geneid | 79902 |
---|---|
ensemblid | ENSG00000125450.11 |
hgncid | 8734 |
symbol | NUP85 |
name | nucleoporin 85 |
refseq_nuc | NM_024844.5 |
refseq_prot | NP_079120.1 |
ensembl_nuc | ENST00000245544.9 |
ensembl_prot | ENSP00000245544.4 |
mane_status | MANE Select |
chr | chr17 |
start | 75205679 |
end | 75235758 |
strand | + |
ver | v1.2 |
region | chr17:75205679-75235758 |
region5000 | chr17:75200679-75240758 |
regionname0 | NUP85_chr17_75205679_75235758 |
regionname5000 | NUP85_chr17_75200679_75240758 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 656 | 271 | 91 | 61 | 64 | 13 | 40 | 38 | NUP85_chr17_75200679_75240758 | NUP85 | copy fasta | chr17 | 75200679 | 75240758 |
a0002 | 0/0 | 656 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | copy fasta | chr17 | 75200679 | 75240758 |
a0003 | 0/0 | 656 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | copy fasta | chr17 | 75200679 | 75240758 |
a0004 | 0/0 | 656 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | copy fasta | chr17 | 75200679 | 75240758 |
a0005 | 0/0 | 656 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | copy fasta | chr17 | 75200679 | 75240758 |
a0006 | 0/0 | 656 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | copy fasta | chr17 | 75200679 | 75240758 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 1971 | 180 | 62 | 40 | 43 | 8 | 26 | NUP85_chr17_75200679_75240758 | NUP85 | copy fasta | chr17 | 75200679 | 75240758 |
c0002 | 0/0 | 1971 | 45 | 17 | 9 | 11 | 0 | 8 | NUP85_chr17_75200679_75240758 | NUP85 | copy fasta | chr17 | 75200679 | 75240758 |
c0003 | 0/0 | 1971 | 24 | 0 | 6 | 10 | 4 | 4 | NUP85_chr17_75200679_75240758 | NUP85 | copy fasta | chr17 | 75200679 | 75240758 |
c0004 | 1/0 | 1971 | 9 | 8 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | copy fasta | chr17 | 75200679 | 75240758 |
c0005 | 0/0 | 1971 | 8 | 1 | 5 | 0 | 1 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | copy fasta | chr17 | 75200679 | 75240758 |
c0006 | 0/0 | 1971 | 3 | 3 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | copy fasta | chr17 | 75200679 | 75240758 |
c0007 | 0/0 | 1971 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | copy fasta | chr17 | 75200679 | 75240758 |
c0008 | 0/0 | 1971 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | copy fasta | chr17 | 75200679 | 75240758 |
c0009 | 0/0 | 1971 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | copy fasta | chr17 | 75200679 | 75240758 |
c0010 | 0/0 | 1971 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | copy fasta | chr17 | 75200679 | 75240758 |
c0011 | 0/0 | 1971 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | copy fasta | chr17 | 75200679 | 75240758 |
c0012 | 0/0 | 1971 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | copy fasta | chr17 | 75200679 | 75240758 |
c0013 | 0/0 | 1971 | 1 | 0 | 0 | 0 | 1 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | copy fasta | chr17 | 75200679 | 75240758 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 162 | 234 | 83 | 50 | 54 | 9 | 37 | NUP85_chr17_75200679_75240758 | NUP85 | copy fasta | chr17 | 75200679 | 75240758 |
t0002 | 1/0 | 163 | 41 | 9 | 11 | 10 | 5 | 5 | NUP85_chr17_75200679_75240758 | NUP85 | copy fasta | chr17 | 75200679 | 75240758 |
t0003 | 0/0 | 162 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | copy fasta | chr17 | 75200679 | 75240758 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0002 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0005 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0006 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0007 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0008 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0115 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 1971 | 180 | 62 | 40 | 43 | 8 | 26 | NUP85_chr17_75200679_75240758 | NUP85 | copy fasta | chr17 | 75200679 | 75240758 |
a0001c0002 | 0/0 | 1971 | 45 | 17 | 9 | 11 | 0 | 8 | NUP85_chr17_75200679_75240758 | NUP85 | copy fasta | chr17 | 75200679 | 75240758 |
a0001c0003 | 0/0 | 1971 | 24 | 0 | 6 | 10 | 4 | 4 | NUP85_chr17_75200679_75240758 | NUP85 | copy fasta | chr17 | 75200679 | 75240758 |
a0001c0004 | 1/0 | 1971 | 9 | 8 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | copy fasta | chr17 | 75200679 | 75240758 |
a0001c0005 | 0/0 | 1971 | 8 | 1 | 5 | 0 | 1 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | copy fasta | chr17 | 75200679 | 75240758 |
a0001c0006 | 0/0 | 1971 | 3 | 3 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | copy fasta | chr17 | 75200679 | 75240758 |
a0001c0008 | 0/0 | 1971 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | copy fasta | chr17 | 75200679 | 75240758 |
a0001c0010 | 0/0 | 1971 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | copy fasta | chr17 | 75200679 | 75240758 |
a0002c0007 | 0/0 | 1971 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | copy fasta | chr17 | 75200679 | 75240758 |
a0003c0013 | 0/0 | 1971 | 1 | 0 | 0 | 0 | 1 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | copy fasta | chr17 | 75200679 | 75240758 |
a0004c0012 | 0/0 | 1971 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | copy fasta | chr17 | 75200679 | 75240758 |
a0005c0011 | 0/0 | 1971 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | copy fasta | chr17 | 75200679 | 75240758 |
a0006c0009 | 0/0 | 1971 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | copy fasta | chr17 | 75200679 | 75240758 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 2132 | 179 | 62 | 39 | 43 | 8 | 26 | NUP85_chr17_75200679_75240758 | NUP85 | copy fasta | chr17 | 75200679 | 75240758 |
a0001c0001t0003 | 0/0 | 2132 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | copy fasta | chr17 | 75200679 | 75240758 |
a0001c0002t0001 | 0/0 | 2132 | 45 | 17 | 9 | 11 | 0 | 8 | NUP85_chr17_75200679_75240758 | NUP85 | copy fasta | chr17 | 75200679 | 75240758 |
a0001c0003t0002 | 0/0 | 2133 | 24 | 0 | 6 | 10 | 4 | 4 | NUP85_chr17_75200679_75240758 | NUP85 | copy fasta | chr17 | 75200679 | 75240758 |
a0001c0004t0002 | 1/0 | 2133 | 9 | 8 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | copy fasta | chr17 | 75200679 | 75240758 |
a0001c0005t0002 | 0/0 | 2133 | 8 | 1 | 5 | 0 | 1 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | copy fasta | chr17 | 75200679 | 75240758 |
a0001c0006t0001 | 0/0 | 2132 | 3 | 3 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | copy fasta | chr17 | 75200679 | 75240758 |
a0001c0008t0001 | 0/0 | 2132 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | copy fasta | chr17 | 75200679 | 75240758 |
a0001c0010t0001 | 0/0 | 2132 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | copy fasta | chr17 | 75200679 | 75240758 |
a0002c0007t0001 | 0/0 | 2132 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | copy fasta | chr17 | 75200679 | 75240758 |
a0003c0013t0001 | 0/0 | 2132 | 1 | 0 | 0 | 0 | 1 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | copy fasta | chr17 | 75200679 | 75240758 |
a0004c0012t0001 | 0/0 | 2132 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | copy fasta | chr17 | 75200679 | 75240758 |
a0005c0011t0001 | 0/0 | 2132 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | copy fasta | chr17 | 75200679 | 75240758 |
a0006c0009t0001 | 0/0 | 2132 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | copy fasta | chr17 | 75200679 | 75240758 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0002 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0006 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0007 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0115 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0003g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0002t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0002t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0002t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0002t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0002t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0002t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0002t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0002t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0002t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0002t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0002t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0002t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0002t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0002t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0002t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0002t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0002t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0002t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0002t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0002t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0002t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0002t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0002t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0002t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0002t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0002t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0003t0002g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0003t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0003t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0003t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0003t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0003t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0003t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0003t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0003t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0003t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0003t0002g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0003t0002g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0003t0002g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0003t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0003t0002g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0003t0002g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0003t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0003t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0003t0002g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0003t0002g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0003t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0003t0002g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0003t0002g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0003t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0004t0002g0005 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0004t0002g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0004t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0004t0002g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0004t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0004t0002g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0004t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0004t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0005t0002g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0005t0002g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0005t0002g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0005t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0005t0002g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0005t0002g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0005t0002g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0005t0002g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0006t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0006t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0006t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0008t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0010t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0002c0007t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0003c0013t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0004c0012t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0005c0011t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0006c0009t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0005 | t0002 | g0171 | EUR | GBR | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0053 | EUR | GBR | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0075 | EUR | FIN | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0072 | EUR | FIN | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG00544 | hp1 | a0001 | c0003 | t0002 | g0180 | EAS | CHS | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | CHS | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG00597 | hp1 | a0001 | c0003 | t0002 | g0179 | EAS | CHS | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | CHS | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | CHS | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | CHS | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | CHS | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | CHS | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | CHS | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG00733 | hp1 | a0001 | c0002 | t0001 | g0228 | AMR | PUR | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG00735 | hp1 | a0001 | c0005 | t0002 | g0186 | AMR | PUR | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01069 | hp1 | a0001 | c0005 | t0002 | g0208 | AMR | PUR | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01070 | hp1 | a0001 | c0003 | t0002 | g0194 | AMR | PUR | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01070 | hp2 | a0001 | c0002 | t0001 | g0230 | AMR | PUR | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01071 | hp1 | a0001 | c0002 | t0001 | g0232 | AMR | PUR | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01071 | hp2 | a0001 | c0005 | t0002 | g0209 | AMR | PUR | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01074 | hp1 | a0001 | c0005 | t0002 | g0168 | AMR | PUR | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01099 | hp1 | a0001 | c0002 | t0001 | g0229 | AMR | PUR | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01106 | hp1 | a0001 | c0002 | t0001 | g0223 | AMR | PUR | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01109 | hp2 | a0001 | c0008 | t0001 | g0187 | AMR | PUR | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01243 | hp2 | a0001 | c0002 | t0001 | g0210 | AMR | PUR | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01255 | hp2 | a0001 | c0001 | t0003 | g0009 | AMR | CLM | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | CLM | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | CLM | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | CLM | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01257 | hp2 | a0001 | c0003 | t0002 | g0196 | AMR | CLM | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01258 | hp1 | a0001 | c0003 | t0002 | g0197 | AMR | CLM | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | CLM | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | CLM | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | CLM | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01358 | hp1 | a0001 | c0002 | t0001 | g0235 | AMR | CLM | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | CLM | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01361 | hp1 | a0001 | c0005 | t0002 | g0170 | AMR | CLM | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01361 | hp2 | a0006 | c0009 | t0001 | g0032 | AMR | CLM | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01433 | hp1 | a0001 | c0003 | t0002 | g0184 | AMR | CLM | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | CLM | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | CLM | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01496 | hp2 | a0001 | c0003 | t0002 | g0193 | AMR | CLM | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0061 | EUR | IBS | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01515 | hp2 | a0001 | c0003 | t0002 | g0195 | EUR | IBS | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0097 | EUR | IBS | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01516 | hp2 | a0001 | c0003 | t0002 | g0191 | EUR | IBS | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0068 | EUR | IBS | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01517 | hp2 | a0001 | c0003 | t0002 | g0198 | EUR | IBS | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | ACB | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01884 | hp2 | a0001 | c0002 | t0001 | g0224 | AFR | ACB | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01891 | hp1 | a0001 | c0005 | t0002 | g0166 | AFR | ACB | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01891 | hp2 | a0004 | c0012 | t0001 | g0167 | AFR | ACB | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PEL | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01928 | hp2 | a0001 | c0003 | t0002 | g0200 | AMR | PEL | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01943 | hp1 | a0001 | c0002 | t0001 | g0231 | AMR | PEL | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PEL | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01975 | hp1 | a0001 | c0002 | t0001 | g0234 | AMR | PEL | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PEL | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | PEL | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PEL | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | PEL | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PEL | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | KHV | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02015 | hp2 | a0001 | c0003 | t0002 | g0175 | EAS | KHV | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02040 | hp1 | a0001 | c0002 | t0001 | g0225 | EAS | KHV | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | KHV | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | ACB | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02055 | hp2 | a0001 | c0002 | t0001 | g0256 | AFR | ACB | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02071 | hp1 | a0001 | c0002 | t0001 | g0255 | EAS | KHV | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | KHV | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02074 | hp1 | a0001 | c0002 | t0001 | g0243 | EAS | KHV | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02080 | hp1 | a0001 | c0002 | t0001 | g0242 | EAS | KHV | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | KHV | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02129 | hp1 | a0001 | c0003 | t0002 | g0173 | EAS | KHV | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02135 | hp1 | a0001 | c0003 | t0002 | g0185 | EAS | KHV | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | KHV | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PEL | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PEL | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02155 | hp1 | a0001 | c0002 | t0001 | g0236 | EAS | CDX | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | CDX | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | ACB | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | ACB | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | ACB | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | ACB | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02451 | hp1 | a0001 | c0004 | t0002 | g0019 | AFR | ACB | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02572 | hp1 | a0001 | c0004 | t0002 | g0025 | AFR | GWD | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0258 | SAS | PJL | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0062 | SAS | PJL | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | GWD | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | GWD | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | GWD | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02630 | hp1 | a0001 | c0002 | t0001 | g0213 | AFR | GWD | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | GWD | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | GWD | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0085 | SAS | PJL | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0135 | SAS | PJL | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02698 | hp2 | a0001 | c0003 | t0002 | g0172 | SAS | PJL | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | GWD | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02723 | hp1 | a0001 | c0004 | t0002 | g0022 | AFR | GWD | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | PJL | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | GWD | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | GWD | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02886 | hp1 | a0001 | c0002 | t0001 | g0250 | AFR | GWD | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02886 | hp2 | a0001 | c0006 | t0001 | g0189 | AFR | GWD | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | GWD | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02895 | hp2 | a0001 | c0002 | t0001 | g0249 | AFR | GWD | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | GWD | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | GWD | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | ESN | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02922 | hp2 | a0001 | c0004 | t0002 | g0020 | AFR | ESN | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | ESN | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02965 | hp2 | a0001 | c0002 | t0001 | g0219 | AFR | ESN | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | ESN | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02970 | hp2 | a0001 | c0002 | t0001 | g0226 | AFR | ESN | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | ESN | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG03017 | hp2 | a0001 | c0002 | t0001 | g0238 | SAS | PJL | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | GWD | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG03041 | hp2 | a0001 | c0004 | t0002 | g0005 | AFR | GWD | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG03098 | hp1 | a0001 | c0002 | t0001 | g0211 | AFR | MSL | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG03139 | hp1 | a0001 | c0006 | t0001 | g0188 | AFR | ESN | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | ESN | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | ESN | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | MSL | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | MSL | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | MSL | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | MSL | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0257 | SAS | PJL | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0070 | SAS | PJL | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | MSL | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG03453 | hp2 | a0001 | c0002 | t0001 | g0227 | AFR | MSL | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG03486 | hp1 | a0001 | c0006 | t0001 | g0190 | AFR | MSL | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | MSL | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG03491 | hp1 | a0001 | c0002 | t0001 | g0237 | SAS | PJL | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0149 | SAS | PJL | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG03492 | hp1 | a0001 | c0002 | t0001 | g0241 | SAS | PJL | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0054 | SAS | PJL | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG03516 | hp1 | a0001 | c0004 | t0002 | g0024 | AFR | ESN | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG03540 | hp1 | a0001 | c0002 | t0001 | g0239 | AFR | GWD | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG03540 | hp2 | a0001 | c0002 | t0001 | g0233 | AFR | GWD | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG03654 | hp1 | a0001 | c0002 | t0001 | g0247 | SAS | PJL | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0123 | SAS | PJL | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG03710 | hp1 | a0002 | c0007 | t0001 | g0246 | SAS | PJL | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG03710 | hp2 | a0001 | c0005 | t0002 | g0169 | SAS | PJL | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0037 | SAS | BEB | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0096 | SAS | BEB | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG03834 | hp1 | a0005 | c0011 | t0001 | g0064 | SAS | BEB | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | BEB | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG03927 | hp1 | a0001 | c0003 | t0002 | g0182 | SAS | BEB | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0088 | SAS | BEB | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG03942 | hp1 | a0001 | c0002 | t0001 | g0251 | SAS | BEB | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG03942 | hp2 | a0001 | c0010 | t0001 | g0078 | SAS | BEB | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG04115 | hp1 | a0001 | c0002 | t0001 | g0248 | SAS | STU | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0034 | SAS | STU | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG04184 | hp1 | a0001 | c0002 | t0001 | g0252 | SAS | BEB | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0084 | SAS | BEB | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG04199 | hp1 | a0001 | c0002 | t0001 | g0253 | SAS | STU | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0083 | SAS | STU | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0137 | SAS | STU | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG04204 | hp2 | a0001 | c0003 | t0002 | g0199 | SAS | STU | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG04228 | hp1 | a0001 | c0003 | t0002 | g0183 | SAS | STU | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | YRI | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA18522 | hp2 | a0001 | c0002 | t0001 | g0245 | AFR | YRI | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA18906 | hp1 | a0001 | c0002 | t0001 | g0217 | AFR | YRI | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA18906 | hp2 | a0001 | c0004 | t0002 | g0023 | AFR | YRI | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA18945 | hp1 | a0001 | c0002 | t0001 | g0220 | EAS | JPT | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA18946 | hp2 | a0001 | c0002 | t0001 | g0254 | EAS | JPT | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA18947 | hp1 | a0001 | c0002 | t0001 | g0221 | EAS | JPT | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA18967 | hp2 | a0001 | c0002 | t0001 | g0240 | EAS | JPT | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA18982 | hp1 | a0001 | c0003 | t0002 | g0174 | EAS | JPT | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA18989 | hp1 | a0001 | c0003 | t0002 | g0177 | EAS | JPT | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA18990 | hp2 | a0001 | c0003 | t0002 | g0181 | EAS | JPT | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA19002 | hp2 | a0001 | c0002 | t0001 | g0222 | EAS | JPT | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | LWK | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | LWK | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | LWK | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | LWK | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA19064 | hp2 | a0001 | c0002 | t0001 | g0244 | EAS | JPT | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA19068 | hp2 | a0001 | c0003 | t0002 | g0176 | EAS | JPT | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA19090 | hp2 | a0001 | c0003 | t0002 | g0178 | EAS | JPT | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | YRI | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA19240 | hp2 | a0001 | c0002 | t0001 | g0216 | AFR | YRI | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | ASW | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA20129 | hp2 | a0001 | c0002 | t0001 | g0214 | AFR | ASW | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA20752 | hp1 | a0003 | c0013 | t0001 | g0027 | EUR | TSI | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0007 | EUR | TSI | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA20805 | hp2 | a0001 | c0003 | t0002 | g0192 | EUR | TSI | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0071 | SAS | GIH | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0136 | SAS | GIH | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | CLM | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | ACB | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0259 | AFR | ACB | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | ACB | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | ACB | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02559 | hp2 | a0001 | c0002 | t0001 | g0212 | AFR | ACB | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG03471 | hp1 | a0001 | c0002 | t0001 | g0215 | AFR | MSL | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | USA | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | USA | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | USA | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA20300 | hp2 | a0001 | c0004 | t0002 | g0021 | AFR | USA | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | LWK | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | LWK | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0115 | REF | REF | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
homoSapiens_grch38 | hp1 | a0001 | c0004 | t0002 | g0005 | REF | REF | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:75208539
|
G | A | 1 | a0002 | 1 | HG03710.hp1 | missense_variant | MODERATE | c.46G>A | p.Val16Met | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 2/19 | 129/2133 | 46/1971 | 16/656 | chr17 | 75208539 | ||
chr17:75225351
|
A | G | 1 | a0003 | 1 | NA20752.hp1 | missense_variant | MODERATE | c.742A>G | p.Thr248Ala | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 9/19 | 825/2133 | 742/1971 | 248/656 | chr17 | 75225351 | ||
chr17:75225432
|
G | A | 1 | a0006 | 1 | HG01361.hp2 | missense_variant | MODERATE | c.823G>A | p.Ala275Thr | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 9/19 | 906/2133 | 823/1971 | 275/656 | chr17 | 75225432 | ||
chr17:75234684
|
G | A | 1 | a0005 | 1 | HG03834.hp1 | missense_variant | MODERATE | c.1663G>A | p.Asp555Asn | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 17/19 | 1746/2133 | 1663/1971 | 555/656 | chr17 | 75234684 | ||
chr17:75234721
|
G | A | 1 | a0004 | 1 | HG01891.hp2 | missense_variant | MODERATE | c.1700G>A | p.Arg567Gln | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 17/19 | 1783/2133 | 1700/1971 | 567/656 | chr17 | 75234721 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:75209881
|
T | C | 1 | a0001c0003 | 24 | HG00544.hp1 HG00597.hp1 HG01070.hp1 others(21): Show |
synonymous_variant | LOW | c.186T>C | p.Asp62Asp | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 3/19 | 269/2133 | 186/1971 | 62/656 | chr17 | 75209881 | ||
chr17:75225344
|
C | T | 8 | a0001c0001a0001c0003a0001c0005others(5): Show | 217 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(214): Show |
splice_region_variant&synonymous_variant | LOW | c.735C>T | p.Pro245Pro | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 9/19 | 818/2133 | 735/1971 | 245/656 | chr17 | 75225344 | ||
chr17:75231840
|
G | A | 1 | a0001c0010 | 1 | HG03942.hp2 | synonymous_variant | LOW | c.1257G>A | p.Leu419Leu | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 14/19 | 1340/2133 | 1257/1971 | 419/656 | chr17 | 75231840 | ||
chr17:75232942
|
C | T | 1 | a0001c0008 | 1 | HG01109.hp2 | synonymous_variant | LOW | c.1488C>T | p.Ala496Ala | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 15/19 | 1571/2133 | 1488/1971 | 496/656 | chr17 | 75232942 | ||
chr17:75234701
|
T | C | 2 | a0001c0002a0002c0007 | 46 | HG00733.hp1 HG01070.hp2 HG01071.hp1 others(43): Show |
synonymous_variant | LOW | c.1680T>C | p.Leu560Leu | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 17/19 | 1763/2133 | 1680/1971 | 560/656 | chr17 | 75234701 | ||
chr17:75234761
|
C | T | 10 | a0001c0001a0001c0002a0001c0006others(7): Show | 235 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(232): Show |
synonymous_variant | LOW | c.1740C>T | p.Asp580Asp | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 17/19 | 1823/2133 | 1740/1971 | 580/656 | chr17 | 75234761 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:75205738
|
T | C | 1 | a0001c0001t0003 | 1 | HG01255.hp2 | 5_prime_UTR_variant | MODIFIER | c.-24T>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 1/19 | 24 | chr17 | 75205738 | |||||
chr17:75235722
|
AT | A | 11 | a0001c0001t0001a0001c0001t0003a0001c0002t0001others(8): Show | 235 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(232): Show |
3_prime_UTR_variant | MODIFIER | c.*50delT | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 19/19 | 50 | INFO_REALIGN_3_PRIME | chr17 | 75235722 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:75205874
|
T | C | 1 | a0001c0001t0001g0014 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.33+80T>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 1/18 | chr17 | 75205874 | ||||||
chr17:75205897
|
G | C | 1 | a0001c0001t0001g0015 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.33+103G>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 1/18 | chr17 | 75205897 | ||||||
chr17:75205905
|
C | T | 2 | a0001c0001t0001g0258a0001c0001t0001g0259 | 2 | HG02486.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.33+111C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 1/18 | chr17 | 75205905 | ||||||
chr17:75206136
|
G | A | 1 | a0001c0001t0001g0016 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.33+342G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 1/18 | chr17 | 75206136 | ||||||
chr17:75206467
|
A | G | 48 | a0001c0001t0001g0218a0001c0001t0001g0257a0001c0002t0001g0210others(45): Show | 48 | HG00733.hp1 HG01070.hp2 HG01071.hp1 others(45): Show |
intron_variant | MODIFIER | c.33+673A>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 1/18 | chr17 | 75206467 | ||||||
chr17:75206526
|
G | A | 2 | a0001c0001t0001g0017a0001c0001t0001g0018 | 2 | HG02109.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.33+732G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 1/18 | chr17 | 75206526 | ||||||
chr17:75206604
|
G | A | 48 | a0001c0001t0001g0218a0001c0001t0001g0257a0001c0002t0001g0210others(45): Show | 48 | HG00733.hp1 HG01070.hp2 HG01071.hp1 others(45): Show |
intron_variant | MODIFIER | c.33+810G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 1/18 | chr17 | 75206604 | ||||||
chr17:75206851
|
C | T | 252 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(249): Show | 267 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.33+1057C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 1/18 | chr17 | 75206851 | ||||||
