geneid | 129401 |
---|---|
ensemblid | ENSG00000163002.13 |
hgncid | 29797 |
symbol | NUP35 |
name | nucleoporin 35 |
refseq_nuc | NM_138285.5 |
refseq_prot | NP_612142.2 |
ensembl_nuc | ENST00000295119.9 |
ensembl_prot | ENSP00000295119.4 |
mane_status | MANE Select |
chr | chr2 |
start | 183124443 |
end | 183161680 |
strand | + |
ver | v1.2 |
region | chr2:183124443-183161680 |
region5000 | chr2:183119443-183166680 |
regionname0 | NUP35_chr2_183124443_183161680 |
regionname5000 | NUP35_chr2_183119443_183166680 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 326 | 401 | 87 | 62 | 192 | 18 | 40 | 146 | NUP35_chr2_183119443_183166680 | NUP35 | copy fasta | chr2 | 183119443 | 183166680 |
a0002 | 0/0 | 326 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | copy fasta | chr2 | 183119443 | 183166680 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 981 | 395 | 82 | 62 | 192 | 18 | 39 | NUP35_chr2_183119443_183166680 | NUP35 | copy fasta | chr2 | 183119443 | 183166680 |
c0002 | 0/0 | 981 | 4 | 4 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | copy fasta | chr2 | 183119443 | 183166680 |
c0003 | 0/0 | 981 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | copy fasta | chr2 | 183119443 | 183166680 |
c0004 | 0/0 | 981 | 1 | 0 | 0 | 0 | 0 | 1 | NUP35_chr2_183119443_183166680 | NUP35 | copy fasta | chr2 | 183119443 | 183166680 |
c0005 | 0/0 | 981 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | copy fasta | chr2 | 183119443 | 183166680 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 565 | 344 | 76 | 54 | 165 | 18 | 29 | NUP35_chr2_183119443_183166680 | NUP35 | copy fasta | chr2 | 183119443 | 183166680 |
t0002 | 0/0 | 565 | 42 | 1 | 4 | 26 | 0 | 11 | NUP35_chr2_183119443_183166680 | NUP35 | copy fasta | chr2 | 183119443 | 183166680 |
t0003 | 0/0 | 565 | 11 | 11 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | copy fasta | chr2 | 183119443 | 183166680 |
t0004 | 0/0 | 565 | 3 | 0 | 3 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | copy fasta | chr2 | 183119443 | 183166680 |
t0005 | 0/0 | 565 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | copy fasta | chr2 | 183119443 | 183166680 |
t0006 | 0/0 | 565 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | copy fasta | chr2 | 183119443 | 183166680 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 15 | 0 | 0 | 15 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0002 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0003 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0004 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0005 | 0/0 | 4 | 0 | 2 | 0 | 0 | 2 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0006 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0007 | 0/0 | 4 | 1 | 2 | 0 | 1 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0008 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0010 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0014 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0023 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0025 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0028 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0030 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0038 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0041 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0071 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0247 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0300 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0302 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 981 | 395 | 82 | 62 | 192 | 18 | 39 | NUP35_chr2_183119443_183166680 | NUP35 | copy fasta | chr2 | 183119443 | 183166680 |
a0001c0002 | 0/0 | 981 | 4 | 4 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | copy fasta | chr2 | 183119443 | 183166680 |
a0001c0003 | 0/0 | 981 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | copy fasta | chr2 | 183119443 | 183166680 |
a0001c0004 | 0/0 | 981 | 1 | 0 | 0 | 0 | 0 | 1 | NUP35_chr2_183119443_183166680 | NUP35 | copy fasta | chr2 | 183119443 | 183166680 |
a0002c0005 | 0/0 | 981 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | copy fasta | chr2 | 183119443 | 183166680 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 1545 | 338 | 71 | 54 | 165 | 18 | 28 | NUP35_chr2_183119443_183166680 | NUP35 | copy fasta | chr2 | 183119443 | 183166680 |
a0001c0001t0002 | 0/0 | 1545 | 41 | 0 | 4 | 26 | 0 | 11 | NUP35_chr2_183119443_183166680 | NUP35 | copy fasta | chr2 | 183119443 | 183166680 |
a0001c0001t0003 | 0/0 | 1545 | 11 | 11 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | copy fasta | chr2 | 183119443 | 183166680 |
a0001c0001t0004 | 0/0 | 1545 | 3 | 0 | 3 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | copy fasta | chr2 | 183119443 | 183166680 |
a0001c0001t0005 | 0/0 | 1545 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | copy fasta | chr2 | 183119443 | 183166680 |
a0001c0001t0006 | 0/0 | 1545 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | copy fasta | chr2 | 183119443 | 183166680 |
a0001c0002t0001 | 0/0 | 1545 | 4 | 4 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | copy fasta | chr2 | 183119443 | 183166680 |
a0001c0003t0002 | 0/0 | 1545 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | copy fasta | chr2 | 183119443 | 183166680 |
a0001c0004t0001 | 0/0 | 1545 | 1 | 0 | 0 | 0 | 0 | 1 | NUP35_chr2_183119443_183166680 | NUP35 | copy fasta | chr2 | 183119443 | 183166680 |
