | HG02922.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.167+5432G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13414628 | ||||||
chr3:13414642
|
G | A | 1 | a0001c0001t0002g0146 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.167+5418C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13414642 | ||||||
chr3:13414659
|
T | C | 59 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(56): Show | 60 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(57): Show |
intron_variant | MODIFIER | c.167+5401A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13414659 | ||||||
chr3:13414882
|
G | T | 59 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(56): Show | 60 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(57): Show |
intron_variant | MODIFIER | c.167+5178C>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13414882 | ||||||
chr3:13415113
|
A | G | 1 | a0001c0001t0002g0073 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.167+4947T>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13415113 | ||||||
chr3:13415125
|
G | A | 1 | a0006c0007t0001g0040 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.167+4935C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13415125 | ||||||
chr3:13415199
|
G | C | 4 | a0005c0003t0001g0303a0005c0003t0001g0304a0005c0003t0001g0306others(1): Show | 4 | HG00735.hp2 HG02486.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.167+4861C>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13415199 | ||||||
chr3:13415291
|
T | G | 1 | a0002c0002t0001g0204 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.167+4769A>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13415291 | ||||||
chr3:13415303
|
C | T | 59 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(56): Show | 60 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(57): Show |
intron_variant | MODIFIER | c.167+4757G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13415303 | ||||||
chr3:13415321
|
C | A | 1 | a0006c0007t0001g0022 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.167+4739G>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13415321 | ||||||
chr3:13415340
|
C | T | 59 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(56): Show | 60 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(57): Show |
intron_variant | MODIFIER | c.167+4720G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13415340 | ||||||
chr3:13415419
|
C | T | 15 | a0002c0002t0001g0217a0002c0002t0001g0218a0002c0002t0001g0219others(12): Show | 15 | HG00280.hp2 HG00323.hp2 HG00642.hp1 others(12): Show |
intron_variant | MODIFIER | c.167+4641G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13415419 | ||||||
chr3:13415546
|
C | G | 1 | a0009c0030t0005g0009 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.167+4514G>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13415546 | ||||||
chr3:13415820
|
C | T | 1 | a0002c0002t0001g0231 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.167+4240G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13415820 | ||||||
chr3:13415922
|
G | C | 1 | a0001c0001t0002g0147 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.167+4138C>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13415922 | ||||||
chr3:13415962
|
T | C | 122 | a0001c0001t0002g0265a0001c0001t0002g0274a0001c0001t0002g0276others(119): Show | 122 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.167+4098A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13415962 | ||||||
chr3:13416050
|
A | G | 1 | a0024c0038t0002g0321 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.167+4010T>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13416050 | ||||||
chr3:13416064
|
G | A | 2 | a0008c0009t0001g0004a0008c0009t0001g0194 | 3 | HG02615.hp2 HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.167+3996C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13416064 | ||||||
chr3:13416110
|
A | G | 216 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(213): Show | 218 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.167+3950T>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13416110 | ||||||
chr3:13416251
|
G | A | 59 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(56): Show | 60 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(57): Show |
intron_variant | MODIFIER | c.167+3809C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13416251 | ||||||
chr3:13416285
|
CTG | C | 59 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(56): Show | 60 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(57): Show |
intron_variant | MODIFIER | c.167+3773_167+3774d others(4): Show |
NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13416285 | ||||||
chr3:13416411
|
A | G | 1 | a0003c0019t0013g0164 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.167+3649T>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13416411 | ||||||
chr3:13416541
|
A | G | 1 | a0003c0005t0005g0023 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.167+3519T>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13416541 | ||||||
chr3:13416632
|
C | T | 1 | a0001c0001t0002g0041 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.167+3428G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13416632 | ||||||
chr3:13416636
|