chr17:75207105
|
C | G | 2 | a0001c0005t0002g0208a0001c0005t0002g0209 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.33+1311C>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 1/18 | chr17 | 75207105 | ||||||
chr17:75207173
|
A | T | 8 | a0001c0001t0001g0004a0001c0001t0001g0201a0001c0001t0001g0202others(5): Show | 10 | HG02055.hp1 HG02109.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.34-1354A>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 1/18 | chr17 | 75207173 | ||||||
chr17:75207254
|
G | A | 8 | a0001c0002t0001g0210a0001c0002t0001g0211a0001c0002t0001g0212others(5): Show | 8 | HG01243.hp2 HG02559.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.34-1273G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 1/18 | chr17 | 75207254 | ||||||
chr17:75207314
|
G | T | 10 | a0001c0003t0002g0191a0001c0003t0002g0192a0001c0003t0002g0193others(7): Show | 10 | HG01070.hp1 HG01257.hp2 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.34-1213G>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 1/18 | chr17 | 75207314 | ||||||
chr17:75207558
|
C | T | 1 | a0001c0001t0001g0257 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.34-969C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 1/18 | chr17 | 75207558 | ||||||
chr17:75207693
|
T | C | 164 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(161): Show | 178 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(175): Show |
intron_variant | MODIFIER | c.34-834T>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 1/18 | chr17 | 75207693 | ||||||
chr17:75207769
|
C | T | 3 | a0001c0006t0001g0188a0001c0006t0001g0189a0001c0006t0001g0190 | 3 | HG02886.hp2 HG03139.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.34-758C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 1/18 | chr17 | 75207769 | ||||||
chr17:75207934
|
G | C | 1 | a0001c0001t0001g0026 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.34-593G>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 1/18 | chr17 | 75207934 | ||||||
chr17:75207937
|
T | C | 201 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(198): Show | 216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.34-590T>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 1/18 | chr17 | 75207937 | ||||||
chr17:75208042
|
C | T | 164 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(161): Show | 178 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(175): Show |
intron_variant | MODIFIER | c.34-485C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 1/18 | chr17 | 75208042 | ||||||
chr17:75208157
|
C | T | 31 | a0001c0003t0002g0172a0001c0003t0002g0173a0001c0003t0002g0174others(28): Show | 31 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(28): Show |
intron_variant | MODIFIER | c.34-370C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 1/18 | chr17 | 75208157 | ||||||
chr17:75208179
|
T | C | 1 | a0003c0013t0001g0027 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.34-348T>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 1/18 | chr17 | 75208179 | ||||||
chr17:75208280
|
G | GA | 36 | a0001c0001t0001g0013a0001c0001t0001g0028a0001c0001t0001g0029others(33): Show | 37 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(34): Show |
intron_variant | MODIFIER | c.34-231dupA | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr17 | 75208280 | |||||
chr17:75208280
|
GA | G | 64 | a0001c0001t0001g0012a0001c0001t0001g0150a0001c0001t0001g0151others(61): Show | 65 | HG00733.hp1 HG00738.hp2 HG01070.hp2 others(62): Show |
intron_variant | MODIFIER | c.34-231delA | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr17 | 75208280 | |||||
chr17:75208435
|
T | C | 164 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(161): Show | 178 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(175): Show |
intron_variant | MODIFIER | c.34-92T>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 1/18 | chr17 | 75208435 | ||||||
chr17:75208440
|
C | CA | 44 | a0001c0001t0001g0257a0001c0002t0001g0210a0001c0002t0001g0211others(41): Show | 44 | HG00733.hp1 HG01070.hp2 HG01071.hp1 others(41): Show |
intron_variant | MODIFIER | c.34-65dupA | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr17 | 75208440 | |||||
chr17:75208440
|
CA | C | 37 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0031others(34): Show | 40 | HG00738.hp2 HG01261.hp1 HG01361.hp2 others(37): Show |
intron_variant | MODIFIER | c.34-65delA | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr17 | 75208440 | |||||
chr17:75208440
|
CAA | C | 125 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(122): Show | 137 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.34-66_34-65delAA | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr17 | 75208440 | |||||
chr17:75208440
|
CAAA | C | 38 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0142others(35): Show | 38 | HG00544.hp1 HG00597.hp1 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.34-67_34-65delAAA | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr17 | 75208440 | |||||
chr17:75208829
|
A | T | 2 | a0001c0001t0001g0138a0001c0001t0001g0139 | 2 | NA18980.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.127+209A>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 2/18 | chr17 | 75208829 | ||||||
chr17:75208964
|
G | A | 201 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(198): Show | 216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.127+344G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 2/18 | chr17 | 75208964 | ||||||
chr17:75208992
|
C | T | 1 | a0001c0001t0001g0137 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.127+372C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 2/18 | chr17 | 75208992 | ||||||
chr17:75209150
|
A | G | 1 | a0003c0013t0001g0027 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.127+530A>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 2/18 | chr17 | 75209150 | ||||||
chr17:75209270
|
G | A | 1 | a0001c0001t0001g0043 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.128-553G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 2/18 | chr17 | 75209270 | ||||||
chr17:75209445
|
C | CT | 7 | a0001c0002t0001g0252a0001c0002t0001g0253a0001c0004t0002g0025others(4): Show | 7 | HG01109.hp2 HG02572.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.128-359dupT | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr17 | 75209445 | |||||
chr17:75209445
|
CT | C | 11 | a0001c0001t0001g0013a0001c0001t0001g0134a0001c0001t0001g0135others(8): Show | 12 | HG00639.hp1 HG01074.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.128-359delT | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr17 | 75209445 | |||||
chr17:75209445
|
CTT | C | 187 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(184): Show | 201 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.128-360_128-359del others(2): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr17 | 75209445 | |||||
chr17:75209470
|
G | A | 8 | a0001c0001t0001g0014a0001c0001t0001g0031a0001c0001t0001g0044others(5): Show | 8 | HG01069.hp2 HG01074.hp2 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.128-353G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 2/18 | chr17 | 75209470 | ||||||
chr17:75209517
|
C | T | 1 | a0001c0001t0001g0133 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.128-306C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 2/18 | chr17 | 75209517 | ||||||
chr17:75209644
|
A | G | 1 | a0001c0001t0001g0148 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.128-179A>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 2/18 | chr17 | 75209644 | ||||||
chr17:75209782
|
T | C | 1 | a0001c0001t0001g0013 | 2 | HG02622.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.128-41T>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 2/18 | chr17 | 75209782 | ||||||
chr17:75209804
|
T | C | 3 | a0001c0006t0001g0188a0001c0006t0001g0189a0001c0006t0001g0190 | 3 | HG02886.hp2 HG03139.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.128-19T>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 2/18 | chr17 | 75209804 | ||||||
chr17:75210140
|
G | A | 1 | a0006c0009t0001g0032 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.290+155G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 3/18 | chr17 | 75210140 | ||||||
chr17:75210226
|
G | C | 201 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(198): Show | 216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.290+241G>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 3/18 | chr17 | 75210226 | ||||||
chr17:75210368
|
C | G | 1 | a0001c0001t0001g0132 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.290+383C>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 3/18 | chr17 | 75210368 | ||||||
chr17:75210384
|
C | T | 32 | a0001c0003t0002g0172a0001c0003t0002g0173a0001c0003t0002g0174others(29): Show | 32 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.290+399C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 3/18 | chr17 | 75210384 | ||||||
chr17:75210482
|
C | T | 5 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(2): Show | 5 | HG01884.hp1 HG02258.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.290+497C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 3/18 | chr17 | 75210482 | ||||||
chr17:75210683
|
G | A | 201 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(198): Show | 216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.290+698G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 3/18 | chr17 | 75210683 | ||||||
chr17:75210762
|
C | T | 1 | a0001c0001t0001g0131 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.290+777C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 3/18 | chr17 | 75210762 | ||||||
chr17:75210784
|
C | T | 2 | a0001c0001t0001g0011a0001c0001t0001g0130 | 3 | HG02965.hp1 HG03139.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.290+799C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 3/18 | chr17 | 75210784 | ||||||
chr17:75210812
|
C | T | 1 | a0001c0001t0001g0206 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.290+827C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 3/18 | chr17 | 75210812 | ||||||
chr17:75210850
|
T | C | 201 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(198): Show | 216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.290+865T>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 3/18 | chr17 | 75210850 | ||||||
chr17:75210981
|
G | A | 1 | a0001c0001t0001g0028 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.290+996G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 3/18 | chr17 | 75210981 | ||||||
chr17:75211003
|
G | GT | 187 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(184): Show | 202 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.291-972dupT | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr17 | 75211003 | |||||
chr17:75211003
|
G | GTT | 18 | a0001c0001t0001g0016a0001c0001t0001g0047a0001c0001t0001g0116others(15): Show | 18 | HG00639.hp2 HG01175.hp1 HG01175.hp2 others(15): Show |
intron_variant | MODIFIER | c.291-973_291-972dup others(2): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr17 | 75211003 | |||||
chr17:75211055
|
T | G | 1 | a0003c0013t0001g0027 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.291-937T>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 3/18 | chr17 | 75211055 | ||||||
chr17:75211064
|
G | A | 47 | a0001c0001t0001g0257a0001c0002t0001g0210a0001c0002t0001g0211others(44): Show | 47 | HG00733.hp1 HG01070.hp2 HG01071.hp1 others(44): Show |
intron_variant | MODIFIER | c.291-928G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 3/18 | chr17 | 75211064 | ||||||
chr17:75211097
|
G | C | 1 | a0001c0003t0002g0193 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.291-895G>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 3/18 | chr17 | 75211097 | ||||||
chr17:75211112
|
C | T | 47 | a0001c0001t0001g0257a0001c0002t0001g0210a0001c0002t0001g0211others(44): Show | 47 | HG00733.hp1 HG01070.hp2 HG01071.hp1 others(44): Show |
intron_variant | MODIFIER | c.291-880C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 3/18 | chr17 | 75211112 | ||||||
chr17:75211168
|
A | G | 32 | a0001c0003t0002g0172a0001c0003t0002g0173a0001c0003t0002g0174others(29): Show | 32 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.291-824A>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 3/18 | chr17 | 75211168 | ||||||
chr17:75211222
|
T | C | 201 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(198): Show | 216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.291-770T>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 3/18 | chr17 | 75211222 | ||||||
chr17:75211224
|
A | C | 1 | a0001c0001t0001g0046 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.291-768A>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 3/18 | chr17 | 75211224 | ||||||
chr17:75211379
|
A | G | 3 | a0001c0001t0001g0013a0001c0001t0001g0165a0004c0012t0001g0167 | 4 | HG01891.hp2 HG02622.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.291-613A>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 3/18 | chr17 | 75211379 | ||||||
chr17:75211411
|
A | T | 1 | a0001c0003t0002g0184 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.291-581A>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 3/18 | chr17 | 75211411 | ||||||
chr17:75211429
|
CT | C | 199 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(196): Show | 214 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.291-548delT | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr17 | 75211429 | |||||
chr17:75211638
|
C | T | 47 | a0001c0001t0001g0257a0001c0002t0001g0210a0001c0002t0001g0211others(44): Show | 47 | HG00733.hp1 HG01070.hp2 HG01071.hp1 others(44): Show |
intron_variant | MODIFIER | c.291-354C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 3/18 | chr17 | 75211638 | ||||||
chr17:75211675
|
G | A | 1 | a0001c0001t0001g0016 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.291-317G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 3/18 | chr17 | 75211675 | ||||||
chr17:75211705
|
C | T | 204 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(201): Show | 219 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.291-287C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 3/18 | chr17 | 75211705 | ||||||
chr17:75211824
|
G | A | 1 | a0001c0001t0001g0016 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.291-168G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 3/18 | chr17 | 75211824 | ||||||
chr17:75212081
|
T | TGC | 32 | a0001c0001t0001g0206a0001c0003t0002g0172a0001c0003t0002g0173others(29): Show | 32 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.361+25_361+26dupCG | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr17 | 75212081 | |||||
chr17:75212083
|
CGCGCGTG others(5): Show |
C | 9 | a0001c0002t0001g0210a0001c0002t0001g0211a0001c0002t0001g0212others(6): Show | 9 | HG01243.hp2 HG02559.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.361+23_361+34delCG others(10): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr17 | 75212083 | |||||
chr17:75212087
|
C | CGT | 3 | a0001c0004t0002g0022a0001c0004t0002g0023a0001c0004t0002g0024 | 3 | HG02723.hp1 HG03516.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.361+47_361+48dupTG | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr17 | 75212087 | |||||
chr17:75212087
|
C | T | 148 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(145): Show | 161 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.361+25C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 4/18 | chr17 | 75212087 | ||||||
chr17:75212087
|
CGT | C | 38 | a0001c0001t0001g0257a0001c0002t0001g0219a0001c0002t0001g0220others(35): Show | 38 | HG00733.hp1 HG01070.hp2 HG01071.hp1 others(35): Show |
intron_variant | MODIFIER | c.361+47_361+48delTG | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr17 | 75212087 | |||||
chr17:75212087
|
CGTGTGTG others(3): Show |
C | 1 | a0001c0008t0001g0187 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.361+39_361+48delTG others(8): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr17 | 75212087 | |||||
chr17:75212089
|
T | C | 8 | a0001c0001t0001g0206a0001c0005t0002g0168a0001c0005t0002g0169others(5): Show | 8 | HG00140.hp1 HG00735.hp1 HG01069.hp1 others(5): Show |
intron_variant | MODIFIER | c.361+27T>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 4/18 | chr17 | 75212089 | ||||||
chr17:75212091
|
T | C | 38 | a0001c0001t0001g0257a0001c0002t0001g0219a0001c0002t0001g0220others(35): Show | 38 | HG00733.hp1 HG01070.hp2 HG01071.hp1 others(35): Show |
intron_variant | MODIFIER | c.361+29T>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 4/18 | chr17 | 75212091 | ||||||
chr17:75212093
|
T | C | 3 | a0001c0002t0001g0220a0001c0002t0001g0221a0001c0002t0001g0222 | 3 | NA18945.hp1 NA18947.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.361+31T>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 4/18 | chr17 | 75212093 | ||||||
chr17:75212110
|
G | GTGTGTGT others(7): Show |
1 | a0001c0001t0001g0218 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.361+48_361+49insTG others(12): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 4/18 | chr17 | 75212110 | ||||||
chr17:75212110
|
G | GTGTGTT | 31 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0031others(28): Show | 32 | HG00140.hp2 HG00621.hp2 HG00673.hp2 others(29): Show |