a0002c0005t0001 | 0/0 | 1545 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | copy fasta | chr2 | 183119443 | 183166680 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 15 | 0 | 0 | 15 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0002 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0003 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0004 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0005 | 0/0 | 4 | 0 | 2 | 0 | 0 | 2 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0006 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0007 | 0/0 | 4 | 1 | 2 | 0 | 1 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0008 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0010 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0071 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0247 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0002g0014 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0002g0038 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0002g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0002g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0002g0041 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0002g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0003g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0003g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0003g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0003g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0003g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0003g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0003g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0003g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0003g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0003g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0004g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0004g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0005g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0001t0006g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0002t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0002t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0002t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0003t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0001c0004t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
a0002c0005t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0007 | EUR | GBR | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0100 | EUR | GBR | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0192 | EUR | GBR | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0160 | EUR | GBR | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0028 | EUR | FIN | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0119 | EUR | FIN | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0239 | EUR | FIN | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0058 | EUR | FIN | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | CHS | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | CHS | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG00423 | hp1 | a0001 | c0001 | t0002 | g0261 | EAS | CHS | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | CHS | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | CHS | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | CHS | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | CHS | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | CHS | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | CHS | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | CHS | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | CHS | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | CHS | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | CHS | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0288 | EAS | CHS | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | PUR | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | CHS | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | CHS | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0211 | AMR | PUR | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0266 | AMR | PUR | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG01069 | hp1 | a0001 | c0001 | t0002 | g0014 | AMR | PUR | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0014 | AMR | PUR | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0298 | AMR | PUR | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | PUR | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG01099 | hp1 | a0001 | c0001 | t0004 | g0076 | AMR | PUR | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0014 | AMR | PUR | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | CLM | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | CLM | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG01256 | hp1 | a0001 | c0001 | t0006 | g0023 | AMR | CLM | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | CLM | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | CLM | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | CLM | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | CLM | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG01358 | hp1 | a0001 | c0001 | t0004 | g0020 | AMR | CLM | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | CLM | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | CLM | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG01361 | hp2 | a0001 | c0001 | t0004 | g0020 | AMR | CLM | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0228 | EUR | IBS | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0131 | EUR | IBS | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0023 | EUR | IBS | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0132 | EUR | IBS | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0094 | EUR | IBS | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0229 | EUR | IBS | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | ACB | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | ACB | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0292 | AMR | PEL | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG01928 | hp2 | a0001 | c0001 | t0002 | g0041 | AMR | PEL | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PEL | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | PEL | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | PEL | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | PEL | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | PEL | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | PEL | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | KHV | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | KHV | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | KHV | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | KHV | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | KHV | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | ACB | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | ACB | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG02056 | hp1 | a0001 | c0001 | t0002 | g0286 | EAS | KHV | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | KHV | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | KHV | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | KHV | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | KHV | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0284 | EAS | KHV | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0039 | EAS | KHV | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | KHV | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | KHV | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | KHV | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | KHV | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG02135 | hp2 | a0001 | c0001 | t0002 | g0272 | EAS | KHV | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | ACB | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | ACB | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0254 | AMR | PEL | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0252 | AMR | PEL | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | CDX | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | CDX | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG02257 | hp1 | a0001 | c0002 | t0001 | g0019 | AFR | ACB | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG02257 | hp2 | a0001 | c0001 | t0003 | g0085 | AFR | ACB | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | ACB | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | ACB | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PEL | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | ACB | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG02280 | hp2 | a0001 | c0002 | t0001 | g0050 | AFR | ACB | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | PEL | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | PEL | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0291 | AMR | PEL | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG02451 | hp1 | a0001 | c0001 | t0003 | g0092 | AFR | ACB | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG02451 | hp2 | a0001 | c0001 | t0003 | g0082 | AFR | ACB | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0279 | EAS | KHV | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | GWD | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | GWD | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | GWD | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | GWD | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | GWD | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0294 | AFR | GWD | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | GWD | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | GWD | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG02683 | hp2 | a0001 | c0001 | t0002 | g0041 | SAS | PJL | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0231 | SAS | PJL | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0054 | SAS | PJL | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | GWD | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG02717 | hp2 | a0001 | c0001 | t0003 | g0069 | AFR | GWD | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | GWD | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | GWD | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0296 | SAS | PJL | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0264 | SAS | PJL | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0260 | SAS | PJL | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG02738 | hp2 | a0001 | c0004 | t0001 | g0232 | SAS | PJL | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0301 | AFR | GWD | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0263 | AFR | GWD | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | GWD | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | GWD | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0319 | AFR | GWD | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | GWD | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | GWD | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | GWD | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0297 | AFR | GWD | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0299 | AFR | GWD | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | ESN | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0307 | AFR | ESN | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | ESN | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG02965 | hp2 | a0001 | c0002 | t0001 | g0019 | AFR | ESN | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | ESN | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | ESN | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | ESN | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0063 | SAS | PJL | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | GWD | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | GWD | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | ESN | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | ESN | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | MSL | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | MSL | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG03225 | hp1 | a0001 | c0002 | t0001 | g0049 | AFR | MSL | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG03225 | hp2 | a0001 | c0001 | t0003 | g0084 | AFR | MSL | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | MSL | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG03453 | hp2 | a0002 | c0005 | t0001 | g0311 | AFR | MSL | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG03486 | hp1 | a0001 | c0001 | t0003 | g0083 | AFR | MSL | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | MSL | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0255 | SAS | PJL | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0317 | SAS | PJL | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0258 | SAS | PJL | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | GWD | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG03540 | hp2 | a0001 | c0001 | t0003 | g0021 | AFR | GWD | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG03579 | hp1 | a0001 | c0001 | t0003 | g0086 | AFR | MSL | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | MSL | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG03669 | hp2 | a0001 | c0001 | t0002 | g0038 | SAS | PJL | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0271 | SAS | PJL | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0150 | SAS | PJL | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0278 | SAS | PJL | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0141 | SAS | PJL | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0269 | SAS | BEB | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0250 | SAS | BEB | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0290 | SAS | BEB | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0095 | SAS | BEB | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0267 | SAS | BEB | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0124 | SAS | BEB | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0318 | SAS | BEB | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0122 | SAS | BEB | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0137 | SAS | STU | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0062 | SAS | STU | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0145 | SAS | BEB | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0038 | SAS | BEB | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0310 | SAS | STU | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0259 | SAS | STU | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0179 | SAS | STU | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0257 | SAS | STU | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | YRI | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0295 | AFR | YRI | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | CHB | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | CHB | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | CHB | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | YRI | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | YRI | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA18939 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA18944 | hp2 | a0001 | c0001 | t0002 | g0276 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA18951 | hp1 | a0001 | c0001 | t0002 | g0282 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA18960 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA18966 | hp1 | a0001 | c0001 | t0002 | g0274 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA18970 | hp2 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA18978 | hp2 | a0001 | c0001 | t0002 | g0285 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA18983 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA18985 | hp1 | a0001 | c0001 | t0002 | g0273 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA18995 | hp1 | a0001 | c0001 | t0002 | g0281 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA18999 | hp2 | a0001 | c0001 | t0002 | g0268 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA19004 | hp1 | a0001 | c0001 | t0002 | g0280 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA19005 | hp1 | a0001 | c0001 | t0005 | g0013 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA19006 | hp2 | a0001 | c0001 | t0002 | g0283 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA19010 | hp1 | a0001 | c0001 | t0002 | g0289 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | LWK | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | LWK | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | LWK | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA19043 | hp2 | a0001 | c0003 | t0002 | g0118 | AFR | LWK | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA19056 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA19062 | hp2 | a0001 | c0001 | t0002 | g0277 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA19078 | hp1 | a0001 | c0001 | t0002 | g0275 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA19080 | hp2 | a0001 | c0001 | t0002 | g0270 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | YRI | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA19240 | hp2 | a0001 | c0001 | t0003 | g0021 | AFR | YRI | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0300 | EUR | TSI | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0104 | EUR | TSI | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0302 | EUR | TSI | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0157 | EUR | TSI | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0265 | SAS | GIH | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0098 | SAS | GIH | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | CLM | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0293 | AMR | CLM | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | ACB | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | ACB | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG02486 | hp1 | a0001 | c0001 | t0003 | g0068 | AFR | ACB | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | ACB | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG02559 | hp1 | a0001 | c0001 | t0003 | g0081 | AFR | ACB | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | MSL | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | MSL | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | USA | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | USA | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA18955 | hp2 | a0001 | c0001 | t0002 | g0287 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | USA | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | USA | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0247 | REF | REF | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0071 | REF | REF | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:183161061
