geneid | 9631 |
---|---|
ensemblid | ENSG00000113569.16 |
hgncid | 8063 |
symbol | NUP155 |
name | nucleoporin 155 |
refseq_nuc | NM_153485.3 |
refseq_prot | NP_705618.1 |
ensembl_nuc | ENST00000231498.8 |
ensembl_prot | ENSP00000231498.3 |
mane_status | MANE Select |
chr | chr5 |
start | 37288137 |
end | 37371106 |
strand | - |
ver | v1.2 |
region | chr5:37288137-37371106 |
region5000 | chr5:37283137-37376106 |
regionname0 | NUP155_chr5_37288137_37371106 |
regionname5000 | NUP155_chr5_37283137_37376106 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 1391 | 290 | 81 | 49 | 114 | 12 | 32 | 82 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
a0002 | 0/0 | 1391 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
a0003 | 0/0 | 1391 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
a0004 | 0/0 | 1391 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
a0005 | 0/0 | 1391 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
a0006 | 0/0 | 1391 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
a0007 | 0/0 | 1391 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
a0008 | 0/0 | 1391 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
a0009 | 0/0 | 1391 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 4176 | 96 | 6 | 22 | 55 | 5 | 8 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
c0002 | 0/0 | 4176 | 91 | 54 | 11 | 12 | 3 | 11 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
c0003 | 0/1 | 4176 | 79 | 2 | 15 | 45 | 4 | 12 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
c0004 | 0/0 | 4176 | 8 | 8 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
c0005 | 0/0 | 4176 | 7 | 7 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
c0006 | 0/0 | 4176 | 2 | 1 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
c0007 | 0/0 | 4176 | 2 | 0 | 2 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
c0008 | 0/0 | 4176 | 2 | 0 | 0 | 2 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
c0009 | 0/0 | 4176 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
c0010 | 0/0 | 4176 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
c0011 | 0/0 | 4176 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
c0012 | 0/0 | 4176 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
c0013 | 0/0 | 4176 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
c0014 | 0/0 | 4176 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
c0015 | 0/0 | 4176 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
c0016 | 0/0 | 4176 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
c0017 | 0/0 | 4176 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
c0018 | 0/0 | 4176 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
c0019 | 1/0 | 4176 | 1 | 0 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
c0020 | 0/0 | 4176 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
c0021 | 0/0 | 4176 | 1 | 0 | 0 | 0 | 0 | 1 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 3902 | 138 | 5 | 33 | 80 | 4 | 15 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
t0002 | 0/0 | 3903 | 15 | 5 | 2 | 5 | 2 | 1 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
t0003 | 0/0 | 3901 | 11 | 0 | 4 | 6 | 0 | 1 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
t0004 | 0/0 | 3895 | 10 | 9 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
t0005 | 1/0 | 3893 | 9 | 5 | 1 | 2 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
t0006 | 0/0 | 3899 | 9 | 0 | 0 | 3 | 0 | 6 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
t0007 | 0/0 | 3897 | 8 | 7 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
t0008 | 0/0 | 3893 | 8 | 7 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
t0009 | 0/0 | 3888 | 7 | 7 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
t0010 | 0/0 | 3903 | 6 | 0 | 0 | 6 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
t0011 | 0/0 | 3908 | 5 | 5 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
t0012 | 0/0 | 3902 | 4 | 0 | 0 | 0 | 3 | 1 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
t0013 | 0/0 | 3903 | 4 | 1 | 3 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
t0014 | 0/0 | 3904 | 4 | 2 | 0 | 0 | 0 | 2 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
t0015 | 0/0 | 3894 | 3 | 3 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
t0016 | 0/0 | 3898 | 3 | 2 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
t0017 | 0/0 | 3894 | 3 | 2 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
t0018 | 0/0 | 3903 | 3 | 0 | 0 | 2 | 0 | 1 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
t0019 | 0/0 | 3903 | 3 | 0 | 0 | 0 | 2 | 1 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
t0020 | 0/0 | 3900 | 3 | 1 | 1 | 0 | 1 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
t0021 | 0/0 | 3903 | 2 | 2 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
t0022 | 0/0 | 3904 | 2 | 0 | 0 | 1 | 0 | 1 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
t0023 | 0/0 | 3904 | 2 | 1 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
t0024 | 0/0 | 3905 | 2 | 2 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
t0025 | 0/0 | 3900 | 2 | 1 | 0 | 0 | 0 | 1 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
t0026 | 0/0 | 3903 | 2 | 0 | 1 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
t0027 | 0/0 | 3898 | 2 | 1 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
t0028 | 0/0 | 3909 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
t0029 | 0/0 | 3910 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
t0030 | 0/0 | 3902 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
t0031 | 0/0 | 3901 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
t0032 | 0/0 | 3891 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
t0033 | 0/0 | 3893 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
t0034 | 0/0 | 3896 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
t0035 | 0/0 | 3896 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
t0036 | 0/0 | 3898 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
t0037 | 0/0 | 3902 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
t0038 | 0/0 | 3901 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
t0039 | 0/0 | 3902 | 1 | 0 | 0 | 0 | 0 | 1 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
t0040 | 0/0 | 3902 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
t0041 | 0/0 | 3893 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
t0042 | 0/0 | 3903 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
t0043 | 0/0 | 3903 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
t0044 | 0/0 | 3904 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
t0045 | 0/0 | 3906 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
t0046 | 0/0 | 3898 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
t0047 | 0/0 | 3899 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
t0048 | 0/0 | 3901 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
t0049 | 0/0 | 3899 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
t0050 | 0/0 | 3902 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
t0051 | 0/0 | 3903 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
t0052 | 0/0 | 3897 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
t0053 | 0/0 | 3907 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
t0054 | 0/0 | 3901 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
t0055 | 0/0 | 3903 | 1 | 0 | 0 | 0 | 0 | 1 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
t0056 | 0/0 | 3835 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
t0057 | 0/0 | 3902 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0060 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0190 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0281 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 4176 | 96 | 6 | 22 | 55 | 5 | 8 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
a0001c0002 | 0/0 | 4176 | 91 | 54 | 11 | 12 | 3 | 11 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
a0001c0003 | 0/1 | 4176 | 79 | 2 | 15 | 45 | 4 | 12 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
a0001c0004 | 0/0 | 4176 | 8 | 8 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
a0001c0005 | 0/0 | 4176 | 7 | 7 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
a0001c0006 | 0/0 | 4176 | 2 | 1 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
a0001c0010 | 0/0 | 4176 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
a0001c0011 | 0/0 | 4176 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
a0001c0015 | 0/0 | 4176 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
a0001c0017 | 0/0 | 4176 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
a0001c0018 | 0/0 | 4176 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
a0001c0019 | 1/0 | 4176 | 1 | 0 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
a0001c0021 | 0/0 | 4176 | 1 | 0 | 0 | 0 | 0 | 1 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
a0002c0008 | 0/0 | 4176 | 2 | 0 | 0 | 2 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
a0003c0007 | 0/0 | 4176 | 2 | 0 | 2 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
a0004c0020 | 0/0 | 4176 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
a0005c0009 | 0/0 | 4176 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
a0006c0016 | 0/0 | 4176 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
a0007c0013 | 0/0 | 4176 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
a0008c0014 | 0/0 | 4176 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
a0009c0012 | 0/0 | 4176 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 8077 | 68 | 3 | 16 | 41 | 2 | 6 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
a0001c0001t0003 | 0/0 | 8076 | 5 | 0 | 3 | 1 | 0 | 1 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
a0001c0001t0010 | 0/0 | 8078 | 4 | 0 | 0 | 4 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
a0001c0001t0012 | 0/0 | 8077 | 4 | 0 | 0 | 0 | 3 | 1 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
a0001c0001t0018 | 0/0 | 8078 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
a0001c0001t0021 | 0/0 | 8078 | 2 | 2 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
a0001c0001t0022 | 0/0 | 8079 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
a0001c0001t0026 | 0/0 | 8078 | 2 | 0 | 1 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
a0001c0001t0030 | 0/0 | 8077 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
a0001c0001t0031 | 0/0 | 8076 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
a0001c0001t0037 | 0/0 | 8077 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
a0001c0001t0038 | 0/0 | 8076 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
a0001c0001t0040 | 0/0 | 8077 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
a0001c0001t0042 | 0/0 | 8078 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
a0001c0001t0043 | 0/0 | 8078 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
a0001c0001t0050 | 0/0 | 8077 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
a0001c0001t0057 | 0/0 | 8077 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
a0001c0002t0002 | 0/0 | 8078 | 15 | 5 | 2 | 5 | 2 | 1 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
a0001c0002t0004 | 0/0 | 8070 | 10 | 9 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
a0001c0002t0005 | 0/0 | 8068 | 5 | 5 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
a0001c0002t0006 | 0/0 | 8074 | 9 | 0 | 0 | 3 | 0 | 6 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
a0001c0002t0007 | 0/0 | 8072 | 8 | 7 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
a0001c0002t0008 | 0/0 | 8068 | 7 | 7 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
a0001c0002t0013 | 0/0 | 8078 | 4 | 1 | 3 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
a0001c0002t0014 | 0/0 | 8079 | 4 | 2 | 0 | 0 | 0 | 2 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
a0001c0002t0015 | 0/0 | 8069 | 3 | 3 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
a0001c0002t0016 | 0/0 | 8073 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
a0001c0002t0017 | 0/0 | 8069 | 2 | 1 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
a0001c0002t0020 | 0/0 | 8075 | 3 | 1 | 1 | 0 | 1 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
a0001c0002t0023 | 0/0 | 8079 | 2 | 1 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
a0001c0002t0024 | 0/0 | 8080 | 2 | 2 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
a0001c0002t0025 | 0/0 | 8075 | 2 | 1 | 0 | 0 | 0 | 1 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
a0001c0002t0027 | 0/0 | 8073 | 2 | 1 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
a0001c0002t0033 | 0/0 | 8068 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
a0001c0002t0034 | 0/0 | 8071 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
a0001c0002t0035 | 0/0 | 8071 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
a0001c0002t0044 | 0/0 | 8079 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
a0001c0002t0045 | 0/0 | 8081 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
a0001c0002t0046 | 0/0 | 8073 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
a0001c0002t0047 | 0/0 | 8074 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
a0001c0002t0048 | 0/0 | 8076 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
a0001c0002t0049 | 0/0 | 8074 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
a0001c0002t0054 | 0/0 | 8076 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
a0001c0002t0055 | 0/0 | 8078 | 1 | 0 | 0 | 0 | 0 | 1 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
a0001c0002t0056 | 0/0 | 8010 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
a0001c0003t0001 | 0/1 | 8077 | 58 | 1 | 13 | 33 | 2 | 8 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
a0001c0003t0003 | 0/0 | 8076 | 6 | 0 | 1 | 5 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
a0001c0003t0005 | 0/0 | 8068 | 3 | 0 | 1 | 2 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
a0001c0003t0010 | 0/0 | 8078 | 2 | 0 | 0 | 2 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
a0001c0003t0018 | 0/0 | 8078 | 2 | 0 | 0 | 1 | 0 | 1 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
a0001c0003t0019 | 0/0 | 8078 | 3 | 0 | 0 | 0 | 2 | 1 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
a0001c0003t0022 | 0/0 | 8079 | 1 | 0 | 0 | 0 | 0 | 1 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
a0001c0003t0032 | 0/0 | 8066 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
a0001c0003t0039 | 0/0 | 8077 | 1 | 0 | 0 | 0 | 0 | 1 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
a0001c0003t0041 | 0/0 | 8068 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
a0001c0003t0051 | 0/0 | 8078 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
a0001c0004t0011 | 0/0 | 8083 | 5 | 5 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
a0001c0004t0029 | 0/0 | 8085 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
a0001c0004t0052 | 0/0 | 8072 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
a0001c0004t0053 | 0/0 | 8082 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
a0001c0005t0009 | 0/0 | 8063 | 7 | 7 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
a0001c0006t0016 | 0/0 | 8073 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
a0001c0006t0036 | 0/0 | 8073 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
a0001c0010t0017 | 0/0 | 8069 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
a0001c0011t0028 | 0/0 | 8084 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
a0001c0015t0001 | 0/0 | 8077 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
a0001c0017t0001 | 0/0 | 8077 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
a0001c0018t0016 | 0/0 | 8073 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
a0001c0019t0005 | 1/0 | 8068 | 1 | 0 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
a0001c0021t0001 | 0/0 | 8077 | 1 | 0 | 0 | 0 | 0 | 1 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
a0002c0008t0001 | 0/0 | 8077 | 2 | 0 | 0 | 2 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
a0003c0007t0001 | 0/0 | 8077 | 2 | 0 | 2 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
a0004c0020t0001 | 0/0 | 8077 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
a0005c0009t0001 | 0/0 | 8077 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
a0006c0016t0001 | 0/0 | 8077 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
a0007c0013t0001 | 0/0 | 8077 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
a0008c0014t0001 | 0/0 | 8077 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
a0009c0012t0008 | 0/0 | 8068 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | copy fasta | chr5 | 37283137 | 37376106 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0001t0003g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0001t0003g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0001t0003g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0001t0010g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0001t0010g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0001t0010g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0001t0010g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0001t0012g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0001t0012g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0001t0012g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0001t0012g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0001t0018g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0001t0021g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0001t0021g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0001t0022g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0001t0026g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0001t0026g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0001t0030g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0001t0031g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0001t0037g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0001t0038g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0001t0040g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0001t0042g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0001t0043g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0001t0050g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0001t0057g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0002t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0002t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0002t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0002t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0002t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0002t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0002t0002g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0002t0002g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0002t0004g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0002t0004g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0002t0004g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0002t0004g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0002t0004g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0002t0004g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0002t0004g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0002t0004g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0002t0004g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0002t0004g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0002t0005g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0002t0005g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0002t0005g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0002t0005g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0002t0005g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0002t0006g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0002t0006g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0002t0006g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0002t0006g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0002t0006g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0002t0006g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0002t0006g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0002t0006g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0002t0006g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0002t0007g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0002t0007g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0002t0007g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0002t0007g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0002t0007g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0002t0007g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0002t0007g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0002t0007g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0002t0008g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0002t0008g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0002t0008g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0002t0008g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0002t0008g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0002t0008g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0002t0008g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0002t0013g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0002t0013g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0002t0013g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0002t0013g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0002t0014g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0002t0014g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0002t0014g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0002t0014g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0002t0015g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0002t0015g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0002t0015g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0002t0016g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0002t0017g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0002t0017g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0002t0020g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0002t0020g0281 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0002t0020g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0002t0023g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0002t0023g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0002t0024g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0002t0024g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0002t0025g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0002t0025g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0002t0027g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0002t0027g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0002t0033g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0002t0034g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0002t0035g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0002t0044g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0002t0045g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0002t0046g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0002t0047g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0002t0048g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0002t0049g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0002t0054g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0002t0055g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0002t0056g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0003t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0003t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0003t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0003t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0003t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0003t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0003t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0003t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0003t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0003t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0003t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0003t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0003t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0003t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0003t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0003t0001g0190 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0003t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0003t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0003t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0003t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0003t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0003t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0003t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0003t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0003t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0003t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0003t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0003t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0003t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0003t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0003t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0003t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0003t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0003t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0003t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0003t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0003t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0003t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0003t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0003t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0003t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0003t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0003t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0003t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0003t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0003t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0003t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0003t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0003t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0003t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0003t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0003t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0003t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0003t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0003t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0003t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0003t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0003t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0003t0003g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0003t0003g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0003t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0003t0003g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0003t0003g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0003t0003g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0003t0005g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0003t0005g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0003t0005g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0003t0010g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0003t0010g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0003t0018g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0003t0018g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0003t0019g0001 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0003t0019g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0003t0022g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0003t0032g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0003t0039g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0003t0041g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0003t0051g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0004t0011g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0004t0011g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0004t0011g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0004t0011g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0004t0011g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0004t0029g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0004t0052g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0004t0053g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0005t0009g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0005t0009g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0005t0009g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0005t0009g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0005t0009g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0005t0009g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0005t0009g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0006t0016g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0006t0036g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0010t0017g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0011t0028g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0015t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0017t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0018t0016g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0019t0005g0060 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0001c0021t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0002c0008t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0002c0008t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0003c0007t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0003c0007t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0004c0020t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0005c0009t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0006c0016t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0007c0013t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0008c0014t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
a0009c0012t0008g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0002 | t0020 | g0281 | EUR | GBR | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG00099 | hp2 | a0001 | c0003 | t0019 | g0001 | EUR | GBR | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG00140 | hp1 | a0001 | c0003 | t0001 | g0240 | EUR | GBR | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0159 | EUR | GBR | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG00323 | hp1 | a0001 | c0001 | t0012 | g0112 | EUR | FIN | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG00323 | hp2 | a0001 | c0003 | t0001 | g0223 | EUR | FIN | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG00408 | hp1 | a0001 | c0003 | t0001 | g0264 | EAS | CHS | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG00408 | hp2 | a0001 | c0002 | t0006 | g0278 | EAS | CHS | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG00423 | hp1 | a0001 | c0003 | t0001 | g0176 | EAS | CHS | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG00423 | hp2 | a0001 | c0002 | t0002 | g0083 | EAS | CHS | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | CHS | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | CHS | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG00639 | hp1 | a0003 | c0007 | t0001 | g0232 | AMR | PUR | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG00642 | hp2 | a0001 | c0002 | t0002 | g0087 | AMR | PUR | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | CHS | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG00673 | hp2 | a0001 | c0003 | t0001 | g0177 | EAS | CHS | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG00735 | hp1 | a0001 | c0003 | t0001 | g0187 | AMR | PUR | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG00735 | hp2 | a0001 | c0002 | t0020 | g0271 | AMR | PUR | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG01069 | hp1 | a0001 | c0002 | t0002 | g0073 | AMR | PUR | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0256 | AMR | PUR | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG01074 | hp1 | a0001 | c0003 | t0003 | g0203 | AMR | PUR | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG01109 | hp1 | a0001 | c0001 | t0042 | g0113 | AMR | PUR | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG01109 | hp2 | a0001 | c0002 | t0007 | g0036 | AMR | PUR | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG01167 | hp1 | a0001 | c0003 | t0001 | g0222 | AMR | PUR | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG01175 | hp1 | a0001 | c0003 | t0005 | g0178 | AMR | PUR | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG01192 | hp1 | a0001 | c0003 | t0001 | g0172 | AMR | PUR | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG01192 | hp2 | a0001 | c0002 | t0004 | g0028 | AMR | PUR | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG01243 | hp1 | a0001 | c0002 | t0027 | g0045 | AMR | PUR | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG01243 | hp2 | a0009 | c0012 | t0008 | g0013 | AMR | PUR | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG01256 | hp1 | a0001 | c0001 | t0003 | g0157 | AMR | CLM | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG01256 | hp2 | a0003 | c0007 | t0001 | g0229 | AMR | CLM | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG01257 | hp1 | a0001 | c0001 | t0003 | g0128 | AMR | CLM | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG01257 | hp2 | a0001 | c0002 | t0013 | g0071 | AMR | CLM | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG01261 | hp1 | a0001 | c0006 | t0016 | g0044 | AMR | CLM | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG01261 | hp2 | a0001 | c0003 | t0001 | g0181 | AMR | CLM | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG01346 | hp1 | a0001 | c0002 | t0017 | g0042 | AMR | CLM | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG01346 | hp2 | a0001 | c0003 | t0001 | g0185 | AMR | CLM | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | CLM | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG01358 | hp2 | a0001 | c0003 | t0001 | g0175 | AMR | CLM | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | CLM | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | CLM | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG01433 | hp1 | a0008 | c0014 | t0001 | g0196 | AMR | CLM | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG01433 | hp2 | a0001 | c0001 | t0057 | g0299 | AMR | CLM | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG01515 | hp1 | a0001 | c0001 | t0012 | g0092 | EUR | IBS | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG01515 | hp2 | a0001 | c0002 | t0002 | g0078 | EUR | IBS | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG01517 | hp1 | a0001 | c0002 | t0002 | g0080 | EUR | IBS | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0253 | EUR | IBS | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG01884 | hp1 | a0001 | c0002 | t0048 | g0288 | AFR | ACB | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG01884 | hp2 | a0001 | c0002 | t0014 | g0079 | AFR | ACB | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | ACB | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG01891 | hp2 | a0001 | c0002 | t0004 | g0023 | AFR | ACB | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG01952 | hp1 | a0001 | c0003 | t0001 | g0173 | AMR | PEL | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PEL | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG01975 | hp1 | a0001 | c0003 | t0001 | g0259 | AMR | PEL | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | PEL | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG01981 | hp1 | a0007 | c0013 | t0001 | g0251 | AMR | PEL | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG01981 | hp2 | a0001 | c0003 | t0001 | g0225 | AMR | PEL | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG01993 | hp1 | a0001 | c0001 | t0003 | g0245 | AMR | PEL | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG01993 | hp2 | a0001 | c0002 | t0044 | g0070 | AMR | PEL | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG02004 | hp1 | a0001 | c0002 | t0013 | g0069 | AMR | PEL | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG02004 | hp2 | a0001 | c0001 | t0026 | g0152 | AMR | PEL | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | KHV | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG02027 | hp2 | a0001 | c0003 | t0001 | g0170 | EAS | KHV | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG02040 | hp1 | a0001 | c0003 | t0001 | g0207 | EAS | KHV | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG02040 | hp2 | a0001 | c0003 | t0001 | g0213 | EAS | KHV | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG02055 | hp1 | a0001 | c0002 | t0005 | g0268 | AFR | ACB | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG02055 | hp2 | a0001 | c0002 | t0015 | g0012 | AFR | ACB | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG02056 | hp1 | a0001 | c0001 | t0022 | g0099 | EAS | KHV | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG02056 | hp2 | a0001 | c0003 | t0001 | g0186 | EAS | KHV | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG02071 | hp1 | a0001 | c0003 | t0001 | g0263 | EAS | KHV | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | KHV | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG02074 | hp1 | a0001 | c0001 | t0010 | g0116 | EAS | KHV | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG02074 | hp2 | a0001 | c0003 | t0001 | g0165 | EAS | KHV | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | KHV | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | KHV | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG02083 | hp1 | a0001 | c0003 | t0001 | g0239 | EAS | KHV | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | KHV | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG02129 | hp1 | a0001 | c0002 | t0002 | g0074 | EAS | KHV | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG02129 | hp2 | a0001 | c0001 | t0038 | g0117 | EAS | KHV | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | KHV | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG02132 | hp2 | a0001 | c0002 | t0002 | g0076 | EAS | KHV | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG02145 | hp1 | a0001 | c0005 | t0009 | g0057 | AFR | ACB | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG02145 | hp2 | a0001 | c0002 | t0025 | g0273 | AFR | ACB | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | PEL | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG02148 | hp2 | a0001 | c0003 | t0001 | g0191 | AMR | PEL | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG02165 | hp1 | a0001 | c0003 | t0001 | g0206 | EAS | CDX | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | CDX | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG02257 | hp1 | a0001 | c0004 | t0011 | g0051 | AFR | ACB | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | ACB | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG02258 | hp1 | a0001 | c0001 | t0030 | g0202 | AFR | ACB | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG02258 | hp2 | a0001 | c0002 | t0007 | g0038 | AFR | ACB | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0242 | AMR | PEL | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG02273 | hp2 | a0001 | c0003 | t0001 | g0235 | AMR | PEL | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG02280 | hp1 | a0001 | c0002 | t0007 | g0048 | AFR | ACB | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG02280 | hp2 | a0001 | c0002 | t0008 | g0017 | AFR | ACB | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | PEL | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PEL | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG02300 | hp1 | a0001 | c0003 | t0001 | g0231 | AMR | PEL | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG02300 | hp2 | a0001 | c0002 | t0013 | g0067 | AMR | PEL | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG02451 | hp1 | a0001 | c0002 | t0023 | g0031 | AFR | ACB | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG02451 | hp2 | a0001 | c0002 | t0004 | g0021 | AFR | ACB | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG02572 | hp1 | a0001 | c0002 | t0014 | g0084 | AFR | GWD | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG02572 | hp2 | a0001 | c0002 | t0045 | g0292 | AFR | GWD | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG02615 | hp1 | a0001 | c0002 | t0024 | g0032 | AFR | GWD | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG02615 | hp2 | a0001 | c0006 | t0036 | g0046 | AFR | GWD | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG02630 | hp1 | a0001 | c0002 | t0007 | g0039 | AFR | GWD | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG02630 | hp2 | a0001 | c0002 | t0004 | g0020 | AFR | GWD | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG02647 | hp1 | a0001 | c0002 | t0005 | g0266 | AFR | GWD | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG02647 | hp2 | a0001 | c0002 | t0027 | g0034 | AFR | GWD | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG02683 | hp1 | a0001 | c0003 | t0019 | g0212 | SAS | PJL | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG02683 | hp2 | a0001 | c0002 | t0014 | g0072 | SAS | PJL | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG02698 | hp1 | a0001 | c0003 | t0001 | g0237 | SAS | PJL | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG02698 | hp2 | a0001 | c0002 | t0055 | g0068 | SAS | PJL | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG02717 | hp1 | a0001 | c0004 | t0052 | g0056 | AFR | GWD | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG02717 | hp2 | a0001 | c0002 | t0007 | g0049 | AFR | GWD | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG02723 | hp1 | a0001 | c0002 | t0002 | g0086 | AFR | GWD | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG02723 | hp2 | a0001 | c0003 | t0001 | g0228 | AFR | GWD | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | PJL | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG02735 | hp2 | a0001 | c0002 | t0006 | g0277 | SAS | PJL | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG02738 | hp1 | a0001 | c0021 | t0001 | g0298 | SAS | PJL | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG02738 | hp2 | a0001 | c0003 | t0001 | g0293 | SAS | PJL | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG02809 | hp1 | a0001 | c0011 | t0028 | g0003 | AFR | GWD | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG02809 | hp2 | a0001 | c0002 | t0007 | g0040 | AFR | GWD | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG02895 | hp1 | a0001 | c0005 | t0009 | g0064 | AFR | GWD | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG02895 | hp2 | a0001 | c0002 | t0013 | g0066 | AFR | GWD | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG02896 | hp1 | a0001 | c0002 | t0007 | g0037 | AFR | GWD | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG02896 | hp2 | a0001 | c0002 | t0004 | g0022 | AFR | GWD | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG02897 | hp1 | a0001 | c0002 | t0004 | g0027 | AFR | GWD | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG02897 | hp2 | a0001 | c0005 | t0009 | g0062 | AFR | GWD | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG02922 | hp1 | a0001 | c0002 | t0008 | g0015 | AFR | ESN | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG02922 | hp2 | a0001 | c0002 | t0017 | g0041 | AFR | ESN | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG02965 | hp1 | a0001 | c0002 | t0035 | g0047 | AFR | ESN | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG02965 | hp2 | a0001 | c0005 | t0009 | g0054 | AFR | ESN | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG02970 | hp1 | a0001 | c0004 | t0011 | g0055 | AFR | ESN | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG02970 | hp2 | a0001 | c0002 | t0024 | g0033 | AFR | ESN | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG02976 | hp1 | a0001 | c0002 | t0015 | g0029 | AFR | ESN | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG02976 | hp2 | a0001 | c0004 | t0029 | g0002 | AFR | ESN | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG03017 | hp1 | a0001 | c0002 | t0006 | g0284 | SAS | PJL | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG03017 | hp2 | a0001 | c0003 | t0001 | g0221 | SAS | PJL | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG03041 | hp1 | a0001 | c0002 | t0005 | g0270 | AFR | GWD | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG03041 | hp2 | a0001 | c0002 | t0015 | g0024 | AFR | GWD | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG03098 | hp1 | a0001 | c0004 | t0053 | g0265 | AFR | MSL | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG03098 | hp2 | a0001 | c0002 | t0056 | g0008 | AFR | MSL | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG03130 | hp1 | a0001 | c0002 | t0033 | g0018 | AFR | ESN | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG03130 | hp2 | a0001 | c0002 | t0004 | g0026 | AFR | ESN | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG03139 | hp1 | a0001 | c0018 | t0016 | g0050 | AFR | ESN | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG03139 | hp2 | a0001 | c0002 | t0002 | g0088 | AFR | ESN | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | MSL | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG03209 | hp2 | a0001 | c0002 | t0016 | g0043 | AFR | MSL | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG03453 | hp1 | a0001 | c0002 | t0008 | g0016 | AFR | MSL | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG03453 | hp2 | a0001 | c0002 | t0049 | g0275 | AFR | MSL | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG03486 | hp1 | a0001 | c0002 | t0008 | g0011 | AFR | MSL | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG03486 | hp2 | a0001 | c0005 | t0009 | g0061 | AFR | MSL | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG03490 | hp1 | a0001 | c0003 | t0001 | g0260 | SAS | PJL | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG03490 | hp2 | a0001 | c0001 | t0003 | g0166 | SAS | PJL | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG03516 | hp1 | a0001 | c0004 | t0011 | g0053 | AFR | ESN | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG03516 | hp2 | a0001 | c0005 | t0009 | g0058 | AFR | ESN | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG03540 | hp1 | a0001 | c0005 | t0009 | g0063 | AFR | GWD | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG03540 | hp2 | a0001 | c0002 | t0008 | g0010 | AFR | GWD | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG03579 | hp1 | a0001 | c0002 | t0002 | g0274 | AFR | MSL | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG03579 | hp2 | a0001 | c0002 | t0004 | g0019 | AFR | MSL | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0142 | SAS | PJL | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG03654 | hp2 | a0001 | c0002 | t0006 | g0285 | SAS | PJL | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG03669 | hp1 | a0001 | c0002 | t0006 | g0287 | SAS | PJL | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0105 | SAS | STU | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG03688 | hp2 | a0001 | c0002 | t0006 | g0272 | SAS | STU | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG03704 | hp1 | a0001 | c0003 | t0001 | g0258 | SAS | PJL | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0163 | SAS | PJL | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG03710 | hp1 | a0001 | c0003 | t0001 | g0205 | SAS | PJL | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG03710 | hp2 | a0001 | c0002 | t0002 | g0081 | SAS | PJL | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG03834 | hp1 | a0001 | c0003 | t0001 | g0197 | SAS | BEB | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG03834 | hp2 | a0001 | c0003 | t0001 | g0198 | SAS | BEB | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG03942 | hp1 | a0001 | c0003 | t0018 | g0180 | SAS | BEB | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG03942 | hp2 | a0001 | c0002 | t0014 | g0075 | SAS | BEB | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG04184 | hp1 | a0001 | c0002 | t0025 | g0279 | SAS | BEB | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0109 | SAS | BEB | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG04199 | hp1 | a0001 | c0001 | t0012 | g0093 | SAS | STU | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG04199 | hp2 | a0001 | c0003 | t0039 | g0262 | SAS | STU | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG04228 | hp1 | a0001 | c0003 | t0022 | g0219 | SAS | STU | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG04228 | hp2 | a0001 | c0002 | t0006 | g0286 | SAS | STU | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
NA18612 | hp1 | a0001 | c0003 | t0005 | g0164 | EAS | CHB | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
NA18612 | hp2 | a0001 | c0001 | t0040 | g0155 | EAS | CHB | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
NA18747 | hp1 | a0001 | c0001 | t0031 | g0154 | EAS | CHB | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
NA18747 | hp2 | a0001 | c0003 | t0001 | g0238 | EAS | CHB | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
NA18906 | hp1 | a0006 | c0016 | t0001 | g0200 | AFR | YRI | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
NA18906 | hp2 | a0001 | c0010 | t0017 | g0035 | AFR | YRI | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
NA18939 | hp1 | a0001 | c0003 | t0001 | g0254 | EAS | JPT | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
NA18939 | hp2 | a0001 | c0002 | t0046 | g0291 | EAS | JPT | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
NA18946 | hp1 | a0001 | c0003 | t0003 | g0261 | EAS | JPT | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
NA18953 | hp1 | a0002 | c0008 | t0001 | g0296 | EAS | JPT | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
NA18953 | hp2 | a0001 | c0001 | t0003 | g0098 | EAS | JPT | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
NA18954 | hp1 | a0001 | c0002 | t0006 | g0282 | EAS | JPT | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
NA18954 | hp2 | a0001 | c0003 | t0001 | g0227 | EAS | JPT | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
NA18956 | hp2 | a0001 | c0003 | t0010 | g0188 | EAS | JPT | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
NA18960 | hp1 | a0001 | c0003 | t0001 | g0215 | EAS | JPT | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
NA18961 | hp2 | a0001 | c0003 | t0003 | g0234 | EAS | JPT | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
NA18968 | hp2 | a0001 | c0002 | t0002 | g0082 | EAS | JPT | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
NA18975 | hp1 | a0001 | c0003 | t0041 | g0226 | EAS | JPT | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
NA18977 | hp1 | a0001 | c0001 | t0043 | g0138 | EAS | JPT | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
NA18977 | hp2 | a0001 | c0003 | t0003 | g0171 | EAS | JPT | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
NA18979 | hp1 | a0001 | c0003 | t0003 | g0210 | EAS | JPT | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
NA18979 | hp2 | a0001 | c0002 | t0023 | g0065 | EAS | JPT | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
NA18983 | hp1 | a0001 | c0003 | t0001 | g0211 | EAS | JPT | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
NA18984 | hp1 | a0001 | c0003 | t0001 | g0204 | EAS | JPT | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
NA18984 | hp2 | a0001 | c0002 | t0006 | g0283 | EAS | JPT | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
NA18986 | hp1 | a0001 | c0003 | t0001 | g0255 | EAS | JPT | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
NA18990 | hp2 | a0001 | c0017 | t0001 | g0189 | EAS | JPT | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
NA18991 | hp1 | a0001 | c0001 | t0010 | g0097 | EAS | JPT | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
NA18991 | hp2 | a0001 | c0003 | t0001 | g0179 | EAS | JPT | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
NA18992 | hp2 | a0001 | c0015 | t0001 | g0230 | EAS | JPT | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
NA18994 | hp1 | a0001 | c0003 | t0003 | g0233 | EAS | JPT | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
NA18998 | hp2 | a0001 | c0003 | t0001 | g0174 | EAS | JPT | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
NA19000 | hp1 | a0001 | c0001 | t0018 | g0094 | EAS | JPT | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
NA19000 | hp2 | a0001 | c0002 | t0054 | g0276 | EAS | JPT | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
NA19001 | hp1 | a0001 | c0002 | t0002 | g0085 | EAS | JPT | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
NA19001 | hp2 | a0001 | c0003 | t0051 | g0195 | EAS | JPT | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
NA19004 | hp2 | a0001 | c0003 | t0001 | g0220 | EAS | JPT | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
NA19006 | hp1 | a0001 | c0003 | t0001 | g0217 | EAS | JPT | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
NA19006 | hp2 | a0001 | c0001 | t0050 | g0125 | EAS | JPT | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
NA19010 | hp1 | a0004 | c0020 | t0001 | g0297 | EAS | JPT | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
NA19010 | hp2 | a0001 | c0003 | t0001 | g0184 | EAS | JPT | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
NA19011 | hp1 | a0001 | c0003 | t0001 | g0214 | EAS | JPT | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
NA19012 | hp1 | a0001 | c0003 | t0001 | g0241 | EAS | JPT | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
NA19043 | hp1 | a0001 | c0002 | t0034 | g0005 | AFR | LWK | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
NA19043 | hp2 | a0001 | c0002 | t0005 | g0269 | AFR | LWK | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
NA19054 | hp1 | a0001 | c0001 | t0026 | g0146 | EAS | JPT | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
NA19054 | hp2 | a0005 | c0009 | t0001 | g0248 | EAS | JPT | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
NA19056 | hp1 | a0001 | c0003 | t0010 | g0209 | EAS | JPT | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
NA19056 | hp2 | a0001 | c0002 | t0047 | g0280 | EAS | JPT | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
NA19065 | hp1 | a0002 | c0008 | t0001 | g0295 | EAS | JPT | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
NA19067 | hp1 | a0001 | c0003 | t0018 | g0182 | EAS | JPT | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
NA19068 | hp1 | a0001 | c0001 | t0010 | g0129 | EAS | JPT | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
NA19070 | hp2 | a0001 | c0003 | t0001 | g0257 | EAS | JPT | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
NA19074 | hp1 | a0001 | c0001 | t0037 | g0091 | EAS | JPT | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
NA19074 | hp2 | a0001 | c0003 | t0001 | g0208 | EAS | JPT | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
NA19078 | hp2 | a0001 | c0001 | t0010 | g0147 | EAS | JPT | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
NA19084 | hp1 | a0001 | c0003 | t0005 | g0167 | EAS | JPT | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
NA19084 | hp2 | a0001 | c0003 | t0001 | g0294 | EAS | JPT | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
NA19087 | hp2 | a0001 | c0003 | t0001 | g0183 | EAS | JPT | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
NA19088 | hp1 | a0001 | c0003 | t0001 | g0244 | EAS | JPT | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
NA19090 | hp2 | a0001 | c0003 | t0001 | g0218 | EAS | JPT | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
NA19091 | hp2 | a0001 | c0003 | t0001 | g0236 | EAS | JPT | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
NA20129 | hp1 | a0001 | c0002 | t0002 | g0077 | AFR | ASW | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
NA20129 | hp2 | a0001 | c0002 | t0005 | g0267 | AFR | ASW | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
NA20752 | hp1 | a0001 | c0003 | t0019 | g0001 | EUR | TSI | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
NA20752 | hp2 | a0001 | c0001 | t0012 | g0111 | EUR | TSI | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | CLM | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG01123 | hp2 | a0001 | c0003 | t0001 | g0224 | AMR | CLM | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG02109 | hp1 | a0001 | c0002 | t0008 | g0014 | AFR | ACB | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG02109 | hp2 | a0001 | c0002 | t0008 | g0009 | AFR | ACB | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG02486 | hp1 | a0001 | c0004 | t0011 | g0052 | AFR | ACB | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG02486 | hp2 | a0001 | c0002 | t0002 | g0290 | AFR | ACB | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG02559 | hp1 | a0001 | c0001 | t0021 | g0006 | AFR | ACB | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG02559 | hp2 | a0001 | c0004 | t0011 | g0059 | AFR | ACB | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG06807 | hp1 | a0001 | c0002 | t0020 | g0289 | AFR | USA | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
HG06807 | hp2 | a0001 | c0002 | t0004 | g0025 | AFR | USA | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
NA18955 | hp1 | a0001 | c0003 | t0001 | g0243 | EAS | JPT | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
NA20300 | hp1 | a0001 | c0003 | t0032 | g0216 | AFR | USA | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
NA20300 | hp2 | a0001 | c0002 | t0007 | g0030 | AFR | USA | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
NA21309 | hp1 | a0001 | c0001 | t0021 | g0007 | AFR | LWK | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
NA21309 | hp2 | a0001 | c0002 | t0004 | g0004 | AFR | LWK | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
homoSapiens_chm13v2 | hp1 | a0001 | c0003 | t0001 | g0190 | REF | REF | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
homoSapiens_grch38 | hp1 | a0001 | c0019 | t0005 | g0060 | REF | REF | NUP155_chr5_37283137_37376106 | NUP155 | chr5 | 37283137 | 37376106 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:37292016
|
G | C | 1 | a0009 | 1 | HG01243.hp2 | missense_variant | MODERATE | c.4060C>G | p.Leu1354Val | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 35/35 | 4189/8068 | 4060/4176 | 1354/1391 | chr5 | 37292016 | ||
chr5:37303350
|
C | T | 1 | a0008 | 1 | HG01433.hp1 | missense_variant | MODERATE | c.3227G>A | p.Arg1076His | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 28/35 | 3356/8068 | 3227/4176 | 1076/1391 | chr5 | 37303350 | ||
chr5:37314277
|
C | T | 1 | a0003 | 2 | HG00639.hp1 HG01256.hp2 |
missense_variant | MODERATE | c.2357G>A | p.Arg786Gln | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 22/35 | 2486/8068 | 2357/4176 | 786/1391 | chr5 | 37314277 | ||
chr5:37327776
|
C | T | 1 | a0007 | 1 | HG01981.hp1 | missense_variant&splice_region_variant | MODERATE | c.1877G>A | p.Gly626Asp | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 18/35 | 2006/8068 | 1877/4176 | 626/1391 | chr5 | 37327776 | ||
chr5:37328393
|
T | C | 1 | a0006 | 1 | NA18906.hp1 | missense_variant | MODERATE | c.1841A>G | p.Tyr614Cys | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 17/35 | 1970/8068 | 1841/4176 | 614/1391 | chr5 | 37328393 | ||
chr5:37341132
|
C | T | 1 | a0005 | 1 | NA19054.hp2 | missense_variant | MODERATE | c.1204G>A | p.Val402Met | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 11/35 | 1333/8068 | 1204/4176 | 402/1391 | chr5 | 37341132 | ||
chr5:37370824
|
G | C | 1 | a0002 | 2 | NA18953.hp1 NA19065.hp1 |
missense_variant | MODERATE | c.154C>G | p.Pro52Ala | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/35 | 283/8068 | 154/4176 | 52/1391 | chr5 | 37370824 | ||
chr5:37370851
|
G | A | 1 | a0004 | 1 | NA19010.hp1 | missense_variant | MODERATE | c.127C>T | p.Leu43Phe | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/35 | 256/8068 | 127/4176 | 43/1391 | chr5 | 37370851 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:37294371
|
T | C | 6 | a0001c0001a0002c0008a0004c0020others(3): Show | 102 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(99): Show |
synonymous_variant | LOW | c.3888A>G | p.Leu1296Leu | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 33/35 | 4017/8068 | 3888/4176 | 1296/1391 | chr5 | 37294371 | ||
chr5:37298905
|
G | A | 1 | a0001c0005 | 7 | HG02145.hp1 HG02895.hp1 HG02897.hp2 others(4): Show |
synonymous_variant | LOW | c.3756C>T | p.Gly1252Gly | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 32/35 | 3885/8068 | 3756/4176 | 1252/1391 | chr5 | 37298905 | ||
chr5:37298947
|
C | T | 2 | a0001c0004a0001c0011 | 9 | HG02257.hp1 HG02486.hp1 HG02559.hp2 others(6): Show |
synonymous_variant | LOW | c.3714G>A | p.Ser1238Ser | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 32/35 | 3843/8068 | 3714/4176 | 1238/1391 | chr5 | 37298947 | ||
chr5:37299479
|
C | T | 1 | a0001c0011 | 1 | HG02809.hp1 | synonymous_variant | LOW | c.3651G>A | p.Val1217Val | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 31/35 | 3780/8068 | 3651/4176 | 1217/1391 | chr5 | 37299479 | ||
chr5:37303268
|
G | A | 1 | a0001c0006 | 2 | HG01261.hp1 HG02615.hp2 |
synonymous_variant | LOW | c.3309C>T | p.Asp1103Asp | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 28/35 | 3438/8068 | 3309/4176 | 1103/1391 | chr5 | 37303268 | ||
chr5:37310663
|
A | G | 1 | a0001c0005 | 7 | HG02145.hp1 HG02895.hp1 HG02897.hp2 others(4): Show |
synonymous_variant | LOW | c.2517T>C | p.Ala839Ala | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 23/35 | 2646/8068 | 2517/4176 | 839/1391 | chr5 | 37310663 | ||
chr5:37314318
|
T | C | 1 | a0001c0015 | 1 | NA18992.hp2 | synonymous_variant | LOW | c.2316A>G | p.Leu772Leu | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 22/35 | 2445/8068 | 2316/4176 | 772/1391 | chr5 | 37314318 | ||
chr5:37333592
|
C | T | 1 | a0001c0010 | 1 | NA18906.hp2 | synonymous_variant | LOW | c.1389G>A | p.Ala463Ala | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 13/35 | 1518/8068 | 1389/4176 | 463/1391 | chr5 | 37333592 | ||
chr5:37333625
|
A | G | 8 | a0001c0002a0001c0004a0001c0005others(5): Show | 112 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(109): Show |
synonymous_variant | LOW | c.1356T>C | p.Ala452Ala | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 13/35 | 1485/8068 | 1356/4176 | 452/1391 | chr5 | 37333625 | ||
chr5:37337821
|
G | C | 1 | a0001c0017 | 1 | NA18990.hp2 | synonymous_variant | LOW | c.1344C>G | p.Thr448Thr | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 12/35 | 1473/8068 | 1344/4176 | 448/1391 | chr5 | 37337821 | ||
chr5:37364341
|
C | T | 18 | a0001c0001a0001c0002a0001c0003others(15): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
synonymous_variant | LOW | c.201G>A | p.Leu67Leu | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 2/35 | 330/8068 | 201/4176 | 67/1391 | chr5 | 37364341 | ||
chr5:37370957
|
G | A | 1 | a0001c0021 | 1 | HG02738.hp1 | synonymous_variant | LOW | c.21C>T | p.Gly7Gly | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/35 | 150/8068 | 21/4176 | 7/1391 | chr5 | 37370957 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:37288288
|
G | A | 1 | a0001c0003t0039 | 1 | HG04199.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3612C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 35/35 | 3612 | chr5 | 37288288 | |||||
chr5:37288340
|
C | A | 1 | a0001c0001t0040 | 1 | NA18612.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3560G>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 35/35 | 3560 | chr5 | 37288340 | |||||
chr5:37288415
|
C | A | 1 | a0001c0003t0051 | 1 | NA19001.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3485G>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 35/35 | 3485 | chr5 | 37288415 | |||||
chr5:37288433
|
A | G | 38 | a0001c0002t0002a0001c0002t0004a0001c0002t0006others(35): Show | 107 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(104): Show |
3_prime_UTR_variant | MODIFIER | c.*3467T>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 35/35 | 3467 | chr5 | 37288433 | |||||
chr5:37288434
|
TAAAC | T | 1 | a0001c0005t0009 | 7 | HG02145.hp1 HG02895.hp1 HG02897.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3462_*3465delGTTT | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 35/35 | 3462 | chr5 | 37288434 | |||||
chr5:37288442
|
T | TA | 1 | a0001c0003t0019 | 3 | HG00099.hp2 HG02683.hp1 NA20752.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3457dupT | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 35/35 | 3457 | chr5 | 37288442 | |||||
chr5:37288547
|
G | A | 1 | a0001c0001t0038 | 1 | HG02129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3353C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 35/35 | 3353 | chr5 | 37288547 | |||||
chr5:37288710
|
G | A | 1 | a0001c0002t0047 | 1 | NA19056.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3190C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 35/35 | 3190 | chr5 | 37288710 | |||||
chr5:37288746
|
T | A | 2 | a0001c0001t0012a0001c0001t0042 | 5 | HG00323.hp1 HG01109.hp1 HG01515.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3154A>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 35/35 | 3154 | chr5 | 37288746 | |||||
chr5:37288747
|
T | A | 2 | a0001c0001t0012a0001c0001t0042 | 5 | HG00323.hp1 HG01109.hp1 HG01515.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3153A>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 35/35 | 3153 | chr5 | 37288747 | |||||
chr5:37288747
|
T | TA | 13 | a0001c0002t0007a0001c0002t0008a0001c0002t0015others(10): Show | 30 | HG01109.hp2 HG01243.hp1 HG01243.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*3152dupT | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 35/35 | 3152 | chr5 | 37288747 | |||||
chr5:37288747
|
T | TAA | 3 | a0001c0002t0004a0001c0004t0052a0001c0004t0053 | 12 | HG01192.hp2 HG01891.hp2 HG02451.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*3151_*3152dupTT | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 35/35 | 3152 | chr5 | 37288747 | |||||
chr5:37288747
|
T | TAAA | 3 | a0001c0004t0011a0001c0004t0029a0001c0011t0028 | 7 | HG02257.hp1 HG02486.hp1 HG02559.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3150_*3152dupTTT | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 35/35 | 3152 | chr5 | 37288747 | |||||
chr5:37288747
|
TAA | T | 1 | a0001c0005t0009 | 7 | HG02145.hp1 HG02895.hp1 HG02897.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3151_*3152delTT | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 35/35 | 3151 | chr5 | 37288747 | |||||
chr5:37288767
|
A | AGTAGGGG others(1): Show |
4 | a0001c0001t0003a0001c0001t0031a0001c0001t0038others(1): Show | 13 | HG01074.hp1 HG01256.hp1 HG01257.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*3132_*3133insCCCC others(4): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 35/35 | 3132 | chr5 | 37288767 | |||||
chr5:37288767
|
A | G | 1 | a0001c0003t0041 | 1 | NA18975.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3133T>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 35/35 | 3133 | chr5 | 37288767 | |||||
chr5:37288768
|
A | AAGTAGGG others(3): Show |
1 | a0001c0001t0021 | 2 | HG02559.hp1 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3131_*3132insCCCC others(6): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 35/35 | 3131 | chr5 | 37288768 | |||||
chr5:37288768
|
A | G | 5 | a0001c0001t0003a0001c0001t0031a0001c0001t0038others(2): Show | 14 | HG01074.hp1 HG01256.hp1 HG01257.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*3132T>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 35/35 | 3132 | chr5 | 37288768 | |||||
chr5:37288771
|
A | AGGGGGGG others(3): Show |
2 | a0001c0001t0018a0001c0003t0018 | 3 | HG03942.hp1 NA19000.hp1 NA19067.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3128_*3129insCACC others(6): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 35/35 | 3128 | chr5 | 37288771 | |||||
chr5:37288771
|
A | AGGGGGGG others(4): Show |
3 | a0001c0001t0022a0001c0002t0044a0001c0003t0022 | 3 | HG01993.hp2 HG02056.hp1 HG04228.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3128_*3129insCCAC others(7): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 35/35 | 3128 | chr5 | 37288771 | |||||
chr5:37288771
|
A | AGGGGGGG others(2): Show |
23 | a0001c0001t0001a0001c0001t0012a0001c0001t0026others(20): Show | 155 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(152): Show |
3_prime_UTR_variant | MODIFIER | c.*3120_*3128dupCACC others(5): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 35/35 | 3128 | chr5 | 37288771 | |||||
chr5:37288771
|
A | AGGGGGGG others(3): Show |
14 | a0001c0001t0010a0001c0001t0042a0001c0002t0002others(11): Show | 49 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*3119_*3128dupCCAC others(6): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 35/35 | 3128 | chr5 | 37288771 | |||||
chr5:37288771
|
A | AGGGGGGG others(4): Show |
5 | a0001c0002t0014a0001c0002t0023a0001c0002t0025others(2): Show | 10 | HG01884.hp2 HG02145.hp2 HG02451.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*3118_*3128dupCCCA others(7): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 35/35 | 3128 | chr5 | 37288771 | |||||
chr5:37288771
|
A | AGGGGGGG others(5): Show |
3 | a0001c0002t0024a0001c0002t0048a0001c0004t0029 | 4 | HG01884.hp1 HG02615.hp1 HG02970.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3117_*3128dupCCCC others(8): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 35/35 | 3128 | chr5 | 37288771 | |||||
chr5:37288771
|
A | AGGGGGGG others(6): Show |
1 | a0001c0002t0045 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3128_*3129insCCCC others(9): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 35/35 | 3128 | chr5 | 37288771 | |||||
chr5:37288771
|
A | G | 6 | a0001c0001t0003a0001c0001t0021a0001c0001t0031others(3): Show | 16 | HG01074.hp1 HG01256.hp1 HG01257.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*3129T>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 35/35 | 3129 | chr5 | 37288771 | |||||
chr5:37288833
|
G | C | 2 | a0001c0002t0002a0001c0002t0014 | 19 | HG00423.hp2 HG00642.hp2 HG01069.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*3067C>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 35/35 | 3067 | chr5 | 37288833 | |||||
chr5:37288882
|
G | A | 1 | a0001c0002t0049 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3018C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 35/35 | 3018 | chr5 | 37288882 | |||||
chr5:37288909
|
C | CA | 14 | a0001c0001t0043a0001c0002t0007a0001c0002t0016others(11): Show | 32 | HG01109.hp2 HG01243.hp1 HG01261.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*2990dupT | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 35/35 | 2990 | chr5 | 37288909 | |||||
chr5:37288947
|
T | A | 16 | a0001c0002t0002a0001c0002t0006a0001c0002t0013others(13): Show | 49 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*2953A>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 35/35 | 2953 | chr5 | 37288947 | |||||
chr5:37289049
|
C | A | 1 | a0001c0004t0053 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2851G>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 35/35 | 2851 | chr5 | 37289049 | |||||
chr5:37289117
|
C | G | 1 | a0001c0002t0055 | 1 | HG02698.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2783G>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 35/35 | 2783 | chr5 | 37289117 | |||||
chr5:37289396
|
CACTG | C | 8 | a0001c0002t0006a0001c0002t0020a0001c0002t0025others(5): Show | 19 | HG00099.hp1 HG00408.hp2 HG00735.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*2500_*2503delCAGT | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 35/35 | 2500 | chr5 | 37289396 | |||||
chr5:37289460
|
C | A | 1 | a0001c0006t0036 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2440G>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 35/35 | 2440 | chr5 | 37289460 | |||||
chr5:37289687
|
T | C | 8 | a0001c0002t0004a0001c0002t0008a0001c0002t0015others(5): Show | 26 | HG01192.hp2 HG01243.hp2 HG01346.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*2213A>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 35/35 | 2213 | chr5 | 37289687 | |||||
chr5:37289702
|
T | C | 1 | a0001c0001t0050 | 1 | NA19006.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2198A>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 35/35 | 2198 | chr5 | 37289702 | |||||
chr5:37289872
|
C | T | 1 | a0001c0001t0030 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2028G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 35/35 | 2028 | chr5 | 37289872 | |||||
chr5:37289974
|
C | T | 1 | a0001c0001t0021 | 2 | HG02559.hp1 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1926G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 35/35 | 1926 | chr5 | 37289974 | |||||
chr5:37290021
|
A | G | 1 | a0001c0002t0056 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1879T>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 35/35 | 1879 | chr5 | 37290021 | |||||
chr5:37290066
|
A | G | 1 | a0001c0001t0037 | 1 | NA19074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1834T>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 35/35 | 1834 | chr5 | 37290066 | |||||
chr5:37290247
|
G | A | 1 | a0001c0003t0051 | 1 | NA19001.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1653C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 35/35 | 1653 | chr5 | 37290247 | |||||
chr5:37290426
|
C | T | 8 | a0001c0002t0007a0001c0002t0016a0001c0002t0027others(5): Show | 16 | HG01109.hp2 HG01243.hp1 HG01261.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1474G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 35/35 | 1474 | chr5 | 37290426 | |||||
chr5:37290478
|
C | CA | 8 | a0001c0001t0026a0001c0002t0020a0001c0002t0054others(5): Show | 15 | HG00099.hp1 HG00735.hp2 HG02004.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1421dupT | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 35/35 | 1421 | chr5 | 37290478 | |||||
chr5:37290478
|
C | CAA | 3 | a0001c0002t0007a0001c0002t0034a0001c0002t0035 | 10 | HG01109.hp2 HG02258.hp2 HG02280.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1420_*1421dupTT | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 35/35 | 1421 | chr5 | 37290478 | |||||
chr5:37290478
|
C | CAAA | 5 | a0001c0002t0016a0001c0002t0027a0001c0006t0016others(2): Show | 6 | HG01243.hp1 HG01261.hp1 HG02615.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1419_*1421dupTTT | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 35/35 | 1421 | chr5 | 37290478 | |||||
chr5:37290734
|
T | A | 2 | a0001c0002t0017a0001c0010t0017 | 3 | HG01346.hp1 HG02922.hp2 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1166A>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 35/35 | 1166 | chr5 | 37290734 | |||||
chr5:37290798
|
A | G | 16 | a0001c0002t0004a0001c0002t0007a0001c0002t0008others(13): Show | 42 | HG01109.hp2 HG01192.hp2 HG01243.hp1 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*1102T>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 35/35 | 1102 | chr5 | 37290798 | |||||
chr5:37290885
|
GTGATGCT others(5): Show |
G | 1 | a0001c0003t0032 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1003_*1014delGCAT others(8): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 35/35 | 1003 | chr5 | 37290885 | |||||
chr5:37291061
|
A | C | 1 | a0001c0002t0056 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*839T>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 35/35 | 839 | chr5 | 37291061 | |||||
chr5:37291337
|
G | A | 1 | a0001c0002t0027 | 2 | HG01243.hp1 HG02647.hp2 |
3_prime_UTR_variant | MODIFIER | c.*563C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 35/35 | 563 | chr5 | 37291337 | |||||
chr5:37291350
|
G | A | 1 | a0001c0005t0009 | 7 | HG02145.hp1 HG02895.hp1 HG02897.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*550C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 35/35 | 550 | chr5 | 37291350 | |||||
chr5:37291387
|
G | A | 1 | a0001c0002t0055 | 1 | HG02698.hp2 | 3_prime_UTR_variant | MODIFIER | c.*513C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 35/35 | 513 | chr5 | 37291387 | |||||
chr5:37291624
|
AATTCAAA others(52): Show |
A | 1 | a0001c0002t0056 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*217_*275delGAGATT others(53): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 35/35 | 217 | chr5 | 37291624 | |||||
chr5:37291646
|
AT | A | 2 | a0001c0002t0008a0009c0012t0008 | 8 | HG01243.hp2 HG02109.hp1 HG02109.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*253delA | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 35/35 | 253 | chr5 | 37291646 | |||||
chr5:37291839
|
C | T | 1 | a0001c0001t0031 | 1 | NA18747.hp1 | 3_prime_UTR_variant | MODIFIER | c.*61G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 35/35 | 61 | chr5 | 37291839 | |||||
chr5:37291859
|
A | G | 1 | a0001c0001t0030 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*41T>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 35/35 | 41 | chr5 | 37291859 | |||||
chr5:37291881
|
T | C | 1 | a0001c0005t0009 | 7 | HG02145.hp1 HG02895.hp1 HG02897.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*19A>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 35/35 | 19 | chr5 | 37291881 | |||||
chr5:37371019
|
C | G | 2 | a0001c0004t0029a0001c0011t0028 | 2 | HG02809.hp1 HG02976.hp2 |
5_prime_UTR_variant | MODIFIER | c.-42G>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/35 | 42 | chr5 | 37371019 | |||||
chr5:37371091
|
G | A | 1 | a0001c0001t0057 | 1 | HG01433.hp2 | 5_prime_UTR_variant | MODIFIER | c.-114C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/35 | 114 | chr5 | 37371091 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:37292137
|
G | A | 112 | a0001c0002t0002g0073a0001c0002t0002g0074a0001c0002t0002g0076others(109): Show | 112 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.4038-99C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 34/34 | chr5 | 37292137 | ||||||
chr5:37292217
|
A | AT | 10 | a0001c0001t0001g0096a0001c0001t0001g0194a0001c0001t0043g0138others(7): Show | 10 | HG01981.hp1 HG02080.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.4038-180dupA | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 34/34 | chr5 | 37292217 | ||||||
chr5:37292217
|
AT | A | 6 | a0001c0002t0005g0266a0001c0002t0005g0267a0001c0002t0005g0268others(3): Show | 6 | HG02055.hp1 HG02647.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.4038-180delA | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 34/34 | chr5 | 37292217 | ||||||
chr5:37292217
|
ATT | A | 15 | a0001c0002t0007g0030a0001c0002t0007g0036a0001c0002t0007g0037others(12): Show | 15 | HG01109.hp2 HG01243.hp1 HG01261.hp1 others(12): Show |
intron_variant | MODIFIER | c.4038-181_4038-180d others(4): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 34/34 | chr5 | 37292217 | ||||||
chr5:37292265
|
C | G | 182 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0095others(179): Show | 182 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.4038-227G>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 34/34 | chr5 | 37292265 | ||||||
chr5:37292284
|
C | T | 1 | a0001c0004t0052g0056 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.4038-246G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 34/34 | chr5 | 37292284 | ||||||
chr5:37292393
|
T | G | 5 | a0001c0002t0005g0266a0001c0002t0005g0267a0001c0002t0005g0268others(2): Show | 5 | HG02055.hp1 HG02647.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.4038-355A>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 34/34 | chr5 | 37292393 | ||||||
chr5:37292406
|
T | C | 112 | a0001c0002t0002g0073a0001c0002t0002g0074a0001c0002t0002g0076others(109): Show | 112 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.4038-368A>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 34/34 | chr5 | 37292406 | ||||||
chr5:37292494
|
T | A | 7 | a0001c0001t0001g0169a0001c0001t0001g0199a0001c0001t0001g0201others(4): Show | 7 | HG01891.hp1 HG02257.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.4037+385A>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 34/34 | chr5 | 37292494 | ||||||
chr5:37293036
|
T | C | 1 | a0001c0002t0005g0270 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3931-51A>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 33/34 | chr5 | 37293036 | ||||||
chr5:37293088
|
G | A | 2 | a0001c0001t0001g0143a0001c0001t0010g0129 | 2 | NA19067.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.3931-103C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 33/34 | chr5 | 37293088 | ||||||
chr5:37293113
|
A | G | 49 | a0001c0002t0002g0073a0001c0002t0002g0074a0001c0002t0002g0076others(46): Show | 49 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(46): Show |
intron_variant | MODIFIER | c.3931-128T>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 33/34 | chr5 | 37293113 | ||||||
chr5:37293249
|
C | T | 12 | a0001c0002t0004g0004a0001c0002t0004g0019a0001c0002t0004g0020others(9): Show | 12 | HG01192.hp2 HG01891.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.3931-264G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 33/34 | chr5 | 37293249 | ||||||
chr5:37293392
|
AC | A | 49 | a0001c0002t0002g0073a0001c0002t0002g0074a0001c0002t0002g0076others(46): Show | 49 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(46): Show |
intron_variant | MODIFIER | c.3931-408delG | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 33/34 | chr5 | 37293392 | ||||||
chr5:37293564
|
T | G | 4 | a0001c0002t0023g0031a0001c0002t0024g0032a0001c0002t0024g0033others(1): Show | 4 | HG02451.hp1 HG02572.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.3931-579A>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 33/34 | chr5 | 37293564 | ||||||