intron_variant | MODIFIER | c.361+48_361+49insTG others(4): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 4/18 | chr17 | 75212110 | ||||||
chr17:75212110
|
G | GTGTT | 120 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(117): Show | 132 | HG00280.hp1 HG00280.hp2 HG00544.hp2 others(129): Show |
intron_variant | MODIFIER | c.361+48_361+49insTG others(2): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 4/18 | chr17 | 75212110 | ||||||
chr17:75212110
|
G | GTT | 13 | a0001c0001t0001g0004a0001c0001t0001g0145a0001c0001t0001g0146others(10): Show | 15 | HG00639.hp1 HG02055.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.361+48_361+49insTT | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 4/18 | chr17 | 75212110 | ||||||
chr17:75212110
|
G | T | 35 | a0001c0001t0001g0048a0001c0001t0001g0115a0001c0001t0001g0206others(32): Show | 35 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(32): Show |
intron_variant | MODIFIER | c.361+48G>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 4/18 | chr17 | 75212110 | ||||||
chr17:75212187
|
T | C | 1 | a0001c0001t0001g0059 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.361+125T>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 4/18 | chr17 | 75212187 | ||||||
chr17:75212228
|
GGTTTTTT others(23): Show |
G | 1 | a0001c0001t0001g0018 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.361+167_361+196del others(30): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 4/18 | chr17 | 75212228 | ||||||
chr17:75212228
|
GGTTTTTT others(24): Show |
G | 10 | a0001c0001t0001g0017a0001c0001t0001g0114a0001c0001t0001g0139others(7): Show | 10 | HG00140.hp1 HG01928.hp2 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.361+167_361+197del others(31): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 4/18 | chr17 | 75212228 | ||||||
chr17:75212228
|
GGTTTTTT others(25): Show |
G | 64 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(61): Show | 67 | HG00544.hp1 HG00597.hp1 HG00597.hp2 others(64): Show |
intron_variant | MODIFIER | c.361+167_361+198del others(32): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 4/18 | chr17 | 75212228 | ||||||
chr17:75212228
|
GGTTTTTT others(26): Show |
G | 122 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(119): Show | 134 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.361+167_361+199del others(33): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 4/18 | chr17 | 75212228 | ||||||
chr17:75212228
|
GGTTTTTT others(27): Show |
G | 2 | a0001c0001t0001g0061a0001c0001t0001g0141 | 2 | HG01256.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.361+167_361+200del others(34): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 4/18 | chr17 | 75212228 | ||||||
chr17:75212228
|
GGTTTTTT others(39): Show |
G | 1 | a0001c0003t0002g0194 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.361+167_361+212del others(46): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 4/18 | chr17 | 75212228 | ||||||
chr17:75212228
|
GGTTTTTT others(41): Show |
G | 1 | a0001c0001t0001g0060 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.361+167_361+214del others(48): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 4/18 | chr17 | 75212228 | ||||||
chr17:75212247
|
G | GTTGTTGT | 5 | a0001c0002t0001g0228a0001c0002t0001g0229a0001c0002t0001g0230others(2): Show | 5 | HG00733.hp1 HG01070.hp2 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.361+187_361+188ins others(7): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr17 | 75212247 | |||||
chr17:75212247
|
G | GTTGTTGT others(1): Show |
9 | a0001c0001t0001g0257a0001c0002t0001g0219a0001c0002t0001g0222others(6): Show | 9 | HG01358.hp1 HG01975.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.361+187_361+188ins others(8): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr17 | 75212247 | |||||
chr17:75212247
|
G | GTTGTTGT others(3): Show |
2 | a0001c0002t0001g0223a0001c0002t0001g0224 | 2 | HG01106.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.361+187_361+188ins others(10): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr17 | 75212247 | |||||
chr17:75212247
|
G | GTTGTTGT others(4): Show |
1 | a0001c0002t0001g0225 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.361+187_361+188ins others(11): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr17 | 75212247 | |||||
chr17:75212247
|
G | GTTGTTGT others(2): Show |
9 | a0001c0002t0001g0210a0001c0002t0001g0239a0001c0002t0001g0240others(6): Show | 9 | HG01243.hp2 HG02071.hp1 HG02074.hp1 others(6): Show |
intron_variant | MODIFIER | c.361+187_361+188ins others(9): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr17 | 75212247 | |||||
chr17:75212247
|
G | GTTGTTGT others(3): Show |
5 | a0001c0002t0001g0211a0001c0002t0001g0212a0001c0002t0001g0213others(2): Show | 5 | HG02559.hp2 HG02630.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.361+187_361+188ins others(10): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr17 | 75212247 | |||||
chr17:75212247
|
G | GTTGTTGT others(4): Show |
3 | a0001c0002t0001g0214a0001c0002t0001g0215a0001c0002t0001g0245 | 3 | HG03471.hp1 NA18522.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.361+187_361+188ins others(11): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr17 | 75212247 | |||||
chr17:75212247
|
G | GTTGTTGT others(5): Show |
1 | a0001c0002t0001g0216 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.361+187_361+188ins others(12): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr17 | 75212247 | |||||
chr17:75212247
|
G | GTTGTTGT others(7): Show |
1 | a0002c0007t0001g0246 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.361+187_361+188ins others(14): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr17 | 75212247 | |||||
chr17:75212247
|
G | GTTGTTGT others(9): Show |
2 | a0001c0002t0001g0217a0001c0002t0001g0256 | 2 | HG02055.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.361+187_361+188ins others(16): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr17 | 75212247 | |||||
chr17:75212247
|
G | GTTGTTGT others(10): Show |
1 | a0001c0002t0001g0247 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.361+187_361+188ins others(17): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr17 | 75212247 | |||||
chr17:75212247
|
GTTTTTTT others(7): Show |
G | 2 | a0001c0002t0001g0226a0001c0002t0001g0227 | 2 | HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.361+211_361+224del others(14): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr17 | 75212247 | |||||
chr17:75212247
|
GTTTTTTT others(8): Show |
G | 2 | a0001c0002t0001g0220a0001c0002t0001g0221 | 2 | NA18945.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.361+210_361+224del others(15): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr17 | 75212247 | |||||
chr17:75212247
|
GTTTTTTT others(10): Show |
G | 3 | a0001c0006t0001g0188a0001c0006t0001g0189a0001c0006t0001g0190 | 3 | HG02886.hp2 HG03139.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.361+208_361+224del others(17): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr17 | 75212247 | |||||
chr17:75212250
|
T | G | 1 | a0001c0002t0001g0248 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.361+188T>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 4/18 | chr17 | 75212250 | ||||||
chr17:75212251
|
T | G | 2 | a0001c0002t0001g0250a0001c0002t0001g0253 | 2 | HG02886.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.361+189T>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 4/18 | chr17 | 75212251 | ||||||
chr17:75212254
|
T | G | 1 | a0001c0002t0001g0250 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.361+192T>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 4/18 | chr17 | 75212254 | ||||||
chr17:75212256
|
T | TG | 7 | a0001c0004t0002g0019a0001c0004t0002g0020a0001c0004t0002g0021others(4): Show | 7 | HG01109.hp2 HG02451.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.361+194_361+195ins others(1): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 4/18 | chr17 | 75212256 | ||||||
chr17:75212264
|
T | G | 2 | a0001c0002t0001g0226a0001c0002t0001g0227 | 2 | HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.361+202T>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 4/18 | chr17 | 75212264 | ||||||
chr17:75212265
|
T | G | 5 | a0001c0001t0001g0013a0001c0001t0001g0165a0001c0002t0001g0220others(2): Show | 6 | HG01891.hp2 HG02622.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.361+203T>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 4/18 | chr17 | 75212265 | ||||||
chr17:75212267
|
T | G | 2 | a0001c0002t0001g0226a0001c0002t0001g0227 | 2 | HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.361+205T>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 4/18 | chr17 | 75212267 | ||||||
chr17:75212268
|
T | G | 2 | a0001c0002t0001g0220a0001c0002t0001g0221 | 2 | NA18945.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.361+206T>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 4/18 | chr17 | 75212268 | ||||||
chr17:75212270
|
T | G | 1 | a0001c0001t0001g0206 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.361+208T>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 4/18 | chr17 | 75212270 | ||||||
chr17:75212307
|
C | T | 4 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(1): Show | 4 | HG00639.hp1 HG02809.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.361+245C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 4/18 | chr17 | 75212307 | ||||||
chr17:75212406
|
C | T | 137 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(134): Show | 148 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.361+344C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 4/18 | chr17 | 75212406 | ||||||
chr17:75212469
|
GTT | G | 45 | a0001c0001t0001g0257a0001c0002t0001g0210a0001c0002t0001g0211others(42): Show | 45 | HG00733.hp1 HG01070.hp2 HG01071.hp1 others(42): Show |
intron_variant | MODIFIER | c.361+433_361+434del others(2): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr17 | 75212469 | |||||
chr17:75212469
|
GTTTTT | G | 57 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0016others(54): Show | 59 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.361+430_361+434del others(5): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr17 | 75212469 | |||||
chr17:75212469
|
GTTTTTT | G | 133 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(130): Show | 144 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.361+429_361+434del others(6): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr17 | 75212469 | |||||
chr17:75212469
|
GTTTTTTT | G | 7 | a0001c0001t0001g0004a0001c0001t0001g0201a0001c0001t0001g0202others(4): Show | 9 | HG02055.hp1 HG02109.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.361+428_361+434del others(7): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr17 | 75212469 | |||||
chr17:75212476
|
T | G | 3 | a0001c0003t0002g0185a0001c0003t0002g0192a0001c0005t0002g0166 | 3 | HG01891.hp1 HG02135.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.361+414T>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 4/18 | chr17 | 75212476 | ||||||
chr17:75212477
|
T | G | 29 | a0001c0003t0002g0172a0001c0003t0002g0173a0001c0003t0002g0174others(26): Show | 29 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(26): Show |
intron_variant | MODIFIER | c.361+415T>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 4/18 | chr17 | 75212477 | ||||||
chr17:75212562
|
G | A | 8 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(5): Show | 8 | HG00621.hp2 HG00673.hp2 HG02602.hp2 others(5): Show |
intron_variant | MODIFIER | c.361+500G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 4/18 | chr17 | 75212562 | ||||||
chr17:75212629
|
T | C | 1 | a0001c0001t0001g0148 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.362-447T>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 4/18 | chr17 | 75212629 | ||||||
chr17:75212677
|
T | C | 1 | a0001c0001t0001g0053 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.362-399T>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 4/18 | chr17 | 75212677 | ||||||
chr17:75213030
|
G | A | 1 | a0001c0002t0001g0239 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.362-46G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 4/18 | chr17 | 75213030 | ||||||
chr17:75213125
|
G | T | 1 | a0001c0001t0001g0016 | 1 | HG01255.hp1 | splice_region_variant&intron_variant | LOW | c.405+6G>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 5/18 | chr17 | 75213125 | ||||||
chr17:75213270
|
C | T | 1 | a0001c0001t0001g0126 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.405+151C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 5/18 | chr17 | 75213270 | ||||||
chr17:75213375
|
G | A | 1 | a0001c0001t0001g0097 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.405+256G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 5/18 | chr17 | 75213375 | ||||||
chr17:75213559
|
G | A | 1 | a0001c0001t0001g0095 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.405+440G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 5/18 | chr17 | 75213559 | ||||||
chr17:75213649
|
G | A | 1 | a0001c0001t0001g0218 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.405+530G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 5/18 | chr17 | 75213649 | ||||||
chr17:75213725
|
A | AT | 48 | a0001c0001t0001g0132a0001c0001t0001g0257a0001c0002t0001g0210others(45): Show | 48 | HG00733.hp1 HG01070.hp2 HG01071.hp1 others(45): Show |
intron_variant | MODIFIER | c.405+616dupT | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr17 | 75213725 | |||||
chr17:75213862
|
G | GT | 6 | a0001c0002t0001g0243a0001c0002t0001g0248a0001c0002t0001g0251others(3): Show | 6 | HG02074.hp1 HG02572.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.405+770dupT | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr17 | 75213862 | |||||
chr17:75213862
|
GT | G | 40 | a0001c0001t0001g0034a0001c0001t0001g0098a0001c0001t0001g0259others(37): Show | 40 | HG00597.hp1 HG00733.hp1 HG01070.hp2 others(37): Show |
intron_variant | MODIFIER | c.405+770delT | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr17 | 75213862 | |||||
chr17:75213862
|
GTT | G | 190 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(187): Show | 205 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.405+769_405+770del others(2): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr17 | 75213862 | |||||
chr17:75213863
|
T | G | 1 | a0001c0003t0002g0180 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.405+744T>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 5/18 | chr17 | 75213863 | ||||||
chr17:75213864
|
T | G | 7 | a0001c0003t0002g0179a0001c0003t0002g0182a0001c0003t0002g0183others(4): Show | 7 | HG00597.hp1 HG01074.hp1 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.405+745T>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 5/18 | chr17 | 75213864 | ||||||
chr17:75213865
|
T | G | 24 | a0001c0003t0002g0172a0001c0003t0002g0173a0001c0003t0002g0174others(21): Show | 24 | HG00140.hp1 HG00735.hp1 HG01069.hp1 others(21): Show |
intron_variant | MODIFIER | c.405+746T>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 5/18 | chr17 | 75213865 | ||||||
chr17:75213870
|
T | G | 1 | a0001c0002t0001g0240 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.405+751T>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 5/18 | chr17 | 75213870 | ||||||
chr17:75213873
|
T | G | 1 | a0001c0001t0001g0098 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.405+754T>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 5/18 | chr17 | 75213873 | ||||||
chr17:75213874
|
T | G | 14 | a0001c0001t0001g0012a0001c0001t0001g0150a0001c0001t0001g0151others(11): Show | 15 | HG00738.hp2 HG02258.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.405+755T>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 5/18 | chr17 | 75213874 | ||||||
chr17:75213877
|
T | G | 2 | a0001c0001t0001g0034a0001c0001t0001g0098 | 2 | HG04115.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.405+758T>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 5/18 | chr17 | 75213877 | ||||||
chr17:75213878
|
T | G | 167 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(164): Show | 182 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(179): Show |
intron_variant | MODIFIER | c.405+759T>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 5/18 | chr17 | 75213878 | ||||||
chr17:75213883
|
T | G | 6 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0117others(3): Show | 8 | HG01081.hp1 HG02451.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.405+764T>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 5/18 | chr17 | 75213883 | ||||||
chr17:75213902
|
C | T | 32 | a0001c0003t0002g0172a0001c0003t0002g0173a0001c0003t0002g0174others(29): Show | 32 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.405+783C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 5/18 | chr17 | 75213902 | ||||||
chr17:75213903
|
T | G | 201 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(198): Show | 216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.405+784T>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 5/18 | chr17 | 75213903 | ||||||
chr17:75214046
|
G | A | 14 | a0001c0001t0001g0012a0001c0001t0001g0150a0001c0001t0001g0151others(11): Show | 15 | HG00738.hp2 HG02258.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.405+927G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 5/18 | chr17 | 75214046 | ||||||