|
C | T | 1 | a0002 | 1 | HG03453.hp2 | missense_variant | MODERATE | c.911C>T | p.Ser304Phe | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 9/9 | 926/1545 | 911/981 | 304/326 | chr2 | 183161061 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:183128357
|
A | G | 1 | a0001c0002 | 4 | HG02257.hp1 HG02280.hp2 HG02965.hp2 others(1): Show |
synonymous_variant | LOW | c.111A>G | p.Gly37Gly | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 2/9 | 126/1545 | 111/981 | 37/326 | chr2 | 183128357 | ||
chr2:183128384
|
G | A | 1 | a0001c0003 | 1 | NA19043.hp2 | synonymous_variant | LOW | c.138G>A | p.Pro46Pro | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 2/9 | 153/1545 | 138/981 | 46/326 | chr2 | 183128384 | ||
chr2:183159613
|
T | C | 1 | a0001c0004 | 1 | HG02738.hp2 | synonymous_variant | LOW | c.864T>C | p.Pro288Pro | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 8/9 | 879/1545 | 864/981 | 288/326 | chr2 | 183159613 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:183161144
|
A | G | 1 | a0001c0001t0006 | 1 | HG01256.hp1 | 3_prime_UTR_variant | MODIFIER | c.*13A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 9/9 | 13 | chr2 | 183161144 | |||||
chr2:183161147
|
G | T | 2 | a0001c0001t0002a0001c0003t0002 | 42 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*16G>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 9/9 | 16 | chr2 | 183161147 | |||||
chr2:183161148
|
A | T | 2 | a0001c0001t0002a0001c0003t0002 | 42 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*17A>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 9/9 | 17 | chr2 | 183161148 | |||||
chr2:183161238
|
A | C | 1 | a0001c0001t0005 | 1 | NA19005.hp1 | 3_prime_UTR_variant | MODIFIER | c.*107A>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 9/9 | 107 | chr2 | 183161238 | |||||
chr2:183161260
|
T | C | 1 | a0001c0001t0003 | 11 | HG02257.hp2 HG02451.hp1 HG02451.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*129T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 9/9 | 129 | chr2 | 183161260 | |||||
chr2:183161340
|
C | T | 1 | a0001c0001t0003 | 11 | HG02257.hp2 HG02451.hp1 HG02451.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*209C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 9/9 | 209 | chr2 | 183161340 | |||||
chr2:183161516
|
A | G | 1 | a0001c0001t0004 | 3 | HG01099.hp1 HG01358.hp1 HG01361.hp2 |
3_prime_UTR_variant | MODIFIER | c.*385A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 9/9 | 385 | chr2 | 183161516 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:183124577
|
C | A | 26 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0018others(23): Show | 34 | HG00323.hp2 HG00642.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.40+80C>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183124577 | ||||||
chr2:183124651
|
C | T | 1 | a0001c0001t0001g0319 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.40+154C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183124651 | ||||||
chr2:183124898
|
G | A | 1 | a0001c0001t0001g0065 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.40+401G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183124898 | ||||||
chr2:183124909
|
C | T | 233 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(230): Show | 298 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(295): Show |
intron_variant | MODIFIER | c.40+412C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183124909 | ||||||
chr2:183124916
|
GTGTGTGG others(550): Show |
G | 2 | a0001c0001t0001g0066a0001c0001t0001g0067 | 2 | HG02886.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.40+422_40+978del | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 183124916 | |||||
chr2:183124950
|
G | T | 306 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(303): Show | 386 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(383): Show |
intron_variant | MODIFIER | c.40+453G>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183124950 | ||||||
chr2:183124988
|
C | T | 1 | a0001c0001t0001g0078 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.40+491C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183124988 | ||||||
chr2:183125135
|
C | T | 233 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(230): Show | 298 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(295): Show |
intron_variant | MODIFIER | c.40+638C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183125135 | ||||||
chr2:183125242
|
G | GA | 14 | a0001c0001t0001g0022a0001c0001t0001g0079a0001c0001t0001g0080others(11): Show | 16 | HG02257.hp2 HG02451.hp2 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.40+752dupA | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 183125242 | |||||
chr2:183125279
|
T | G | 8 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0043others(5): Show | 13 | HG02055.hp2 HG02258.hp1 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.40+782T>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183125279 | ||||||
chr2:183125293
|
G | A | 1 | a0001c0001t0001g0043 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.40+796G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183125293 | ||||||
chr2:183125351
|
G | C | 1 | a0001c0001t0001g0091 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.40+854G>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183125351 | ||||||
chr2:183125429
|
G | A | 307 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(304): Show | 387 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(384): Show |