chr5:37293697
|
TTAAAGCA others(324): Show |
T | 112 | a0001c0002t0002g0073a0001c0002t0002g0074a0001c0002t0002g0076others(109): Show | 112 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.3930+301_3930+631d others(2): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 33/34 | chr5 | 37293697 | ||||||
chr5:37293826
|
C | T | 1 | a0001c0001t0001g0122 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.3930+503G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 33/34 | chr5 | 37293826 | ||||||
chr5:37293862
|
G | A | 10 | a0001c0003t0001g0165a0001c0003t0001g0170a0001c0003t0001g0174others(7): Show | 10 | HG00423.hp1 HG00673.hp2 HG02027.hp2 others(7): Show |
intron_variant | MODIFIER | c.3930+467C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 33/34 | chr5 | 37293862 | ||||||
chr5:37293993
|
G | A | 1 | a0001c0001t0012g0092 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.3930+336C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 33/34 | chr5 | 37293993 | ||||||
chr5:37294005
|
C | CAAAAAAA others(3): Show |
2 | a0001c0001t0001g0104a0001c0001t0001g0145 | 2 | HG01952.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.3930+314_3930+323d others(12): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 33/34 | chr5 | 37294005 | ||||||
chr5:37294005
|
C | CAAAAAAA others(4): Show |
1 | a0001c0001t0001g0134 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.3930+313_3930+323d others(13): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 33/34 | chr5 | 37294005 | ||||||
chr5:37294005
|
C | CAAAAAAA others(7): Show |
5 | a0001c0001t0001g0118a0001c0001t0001g0120a0001c0001t0001g0127others(2): Show | 5 | HG00639.hp2 HG01074.hp2 HG01123.hp1 others(2): Show |
intron_variant | MODIFIER | c.3930+310_3930+323d others(16): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 33/34 | chr5 | 37294005 | ||||||
chr5:37294005
|
C | CAAAAAAA others(8): Show |
3 | a0001c0001t0001g0140a0001c0001t0001g0144a0001c0001t0012g0092 | 3 | HG00642.hp1 HG01167.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.3930+309_3930+323d others(17): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 33/34 | chr5 | 37294005 | ||||||
chr5:37294005
|
C | CAAAAAAA others(9): Show |
3 | a0001c0001t0001g0156a0001c0001t0012g0111a0001c0001t0022g0099 | 3 | HG01358.hp1 HG02056.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.3930+308_3930+323d others(18): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 33/34 | chr5 | 37294005 | ||||||
chr5:37294005
|
C | CAAAAAAA others(10): Show |
1 | a0001c0001t0012g0093 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.3930+307_3930+323d others(19): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 33/34 | chr5 | 37294005 | ||||||
chr5:37294005
|
C | CAAAAAAA others(12): Show |
6 | a0001c0001t0001g0090a0001c0001t0001g0106a0001c0001t0001g0135others(3): Show | 6 | HG01975.hp2 NA18612.hp2 NA18961.hp1 others(3): Show |
intron_variant | MODIFIER | c.3930+305_3930+323d others(21): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 33/34 | chr5 | 37294005 | ||||||
chr5:37294005
|
C | CAAAAAAA others(13): Show |
5 | a0001c0001t0001g0109a0001c0001t0001g0115a0001c0001t0001g0142others(2): Show | 5 | HG03654.hp1 HG04184.hp2 NA18946.hp2 others(2): Show |
intron_variant | MODIFIER | c.3930+304_3930+323d others(22): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 33/34 | chr5 | 37294005 | ||||||
chr5:37294005
|
C | CAAAAAAA others(14): Show |
4 | a0001c0001t0001g0126a0001c0001t0001g0163a0001c0001t0010g0147others(1): Show | 4 | HG00323.hp1 HG02083.hp2 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.3930+303_3930+323d others(23): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 33/34 | chr5 | 37294005 | ||||||
chr5:37294005
|
C | CAAAAAAA others(15): Show |
3 | a0001c0001t0001g0160a0001c0001t0001g0162a0001c0001t0057g0299 | 3 | HG01433.hp2 NA18975.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.3930+302_3930+323d others(24): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 33/34 | chr5 | 37294005 | ||||||
chr5:37294005
|
C | CAAAAAAA others(16): Show |
1 | a0001c0001t0037g0091 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.3930+301_3930+323d others(25): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 33/34 | chr5 | 37294005 | ||||||
chr5:37294005
|
C | CAAAAAAA others(17): Show |
3 | a0001c0001t0001g0110a0001c0001t0001g0131a0001c0001t0001g0153 | 3 | HG00438.hp1 HG02132.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.3930+323_3930+324i others(26): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 33/34 | chr5 | 37294005 | ||||||
chr5:37294005
|
C | CAAAAAAA others(18): Show |
3 | a0001c0001t0001g0143a0001c0001t0001g0148a0001c0001t0026g0152 | 3 | HG00673.hp1 HG02004.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.3930+323_3930+324i others(27): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 33/34 | chr5 | 37294005 | ||||||
chr5:37294005
|
C | CAAAAAAA others(19): Show |
9 | a0001c0001t0001g0089a0001c0001t0001g0108a0001c0001t0001g0123others(6): Show | 9 | HG00140.hp2 HG01175.hp2 HG02074.hp1 others(6): Show |
intron_variant | MODIFIER | c.3930+323_3930+324i others(28): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 33/34 | chr5 | 37294005 | ||||||
chr5:37294005
|
C | CAAAAAAA others(20): Show |
7 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0124others(4): Show | 7 | HG00438.hp2 HG01361.hp1 HG02071.hp2 others(4): Show |
intron_variant | MODIFIER | c.3930+323_3930+324i others(29): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 33/34 | chr5 | 37294005 | ||||||
chr5:37294005
|
C | CAAAAAAA others(21): Show |
3 | a0001c0001t0001g0095a0001c0001t0001g0102a0001c0001t0001g0119 | 3 | NA18994.hp2 NA19004.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.3930+323_3930+324i others(30): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 33/34 | chr5 | 37294005 | ||||||
chr5:37294005
|
C | CAAAAAAA others(22): Show |
1 | a0001c0001t0001g0141 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.3930+323_3930+324i others(31): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 33/34 | chr5 | 37294005 | ||||||
chr5:37294005
|
C | CAAAAAAA others(23): Show |
3 | a0001c0001t0001g0130a0001c0001t0001g0132a0001c0001t0003g0157 | 3 | HG01256.hp1 HG02735.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.3930+323_3930+324i others(32): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 33/34 | chr5 | 37294005 | ||||||
chr5:37294005
|
C | CAAAAAAA others(24): Show |
2 | a0001c0001t0001g0149a0001c0001t0010g0097 | 2 | HG02165.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.3930+323_3930+324i others(33): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 33/34 | chr5 | 37294005 | ||||||
chr5:37294005
|
C | CAAAAAAA others(25): Show |
1 | a0001c0001t0001g0096 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.3930+323_3930+324i others(34): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 33/34 | chr5 | 37294005 | ||||||
chr5:37294005
|
C | CAAAAAAA others(26): Show |
1 | a0001c0001t0001g0103 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.3930+323_3930+324i others(35): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 33/34 | chr5 | 37294005 | ||||||
chr5:37294005
|
C | CAAAAAAA others(27): Show |
1 | a0001c0001t0018g0094 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.3930+323_3930+324i others(36): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 33/34 | chr5 | 37294005 | ||||||
chr5:37294005
|
C | CAAAAAAA others(28): Show |
1 | a0001c0001t0050g0125 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.3930+323_3930+324i others(37): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 33/34 | chr5 | 37294005 | ||||||
chr5:37294005
|
C | CAAAAAAA others(30): Show |
1 | a0001c0001t0001g0150 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.3930+323_3930+324i others(39): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 33/34 | chr5 | 37294005 | ||||||
chr5:37294005
|
CA | C | 92 | a0001c0001t0001g0168a0001c0001t0001g0192a0001c0001t0001g0193others(89): Show | 93 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(90): Show |
intron_variant | MODIFIER | c.3930+323delT | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 33/34 | chr5 | 37294005 | ||||||
chr5:37294005
|
CAA | C | 6 | a0001c0001t0001g0169a0001c0001t0001g0199a0001c0001t0001g0201others(3): Show | 6 | HG01069.hp2 HG01109.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.3930+322_3930+323d others(4): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 33/34 | chr5 | 37294005 | ||||||
chr5:37294024
|
A | AAAAAAAA others(19): Show |
2 | a0001c0001t0001g0114a0001c0001t0001g0121 | 2 | NA18960.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.3930+304_3930+305i others(28): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 33/34 | chr5 | 37294024 | ||||||
chr5:37294025
|
A | AAAAAAAA others(19): Show |
1 | a0001c0001t0001g0122 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.3930+303_3930+304i others(28): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 33/34 | chr5 | 37294025 | ||||||
chr5:37294025
|
A | T | 1 | a0001c0003t0001g0243 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.3930+304T>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 33/34 | chr5 | 37294025 | ||||||
chr5:37294268
|
A | G | 1 | a0001c0002t0002g0073 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.3930+61T>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 33/34 | chr5 | 37294268 | ||||||
chr5:37294294
|
G | T | 7 | a0001c0005t0009g0054a0001c0005t0009g0057a0001c0005t0009g0058others(4): Show | 7 | HG02145.hp1 HG02895.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.3930+35C>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 33/34 | chr5 | 37294294 | ||||||
chr5:37294597
|
G | GT | 10 | a0001c0001t0001g0103a0001c0001t0001g0150a0001c0001t0001g0249others(7): Show | 10 | HG00673.hp2 HG01261.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.3794-133dupA | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 32/34 | chr5 | 37294597 | ||||||
chr5:37294597
|
G | T | 1 | a0001c0006t0036g0046 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.3794-132C>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 32/34 | chr5 | 37294597 | ||||||
chr5:37294784
|
A | G | 2 | a0001c0001t0001g0131a0001c0001t0001g0153 | 2 | HG00438.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.3794-319T>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 32/34 | chr5 | 37294784 | ||||||
chr5:37294819
|
G | C | 1 | a0001c0011t0028g0003 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3794-354C>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 32/34 | chr5 | 37294819 | ||||||
chr5:37294886
|
T | C | 7 | a0001c0005t0009g0054a0001c0005t0009g0057a0001c0005t0009g0058others(4): Show | 7 | HG02145.hp1 HG02895.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.3794-421A>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 32/34 | chr5 | 37294886 | ||||||
chr5:37294930
|
A | G | 1 | a0001c0003t0001g0207 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.3794-465T>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 32/34 | chr5 | 37294930 | ||||||
chr5:37295193
|
C | T | 1 | a0001c0003t0005g0164 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.3794-728G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 32/34 | chr5 | 37295193 | ||||||
chr5:37295204
|
G | A | 23 | a0001c0002t0004g0004a0001c0002t0004g0019a0001c0002t0004g0020others(20): Show | 23 | HG01192.hp2 HG01243.hp2 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.3794-739C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 32/34 | chr5 | 37295204 | ||||||
chr5:37295218
|
C | T | 7 | a0001c0005t0009g0054a0001c0005t0009g0057a0001c0005t0009g0058others(4): Show | 7 | HG02145.hp1 HG02895.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.3794-753G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 32/34 | chr5 | 37295218 | ||||||
chr5:37295245
|
T | C | 107 | a0001c0002t0002g0073a0001c0002t0002g0074a0001c0002t0002g0076others(104): Show | 107 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.3794-780A>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 32/34 | chr5 | 37295245 | ||||||
chr5:37295281
|
G | A | 2 | a0001c0002t0002g0087a0001c0002t0014g0072 | 2 | HG00642.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.3794-816C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 32/34 | chr5 | 37295281 | ||||||
chr5:37295316
|
C | T | 1 | a0001c0002t0002g0087 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.3794-851G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 32/34 | chr5 | 37295316 | ||||||
chr5:37295368
|
G | A | 5 | a0001c0004t0011g0051a0001c0004t0011g0052a0001c0004t0011g0053others(2): Show | 5 | HG02257.hp1 HG02486.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.3794-903C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 32/34 | chr5 | 37295368 | ||||||
chr5:37295379
|
C | T | 2 | a0001c0006t0016g0044a0001c0006t0036g0046 | 2 | HG01261.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.3794-914G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 32/34 | chr5 | 37295379 | ||||||
chr5:37295393
|
C | G | 7 | a0001c0005t0009g0054a0001c0005t0009g0057a0001c0005t0009g0058others(4): Show | 7 | HG02145.hp1 HG02895.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.3794-928G>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 32/34 | chr5 | 37295393 | ||||||
chr5:37295401
|
A | C | 7 | a0001c0005t0009g0054a0001c0005t0009g0057a0001c0005t0009g0058others(4): Show | 7 | HG02145.hp1 HG02895.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.3794-936T>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 32/34 | chr5 | 37295401 | ||||||
chr5:37295429
|
T | C | 2 | a0001c0003t0001g0197a0001c0003t0001g0293 | 2 | HG02738.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.3794-964A>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 32/34 | chr5 | 37295429 | ||||||
chr5:37295464
|
G | A | 3 | a0001c0002t0002g0086a0001c0002t0002g0088a0001c0002t0014g0079 | 3 | HG01884.hp2 HG02723.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.3794-999C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 32/34 | chr5 | 37295464 | ||||||
chr5:37295465
|
C | T | 4 | a0001c0002t0023g0031a0001c0002t0024g0032a0001c0002t0024g0033others(1): Show | 4 | HG02451.hp1 HG02572.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.3794-1000G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 32/34 | chr5 | 37295465 | ||||||
chr5:37295490
|
G | A | 49 | a0001c0002t0002g0073a0001c0002t0002g0074a0001c0002t0002g0076others(46): Show | 49 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(46): Show |
intron_variant | MODIFIER | c.3794-1025C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 32/34 | chr5 | 37295490 | ||||||
chr5:37295566
|
A | G | 1 | a0001c0004t0011g0051 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3794-1101T>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 32/34 | chr5 | 37295566 | ||||||
chr5:37295576
|
A | G | 1 | a0001c0004t0011g0051 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3794-1111T>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 32/34 | chr5 | 37295576 | ||||||
chr5:37295576
|
AGCCGCCA others(33): Show |
A | 57 | a0001c0001t0001g0105a0001c0001t0001g0120a0001c0001t0001g0127others(54): Show | 57 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(54): Show |
intron_variant | MODIFIER | c.3794-1151_3794-111 others(44): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 32/34 | chr5 | 37295576 | ||||||
chr5:37295579
|
C | T | 2 | a0001c0002t0007g0040a0001c0002t0007g0048 | 2 | HG02280.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.3794-1114G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 32/34 | chr5 | 37295579 | ||||||
chr5:37295655
|
C | T | 16 | a0001c0002t0007g0030a0001c0002t0007g0036a0001c0002t0007g0037others(13): Show | 16 | HG01109.hp2 HG01243.hp1 HG01261.hp1 others(13): Show |
intron_variant | MODIFIER | c.3794-1190G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 32/34 | chr5 | 37295655 | ||||||
chr5:37295684
|
C | T | 28 | a0001c0002t0002g0073a0001c0002t0002g0074a0001c0002t0002g0076others(25): Show | 28 | HG00423.hp2 HG00642.hp2 HG01069.hp1 others(25): Show |
intron_variant | MODIFIER | c.3794-1219G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 32/34 | chr5 | 37295684 | ||||||
chr5:37295704
|
G | A | 5 | a0001c0005t0009g0057a0001c0005t0009g0061a0001c0005t0009g0062others(2): Show | 5 | HG02145.hp1 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.3794-1239C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 32/34 | chr5 | 37295704 | ||||||
chr5:37295708
|
G | A | 49 | a0001c0002t0002g0073a0001c0002t0002g0074a0001c0002t0002g0076others(46): Show | 49 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(46): Show |
intron_variant | MODIFIER | c.3794-1243C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 32/34 | chr5 | 37295708 | ||||||
chr5:37295721
|
C | T | 1 | a0001c0001t0026g0152 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.3794-1256G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 32/34 | chr5 | 37295721 | ||||||
chr5:37295780
|
T | TGTCTGAG others(33): Show |
1 | a0001c0003t0005g0167 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.3794-1355_3794-131 others(44): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 32/34 | chr5 | 37295780 | ||||||
chr5:37295815
|
C | T | 7 | a0001c0005t0009g0054a0001c0005t0009g0057a0001c0005t0009g0058others(4): Show | 7 | HG02145.hp1 HG02895.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.3794-1350G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 32/34 | chr5 | 37295815 | ||||||
chr5:37295826
|
A | G | 1 | a0001c0002t0055g0068 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.3794-1361T>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 32/34 | chr5 | 37295826 | ||||||
chr5:37295860
|
C | T | 14 | a0001c0001t0001g0168a0001c0001t0001g0192a0001c0001t0001g0194others(11): Show | 14 | HG01069.hp2 HG01993.hp1 HG02080.hp2 others(11): Show |
intron_variant | MODIFIER | c.3794-1395G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 32/34 | chr5 | 37295860 | ||||||
chr5:37295860
|
CGTCCGGG others(170): Show |
C | 2 | a0001c0004t0029g0002a0001c0011t0028g0003 | 2 | HG02809.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.3794-1572_3794-139 others(4): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 32/34 | chr5 | 37295860 | ||||||
chr5:37295876
|
T | G | 110 | a0001c0002t0002g0073a0001c0002t0002g0074a0001c0002t0002g0076others(107): Show | 110 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.3794-1411A>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 32/34 | chr5 | 37295876 | ||||||
chr5:37295928
|
G | A | 1 | a0001c0003t0001g0187 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.3794-1463C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 32/34 | chr5 | 37295928 | ||||||
chr5:37295928
|
GCCTCTGC others(170): Show |
G | 19 | a0001c0002t0006g0272a0001c0002t0006g0277a0001c0002t0006g0278others(16): Show | 19 | HG00099.hp1 HG00408.hp2 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.3794-1640_3794-146 others(4): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 32/34 | chr5 | 37295928 | ||||||
chr5:37295931
|
T | G | 2 | a0001c0001t0001g0123a0001c0001t0010g0097 | 2 | NA18955.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.3794-1466A>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 32/34 | chr5 | 37295931 | ||||||
chr5:37295932
|
C | T | 2 | a0001c0001t0001g0123a0001c0001t0010g0097 | 2 | NA18955.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.3794-1467G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 32/34 | chr5 | 37295932 | ||||||
chr5:37295966
|
C | G | 2 | a0001c0003t0001g0221a0001c0003t0039g0262 | 2 | HG03017.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.3794-1501G>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 32/34 | chr5 | 37295966 | ||||||
chr5:37295970
|
TGCCCGGC others(43): Show |
T | 2 | a0001c0003t0001g0221a0001c0003t0039g0262 | 2 | HG03017.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.3794-1555_3794-150 others(54): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 32/34 | chr5 | 37295970 | ||||||
chr5:37295992
|
G | A | 2 | a0001c0002t0015g0012a0001c0002t0033g0018 | 2 | HG02055.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.3794-1527C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 32/34 | chr5 | 37295992 | ||||||
chr5:37296037
|
T | C | 23 | a0001c0002t0004g0004a0001c0002t0004g0019a0001c0002t0004g0020others(20): Show | 23 | HG01192.hp2 HG01243.hp2 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.3794-1572A>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 32/34 | chr5 | 37296037 | ||||||
chr5:37296037
|
TGTCCGGG others(42): Show |
T | 1 | a0001c0001t0001g0110 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.3794-1621_3794-157 others(53): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 32/34 | chr5 | 37296037 | ||||||
chr5:37296073
|
C | T | 1 | a0001c0003t0001g0181 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.3794-1608G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 32/34 | chr5 | 37296073 | ||||||
chr5:37296085
|
C | A | 1 | a0001c0003t0001g0205 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.3794-1620G>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 32/34 | chr5 | 37296085 | ||||||
chr5:37296091
|
G | A | 16 | a0001c0002t0007g0030a0001c0002t0007g0036a0001c0002t0007g0037others(13): Show | 16 | HG01109.hp2 HG01243.hp1 HG01261.hp1 others(13): Show |
intron_variant | MODIFIER | c.3794-1626C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 32/34 | chr5 | 37296091 | ||||||
chr5:37296104
|
C | T | 1 | a0001c0001t0001g0153 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.3794-1639G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 32/34 | chr5 | 37296104 | ||||||
chr5:37296105
|
A | G | 3 | a0001c0001t0001g0153a0001c0004t0029g0002a0001c0011t0028g0003 | 3 | HG02132.hp1 HG02809.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.3794-1640T>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 32/34 | chr5 | 37296105 | ||||||
chr5:37296115
|
G | A | 1 | a0001c0001t0031g0154 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.3794-1650C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 32/34 | chr5 | 37296115 | ||||||
chr5:37296156
|
A | G | 2 | a0001c0001t0001g0101a0001c0001t0001g0118 | 2 | NA18983.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.3794-1691T>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 32/34 | chr5 | 37296156 | ||||||
chr5:37296213
|
T | C | 84 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0095others(81): Show | 84 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.3794-1748A>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 32/34 | chr5 | 37296213 | ||||||
chr5:37296262
|
A | G | 188 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0095others(185): Show | 188 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.3794-1797T>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 32/34 | chr5 | 37296262 | ||||||
chr5:37296286
|
A | G | 1 | a0001c0001t0021g0006 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.3794-1821T>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 32/34 | chr5 | 37296286 | ||||||
chr5:37296297
|
T | C | 73 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0095others(70): Show | 73 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.3794-1832A>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 32/34 | chr5 | 37296297 | ||||||
chr5:37296315
|
C | A | 77 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0095others(74): Show | 77 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.3794-1850G>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 32/34 | chr5 | 37296315 | ||||||
chr5:37296386
|
T | A | 1 | a0001c0001t0001g0150 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.3794-1921A>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 32/34 | chr5 | 37296386 | ||||||
chr5:37296453
|
T | G | 9 | a0001c0002t0008g0009a0001c0002t0008g0010a0001c0002t0008g0011others(6): Show | 9 | HG01243.hp2 HG02109.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.3794-1988A>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 32/34 | chr5 | 37296453 | ||||||
chr5:37296473
|
AGGCAGCA others(3): Show |
A | 2 | a0001c0004t0029g0002a0001c0011t0028g0003 | 2 | HG02809.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.3794-2018_3794-200 others(14): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 32/34 | chr5 | 37296473 | ||||||
chr5:37296495
|
T | C | 196 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0095others(193): Show | 196 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.3794-2030A>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 32/34 | chr5 | 37296495 | ||||||
chr5:37296545
|
G | A | 1 | a0001c0004t0052g0056 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3794-2080C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 32/34 | chr5 | 37296545 | ||||||
chr5:37296556
|
C | CCGGAA | 50 | a0001c0002t0002g0073a0001c0002t0002g0074a0001c0002t0002g0076others(47): Show | 50 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(47): Show |
intron_variant | MODIFIER | c.3794-2092_3794-209 others(9): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 32/34 | chr5 | 37296556 | ||||||
chr5:37296557
|
A | G | 50 | a0001c0002t0002g0073a0001c0002t0002g0074a0001c0002t0002g0076others(47): Show | 50 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(47): Show |
intron_variant | MODIFIER | c.3794-2092T>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 32/34 | chr5 | 37296557 | ||||||
chr5:37296688
|
A | AAAAT | 6 | a0001c0001t0001g0090a0001c0002t0004g0025a0001c0002t0025g0279others(3): Show | 7 | HG00099.hp2 HG01975.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.3793+2176_3793+217 others(8): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 32/34 | chr5 | 37296688 | ||||||
chr5:37296688
|
A | AAAATAAA others(1): Show |
21 | a0001c0002t0004g0004a0001c0002t0004g0019a0001c0002t0004g0020others(18): Show | 21 | HG01192.hp2 HG01346.hp1 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.3793+2172_3793+217 others(12): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 32/34 | chr5 | 37296688 | ||||||
chr5:37296688
|
A | AAAATAAA others(5): Show |
22 | a0001c0002t0004g0021a0001c0002t0007g0030a0001c0002t0007g0036others(19): Show | 22 | HG01109.hp2 HG01243.hp1 HG01261.hp1 others(19): Show |
intron_variant | MODIFIER | c.3793+2168_3793+217 others(16): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 32/34 | chr5 | 37296688 | ||||||
chr5:37296688
|
A | AAAATAAA others(9): Show |
10 | a0001c0002t0007g0040a0001c0002t0007g0048a0001c0002t0008g0009others(7): Show | 10 | HG01243.hp2 HG02109.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.3793+2164_3793+217 others(20): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 32/34 | chr5 | 37296688 | ||||||
chr5:37296688
|
A | AAAATAAA others(13): Show |
2 | a0001c0002t0007g0038a0001c0005t0009g0063 | 2 | HG02258.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.3793+2160_3793+217 others(24): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 32/34 | chr5 | 37296688 | ||||||
chr5:37296718
|
G | C | 1 | a0001c0001t0001g0132 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.3793+2150C>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 32/34 | chr5 | 37296718 | ||||||
chr5:37296853
|
G | C | 4 | a0001c0002t0008g0009a0001c0002t0008g0010a0001c0002t0008g0015others(1): Show | 4 | HG02109.hp2 HG02922.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.3793+2015C>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 32/34 | chr5 | 37296853 | ||||||
chr5:37296913
|
G | A | 5 | a0001c0002t0005g0266a0001c0002t0005g0267a0001c0002t0005g0268others(2): Show | 5 | HG02055.hp1 HG02647.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.3793+1955C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 32/34 | chr5 | 37296913 | ||||||
chr5:37296917
|
C | T | 7 | a0001c0005t0009g0054a0001c0005t0009g0057a0001c0005t0009g0058others(4): Show | 7 | HG02145.hp1 HG02895.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.3793+1951G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 32/34 | chr5 | 37296917 | ||||||
chr5:37296955
|
T | A | 4 | a0001c0002t0008g0009a0001c0002t0008g0010a0001c0002t0008g0015others(1): Show | 4 | HG02109.hp2 HG02922.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.3793+1913A>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 32/34 | chr5 | 37296955 | ||||||
chr5:37297039
|
T | C | 112 | a0001c0002t0002g0073a0001c0002t0002g0074a0001c0002t0002g0076others(109): Show | 112 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.3793+1829A>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 32/34 | chr5 | 37297039 | ||||||
chr5:37297168
|
C | T | 49 | a0001c0002t0002g0073a0001c0002t0002g0074a0001c0002t0002g0076others(46): Show | 49 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(46): Show |
intron_variant | MODIFIER | c.3793+1700G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 32/34 | chr5 | 37297168 | ||||||
chr5:37297211
|
G | A | 49 | a0001c0002t0002g0073a0001c0002t0002g0074a0001c0002t0002g0076others(46): Show | 49 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(46): Show |
intron_variant | MODIFIER | c.3793+1657C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 32/34 | chr5 | 37297211 | ||||||
chr5:37297369
|
A | G | 49 | a0001c0002t0002g0073a0001c0002t0002g0074a0001c0002t0002g0076others(46): Show | 49 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(46): Show |
intron_variant | MODIFIER | c.3793+1499T>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 32/34 | chr5 | 37297369 | ||||||
chr5:37297379
|
G | GTTAT | 7 | a0001c0005t0009g0054a0001c0005t0009g0057a0001c0005t0009g0058others(4): Show | 7 | HG02145.hp1 HG02895.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.3793+1485_3793+148 others(8): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 32/34 | chr5 | 37297379 | ||||||
chr5:37297441
|
C | T | 2 | a0001c0002t0020g0281a0001c0002t0020g0289 | 2 | HG00099.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.3793+1427G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 32/34 | chr5 | 37297441 | ||||||
chr5:37297445
|
C | T | 5 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0003g0098others(2): Show | 5 | HG00438.hp2 HG02074.hp1 NA18953.hp2 others(2): Show |
intron_variant | MODIFIER | c.3793+1423G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 32/34 | chr5 | 37297445 | ||||||
chr5:37297626
|
C | G | 18 | a0001c0001t0001g0168a0001c0001t0001g0192a0001c0001t0001g0193others(15): Show | 18 | HG01069.hp2 HG01361.hp2 HG01517.hp2 others(15): Show |
intron_variant | MODIFIER | c.3793+1242G>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 32/34 | chr5 | 37297626 | ||||||
chr5:37297627
|
G | T | 1 | a0001c0002t0008g0014 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3793+1241C>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 32/34 | chr5 | 37297627 | ||||||
chr5:37297813
|
C | T | 1 | a0009c0012t0008g0013 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.3793+1055G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 32/34 | chr5 | 37297813 | ||||||
chr5:37297859
|
TTTATTTC others(8): Show |
T | 25 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0192others(22): Show | 25 | HG01069.hp2 HG01361.hp2 HG01517.hp2 others(22): Show |
intron_variant | MODIFIER | c.3793+994_3793+1008 others(18): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 32/34 | chr5 | 37297859 | ||||||
chr5:37297876
|
C | G | 25 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0192others(22): Show | 25 | HG01069.hp2 HG01361.hp2 HG01517.hp2 others(22): Show |
intron_variant | MODIFIER | c.3793+992G>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 32/34 | chr5 | 37297876 | ||||||
chr5:37297932
|
T | C | 1 | a0001c0003t0001g0177 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.3793+936A>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 32/34 | chr5 | 37297932 | ||||||
chr5:37297934
|
GA | G | 158 | a0001c0001t0001g0090a0001c0001t0001g0095a0001c0001t0001g0105others(155): Show | 158 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(155): Show |
intron_variant | MODIFIER | c.3793+933delT | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 32/34 | chr5 | 37297934 | ||||||
chr5:37298237
|
C | CA | 12 | a0001c0001t0001g0194a0001c0002t0002g0081a0001c0002t0002g0088others(9): Show | 12 | HG02055.hp2 HG02080.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.3793+630dupT | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 32/34 | chr5 | 37298237 | ||||||
chr5:37298237
|
CA | C | 17 | a0001c0001t0001g0246a0001c0001t0001g0247a0001c0001t0022g0099others(14): Show | 17 | HG01192.hp1 HG01192.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.3793+630delT | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 32/34 | chr5 | 37298237 | ||||||
chr5:37298779
|
T | C | 7 | a0001c0005t0009g0054a0001c0005t0009g0057a0001c0005t0009g0058others(4): Show | 7 | HG02145.hp1 HG02895.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.3793+89A>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 32/34 | chr5 | 37298779 | ||||||
chr5:37298985
|
C | A | 1 | a0001c0003t0001g0183 | 1 | NA19087.hp2 | splice_region_variant&intron_variant | LOW | c.3683-7G>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 31/34 | chr5 | 37298985 | ||||||
chr5:37299060
|
A | G | 9 | a0001c0004t0011g0051a0001c0004t0011g0052a0001c0004t0011g0053others(6): Show | 9 | HG02257.hp1 HG02486.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.3683-82T>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 31/34 | chr5 | 37299060 | ||||||
chr5:37299154
|
G | A | 2 | a0001c0003t0001g0165a0001c0003t0001g0176 | 2 | HG00423.hp1 HG02074.hp2 |
intron_variant | MODIFIER | c.3683-176C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 31/34 | chr5 | 37299154 | ||||||
chr5:37299161
|
T | C | 2 | a0001c0001t0001g0126a0001c0001t0038g0117 | 2 | HG02083.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.3683-183A>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 31/34 | chr5 | 37299161 | ||||||
chr5:37299298
|
A | AC | 4 | a0001c0002t0023g0031a0001c0002t0024g0032a0001c0002t0024g0033others(1): Show | 4 | HG02451.hp1 HG02572.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.3682+149dupG | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 31/34 | chr5 | 37299298 | ||||||
chr5:37299681
|
T | C | 9 | a0001c0004t0011g0051a0001c0004t0011g0052a0001c0004t0011g0053others(6): Show | 9 | HG02257.hp1 HG02486.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.3562-113A>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 30/34 | chr5 | 37299681 | ||||||
chr5:37299692
|
A | C | 26 | a0001c0002t0002g0073a0001c0002t0002g0074a0001c0002t0002g0076others(23): Show | 26 | HG00423.hp2 HG00642.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.3562-124T>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 30/34 | chr5 | 37299692 | ||||||
chr5:37299722
|
A | G | 9 | a0001c0004t0011g0051a0001c0004t0011g0052a0001c0004t0011g0053others(6): Show | 9 | HG02257.hp1 HG02486.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.3562-154T>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 30/34 | chr5 | 37299722 | ||||||
chr5:37299877
|
TA | T | 104 | a0001c0002t0002g0073a0001c0002t0002g0074a0001c0002t0002g0076others(101): Show | 104 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.3562-310delT | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 30/34 | chr5 | 37299877 | ||||||
chr5:37299877
|
TAA | T | 7 | a0001c0005t0009g0054a0001c0005t0009g0057a0001c0005t0009g0058others(4): Show | 7 | HG02145.hp1 HG02895.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.3562-311_3562-310d others(4): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 30/34 | chr5 | 37299877 | ||||||
chr5:37299991
|
C | T | 1 | a0001c0004t0053g0265 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3562-423G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 30/34 | chr5 | 37299991 | ||||||
chr5:37300025
|
C | CA | 11 | a0001c0001t0001g0133a0001c0002t0002g0077a0001c0002t0008g0009others(8): Show | 11 | HG01243.hp2 HG02109.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.3562-458dupT | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 30/34 | chr5 | 37300025 | ||||||
chr5:37300193
|
T | C | 49 | a0001c0002t0002g0073a0001c0002t0002g0074a0001c0002t0002g0076others(46): Show | 49 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(46): Show |
intron_variant | MODIFIER | c.3562-625A>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 30/34 | chr5 | 37300193 | ||||||
chr5:37300215
|
TAC | T | 5 | a0001c0002t0005g0266a0001c0002t0005g0267a0001c0002t0005g0268others(2): Show | 5 | HG02055.hp1 HG02647.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.3562-649_3562-648d others(4): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 30/34 | chr5 | 37300215 | ||||||
chr5:37300494
|
CAA | C | 103 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0095others(100): Show | 103 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.3562-928_3562-927d others(4): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 30/34 | chr5 | 37300494 | ||||||
chr5:37300503
|
T | G | 7 | a0001c0005t0009g0054a0001c0005t0009g0057a0001c0005t0009g0058others(4): Show | 7 | HG02145.hp1 HG02895.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.3561+934A>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 30/34 | chr5 | 37300503 | ||||||
chr5:37300556
|
G | C | 73 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0095others(70): Show | 73 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.3561+881C>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 30/34 | chr5 | 37300556 | ||||||
chr5:37300659
|
G | GT | 9 | a0001c0001t0001g0194a0001c0003t0001g0183a0001c0005t0009g0054others(6): Show | 9 | HG02080.hp2 HG02145.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.3561+777dupA | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 30/34 | chr5 | 37300659 | ||||||
chr5:37300687
|
C | CA | 5 | a0001c0004t0011g0051a0001c0004t0011g0052a0001c0004t0011g0053others(2): Show | 5 | HG02257.hp1 HG02486.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.3561+749dupT | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 30/34 | chr5 | 37300687 | ||||||
chr5:37300822
|
A | AT | 12 | a0001c0001t0001g0105a0001c0001t0001g0109a0001c0001t0001g0162others(9): Show | 12 | HG00323.hp1 HG00408.hp1 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.3561+614dupA | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 30/34 | chr5 | 37300822 | ||||||
chr5:37300822
|
AT | A | 32 | a0001c0001t0001g0115a0001c0001t0001g0120a0001c0001t0001g0140others(29): Show | 32 | HG01069.hp2 HG01074.hp2 HG01167.hp2 others(29): Show |
intron_variant | MODIFIER | c.3561+614delA | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 30/34 | chr5 | 37300822 | ||||||
chr5:37300843
|
T | C | 4 | a0001c0002t0023g0031a0001c0002t0024g0032a0001c0002t0024g0033others(1): Show | 4 | HG02451.hp1 HG02572.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.3561+594A>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 30/34 | chr5 | 37300843 | ||||||
chr5:37301065
|
C | G | 1 | a0001c0001t0042g0113 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.3561+372G>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 30/34 | chr5 | 37301065 | ||||||
chr5:37301235
|
C | T | 1 | a0001c0002t0014g0084 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3561+202G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 30/34 | chr5 | 37301235 | ||||||
chr5:37301350
|
T | C | 7 | a0001c0005t0009g0054a0001c0005t0009g0057a0001c0005t0009g0058others(4): Show | 7 | HG02145.hp1 HG02895.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.3561+87A>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 30/34 | chr5 | 37301350 | ||||||
chr5:37301659
|
A | C | 2 | a0001c0003t0001g0179a0001c0003t0001g0215 | 2 | NA18960.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.3448-109T>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 29/34 | chr5 | 37301659 | ||||||
chr5:37301702
|
C | T | 4 | a0001c0002t0023g0031a0001c0002t0024g0032a0001c0002t0024g0033others(1): Show | 4 | HG02451.hp1 HG02572.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.3448-152G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 29/34 | chr5 | 37301702 | ||||||
chr5:37301794
|
G | A | 3 | a0001c0002t0002g0086a0001c0002t0002g0088a0001c0002t0014g0079 | 3 | HG01884.hp2 HG02723.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.3448-244C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 29/34 | chr5 | 37301794 | ||||||
chr5:37301822
|
T | C | 2 | a0001c0002t0006g0277a0001c0002t0006g0285 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.3448-272A>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 29/34 | chr5 | 37301822 | ||||||