chr17:75214080
|
G | A | 2 | a0001c0002t0001g0228a0001c0002t0001g0251 | 2 | HG00733.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.405+961G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 5/18 | chr17 | 75214080 | ||||||
chr17:75214245
|
C | T | 1 | a0001c0001t0001g0164 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.405+1126C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 5/18 | chr17 | 75214245 | ||||||
chr17:75214393
|
G | A | 2 | a0001c0001t0001g0013a0001c0001t0001g0165 | 3 | HG02622.hp1 HG02630.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.405+1274G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 5/18 | chr17 | 75214393 | ||||||
chr17:75214482
|
C | T | 1 | a0001c0001t0001g0094 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.406-1272C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 5/18 | chr17 | 75214482 | ||||||
chr17:75214610
|
G | A | 4 | a0001c0001t0001g0013a0001c0001t0001g0165a0001c0001t0001g0218others(1): Show | 5 | HG01891.hp2 HG02622.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.406-1144G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 5/18 | chr17 | 75214610 | ||||||
chr17:75214856
|
CAAAA | C | 169 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(166): Show | 184 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(181): Show |
intron_variant | MODIFIER | c.406-890_406-887del others(4): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr17 | 75214856 | |||||
chr17:75214866
|
A | C | 3 | a0001c0006t0001g0188a0001c0006t0001g0189a0001c0006t0001g0190 | 3 | HG02886.hp2 HG03139.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.406-888A>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 5/18 | chr17 | 75214866 | ||||||
chr17:75214948
|
T | G | 251 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(248): Show | 266 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.406-806T>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 5/18 | chr17 | 75214948 | ||||||
chr17:75215062
|
T | G | 2 | a0001c0001t0001g0145a0001c0001t0001g0148 | 2 | HG02809.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.406-692T>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 5/18 | chr17 | 75215062 | ||||||
chr17:75215225
|
T | A | 1 | a0001c0001t0001g0014 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.406-529T>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 5/18 | chr17 | 75215225 | ||||||
chr17:75215324
|
C | G | 2 | a0001c0001t0001g0093a0001c0001t0001g0144 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.406-430C>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 5/18 | chr17 | 75215324 | ||||||
chr17:75215451
|
C | T | 16 | a0001c0002t0001g0220a0001c0002t0001g0221a0001c0002t0001g0222others(13): Show | 16 | HG00733.hp1 HG01070.hp2 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.406-303C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 5/18 | chr17 | 75215451 | ||||||
chr17:75215489
|
A | C | 201 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(198): Show | 216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.406-265A>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 5/18 | chr17 | 75215489 | ||||||
chr17:75215490
|
A | G | 201 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(198): Show | 216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.406-264A>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 5/18 | chr17 | 75215490 | ||||||
chr17:75215530
|
A | G | 1 | a0001c0001t0001g0043 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.406-224A>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 5/18 | chr17 | 75215530 | ||||||
chr17:75215547
|
A | G | 169 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(166): Show | 184 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(181): Show |
intron_variant | MODIFIER | c.406-207A>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 5/18 | chr17 | 75215547 | ||||||
chr17:75215576
|
A | G | 1 | a0001c0002t0001g0239 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.406-178A>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 5/18 | chr17 | 75215576 | ||||||
chr17:75215651
|
A | C | 1 | a0001c0001t0001g0218 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.406-103A>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 5/18 | chr17 | 75215651 | ||||||
chr17:75215673
|
C | G | 1 | a0001c0001t0001g0206 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.406-81C>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 5/18 | chr17 | 75215673 | ||||||
chr17:75215855
|
A | C | 1 | a0001c0002t0001g0239 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.475+32A>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 6/18 | chr17 | 75215855 | ||||||
chr17:75216269
|
C | CT | 5 | a0001c0001t0001g0031a0001c0001t0001g0134a0001c0006t0001g0188others(2): Show | 5 | HG01074.hp2 HG01261.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.475+459dupT | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr17 | 75216269 | |||||
chr17:75216329
|
G | A | 47 | a0001c0001t0001g0257a0001c0002t0001g0210a0001c0002t0001g0211others(44): Show | 47 | HG00733.hp1 HG01070.hp2 HG01071.hp1 others(44): Show |
intron_variant | MODIFIER | c.475+506G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 6/18 | chr17 | 75216329 | ||||||
chr17:75216332
|
C | G | 1 | a0001c0002t0001g0236 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.475+509C>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 6/18 | chr17 | 75216332 | ||||||
chr17:75216342
|
C | T | 32 | a0001c0003t0002g0172a0001c0003t0002g0173a0001c0003t0002g0174others(29): Show | 32 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.475+519C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 6/18 | chr17 | 75216342 | ||||||
chr17:75216354
|
C | T | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 149 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.475+531C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 6/18 | chr17 | 75216354 | ||||||
chr17:75216384
|
A | G | 204 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(201): Show | 219 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.475+561A>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 6/18 | chr17 | 75216384 | ||||||
chr17:75216395
|
A | G | 47 | a0001c0001t0001g0257a0001c0002t0001g0210a0001c0002t0001g0211others(44): Show | 47 | HG00733.hp1 HG01070.hp2 HG01071.hp1 others(44): Show |
intron_variant | MODIFIER | c.475+572A>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 6/18 | chr17 | 75216395 | ||||||
chr17:75216558
|
C | T | 2 | a0001c0001t0001g0017a0001c0001t0001g0018 | 2 | HG02109.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.475+735C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 6/18 | chr17 | 75216558 | ||||||
chr17:75217033
|
G | A | 1 | a0001c0001t0001g0063 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.476-1152G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 6/18 | chr17 | 75217033 | ||||||
chr17:75217123
|
C | T | 3 | a0001c0001t0001g0013a0001c0001t0001g0165a0004c0012t0001g0167 | 4 | HG01891.hp2 HG02622.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.476-1062C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 6/18 | chr17 | 75217123 | ||||||
chr17:75217373
|
A | AT | 15 | a0001c0001t0001g0012a0001c0001t0001g0150a0001c0001t0001g0151others(12): Show | 16 | HG00738.hp2 HG02258.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.476-803dupT | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr17 | 75217373 | |||||
chr17:75217373
|
A | ATT | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 149 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.476-804_476-803dup others(2): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr17 | 75217373 | |||||
chr17:75217377
|
T | TTA | 11 | a0001c0001t0001g0004a0001c0001t0001g0145a0001c0001t0001g0146others(8): Show | 13 | HG00639.hp1 HG02055.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.476-807_476-806ins others(2): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr17 | 75217377 | |||||
chr17:75217604
|
G | A | 1 | a0001c0001t0001g0113 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.476-581G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 6/18 | chr17 | 75217604 | ||||||
chr17:75217790
|
C | G | 1 | a0001c0005t0002g0170 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.476-395C>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 6/18 | chr17 | 75217790 | ||||||
chr17:75217924
|
T | C | 1 | a0001c0001t0001g0206 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.476-261T>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 6/18 | chr17 | 75217924 | ||||||
chr17:75218050
|
A | G | 1 | a0001c0005t0002g0186 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.476-135A>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 6/18 | chr17 | 75218050 | ||||||
chr17:75218173
|
C | G | 1 | a0002c0007t0001g0246 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.476-12C>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 6/18 | chr17 | 75218173 | ||||||
chr17:75218588
|
G | GTT | 30 | a0001c0002t0001g0210a0001c0002t0001g0212a0001c0002t0001g0214others(27): Show | 30 | HG00733.hp1 HG01070.hp2 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.597+300_597+301dup others(2): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr17 | 75218588 | |||||
chr17:75218588
|
G | GTTT | 20 | a0001c0001t0001g0016a0001c0001t0001g0206a0001c0002t0001g0211others(17): Show | 20 | HG01106.hp1 HG01255.hp1 HG01358.hp1 others(17): Show |
intron_variant | MODIFIER | c.597+299_597+301dup others(3): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr17 | 75218588 | |||||
chr17:75218588
|
G | GTTTT | 31 | a0001c0001t0001g0034a0001c0001t0001g0099a0001c0001t0001g0118others(28): Show | 31 | HG00140.hp1 HG00544.hp1 HG00639.hp2 others(28): Show |
intron_variant | MODIFIER | c.597+298_597+301dup others(4): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr17 | 75218588 | |||||
chr17:75218588
|
G | GTTTTT | 100 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(97): Show | 106 | HG00280.hp1 HG00280.hp2 HG00597.hp1 others(103): Show |
intron_variant | MODIFIER | c.597+297_597+301dup others(5): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr17 | 75218588 | |||||
chr17:75218588
|
G | GTTTTTT | 64 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(61): Show | 73 | HG00140.hp2 HG00544.hp2 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.597+296_597+301dup others(6): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr17 | 75218588 | |||||
chr17:75218588
|
G | GTTTTTTT | 6 | a0001c0001t0001g0017a0001c0001t0001g0035a0001c0001t0001g0055others(3): Show | 6 | HG01123.hp1 HG02055.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.597+295_597+301dup others(7): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr17 | 75218588 | |||||
chr17:75218839
|
C | T | 1 | a0001c0001t0001g0014 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.597+533C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75218839 | ||||||
chr17:75218911
|
G | C | 202 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(199): Show | 217 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.597+605G>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75218911 | ||||||
chr17:75218977
|
C | T | 32 | a0001c0003t0002g0172a0001c0003t0002g0173a0001c0003t0002g0174others(29): Show | 32 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.597+671C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75218977 | ||||||
chr17:75218978
|
A | G | 202 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(199): Show | 217 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.597+672A>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75218978 | ||||||
chr17:75219045
|
G | A | 6 | a0001c0001t0001g0009a0001c0001t0001g0063a0001c0001t0001g0093others(3): Show | 6 | HG00741.hp1 HG01123.hp2 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.597+739G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75219045 | ||||||
chr17:75219143
|
A | G | 1 | a0001c0001t0001g0090 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.597+837A>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75219143 | ||||||
chr17:75219173
|
G | A | 32 | a0001c0003t0002g0172a0001c0003t0002g0173a0001c0003t0002g0174others(29): Show | 32 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.597+867G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75219173 | ||||||
chr17:75219241
|
G | A | 1 | a0005c0011t0001g0064 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.597+935G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75219241 | ||||||
chr17:75219318
|
C | A | 1 | a0001c0001t0001g0043 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.597+1012C>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75219318 | ||||||
chr17:75219324
|
G | A | 1 | a0001c0001t0001g0016 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.597+1018G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75219324 | ||||||
chr17:75219511
|
C | G | 14 | a0001c0001t0001g0012a0001c0001t0001g0150a0001c0001t0001g0151others(11): Show | 15 | HG00738.hp2 HG02258.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.597+1205C>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75219511 | ||||||
chr17:75219655
|
C | T | 5 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(2): Show | 5 | HG01884.hp1 HG02258.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.597+1349C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75219655 | ||||||
chr17:75219896
|
T | C | 2 | a0001c0001t0001g0100a0001c0001t0001g0105 | 2 | HG01993.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.597+1590T>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75219896 | ||||||
chr17:75220210
|
T | C | 1 | a0001c0001t0001g0065 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.597+1904T>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75220210 | ||||||
chr17:75220261
|
ACTACAGG others(10): Show |
A | 32 | a0001c0003t0002g0172a0001c0003t0002g0173a0001c0003t0002g0174others(29): Show | 32 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.597+1957_597+1973d others(19): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr17 | 75220261 | |||||
chr17:75220270
|
G | A | 1 | a0001c0006t0001g0190 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.597+1964G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75220270 | ||||||
chr17:75220290
|
A | C | 1 | a0001c0001t0001g0161 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.597+1984A>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75220290 | ||||||
chr17:75220422
|
C | CT | 13 | a0001c0001t0001g0035a0001c0001t0001g0052a0001c0001t0001g0056others(10): Show | 13 | HG00597.hp2 HG00673.hp2 HG01358.hp2 others(10): Show |
intron_variant | MODIFIER | c.597+2131dupT | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr17 | 75220422 | |||||
chr17:75220437
|
T | A | 2 | a0001c0001t0001g0016a0001c0001t0001g0106 | 2 | HG00673.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.597+2131T>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75220437 | ||||||
chr17:75220484
|
G | C | 203 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(200): Show | 218 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.597+2178G>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75220484 | ||||||
chr17:75220734
|
G | A | 3 | a0001c0001t0001g0013a0001c0001t0001g0165a0004c0012t0001g0167 | 4 | HG01891.hp2 HG02622.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.597+2428G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75220734 | ||||||
chr17:75220752
|
TTTTTG | T | 4 | a0001c0001t0001g0006a0001c0001t0001g0089a0001c0001t0001g0258others(1): Show | 5 | HG01081.hp1 HG01081.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.597+2466_597+2470d others(7): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr17 | 75220752 | |||||
chr17:75220878
|
A | AT | 116 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(113): Show | 127 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.597+2594dupT | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr17 | 75220878 | |||||
chr17:75220893
|
T | C | 1 | a0001c0001t0001g0031 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.597+2587T>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75220893 | ||||||
chr17:75220918
|
A | G | 1 | a0004c0012t0001g0167 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.597+2612A>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75220918 | ||||||
chr17:75220944
|
C | T | 1 | a0001c0002t0001g0250 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.597+2638C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75220944 | ||||||
chr17:75220955
|
C | T | 7 | a0001c0001t0001g0004a0001c0001t0001g0201a0001c0001t0001g0202others(4): Show | 9 | HG02055.hp1 HG02109.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.597+2649C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75220955 | ||||||
chr17:75220968
|
G | A | 202 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(199): Show | 217 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.597+2662G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75220968 | ||||||
chr17:75221039
|
G | A | 46 | a0001c0002t0001g0210a0001c0002t0001g0211a0001c0002t0001g0212others(43): Show | 46 | HG00733.hp1 HG01070.hp2 HG01071.hp1 others(43): Show |
intron_variant | MODIFIER | c.597+2733G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75221039 | ||||||