intron_variant | MODIFIER | c.40+932G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183125429 | ||||||
chr2:183125497
|
A | G | 2 | a0001c0001t0001g0317a0001c0001t0001g0318 | 2 | HG03491.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.40+1000A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183125497 | ||||||
chr2:183125509
|
C | G | 2 | a0001c0001t0001g0078a0001c0003t0002g0118 | 2 | HG02723.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.40+1012C>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183125509 | ||||||
chr2:183125560
|
T | C | 310 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(307): Show | 390 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(387): Show |
intron_variant | MODIFIER | c.40+1063T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183125560 | ||||||
chr2:183125698
|
TG | T | 28 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0018others(25): Show | 37 | HG00323.hp2 HG00642.hp1 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.40+1205delG | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 183125698 | |||||
chr2:183125762
|
A | G | 1 | a0001c0001t0001g0091 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.40+1265A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183125762 | ||||||
chr2:183125797
|
C | G | 5 | a0001c0001t0001g0312a0001c0001t0001g0313a0001c0001t0001g0314others(2): Show | 5 | NA18962.hp1 NA19011.hp2 NA19055.hp1 others(2): Show |
intron_variant | MODIFIER | c.40+1300C>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183125797 | ||||||
chr2:183125831
|
G | A | 1 | a0001c0001t0001g0079 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.40+1334G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183125831 | ||||||
chr2:183125837
|
A | G | 3 | a0001c0001t0001g0077a0001c0001t0001g0091a0002c0005t0001g0311 | 3 | HG02145.hp1 HG02818.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.40+1340A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183125837 | ||||||
chr2:183125978
|
C | T | 12 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0107others(9): Show | 12 | HG01255.hp1 HG01261.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.40+1481C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183125978 | ||||||
chr2:183126048
|
C | G | 38 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(35): Show | 66 | HG00323.hp2 HG00438.hp1 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.40+1551C>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183126048 | ||||||
chr2:183126071
|
G | A | 175 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(172): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.40+1574G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183126071 | ||||||
chr2:183126101
|
G | A | 184 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(181): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.40+1604G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183126101 | ||||||
chr2:183126123
|
C | G | 231 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(228): Show | 300 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(297): Show |
intron_variant | MODIFIER | c.40+1626C>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183126123 | ||||||
chr2:183126124
|
C | T | 1 | a0001c0001t0001g0262 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.40+1627C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183126124 | ||||||
chr2:183126127
|
C | G | 40 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(37): Show | 68 | HG00323.hp2 HG00438.hp1 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.40+1630C>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183126127 | ||||||
chr2:183126167
|
T | G | 1 | a0001c0001t0001g0262 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.40+1670T>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183126167 | ||||||
chr2:183126312
|
C | A | 95 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(92): Show | 132 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.40+1815C>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183126312 | ||||||
chr2:183126320
|
A | G | 22 | a0001c0001t0001g0005a0001c0001t0001g0023a0001c0001t0001g0024others(19): Show | 27 | HG00099.hp2 HG00597.hp1 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.40+1823A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183126320 | ||||||
chr2:183126491
|
T | C | 47 | a0001c0001t0001g0005a0001c0001t0001g0023a0001c0001t0001g0024others(44): Show | 53 | HG00099.hp2 HG00597.hp1 HG00741.hp2 others(50): Show |
intron_variant | MODIFIER | c.41-1796T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183126491 | ||||||
chr2:183126538
|
C | T | 192 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(189): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(251): Show |
intron_variant | MODIFIER | c.41-1749C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183126538 | ||||||
chr2:183126642
|
G | GT | 7 | a0001c0001t0001g0003a0001c0001t0001g0191a0001c0001t0001g0255others(4): Show | 11 | HG02165.hp1 HG03490.hp1 HG03492.hp2 others(8): Show |
intron_variant | MODIFIER | c.41-1634dupT | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 183126642 | |||||
chr2:183126642
|
G | GTT | 8 | a0001c0001t0001g0052a0001c0001t0001g0070a0001c0001t0001g0075others(5): Show | 9 | HG01099.hp1 HG01358.hp1 HG01361.hp2 others(6): Show |
intron_variant | MODIFIER | c.41-1635_41-1634dup others(2): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 183126642 | |||||
chr2:183126642
|
G | GTTTT | 33 | a0001c0001t0001g0291a0001c0001t0001g0292a0001c0001t0002g0014others(30): Show | 40 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(37): Show |
intron_variant | MODIFIER | c.41-1637_41-1634dup others(4): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 183126642 | |||||
chr2:183126642
|
GT | G | 90 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(87): Show | 126 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.41-1634delT | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 183126642 | |||||