chr5:37301875
|
G | A | 2 | a0001c0003t0001g0184a0001c0003t0010g0188 | 2 | NA18956.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.3448-325C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 29/34 | chr5 | 37301875 | ||||||
chr5:37301965
|
C | T | 49 | a0001c0002t0002g0073a0001c0002t0002g0074a0001c0002t0002g0076others(46): Show | 49 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(46): Show |
intron_variant | MODIFIER | c.3448-415G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 29/34 | chr5 | 37301965 | ||||||
chr5:37302079
|
CT | C | 16 | a0001c0002t0007g0030a0001c0002t0007g0036a0001c0002t0007g0037others(13): Show | 16 | HG01109.hp2 HG01243.hp1 HG01261.hp1 others(13): Show |
intron_variant | MODIFIER | c.3448-530delA | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 29/34 | chr5 | 37302079 | ||||||
chr5:37302105
|
T | C | 7 | a0001c0005t0009g0054a0001c0005t0009g0057a0001c0005t0009g0058others(4): Show | 7 | HG02145.hp1 HG02895.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.3448-555A>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 29/34 | chr5 | 37302105 | ||||||
chr5:37302232
|
T | A | 6 | a0001c0004t0011g0051a0001c0004t0011g0052a0001c0004t0011g0053others(3): Show | 6 | HG02257.hp1 HG02486.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.3447+547A>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 29/34 | chr5 | 37302232 | ||||||
chr5:37302314
|
C | A | 1 | a0001c0001t0030g0202 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3447+465G>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 29/34 | chr5 | 37302314 | ||||||
chr5:37302345
|
G | A | 26 | a0001c0002t0004g0004a0001c0002t0004g0019a0001c0002t0004g0020others(23): Show | 26 | HG01192.hp2 HG01243.hp2 HG01346.hp1 others(23): Show |
intron_variant | MODIFIER | c.3447+434C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 29/34 | chr5 | 37302345 | ||||||
chr5:37302401
|
TC | T | 7 | a0001c0005t0009g0054a0001c0005t0009g0057a0001c0005t0009g0058others(4): Show | 7 | HG02145.hp1 HG02895.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.3447+377delG | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 29/34 | chr5 | 37302401 | ||||||
chr5:37302402
|
C | T | 100 | a0001c0002t0002g0073a0001c0002t0002g0074a0001c0002t0002g0076others(97): Show | 100 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.3447+377G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 29/34 | chr5 | 37302402 | ||||||
chr5:37302426
|
A | C | 9 | a0001c0004t0011g0051a0001c0004t0011g0052a0001c0004t0011g0053others(6): Show | 9 | HG02257.hp1 HG02486.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.3447+353T>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 29/34 | chr5 | 37302426 | ||||||
chr5:37302428
|
G | C | 2 | a0002c0008t0001g0295a0002c0008t0001g0296 | 2 | NA18953.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.3447+351C>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 29/34 | chr5 | 37302428 | ||||||
chr5:37302432
|
C | T | 1 | a0001c0002t0006g0272 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.3447+347G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 29/34 | chr5 | 37302432 | ||||||
chr5:37302968
|
A | G | 5 | a0001c0004t0011g0051a0001c0004t0011g0052a0001c0004t0011g0053others(2): Show | 5 | HG02257.hp1 HG02486.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.3318-60T>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 28/34 | chr5 | 37302968 | ||||||
chr5:37302969
|
C | T | 8 | a0001c0002t0007g0030a0001c0002t0007g0036a0001c0002t0007g0037others(5): Show | 8 | HG01109.hp2 HG02258.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.3318-61G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 28/34 | chr5 | 37302969 | ||||||
chr5:37302970
|
G | A | 3 | a0001c0001t0001g0169a0001c0001t0001g0199a0001c0001t0001g0201 | 3 | HG01891.hp1 HG02257.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.3318-62C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 28/34 | chr5 | 37302970 | ||||||
chr5:37303021
|
A | C | 1 | a0001c0002t0008g0014 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3318-113T>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 28/34 | chr5 | 37303021 | ||||||
chr5:37303035
|
T | C | 1 | a0001c0001t0001g0130 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.3318-127A>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 28/34 | chr5 | 37303035 | ||||||
chr5:37303776
|
C | T | 16 | a0001c0002t0007g0030a0001c0002t0007g0036a0001c0002t0007g0037others(13): Show | 16 | HG01109.hp2 HG01243.hp1 HG01261.hp1 others(13): Show |
intron_variant | MODIFIER | c.3163-362G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 27/34 | chr5 | 37303776 | ||||||
chr5:37303903
|
T | C | 1 | a0001c0002t0024g0032 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3163-489A>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 27/34 | chr5 | 37303903 | ||||||
chr5:37303932
|
T | C | 2 | a0001c0002t0027g0034a0001c0002t0027g0045 | 2 | HG01243.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.3163-518A>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 27/34 | chr5 | 37303932 | ||||||
chr5:37303939
|
C | T | 3 | a0001c0002t0017g0041a0001c0002t0017g0042a0001c0010t0017g0035 | 3 | HG01346.hp1 HG02922.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.3163-525G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 27/34 | chr5 | 37303939 | ||||||
chr5:37303999
|
G | A | 1 | a0001c0002t0055g0068 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.3163-585C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 27/34 | chr5 | 37303999 | ||||||
chr5:37304000
|
C | A | 1 | a0001c0002t0055g0068 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.3163-586G>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 27/34 | chr5 | 37304000 | ||||||
chr5:37304029
|
C | G | 23 | a0001c0002t0006g0272a0001c0002t0006g0277a0001c0002t0006g0278others(20): Show | 23 | HG00099.hp1 HG00408.hp2 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.3163-615G>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 27/34 | chr5 | 37304029 | ||||||
chr5:37304077
|
G | A | 1 | a0001c0003t0001g0239 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.3162+662C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 27/34 | chr5 | 37304077 | ||||||
chr5:37304078
|
T | G | 35 | a0001c0002t0002g0073a0001c0002t0002g0074a0001c0002t0002g0076others(32): Show | 35 | HG00423.hp2 HG00642.hp2 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.3162+661A>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 27/34 | chr5 | 37304078 | ||||||
chr5:37304083
|
A | G | 4 | a0001c0002t0023g0031a0001c0002t0024g0032a0001c0002t0024g0033others(1): Show | 4 | HG02451.hp1 HG02572.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.3162+656T>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 27/34 | chr5 | 37304083 | ||||||
chr5:37304102
|
T | A | 2 | a0001c0001t0001g0246a0001c0001t0001g0247 | 2 | NA18952.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.3162+637A>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 27/34 | chr5 | 37304102 | ||||||
chr5:37304248
|
T | C | 1 | a0001c0002t0013g0066 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.3162+491A>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 27/34 | chr5 | 37304248 | ||||||
chr5:37304249
|
C | CA | 14 | a0001c0001t0001g0168a0001c0001t0001g0256a0001c0001t0012g0093others(11): Show | 14 | HG00735.hp2 HG01069.hp2 HG02074.hp2 others(11): Show |
intron_variant | MODIFIER | c.3162+489dupT | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 27/34 | chr5 | 37304249 | ||||||
chr5:37304268
|
AAAAAAG | A | 22 | a0001c0002t0002g0073a0001c0002t0002g0074a0001c0002t0002g0076others(19): Show | 22 | HG00423.hp2 HG00642.hp2 HG01069.hp1 others(19): Show |
intron_variant | MODIFIER | c.3162+465_3162+470d others(8): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 27/34 | chr5 | 37304268 | ||||||
chr5:37304269
|
AAAAAG | A | 10 | a0001c0002t0013g0067a0001c0002t0013g0069a0001c0002t0013g0071others(7): Show | 10 | HG01257.hp2 HG01993.hp2 HG02004.hp1 others(7): Show |
intron_variant | MODIFIER | c.3162+465_3162+469d others(7): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 27/34 | chr5 | 37304269 | ||||||
chr5:37304272
|
AAG | A | 19 | a0001c0002t0005g0267a0001c0002t0005g0268a0001c0002t0005g0269others(16): Show | 19 | HG01109.hp2 HG01243.hp1 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.3162+465_3162+466d others(4): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 27/34 | chr5 | 37304272 | ||||||
chr5:37304273
|
AG | A | 98 | a0001c0001t0001g0090a0001c0001t0001g0095a0001c0001t0001g0100others(95): Show | 98 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.3162+465delC | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 27/34 | chr5 | 37304273 | ||||||
chr5:37304274
|
G | A | 147 | a0001c0001t0001g0089a0001c0001t0001g0096a0001c0001t0001g0119others(144): Show | 148 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(145): Show |
intron_variant | MODIFIER | c.3162+465C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 27/34 | chr5 | 37304274 | ||||||
chr5:37304422
|
G | C | 1 | a0001c0003t0005g0167 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.3162+317C>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 27/34 | chr5 | 37304422 | ||||||
chr5:37304445
|
C | T | 23 | a0001c0002t0006g0272a0001c0002t0006g0277a0001c0002t0006g0278others(20): Show | 23 | HG00099.hp1 HG00408.hp2 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.3162+294G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 27/34 | chr5 | 37304445 | ||||||
chr5:37304500
|
T | C | 1 | a0001c0001t0001g0108 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3162+239A>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 27/34 | chr5 | 37304500 | ||||||
chr5:37304725
|
A | G | 7 | a0001c0005t0009g0054a0001c0005t0009g0057a0001c0005t0009g0058others(4): Show | 7 | HG02145.hp1 HG02895.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.3162+14T>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 27/34 | chr5 | 37304725 | ||||||
chr5:37304959
|
A | G | 2 | a0001c0001t0021g0006a0001c0001t0021g0007 | 2 | HG02559.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.3057+98T>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 26/34 | chr5 | 37304959 | ||||||
chr5:37305249
|
C | G | 2 | a0001c0005t0009g0054a0001c0005t0009g0058 | 2 | HG02965.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2904-39G>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 25/34 | chr5 | 37305249 | ||||||
chr5:37305366
|
G | A | 1 | a0001c0001t0010g0147 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.2904-156C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 25/34 | chr5 | 37305366 | ||||||
chr5:37305373
|
C | T | 1 | a0001c0003t0001g0173 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.2904-163G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 25/34 | chr5 | 37305373 | ||||||
chr5:37305387
|
A | C | 1 | a0001c0003t0039g0262 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2904-177T>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 25/34 | chr5 | 37305387 | ||||||
chr5:37305390
|
CA | C | 112 | a0001c0002t0002g0073a0001c0002t0002g0074a0001c0002t0002g0076others(109): Show | 112 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.2904-181delT | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 25/34 | chr5 | 37305390 | ||||||
chr5:37305474
|
G | T | 4 | a0001c0002t0023g0031a0001c0002t0024g0032a0001c0002t0024g0033others(1): Show | 4 | HG02451.hp1 HG02572.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.2904-264C>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 25/34 | chr5 | 37305474 | ||||||
chr5:37305511
|
G | A | 1 | a0001c0003t0001g0173 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.2904-301C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 25/34 | chr5 | 37305511 | ||||||
chr5:37305546
|
G | A | 4 | a0001c0002t0005g0267a0001c0002t0005g0268a0001c0002t0005g0269others(1): Show | 4 | HG02055.hp1 HG03041.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.2904-336C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 25/34 | chr5 | 37305546 | ||||||
chr5:37305671
|
C | A | 1 | a0001c0004t0052g0056 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2904-461G>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 25/34 | chr5 | 37305671 | ||||||
chr5:37305682
|
A | G | 2 | a0001c0002t0004g0028a0001c0002t0015g0029 | 2 | HG01192.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.2904-472T>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 25/34 | chr5 | 37305682 | ||||||
chr5:37305912
|
A | C | 2 | a0001c0003t0001g0207a0001c0003t0001g0263 | 2 | HG02040.hp1 HG02071.hp1 |
intron_variant | MODIFIER | c.2904-702T>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 25/34 | chr5 | 37305912 | ||||||
chr5:37305954
|
T | C | 35 | a0001c0002t0002g0073a0001c0002t0002g0074a0001c0002t0002g0076others(32): Show | 35 | HG00423.hp2 HG00642.hp2 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.2904-744A>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 25/34 | chr5 | 37305954 | ||||||
chr5:37306117
|
G | T | 25 | a0001c0001t0012g0092a0001c0001t0042g0113a0001c0002t0006g0272others(22): Show | 25 | HG00099.hp1 HG00408.hp2 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.2904-907C>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 25/34 | chr5 | 37306117 | ||||||
chr5:37306240
|
G | GA | 7 | a0001c0001t0001g0169a0001c0001t0001g0199a0001c0001t0001g0201others(4): Show | 7 | HG01891.hp1 HG02257.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.2904-1031dupT | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 25/34 | chr5 | 37306240 | ||||||
chr5:37306256
|
C | T | 1 | a0001c0003t0005g0167 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.2903+1041G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 25/34 | chr5 | 37306256 | ||||||
chr5:37306328
|
A | G | 16 | a0001c0002t0007g0030a0001c0002t0007g0036a0001c0002t0007g0037others(13): Show | 16 | HG01109.hp2 HG01243.hp1 HG01261.hp1 others(13): Show |
intron_variant | MODIFIER | c.2903+969T>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 25/34 | chr5 | 37306328 | ||||||
chr5:37306424
|
C | CA | 5 | a0001c0002t0006g0278a0001c0002t0006g0282a0001c0002t0006g0283others(2): Show | 5 | HG00408.hp2 NA18939.hp2 NA18954.hp1 others(2): Show |
intron_variant | MODIFIER | c.2903+872dupT | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 25/34 | chr5 | 37306424 | ||||||
chr5:37306456
|
T | A | 1 | a0001c0003t0001g0207 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2903+841A>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 25/34 | chr5 | 37306456 | ||||||
chr5:37306560
|
C | T | 1 | a0001c0001t0038g0117 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2903+737G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 25/34 | chr5 | 37306560 | ||||||
chr5:37306563
|
G | A | 1 | a0001c0003t0001g0263 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2903+734C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 25/34 | chr5 | 37306563 | ||||||
chr5:37306602
|
G | A | 23 | a0001c0002t0006g0272a0001c0002t0006g0277a0001c0002t0006g0278others(20): Show | 23 | HG00099.hp1 HG00408.hp2 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.2903+695C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 25/34 | chr5 | 37306602 | ||||||
chr5:37306619
|
C | A | 1 | a0001c0003t0001g0165 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.2903+678G>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 25/34 | chr5 | 37306619 | ||||||
chr5:37306620
|
A | G | 26 | a0001c0002t0004g0004a0001c0002t0004g0019a0001c0002t0004g0020others(23): Show | 26 | HG01192.hp2 HG01243.hp2 HG01346.hp1 others(23): Show |
intron_variant | MODIFIER | c.2903+677T>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 25/34 | chr5 | 37306620 | ||||||
chr5:37306826
|
A | C | 35 | a0001c0002t0002g0073a0001c0002t0002g0074a0001c0002t0002g0076others(32): Show | 35 | HG00423.hp2 HG00642.hp2 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.2903+471T>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 25/34 | chr5 | 37306826 | ||||||
chr5:37306836
|
C | T | 23 | a0001c0002t0004g0004a0001c0002t0004g0019a0001c0002t0004g0020others(20): Show | 23 | HG01192.hp2 HG01243.hp2 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.2903+461G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 25/34 | chr5 | 37306836 | ||||||
chr5:37306902
|
C | A | 23 | a0001c0002t0004g0004a0001c0002t0004g0019a0001c0002t0004g0020others(20): Show | 23 | HG01192.hp2 HG01243.hp2 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.2903+395G>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 25/34 | chr5 | 37306902 | ||||||
chr5:37306925
|
C | T | 4 | a0001c0002t0023g0031a0001c0002t0024g0032a0001c0002t0024g0033others(1): Show | 4 | HG02451.hp1 HG02572.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.2903+372G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 25/34 | chr5 | 37306925 | ||||||
chr5:37307028
|
T | C | 1 | a0001c0002t0008g0014 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2903+269A>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 25/34 | chr5 | 37307028 | ||||||
chr5:37307082
|
C | T | 7 | a0001c0005t0009g0054a0001c0005t0009g0057a0001c0005t0009g0058others(4): Show | 7 | HG02145.hp1 HG02895.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.2903+215G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 25/34 | chr5 | 37307082 | ||||||
chr5:37307197
|
C | CA | 11 | a0001c0001t0001g0120a0001c0001t0001g0127a0001c0001t0001g0140others(8): Show | 11 | HG00639.hp2 HG00642.hp1 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.2903+99dupT | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 25/34 | chr5 | 37307197 | ||||||
chr5:37307197
|
C | CAAA | 15 | a0001c0002t0007g0030a0001c0002t0007g0036a0001c0002t0007g0037others(12): Show | 15 | HG01109.hp2 HG01243.hp1 HG01261.hp1 others(12): Show |
intron_variant | MODIFIER | c.2903+97_2903+99dup others(3): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 25/34 | chr5 | 37307197 | ||||||
chr5:37307287
|
T | C | 23 | a0001c0002t0006g0272a0001c0002t0006g0277a0001c0002t0006g0278others(20): Show | 23 | HG00099.hp1 HG00408.hp2 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.2903+10A>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 25/34 | chr5 | 37307287 | ||||||
chr5:37307738
|
A | G | 1 | a0001c0001t0001g0142 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2768-306T>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 24/34 | chr5 | 37307738 | ||||||
chr5:37307745
|
A | C | 1 | a0001c0003t0001g0198 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2768-313T>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 24/34 | chr5 | 37307745 | ||||||
chr5:37307812
|
C | G | 6 | a0001c0003t0001g0175a0001c0003t0001g0191a0001c0003t0001g0225others(3): Show | 6 | HG01358.hp2 HG01433.hp1 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.2768-380G>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 24/34 | chr5 | 37307812 | ||||||
chr5:37307832
|
G | C | 2 | a0001c0003t0019g0001a0001c0003t0019g0212 | 3 | HG00099.hp2 HG02683.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.2768-400C>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 24/34 | chr5 | 37307832 | ||||||
chr5:37307848
|
C | T | 1 | a0001c0001t0030g0202 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2768-416G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 24/34 | chr5 | 37307848 | ||||||
chr5:37307921
|
C | CA | 41 | a0001c0002t0004g0004a0001c0002t0004g0019a0001c0002t0004g0020others(38): Show | 41 | HG01109.hp2 HG01192.hp2 HG01243.hp1 others(38): Show |
intron_variant | MODIFIER | c.2768-490dupT | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 24/34 | chr5 | 37307921 | ||||||
chr5:37307923
|
C | A | 77 | a0001c0002t0002g0073a0001c0002t0002g0074a0001c0002t0002g0076others(74): Show | 77 | HG00423.hp2 HG00642.hp2 HG01069.hp1 others(74): Show |
intron_variant | MODIFIER | c.2768-491G>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 24/34 | chr5 | 37307923 | ||||||
chr5:37307924
|
A | G | 2 | a0001c0001t0001g0103a0001c0001t0037g0091 | 2 | HG02080.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.2768-492T>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 24/34 | chr5 | 37307924 | ||||||
chr5:37307942
|
GA | G | 24 | a0001c0001t0001g0107a0001c0002t0007g0030a0001c0002t0007g0036others(21): Show | 24 | HG01109.hp2 HG01243.hp1 HG01261.hp1 others(21): Show |
intron_variant | MODIFIER | c.2768-511delT | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 24/34 | chr5 | 37307942 | ||||||
chr5:37307942
|
GAA | G | 83 | a0001c0002t0002g0074a0001c0002t0002g0076a0001c0002t0002g0077others(80): Show | 83 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.2768-512_2768-511d others(4): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 24/34 | chr5 | 37307942 | ||||||
chr5:37307951
|
AAAT | A | 70 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0095others(67): Show | 70 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.2768-522_2768-520d others(5): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 24/34 | chr5 | 37307951 | ||||||
chr5:37307952
|
A | T | 13 | a0001c0002t0002g0077a0001c0002t0004g0025a0001c0002t0007g0040others(10): Show | 13 | HG01243.hp1 HG01261.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.2768-520T>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 24/34 | chr5 | 37307952 | ||||||
chr5:37307952
|
AAT | A | 13 | a0001c0001t0001g0096a0001c0001t0001g0169a0001c0001t0001g0199others(10): Show | 13 | HG01069.hp1 HG01346.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.2768-522_2768-521d others(4): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 24/34 | chr5 | 37307952 | ||||||
chr5:37307953
|
AT | A | 93 | a0001c0001t0001g0119a0001c0001t0001g0168a0001c0001t0001g0192others(90): Show | 94 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.2768-522delA | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 24/34 | chr5 | 37307953 | ||||||
chr5:37307953
|
ATAT | A | 3 | a0001c0001t0001g0103a0001c0001t0021g0006a0001c0001t0021g0007 | 3 | HG02080.hp1 HG02559.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2768-524_2768-522d others(5): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 24/34 | chr5 | 37307953 | ||||||
chr5:37307956
|
T | A | 7 | a0001c0001t0001g0169a0001c0001t0001g0193a0001c0001t0001g0199others(4): Show | 8 | HG00099.hp2 HG01361.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.2768-524A>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 24/34 | chr5 | 37307956 | ||||||
chr5:37307958
|
T | A | 1 | a0001c0001t0001g0201 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2768-526A>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 24/34 | chr5 | 37307958 | ||||||
chr5:37308373
|
T | G | 16 | a0001c0002t0007g0030a0001c0002t0007g0036a0001c0002t0007g0037others(13): Show | 16 | HG01109.hp2 HG01243.hp1 HG01261.hp1 others(13): Show |
intron_variant | MODIFIER | c.2767+756A>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 24/34 | chr5 | 37308373 | ||||||
chr5:37308421
|
G | A | 2 | a0001c0005t0009g0054a0001c0005t0009g0058 | 2 | HG02965.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2767+708C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 24/34 | chr5 | 37308421 | ||||||
chr5:37308555
|
G | A | 1 | a0001c0001t0001g0142 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2767+574C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 24/34 | chr5 | 37308555 | ||||||
chr5:37308649
|
C | T | 1 | a0001c0001t0001g0253 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.2767+480G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 24/34 | chr5 | 37308649 | ||||||
chr5:37308650
|
G | A | 1 | a0001c0002t0056g0008 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2767+479C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 24/34 | chr5 | 37308650 | ||||||
chr5:37308793
|
T | A | 1 | a0001c0005t0009g0057 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2767+336A>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 24/34 | chr5 | 37308793 | ||||||
chr5:37308815
|
G | A | 2 | a0001c0002t0027g0034a0001c0002t0027g0045 | 2 | HG01243.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.2767+314C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 24/34 | chr5 | 37308815 | ||||||
chr5:37308875
|
C | CA | 8 | a0001c0001t0001g0169a0001c0003t0001g0186a0001c0003t0001g0198others(5): Show | 8 | HG01891.hp1 HG02040.hp1 HG02056.hp2 others(5): Show |
intron_variant | MODIFIER | c.2767+253dupT | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 24/34 | chr5 | 37308875 | ||||||
chr5:37308875
|
C | CAAAA | 6 | a0001c0004t0011g0051a0001c0004t0011g0052a0001c0004t0011g0053others(3): Show | 6 | HG02257.hp1 HG02486.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.2767+250_2767+253d others(6): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 24/34 | chr5 | 37308875 | ||||||
chr5:37308875
|
CA | C | 9 | a0001c0001t0001g0194a0001c0002t0020g0271a0001c0003t0001g0197others(6): Show | 9 | HG00735.hp2 HG02080.hp2 HG03834.hp1 others(6): Show |
intron_variant | MODIFIER | c.2767+253delT | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 24/34 | chr5 | 37308875 | ||||||
chr5:37308875
|
CAA | C | 29 | a0001c0002t0005g0266a0001c0002t0005g0267a0001c0002t0005g0268others(26): Show | 29 | HG00099.hp1 HG00408.hp2 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.2767+252_2767+253d others(4): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 24/34 | chr5 | 37308875 | ||||||
chr5:37308875
|
CAAA | C | 46 | a0001c0002t0004g0004a0001c0002t0004g0019a0001c0002t0004g0020others(43): Show | 46 | HG01109.hp2 HG01192.hp2 HG01243.hp1 others(43): Show |
intron_variant | MODIFIER | c.2767+251_2767+253d others(5): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 24/34 | chr5 | 37308875 | ||||||
chr5:37308875
|
CAAAAAAA | C | 23 | a0001c0002t0002g0073a0001c0002t0002g0074a0001c0002t0002g0076others(20): Show | 23 | HG00423.hp2 HG00642.hp2 HG01069.hp1 others(20): Show |
intron_variant | MODIFIER | c.2767+247_2767+253d others(9): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 24/34 | chr5 | 37308875 | ||||||
chr5:37308875
|
CAAAAAAA others(3): Show |
C | 77 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0095others(74): Show | 77 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.2767+244_2767+253d others(12): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 24/34 | chr5 | 37308875 | ||||||
chr5:37309002
|
C | T | 25 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0192others(22): Show | 25 | HG01069.hp2 HG01361.hp2 HG01517.hp2 others(22): Show |
intron_variant | MODIFIER | c.2767+127G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 24/34 | chr5 | 37309002 | ||||||
chr5:37309269
|
TAGA | T | 102 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0095others(99): Show | 102 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(99): Show |
splice_region_variant&intron_variant | LOW | c.2629-5_2629-3delTC others(1): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 23/34 | chr5 | 37309269 | ||||||
chr5:37309585
|
A | T | 1 | a0001c0001t0001g0160 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.2629-318T>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 23/34 | chr5 | 37309585 | ||||||
chr5:37309780
|
C | A | 23 | a0001c0002t0006g0272a0001c0002t0006g0277a0001c0002t0006g0278others(20): Show | 23 | HG00099.hp1 HG00408.hp2 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.2629-513G>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 23/34 | chr5 | 37309780 | ||||||
chr5:37309788
|
C | T | 1 | a0001c0003t0001g0231 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.2629-521G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 23/34 | chr5 | 37309788 | ||||||
chr5:37309790
|
C | T | 16 | a0001c0002t0007g0030a0001c0002t0007g0036a0001c0002t0007g0037others(13): Show | 16 | HG01109.hp2 HG01243.hp1 HG01261.hp1 others(13): Show |
intron_variant | MODIFIER | c.2629-523G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 23/34 | chr5 | 37309790 | ||||||
chr5:37310040
|
T | A | 102 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0095others(99): Show | 102 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.2628+512A>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 23/34 | chr5 | 37310040 | ||||||
chr5:37310130
|
A | G | 17 | a0001c0002t0006g0272a0001c0002t0006g0277a0001c0002t0006g0278others(14): Show | 17 | HG00099.hp1 HG00408.hp2 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.2628+422T>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 23/34 | chr5 | 37310130 | ||||||
chr5:37311462
|
AAATAT | A | 23 | a0001c0002t0004g0004a0001c0002t0004g0019a0001c0002t0004g0020others(20): Show | 23 | HG01192.hp2 HG01243.hp2 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.2437-724_2437-720d others(7): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 22/34 | chr5 | 37311462 | ||||||
chr5:37311663
|
A | AT | 9 | a0001c0002t0002g0073a0001c0002t0002g0081a0001c0002t0007g0030others(6): Show | 9 | HG01069.hp1 HG01175.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.2437-921dupA | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 22/34 | chr5 | 37311663 | ||||||
chr5:37311663
|
A | T | 1 | a0001c0003t0018g0182 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.2437-920T>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 22/34 | chr5 | 37311663 | ||||||
chr5:37311774
|
CT | C | 12 | a0001c0002t0004g0004a0001c0002t0004g0019a0001c0002t0004g0020others(9): Show | 12 | HG01192.hp2 HG01891.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.2437-1032delA | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 22/34 | chr5 | 37311774 | ||||||
chr5:37312042
|
A | G | 35 | a0001c0002t0002g0073a0001c0002t0002g0074a0001c0002t0002g0076others(32): Show | 35 | HG00423.hp2 HG00642.hp2 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.2437-1299T>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 22/34 | chr5 | 37312042 | ||||||
chr5:37312111
|
G | A | 1 | a0001c0003t0001g0240 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2437-1368C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 22/34 | chr5 | 37312111 | ||||||
chr5:37312356
|
G | A | 1 | a0001c0001t0001g0127 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2437-1613C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 22/34 | chr5 | 37312356 | ||||||
chr5:37312370
|
TA | T | 103 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0095others(100): Show | 103 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.2437-1628delT | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 22/34 | chr5 | 37312370 | ||||||
chr5:37312442
|
A | C | 4 | a0001c0002t0023g0031a0001c0002t0024g0032a0001c0002t0024g0033others(1): Show | 4 | HG02451.hp1 HG02572.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.2437-1699T>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 22/34 | chr5 | 37312442 | ||||||
chr5:37312560
|
C | T | 2 | a0001c0002t0007g0038a0001c0002t0035g0047 | 2 | HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.2436+1638G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 22/34 | chr5 | 37312560 | ||||||
chr5:37312606
|
T | C | 1 | a0001c0001t0001g0105 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2436+1592A>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 22/34 | chr5 | 37312606 | ||||||
chr5:37312699
|
C | T | 2 | a0001c0002t0025g0273a0001c0002t0048g0288 | 2 | HG01884.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.2436+1499G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 22/34 | chr5 | 37312699 | ||||||
chr5:37312816
|
C | T | 7 | a0001c0005t0009g0054a0001c0005t0009g0057a0001c0005t0009g0058others(4): Show | 7 | HG02145.hp1 HG02895.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.2436+1382G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 22/34 | chr5 | 37312816 | ||||||
chr5:37312964
|
T | A | 2 | a0001c0002t0015g0012a0001c0002t0033g0018 | 2 | HG02055.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.2436+1234A>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 22/34 | chr5 | 37312964 | ||||||
chr5:37313197
|
G | A | 1 | a0001c0005t0009g0058 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2436+1001C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 22/34 | chr5 | 37313197 | ||||||
chr5:37313201
|
C | T | 1 | a0001c0002t0002g0274 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2436+997G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 22/34 | chr5 | 37313201 | ||||||
chr5:37313259
|
C | G | 2 | a0001c0002t0025g0273a0001c0002t0048g0288 | 2 | HG01884.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.2436+939G>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 22/34 | chr5 | 37313259 | ||||||
chr5:37313473
|
A | ATG | 31 | a0001c0002t0006g0272a0001c0002t0006g0277a0001c0002t0006g0278others(28): Show | 31 | HG00099.hp1 HG00408.hp2 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.2436+723_2436+724d others(4): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 22/34 | chr5 | 37313473 | ||||||
chr5:37313473
|
ATG | A | 33 | a0001c0001t0001g0109a0001c0002t0002g0081a0001c0002t0007g0030others(30): Show | 33 | HG01109.hp2 HG01243.hp1 HG01261.hp1 others(30): Show |
intron_variant | MODIFIER | c.2436+723_2436+724d others(4): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 22/34 | chr5 | 37313473 | ||||||
chr5:37313473
|
ATGTG | A | 132 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0095others(129): Show | 132 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(129): Show |
intron_variant | MODIFIER | c.2436+721_2436+724d others(6): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 22/34 | chr5 | 37313473 | ||||||
chr5:37313504
|
T | A | 13 | a0001c0002t0008g0009a0001c0002t0008g0010a0001c0002t0008g0011others(10): Show | 13 | HG01243.hp2 HG01346.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.2436+694A>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 22/34 | chr5 | 37313504 | ||||||
chr5:37313504
|
T | TGTGA | 12 | a0001c0002t0004g0004a0001c0002t0004g0019a0001c0002t0004g0020others(9): Show | 12 | HG01192.hp2 HG01891.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.2436+693_2436+694i others(6): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 22/34 | chr5 | 37313504 | ||||||
chr5:37313509
|
G | C | 102 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0095others(99): Show | 102 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.2436+689C>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 22/34 | chr5 | 37313509 | ||||||
chr5:37313896
|
G | A | 18 | a0001c0001t0001g0168a0001c0001t0001g0192a0001c0001t0001g0193others(15): Show | 18 | HG01069.hp2 HG01361.hp2 HG01517.hp2 others(15): Show |
intron_variant | MODIFIER | c.2436+302C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 22/34 | chr5 | 37313896 | ||||||
chr5:37313964
|
AAT | A | 6 | a0001c0002t0008g0010a0001c0002t0008g0011a0001c0002t0008g0015others(3): Show | 6 | HG02280.hp2 HG02922.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.2436+232_2436+233d others(4): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 22/34 | chr5 | 37313964 | ||||||
chr5:37313975
|
T | A | 77 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0095others(74): Show | 77 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.2436+223A>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 22/34 | chr5 | 37313975 | ||||||
chr5:37314030
|
T | C | 3 | a0001c0003t0001g0173a0001c0003t0001g0205a0001c0003t0001g0228 | 3 | HG01952.hp1 HG02723.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.2436+168A>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 22/34 | chr5 | 37314030 | ||||||
chr5:37314366
|
T | C | 1 | a0001c0001t0001g0148 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2306-38A>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 21/34 | chr5 | 37314366 | ||||||
chr5:37314429
|
T | A | 1 | a0001c0004t0052g0056 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2306-101A>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 21/34 | chr5 | 37314429 | ||||||
chr5:37314587
|
C | T | 23 | a0001c0002t0006g0272a0001c0002t0006g0277a0001c0002t0006g0278others(20): Show | 23 | HG00099.hp1 HG00408.hp2 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.2306-259G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 21/34 | chr5 | 37314587 | ||||||
chr5:37314697
|
G | T | 1 | a0001c0001t0042g0113 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2306-369C>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 21/34 | chr5 | 37314697 | ||||||
chr5:37314970
|
G | C | 1 | a0001c0003t0001g0204 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.2306-642C>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 21/34 | chr5 | 37314970 | ||||||
chr5:37315162
|
G | C | 4 | a0001c0002t0023g0031a0001c0002t0024g0032a0001c0002t0024g0033others(1): Show | 4 | HG02451.hp1 HG02572.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.2306-834C>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 21/34 | chr5 | 37315162 | ||||||
chr5:37315208
|
G | A | 2 | a0001c0005t0009g0062a0001c0005t0009g0064 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2306-880C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 21/34 | chr5 | 37315208 | ||||||
chr5:37315388
|
T | G | 1 | a0007c0013t0001g0251 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.2306-1060A>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 21/34 | chr5 | 37315388 | ||||||
chr5:37315535
|
AGATGCCA others(44): Show |
A | 8 | a0001c0005t0009g0054a0001c0005t0009g0057a0001c0005t0009g0058others(5): Show | 8 | HG02145.hp1 HG02895.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.2306-1258_2306-120 others(55): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 21/34 | chr5 | 37315535 | ||||||
chr5:37315634
|
C | T | 22 | a0001c0002t0006g0272a0001c0002t0006g0277a0001c0002t0006g0278others(19): Show | 22 | HG00099.hp1 HG00408.hp2 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.2306-1306G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 21/34 | chr5 | 37315634 | ||||||
chr5:37315654
|
T | C | 35 | a0001c0002t0002g0073a0001c0002t0002g0074a0001c0002t0002g0076others(32): Show | 35 | HG00423.hp2 HG00642.hp2 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.2306-1326A>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 21/34 | chr5 | 37315654 | ||||||
chr5:37315853
|
T | C | 1 | a0001c0001t0001g0109 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2306-1525A>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 21/34 | chr5 | 37315853 | ||||||
chr5:37315934
|
C | G | 1 | a0006c0016t0001g0200 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2306-1606G>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 21/34 | chr5 | 37315934 | ||||||
chr5:37315997
|
T | C | 2 | a0001c0002t0002g0081a0001c0002t0014g0075 | 2 | HG03710.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.2306-1669A>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 21/34 | chr5 | 37315997 | ||||||
chr5:37316148
|
C | T | 1 | a0001c0001t0001g0131 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.2306-1820G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 21/34 | chr5 | 37316148 | ||||||
chr5:37316203
|
G | A | 2 | a0001c0006t0016g0044a0001c0006t0036g0046 | 2 | HG01261.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.2305+1785C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 21/34 | chr5 | 37316203 | ||||||
chr5:37316227
|
T | C | 2 | a0001c0004t0029g0002a0001c0011t0028g0003 | 2 | HG02809.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.2305+1761A>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 21/34 | chr5 | 37316227 | ||||||
chr5:37316845
|
T | TGCCACTG others(3): Show |
19 | a0001c0002t0006g0272a0001c0002t0006g0277a0001c0002t0006g0278others(16): Show | 19 | HG00099.hp1 HG00408.hp2 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.2305+1133_2305+114 others(14): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 21/34 | chr5 | 37316845 | ||||||
chr5:37316858
|
T | C | 35 | a0001c0002t0002g0073a0001c0002t0002g0074a0001c0002t0002g0076others(32): Show | 35 | HG00423.hp2 HG00642.hp2 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.2305+1130A>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 21/34 | chr5 | 37316858 | ||||||
chr5:37316919
|
T | C | 8 | a0001c0005t0009g0054a0001c0005t0009g0057a0001c0005t0009g0058others(5): Show | 8 | HG02145.hp1 HG02895.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.2305+1069A>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 21/34 | chr5 | 37316919 | ||||||
chr5:37317007
|
C | CA | 26 | a0001c0002t0004g0004a0001c0002t0004g0019a0001c0002t0004g0020others(23): Show | 26 | HG01192.hp2 HG01243.hp2 HG01346.hp1 others(23): Show |
intron_variant | MODIFIER | c.2305+980dupT | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 21/34 | chr5 | 37317007 | ||||||