T | C | 59 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(56): Show | 60 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(57): Show |
intron_variant | MODIFIER | c.167+3424A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13416636 | ||||||
chr3:13416671
|
A | G | 94 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(91): Show | 96 | HG00140.hp2 HG00544.hp1 HG00639.hp2 others(93): Show |
intron_variant | MODIFIER | c.167+3389T>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13416671 | ||||||
chr3:13416822
|
G | A | 122 | a0001c0001t0002g0265a0001c0001t0002g0274a0001c0001t0002g0276others(119): Show | 122 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.167+3238C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13416822 | ||||||
chr3:13416919
|
A | G | 23 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(20): Show | 23 | HG01243.hp2 HG01346.hp1 HG01978.hp2 others(20): Show |
intron_variant | MODIFIER | c.167+3141T>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13416919 | ||||||
chr3:13416938
|
G | A | 3 | a0001c0001t0002g0148a0003c0011t0001g0035a0003c0011t0001g0036 | 3 | HG02738.hp2 HG02922.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.167+3122C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13416938 | ||||||
chr3:13417083
|
G | A | 2 | a0004c0004t0003g0188a0004c0004t0003g0189 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.167+2977C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13417083 | ||||||
chr3:13417112
|
T | C | 1 | a0002c0002t0001g0230 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.167+2948A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13417112 | ||||||
chr3:13417284
|
A | G | 59 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(56): Show | 60 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(57): Show |
intron_variant | MODIFIER | c.167+2776T>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13417284 | ||||||
chr3:13417422
|
G | A | 1 | a0003c0005t0005g0037 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.167+2638C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13417422 | ||||||
chr3:13417603
|
C | T | 59 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(56): Show | 60 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(57): Show |
intron_variant | MODIFIER | c.167+2457G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13417603 | ||||||
chr3:13417734
|
A | G | 59 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(56): Show | 60 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(57): Show |
intron_variant | MODIFIER | c.167+2326T>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13417734 | ||||||
chr3:13417822
|
T | C | 23 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(20): Show | 23 | HG01243.hp2 HG01346.hp1 HG01978.hp2 others(20): Show |
intron_variant | MODIFIER | c.167+2238A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13417822 | ||||||
chr3:13418357
|
C | T | 33 | a0002c0002t0001g0160a0002c0002t0001g0161a0002c0002t0001g0162others(30): Show | 33 | HG00544.hp1 HG01081.hp1 HG01516.hp2 others(30): Show |
intron_variant | MODIFIER | c.167+1703G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13418357 | ||||||
chr3:13418454
|
A | G | 1 | a0002c0002t0004g0038 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.167+1606T>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13418454 | ||||||
chr3:13418461
|
G | A | 20 | a0005c0003t0001g0215a0005c0003t0001g0216a0005c0003t0001g0291others(17): Show | 20 | HG00140.hp1 HG00642.hp2 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.167+1599C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13418461 | ||||||
chr3:13418519
|
T | C | 59 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(56): Show | 60 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(57): Show |
intron_variant | MODIFIER | c.167+1541A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13418519 | ||||||
chr3:13418524
|
GAGTTCTC others(8): Show |
G | 59 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(56): Show | 60 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(57): Show |
intron_variant | MODIFIER | c.167+1521_167+1535d others(17): Show |
NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13418524 | ||||||
chr3:13418541
|
G | C | 59 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(56): Show | 60 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(57): Show |
intron_variant | MODIFIER | c.167+1519C>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13418541 | ||||||
chr3:13418672
|
C | G | 15 | a0002c0002t0001g0217a0002c0002t0001g0218a0002c0002t0001g0219others(12): Show | 15 | HG00280.hp2 HG00323.hp2 HG00642.hp1 others(12): Show |
intron_variant | MODIFIER | c.167+1388G>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13418672 | ||||||
chr3:13418689
|
G | A | 1 | a0001c0001t0002g0149 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.167+1371C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13418689 | ||||||
chr3:13418948
|
C | CA | 11 | a0001c0001t0002g0150a0001c0001t0002g0151a0001c0001t0002g0152others(8): Show | 11 | HG00558.hp2 HG00597.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.167+1111dupT | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13418948 | ||||||
chr3:13418948