chr17:75221054
|
T | A | 3 | a0001c0001t0001g0013a0001c0001t0001g0165a0004c0012t0001g0167 | 4 | HG01891.hp2 HG02622.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.597+2748T>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75221054 | ||||||
chr17:75221102
|
C | G | 2 | a0001c0001t0001g0014a0001c0001t0001g0046 | 2 | HG02818.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.597+2796C>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75221102 | ||||||
chr17:75221166
|
C | T | 3 | a0001c0006t0001g0188a0001c0006t0001g0189a0001c0006t0001g0190 | 3 | HG02886.hp2 HG03139.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.597+2860C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75221166 | ||||||
chr17:75221171
|
C | T | 2 | a0001c0005t0002g0208a0001c0005t0002g0209 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.597+2865C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75221171 | ||||||
chr17:75221176
|
G | A | 46 | a0001c0002t0001g0210a0001c0002t0001g0211a0001c0002t0001g0212others(43): Show | 46 | HG00733.hp1 HG01070.hp2 HG01071.hp1 others(43): Show |
intron_variant | MODIFIER | c.597+2870G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75221176 | ||||||
chr17:75221247
|
A | G | 205 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(202): Show | 220 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.597+2941A>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75221247 | ||||||
chr17:75221535
|
C | A | 1 | a0001c0001t0001g0137 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.597+3229C>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75221535 | ||||||
chr17:75221678
|
C | T | 201 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(198): Show | 216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.597+3372C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75221678 | ||||||
chr17:75221734
|
G | A | 2 | a0001c0001t0001g0070a0001c0001t0001g0083 | 2 | HG03239.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.598-3369G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75221734 | ||||||
chr17:75221812
|
A | G | 3 | a0001c0006t0001g0188a0001c0006t0001g0189a0001c0006t0001g0190 | 3 | HG02886.hp2 HG03139.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.598-3291A>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75221812 | ||||||
chr17:75221910
|
G | C | 1 | a0001c0001t0001g0028 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.598-3193G>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75221910 | ||||||
chr17:75222022
|
CGTGT | C | 3 | a0001c0006t0001g0188a0001c0006t0001g0189a0001c0006t0001g0190 | 3 | HG02886.hp2 HG03139.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.598-3070_598-3067d others(6): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr17 | 75222022 | |||||
chr17:75222041
|
TTTTG | T | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 149 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.598-3042_598-3039d others(6): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr17 | 75222041 | |||||
chr17:75222062
|
T | C | 1 | a0001c0001t0001g0034 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.598-3041T>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75222062 | ||||||
chr17:75222161
|
A | C | 202 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(199): Show | 217 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.598-2942A>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75222161 | ||||||
chr17:75222234
|
G | A | 7 | a0001c0001t0001g0004a0001c0001t0001g0201a0001c0001t0001g0202others(4): Show | 9 | HG02055.hp1 HG02109.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.598-2869G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75222234 | ||||||
chr17:75222388
|
A | G | 32 | a0001c0003t0002g0172a0001c0003t0002g0173a0001c0003t0002g0174others(29): Show | 32 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.598-2715A>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75222388 | ||||||
chr17:75222478
|
A | G | 7 | a0001c0001t0001g0004a0001c0001t0001g0201a0001c0001t0001g0202others(4): Show | 9 | HG02055.hp1 HG02109.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.598-2625A>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75222478 | ||||||
chr17:75222495
|
ATTT | A | 6 | a0001c0002t0001g0243a0001c0002t0001g0248a0001c0002t0001g0256others(3): Show | 6 | HG02055.hp2 HG02074.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.598-2581_598-2579d others(5): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr17 | 75222495 | |||||
chr17:75222495
|
ATTTT | A | 48 | a0001c0001t0001g0013a0001c0001t0001g0165a0001c0002t0001g0210others(45): Show | 49 | HG00733.hp1 HG00735.hp1 HG01070.hp2 others(46): Show |
intron_variant | MODIFIER | c.598-2582_598-2579d others(6): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr17 | 75222495 | |||||
chr17:75222495
|
ATTTTT | A | 31 | a0001c0001t0001g0047a0001c0001t0001g0218a0001c0002t0001g0214others(28): Show | 31 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(28): Show |
intron_variant | MODIFIER | c.598-2583_598-2579d others(7): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr17 | 75222495 | |||||
chr17:75222495
|
ATTTTTT | A | 21 | a0001c0001t0001g0014a0001c0001t0001g0031a0001c0001t0001g0033others(18): Show | 21 | HG00140.hp2 HG00733.hp2 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.598-2584_598-2579d others(8): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr17 | 75222495 | |||||
chr17:75222495
|
ATTTTTTT | A | 142 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(139): Show | 156 | HG00280.hp1 HG00280.hp2 HG00544.hp2 others(153): Show |
intron_variant | MODIFIER | c.598-2585_598-2579d others(9): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr17 | 75222495 | |||||
chr17:75222658
|
A | G | 1 | a0001c0001t0001g0013 | 2 | HG02622.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.598-2445A>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75222658 | ||||||
chr17:75222843
|
G | A | 17 | a0001c0001t0001g0014a0001c0001t0001g0031a0001c0001t0001g0033others(14): Show | 17 | HG01069.hp2 HG01074.hp2 HG01261.hp1 others(14): Show |
intron_variant | MODIFIER | c.598-2260G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75222843 | ||||||
chr17:75222928
|
G | A | 1 | a0001c0003t0002g0183 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.598-2175G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75222928 | ||||||
chr17:75222976
|
A | G | 1 | a0001c0001t0001g0206 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.598-2127A>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75222976 | ||||||
chr17:75223032
|
C | CA | 41 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0039others(38): Show | 44 | HG00597.hp1 HG00639.hp1 HG01069.hp2 others(41): Show |
intron_variant | MODIFIER | c.598-2049dupA | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr17 | 75223032 | |||||
chr17:75223032
|
C | CAA | 20 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0031others(17): Show | 20 | HG00738.hp2 HG01255.hp1 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.598-2050_598-2049d others(4): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr17 | 75223032 | |||||
chr17:75223044
|
A | AC | 117 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(114): Show | 128 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.598-2059_598-2058i others(3): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75223044 | ||||||
chr17:75223044
|
A | C | 1 | a0001c0001t0001g0111 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.598-2059A>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75223044 | ||||||
chr17:75223130
|
A | G | 1 | a0001c0001t0001g0218 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.598-1973A>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75223130 | ||||||
chr17:75223157
|
G | A | 1 | a0001c0001t0001g0091 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.598-1946G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75223157 | ||||||
chr17:75223369
|
A | G | 1 | a0001c0001t0001g0092 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.598-1734A>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75223369 | ||||||
chr17:75223382
|
TTTATG | T | 5 | a0001c0001t0001g0004a0001c0001t0001g0156a0001c0001t0001g0202others(2): Show | 7 | HG02109.hp2 HG02717.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.598-1706_598-1702d others(7): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr17 | 75223382 | |||||
chr17:75223511
|
C | T | 1 | a0001c0004t0002g0021 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.598-1592C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75223511 | ||||||
chr17:75223513
|
G | A | 11 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0037others(8): Show | 14 | HG00735.hp2 HG01123.hp1 HG02683.hp2 others(11): Show |
intron_variant | MODIFIER | c.598-1590G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75223513 | ||||||
chr17:75223549
|
G | A | 150 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(147): Show | 163 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.598-1554G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75223549 | ||||||
chr17:75223959
|
G | A | 1 | a0001c0003t0002g0181 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.598-1144G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75223959 | ||||||
chr17:75223992
|
C | T | 202 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(199): Show | 217 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.598-1111C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75223992 | ||||||
chr17:75224031
|
A | G | 251 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(248): Show | 266 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.598-1072A>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75224031 | ||||||
chr17:75224086
|
T | C | 251 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(248): Show | 266 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.598-1017T>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75224086 | ||||||
chr17:75224127
|
C | T | 8 | a0001c0001t0001g0014a0001c0001t0001g0031a0001c0001t0001g0044others(5): Show | 8 | HG01069.hp2 HG01074.hp2 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.598-976C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75224127 | ||||||
chr17:75224202
|
C | G | 1 | a0001c0001t0001g0164 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.598-901C>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75224202 | ||||||
chr17:75224261
|
G | A | 7 | a0001c0001t0001g0099a0001c0001t0001g0118a0001c0001t0001g0119others(4): Show | 7 | HG00639.hp2 HG01175.hp1 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.598-842G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75224261 | ||||||
chr17:75224288
|
G | C | 1 | a0001c0003t0002g0173 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.598-815G>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75224288 | ||||||
chr17:75224337
|
G | A | 5 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(2): Show | 5 | HG00639.hp1 HG02809.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.598-766G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75224337 | ||||||
chr17:75224719
|
C | G | 1 | a0001c0001t0001g0146 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.598-384C>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75224719 | ||||||
chr17:75224729
|
G | T | 24 | a0001c0003t0002g0172a0001c0003t0002g0173a0001c0003t0002g0174others(21): Show | 24 | HG00544.hp1 HG00597.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.598-374G>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75224729 | ||||||
chr17:75224756
|
C | T | 9 | a0001c0001t0001g0012a0001c0001t0001g0150a0001c0001t0001g0153others(6): Show | 10 | HG00738.hp2 HG02258.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.598-347C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75224756 | ||||||
chr17:75224814
|
A | C | 1 | a0001c0001t0001g0218 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.598-289A>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75224814 | ||||||
chr17:75224829
|
G | GA | 178 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(175): Show | 192 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.598-258dupA | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr17 | 75224829 | |||||
chr17:75224829
|
G | GAA | 6 | a0001c0001t0001g0035a0001c0001t0001g0055a0001c0001t0001g0110others(3): Show | 6 | HG00140.hp1 HG02148.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.598-259_598-258dup others(2): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr17 | 75224829 | |||||
chr17:75224904
|
C | T | 165 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(162): Show | 179 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(176): Show |
intron_variant | MODIFIER | c.598-199C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75224904 | ||||||
chr17:75224979
|
T | G | 251 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(248): Show | 266 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.598-124T>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75224979 | ||||||
chr17:75225557
|
A | G | 3 | a0001c0001t0001g0013a0001c0001t0001g0165a0004c0012t0001g0167 | 4 | HG01891.hp2 HG02622.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.855+93A>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 9/18 | chr17 | 75225557 | ||||||
chr17:75225975
|
C | T | 1 | a0001c0001t0001g0079 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.988-76C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 10/18 | chr17 | 75225975 | ||||||
chr17:75225992
|
G | T | 1 | a0001c0001t0001g0150 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.988-59G>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 10/18 | chr17 | 75225992 | ||||||
chr17:75226178
|
C | G | 1 | a0001c0001t0001g0218 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1094+21C>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75226178 | ||||||
chr17:75226285
|
C | T | 1 | a0001c0002t0001g0213 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1094+128C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75226285 | ||||||
chr17:75226293
|
T | C | 2 | a0001c0001t0001g0017a0001c0001t0001g0018 | 2 | HG02109.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1094+136T>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75226293 | ||||||
chr17:75226357
|
C | T | 32 | a0001c0003t0002g0172a0001c0003t0002g0173a0001c0003t0002g0174others(29): Show | 32 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.1094+200C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75226357 | ||||||
chr17:75226724
|
A | G | 4 | a0001c0001t0001g0055a0001c0006t0001g0188a0001c0006t0001g0189others(1): Show | 4 | HG02622.hp2 HG02886.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1094+567A>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75226724 | ||||||
chr17:75226752
|
C | T | 251 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(248): Show | 266 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.1094+595C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75226752 | ||||||
chr17:75226770
|
G | A | 116 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(113): Show | 126 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.1094+613G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75226770 | ||||||
chr17:75226931
|
C | G | 1 | a0001c0001t0001g0146 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1094+774C>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75226931 | ||||||
chr17:75227002
|
A | C | 1 | a0001c0001t0001g0133 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1094+845A>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75227002 | ||||||
chr17:75227003
|
TAATC | T | 7 | a0001c0001t0001g0124a0001c0003t0002g0173a0001c0003t0002g0174others(4): Show | 7 | HG00597.hp1 HG02015.hp2 HG02129.hp1 others(4): Show |
intron_variant | MODIFIER | c.1094+853_1094+856d others(6): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr17 | 75227003 | |||||
chr17:75227073
|
G | C | 205 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(202): Show | 220 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.1094+916G>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75227073 | ||||||
chr17:75227299
|
A | G | 2 | a0001c0001t0001g0138a0001c0001t0001g0139 | 2 | NA18980.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.1094+1142A>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75227299 | ||||||
chr17:75227326
|
G | GTTT | 14 | a0001c0003t0002g0172a0001c0003t0002g0173a0001c0003t0002g0174others(11): Show | 14 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(11): Show |
intron_variant | MODIFIER | c.1094+1193_1094+119 others(7): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr17 | 75227326 | |||||
chr17:75227326
|
G | GTTTT | 7 | a0001c0003t0002g0176a0001c0003t0002g0177a0001c0003t0002g0178others(4): Show | 7 | HG01361.hp1 HG02135.hp1 HG03710.hp2 others(4): Show |
intron_variant | MODIFIER | c.1094+1192_1094+119 others(8): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr17 | 75227326 | |||||
chr17:75227326
|
GT | G | 32 | a0001c0001t0001g0011a0001c0001t0001g0017a0001c0001t0001g0018others(29): Show | 33 | HG01070.hp1 HG01099.hp1 HG01257.hp2 others(30): Show |
intron_variant | MODIFIER | c.1094+1195delT | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr17 | 75227326 | |||||
chr17:75227326
|