chr5:37317062
|
A | G | 35 | a0001c0002t0002g0073a0001c0002t0002g0074a0001c0002t0002g0076others(32): Show | 35 | HG00423.hp2 HG00642.hp2 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.2305+926T>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 21/34 | chr5 | 37317062 | ||||||
chr5:37317105
|
C | T | 1 | a0001c0001t0057g0299 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2305+883G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 21/34 | chr5 | 37317105 | ||||||
chr5:37317108
|
G | C | 2 | a0001c0001t0001g0246a0001c0001t0001g0247 | 2 | NA18952.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.2305+880C>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 21/34 | chr5 | 37317108 | ||||||
chr5:37317449
|
T | G | 2 | a0001c0002t0027g0034a0001c0002t0027g0045 | 2 | HG01243.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.2305+539A>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 21/34 | chr5 | 37317449 | ||||||
chr5:37317688
|
C | CT | 273 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0095others(270): Show | 274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.2305+299dupA | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 21/34 | chr5 | 37317688 | ||||||
chr5:37317688
|
C | CTT | 16 | a0001c0001t0001g0247a0001c0001t0001g0256a0001c0002t0002g0085others(13): Show | 16 | HG01069.hp2 HG01243.hp2 NA18906.hp2 others(13): Show |
intron_variant | MODIFIER | c.2305+298_2305+299d others(4): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 21/34 | chr5 | 37317688 | ||||||
chr5:37317688
|
C | T | 1 | a0001c0003t0001g0211 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.2305+300G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 21/34 | chr5 | 37317688 | ||||||
chr5:37317771
|
T | A | 1 | a0001c0001t0001g0090 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.2305+217A>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 21/34 | chr5 | 37317771 | ||||||
chr5:37318193
|
G | T | 208 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0095others(205): Show | 208 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.2208-108C>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 20/34 | chr5 | 37318193 | ||||||
chr5:37318239
|
T | G | 2 | a0001c0003t0003g0233a0001c0003t0041g0226 | 2 | NA18975.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.2208-154A>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 20/34 | chr5 | 37318239 | ||||||
chr5:37318272
|
T | C | 49 | a0001c0002t0002g0073a0001c0002t0002g0074a0001c0002t0002g0076others(46): Show | 49 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(46): Show |
intron_variant | MODIFIER | c.2208-187A>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 20/34 | chr5 | 37318272 | ||||||
chr5:37318393
|
G | A | 16 | a0001c0002t0007g0030a0001c0002t0007g0036a0001c0002t0007g0037others(13): Show | 16 | HG01109.hp2 HG01243.hp1 HG01261.hp1 others(13): Show |
intron_variant | MODIFIER | c.2208-308C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 20/34 | chr5 | 37318393 | ||||||
chr5:37318439
|
C | T | 3 | a0001c0002t0020g0271a0001c0002t0020g0281a0001c0002t0020g0289 | 3 | HG00099.hp1 HG00735.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2208-354G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 20/34 | chr5 | 37318439 | ||||||
chr5:37318448
|
T | G | 2 | a0001c0004t0029g0002a0001c0011t0028g0003 | 2 | HG02809.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.2208-363A>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 20/34 | chr5 | 37318448 | ||||||
chr5:37318482
|
T | TA | 23 | a0001c0002t0004g0004a0001c0002t0004g0019a0001c0002t0004g0020others(20): Show | 23 | HG01192.hp2 HG01243.hp2 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.2208-398dupT | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 20/34 | chr5 | 37318482 | ||||||
chr5:37318498
|
CATCTGAA others(10): Show |
C | 23 | a0001c0002t0006g0272a0001c0002t0006g0277a0001c0002t0006g0278others(20): Show | 23 | HG00099.hp1 HG00408.hp2 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.2208-430_2208-414d others(19): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 20/34 | chr5 | 37318498 | ||||||
chr5:37318525
|
G | A | 4 | a0001c0002t0023g0031a0001c0002t0024g0032a0001c0002t0024g0033others(1): Show | 4 | HG02451.hp1 HG02572.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.2208-440C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 20/34 | chr5 | 37318525 | ||||||
chr5:37318860
|
A | G | 3 | a0001c0003t0003g0210a0001c0003t0003g0233a0001c0003t0041g0226 | 3 | NA18975.hp1 NA18979.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.2208-775T>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 20/34 | chr5 | 37318860 | ||||||
chr5:37318951
|
T | C | 4 | a0001c0002t0023g0031a0001c0002t0024g0032a0001c0002t0024g0033others(1): Show | 4 | HG02451.hp1 HG02572.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.2208-866A>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 20/34 | chr5 | 37318951 | ||||||
chr5:37318991
|
C | T | 8 | a0001c0005t0009g0054a0001c0005t0009g0057a0001c0005t0009g0058others(5): Show | 8 | HG02145.hp1 HG02895.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.2208-906G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 20/34 | chr5 | 37318991 | ||||||
chr5:37319057
|
T | C | 5 | a0001c0002t0005g0266a0001c0002t0005g0267a0001c0002t0005g0268others(2): Show | 5 | HG02055.hp1 HG02647.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.2208-972A>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 20/34 | chr5 | 37319057 | ||||||
chr5:37319148
|
C | A | 1 | a0001c0002t0004g0025 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2208-1063G>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 20/34 | chr5 | 37319148 | ||||||
chr5:37319592
|
C | T | 1 | a0001c0002t0004g0023 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2208-1507G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 20/34 | chr5 | 37319592 | ||||||
chr5:37319672
|
C | T | 1 | a0001c0002t0002g0081 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2208-1587G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 20/34 | chr5 | 37319672 | ||||||
chr5:37319738
|
G | A | 1 | a0001c0004t0052g0056 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2208-1653C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 20/34 | chr5 | 37319738 | ||||||
chr5:37319749
|
T | G | 1 | a0001c0011t0028g0003 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2208-1664A>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 20/34 | chr5 | 37319749 | ||||||
chr5:37320110
|
G | C | 1 | a0001c0001t0001g0142 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2208-2025C>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 20/34 | chr5 | 37320110 | ||||||
chr5:37320203
|
C | T | 26 | a0001c0002t0004g0004a0001c0002t0004g0019a0001c0002t0004g0020others(23): Show | 26 | HG01192.hp2 HG01243.hp2 HG01346.hp1 others(23): Show |
intron_variant | MODIFIER | c.2208-2118G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 20/34 | chr5 | 37320203 | ||||||
chr5:37320303
|
C | A | 1 | a0001c0002t0007g0048 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2208-2218G>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 20/34 | chr5 | 37320303 | ||||||
chr5:37320339
|
T | C | 26 | a0001c0002t0004g0004a0001c0002t0004g0019a0001c0002t0004g0020others(23): Show | 26 | HG01192.hp2 HG01243.hp2 HG01346.hp1 others(23): Show |
intron_variant | MODIFIER | c.2208-2254A>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 20/34 | chr5 | 37320339 | ||||||
chr5:37320359
|
C | T | 1 | a0001c0001t0010g0116 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.2208-2274G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 20/34 | chr5 | 37320359 | ||||||
chr5:37320892
|
T | G | 1 | a0001c0003t0001g0207 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2208-2807A>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 20/34 | chr5 | 37320892 | ||||||
chr5:37321114
|
T | TGAA | 107 | a0001c0002t0002g0073a0001c0002t0002g0074a0001c0002t0002g0076others(104): Show | 107 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.2207+2875_2207+287 others(7): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 20/34 | chr5 | 37321114 | ||||||
chr5:37321268
|
C | A | 4 | a0001c0002t0023g0031a0001c0002t0024g0032a0001c0002t0024g0033others(1): Show | 4 | HG02451.hp1 HG02572.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.2207+2724G>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 20/34 | chr5 | 37321268 | ||||||
chr5:37321445
|
G | A | 1 | a0001c0015t0001g0230 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.2207+2547C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 20/34 | chr5 | 37321445 | ||||||
chr5:37321446
|
C | T | 1 | a0001c0003t0003g0203 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2207+2546G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 20/34 | chr5 | 37321446 | ||||||
chr5:37321670
|
T | C | 1 | a0009c0012t0008g0013 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2207+2322A>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 20/34 | chr5 | 37321670 | ||||||
chr5:37321815
|
C | G | 1 | a0001c0002t0017g0042 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2207+2177G>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 20/34 | chr5 | 37321815 | ||||||
chr5:37322002
|
T | C | 1 | a0001c0001t0001g0142 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2207+1990A>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 20/34 | chr5 | 37322002 | ||||||
chr5:37322124
|
G | T | 7 | a0001c0005t0009g0054a0001c0005t0009g0057a0001c0005t0009g0058others(4): Show | 7 | HG02145.hp1 HG02895.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.2207+1868C>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 20/34 | chr5 | 37322124 | ||||||
chr5:37322149
|
C | T | 1 | a0001c0001t0038g0117 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2207+1843G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 20/34 | chr5 | 37322149 | ||||||
chr5:37322187
|
A | G | 1 | a0001c0021t0001g0298 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2207+1805T>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 20/34 | chr5 | 37322187 | ||||||
chr5:37322207
|
G | C | 2 | a0001c0004t0029g0002a0001c0011t0028g0003 | 2 | HG02809.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.2207+1785C>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 20/34 | chr5 | 37322207 | ||||||
chr5:37322359
|
G | A | 5 | a0001c0002t0005g0266a0001c0002t0005g0267a0001c0002t0005g0268others(2): Show | 5 | HG02055.hp1 HG02647.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.2207+1633C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 20/34 | chr5 | 37322359 | ||||||
chr5:37322372
|
T | G | 2 | a0001c0001t0021g0006a0001c0001t0021g0007 | 2 | HG02559.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2207+1620A>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 20/34 | chr5 | 37322372 | ||||||
chr5:37322409
|
T | C | 3 | a0001c0003t0001g0198a0001c0003t0001g0240a0001c0003t0001g0260 | 3 | HG00140.hp1 HG03490.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.2207+1583A>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 20/34 | chr5 | 37322409 | ||||||
chr5:37322451
|
T | G | 8 | a0001c0005t0009g0054a0001c0005t0009g0057a0001c0005t0009g0058others(5): Show | 8 | HG02145.hp1 HG02895.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.2207+1541A>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 20/34 | chr5 | 37322451 | ||||||
chr5:37322638
|
C | T | 1 | a0009c0012t0008g0013 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2207+1354G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 20/34 | chr5 | 37322638 | ||||||
chr5:37322686
|
G | A | 7 | a0001c0005t0009g0054a0001c0005t0009g0057a0001c0005t0009g0058others(4): Show | 7 | HG02145.hp1 HG02895.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.2207+1306C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 20/34 | chr5 | 37322686 | ||||||
chr5:37322706
|
C | CA | 39 | a0001c0001t0001g0107a0001c0001t0001g0109a0001c0001t0001g0110others(36): Show | 39 | HG00423.hp2 HG00642.hp2 HG01069.hp1 others(36): Show |
intron_variant | MODIFIER | c.2207+1285dupT | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 20/34 | chr5 | 37322706 | ||||||
chr5:37322706
|
C | CAA | 12 | a0001c0001t0001g0143a0001c0002t0023g0065a0001c0003t0001g0165others(9): Show | 12 | HG00423.hp1 HG00673.hp2 HG02027.hp2 others(9): Show |
intron_variant | MODIFIER | c.2207+1284_2207+128 others(6): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 20/34 | chr5 | 37322706 | ||||||
chr5:37322954
|
C | T | 35 | a0001c0002t0002g0073a0001c0002t0002g0074a0001c0002t0002g0076others(32): Show | 35 | HG00423.hp2 HG00642.hp2 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.2207+1038G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 20/34 | chr5 | 37322954 | ||||||
chr5:37322957
|
G | C | 1 | a0001c0004t0052g0056 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2207+1035C>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 20/34 | chr5 | 37322957 | ||||||
chr5:37322973
|
C | CA | 17 | a0001c0002t0007g0030a0001c0002t0007g0036a0001c0002t0007g0037others(14): Show | 17 | HG01109.hp2 HG01243.hp1 HG01261.hp1 others(14): Show |
intron_variant | MODIFIER | c.2207+1018dupT | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 20/34 | chr5 | 37322973 | ||||||
chr5:37322983
|
A | C | 2 | a0001c0001t0001g0123a0001c0001t0010g0097 | 2 | NA18955.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.2207+1009T>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 20/34 | chr5 | 37322983 | ||||||
chr5:37323192
|
GGAGAA | G | 26 | a0001c0002t0004g0004a0001c0002t0004g0019a0001c0002t0004g0020others(23): Show | 26 | HG01192.hp2 HG01243.hp2 HG01346.hp1 others(23): Show |
intron_variant | MODIFIER | c.2207+795_2207+799d others(7): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 20/34 | chr5 | 37323192 | ||||||
chr5:37323199
|
T | A | 26 | a0001c0002t0004g0004a0001c0002t0004g0019a0001c0002t0004g0020others(23): Show | 26 | HG01192.hp2 HG01243.hp2 HG01346.hp1 others(23): Show |
intron_variant | MODIFIER | c.2207+793A>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 20/34 | chr5 | 37323199 | ||||||
chr5:37323322
|
A | G | 1 | a0001c0002t0006g0277 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2207+670T>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 20/34 | chr5 | 37323322 | ||||||
chr5:37323471
|
G | A | 1 | a0001c0002t0002g0087 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2207+521C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 20/34 | chr5 | 37323471 | ||||||
chr5:37323602
|
ATATAAC | A | 25 | a0001c0002t0002g0274a0001c0002t0002g0290a0001c0002t0006g0272others(22): Show | 25 | HG00099.hp1 HG00408.hp2 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.2207+384_2207+389d others(8): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 20/34 | chr5 | 37323602 | ||||||
chr5:37323688
|
A | G | 1 | a0001c0003t0001g0186 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2207+304T>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 20/34 | chr5 | 37323688 | ||||||
chr5:37323759
|
C | G | 5 | a0001c0001t0001g0106a0001c0001t0001g0115a0001c0001t0001g0135others(2): Show | 5 | NA18946.hp2 NA18961.hp1 NA18986.hp2 others(2): Show |
intron_variant | MODIFIER | c.2207+233G>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 20/34 | chr5 | 37323759 | ||||||
chr5:37323947
|
C | G | 2 | a0001c0002t0017g0041a0001c0002t0017g0042 | 2 | HG01346.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.2207+45G>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 20/34 | chr5 | 37323947 | ||||||
chr5:37324223
|
C | A | 1 | a0001c0003t0001g0237 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2092-116G>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 19/34 | chr5 | 37324223 | ||||||
chr5:37324281
|
T | C | 1 | a0001c0001t0001g0149 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2092-174A>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 19/34 | chr5 | 37324281 | ||||||
chr5:37324562
|
C | CT | 23 | a0001c0002t0004g0004a0001c0002t0004g0019a0001c0002t0004g0020others(20): Show | 23 | HG01192.hp2 HG01243.hp2 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.2092-456dupA | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 19/34 | chr5 | 37324562 | ||||||
chr5:37324575
|
G | A | 1 | a0001c0001t0001g0148 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2092-468C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 19/34 | chr5 | 37324575 | ||||||
chr5:37324682
|
G | A | 2 | a0001c0002t0017g0041a0001c0002t0017g0042 | 2 | HG01346.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.2092-575C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 19/34 | chr5 | 37324682 | ||||||
chr5:37324721
|
C | T | 23 | a0001c0002t0004g0004a0001c0002t0004g0019a0001c0002t0004g0020others(20): Show | 23 | HG01192.hp2 HG01243.hp2 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.2092-614G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 19/34 | chr5 | 37324721 | ||||||
chr5:37324928
|
T | A | 5 | a0001c0004t0011g0051a0001c0004t0011g0052a0001c0004t0011g0053others(2): Show | 5 | HG02257.hp1 HG02486.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.2092-821A>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 19/34 | chr5 | 37324928 | ||||||
chr5:37324982
|
T | A | 2 | a0001c0002t0015g0012a0001c0002t0033g0018 | 2 | HG02055.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.2092-875A>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 19/34 | chr5 | 37324982 | ||||||
chr5:37325184
|
C | A | 16 | a0001c0002t0007g0030a0001c0002t0007g0036a0001c0002t0007g0037others(13): Show | 16 | HG01109.hp2 HG01243.hp1 HG01261.hp1 others(13): Show |
intron_variant | MODIFIER | c.2091+717G>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 19/34 | chr5 | 37325184 | ||||||
chr5:37325213
|
A | C | 1 | a0001c0005t0009g0063 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2091+688T>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 19/34 | chr5 | 37325213 | ||||||
chr5:37325251
|
G | A | 2 | a0001c0004t0029g0002a0001c0011t0028g0003 | 2 | HG02809.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.2091+650C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 19/34 | chr5 | 37325251 | ||||||
chr5:37325410
|
G | A | 1 | a0001c0003t0019g0212 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2091+491C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 19/34 | chr5 | 37325410 | ||||||
chr5:37325709
|
C | T | 16 | a0001c0002t0007g0030a0001c0002t0007g0036a0001c0002t0007g0037others(13): Show | 16 | HG01109.hp2 HG01243.hp1 HG01261.hp1 others(13): Show |
intron_variant | MODIFIER | c.2091+192G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 19/34 | chr5 | 37325709 | ||||||
chr5:37325768
|
C | CA | 87 | a0001c0001t0001g0096a0001c0001t0001g0102a0001c0001t0001g0109others(84): Show | 88 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.2091+132dupT | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 19/34 | chr5 | 37325768 | ||||||
chr5:37325768
|
C | CAA | 21 | a0001c0001t0042g0113a0001c0002t0002g0087a0001c0002t0002g0088others(18): Show | 21 | HG00099.hp1 HG00408.hp2 HG00642.hp2 others(18): Show |
intron_variant | MODIFIER | c.2091+131_2091+132d others(4): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 19/34 | chr5 | 37325768 | ||||||
chr5:37325768
|
CA | C | 13 | a0001c0001t0001g0132a0001c0001t0001g0150a0001c0002t0008g0009others(10): Show | 13 | HG01346.hp1 HG02055.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.2091+132delT | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 19/34 | chr5 | 37325768 | ||||||
chr5:37325792
|
T | A | 8 | a0001c0002t0002g0082a0001c0002t0002g0085a0001c0004t0011g0051others(5): Show | 8 | HG02257.hp1 HG02486.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.2091+109A>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 19/34 | chr5 | 37325792 | ||||||
chr5:37325800
|
G | C | 1 | a0001c0002t0014g0075 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2091+101C>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 19/34 | chr5 | 37325800 | ||||||
chr5:37325817
|
A | C | 19 | a0001c0002t0006g0272a0001c0002t0006g0277a0001c0002t0006g0278others(16): Show | 19 | HG00099.hp1 HG00408.hp2 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.2091+84T>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 19/34 | chr5 | 37325817 | ||||||
chr5:37325838
|
T | C | 45 | a0001c0002t0002g0073a0001c0002t0002g0074a0001c0002t0002g0076others(42): Show | 45 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(42): Show |
intron_variant | MODIFIER | c.2091+63A>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 19/34 | chr5 | 37325838 | ||||||
chr5:37325892
|
C | T | 1 | a0001c0003t0001g0197 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2091+9G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 19/34 | chr5 | 37325892 | ||||||
chr5:37326240
|
A | G | 1 | a0001c0004t0052g0056 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2025-273T>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 18/34 | chr5 | 37326240 | ||||||
chr5:37326410
|
T | A | 1 | a0001c0001t0057g0299 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2025-443A>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 18/34 | chr5 | 37326410 | ||||||
chr5:37326536
|
G | A | 16 | a0001c0002t0007g0030a0001c0002t0007g0036a0001c0002t0007g0037others(13): Show | 16 | HG01109.hp2 HG01243.hp1 HG01261.hp1 others(13): Show |
intron_variant | MODIFIER | c.2025-569C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 18/34 | chr5 | 37326536 | ||||||
chr5:37326696
|
G | C | 7 | a0001c0005t0009g0054a0001c0005t0009g0057a0001c0005t0009g0058others(4): Show | 7 | HG02145.hp1 HG02895.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.2025-729C>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 18/34 | chr5 | 37326696 | ||||||
chr5:37326701
|
T | C | 1 | a0001c0001t0010g0129 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.2025-734A>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 18/34 | chr5 | 37326701 | ||||||
chr5:37327051
|
TCTTC | T | 18 | a0001c0001t0001g0168a0001c0001t0001g0192a0001c0001t0001g0193others(15): Show | 18 | HG01069.hp2 HG01361.hp2 HG01517.hp2 others(15): Show |
intron_variant | MODIFIER | c.2024+574_2024+577d others(6): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 18/34 | chr5 | 37327051 | ||||||
chr5:37327123
|
A | G | 8 | a0001c0005t0009g0054a0001c0005t0009g0057a0001c0005t0009g0058others(5): Show | 8 | HG02145.hp1 HG02895.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.2024+506T>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 18/34 | chr5 | 37327123 | ||||||
chr5:37327370
|
C | T | 18 | a0001c0001t0001g0168a0001c0001t0001g0192a0001c0001t0001g0193others(15): Show | 18 | HG01069.hp2 HG01361.hp2 HG01517.hp2 others(15): Show |
intron_variant | MODIFIER | c.2024+259G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 18/34 | chr5 | 37327370 | ||||||
chr5:37327460
|
T | C | 1 | a0001c0001t0003g0166 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.2024+169A>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 18/34 | chr5 | 37327460 | ||||||
chr5:37327781
|
T | C | 1 | a0001c0010t0017g0035 | 1 | NA18906.hp2 | splice_region_variant&intron_variant | LOW | c.1877-5A>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 17/34 | chr5 | 37327781 | ||||||
chr5:37328092
|
G | A | 1 | a0001c0001t0001g0153 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1876+266C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 17/34 | chr5 | 37328092 | ||||||
chr5:37328573
|
G | A | 19 | a0001c0002t0006g0272a0001c0002t0006g0277a0001c0002t0006g0278others(16): Show | 19 | HG00099.hp1 HG00408.hp2 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.1814-153C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 16/34 | chr5 | 37328573 | ||||||
chr5:37328606
|
C | T | 6 | a0001c0001t0021g0006a0001c0004t0011g0051a0001c0004t0011g0052others(3): Show | 6 | HG02257.hp1 HG02486.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.1814-186G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 16/34 | chr5 | 37328606 | ||||||
chr5:37328845
|
G | A | 9 | a0001c0004t0011g0051a0001c0004t0011g0052a0001c0004t0011g0053others(6): Show | 9 | HG02257.hp1 HG02486.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1813+345C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 16/34 | chr5 | 37328845 | ||||||
chr5:37328852
|
G | C | 1 | a0001c0004t0053g0265 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1813+338C>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 16/34 | chr5 | 37328852 | ||||||
chr5:37328892
|
C | T | 1 | a0001c0003t0001g0204 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1813+298G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 16/34 | chr5 | 37328892 | ||||||
chr5:37328981
|
T | C | 1 | a0001c0001t0030g0202 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1813+209A>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 16/34 | chr5 | 37328981 | ||||||
chr5:37329381
|
A | C | 1 | a0001c0001t0043g0138 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1725-103T>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 15/34 | chr5 | 37329381 | ||||||
chr5:37329399
|
T | C | 1 | a0001c0001t0001g0115 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1725-121A>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 15/34 | chr5 | 37329399 | ||||||
chr5:37329477
|
A | G | 2 | a0001c0001t0018g0094a0001c0001t0026g0146 | 2 | NA19000.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.1725-199T>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 15/34 | chr5 | 37329477 | ||||||
chr5:37329504
|
T | C | 1 | a0001c0002t0020g0289 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1725-226A>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 15/34 | chr5 | 37329504 | ||||||
chr5:37329749
|
T | C | 4 | a0001c0002t0017g0041a0001c0002t0017g0042a0001c0003t0001g0293others(1): Show | 4 | HG01346.hp1 HG02738.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1724+289A>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 15/34 | chr5 | 37329749 | ||||||
chr5:37329841
|
T | C | 9 | a0001c0004t0011g0051a0001c0004t0011g0052a0001c0004t0011g0053others(6): Show | 9 | HG02257.hp1 HG02486.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1724+197A>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 15/34 | chr5 | 37329841 | ||||||
chr5:37330168
|
T | C | 1 | a0001c0001t0001g0139 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1630-36A>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 14/34 | chr5 | 37330168 | ||||||
chr5:37330237
|
A | G | 51 | a0001c0002t0004g0004a0001c0002t0004g0019a0001c0002t0004g0020others(48): Show | 51 | HG01109.hp2 HG01192.hp2 HG01243.hp1 others(48): Show |
intron_variant | MODIFIER | c.1630-105T>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 14/34 | chr5 | 37330237 | ||||||
chr5:37330243
|
T | G | 1 | a0001c0001t0040g0155 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1630-111A>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 14/34 | chr5 | 37330243 | ||||||
chr5:37330370
|
T | G | 23 | a0001c0002t0004g0004a0001c0002t0004g0019a0001c0002t0004g0020others(20): Show | 23 | HG01192.hp2 HG01243.hp2 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.1630-238A>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 14/34 | chr5 | 37330370 | ||||||
chr5:37330378
|
G | A | 16 | a0001c0002t0007g0030a0001c0002t0007g0036a0001c0002t0007g0037others(13): Show | 16 | HG01109.hp2 HG01243.hp1 HG01261.hp1 others(13): Show |
intron_variant | MODIFIER | c.1630-246C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 14/34 | chr5 | 37330378 | ||||||
chr5:37330487
|
G | C | 1 | a0001c0001t0001g0193 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1630-355C>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 14/34 | chr5 | 37330487 | ||||||
chr5:37330502
|
C | T | 3 | a0001c0001t0001g0107a0001c0001t0001g0130a0001c0001t0022g0099 | 3 | HG02056.hp1 NA19011.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.1630-370G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 14/34 | chr5 | 37330502 | ||||||
chr5:37330523
|
G | A | 2 | a0001c0001t0021g0006a0001c0001t0021g0007 | 2 | HG02559.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1630-391C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 14/34 | chr5 | 37330523 | ||||||
chr5:37330799
|
A | G | 3 | a0001c0001t0001g0160a0001c0001t0018g0094a0001c0001t0026g0146 | 3 | NA18975.hp2 NA19000.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.1630-667T>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 14/34 | chr5 | 37330799 | ||||||
chr5:37330840
|
A | T | 49 | a0001c0002t0002g0073a0001c0002t0002g0074a0001c0002t0002g0076others(46): Show | 49 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(46): Show |
intron_variant | MODIFIER | c.1630-708T>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 14/34 | chr5 | 37330840 | ||||||
chr5:37330920
|
C | T | 1 | a0001c0015t0001g0230 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1629+765G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 14/34 | chr5 | 37330920 | ||||||
chr5:37330940
|
G | C | 8 | a0001c0002t0008g0009a0001c0002t0008g0010a0001c0002t0008g0011others(5): Show | 8 | HG01243.hp2 HG02109.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1629+745C>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 14/34 | chr5 | 37330940 | ||||||
chr5:37331013
|
G | T | 1 | a0003c0007t0001g0229 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1629+672C>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 14/34 | chr5 | 37331013 | ||||||
chr5:37331018
|
G | A | 1 | a0001c0003t0001g0222 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1629+667C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 14/34 | chr5 | 37331018 | ||||||
chr5:37331106
|
G | A | 3 | a0001c0002t0017g0041a0001c0002t0017g0042a0001c0010t0017g0035 | 3 | HG01346.hp1 HG02922.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1629+579C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 14/34 | chr5 | 37331106 | ||||||
chr5:37331129
|
A | G | 7 | a0001c0005t0009g0054a0001c0005t0009g0057a0001c0005t0009g0058others(4): Show | 7 | HG02145.hp1 HG02895.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.1629+556T>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 14/34 | chr5 | 37331129 | ||||||
chr5:37331146
|
C | T | 2 | a0001c0003t0001g0214a0001c0003t0003g0171 | 2 | NA18977.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.1629+539G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 14/34 | chr5 | 37331146 | ||||||
chr5:37331148
|
C | CA | 70 | a0001c0001t0021g0006a0001c0001t0021g0007a0001c0002t0002g0073others(67): Show | 70 | HG00423.hp2 HG00642.hp2 HG01069.hp1 others(67): Show |
intron_variant | MODIFIER | c.1629+536dupT | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 14/34 | chr5 | 37331148 | ||||||
chr5:37331312
|
G | A | 1 | a0001c0002t0015g0029 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1629+373C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 14/34 | chr5 | 37331312 | ||||||
chr5:37331561
|
C | T | 7 | a0001c0005t0009g0054a0001c0005t0009g0057a0001c0005t0009g0058others(4): Show | 7 | HG02145.hp1 HG02895.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.1629+124G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 14/34 | chr5 | 37331561 | ||||||
chr5:37331883
|
G | T | 77 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0095others(74): Show | 77 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.1519-88C>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 13/34 | chr5 | 37331883 | ||||||
chr5:37331935
|
C | T | 26 | a0001c0002t0004g0004a0001c0002t0004g0019a0001c0002t0004g0020others(23): Show | 26 | HG01192.hp2 HG01243.hp2 HG01346.hp1 others(23): Show |
intron_variant | MODIFIER | c.1519-140G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 13/34 | chr5 | 37331935 | ||||||
chr5:37331980
|
A | G | 4 | a0001c0002t0008g0009a0001c0002t0008g0010a0001c0002t0008g0015others(1): Show | 4 | HG02109.hp2 HG02922.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1519-185T>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 13/34 | chr5 | 37331980 | ||||||
chr5:37332168
|
C | CA | 38 | a0001c0001t0001g0168a0001c0001t0001g0201a0001c0002t0002g0073others(35): Show | 38 | HG00099.hp1 HG00735.hp2 HG01069.hp1 others(35): Show |
intron_variant | MODIFIER | c.1519-374dupT | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 13/34 | chr5 | 37332168 | ||||||
chr5:37332168
|
C | CAA | 18 | a0001c0001t0001g0249a0001c0002t0002g0074a0001c0002t0002g0076others(15): Show | 18 | HG00423.hp2 HG00642.hp2 HG01257.hp2 others(15): Show |
intron_variant | MODIFIER | c.1519-375_1519-374d others(4): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 13/34 | chr5 | 37332168 | ||||||
chr5:37332168
|
CA | C | 86 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0095others(83): Show | 86 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.1519-374delT | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 13/34 | chr5 | 37332168 | ||||||
chr5:37332168
|
CAA | C | 43 | a0001c0002t0004g0004a0001c0002t0004g0019a0001c0002t0004g0020others(40): Show | 43 | HG01192.hp2 HG01243.hp2 HG01346.hp1 others(40): Show |
intron_variant | MODIFIER | c.1519-375_1519-374d others(4): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 13/34 | chr5 | 37332168 | ||||||
chr5:37332206
|
C | T | 5 | a0001c0002t0005g0266a0001c0002t0005g0267a0001c0002t0005g0268others(2): Show | 5 | HG02055.hp1 HG02647.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1519-411G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 13/34 | chr5 | 37332206 | ||||||
chr5:37332313
|
C | CT | 48 | a0001c0001t0001g0102a0001c0001t0001g0106a0001c0001t0001g0121others(45): Show | 48 | HG00423.hp1 HG00438.hp2 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.1519-519dupA | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 13/34 | chr5 | 37332313 | ||||||
chr5:37332313
|
C | CTTTT | 6 | a0001c0002t0004g0025a0001c0002t0008g0010a0001c0002t0008g0015others(3): Show | 6 | HG02922.hp1 HG03041.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.1519-522_1519-519d others(6): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 13/34 | chr5 | 37332313 | ||||||
chr5:37332313
|
C | CTTTTT | 7 | a0001c0002t0004g0004a0001c0002t0004g0020a0001c0002t0004g0022others(4): Show | 7 | HG02280.hp2 HG02630.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1519-523_1519-519d others(7): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 13/34 | chr5 | 37332313 | ||||||
chr5:37332313
|
C | CTTTTTTT others(3): Show |
1 | a0009c0012t0008g0013 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1519-528_1519-519d others(12): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 13/34 | chr5 | 37332313 | ||||||
chr5:37332313
|
C | CTTTTTTT others(6): Show |
1 | a0001c0010t0017g0035 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1519-531_1519-519d others(15): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 13/34 | chr5 | 37332313 | ||||||
chr5:37332313
|
CT | C | 51 | a0001c0001t0001g0132a0001c0001t0001g0150a0001c0001t0001g0151others(48): Show | 51 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(48): Show |
intron_variant | MODIFIER | c.1519-519delA | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 13/34 | chr5 | 37332313 | ||||||
chr5:37332313
|
CTT | C | 7 | a0001c0004t0011g0051a0001c0004t0011g0052a0001c0004t0011g0053others(4): Show | 7 | HG02257.hp1 HG02486.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1519-520_1519-519d others(4): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 13/34 | chr5 | 37332313 | ||||||
chr5:37332415
|
G | A | 3 | a0001c0002t0017g0041a0001c0002t0017g0042a0001c0010t0017g0035 | 3 | HG01346.hp1 HG02922.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1519-620C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 13/34 | chr5 | 37332415 | ||||||
chr5:37332422
|
T | C | 107 | a0001c0002t0002g0073a0001c0002t0002g0074a0001c0002t0002g0076others(104): Show | 107 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.1519-627A>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 13/34 | chr5 | 37332422 | ||||||
chr5:37332495
|
T | G | 1 | a0001c0010t0017g0035 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1519-700A>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 13/34 | chr5 | 37332495 | ||||||
chr5:37332513
|
C | T | 7 | a0001c0005t0009g0054a0001c0005t0009g0057a0001c0005t0009g0058others(4): Show | 7 | HG02145.hp1 HG02895.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.1519-718G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 13/34 | chr5 | 37332513 | ||||||
chr5:37332516
|
G | C | 1 | a0001c0002t0006g0285 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1519-721C>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 13/34 | chr5 | 37332516 | ||||||
chr5:37332688
|
T | C | 1 | a0001c0003t0005g0167 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1518+775A>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 13/34 | chr5 | 37332688 | ||||||
chr5:37332712
|
A | T | 19 | a0001c0001t0001g0089a0001c0001t0001g0095a0001c0001t0001g0096others(16): Show | 19 | HG00438.hp2 HG02027.hp1 HG02071.hp2 others(16): Show |
intron_variant | MODIFIER | c.1518+751T>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 13/34 | chr5 | 37332712 | ||||||
chr5:37332822
|
T | G | 1 | a0001c0001t0001g0136 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1518+641A>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 13/34 | chr5 | 37332822 | ||||||
chr5:37332922
|
C | G | 2 | a0001c0001t0001g0101a0001c0001t0001g0118 | 2 | NA18983.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.1518+541G>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 13/34 | chr5 | 37332922 | ||||||
chr5:37333097
|
G | A | 49 | a0001c0002t0002g0073a0001c0002t0002g0074a0001c0002t0002g0076others(46): Show | 49 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(46): Show |
intron_variant | MODIFIER | c.1518+366C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 13/34 | chr5 | 37333097 | ||||||
chr5:37333423
|
C | T | 7 | a0001c0005t0009g0054a0001c0005t0009g0057a0001c0005t0009g0058others(4): Show | 7 | HG02145.hp1 HG02895.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.1518+40G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 13/34 | chr5 | 37333423 | ||||||
chr5:37333963
|
A | G | 2 | a0001c0002t0015g0012a0001c0002t0033g0018 | 2 | HG02055.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1348-330T>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 12/34 | chr5 | 37333963 | ||||||
chr5:37334044
|
G | A | 24 | a0001c0002t0002g0073a0001c0002t0002g0074a0001c0002t0002g0076others(21): Show | 24 | HG00423.hp2 HG00642.hp2 HG01069.hp1 others(21): Show |
intron_variant | MODIFIER | c.1348-411C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 12/34 | chr5 | 37334044 | ||||||
chr5:37334102
|
C | T | 1 | a0001c0001t0001g0107 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1348-469G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 12/34 | chr5 | 37334102 | ||||||
chr5:37334104
|
G | C | 1 | a0001c0003t0039g0262 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1348-471C>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 12/34 | chr5 | 37334104 | ||||||
chr5:37334129
|
T | C | 26 | a0001c0002t0004g0004a0001c0002t0004g0019a0001c0002t0004g0020others(23): Show | 26 | HG01192.hp2 HG01243.hp2 HG01346.hp1 others(23): Show |
intron_variant | MODIFIER | c.1348-496A>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 12/34 | chr5 | 37334129 | ||||||
chr5:37334204
|
T | C | 7 | a0001c0005t0009g0054a0001c0005t0009g0057a0001c0005t0009g0058others(4): Show | 7 | HG02145.hp1 HG02895.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.1348-571A>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 12/34 | chr5 | 37334204 | ||||||
chr5:37334259
|
C | T | 1 | a0001c0002t0014g0079 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1348-626G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 12/34 | chr5 | 37334259 | ||||||
chr5:37334322
|
C | T | 1 | a0001c0002t0025g0279 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1348-689G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 12/34 | chr5 | 37334322 | ||||||
chr5:37334384
|
C | CT | 42 | a0001c0002t0004g0004a0001c0002t0004g0019a0001c0002t0004g0020others(39): Show | 42 | HG01109.hp2 HG01192.hp2 HG01243.hp1 others(39): Show |
intron_variant | MODIFIER | c.1348-752dupA | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 12/34 | chr5 | 37334384 | ||||||
chr5:37334501
|
C | G | 1 | a0001c0004t0052g0056 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1348-868G>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 12/34 | chr5 | 37334501 | ||||||
chr5:37334520
|