|
CA | C | 9 | a0001c0001t0002g0064a0001c0001t0002g0065a0001c0001t0002g0066others(6): Show | 9 | HG01516.hp1 HG02132.hp1 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.167+1111delT | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13418948 | ||||||
chr3:13418948
|
CAAAAAAA others(4): Show |
C | 3 | a0004c0004t0003g0192a0004c0016t0005g0190a0004c0016t0005g0191 | 3 | HG01081.hp1 HG02622.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.167+1101_167+1111d others(13): Show |
NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13418948 | ||||||
chr3:13418948
|
CAAAAAAA others(5): Show |
C | 43 | a0002c0002t0001g0160a0002c0002t0001g0161a0002c0002t0001g0162others(40): Show | 44 | HG00140.hp2 HG00544.hp1 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.167+1100_167+1111d others(14): Show |
NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13418948 | ||||||
chr3:13418948
|
CAAAAAAA others(6): Show |
C | 2 | a0004c0004t0003g0165a0004c0004t0003g0166 | 2 | NA18962.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.167+1099_167+1111d others(15): Show |
NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13418948 | ||||||
chr3:13418970
|
A | G | 3 | a0001c0001t0002g0063a0001c0001t0002g0159a0003c0019t0013g0164 | 3 | HG03098.hp1 NA19058.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.167+1090T>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13418970 | ||||||
chr3:13418972
|
AAG | A | 29 | a0002c0002t0001g0199a0002c0002t0001g0206a0002c0002t0001g0207others(26): Show | 29 | HG01074.hp2 HG01099.hp2 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.167+1086_167+1087d others(4): Show |
NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13418972 | ||||||
chr3:13418973
|
AG | A | 111 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(108): Show | 111 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(108): Show |
intron_variant | MODIFIER | c.167+1086delC | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13418973 | ||||||
chr3:13418974
|
G | A | 24 | a0002c0002t0001g0050a0002c0002t0001g0204a0002c0002t0001g0308others(21): Show | 24 | HG00099.hp1 HG00642.hp2 HG01361.hp1 others(21): Show |
intron_variant | MODIFIER | c.167+1086C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13418974 | ||||||
chr3:13419001
|
A | C | 1 | a0003c0006t0005g0008 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.167+1059T>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13419001 | ||||||
chr3:13419161
|
AACAGAAA others(5): Show |
A | 2 | a0003c0005t0005g0060a0003c0005t0005g0061 | 2 | HG02280.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.167+887_167+898del others(12): Show |
NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13419161 | ||||||
chr3:13419230
|
C | T | 1 | a0001c0001t0002g0062 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.167+830G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13419230 | ||||||
chr3:13419308
|
C | T | 1 | a0002c0002t0004g0205 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.167+752G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13419308 | ||||||
chr3:13419398
|
C | T | 6 | a0002c0002t0001g0199a0002c0002t0001g0200a0002c0002t0001g0201others(3): Show | 6 | HG01099.hp2 HG02280.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.167+662G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13419398 | ||||||
chr3:13419460
|
G | A | 1 | a0001c0001t0002g0159 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.167+600C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13419460 | ||||||
chr3:13419611
|
T | C | 216 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(213): Show | 218 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.167+449A>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13419611 | ||||||
chr3:13419623
|
C | T | 4 | a0002c0002t0001g0160a0002c0002t0001g0161a0002c0002t0001g0162others(1): Show | 4 | HG02145.hp1 HG03041.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.167+437G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13419623 | ||||||
chr3:13419678
|
T | G | 216 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(213): Show | 218 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.167+382A>C | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13419678 | ||||||
chr3:13419810
|
G | C | 4 | a0001c0001t0009g0195a0001c0001t0009g0196a0001c0001t0009g0198others(1): Show | 4 | HG01884.hp2 HG02258.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.167+250C>G | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13419810 | ||||||
chr3:13419856
|
G | A | 122 | a0001c0001t0002g0265a0001c0001t0002g0274a0001c0001t0002g0276others(119): Show | 122 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.167+204C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13419856 | ||||||
chr3:13419865
|
G | A | 1 | a0002c0002t0004g0320 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.167+195C>T | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13419865 | ||||||
chr3:13419930
|
C | T | 58 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(55): Show | 59 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(56): Show |
intron_variant | MODIFIER | c.167+130G>A | NUP210 | ENSG00000132182.13 | transcript | ENST00000254508.7 | protein_coding | 1/39 | chr3 | 13419930 |