GTT | G | 190 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(187): Show | 203 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.1094+1194_1094+119 others(6): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr17 | 75227326 | |||||
chr17:75227334
|
T | G | 12 | a0001c0001t0001g0011a0001c0001t0001g0017a0001c0001t0001g0018others(9): Show | 13 | HG01361.hp2 HG01496.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.1094+1177T>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75227334 | ||||||
chr17:75227335
|
T | G | 153 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(150): Show | 166 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.1094+1178T>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75227335 | ||||||
chr17:75227336
|
T | G | 4 | a0001c0001t0001g0055a0001c0006t0001g0188a0001c0006t0001g0189others(1): Show | 4 | HG02622.hp2 HG02886.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1094+1179T>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75227336 | ||||||
chr17:75227340
|
T | G | 2 | a0001c0001t0001g0044a0001c0001t0001g0140 | 2 | HG01069.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.1094+1183T>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75227340 | ||||||
chr17:75227422
|
A | G | 251 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(248): Show | 266 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.1094+1265A>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75227422 | ||||||
chr17:75227429
|
G | A | 2 | a0001c0001t0001g0202a0001c0001t0001g0203 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1094+1272G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75227429 | ||||||
chr17:75227579
|
C | G | 204 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(201): Show | 219 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.1094+1422C>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75227579 | ||||||
chr17:75227662
|
G | A | 1 | a0001c0001t0001g0016 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1094+1505G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75227662 | ||||||
chr17:75227750
|
G | A | 4 | a0001c0001t0001g0055a0001c0006t0001g0188a0001c0006t0001g0189others(1): Show | 4 | HG02622.hp2 HG02886.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1094+1593G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75227750 | ||||||
chr17:75227771
|
A | G | 201 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(198): Show | 216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1094+1614A>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75227771 | ||||||
chr17:75227772
|
G | A | 1 | a0004c0012t0001g0167 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1094+1615G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75227772 | ||||||
chr17:75227779
|
A | C | 1 | a0001c0002t0001g0225 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1094+1622A>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75227779 | ||||||
chr17:75227810
|
A | T | 1 | a0001c0001t0001g0109 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1094+1653A>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75227810 | ||||||
chr17:75227887
|
T | C | 1 | a0001c0001t0001g0218 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1094+1730T>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75227887 | ||||||
chr17:75227937
|
G | A | 3 | a0001c0001t0001g0033a0001c0001t0001g0066a0001c0001t0001g0142 | 3 | HG02895.hp1 HG02897.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1094+1780G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75227937 | ||||||
chr17:75228107
|
A | T | 1 | a0001c0006t0001g0189 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1094+1950A>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75228107 | ||||||
chr17:75228130
|
C | A | 1 | a0001c0001t0001g0206 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1094+1973C>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75228130 | ||||||
chr17:75228284
|
A | T | 9 | a0001c0002t0001g0210a0001c0002t0001g0211a0001c0002t0001g0212others(6): Show | 9 | HG01243.hp2 HG02559.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1094+2127A>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75228284 | ||||||
chr17:75228292
|
C | T | 4 | a0001c0001t0001g0055a0001c0006t0001g0188a0001c0006t0001g0189others(1): Show | 4 | HG02622.hp2 HG02886.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1094+2135C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75228292 | ||||||
chr17:75228544
|
G | C | 169 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(166): Show | 184 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(181): Show |
intron_variant | MODIFIER | c.1094+2387G>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75228544 | ||||||
chr17:75228558
|
T | G | 3 | a0001c0005t0002g0169a0001c0005t0002g0170a0001c0005t0002g0171 | 3 | HG00140.hp1 HG01361.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.1094+2401T>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75228558 | ||||||
chr17:75228646
|
C | T | 1 | a0001c0001t0001g0082 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1094+2489C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75228646 | ||||||
chr17:75228700
|
A | C | 32 | a0001c0003t0002g0172a0001c0003t0002g0173a0001c0003t0002g0174others(29): Show | 32 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.1094+2543A>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75228700 | ||||||
chr17:75228984
|
C | T | 1 | a0001c0001t0001g0056 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1095-2356C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75228984 | ||||||
chr17:75229043
|
A | G | 1 | a0001c0001t0001g0122 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1095-2297A>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75229043 | ||||||
chr17:75229154
|
C | T | 5 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(2): Show | 5 | HG00639.hp1 HG02809.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1095-2186C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75229154 | ||||||
chr17:75229224
|
A | G | 1 | a0001c0001t0001g0041 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1095-2116A>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75229224 | ||||||
chr17:75229277
|
A | T | 3 | a0001c0003t0002g0173a0001c0003t0002g0175a0001c0003t0002g0177 | 3 | HG02015.hp2 HG02129.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.1095-2063A>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75229277 | ||||||
chr17:75229278
|
T | G | 14 | a0001c0001t0001g0012a0001c0001t0001g0150a0001c0001t0001g0151others(11): Show | 15 | HG00738.hp2 HG02258.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.1095-2062T>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75229278 | ||||||
chr17:75229441
|
C | T | 1 | a0001c0001t0001g0218 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1095-1899C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75229441 | ||||||
chr17:75229527
|
G | A | 1 | a0004c0012t0001g0167 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1095-1813G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75229527 | ||||||
chr17:75229664
|
G | A | 7 | a0001c0001t0001g0004a0001c0001t0001g0201a0001c0001t0001g0202others(4): Show | 9 | HG02055.hp1 HG02109.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1095-1676G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75229664 | ||||||
chr17:75229679
|
A | G | 6 | a0001c0002t0001g0210a0001c0002t0001g0212a0001c0002t0001g0213others(3): Show | 6 | HG01243.hp2 HG02559.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.1095-1661A>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75229679 | ||||||
chr17:75229778
|
C | T | 1 | a0001c0002t0001g0214 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1095-1562C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75229778 | ||||||
chr17:75229820
|
C | T | 14 | a0001c0001t0001g0012a0001c0001t0001g0150a0001c0001t0001g0151others(11): Show | 15 | HG00738.hp2 HG02258.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.1095-1520C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75229820 | ||||||
chr17:75229861
|
A | G | 1 | a0001c0001t0001g0119 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1095-1479A>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75229861 | ||||||
chr17:75230044
|
A | AT | 17 | a0001c0001t0001g0004a0001c0001t0001g0056a0001c0001t0001g0097others(14): Show | 19 | HG00639.hp1 HG01516.hp1 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.1095-1280dupT | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr17 | 75230044 | |||||
chr17:75230044
|
A | ATT | 120 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(117): Show | 128 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.1095-1281_1095-128 others(6): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr17 | 75230044 | |||||
chr17:75230044
|
A | ATTT | 14 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0037others(11): Show | 17 | HG00735.hp2 HG01123.hp1 HG01433.hp2 others(14): Show |
intron_variant | MODIFIER | c.1095-1282_1095-128 others(7): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr17 | 75230044 | |||||
chr17:75230105
|
A | G | 201 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(198): Show | 216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1095-1235A>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75230105 | ||||||
chr17:75230124
|
G | A | 201 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(198): Show | 216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1095-1216G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75230124 | ||||||
chr17:75230285
|
C | T | 5 | a0001c0001t0001g0026a0001c0001t0001g0036a0001c0001t0001g0108others(2): Show | 5 | HG01256.hp2 HG01981.hp1 NA18947.hp2 others(2): Show |
intron_variant | MODIFIER | c.1095-1055C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75230285 | ||||||
chr17:75230306
|
G | A | 1 | a0001c0002t0001g0249 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1095-1034G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75230306 | ||||||
chr17:75230362
|
G | GT | 65 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0016others(62): Show | 67 | HG00639.hp1 HG00733.hp1 HG00738.hp2 others(64): Show |
intron_variant | MODIFIER | c.1095-963dupT | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr17 | 75230362 | |||||
chr17:75230362
|
G | GTT | 38 | a0001c0001t0001g0004a0001c0001t0001g0202a0001c0001t0001g0203others(35): Show | 40 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.1095-964_1095-963d others(4): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr17 | 75230362 | |||||
chr17:75230362
|
G | T | 3 | a0001c0003t0002g0176a0001c0003t0002g0178a0001c0003t0002g0181 | 3 | NA18990.hp2 NA19068.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1095-978G>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75230362 | ||||||
chr17:75230364
|
T | TG | 136 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(133): Show | 147 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.1095-976_1095-975i others(3): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75230364 | ||||||
chr17:75230382
|
T | C | 201 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(198): Show | 216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1095-958T>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75230382 | ||||||
chr17:75230520
|
C | T | 1 | a0001c0001t0001g0098 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1095-820C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75230520 | ||||||
chr17:75230705
|
A | G | 2 | a0001c0001t0001g0069a0001c0001t0001g0076 | 2 | HG01109.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.1095-635A>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75230705 | ||||||
chr17:75230722
|
T | C | 164 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(161): Show | 178 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(175): Show |
intron_variant | MODIFIER | c.1095-618T>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75230722 | ||||||
chr17:75230722
|
T | G | 32 | a0001c0003t0002g0172a0001c0003t0002g0173a0001c0003t0002g0174others(29): Show | 32 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.1095-618T>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75230722 | ||||||
chr17:75230742
|
G | A | 1 | a0001c0001t0001g0137 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1095-598G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75230742 | ||||||
chr17:75230903
|
G | A | 1 | a0001c0002t0001g0224 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1095-437G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75230903 | ||||||
chr17:75230936
|
A | ATTT | 35 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0165others(32): Show | 36 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(33): Show |
intron_variant | MODIFIER | c.1095-393_1095-391d others(5): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr17 | 75230936 | |||||
chr17:75230936
|
A | ATTTT | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 168 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.1095-394_1095-391d others(6): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr17 | 75230936 | |||||
chr17:75230936
|
A | ATTTTT | 10 | a0001c0001t0001g0031a0001c0001t0001g0035a0001c0001t0001g0056others(7): Show | 10 | HG00544.hp2 HG00673.hp1 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.1095-395_1095-391d others(7): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr17 | 75230936 | |||||
chr17:75230959
|
T | C | 1 | a0001c0001t0001g0120 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1095-381T>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75230959 | ||||||
chr17:75230987
|
G | A | 201 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(198): Show | 216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1095-353G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75230987 | ||||||
chr17:75231057
|
G | A | 1 | a0001c0001t0001g0058 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1095-283G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75231057 | ||||||
chr17:75231315
|
C | A | 4 | a0001c0001t0001g0013a0001c0001t0001g0165a0001c0001t0001g0218others(1): Show | 5 | HG01891.hp2 HG02622.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1095-25C>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75231315 | ||||||
chr17:75231434
|
G | A | 1 | a0001c0001t0001g0016 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1178+11G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 12/18 | chr17 | 75231434 | ||||||
chr17:75231473
|
G | A | 2 | a0001c0001t0001g0017a0001c0001t0001g0018 | 2 | HG02109.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1178+50G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 12/18 | chr17 | 75231473 | ||||||
chr17:75231665
|
TATGCGGG others(11): Show |
T | 38 | a0001c0001t0001g0218a0001c0002t0001g0219a0001c0002t0001g0220others(35): Show | 38 | HG00733.hp1 HG01070.hp2 HG01071.hp1 others(35): Show |
intron_variant | MODIFIER | c.1244+38_1244+55del others(18): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr17 | 75231665 | |||||
chr17:75231666
|
A | G | 2 | a0001c0001t0001g0016a0001c0001t0001g0055 | 2 | HG01255.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.1244+28A>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 13/18 | chr17 | 75231666 | ||||||
chr17:75231671
|
G | A | 1 | a0001c0001t0001g0126 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1244+33G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 13/18 | chr17 | 75231671 | ||||||
chr17:75231732
|
G | GT | 7 | a0001c0001t0001g0009a0001c0001t0001g0063a0001c0001t0001g0093others(4): Show | 7 | HG00741.hp1 HG01123.hp2 HG01255.hp2 others(4): Show |
intron_variant | MODIFIER | c.1244+94_1244+95ins others(1): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 13/18 | chr17 | 75231732 | ||||||
chr17:75231779
|
C | T | 1 | a0001c0001t0001g0104 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1245-49C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 13/18 | chr17 | 75231779 | ||||||
chr17:75232004
|
A | G | 6 | a0001c0001t0001g0055a0001c0002t0001g0226a0001c0002t0001g0227others(3): Show | 6 | HG02622.hp2 HG02886.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1396+25A>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 14/18 | chr17 | 75232004 | ||||||
chr17:75232006
|
T | C | 251 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(248): Show | 266 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.1396+27T>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 14/18 | chr17 | 75232006 | ||||||
chr17:75232049
|
T | C | 38 | a0001c0001t0001g0014a0001c0001t0001g0044a0001c0001t0001g0045others(35): Show | 38 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.1396+70T>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 14/18 | chr17 | 75232049 | ||||||
chr17:75232078
|
C | T | 35 | a0001c0001t0001g0013a0001c0001t0001g0165a0001c0001t0001g0218others(32): Show | 36 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(33): Show |
intron_variant | MODIFIER | c.1396+99C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 14/18 | chr17 | 75232078 | ||||||
chr17:75232141
|
C | T | 205 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(202): Show | 220 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.1396+162C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 14/18 | chr17 | 75232141 | ||||||