A | G | 1 | a0001c0002t0007g0049 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1348-887T>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 12/34 | chr5 | 37334520 | ||||||
chr5:37334747
|
T | C | 3 | a0001c0002t0020g0271a0001c0002t0020g0281a0001c0002t0020g0289 | 3 | HG00099.hp1 HG00735.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1348-1114A>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 12/34 | chr5 | 37334747 | ||||||
chr5:37334869
|
T | A | 1 | a0001c0004t0052g0056 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1348-1236A>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 12/34 | chr5 | 37334869 | ||||||
chr5:37335015
|
G | A | 1 | a0001c0003t0010g0188 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1348-1382C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 12/34 | chr5 | 37335015 | ||||||
chr5:37335136
|
C | T | 10 | a0001c0004t0011g0051a0001c0004t0011g0052a0001c0004t0011g0053others(7): Show | 10 | HG02257.hp1 HG02486.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.1348-1503G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 12/34 | chr5 | 37335136 | ||||||
chr5:37335137
|
G | A | 7 | a0001c0005t0009g0054a0001c0005t0009g0057a0001c0005t0009g0058others(4): Show | 7 | HG02145.hp1 HG02895.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.1348-1504C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 12/34 | chr5 | 37335137 | ||||||
chr5:37335157
|
C | CA | 45 | a0001c0001t0001g0120a0001c0001t0001g0136a0001c0001t0003g0098others(42): Show | 45 | HG00099.hp1 HG00408.hp2 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.1348-1525dupT | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 12/34 | chr5 | 37335157 | ||||||
chr5:37335239
|
G | A | 1 | a0006c0016t0001g0200 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1348-1606C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 12/34 | chr5 | 37335239 | ||||||
chr5:37335255
|
C | T | 9 | a0001c0002t0008g0009a0001c0002t0008g0010a0001c0002t0008g0011others(6): Show | 9 | HG01243.hp2 HG02109.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1348-1622G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 12/34 | chr5 | 37335255 | ||||||
chr5:37335288
|
G | A | 1 | a0001c0001t0001g0105 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1348-1655C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 12/34 | chr5 | 37335288 | ||||||
chr5:37335332
|
CT | C | 112 | a0001c0002t0002g0073a0001c0002t0002g0074a0001c0002t0002g0076others(109): Show | 112 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.1348-1700delA | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 12/34 | chr5 | 37335332 | ||||||
chr5:37335380
|
G | GA | 22 | a0001c0002t0002g0274a0001c0002t0002g0290a0001c0002t0005g0270others(19): Show | 22 | HG00099.hp1 HG00408.hp2 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.1348-1748dupT | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 12/34 | chr5 | 37335380 | ||||||
chr5:37335380
|
G | GAA | 15 | a0001c0002t0007g0030a0001c0002t0007g0037a0001c0002t0007g0038others(12): Show | 15 | HG01243.hp1 HG01261.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1348-1749_1348-174 others(6): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 12/34 | chr5 | 37335380 | ||||||
chr5:37335380
|
GA | G | 183 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0095others(180): Show | 184 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.1348-1748delT | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 12/34 | chr5 | 37335380 | ||||||
chr5:37335571
|
T | C | 1 | a0001c0004t0011g0053 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1348-1938A>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 12/34 | chr5 | 37335571 | ||||||
chr5:37335587
|
C | T | 1 | a0001c0002t0005g0266 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1348-1954G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 12/34 | chr5 | 37335587 | ||||||
chr5:37335653
|
TTTAAAAA others(5): Show |
T | 3 | a0001c0003t0001g0173a0001c0003t0001g0205a0001c0003t0001g0228 | 3 | HG01952.hp1 HG02723.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.1348-2032_1348-202 others(16): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 12/34 | chr5 | 37335653 | ||||||
chr5:37335777
|
C | T | 1 | a0001c0001t0001g0095 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1347+2041G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 12/34 | chr5 | 37335777 | ||||||
chr5:37335852
|
A | AG | 7 | a0001c0001t0001g0110a0001c0001t0001g0168a0001c0001t0043g0138others(4): Show | 7 | HG01358.hp2 HG02027.hp2 HG03669.hp2 others(4): Show |
intron_variant | MODIFIER | c.1347+1965dupC | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 12/34 | chr5 | 37335852 | ||||||
chr5:37335901
|
G | C | 1 | a0001c0003t0001g0207 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1347+1917C>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 12/34 | chr5 | 37335901 | ||||||
chr5:37336097
|
T | C | 9 | a0001c0001t0001g0106a0001c0001t0001g0115a0001c0001t0001g0135others(6): Show | 9 | NA18612.hp2 NA18946.hp2 NA18961.hp1 others(6): Show |
intron_variant | MODIFIER | c.1347+1721A>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 12/34 | chr5 | 37336097 | ||||||
chr5:37336099
|
A | G | 1 | a0009c0012t0008g0013 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1347+1719T>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 12/34 | chr5 | 37336099 | ||||||
chr5:37336126
|
C | T | 5 | a0001c0002t0005g0266a0001c0002t0005g0267a0001c0002t0005g0268others(2): Show | 5 | HG02055.hp1 HG02647.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1347+1692G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 12/34 | chr5 | 37336126 | ||||||
chr5:37336253
|
G | A | 1 | a0001c0003t0001g0186 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1347+1565C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 12/34 | chr5 | 37336253 | ||||||
chr5:37336261
|
G | A | 1 | a0001c0001t0001g0194 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1347+1557C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 12/34 | chr5 | 37336261 | ||||||
chr5:37336385
|
G | T | 49 | a0001c0002t0002g0073a0001c0002t0002g0074a0001c0002t0002g0076others(46): Show | 49 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(46): Show |
intron_variant | MODIFIER | c.1347+1433C>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 12/34 | chr5 | 37336385 | ||||||
chr5:37336609
|
A | G | 107 | a0001c0002t0002g0073a0001c0002t0002g0074a0001c0002t0002g0076others(104): Show | 107 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.1347+1209T>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 12/34 | chr5 | 37336609 | ||||||
chr5:37336621
|
C | T | 1 | a0001c0003t0001g0228 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1347+1197G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 12/34 | chr5 | 37336621 | ||||||
chr5:37337045
|
C | T | 189 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0095others(186): Show | 189 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.1347+773G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 12/34 | chr5 | 37337045 | ||||||
chr5:37337342
|
T | C | 1 | a0001c0004t0011g0052 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1347+476A>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 12/34 | chr5 | 37337342 | ||||||
chr5:37337528
|
G | GA | 8 | a0001c0001t0001g0123a0001c0005t0009g0054a0001c0005t0009g0057others(5): Show | 8 | HG02145.hp1 HG02895.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.1347+289dupT | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 12/34 | chr5 | 37337528 | ||||||
chr5:37337627
|
T | A | 1 | a0001c0002t0002g0082 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1347+191A>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 12/34 | chr5 | 37337627 | ||||||
chr5:37338190
|
C | A | 2 | a0001c0002t0025g0273a0001c0002t0048g0288 | 2 | HG01884.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.1247-272G>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 11/34 | chr5 | 37338190 | ||||||
chr5:37338310
|
T | C | 49 | a0001c0002t0002g0073a0001c0002t0002g0074a0001c0002t0002g0076others(46): Show | 49 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(46): Show |
intron_variant | MODIFIER | c.1247-392A>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 11/34 | chr5 | 37338310 | ||||||
chr5:37338317
|
C | CA | 63 | a0001c0001t0001g0104a0001c0001t0001g0121a0001c0001t0001g0122others(60): Show | 63 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.1247-400dupT | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 11/34 | chr5 | 37338317 | ||||||
chr5:37338317
|
C | CAA | 6 | a0001c0002t0004g0020a0001c0002t0004g0026a0001c0002t0008g0009others(3): Show | 6 | HG01884.hp1 HG02109.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.1247-401_1247-400d others(4): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 11/34 | chr5 | 37338317 | ||||||
chr5:37338317
|
CA | C | 19 | a0001c0002t0007g0030a0001c0002t0007g0036a0001c0002t0007g0037others(16): Show | 19 | HG01109.hp2 HG01243.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.1247-400delT | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 11/34 | chr5 | 37338317 | ||||||
chr5:37338431
|
C | T | 5 | a0001c0002t0005g0266a0001c0002t0005g0267a0001c0002t0005g0268others(2): Show | 5 | HG02055.hp1 HG02647.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1247-513G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 11/34 | chr5 | 37338431 | ||||||
chr5:37338468
|
G | A | 21 | a0001c0002t0002g0274a0001c0002t0002g0290a0001c0002t0006g0272others(18): Show | 21 | HG00099.hp1 HG00408.hp2 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.1247-550C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 11/34 | chr5 | 37338468 | ||||||
chr5:37338476
|
G | A | 1 | a0001c0002t0008g0016 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1247-558C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 11/34 | chr5 | 37338476 | ||||||
chr5:37338500
|
G | A | 26 | a0001c0002t0004g0004a0001c0002t0004g0019a0001c0002t0004g0020others(23): Show | 26 | HG01192.hp2 HG01243.hp2 HG01346.hp1 others(23): Show |
intron_variant | MODIFIER | c.1247-582C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 11/34 | chr5 | 37338500 | ||||||
chr5:37338544
|
C | A | 77 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0095others(74): Show | 77 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.1247-626G>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 11/34 | chr5 | 37338544 | ||||||
chr5:37338563
|
G | A | 1 | a0001c0003t0003g0203 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1247-645C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 11/34 | chr5 | 37338563 | ||||||
chr5:37338621
|
G | C | 1 | a0001c0002t0005g0266 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1247-703C>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 11/34 | chr5 | 37338621 | ||||||
chr5:37338626
|
C | T | 2 | a0001c0002t0002g0086a0001c0002t0002g0088 | 2 | HG02723.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1247-708G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 11/34 | chr5 | 37338626 | ||||||
chr5:37338757
|
A | G | 12 | a0001c0002t0004g0004a0001c0002t0004g0019a0001c0002t0004g0020others(9): Show | 12 | HG01192.hp2 HG01891.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.1247-839T>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 11/34 | chr5 | 37338757 | ||||||
chr5:37338860
|
C | T | 1 | a0001c0004t0053g0265 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1247-942G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 11/34 | chr5 | 37338860 | ||||||
chr5:37338891
|
T | A | 5 | a0001c0002t0005g0266a0001c0002t0005g0267a0001c0002t0005g0268others(2): Show | 5 | HG02055.hp1 HG02647.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1247-973A>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 11/34 | chr5 | 37338891 | ||||||
chr5:37339064
|
T | C | 1 | a0001c0001t0001g0137 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1247-1146A>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 11/34 | chr5 | 37339064 | ||||||
chr5:37339139
|
C | T | 49 | a0001c0002t0002g0073a0001c0002t0002g0074a0001c0002t0002g0076others(46): Show | 49 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(46): Show |
intron_variant | MODIFIER | c.1247-1221G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 11/34 | chr5 | 37339139 | ||||||
chr5:37339196
|
T | C | 4 | a0001c0002t0023g0031a0001c0002t0024g0032a0001c0002t0024g0033others(1): Show | 4 | HG02451.hp1 HG02572.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.1247-1278A>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 11/34 | chr5 | 37339196 | ||||||
chr5:37339293
|
A | G | 2 | a0001c0002t0015g0012a0001c0002t0033g0018 | 2 | HG02055.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1247-1375T>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 11/34 | chr5 | 37339293 | ||||||
chr5:37339307
|
C | CA | 17 | a0001c0001t0001g0122a0001c0001t0001g0137a0001c0002t0005g0266others(14): Show | 17 | HG02027.hp1 HG02055.hp1 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.1247-1390dupT | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 11/34 | chr5 | 37339307 | ||||||
chr5:37339307
|
C | CAAA | 16 | a0001c0002t0007g0030a0001c0002t0007g0036a0001c0002t0007g0037others(13): Show | 16 | HG01109.hp2 HG01243.hp1 HG01261.hp1 others(13): Show |
intron_variant | MODIFIER | c.1247-1392_1247-139 others(7): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 11/34 | chr5 | 37339307 | ||||||
chr5:37339428
|
G | A | 9 | a0001c0002t0008g0009a0001c0002t0008g0010a0001c0002t0008g0011others(6): Show | 9 | HG01243.hp2 HG02109.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1247-1510C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 11/34 | chr5 | 37339428 | ||||||
chr5:37339545
|
C | T | 3 | a0001c0002t0017g0041a0001c0002t0017g0042a0001c0010t0017g0035 | 3 | HG01346.hp1 HG02922.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1246+1545G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 11/34 | chr5 | 37339545 | ||||||
chr5:37339571
|
T | G | 23 | a0001c0002t0004g0004a0001c0002t0004g0019a0001c0002t0004g0020others(20): Show | 23 | HG01192.hp2 HG01243.hp2 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.1246+1519A>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 11/34 | chr5 | 37339571 | ||||||
chr5:37339701
|
A | G | 16 | a0001c0002t0007g0030a0001c0002t0007g0036a0001c0002t0007g0037others(13): Show | 16 | HG01109.hp2 HG01243.hp1 HG01261.hp1 others(13): Show |
intron_variant | MODIFIER | c.1246+1389T>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 11/34 | chr5 | 37339701 | ||||||
chr5:37339790
|
G | A | 26 | a0001c0002t0004g0004a0001c0002t0004g0019a0001c0002t0004g0020others(23): Show | 26 | HG01192.hp2 HG01243.hp2 HG01346.hp1 others(23): Show |
intron_variant | MODIFIER | c.1246+1300C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 11/34 | chr5 | 37339790 | ||||||
chr5:37339819
|
A | T | 5 | a0001c0002t0006g0278a0001c0002t0006g0282a0001c0002t0006g0283others(2): Show | 5 | HG00408.hp2 NA18939.hp2 NA18954.hp1 others(2): Show |
intron_variant | MODIFIER | c.1246+1271T>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 11/34 | chr5 | 37339819 | ||||||
chr5:37339923
|
G | A | 7 | a0001c0005t0009g0054a0001c0005t0009g0057a0001c0005t0009g0058others(4): Show | 7 | HG02145.hp1 HG02895.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.1246+1167C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 11/34 | chr5 | 37339923 | ||||||
chr5:37339966
|
T | C | 8 | a0001c0005t0009g0054a0001c0005t0009g0057a0001c0005t0009g0058others(5): Show | 8 | HG02145.hp1 HG02895.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.1246+1124A>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 11/34 | chr5 | 37339966 | ||||||
chr5:37340024
|
G | A | 77 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0095others(74): Show | 77 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.1246+1066C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 11/34 | chr5 | 37340024 | ||||||
chr5:37340050
|
C | T | 1 | a0001c0003t0041g0226 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1246+1040G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 11/34 | chr5 | 37340050 | ||||||
chr5:37340167
|
A | G | 1 | a0001c0001t0022g0099 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1246+923T>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 11/34 | chr5 | 37340167 | ||||||
chr5:37340311
|
C | A | 1 | a0001c0002t0045g0292 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1246+779G>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 11/34 | chr5 | 37340311 | ||||||
chr5:37340442
|
CA | C | 8 | a0001c0003t0001g0254a0001c0005t0009g0054a0001c0005t0009g0057others(5): Show | 8 | HG02145.hp1 HG02895.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.1246+647delT | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 11/34 | chr5 | 37340442 | ||||||
chr5:37340594
|
C | T | 49 | a0001c0002t0002g0073a0001c0002t0002g0074a0001c0002t0002g0076others(46): Show | 49 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(46): Show |
intron_variant | MODIFIER | c.1246+496G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 11/34 | chr5 | 37340594 | ||||||
chr5:37340595
|
G | A | 1 | a0001c0001t0001g0132 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1246+495C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 11/34 | chr5 | 37340595 | ||||||
chr5:37340676
|
C | G | 8 | a0001c0002t0008g0009a0001c0002t0008g0010a0001c0002t0008g0011others(5): Show | 8 | HG01243.hp2 HG02109.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1246+414G>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 11/34 | chr5 | 37340676 | ||||||
chr5:37340935
|
C | A | 34 | a0001c0002t0004g0004a0001c0002t0004g0019a0001c0002t0004g0020others(31): Show | 34 | HG01192.hp2 HG01243.hp2 HG01346.hp1 others(31): Show |
intron_variant | MODIFIER | c.1246+155G>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 11/34 | chr5 | 37340935 | ||||||
chr5:37341085
|
C | G | 2 | a0001c0001t0001g0126a0001c0001t0038g0117 | 2 | HG02083.hp2 HG02129.hp2 |
splice_region_variant&intron_variant | LOW | c.1246+5G>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 11/34 | chr5 | 37341085 | ||||||
chr5:37341250
|
T | C | 77 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0095others(74): Show | 77 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(74): Show |
splice_region_variant&intron_variant | LOW | c.1094-8A>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 10/34 | chr5 | 37341250 | ||||||
chr5:37341301
|
G | A | 1 | a0001c0006t0036g0046 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1094-59C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 10/34 | chr5 | 37341301 | ||||||
chr5:37341400
|
C | T | 65 | a0001c0002t0002g0073a0001c0002t0002g0074a0001c0002t0002g0076others(62): Show | 65 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.1094-158G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 10/34 | chr5 | 37341400 | ||||||
chr5:37341401
|
G | A | 10 | a0001c0003t0001g0197a0001c0003t0001g0293a0001c0003t0022g0219others(7): Show | 10 | HG02145.hp1 HG02738.hp2 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.1094-159C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 10/34 | chr5 | 37341401 | ||||||
chr5:37341858
|
T | C | 5 | a0001c0002t0006g0278a0001c0002t0006g0282a0001c0002t0006g0283others(2): Show | 5 | HG00408.hp2 NA18939.hp2 NA18954.hp1 others(2): Show |
intron_variant | MODIFIER | c.1094-616A>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 10/34 | chr5 | 37341858 | ||||||
chr5:37342014
|
C | A | 24 | a0001c0002t0002g0073a0001c0002t0002g0074a0001c0002t0002g0076others(21): Show | 24 | HG00423.hp2 HG00642.hp2 HG01069.hp1 others(21): Show |
intron_variant | MODIFIER | c.1093+535G>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 10/34 | chr5 | 37342014 | ||||||
chr5:37342200
|
A | G | 7 | a0001c0005t0009g0054a0001c0005t0009g0057a0001c0005t0009g0058others(4): Show | 7 | HG02145.hp1 HG02895.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.1093+349T>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 10/34 | chr5 | 37342200 | ||||||
chr5:37342699
|
TA | T | 7 | a0001c0005t0009g0054a0001c0005t0009g0057a0001c0005t0009g0058others(4): Show | 7 | HG02145.hp1 HG02895.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.996-54delT | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 9/34 | chr5 | 37342699 | ||||||
chr5:37342936
|
C | T | 65 | a0001c0002t0002g0073a0001c0002t0002g0074a0001c0002t0002g0076others(62): Show | 65 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.996-290G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 9/34 | chr5 | 37342936 | ||||||
chr5:37343282
|
G | A | 1 | a0001c0010t0017g0035 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.996-636C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 9/34 | chr5 | 37343282 | ||||||
chr5:37343287
|
G | A | 1 | a0001c0002t0006g0287 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.996-641C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 9/34 | chr5 | 37343287 | ||||||
chr5:37343317
|
G | A | 3 | a0001c0002t0017g0041a0001c0002t0017g0042a0001c0010t0017g0035 | 3 | HG01346.hp1 HG02922.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.996-671C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 9/34 | chr5 | 37343317 | ||||||
chr5:37343418
|
G | A | 1 | a0001c0002t0002g0074 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.996-772C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 9/34 | chr5 | 37343418 | ||||||
chr5:37343444
|
C | G | 1 | a0006c0016t0001g0200 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.996-798G>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 9/34 | chr5 | 37343444 | ||||||
chr5:37343447
|
G | T | 2 | a0001c0001t0001g0103a0001c0001t0037g0091 | 2 | HG02080.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.996-801C>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 9/34 | chr5 | 37343447 | ||||||
chr5:37343448
|
A | T | 2 | a0001c0001t0001g0103a0001c0001t0037g0091 | 2 | HG02080.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.996-802T>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 9/34 | chr5 | 37343448 | ||||||
chr5:37343449
|
A | C | 2 | a0001c0001t0001g0103a0001c0001t0037g0091 | 2 | HG02080.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.996-803T>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 9/34 | chr5 | 37343449 | ||||||
chr5:37343450
|
A | C | 2 | a0001c0001t0001g0103a0001c0001t0037g0091 | 2 | HG02080.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.996-804T>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 9/34 | chr5 | 37343450 | ||||||
chr5:37343452
|
A | G | 2 | a0001c0001t0001g0103a0001c0001t0037g0091 | 2 | HG02080.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.996-806T>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 9/34 | chr5 | 37343452 | ||||||
chr5:37343453
|
C | T | 2 | a0001c0001t0001g0103a0001c0001t0037g0091 | 2 | HG02080.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.996-807G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 9/34 | chr5 | 37343453 | ||||||
chr5:37343581
|
T | C | 9 | a0001c0004t0011g0051a0001c0004t0011g0052a0001c0004t0011g0053others(6): Show | 9 | HG02257.hp1 HG02486.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.996-935A>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 9/34 | chr5 | 37343581 | ||||||
chr5:37343752
|
G | A | 1 | a0001c0002t0008g0014 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.996-1106C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 9/34 | chr5 | 37343752 | ||||||
chr5:37343791
|
G | A | 7 | a0001c0005t0009g0054a0001c0005t0009g0057a0001c0005t0009g0058others(4): Show | 7 | HG02145.hp1 HG02895.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.996-1145C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 9/34 | chr5 | 37343791 | ||||||
chr5:37343915
|
T | C | 1 | a0001c0001t0001g0137 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.996-1269A>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 9/34 | chr5 | 37343915 | ||||||
chr5:37344211
|
C | T | 1 | a0001c0003t0005g0164 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.996-1565G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 9/34 | chr5 | 37344211 | ||||||
chr5:37344417
|
C | T | 1 | a0001c0003t0003g0210 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.996-1771G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 9/34 | chr5 | 37344417 | ||||||
chr5:37344444
|
T | A | 196 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0095others(193): Show | 196 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.996-1798A>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 9/34 | chr5 | 37344444 | ||||||
chr5:37344474
|
T | C | 1 | a0001c0001t0001g0142 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.996-1828A>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 9/34 | chr5 | 37344474 | ||||||
chr5:37344628
|
C | T | 77 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0095others(74): Show | 77 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.996-1982G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 9/34 | chr5 | 37344628 | ||||||
chr5:37344871
|
C | CA | 23 | a0001c0001t0001g0108a0001c0001t0001g0150a0001c0001t0001g0199others(20): Show | 23 | HG00423.hp2 HG00642.hp2 HG00673.hp2 others(20): Show |
intron_variant | MODIFIER | c.996-2226dupT | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 9/34 | chr5 | 37344871 | ||||||
chr5:37345050
|
G | A | 1 | a0001c0001t0001g0109 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.996-2404C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 9/34 | chr5 | 37345050 | ||||||
chr5:37345072
|
GC | G | 23 | a0001c0002t0004g0004a0001c0002t0004g0019a0001c0002t0004g0020others(20): Show | 23 | HG01192.hp2 HG01243.hp2 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.996-2427delG | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 9/34 | chr5 | 37345072 | ||||||
chr5:37345139
|
G | A | 2 | a0001c0002t0025g0273a0001c0002t0048g0288 | 2 | HG01884.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.996-2493C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 9/34 | chr5 | 37345139 | ||||||
chr5:37345281
|
G | A | 3 | a0001c0002t0002g0086a0001c0002t0002g0088a0001c0002t0014g0079 | 3 | HG01884.hp2 HG02723.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.996-2635C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 9/34 | chr5 | 37345281 | ||||||
chr5:37345438
|
G | A | 14 | a0001c0002t0004g0004a0001c0002t0004g0019a0001c0002t0004g0020others(11): Show | 14 | HG01192.hp2 HG01891.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.996-2792C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 9/34 | chr5 | 37345438 | ||||||
chr5:37345510
|
C | CA | 59 | a0001c0001t0001g0124a0001c0001t0001g0143a0001c0001t0001g0161others(56): Show | 59 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.996-2865dupT | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 9/34 | chr5 | 37345510 | ||||||
chr5:37345510
|
C | CAA | 12 | a0001c0002t0002g0087a0001c0002t0004g0021a0001c0002t0008g0009others(9): Show | 12 | HG00642.hp2 HG02109.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.996-2866_996-2865d others(4): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 9/34 | chr5 | 37345510 | ||||||
chr5:37345510
|
CA | C | 8 | a0001c0001t0026g0152a0001c0001t0031g0154a0001c0001t0043g0138others(5): Show | 8 | HG01167.hp1 HG02004.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.996-2865delT | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 9/34 | chr5 | 37345510 | ||||||
chr5:37345567
|
A | G | 4 | a0001c0002t0005g0267a0001c0002t0005g0268a0001c0002t0005g0269others(1): Show | 4 | HG02055.hp1 HG03041.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.996-2921T>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 9/34 | chr5 | 37345567 | ||||||
chr5:37345746
|
T | C | 1 | a0001c0001t0001g0122 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.995+2759A>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 9/34 | chr5 | 37345746 | ||||||
chr5:37345775
|
G | A | 5 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0003g0098others(2): Show | 5 | HG00438.hp2 HG02074.hp1 NA18953.hp2 others(2): Show |
intron_variant | MODIFIER | c.995+2730C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 9/34 | chr5 | 37345775 | ||||||
chr5:37345776
|
C | T | 1 | a0001c0002t0055g0068 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.995+2729G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 9/34 | chr5 | 37345776 | ||||||
chr5:37345814
|
G | A | 1 | a0001c0002t0020g0289 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.995+2691C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 9/34 | chr5 | 37345814 | ||||||
chr5:37345894
|
G | C | 1 | a0001c0002t0013g0067 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.995+2611C>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 9/34 | chr5 | 37345894 | ||||||
chr5:37345908
|
C | CA | 8 | a0001c0001t0001g0193a0001c0001t0003g0166a0001c0001t0043g0138others(5): Show | 8 | HG00642.hp2 HG01361.hp2 HG01981.hp1 others(5): Show |
intron_variant | MODIFIER | c.995+2596dupT | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 9/34 | chr5 | 37345908 | ||||||
chr5:37345908
|
CA | C | 38 | a0001c0001t0001g0162a0001c0002t0002g0074a0001c0002t0004g0004others(35): Show | 38 | HG01192.hp2 HG01243.hp2 HG01346.hp1 others(35): Show |
intron_variant | MODIFIER | c.995+2596delT | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 9/34 | chr5 | 37345908 | ||||||
chr5:37345908
|
CAA | C | 8 | a0001c0002t0004g0022a0001c0004t0011g0051a0001c0004t0011g0052others(5): Show | 8 | HG02257.hp1 HG02486.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.995+2595_995+2596d others(4): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 9/34 | chr5 | 37345908 | ||||||
chr5:37346277
|
GA | G | 7 | a0001c0005t0009g0054a0001c0005t0009g0057a0001c0005t0009g0058others(4): Show | 7 | HG02145.hp1 HG02895.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.995+2227delT | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 9/34 | chr5 | 37346277 | ||||||
chr5:37346411
|
C | T | 8 | a0001c0003t0001g0175a0001c0003t0001g0191a0001c0003t0001g0220others(5): Show | 8 | HG01358.hp2 HG01433.hp1 HG01975.hp1 others(5): Show |
intron_variant | MODIFIER | c.995+2094G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 9/34 | chr5 | 37346411 | ||||||
chr5:37346529
|
A | T | 1 | a0007c0013t0001g0251 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.995+1976T>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 9/34 | chr5 | 37346529 | ||||||
chr5:37346676
|
AC | A | 5 | a0001c0002t0005g0266a0001c0002t0005g0267a0001c0002t0005g0268others(2): Show | 5 | HG02055.hp1 HG02647.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.995+1828delG | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 9/34 | chr5 | 37346676 | ||||||
chr5:37346677
|
C | A | 107 | a0001c0002t0002g0073a0001c0002t0002g0074a0001c0002t0002g0076others(104): Show | 107 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.995+1828G>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 9/34 | chr5 | 37346677 | ||||||
chr5:37346853
|
T | C | 1 | a0001c0003t0001g0175 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.995+1652A>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 9/34 | chr5 | 37346853 | ||||||
chr5:37346952
|
G | A | 2 | a0001c0004t0029g0002a0001c0011t0028g0003 | 2 | HG02809.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.995+1553C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 9/34 | chr5 | 37346952 | ||||||
chr5:37346962
|
T | A | 65 | a0001c0002t0002g0073a0001c0002t0002g0074a0001c0002t0002g0076others(62): Show | 65 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.995+1543A>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 9/34 | chr5 | 37346962 | ||||||
chr5:37347064
|
T | A | 3 | a0001c0002t0004g0019a0001c0002t0004g0022a0001c0002t0004g0027 | 3 | HG02896.hp2 HG02897.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.995+1441A>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 9/34 | chr5 | 37347064 | ||||||
chr5:37347170
|
G | A | 2 | a0001c0002t0002g0274a0001c0002t0002g0290 | 2 | HG02486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.995+1335C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 9/34 | chr5 | 37347170 | ||||||
chr5:37347315
|
G | A | 24 | a0001c0002t0002g0073a0001c0002t0002g0074a0001c0002t0002g0076others(21): Show | 24 | HG00423.hp2 HG00642.hp2 HG01069.hp1 others(21): Show |
intron_variant | MODIFIER | c.995+1190C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 9/34 | chr5 | 37347315 | ||||||
chr5:37347336
|
C | CAT | 112 | a0001c0002t0002g0073a0001c0002t0002g0074a0001c0002t0002g0076others(109): Show | 112 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.995+1168_995+1169i others(4): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 9/34 | chr5 | 37347336 | ||||||
chr5:37347384
|
A | G | 8 | a0001c0005t0009g0054a0001c0005t0009g0057a0001c0005t0009g0058others(5): Show | 8 | HG02145.hp1 HG02895.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.995+1121T>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 9/34 | chr5 | 37347384 | ||||||
chr5:37347405
|
A | G | 2 | a0001c0002t0007g0040a0001c0002t0007g0048 | 2 | HG02280.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.995+1100T>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 9/34 | chr5 | 37347405 | ||||||
chr5:37347631
|
G | C | 5 | a0001c0004t0011g0051a0001c0004t0011g0052a0001c0004t0011g0053others(2): Show | 5 | HG02257.hp1 HG02486.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.995+874C>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 9/34 | chr5 | 37347631 | ||||||
chr5:37347637
|
A | C | 1 | a0001c0001t0001g0194 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.995+868T>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 9/34 | chr5 | 37347637 | ||||||
chr5:37347696
|
C | CA | 18 | a0001c0001t0001g0144a0001c0001t0018g0094a0001c0002t0007g0038others(15): Show | 18 | HG00423.hp1 HG00642.hp1 HG01175.hp1 others(15): Show |
intron_variant | MODIFIER | c.995+808dupT | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 9/34 | chr5 | 37347696 | ||||||
chr5:37347821
|
C | T | 2 | a0001c0004t0029g0002a0001c0011t0028g0003 | 2 | HG02809.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.995+684G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 9/34 | chr5 | 37347821 | ||||||
chr5:37347832
|
C | T | 9 | a0001c0004t0011g0051a0001c0004t0011g0052a0001c0004t0011g0053others(6): Show | 9 | HG02257.hp1 HG02486.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.995+673G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 9/34 | chr5 | 37347832 | ||||||
chr5:37347838
|
T | A | 8 | a0001c0002t0007g0030a0001c0002t0007g0036a0001c0002t0007g0037others(5): Show | 8 | HG01109.hp2 HG02258.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.995+667A>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 9/34 | chr5 | 37347838 | ||||||
chr5:37347907
|
C | T | 2 | a0001c0002t0027g0034a0001c0002t0027g0045 | 2 | HG01243.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.995+598G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 9/34 | chr5 | 37347907 | ||||||
chr5:37347919
|
G | A | 3 | a0001c0002t0005g0267a0001c0002t0005g0268a0001c0002t0005g0269 | 3 | HG02055.hp1 NA19043.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.995+586C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 9/34 | chr5 | 37347919 | ||||||
chr5:37348006
|
T | C | 1 | a0001c0001t0037g0091 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.995+499A>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 9/34 | chr5 | 37348006 | ||||||
chr5:37348020
|
A | G | 112 | a0001c0002t0002g0073a0001c0002t0002g0074a0001c0002t0002g0076others(109): Show | 112 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.995+485T>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 9/34 | chr5 | 37348020 | ||||||
chr5:37348061
|
G | A | 1 | a0001c0002t0023g0065 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.995+444C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 9/34 | chr5 | 37348061 | ||||||
chr5:37348074
|
C | T | 9 | a0001c0004t0011g0051a0001c0004t0011g0052a0001c0004t0011g0053others(6): Show | 9 | HG02257.hp1 HG02486.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.995+431G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 9/34 | chr5 | 37348074 | ||||||
chr5:37348095
|
C | A | 1 | a0006c0016t0001g0200 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.995+410G>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 9/34 | chr5 | 37348095 | ||||||
chr5:37348133
|
T | G | 77 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0095others(74): Show | 77 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.995+372A>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 9/34 | chr5 | 37348133 | ||||||
chr5:37348141
|
A | T | 28 | a0001c0002t0007g0030a0001c0002t0007g0036a0001c0002t0007g0037others(25): Show | 28 | HG01109.hp2 HG01243.hp1 HG01261.hp1 others(25): Show |
intron_variant | MODIFIER | c.995+364T>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 9/34 | chr5 | 37348141 | ||||||
chr5:37348307
|
A | AAAAT | 26 | a0001c0001t0001g0168a0001c0001t0001g0192a0001c0001t0001g0193others(23): Show | 26 | HG01069.hp2 HG01361.hp2 HG01517.hp2 others(23): Show |
intron_variant | MODIFIER | c.995+194_995+197dup others(4): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 9/34 | chr5 | 37348307 | ||||||
chr5:37348370
|
G | A | 3 | a0001c0002t0016g0043a0001c0006t0016g0044a0001c0006t0036g0046 | 3 | HG01261.hp1 HG02615.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.995+135C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 9/34 | chr5 | 37348370 | ||||||
chr5:37348469
|
T | C | 2 | a0001c0004t0029g0002a0001c0011t0028g0003 | 2 | HG02809.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.995+36A>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 9/34 | chr5 | 37348469 | ||||||
chr5:37348471
|
C | A | 4 | a0001c0002t0005g0267a0001c0002t0005g0268a0001c0002t0005g0269others(1): Show | 4 | HG02055.hp1 HG03041.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.995+34G>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 9/34 | chr5 | 37348471 | ||||||
chr5:37348497
|
CAT | C | 10 | a0001c0003t0001g0165a0001c0003t0001g0170a0001c0003t0001g0174others(7): Show | 10 | HG00423.hp1 HG00673.hp2 HG02027.hp2 others(7): Show |
splice_region_variant&intron_variant | LOW | c.995+6_995+7delAT | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 9/34 | chr5 | 37348497 | ||||||
chr5:37349016
|
A | C | 2 | a0001c0002t0006g0282a0001c0002t0006g0283 | 2 | NA18954.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.903+156T>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 8/34 | chr5 | 37349016 | ||||||
chr5:37349038
|
G | A | 5 | a0001c0002t0005g0266a0001c0002t0005g0267a0001c0002t0005g0268others(2): Show | 5 | HG02055.hp1 HG02647.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.903+134C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 8/34 | chr5 | 37349038 | ||||||
chr5:37349049
|
C | A | 1 | a0001c0003t0001g0239 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.903+123G>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 8/34 | chr5 | 37349049 | ||||||
chr5:37349058
|
C | CT | 71 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0095others(68): Show | 71 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.903+113dupA | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 8/34 | chr5 | 37349058 | ||||||
chr5:37349058
|
CT | C | 10 | a0001c0001t0037g0091a0001c0004t0011g0051a0001c0004t0011g0052others(7): Show | 10 | HG02257.hp1 HG02486.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.903+113delA | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 8/34 | chr5 | 37349058 | ||||||
chr5:37349258
|
C | CA | 6 | a0001c0001t0001g0169a0001c0001t0001g0199a0001c0001t0001g0201others(3): Show | 6 | HG01891.hp1 HG02257.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.830-14dupT | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 7/34 | chr5 | 37349258 | ||||||
chr5:37349306
|
T | C | 1 | a0001c0005t0009g0054 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.830-61A>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 7/34 | chr5 | 37349306 | ||||||
chr5:37349464
|
G | A | 1 | a0001c0010t0017g0035 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.830-219C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 7/34 | chr5 | 37349464 | ||||||
chr5:37349678
|
G | C | 1 | a0001c0003t0001g0237 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.830-433C>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 7/34 | chr5 | 37349678 | ||||||
chr5:37349710
|
G | A | 1 | a0001c0001t0001g0153 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.829+450C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 7/34 | chr5 | 37349710 | ||||||
chr5:37349793
|
T | C | 72 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0095others(69): Show | 72 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.829+367A>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 7/34 | chr5 | 37349793 | ||||||
chr5:37349854
|
A | AT | 3 | a0001c0002t0002g0086a0001c0002t0002g0088a0001c0002t0014g0079 | 3 | HG01884.hp2 HG02723.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.829+305dupA | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 7/34 | chr5 | 37349854 | ||||||
chr5:37349866
|
A | C | 1 | a0001c0003t0005g0178 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.829+294T>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 7/34 | chr5 | 37349866 | ||||||
chr5:37349893
|
C | A | 5 | a0001c0004t0011g0051a0001c0004t0011g0052a0001c0004t0011g0053others(2): Show | 5 | HG02257.hp1 HG02486.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.829+267G>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 7/34 | chr5 | 37349893 | ||||||
chr5:37349928
|
C | T | 1 | a0001c0002t0004g0028 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.829+232G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 7/34 | chr5 | 37349928 | ||||||
chr5:37350050
|
TTAACA | T | 12 | a0001c0002t0004g0004a0001c0002t0004g0019a0001c0002t0004g0020others(9): Show | 12 | HG01192.hp2 HG01891.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.829+105_829+109del others(5): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 7/34 | chr5 | 37350050 | ||||||
chr5:37350288
|
C | A | 107 | a0001c0002t0002g0073a0001c0002t0002g0074a0001c0002t0002g0076others(104): Show | 107 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.724-23G>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 6/34 | chr5 | 37350288 | ||||||
chr5:37350325
|
C | T | 7 | a0001c0005t0009g0054a0001c0005t0009g0057a0001c0005t0009g0058others(4): Show | 7 | HG02145.hp1 HG02895.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.724-60G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 6/34 | chr5 | 37350325 | ||||||
chr5:37350362
|
T | C | 2 | a0001c0002t0015g0012a0001c0002t0033g0018 | 2 | HG02055.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.724-97A>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 6/34 | chr5 | 37350362 | ||||||
chr5:37350748
|
A | C | 23 | a0001c0002t0004g0004a0001c0002t0004g0019a0001c0002t0004g0020others(20): Show | 23 | HG01192.hp2 HG01243.hp2 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.723+442T>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 6/34 | chr5 | 37350748 | ||||||
chr5:37350819
|
T | TA | 33 | a0001c0001t0001g0109a0001c0001t0001g0139a0001c0001t0001g0169others(30): Show | 33 | HG00423.hp1 HG01109.hp2 HG01175.hp1 others(30): Show |
intron_variant | MODIFIER | c.723+370dupT | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 6/34 | chr5 | 37350819 | ||||||
chr5:37350819
|
TA | T | 36 | a0001c0001t0001g0140a0001c0001t0003g0157a0001c0001t0037g0091others(33): Show | 36 | HG00423.hp2 HG00642.hp2 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.723+370delT | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 6/34 | chr5 | 37350819 | ||||||
chr5:37350819
|
TAA | T | 10 | a0001c0002t0017g0041a0001c0002t0017g0042a0001c0004t0011g0051others(7): Show | 10 | HG01346.hp1 HG02257.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.723+369_723+370del others(2): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 6/34 | chr5 | 37350819 | ||||||
chr5:37350905
|
T | G | 65 | a0001c0002t0002g0073a0001c0002t0002g0074a0001c0002t0002g0076others(62): Show | 65 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.723+285A>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 6/34 | chr5 | 37350905 | ||||||
chr5:37351066
|
T | C | 17 | a0001c0002t0006g0272a0001c0002t0006g0277a0001c0002t0006g0278others(14): Show | 17 | HG00099.hp1 HG00408.hp2 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.723+124A>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 6/34 | chr5 | 37351066 | ||||||
chr5:37351150
|
T | C | 1 | a0001c0003t0003g0261 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.723+40A>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 6/34 | chr5 | 37351150 | ||||||
chr5:37351510
|
G | C | 1 | a0001c0002t0005g0266 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.557-154C>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 5/34 | chr5 | 37351510 | ||||||
chr5:37351582
|
G | A | 8 | a0001c0005t0009g0054a0001c0005t0009g0057a0001c0005t0009g0058others(5): Show | 8 | HG02145.hp1 HG02895.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.557-226C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 5/34 | chr5 | 37351582 | ||||||
chr5:37351596
|
G | A | 1 | a0001c0003t0001g0177 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.557-240C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 5/34 | chr5 | 37351596 | ||||||
chr5:37351736
|
AC | A | 64 | a0001c0002t0002g0073a0001c0002t0002g0074a0001c0002t0002g0076others(61): Show | 64 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.557-381delG | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 5/34 | chr5 | 37351736 | ||||||
chr5:37351813
|
TAAAAG | T | 8 | a0001c0005t0009g0054a0001c0005t0009g0057a0001c0005t0009g0058others(5): Show | 8 | HG02145.hp1 HG02895.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.557-462_557-458del others(5): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 5/34 | chr5 | 37351813 | ||||||
chr5:37351825
|
G | A | 2 | a0001c0003t0001g0179a0001c0003t0001g0215 | 2 | NA18960.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.557-469C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 5/34 | chr5 | 37351825 | ||||||
chr5:37351871
|
A | AGT | 39 | a0001c0001t0001g0106a0001c0001t0001g0115a0001c0001t0001g0133others(36): Show | 39 | HG00423.hp2 HG00642.hp2 HG01069.hp1 others(36): Show |
intron_variant | MODIFIER | c.557-517_557-516dup others(2): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 5/34 | chr5 | 37351871 | ||||||
chr5:37351871
|
AGT | A | 9 | a0001c0003t0003g0261a0001c0004t0011g0051a0001c0004t0011g0052others(6): Show | 9 | HG02257.hp1 HG02486.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.557-517_557-516del others(2): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 5/34 | chr5 | 37351871 | ||||||
chr5:37351871
|
AGTGT | A | 26 | a0001c0002t0004g0004a0001c0002t0004g0019a0001c0002t0004g0020others(23): Show | 26 | HG01192.hp2 HG01243.hp2 HG01346.hp1 others(23): Show |
intron_variant | MODIFIER | c.557-519_557-516del others(4): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 5/34 | chr5 | 37351871 | ||||||
chr5:37351891
|
T | C | 2 | a0001c0002t0015g0012a0001c0002t0033g0018 | 2 | HG02055.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.557-535A>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 5/34 | chr5 | 37351891 | ||||||
chr5:37351893
|
T | C | 1 | a0001c0001t0003g0098 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.557-537A>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 5/34 | chr5 | 37351893 | ||||||
chr5:37351945
|
G | A | 8 | a0001c0005t0009g0054a0001c0005t0009g0057a0001c0005t0009g0058others(5): Show | 8 | HG02145.hp1 HG02895.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.557-589C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 5/34 | chr5 | 37351945 | ||||||
chr5:37351995
|
G | C | 15 | a0001c0002t0007g0030a0001c0002t0007g0036a0001c0002t0007g0037others(12): Show | 15 | HG01109.hp2 HG01243.hp1 HG01261.hp1 others(12): Show |
intron_variant | MODIFIER | c.557-639C>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 5/34 | chr5 | 37351995 | ||||||
chr5:37352080
|
G | A | 6 | a0001c0003t0001g0207a0001c0003t0001g0213a0001c0003t0001g0236others(3): Show | 6 | HG02040.hp1 HG02040.hp2 HG02071.hp1 others(3): Show |
intron_variant | MODIFIER | c.556+657C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 5/34 | chr5 | 37352080 | ||||||
chr5:37352223
|
T | C | 2 | a0001c0002t0015g0012a0001c0002t0033g0018 | 2 | HG02055.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.556+514A>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 5/34 | chr5 | 37352223 | ||||||
chr5:37352533
|
C | T | 23 | a0001c0002t0004g0004a0001c0002t0004g0019a0001c0002t0004g0020others(20): Show | 23 | HG01192.hp2 HG01243.hp2 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.556+204G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 5/34 | chr5 | 37352533 | ||||||
chr5:37352698
|
C | G | 1 | a0001c0021t0001g0298 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.556+39G>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 5/34 | chr5 | 37352698 | ||||||
chr5:37352727
|
G | A | 26 | a0001c0002t0004g0004a0001c0002t0004g0019a0001c0002t0004g0020others(23): Show | 26 | HG01192.hp2 HG01243.hp2 HG01346.hp1 others(23): Show |
intron_variant | MODIFIER | c.556+10C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 5/34 | chr5 | 37352727 | ||||||
chr5:37352882
|
AGAGT | A | 12 | a0001c0002t0004g0004a0001c0002t0004g0019a0001c0002t0004g0020others(9): Show | 12 | HG01192.hp2 HG01891.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.464-57_464-54delAC others(2): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 4/34 | chr5 | 37352882 | ||||||
chr5:37353062
|
C | A | 1 | a0001c0002t0027g0045 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.464-233G>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 4/34 | chr5 | 37353062 | ||||||
chr5:37353110
|
T | TTATATTA others(19): Show |
1 | a0001c0004t0053g0265 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.464-282_464-281ins others(26): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 4/34 | chr5 | 37353110 | ||||||
chr5:37353227
|
C | T | 26 | a0001c0002t0004g0004a0001c0002t0004g0019a0001c0002t0004g0020others(23): Show | 26 | HG01192.hp2 HG01243.hp2 HG01346.hp1 others(23): Show |
intron_variant | MODIFIER | c.464-398G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 4/34 | chr5 | 37353227 | ||||||
chr5:37353251
|
C | CAT | 8 | a0001c0005t0009g0054a0001c0005t0009g0057a0001c0005t0009g0058others(5): Show | 8 | HG02145.hp1 HG02895.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.464-424_464-423dup others(2): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 4/34 | chr5 | 37353251 | ||||||
chr5:37353259
|
T | C | 49 | a0001c0002t0002g0073a0001c0002t0002g0074a0001c0002t0002g0076others(46): Show | 49 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(46): Show |
intron_variant | MODIFIER | c.464-430A>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 4/34 | chr5 | 37353259 | ||||||
chr5:37353260
|
A | T | 26 | a0001c0002t0004g0004a0001c0002t0004g0019a0001c0002t0004g0020others(23): Show | 26 | HG01192.hp2 HG01243.hp2 HG01346.hp1 others(23): Show |
intron_variant | MODIFIER | c.464-431T>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 4/34 | chr5 | 37353260 | ||||||
chr5:37353286
|
A | C | 2 | a0001c0002t0025g0273a0001c0002t0048g0288 | 2 | HG01884.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.464-457T>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 4/34 | chr5 | 37353286 | ||||||
chr5:37353320
|
C | T | 3 | a0001c0003t0001g0223a0001c0003t0001g0224a0001c0003t0001g0258 | 3 | HG00323.hp2 HG01123.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.464-491G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 4/34 | chr5 | 37353320 | ||||||
chr5:37353326
|
C | A | 77 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0095others(74): Show | 77 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.464-497G>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 4/34 | chr5 | 37353326 | ||||||
chr5:37353340
|
T | C | 1 | a0001c0002t0024g0033 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.464-511A>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 4/34 | chr5 | 37353340 | ||||||
chr5:37353380
|
T | C | 112 | a0001c0002t0002g0073a0001c0002t0002g0074a0001c0002t0002g0076others(109): Show | 112 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.464-551A>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 4/34 | chr5 | 37353380 | ||||||
chr5:37353496
|
T | C | 8 | a0001c0005t0009g0054a0001c0005t0009g0057a0001c0005t0009g0058others(5): Show | 8 | HG02145.hp1 HG02895.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.464-667A>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 4/34 | chr5 | 37353496 | ||||||
chr5:37353521
|
G | A | 9 | a0001c0004t0011g0051a0001c0004t0011g0052a0001c0004t0011g0053others(6): Show | 9 | HG02257.hp1 HG02486.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.464-692C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 4/34 | chr5 | 37353521 | ||||||
chr5:37353534
|
A | T | 64 | a0001c0002t0002g0073a0001c0002t0002g0074a0001c0002t0002g0076others(61): Show | 64 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.464-705T>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 4/34 | chr5 | 37353534 | ||||||
chr5:37353538
|
C | G | 1 | a0001c0002t0005g0269 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.464-709G>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 4/34 | chr5 | 37353538 | ||||||
chr5:37353561
|
G | A | 1 | a0001c0002t0023g0031 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.464-732C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 4/34 | chr5 | 37353561 | ||||||
chr5:37353872
|
T | G | 107 | a0001c0002t0002g0073a0001c0002t0002g0074a0001c0002t0002g0076others(104): Show | 107 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.464-1043A>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 4/34 | chr5 | 37353872 | ||||||
chr5:37353985
|
A | T | 1 | a0001c0004t0052g0056 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.464-1156T>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 4/34 | chr5 | 37353985 | ||||||
chr5:37354104
|
C | T | 21 | a0001c0002t0002g0274a0001c0002t0002g0290a0001c0002t0006g0272others(18): Show | 21 | HG00099.hp1 HG00408.hp2 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.464-1275G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 4/34 | chr5 | 37354104 | ||||||
chr5:37354104
|
CTT | C | 5 | a0001c0005t0009g0057a0001c0005t0009g0061a0001c0005t0009g0062others(2): Show | 5 | HG02145.hp1 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.464-1277_464-1276d others(4): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 4/34 | chr5 | 37354104 | ||||||
chr5:37354139
|
A | G | 1 | a0001c0001t0031g0154 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.464-1310T>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 4/34 | chr5 | 37354139 | ||||||
chr5:37354157
|
T | G | 8 | a0001c0005t0009g0054a0001c0005t0009g0057a0001c0005t0009g0058others(5): Show | 8 | HG02145.hp1 HG02895.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.464-1328A>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 4/34 | chr5 | 37354157 | ||||||
chr5:37354240
|
G | A | 4 | a0001c0002t0008g0009a0001c0002t0008g0010a0001c0002t0008g0015others(1): Show | 4 | HG02109.hp2 HG02922.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.464-1411C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 4/34 | chr5 | 37354240 | ||||||
chr5:37354344
|
C | T | 1 | a0001c0003t0001g0204 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.464-1515G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 4/34 | chr5 | 37354344 | ||||||
chr5:37354434
|
C | T | 23 | a0001c0002t0004g0004a0001c0002t0004g0019a0001c0002t0004g0020others(20): Show | 23 | HG01192.hp2 HG01243.hp2 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.464-1605G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 4/34 | chr5 | 37354434 | ||||||
chr5:37354457
|
C | CT | 9 | a0001c0002t0005g0266a0001c0002t0005g0267a0001c0002t0005g0268others(6): Show | 9 | HG02055.hp1 HG02280.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.464-1629dupA | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 4/34 | chr5 | 37354457 | ||||||
chr5:37354457
|
CT | C | 157 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0095others(154): Show | 157 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.464-1629delA | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 4/34 | chr5 | 37354457 | ||||||
chr5:37354459
|
T | A | 3 | a0001c0001t0001g0160a0001c0001t0018g0094a0001c0001t0026g0146 | 3 | NA18975.hp2 NA19000.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.464-1630A>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 4/34 | chr5 | 37354459 | ||||||
chr5:37354461
|
T | C | 14 | a0001c0002t0007g0030a0001c0002t0007g0036a0001c0002t0007g0037others(11): Show | 14 | HG01109.hp2 HG01243.hp1 HG01261.hp1 others(11): Show |
intron_variant | MODIFIER | c.464-1632A>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 4/34 | chr5 | 37354461 | ||||||
chr5:37354462
|
T | C | 1 | a0001c0002t0035g0047 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.464-1633A>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 4/34 | chr5 | 37354462 | ||||||
chr5:37354549
|
C | T | 1 | a0001c0002t0006g0284 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.464-1720G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 4/34 | chr5 | 37354549 | ||||||
chr5:37354644
|
A | G | 26 | a0001c0002t0004g0004a0001c0002t0004g0019a0001c0002t0004g0020others(23): Show | 26 | HG01192.hp2 HG01243.hp2 HG01346.hp1 others(23): Show |
intron_variant | MODIFIER | c.464-1815T>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 4/34 | chr5 | 37354644 | ||||||
chr5:37354803
|
C | T | 15 | a0001c0002t0007g0030a0001c0002t0007g0036a0001c0002t0007g0037others(12): Show | 15 | HG01109.hp2 HG01243.hp1 HG01261.hp1 others(12): Show |
intron_variant | MODIFIER | c.464-1974G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 4/34 | chr5 | 37354803 | ||||||
chr5:37354863
|
G | A | 1 | a0001c0003t0001g0260 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.464-2034C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 4/34 | chr5 | 37354863 | ||||||
chr5:37354949
|
G | A | 5 | a0001c0004t0011g0051a0001c0004t0011g0052a0001c0004t0011g0053others(2): Show | 5 | HG02257.hp1 HG02486.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.464-2120C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 4/34 | chr5 | 37354949 | ||||||
chr5:37355048
|
T | C | 1 | a0001c0001t0012g0112 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.464-2219A>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 4/34 | chr5 | 37355048 | ||||||
chr5:37355266
|
G | C | 1 | a0001c0003t0001g0260 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.464-2437C>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 4/34 | chr5 | 37355266 | ||||||
chr5:37355282
|
C | T | 1 | a0001c0001t0030g0202 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.464-2453G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 4/34 | chr5 | 37355282 | ||||||
chr5:37355288
|
G | A | 26 | a0001c0002t0004g0004a0001c0002t0004g0019a0001c0002t0004g0020others(23): Show | 26 | HG01192.hp2 HG01243.hp2 HG01346.hp1 others(23): Show |
intron_variant | MODIFIER | c.464-2459C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 4/34 | chr5 | 37355288 | ||||||
chr5:37355422
|
C | T | 1 | a0001c0010t0017g0035 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.464-2593G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 4/34 | chr5 | 37355422 | ||||||
chr5:37355533
|
A | ATG | 3 | a0001c0001t0012g0092a0001c0004t0029g0002a0001c0011t0028g0003 | 3 | HG01515.hp1 HG02809.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.463+2546_463+2547d others(4): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 4/34 | chr5 | 37355533 | ||||||
chr5:37355533
|
A | ATGTG | 11 | a0001c0002t0008g0009a0001c0002t0008g0010a0001c0002t0008g0011others(8): Show | 11 | HG01243.hp2 HG02055.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.463+2544_463+2547d others(6): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 4/34 | chr5 | 37355533 | ||||||
chr5:37355547
|
G | A | 60 | a0001c0002t0002g0073a0001c0002t0002g0074a0001c0002t0002g0076others(57): Show | 60 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(57): Show |
intron_variant | MODIFIER | c.463+2534C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 4/34 | chr5 | 37355547 | ||||||
chr5:37355547
|
G | GTGTGTAT others(3): Show |
1 | a0001c0002t0005g0266 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.463+2533_463+2534i others(12): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 4/34 | chr5 | 37355547 | ||||||
chr5:37355549
|
A | G | 15 | a0001c0002t0004g0004a0001c0002t0004g0019a0001c0002t0004g0020others(12): Show | 15 | HG01192.hp2 HG01346.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.463+2532T>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 4/34 | chr5 | 37355549 | ||||||
chr5:37355551
|
A | G | 12 | a0001c0002t0004g0004a0001c0002t0004g0019a0001c0002t0004g0020others(9): Show | 12 | HG01192.hp2 HG01891.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.463+2530T>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 4/34 | chr5 | 37355551 | ||||||
chr5:37355559
|
A | ATATATAT others(3): Show |
3 | a0001c0002t0005g0267a0001c0002t0005g0268a0001c0002t0005g0270 | 3 | HG02055.hp1 HG03041.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.463+2521_463+2522i others(12): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 4/34 | chr5 | 37355559 | ||||||
chr5:37355559
|
A | T | 11 | a0001c0002t0008g0009a0001c0002t0008g0010a0001c0002t0008g0011others(8): Show | 11 | HG01243.hp2 HG02055.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.463+2522T>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 4/34 | chr5 | 37355559 | ||||||
chr5:37355561
|
ATTTATT | A | 25 | a0001c0002t0002g0274a0001c0002t0002g0290a0001c0002t0006g0272others(22): Show | 25 | HG00099.hp1 HG00408.hp2 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.463+2514_463+2519d others(8): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 4/34 | chr5 | 37355561 | ||||||
chr5:37355563
|
T | A | 24 | a0001c0002t0002g0073a0001c0002t0002g0074a0001c0002t0002g0076others(21): Show | 24 | HG00423.hp2 HG00642.hp2 HG01069.hp1 others(21): Show |
intron_variant | MODIFIER | c.463+2518A>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 4/34 | chr5 | 37355563 | ||||||
chr5:37355569
|
A | ATTTG | 23 | a0001c0001t0001g0169a0001c0001t0001g0199a0001c0001t0001g0201others(20): Show | 23 | HG00323.hp1 HG01109.hp1 HG01346.hp1 others(20): Show |
intron_variant | MODIFIER | c.463+2508_463+2511d others(6): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 4/34 | chr5 | 37355569 | ||||||
chr5:37355569
|
A | G | 17 | a0001c0001t0001g0131a0001c0002t0005g0267a0001c0002t0005g0268others(14): Show | 17 | HG00438.hp1 HG01243.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.463+2512T>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 4/34 | chr5 | 37355569 | ||||||
chr5:37355569
|
ATTTG | A | 39 | a0001c0002t0002g0073a0001c0002t0002g0074a0001c0002t0002g0076others(36): Show | 39 | HG00423.hp2 HG00642.hp2 HG01069.hp1 others(36): Show |
intron_variant | MODIFIER | c.463+2508_463+2511d others(6): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 4/34 | chr5 | 37355569 | ||||||
chr5:37355573
|
G | A | 25 | a0001c0002t0002g0274a0001c0002t0002g0290a0001c0002t0006g0272others(22): Show | 25 | HG00099.hp1 HG00408.hp2 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.463+2508C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 4/34 | chr5 | 37355573 | ||||||
chr5:37355577
|
G | A | 64 | a0001c0002t0002g0073a0001c0002t0002g0074a0001c0002t0002g0076others(61): Show | 64 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.463+2504C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 4/34 | chr5 | 37355577 | ||||||
chr5:37355595
|
C | T | 290 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0095others(287): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.463+2486G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 4/34 | chr5 | 37355595 | ||||||
chr5:37355604
|
T | A | 290 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0095others(287): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.463+2477A>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 4/34 | chr5 | 37355604 | ||||||
chr5:37355948
|
G | A | 1 | a0001c0002t0025g0279 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.463+2133C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 4/34 | chr5 | 37355948 | ||||||
chr5:37356019
|
C | T | 1 | a0001c0002t0005g0266 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.463+2062G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 4/34 | chr5 | 37356019 | ||||||
chr5:37356090
|
G | A | 77 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0095others(74): Show | 77 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.463+1991C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 4/34 | chr5 | 37356090 | ||||||
chr5:37356186
|
G | A | 1 | a0001c0001t0010g0129 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.463+1895C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 4/34 | chr5 | 37356186 | ||||||
chr5:37356229
|
C | CA | 107 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0095others(104): Show | 107 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.463+1851dupT | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 4/34 | chr5 | 37356229 | ||||||
chr5:37356440
|
C | T | 1 | a0001c0002t0034g0005 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.463+1641G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 4/34 | chr5 | 37356440 | ||||||
chr5:37356464
|
G | A | 1 | a0001c0002t0045g0292 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.463+1617C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 4/34 | chr5 | 37356464 | ||||||
chr5:37356623
|
G | C | 72 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0095others(69): Show | 72 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.463+1458C>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 4/34 | chr5 | 37356623 | ||||||
chr5:37356760
|
T | C | 1 | a0001c0002t0046g0291 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.463+1321A>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 4/34 | chr5 | 37356760 | ||||||
chr5:37356809
|
G | A | 23 | a0001c0002t0004g0004a0001c0002t0004g0019a0001c0002t0004g0020others(20): Show | 23 | HG01192.hp2 HG01243.hp2 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.463+1272C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 4/34 | chr5 | 37356809 | ||||||
chr5:37356928
|
C | T | 15 | a0001c0002t0007g0030a0001c0002t0007g0036a0001c0002t0007g0037others(12): Show | 15 | HG01109.hp2 HG01243.hp1 HG01261.hp1 others(12): Show |
intron_variant | MODIFIER | c.463+1153G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 4/34 | chr5 | 37356928 | ||||||
chr5:37357054
|
C | T | 21 | a0001c0002t0002g0274a0001c0002t0002g0290a0001c0002t0006g0272others(18): Show | 21 | HG00099.hp1 HG00408.hp2 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.463+1027G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 4/34 | chr5 | 37357054 | ||||||
chr5:37357063
|
C | T | 1 | a0001c0003t0001g0220 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.463+1018G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 4/34 | chr5 | 37357063 | ||||||
chr5:37357348
|
G | A | 5 | a0001c0002t0006g0278a0001c0002t0006g0282a0001c0002t0006g0283others(2): Show | 5 | HG00408.hp2 NA18939.hp2 NA18954.hp1 others(2): Show |
intron_variant | MODIFIER | c.463+733C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 4/34 | chr5 | 37357348 | ||||||
chr5:37357399
|
C | CA | 101 | a0001c0001t0001g0192a0001c0001t0001g0242a0001c0001t0001g0247others(98): Show | 102 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.463+681dupT | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 4/34 | chr5 | 37357399 | ||||||
chr5:37357399
|
C | CAA | 30 | a0001c0002t0002g0078a0001c0002t0002g0080a0001c0002t0002g0083others(27): Show | 30 | HG00423.hp2 HG01109.hp2 HG01192.hp2 others(27): Show |
intron_variant | MODIFIER | c.463+680_463+681dup others(2): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 4/34 | chr5 | 37357399 | ||||||
chr5:37357399
|
CA | C | 74 | a0001c0001t0001g0089a0001c0001t0001g0096a0001c0001t0001g0100others(71): Show | 74 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.463+681delT | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 4/34 | chr5 | 37357399 | ||||||
chr5:37357399
|
CAA | C | 6 | a0001c0001t0001g0090a0001c0001t0001g0095a0001c0001t0001g0115others(3): Show | 6 | HG01975.hp2 HG02004.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.463+680_463+681del others(2): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 4/34 | chr5 | 37357399 | ||||||
chr5:37357490
|
A | T | 1 | a0001c0003t0001g0207 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.463+591T>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 4/34 | chr5 | 37357490 | ||||||
chr5:37357809
|
A | G | 1 | a0001c0003t0001g0260 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.463+272T>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 4/34 | chr5 | 37357809 | ||||||
chr5:37357861
|
C | T | 49 | a0001c0002t0002g0073a0001c0002t0002g0074a0001c0002t0002g0076others(46): Show | 49 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(46): Show |
intron_variant | MODIFIER | c.463+220G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 4/34 | chr5 | 37357861 | ||||||
chr5:37357906
|
C | A | 1 | a0001c0003t0001g0228 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.463+175G>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 4/34 | chr5 | 37357906 | ||||||
chr5:37358063
|
T | C | 1 | a0001c0002t0002g0082 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.463+18A>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 4/34 | chr5 | 37358063 | ||||||
chr5:37358567
|
T | C | 9 | a0001c0004t0011g0051a0001c0004t0011g0052a0001c0004t0011g0053others(6): Show | 9 | HG02257.hp1 HG02486.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.393-416A>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 3/34 | chr5 | 37358567 | ||||||
chr5:37358568
|
G | A | 1 | a0003c0007t0001g0229 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.393-417C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 3/34 | chr5 | 37358568 | ||||||
chr5:37358739
|
G | C | 291 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0095others(288): Show | 292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.393-588C>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 3/34 | chr5 | 37358739 | ||||||
chr5:37358770
|
G | A | 1 | a0001c0002t0006g0272 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.393-619C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 3/34 | chr5 | 37358770 | ||||||
chr5:37358785
|
G | A | 1 | a0001c0015t0001g0230 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.393-634C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 3/34 | chr5 | 37358785 | ||||||
chr5:37358894
|
G | A | 2 | a0001c0003t0001g0185a0001c0003t0001g0187 | 2 | HG00735.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.393-743C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 3/34 | chr5 | 37358894 | ||||||
chr5:37358941
|
C | G | 2 | a0001c0001t0001g0131a0001c0001t0001g0153 | 2 | HG00438.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.393-790G>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 3/34 | chr5 | 37358941 | ||||||
chr5:37359014
|
C | CA | 30 | a0001c0002t0004g0004a0001c0002t0004g0019a0001c0002t0004g0020others(27): Show | 30 | HG01192.hp2 HG01243.hp2 HG01346.hp1 others(27): Show |
intron_variant | MODIFIER | c.393-864dupT | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 3/34 | chr5 | 37359014 | ||||||
chr5:37359061
|
C | G | 25 | a0001c0002t0004g0004a0001c0002t0004g0019a0001c0002t0004g0020others(22): Show | 25 | HG01192.hp2 HG01243.hp2 HG01346.hp1 others(22): Show |
intron_variant | MODIFIER | c.393-910G>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 3/34 | chr5 | 37359061 | ||||||
chr5:37359069
|
G | A | 4 | a0001c0002t0016g0043a0001c0006t0016g0044a0001c0006t0036g0046others(1): Show | 4 | HG01261.hp1 HG02615.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.393-918C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 3/34 | chr5 | 37359069 | ||||||
chr5:37359102
|
C | T | 9 | a0001c0004t0011g0051a0001c0004t0011g0052a0001c0004t0011g0053others(6): Show | 9 | HG02257.hp1 HG02486.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.393-951G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 3/34 | chr5 | 37359102 | ||||||
chr5:37359141
|
T | TTA | 14 | a0001c0002t0004g0004a0001c0002t0004g0019a0001c0002t0004g0020others(11): Show | 14 | HG01192.hp2 HG01891.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.393-992_393-991dup others(2): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 3/34 | chr5 | 37359141 | ||||||
chr5:37359255
|
C | G | 2 | a0001c0004t0029g0002a0001c0011t0028g0003 | 2 | HG02809.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.393-1104G>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 3/34 | chr5 | 37359255 | ||||||
chr5:37359331
|
C | T | 4 | a0001c0002t0023g0031a0001c0002t0024g0032a0001c0002t0024g0033others(1): Show | 4 | HG02451.hp1 HG02572.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.393-1180G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 3/34 | chr5 | 37359331 | ||||||
chr5:37359674
|
T | G | 16 | a0001c0002t0007g0030a0001c0002t0007g0036a0001c0002t0007g0037others(13): Show | 16 | HG01109.hp2 HG01243.hp1 HG01261.hp1 others(13): Show |
intron_variant | MODIFIER | c.393-1523A>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 3/34 | chr5 | 37359674 | ||||||
chr5:37359985
|
T | G | 290 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0095others(287): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.393-1834A>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 3/34 | chr5 | 37359985 | ||||||
chr5:37360011
|
C | T | 1 | a0001c0003t0022g0219 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.393-1860G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 3/34 | chr5 | 37360011 | ||||||
chr5:37360032
|
C | A | 3 | a0001c0001t0001g0160a0001c0001t0018g0094a0001c0001t0026g0146 | 3 | NA18975.hp2 NA19000.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.393-1881G>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 3/34 | chr5 | 37360032 | ||||||
chr5:37360105
|
G | A | 1 | a0001c0003t0001g0238 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.393-1954C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 3/34 | chr5 | 37360105 | ||||||
chr5:37360168
|
G | A | 21 | a0001c0002t0002g0274a0001c0002t0002g0290a0001c0002t0006g0272others(18): Show | 21 | HG00099.hp1 HG00408.hp2 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.393-2017C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 3/34 | chr5 | 37360168 | ||||||
chr5:37360198
|
C | T | 9 | a0001c0004t0011g0051a0001c0004t0011g0052a0001c0004t0011g0053others(6): Show | 9 | HG02257.hp1 HG02486.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.393-2047G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 3/34 | chr5 | 37360198 | ||||||
chr5:37360297
|
C | T | 1 | a0001c0003t0018g0180 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.393-2146G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 3/34 | chr5 | 37360297 | ||||||
chr5:37360299
|
T | C | 21 | a0001c0002t0002g0274a0001c0002t0002g0290a0001c0002t0006g0272others(18): Show | 21 | HG00099.hp1 HG00408.hp2 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.393-2148A>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 3/34 | chr5 | 37360299 | ||||||
chr5:37360358
|
G | A | 4 | a0001c0002t0006g0284a0001c0002t0006g0286a0001c0002t0006g0287others(1): Show | 4 | HG03017.hp1 HG03669.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.393-2207C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 3/34 | chr5 | 37360358 | ||||||
chr5:37360436
|
G | C | 1 | a0001c0003t0005g0164 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.393-2285C>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 3/34 | chr5 | 37360436 | ||||||
chr5:37360484
|
CA | C | 9 | a0001c0004t0011g0051a0001c0004t0011g0052a0001c0004t0011g0053others(6): Show | 9 | HG02257.hp1 HG02486.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.393-2334delT | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 3/34 | chr5 | 37360484 | ||||||
chr5:37360513
|
C | T | 9 | a0001c0004t0011g0051a0001c0004t0011g0052a0001c0004t0011g0053others(6): Show | 9 | HG02257.hp1 HG02486.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.393-2362G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 3/34 | chr5 | 37360513 | ||||||
chr5:37360617
|
C | T | 1 | a0001c0001t0012g0112 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.393-2466G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 3/34 | chr5 | 37360617 | ||||||
chr5:37360718
|
T | A | 1 | a0007c0013t0001g0251 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.393-2567A>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 3/34 | chr5 | 37360718 | ||||||
chr5:37360777
|
TA | T | 17 | a0001c0002t0002g0274a0001c0002t0002g0290a0001c0002t0006g0277others(14): Show | 17 | HG00099.hp1 HG01884.hp1 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.393-2627delT | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 3/34 | chr5 | 37360777 | ||||||
chr5:37360786
|
A | AG | 18 | a0001c0002t0004g0028a0001c0002t0005g0267a0001c0002t0005g0269others(15): Show | 18 | HG00423.hp1 HG00673.hp2 HG01175.hp1 others(15): Show |
intron_variant | MODIFIER | c.393-2636dupC | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 3/34 | chr5 | 37360786 | ||||||
chr5:37360786
|
A | G | 4 | a0001c0002t0006g0272a0001c0002t0006g0278a0001c0002t0020g0271others(1): Show | 4 | HG00408.hp2 HG00735.hp2 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.393-2635T>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 3/34 | chr5 | 37360786 | ||||||
chr5:37360789
|
G | T | 2 | a0001c0003t0001g0197a0001c0003t0001g0293 | 2 | HG02738.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.393-2638C>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 3/34 | chr5 | 37360789 | ||||||
chr5:37360794
|
G | A | 77 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0095others(74): Show | 77 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.393-2643C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 3/34 | chr5 | 37360794 | ||||||
chr5:37360803
|
C | A | 1 | a0001c0002t0007g0049 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.393-2652G>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 3/34 | chr5 | 37360803 | ||||||
chr5:37360833
|
T | C | 1 | a0001c0003t0001g0186 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.393-2682A>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 3/34 | chr5 | 37360833 | ||||||
chr5:37361244
|
C | T | 1 | a0001c0002t0008g0014 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.392+2644G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 3/34 | chr5 | 37361244 | ||||||
chr5:37361265
|
C | CA | 85 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0095others(82): Show | 85 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.392+2622dupT | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 3/34 | chr5 | 37361265 | ||||||
chr5:37361265
|
C | CAA | 8 | a0001c0001t0001g0102a0001c0001t0001g0106a0001c0001t0001g0151others(5): Show | 8 | HG01361.hp1 HG02647.hp1 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.392+2621_392+2622d others(4): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 3/34 | chr5 | 37361265 | ||||||
chr5:37361265
|
CAAAAAAA others(3): Show |
C | 49 | a0001c0002t0002g0073a0001c0002t0002g0074a0001c0002t0002g0076others(46): Show | 49 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(46): Show |
intron_variant | MODIFIER | c.392+2613_392+2622d others(12): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 3/34 | chr5 | 37361265 | ||||||
chr5:37361285
|
A | AAAAG | 37 | a0001c0002t0004g0004a0001c0002t0004g0019a0001c0002t0004g0020others(34): Show | 37 | HG01109.hp2 HG01192.hp2 HG01243.hp1 others(34): Show |
intron_variant | MODIFIER | c.392+2602_392+2603i others(6): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 3/34 | chr5 | 37361285 | ||||||
chr5:37361291
|
T | C | 1 | a0009c0012t0008g0013 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.392+2597A>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 3/34 | chr5 | 37361291 | ||||||
chr5:37361323
|
A | C | 1 | a0001c0002t0005g0266 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.392+2565T>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 3/34 | chr5 | 37361323 | ||||||
chr5:37361567
|
C | T | 291 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0095others(288): Show | 292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.392+2321G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 3/34 | chr5 | 37361567 | ||||||
chr5:37361581
|
T | G | 1 | a0001c0010t0017g0035 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.392+2307A>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 3/34 | chr5 | 37361581 | ||||||
chr5:37361626
|