chr17:75232216
|
C | T | 3 | a0001c0006t0001g0188a0001c0006t0001g0189a0001c0006t0001g0190 | 3 | HG02886.hp2 HG03139.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1396+237C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 14/18 | chr17 | 75232216 | ||||||
chr17:75232290
|
G | C | 11 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0037others(8): Show | 14 | HG00735.hp2 HG01123.hp1 HG02683.hp2 others(11): Show |
intron_variant | MODIFIER | c.1396+311G>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 14/18 | chr17 | 75232290 | ||||||
chr17:75232383
|
C | T | 3 | a0001c0006t0001g0188a0001c0006t0001g0189a0001c0006t0001g0190 | 3 | HG02886.hp2 HG03139.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1396+404C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 14/18 | chr17 | 75232383 | ||||||
chr17:75232458
|
C | T | 3 | a0001c0006t0001g0188a0001c0006t0001g0189a0001c0006t0001g0190 | 3 | HG02886.hp2 HG03139.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1397-393C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 14/18 | chr17 | 75232458 | ||||||
chr17:75232472
|
A | G | 203 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(200): Show | 218 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.1397-379A>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 14/18 | chr17 | 75232472 | ||||||
chr17:75232544
|
G | A | 37 | a0001c0002t0001g0219a0001c0002t0001g0220a0001c0002t0001g0221others(34): Show | 37 | HG00733.hp1 HG01070.hp2 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.1397-307G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 14/18 | chr17 | 75232544 | ||||||
chr17:75232564
|
A | G | 47 | a0001c0001t0001g0146a0001c0002t0001g0210a0001c0002t0001g0211others(44): Show | 47 | HG00733.hp1 HG01070.hp2 HG01071.hp1 others(44): Show |
intron_variant | MODIFIER | c.1397-287A>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 14/18 | chr17 | 75232564 | ||||||
chr17:75232609
|
C | A | 183 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(180): Show | 196 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.1397-242C>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 14/18 | chr17 | 75232609 | ||||||
chr17:75232983
|
T | C | 1 | a0001c0001t0001g0257 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1514+15T>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 15/18 | chr17 | 75232983 | ||||||
chr17:75232997
|
G | A | 13 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0033others(10): Show | 15 | HG00738.hp2 HG01069.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.1514+29G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 15/18 | chr17 | 75232997 | ||||||
chr17:75233002
|
G | C | 1 | a0001c0001t0001g0071 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1514+34G>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 15/18 | chr17 | 75233002 | ||||||
chr17:75233294
|
G | A | 5 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(2): Show | 5 | HG00639.hp1 HG02809.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1615+136G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 16/18 | chr17 | 75233294 | ||||||
chr17:75233315
|
T | G | 1 | a0001c0001t0001g0028 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1615+157T>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 16/18 | chr17 | 75233315 | ||||||
chr17:75233343
|
A | ATGTT | 7 | a0001c0001t0001g0004a0001c0001t0001g0201a0001c0001t0001g0202others(4): Show | 9 | HG02055.hp1 HG02109.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1615+207_1615+210d others(6): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr17 | 75233343 | |||||
chr17:75233363
|
T | A | 8 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(5): Show | 8 | HG00621.hp2 HG00673.hp2 HG02602.hp2 others(5): Show |
intron_variant | MODIFIER | c.1615+205T>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 16/18 | chr17 | 75233363 | ||||||
chr17:75233367
|
TTTTC | T | 4 | a0001c0001t0001g0067a0001c0001t0001g0077a0001c0001t0001g0113others(1): Show | 4 | HG01099.hp2 HG01496.hp1 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.1615+219_1615+222d others(6): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr17 | 75233367 | |||||
chr17:75233373
|
T | TTC | 46 | a0001c0002t0001g0210a0001c0002t0001g0211a0001c0002t0001g0212others(43): Show | 46 | HG00733.hp1 HG01070.hp2 HG01071.hp1 others(43): Show |
intron_variant | MODIFIER | c.1615+217_1615+218d others(4): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr17 | 75233373 | |||||
chr17:75233377
|
T | C | 46 | a0001c0002t0001g0210a0001c0002t0001g0211a0001c0002t0001g0212others(43): Show | 46 | HG00733.hp1 HG01070.hp2 HG01071.hp1 others(43): Show |
intron_variant | MODIFIER | c.1615+219T>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 16/18 | chr17 | 75233377 | ||||||
chr17:75233377
|
T | TTCTC | 6 | a0001c0001t0001g0055a0001c0005t0002g0166a0001c0006t0001g0188others(3): Show | 6 | HG01109.hp2 HG01891.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1615+223_1615+226d others(6): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr17 | 75233377 | |||||
chr17:75233377
|
TTCTC | T | 4 | a0001c0001t0001g0013a0001c0001t0001g0150a0001c0001t0001g0165others(1): Show | 5 | HG00738.hp2 HG01891.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1615+223_1615+226d others(6): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr17 | 75233377 | |||||
chr17:75233379
|
CTCTCTTT others(3): Show |
C | 1 | a0005c0011t0001g0064 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1615+231_1615+240d others(12): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr17 | 75233379 | |||||
chr17:75233385
|
TTCTTTC | T | 135 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(132): Show | 146 | HG00140.hp2 HG00280.hp1 HG00544.hp2 others(143): Show |
intron_variant | MODIFIER | c.1615+247_1615+252d others(8): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr17 | 75233385 | |||||
chr17:75233386
|
T | G | 4 | a0001c0001t0001g0055a0001c0006t0001g0188a0001c0006t0001g0189others(1): Show | 4 | HG02622.hp2 HG02886.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1615+228T>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 16/18 | chr17 | 75233386 | ||||||
chr17:75233393
|
C | CTTTCTCT others(1): Show |
47 | a0001c0002t0001g0210a0001c0002t0001g0211a0001c0002t0001g0212others(44): Show | 47 | HG00733.hp1 HG01070.hp2 HG01071.hp1 others(44): Show |
intron_variant | MODIFIER | c.1615+237_1615+244d others(10): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr17 | 75233393 | |||||
chr17:75233396
|
T | TCTCTTTT others(3): Show |
1 | a0001c0002t0001g0240 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1615+244_1615+245i others(12): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr17 | 75233396 | |||||
chr17:75233397
|
CTCTTTCT others(3): Show |
C | 2 | a0001c0001t0001g0091a0001c0001t0001g0119 | 2 | HG00639.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.1615+247_1615+256d others(12): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr17 | 75233397 | |||||
chr17:75233399
|
C | CTT | 4 | a0001c0001t0001g0055a0001c0006t0001g0188a0001c0006t0001g0189others(1): Show | 4 | HG02622.hp2 HG02886.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1615+243_1615+244d others(4): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr17 | 75233399 | |||||
chr17:75233420
|
C | CT | 52 | a0001c0001t0001g0055a0001c0002t0001g0210a0001c0002t0001g0211others(49): Show | 52 | HG00733.hp1 HG01070.hp2 HG01071.hp1 others(49): Show |
intron_variant | MODIFIER | c.1615+266dupT | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr17 | 75233420 | |||||
chr17:75233424
|
T | C | 3 | a0001c0001t0001g0013a0001c0001t0001g0165a0004c0012t0001g0167 | 4 | HG01891.hp2 HG02622.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1615+266T>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 16/18 | chr17 | 75233424 | ||||||
chr17:75233426
|
TTTTATTT others(4): Show |
T | 3 | a0001c0001t0001g0145a0001c0001t0001g0147a0001c0001t0001g0148 | 3 | HG00639.hp1 HG02809.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1615+272_1615+282d others(13): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr17 | 75233426 | |||||
chr17:75233430
|
A | T | 218 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(215): Show | 233 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.1615+272A>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 16/18 | chr17 | 75233430 | ||||||
chr17:75233436
|
T | C | 2 | a0001c0001t0001g0153a0001c0001t0001g0206 | 2 | HG03041.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1615+278T>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 16/18 | chr17 | 75233436 | ||||||
chr17:75233437
|
C | CT | 180 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(177): Show | 193 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.1615+294dupT | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr17 | 75233437 | |||||
chr17:75233437
|
C | CTT | 6 | a0001c0001t0001g0014a0001c0001t0001g0046a0001c0001t0001g0055others(3): Show | 6 | HG01070.hp2 HG01109.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.1615+293_1615+294d others(4): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr17 | 75233437 | |||||
chr17:75233437
|
C | CTTT | 45 | a0001c0002t0001g0210a0001c0002t0001g0211a0001c0002t0001g0212others(42): Show | 45 | HG00733.hp1 HG01071.hp1 HG01099.hp1 others(42): Show |
intron_variant | MODIFIER | c.1615+292_1615+294d others(5): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr17 | 75233437 | |||||
chr17:75233437
|
C | T | 2 | a0001c0001t0001g0153a0001c0001t0001g0206 | 2 | HG03041.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1615+279C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 16/18 | chr17 | 75233437 | ||||||
chr17:75233469
|
C | T | 169 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(166): Show | 184 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(181): Show |
intron_variant | MODIFIER | c.1615+311C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 16/18 | chr17 | 75233469 | ||||||
chr17:75233512
|
C | T | 1 | a0001c0001t0001g0085 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1615+354C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 16/18 | chr17 | 75233512 | ||||||
chr17:75233532
|
G | A | 46 | a0001c0002t0001g0210a0001c0002t0001g0211a0001c0002t0001g0212others(43): Show | 46 | HG00733.hp1 HG01070.hp2 HG01071.hp1 others(43): Show |
intron_variant | MODIFIER | c.1615+374G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 16/18 | chr17 | 75233532 | ||||||
chr17:75233565
|
G | A | 7 | a0001c0004t0002g0019a0001c0004t0002g0020a0001c0004t0002g0021others(4): Show | 7 | HG02451.hp1 HG02572.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1615+407G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 16/18 | chr17 | 75233565 | ||||||
chr17:75233569
|
G | A | 4 | a0001c0001t0001g0073a0001c0001t0001g0086a0001c0001t0001g0089others(1): Show | 4 | HG00544.hp2 HG00597.hp2 HG01081.hp2 others(1): Show |
intron_variant | MODIFIER | c.1615+411G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 16/18 | chr17 | 75233569 | ||||||
chr17:75233677
|
C | T | 1 | a0001c0005t0002g0186 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1615+519C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 16/18 | chr17 | 75233677 | ||||||
chr17:75233721
|
C | T | 1 | a0001c0001t0001g0122 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1615+563C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 16/18 | chr17 | 75233721 | ||||||
chr17:75233761
|
G | C | 46 | a0001c0002t0001g0210a0001c0002t0001g0211a0001c0002t0001g0212others(43): Show | 46 | HG00733.hp1 HG01070.hp2 HG01071.hp1 others(43): Show |
intron_variant | MODIFIER | c.1615+603G>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 16/18 | chr17 | 75233761 | ||||||
chr17:75233825
|
C | G | 1 | a0001c0002t0001g0238 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1615+667C>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 16/18 | chr17 | 75233825 | ||||||
chr17:75233889
|
C | T | 1 | a0001c0001t0001g0218 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1615+731C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 16/18 | chr17 | 75233889 | ||||||
chr17:75233894
|
C | T | 4 | a0001c0001t0001g0013a0001c0001t0001g0165a0001c0003t0002g0184others(1): Show | 5 | HG01433.hp1 HG01891.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1615+736C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 16/18 | chr17 | 75233894 | ||||||
chr17:75233986
|
G | A | 14 | a0001c0001t0001g0012a0001c0001t0001g0150a0001c0001t0001g0151others(11): Show | 15 | HG00738.hp2 HG02258.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.1616-651G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 16/18 | chr17 | 75233986 | ||||||
chr17:75234049
|
CTTCTTT | C | 47 | a0001c0002t0001g0210a0001c0002t0001g0211a0001c0002t0001g0212others(44): Show | 47 | HG00733.hp1 HG01070.hp2 HG01071.hp1 others(44): Show |
intron_variant | MODIFIER | c.1616-585_1616-580d others(8): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr17 | 75234049 | |||||
chr17:75234052
|
C | CT | 28 | a0001c0003t0002g0172a0001c0003t0002g0173a0001c0003t0002g0174others(25): Show | 28 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(25): Show |
intron_variant | MODIFIER | c.1616-568dupT | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr17 | 75234052 | |||||
chr17:75234052
|
CT | C | 159 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(156): Show | 173 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.1616-568delT | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr17 | 75234052 | |||||
chr17:75234058
|
T | C | 5 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0074others(2): Show | 5 | HG02071.hp2 HG02080.hp2 HG02135.hp2 others(2): Show |
intron_variant | MODIFIER | c.1616-579T>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 16/18 | chr17 | 75234058 | ||||||
chr17:75234063
|
T | C | 2 | a0001c0001t0001g0011a0001c0001t0001g0130 | 3 | HG02965.hp1 HG03139.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1616-574T>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 16/18 | chr17 | 75234063 | ||||||
chr17:75234096
|
C | G | 46 | a0001c0002t0001g0210a0001c0002t0001g0211a0001c0002t0001g0212others(43): Show | 46 | HG00733.hp1 HG01070.hp2 HG01071.hp1 others(43): Show |
intron_variant | MODIFIER | c.1616-541C>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 16/18 | chr17 | 75234096 | ||||||
chr17:75234115
|
A | G | 46 | a0001c0002t0001g0210a0001c0002t0001g0211a0001c0002t0001g0212others(43): Show | 46 | HG00733.hp1 HG01070.hp2 HG01071.hp1 others(43): Show |
intron_variant | MODIFIER | c.1616-522A>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 16/18 | chr17 | 75234115 | ||||||
chr17:75234133
|
C | T | 1 | a0001c0003t0002g0195 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1616-504C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 16/18 | chr17 | 75234133 | ||||||
chr17:75234134
|
C | T | 1 | a0001c0005t0002g0166 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1616-503C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 16/18 | chr17 | 75234134 | ||||||
chr17:75234286
|
A | T | 1 | a0001c0002t0001g0238 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1616-351A>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 16/18 | chr17 | 75234286 | ||||||
chr17:75234360
|
G | T | 1 | a0001c0002t0001g0238 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1616-277G>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 16/18 | chr17 | 75234360 | ||||||
chr17:75234841
|
TTA | T | 46 | a0001c0002t0001g0210a0001c0002t0001g0211a0001c0002t0001g0212others(43): Show | 46 | HG00733.hp1 HG01070.hp2 HG01071.hp1 others(43): Show |
intron_variant | MODIFIER | c.1767+54_1767+55del others(2): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 17/18 | chr17 | 75234841 | ||||||
chr17:75234865
|
T | G | 1 | a0001c0001t0001g0131 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1767+77T>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 17/18 | chr17 | 75234865 | ||||||
chr17:75234868
|
G | A | 46 | a0001c0002t0001g0210a0001c0002t0001g0211a0001c0002t0001g0212others(43): Show | 46 | HG00733.hp1 HG01070.hp2 HG01071.hp1 others(43): Show |
intron_variant | MODIFIER | c.1767+80G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 17/18 | chr17 | 75234868 | ||||||
chr17:75234899
|
C | T | 1 | a0001c0001t0001g0151 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1767+111C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 17/18 | chr17 | 75234899 | ||||||
chr17:75235001
|
G | A | 4 | a0001c0001t0001g0055a0001c0006t0001g0188a0001c0006t0001g0189others(1): Show | 4 | HG02622.hp2 HG02886.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1768-99G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 17/18 | chr17 | 75235001 | ||||||
chr17:75235053
|
C | G | 46 | a0001c0002t0001g0210a0001c0002t0001g0211a0001c0002t0001g0212others(43): Show | 46 | HG00733.hp1 HG01070.hp2 HG01071.hp1 others(43): Show |
intron_variant | MODIFIER | c.1768-47C>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 17/18 | chr17 | 75235053 | ||||||
chr17:75235543
|
G | A | 11 | a0001c0001t0001g0010a0001c0001t0001g0061a0001c0001t0001g0068others(8): Show | 12 | HG00280.hp1 HG00741.hp2 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.1870-35G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 18/18 | chr17 | 75235543 |