T | C | 49 | a0001c0002t0002g0073a0001c0002t0002g0074a0001c0002t0002g0076others(46): Show | 49 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(46): Show |
intron_variant | MODIFIER | c.392+2262A>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 3/34 | chr5 | 37361626 | ||||||
chr5:37361644
|
A | G | 1 | a0001c0001t0001g0100 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.392+2244T>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 3/34 | chr5 | 37361644 | ||||||
chr5:37361657
|
A | G | 4 | a0001c0002t0023g0031a0001c0002t0024g0032a0001c0002t0024g0033others(1): Show | 4 | HG02451.hp1 HG02572.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.392+2231T>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 3/34 | chr5 | 37361657 | ||||||
chr5:37361740
|
G | A | 1 | a0001c0004t0052g0056 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.392+2148C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 3/34 | chr5 | 37361740 | ||||||
chr5:37361775
|
A | G | 1 | a0001c0001t0003g0166 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.392+2113T>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 3/34 | chr5 | 37361775 | ||||||
chr5:37361780
|
T | C | 49 | a0001c0002t0002g0073a0001c0002t0002g0074a0001c0002t0002g0076others(46): Show | 49 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(46): Show |
intron_variant | MODIFIER | c.392+2108A>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 3/34 | chr5 | 37361780 | ||||||
chr5:37361933
|
G | A | 1 | a0001c0002t0005g0266 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.392+1955C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 3/34 | chr5 | 37361933 | ||||||
chr5:37361978
|
T | C | 42 | a0001c0002t0004g0004a0001c0002t0004g0019a0001c0002t0004g0020others(39): Show | 42 | HG01109.hp2 HG01192.hp2 HG01243.hp1 others(39): Show |
intron_variant | MODIFIER | c.392+1910A>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 3/34 | chr5 | 37361978 | ||||||
chr5:37362015
|
T | C | 1 | a0001c0001t0001g0150 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.392+1873A>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 3/34 | chr5 | 37362015 | ||||||
chr5:37362043
|
C | T | 1 | a0001c0005t0009g0054 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.392+1845G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 3/34 | chr5 | 37362043 | ||||||
chr5:37362074
|
AG | A | 6 | a0001c0004t0011g0051a0001c0004t0011g0052a0001c0004t0011g0053others(3): Show | 6 | HG02257.hp1 HG02486.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.392+1813delC | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 3/34 | chr5 | 37362074 | ||||||
chr5:37362117
|
G | C | 1 | a0001c0003t0001g0238 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.392+1771C>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 3/34 | chr5 | 37362117 | ||||||
chr5:37362198
|
T | TACCACAA others(4): Show |
1 | a0001c0002t0005g0270 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.392+1679_392+1689d others(13): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 3/34 | chr5 | 37362198 | ||||||
chr5:37362221
|
C | T | 1 | a0001c0002t0006g0277 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.392+1667G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 3/34 | chr5 | 37362221 | ||||||
chr5:37362523
|
G | C | 1 | a0001c0004t0052g0056 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.392+1365C>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 3/34 | chr5 | 37362523 | ||||||
chr5:37362588
|
G | A | 2 | a0001c0004t0029g0002a0001c0011t0028g0003 | 2 | HG02809.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.392+1300C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 3/34 | chr5 | 37362588 | ||||||
chr5:37362791
|
A | T | 1 | a0001c0001t0001g0127 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.392+1097T>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 3/34 | chr5 | 37362791 | ||||||
chr5:37362984
|
C | T | 1 | a0001c0001t0012g0111 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.392+904G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 3/34 | chr5 | 37362984 | ||||||
chr5:37363063
|
C | T | 1 | a0001c0003t0001g0206 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.392+825G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 3/34 | chr5 | 37363063 | ||||||
chr5:37363137
|
C | T | 1 | a0009c0012t0008g0013 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.392+751G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 3/34 | chr5 | 37363137 | ||||||
chr5:37363203
|
C | T | 1 | a0001c0001t0001g0130 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.392+685G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 3/34 | chr5 | 37363203 | ||||||
chr5:37363204
|
G | A | 12 | a0001c0002t0004g0004a0001c0002t0004g0019a0001c0002t0004g0020others(9): Show | 12 | HG01192.hp2 HG01891.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.392+684C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 3/34 | chr5 | 37363204 | ||||||
chr5:37363208
|
T | G | 2 | a0001c0004t0029g0002a0001c0011t0028g0003 | 2 | HG02809.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.392+680A>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 3/34 | chr5 | 37363208 | ||||||
chr5:37363392
|
C | A | 1 | a0001c0003t0001g0238 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.392+496G>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 3/34 | chr5 | 37363392 | ||||||
chr5:37363518
|
C | T | 1 | a0001c0001t0030g0202 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.392+370G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 3/34 | chr5 | 37363518 | ||||||
chr5:37363564
|
C | T | 8 | a0001c0002t0004g0004a0001c0002t0004g0019a0001c0002t0004g0021others(5): Show | 8 | HG01891.hp2 HG02451.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.392+324G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 3/34 | chr5 | 37363564 | ||||||
chr5:37363601
|
C | T | 15 | a0001c0002t0007g0030a0001c0002t0007g0036a0001c0002t0007g0037others(12): Show | 15 | HG01109.hp2 HG01243.hp1 HG01261.hp1 others(12): Show |
intron_variant | MODIFIER | c.392+287G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 3/34 | chr5 | 37363601 | ||||||
chr5:37364031
|
CTTT | C | 5 | a0001c0002t0005g0266a0001c0002t0005g0267a0001c0002t0005g0268others(2): Show | 5 | HG02055.hp1 HG02647.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.296-50_296-48delAA others(1): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 2/34 | chr5 | 37364031 | ||||||
chr5:37364045
|
A | G | 1 | a0001c0001t0010g0129 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.296-61T>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 2/34 | chr5 | 37364045 | ||||||
chr5:37364542
|
C | T | 2 | a0001c0002t0015g0012a0001c0002t0033g0018 | 2 | HG02055.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.158-158G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37364542 | ||||||
chr5:37364591
|
A | G | 284 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0095others(281): Show | 285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.158-207T>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37364591 | ||||||
chr5:37364640
|
A | AT | 50 | a0001c0001t0001g0246a0001c0001t0001g0247a0001c0002t0002g0073others(47): Show | 50 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(47): Show |
intron_variant | MODIFIER | c.158-257dupA | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37364640 | ||||||
chr5:37364644
|
T | TA | 236 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0095others(233): Show | 237 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.158-261_158-260ins others(1): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37364644 | ||||||
chr5:37364698
|
A | G | 291 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0095others(288): Show | 292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.158-314T>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37364698 | ||||||
chr5:37364828
|
G | C | 23 | a0001c0002t0004g0004a0001c0002t0004g0019a0001c0002t0004g0020others(20): Show | 23 | HG01192.hp2 HG01243.hp2 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.158-444C>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37364828 | ||||||
chr5:37364838
|
G | A | 41 | a0001c0002t0004g0004a0001c0002t0004g0019a0001c0002t0004g0020others(38): Show | 41 | HG01109.hp2 HG01192.hp2 HG01243.hp1 others(38): Show |
intron_variant | MODIFIER | c.158-454C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37364838 | ||||||
chr5:37364866
|
G | C | 9 | a0001c0004t0011g0051a0001c0004t0011g0052a0001c0004t0011g0053others(6): Show | 9 | HG02257.hp1 HG02486.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.158-482C>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37364866 | ||||||
chr5:37364957
|
T | C | 5 | a0001c0001t0012g0092a0001c0001t0012g0093a0001c0001t0012g0111others(2): Show | 5 | HG00323.hp1 HG01109.hp1 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.158-573A>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37364957 | ||||||
chr5:37365156
|
G | A | 15 | a0001c0002t0007g0030a0001c0002t0007g0036a0001c0002t0007g0037others(12): Show | 15 | HG01109.hp2 HG01243.hp1 HG01261.hp1 others(12): Show |
intron_variant | MODIFIER | c.158-772C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37365156 | ||||||
chr5:37365183
|
C | T | 3 | a0001c0004t0029g0002a0001c0004t0052g0056a0001c0011t0028g0003 | 3 | HG02717.hp1 HG02809.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.158-799G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37365183 | ||||||
chr5:37365260
|
A | AAAAT | 109 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0192others(106): Show | 110 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.158-880_158-877dup others(4): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37365260 | ||||||
chr5:37365313
|
G | C | 1 | a0001c0001t0001g0148 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.158-929C>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37365313 | ||||||
chr5:37365342
|
T | C | 1 | a0001c0002t0005g0266 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.158-958A>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37365342 | ||||||
chr5:37365368
|
T | C | 21 | a0001c0002t0002g0274a0001c0002t0002g0290a0001c0002t0006g0272others(18): Show | 21 | HG00099.hp1 HG00408.hp2 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.158-984A>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37365368 | ||||||
chr5:37365435
|
C | T | 49 | a0001c0002t0002g0073a0001c0002t0002g0074a0001c0002t0002g0076others(46): Show | 49 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(46): Show |
intron_variant | MODIFIER | c.158-1051G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37365435 | ||||||
chr5:37365484
|
G | A | 2 | a0001c0004t0029g0002a0001c0011t0028g0003 | 2 | HG02809.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.158-1100C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37365484 | ||||||
chr5:37365637
|
G | A | 41 | a0001c0002t0004g0004a0001c0002t0004g0019a0001c0002t0004g0020others(38): Show | 41 | HG01109.hp2 HG01192.hp2 HG01243.hp1 others(38): Show |
intron_variant | MODIFIER | c.158-1253C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37365637 | ||||||
chr5:37365707
|
C | CG | 4 | a0001c0003t0001g0237a0001c0003t0001g0238a0001c0003t0001g0243others(1): Show | 4 | HG02698.hp1 NA18747.hp2 NA18955.hp1 others(1): Show |
intron_variant | MODIFIER | c.158-1324dupC | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37365707 | ||||||
chr5:37365710
|
GGA | G | 3 | a0001c0002t0024g0032a0001c0004t0011g0051a0001c0004t0011g0052 | 3 | HG02257.hp1 HG02486.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.158-1328_158-1327d others(4): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37365710 | ||||||
chr5:37365711
|
GA | G | 65 | a0001c0001t0001g0108a0001c0001t0001g0252a0001c0001t0003g0245others(62): Show | 66 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(63): Show |
intron_variant | MODIFIER | c.158-1328delT | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37365711 | ||||||
chr5:37365711
|
GAGA | G | 6 | a0001c0002t0005g0266a0001c0002t0008g0009a0001c0002t0008g0015others(3): Show | 6 | HG01346.hp1 HG02109.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.158-1330_158-1328d others(5): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37365711 | ||||||
chr5:37365712
|
A | G | 56 | a0001c0001t0001g0168a0001c0001t0001g0192a0001c0001t0001g0193others(53): Show | 56 | HG00408.hp1 HG00639.hp1 HG01069.hp2 others(53): Show |
intron_variant | MODIFIER | c.158-1328T>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37365712 | ||||||
chr5:37365712
|
AG | A | 40 | a0001c0001t0001g0089a0001c0001t0001g0095a0001c0001t0001g0096others(37): Show | 40 | HG00438.hp2 HG01074.hp2 HG01891.hp2 others(37): Show |
intron_variant | MODIFIER | c.158-1329delC | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37365712 | ||||||
chr5:37365713
|
G | A | 167 | a0001c0001t0001g0090a0001c0001t0001g0100a0001c0001t0001g0101others(164): Show | 167 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.158-1329C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37365713 | ||||||
chr5:37365715
|
A | G | 1 | a0001c0002t0005g0266 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.158-1331T>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37365715 | ||||||
chr5:37365728
|
A | T | 1 | a0001c0002t0023g0031 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.158-1344T>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37365728 | ||||||
chr5:37365730
|
A | T | 1 | a0001c0002t0023g0031 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.158-1346T>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37365730 | ||||||
chr5:37365732
|
A | AT | 3 | a0001c0001t0001g0103a0001c0001t0001g0126a0001c0002t0004g0019 | 3 | HG02080.hp1 HG02083.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.158-1349_158-1348i others(3): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37365732 | ||||||
chr5:37365732
|
A | T | 6 | a0001c0002t0015g0012a0001c0002t0023g0031a0001c0002t0024g0032others(3): Show | 6 | HG02055.hp2 HG02451.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.158-1348T>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37365732 | ||||||
chr5:37365734
|
A | AT | 35 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106others(32): Show | 35 | HG00140.hp2 HG00438.hp1 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.158-1351_158-1350i others(3): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37365734 | ||||||
chr5:37365734
|
A | T | 29 | a0001c0001t0001g0103a0001c0001t0001g0115a0001c0001t0001g0126others(26): Show | 29 | HG00639.hp2 HG01257.hp1 HG02004.hp2 others(26): Show |
intron_variant | MODIFIER | c.158-1350T>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37365734 | ||||||
chr5:37365736
|
A | ATAT | 5 | a0001c0001t0012g0092a0001c0001t0012g0111a0001c0001t0012g0112others(2): Show | 5 | HG00323.hp1 HG01109.hp1 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.158-1353_158-1352i others(5): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37365736 | ||||||
chr5:37365736
|
A | T | 109 | a0001c0001t0001g0089a0001c0001t0001g0095a0001c0001t0001g0096others(106): Show | 109 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.158-1352T>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37365736 | ||||||
chr5:37365738
|
A | AAAAAAAA others(9): Show |
1 | a0001c0001t0030g0202 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.158-1355_158-1354i others(18): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37365738 | ||||||
chr5:37365738
|
A | AAAAAAAA others(10): Show |
3 | a0001c0001t0021g0006a0001c0001t0021g0007a0006c0016t0001g0200 | 3 | HG02559.hp1 NA18906.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.158-1355_158-1354i others(19): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37365738 | ||||||
chr5:37365738
|
A | AAAAATAT others(2): Show |
13 | a0001c0001t0001g0249a0001c0002t0006g0278a0001c0002t0006g0282others(10): Show | 13 | HG00099.hp1 HG00408.hp2 HG03017.hp1 others(10): Show |
intron_variant | MODIFIER | c.158-1355_158-1354i others(11): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37365738 | ||||||
chr5:37365738
|
A | AAATATAT others(6): Show |
1 | a0001c0001t0001g0169 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.158-1355_158-1354i others(15): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37365738 | ||||||
chr5:37365738
|
A | AATATATA others(1): Show |
7 | a0001c0001t0001g0168a0001c0001t0001g0246a0001c0001t0001g0247others(4): Show | 7 | HG01069.hp2 NA18952.hp2 NA18953.hp1 others(4): Show |
intron_variant | MODIFIER | c.158-1362_158-1355d others(10): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37365738 | ||||||
chr5:37365738
|
A | ATAT | 5 | a0001c0002t0013g0067a0001c0002t0013g0069a0001c0002t0055g0068others(2): Show | 5 | HG02004.hp1 HG02148.hp2 HG02273.hp2 others(2): Show |
intron_variant | MODIFIER | c.158-1355_158-1354i others(5): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37365738 | ||||||
chr5:37365738
|
A | ATATATAT | 3 | a0001c0001t0001g0192a0001c0001t0003g0245a0001c0002t0014g0075 | 3 | HG01993.hp1 HG02148.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.158-1355_158-1354i others(9): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37365738 | ||||||
chr5:37365738
|
A | T | 145 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0095others(142): Show | 145 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.158-1354T>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37365738 | ||||||
chr5:37365740
|
T | A | 72 | a0001c0002t0006g0277a0001c0003t0001g0165a0001c0003t0001g0170others(69): Show | 73 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.158-1356A>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37365740 | ||||||
chr5:37365742
|
T | A | 40 | a0001c0003t0001g0165a0001c0003t0001g0170a0001c0003t0001g0172others(37): Show | 40 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(37): Show |
intron_variant | MODIFIER | c.158-1358A>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37365742 | ||||||
chr5:37365750
|
T | C | 5 | a0001c0001t0001g0108a0001c0001t0001g0158a0001c0001t0001g0159others(2): Show | 5 | HG00140.hp2 HG01123.hp1 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.158-1366A>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37365750 | ||||||
chr5:37365752
|
T | C | 57 | a0001c0001t0001g0090a0001c0001t0001g0103a0001c0001t0001g0104others(54): Show | 57 | HG00140.hp2 HG00438.hp1 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.158-1368A>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37365752 | ||||||
chr5:37365752
|
T | TAC | 3 | a0001c0001t0001g0107a0001c0002t0033g0018a0001c0005t0009g0061 | 3 | HG03130.hp1 HG03486.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.158-1370_158-1369d others(4): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37365752 | ||||||
chr5:37365752
|
T | TACAC | 14 | a0001c0001t0001g0153a0001c0001t0001g0156a0001c0001t0026g0152others(11): Show | 14 | HG01243.hp2 HG01358.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.158-1372_158-1369d others(6): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37365752 | ||||||
chr5:37365752
|
T | TACACAC | 7 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0037g0091others(4): Show | 7 | HG00408.hp2 HG02145.hp2 HG03669.hp2 others(4): Show |
intron_variant | MODIFIER | c.158-1374_158-1369d others(8): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37365752 | ||||||
chr5:37365752
|
T | TACACACA others(1): Show |
9 | a0001c0001t0030g0202a0001c0002t0002g0274a0001c0002t0004g0026others(6): Show | 9 | HG00099.hp1 HG02258.hp1 HG03017.hp1 others(6): Show |
intron_variant | MODIFIER | c.158-1376_158-1369d others(10): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37365752 | ||||||
chr5:37365752
|
T | TACACACA others(3): Show |
2 | a0001c0002t0006g0286a0001c0002t0006g0287 | 2 | HG03669.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.158-1378_158-1369d others(12): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37365752 | ||||||
chr5:37365752
|
T | TACACACA others(5): Show |
3 | a0001c0002t0020g0289a0001c0002t0046g0291a0001c0002t0049g0275 | 3 | HG03453.hp2 HG06807.hp1 NA18939.hp2 |
intron_variant | MODIFIER | c.158-1380_158-1369d others(14): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37365752 | ||||||
chr5:37365752
|
T | TACACACA others(9): Show |
1 | a0001c0002t0002g0290 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.158-1384_158-1369d others(18): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37365752 | ||||||
chr5:37365752
|
T | TATAC | 3 | a0001c0002t0015g0012a0001c0003t0001g0254a0001c0005t0009g0057 | 3 | HG02055.hp2 HG02145.hp1 NA18939.hp1 |
intron_variant | MODIFIER | c.158-1369_158-1368i others(6): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37365752 | ||||||
chr5:37365752
|
T | TATACAC | 3 | a0001c0002t0002g0081a0001c0003t0001g0255a0001c0004t0053g0265 | 3 | HG03098.hp1 HG03710.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.158-1369_158-1368i others(8): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37365752 | ||||||
chr5:37365752
|
T | TATATACA others(1): Show |
7 | a0001c0002t0002g0077a0001c0002t0002g0078a0001c0002t0002g0080others(4): Show | 7 | HG01257.hp2 HG01515.hp2 HG01517.hp1 others(4): Show |
intron_variant | MODIFIER | c.158-1369_158-1368i others(10): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37365752 | ||||||
chr5:37365752
|
T | TATATACA others(3): Show |
6 | a0001c0001t0012g0093a0001c0002t0002g0083a0001c0002t0002g0085others(3): Show | 6 | HG00423.hp2 HG02572.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.158-1369_158-1368i others(12): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37365752 | ||||||
chr5:37365752
|
T | TATATACA others(5): Show |
1 | a0001c0002t0002g0087 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.158-1369_158-1368i others(14): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37365752 | ||||||
chr5:37365752
|
T | TATATACA others(7): Show |
1 | a0001c0002t0002g0088 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.158-1369_158-1368i others(16): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37365752 | ||||||
chr5:37365752
|
T | TATATATA others(1): Show |
3 | a0001c0001t0001g0194a0001c0001t0001g0252a0001c0001t0001g0253 | 3 | HG01517.hp2 HG02080.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.158-1369_158-1368i others(10): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37365752 | ||||||
chr5:37365752
|
T | TATATATA others(11): Show |
1 | a0001c0002t0048g0288 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.158-1369_158-1368i others(20): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37365752 | ||||||
chr5:37365752
|
T | TATATATA others(3): Show |
1 | a0001c0002t0002g0074 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.158-1369_158-1368i others(12): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37365752 | ||||||
chr5:37365752
|
T | TATATATA others(5): Show |
1 | a0001c0002t0002g0076 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.158-1369_158-1368i others(14): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37365752 | ||||||
chr5:37365752
|
T | TATATATA others(5): Show |
1 | a0001c0001t0001g0201 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.158-1369_158-1368i others(14): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37365752 | ||||||
chr5:37365752
|
TAC | T | 9 | a0001c0003t0001g0175a0001c0003t0001g0190a0001c0003t0001g0220others(6): Show | 9 | HG01358.hp2 HG01433.hp1 HG01975.hp1 others(6): Show |
intron_variant | MODIFIER | c.158-1370_158-1369d others(4): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37365752 | ||||||
chr5:37365754
|
C | T | 119 | a0001c0001t0001g0114a0001c0001t0001g0199a0001c0001t0001g0242others(116): Show | 120 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.158-1370G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37365754 | ||||||
chr5:37365756
|
C | T | 116 | a0001c0001t0001g0114a0001c0001t0003g0166a0001c0001t0012g0092others(113): Show | 117 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.158-1372G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37365756 | ||||||
chr5:37365758
|
C | T | 91 | a0001c0002t0005g0266a0001c0002t0006g0277a0001c0002t0007g0030others(88): Show | 92 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.158-1374G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37365758 | ||||||
chr5:37365760
|
C | T | 14 | a0001c0002t0006g0277a0001c0002t0007g0037a0001c0002t0016g0043others(11): Show | 14 | HG01192.hp1 HG01243.hp1 HG01261.hp1 others(11): Show |
intron_variant | MODIFIER | c.158-1376G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37365760 | ||||||
chr5:37365762
|
C | T | 9 | a0001c0002t0006g0277a0001c0002t0017g0041a0001c0002t0017g0042others(6): Show | 9 | HG01192.hp1 HG01346.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.158-1378G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37365762 | ||||||
chr5:37365764
|
C | T | 4 | a0001c0002t0024g0032a0001c0002t0024g0033a0001c0002t0045g0292others(1): Show | 4 | HG02572.hp2 HG02615.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.158-1380G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37365764 | ||||||
chr5:37365810
|
A | C | 290 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0095others(287): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.158-1426T>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37365810 | ||||||
chr5:37365832
|
A | T | 1 | a0001c0002t0005g0270 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.158-1448T>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37365832 | ||||||
chr5:37365982
|
T | C | 9 | a0001c0002t0007g0036a0001c0002t0007g0037a0001c0002t0007g0038others(6): Show | 9 | HG01109.hp2 HG02258.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.158-1598A>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37365982 | ||||||
chr5:37365989
|
AAAC | A | 12 | a0001c0002t0004g0004a0001c0002t0004g0019a0001c0002t0004g0020others(9): Show | 12 | HG01192.hp2 HG01891.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.158-1608_158-1606d others(5): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37365989 | ||||||
chr5:37366121
|
C | T | 1 | a0001c0002t0016g0043 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.158-1737G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37366121 | ||||||
chr5:37366142
|
C | G | 1 | a0001c0003t0003g0203 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.158-1758G>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37366142 | ||||||
chr5:37366456
|
T | C | 1 | a0001c0002t0008g0014 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.158-2072A>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37366456 | ||||||
chr5:37366541
|
G | A | 1 | a0001c0002t0046g0291 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.158-2157C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37366541 | ||||||
chr5:37366585
|
T | C | 1 | a0001c0001t0001g0256 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.158-2201A>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37366585 | ||||||
chr5:37366662
|
CT | C | 260 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0095others(257): Show | 261 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(258): Show |
intron_variant | MODIFIER | c.158-2279delA | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37366662 | ||||||
chr5:37366662
|
CTT | C | 26 | a0001c0001t0001g0161a0001c0002t0002g0274a0001c0002t0002g0290others(23): Show | 26 | HG00099.hp1 HG00408.hp2 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.158-2280_158-2279d others(4): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37366662 | ||||||
chr5:37366684
|
C | T | 1 | a0001c0003t0001g0170 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.158-2300G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37366684 | ||||||
chr5:37366703
|
G | A | 1 | a0001c0002t0007g0030 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.158-2319C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37366703 | ||||||
chr5:37366710
|
G | A | 1 | a0001c0003t0001g0260 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.158-2326C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37366710 | ||||||
chr5:37366711
|
G | A | 5 | a0001c0002t0005g0266a0001c0002t0005g0267a0001c0002t0005g0268others(2): Show | 5 | HG02055.hp1 HG02647.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.158-2327C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37366711 | ||||||
chr5:37366870
|
T | G | 1 | a0001c0001t0001g0110 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.158-2486A>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37366870 | ||||||
chr5:37367033
|
C | T | 21 | a0001c0002t0002g0274a0001c0002t0002g0290a0001c0002t0006g0272others(18): Show | 21 | HG00099.hp1 HG00408.hp2 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.158-2649G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37367033 | ||||||
chr5:37367047
|
C | CT | 10 | a0001c0001t0018g0094a0001c0004t0011g0051a0001c0004t0011g0052others(7): Show | 10 | HG02257.hp1 HG02486.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.158-2664dupA | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37367047 | ||||||
chr5:37367047
|
CT | C | 19 | a0001c0002t0005g0270a0001c0002t0007g0036a0001c0002t0007g0037others(16): Show | 19 | HG01109.hp2 HG01243.hp1 HG01261.hp1 others(16): Show |
intron_variant | MODIFIER | c.158-2664delA | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37367047 | ||||||
chr5:37367119
|
C | A | 5 | a0001c0001t0012g0092a0001c0001t0012g0093a0001c0001t0012g0111others(2): Show | 5 | HG00323.hp1 HG01109.hp1 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.158-2735G>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37367119 | ||||||
chr5:37367135
|
T | C | 102 | a0001c0001t0001g0168a0001c0001t0001g0192a0001c0001t0001g0193others(99): Show | 103 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.158-2751A>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37367135 | ||||||
chr5:37367180
|
G | A | 109 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0192others(106): Show | 110 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.158-2796C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37367180 | ||||||
chr5:37367231
|
G | GT | 7 | a0001c0001t0001g0168a0001c0002t0023g0065a0001c0002t0054g0276others(4): Show | 7 | HG01433.hp1 HG03834.hp1 HG03834.hp2 others(4): Show |
intron_variant | MODIFIER | c.158-2848dupA | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37367231 | ||||||
chr5:37367284
|
G | A | 50 | a0001c0002t0002g0073a0001c0002t0002g0074a0001c0002t0002g0076others(47): Show | 50 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(47): Show |
intron_variant | MODIFIER | c.158-2900C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37367284 | ||||||
chr5:37367360
|
G | A | 109 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0192others(106): Show | 110 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.158-2976C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37367360 | ||||||
chr5:37367535
|
CT | C | 55 | a0001c0001t0001g0090a0001c0001t0001g0162a0001c0001t0037g0091others(52): Show | 55 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(52): Show |
intron_variant | MODIFIER | c.158-3152delA | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37367535 | ||||||
chr5:37367616
|
T | G | 186 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0095others(183): Show | 187 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(184): Show |
intron_variant | MODIFIER | c.157+3205A>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37367616 | ||||||
chr5:37367625
|
C | T | 109 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0192others(106): Show | 110 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.157+3196G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37367625 | ||||||
chr5:37367649
|
C | T | 1 | a0001c0003t0005g0167 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.157+3172G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37367649 | ||||||
chr5:37367650
|
A | G | 3 | a0001c0002t0017g0041a0001c0002t0017g0042a0001c0010t0017g0035 | 3 | HG01346.hp1 HG02922.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.157+3171T>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37367650 | ||||||
chr5:37367693
|
C | T | 72 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0095others(69): Show | 72 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.157+3128G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37367693 | ||||||
chr5:37367986
|
G | A | 1 | a0001c0001t0001g0163 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.157+2835C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37367986 | ||||||
chr5:37368006
|
A | T | 24 | a0001c0002t0002g0073a0001c0002t0002g0074a0001c0002t0002g0076others(21): Show | 24 | HG00423.hp2 HG00642.hp2 HG01069.hp1 others(21): Show |
intron_variant | MODIFIER | c.157+2815T>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37368006 | ||||||
chr5:37368060
|
C | T | 1 | a0002c0008t0001g0295 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.157+2761G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37368060 | ||||||
chr5:37368071
|
G | A | 2 | a0001c0002t0004g0028a0001c0002t0015g0029 | 2 | HG01192.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.157+2750C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37368071 | ||||||
chr5:37368149
|
T | G | 1 | a0001c0003t0039g0262 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.157+2672A>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37368149 | ||||||
chr5:37368209
|
C | CT | 28 | a0001c0002t0002g0274a0001c0002t0004g0004a0001c0002t0004g0021others(25): Show | 28 | HG00735.hp2 HG01192.hp2 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.157+2611dupA | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37368209 | ||||||
chr5:37368209
|
C | CTT | 16 | a0001c0002t0004g0019a0001c0002t0004g0020a0001c0002t0007g0036others(13): Show | 16 | HG01109.hp2 HG01243.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.157+2610_157+2611d others(4): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37368209 | ||||||
chr5:37368209
|
CT | C | 55 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0100others(52): Show | 55 | HG00323.hp1 HG00423.hp1 HG00673.hp2 others(52): Show |
intron_variant | MODIFIER | c.157+2611delA | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37368209 | ||||||
chr5:37368209
|
CTT | C | 129 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0118others(126): Show | 130 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.157+2610_157+2611d others(4): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37368209 | ||||||
chr5:37368209
|
CTTTTTTT others(3): Show |
C | 17 | a0001c0002t0002g0073a0001c0002t0002g0074a0001c0002t0002g0076others(14): Show | 17 | HG00423.hp2 HG00642.hp2 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.157+2602_157+2611d others(12): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37368209 | ||||||
chr5:37368624
|
A | C | 2 | a0001c0004t0029g0002a0001c0011t0028g0003 | 2 | HG02809.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.157+2197T>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37368624 | ||||||
chr5:37368960
|
C | T | 3 | a0001c0002t0005g0267a0001c0002t0005g0268a0001c0002t0005g0269 | 3 | HG02055.hp1 NA19043.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.157+1861G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37368960 | ||||||
chr5:37369200
|
T | G | 1 | a0001c0003t0001g0263 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.157+1621A>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37369200 | ||||||
chr5:37369300
|
T | A | 2 | a0001c0002t0004g0028a0001c0002t0015g0029 | 2 | HG01192.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.157+1521A>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37369300 | ||||||
chr5:37369306
|
G | A | 191 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0095others(188): Show | 192 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.157+1515C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37369306 | ||||||
chr5:37369358
|
A | C | 17 | a0001c0002t0007g0036a0001c0002t0007g0037a0001c0002t0007g0038others(14): Show | 17 | HG01109.hp2 HG01243.hp1 HG01261.hp1 others(14): Show |
intron_variant | MODIFIER | c.157+1463T>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37369358 | ||||||
chr5:37369513
|
A | G | 41 | a0001c0002t0004g0004a0001c0002t0004g0019a0001c0002t0004g0020others(38): Show | 41 | HG01109.hp2 HG01192.hp2 HG01243.hp1 others(38): Show |
intron_variant | MODIFIER | c.157+1308T>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37369513 | ||||||
chr5:37369552
|
TCTTGTTT others(79): Show |
T | 1 | a0001c0002t0027g0034 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.157+1183_157+1268d others(88): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37369552 | ||||||
chr5:37369609
|
CTAATAGG others(9): Show |
C | 12 | a0001c0002t0004g0004a0001c0002t0004g0019a0001c0002t0004g0020others(9): Show | 12 | HG01192.hp2 HG01891.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.157+1196_157+1211d others(18): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37369609 | ||||||
chr5:37369639
|
G | A | 50 | a0001c0002t0002g0073a0001c0002t0002g0074a0001c0002t0002g0076others(47): Show | 50 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(47): Show |
intron_variant | MODIFIER | c.157+1182C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37369639 | ||||||
chr5:37369742
|
C | T | 5 | a0001c0002t0007g0030a0001c0002t0023g0031a0001c0002t0024g0032others(2): Show | 5 | HG02451.hp1 HG02572.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.157+1079G>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37369742 | ||||||
chr5:37369856
|
A | C | 23 | a0001c0002t0004g0004a0001c0002t0004g0019a0001c0002t0004g0020others(20): Show | 23 | HG01192.hp2 HG01243.hp2 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.157+965T>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37369856 | ||||||
chr5:37369875
|
G | A | 1 | a0001c0003t0001g0264 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.157+946C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37369875 | ||||||
chr5:37370018
|
C | G | 77 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0095others(74): Show | 77 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.157+803G>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37370018 | ||||||
chr5:37370133
|
G | A | 186 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0095others(183): Show | 187 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(184): Show |
intron_variant | MODIFIER | c.157+688C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37370133 | ||||||
chr5:37370235
|
G | C | 1 | a0001c0004t0053g0265 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.157+586C>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37370235 | ||||||
chr5:37370252
|
A | T | 1 | a0001c0002t0005g0266 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.157+569T>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37370252 | ||||||
chr5:37370383
|
CAAAT | C | 5 | a0001c0002t0005g0266a0001c0002t0005g0267a0001c0002t0005g0268others(2): Show | 5 | HG02055.hp1 HG02647.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.157+434_157+437del others(4): Show |
NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37370383 | ||||||
chr5:37370387
|
T | C | 21 | a0001c0002t0002g0274a0001c0002t0002g0290a0001c0002t0006g0272others(18): Show | 21 | HG00099.hp1 HG00408.hp2 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.157+434A>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37370387 | ||||||
chr5:37370397
|
G | A | 1 | a0001c0002t0045g0292 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.157+424C>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37370397 | ||||||
chr5:37370520
|
A | G | 2 | a0001c0001t0021g0006a0001c0001t0021g0007 | 2 | HG02559.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.157+301T>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37370520 | ||||||
chr5:37370666
|
C | A | 1 | a0001c0003t0001g0293 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.157+155G>T | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37370666 | ||||||
chr5:37370751
|
G | C | 1 | a0001c0003t0001g0294 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.157+70C>G | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37370751 | ||||||
chr5:37370799
|
A | G | 1 | a0001c0002t0034g0005 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.157+22T>C | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37370799 | ||||||
chr5:37370805
|
G | T | 1 | a0001c0002t0004g0004 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.157+16C>A | NUP155 | ENSG00000113569.16 | transcript | ENST00000231498.8 | protein_coding | 1/34 | chr5 | 37370805 |