chr2:183126681
|
T | A | 1 | a0001c0001t0001g0195 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.41-1606T>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183126681 | ||||||
chr2:183126703
|
A | G | 1 | a0001c0001t0001g0026 | 2 | HG02145.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.41-1584A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183126703 | ||||||
chr2:183126812
|
A | G | 1 | a0001c0001t0001g0318 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.41-1475A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183126812 | ||||||
chr2:183126836
|
A | G | 3 | a0001c0002t0001g0019a0001c0002t0001g0049a0001c0002t0001g0050 | 4 | HG02257.hp1 HG02280.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.41-1451A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183126836 | ||||||
chr2:183126862
|
A | G | 6 | a0001c0001t0001g0052a0001c0001t0001g0070a0001c0001t0001g0075others(3): Show | 7 | HG01099.hp1 HG01358.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.41-1425A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183126862 | ||||||
chr2:183126973
|
C | CCTAA | 42 | a0001c0001t0001g0052a0001c0001t0001g0070a0001c0001t0001g0075others(39): Show | 50 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(47): Show |
intron_variant | MODIFIER | c.41-1312_41-1311ins others(4): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 183126973 | |||||
chr2:183126984
|
G | GTGCTCAA others(21): Show |
2 | a0001c0001t0001g0063a0001c0001t0001g0064 | 2 | HG01109.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.41-1303_41-1302ins others(28): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183126984 | ||||||
chr2:183126985
|
G | A | 2 | a0001c0001t0001g0063a0001c0001t0001g0064 | 2 | HG01109.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.41-1302G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183126985 | ||||||
chr2:183126986
|
T | A | 2 | a0001c0001t0001g0063a0001c0001t0001g0064 | 2 | HG01109.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.41-1301T>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183126986 | ||||||
chr2:183126988
|
C | G | 2 | a0001c0001t0001g0063a0001c0001t0001g0064 | 2 | HG01109.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.41-1299C>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183126988 | ||||||
chr2:183127101
|
C | G | 1 | a0001c0001t0001g0091 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.41-1186C>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183127101 | ||||||
chr2:183127221
|
G | C | 108 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(105): Show | 134 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.41-1066G>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183127221 | ||||||
chr2:183127221
|
G | T | 34 | a0001c0001t0002g0014a0001c0001t0002g0038a0001c0001t0002g0039others(31): Show | 41 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.41-1066G>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183127221 | ||||||
chr2:183127235
|
A | G | 1 | a0002c0005t0001g0311 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.41-1052A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183127235 | ||||||
chr2:183127251
|
A | G | 1 | a0001c0001t0001g0254 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.41-1036A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183127251 | ||||||
chr2:183127278
|
A | AT | 82 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0013others(79): Show | 93 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(90): Show |
intron_variant | MODIFIER | c.41-994dupT | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 183127278 | |||||
chr2:183127373
|
C | T | 1 | a0001c0001t0001g0253 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.41-914C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183127373 | ||||||
chr2:183127398
|
G | A | 4 | a0001c0001t0001g0025a0001c0001t0001g0117a0001c0001t0001g0119others(1): Show | 5 | HG00280.hp2 HG00639.hp2 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.41-889G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183127398 | ||||||
chr2:183127401
|
A | G | 1 | a0001c0001t0001g0309 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.41-886A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183127401 | ||||||
chr2:183127458
|
T | A | 1 | a0001c0003t0002g0118 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.41-829T>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183127458 | ||||||
chr2:183127549
|
G | T | 1 | a0002c0005t0001g0311 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.41-738G>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183127549 | ||||||
chr2:183127555
|
G | C | 1 | a0001c0001t0001g0124 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.41-732G>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183127555 | ||||||
chr2:183127664
|
G | T | 1 | a0001c0001t0001g0120 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.41-623G>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183127664 | ||||||
chr2:183127666
|
C | T | 2 | a0001c0001t0001g0077a0001c0001t0001g0091 | 2 | HG02145.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.41-621C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183127666 | ||||||
chr2:183127679
|
T | C | 42 | a0001c0001t0001g0052a0001c0001t0001g0070a0001c0001t0001g0075others(39): Show | 50 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(47): Show |
intron_variant | MODIFIER | c.41-608T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183127679 | ||||||
chr2:183127779
|
A | T | 42 | a0001c0001t0001g0052a0001c0001t0001g0070a0001c0001t0001g0075others(39): Show | 50 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(47): Show |
intron_variant | MODIFIER | c.41-508A>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183127779 | ||||||
chr2:183127798
|
G | T | 1 | a0001c0001t0001g0078 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.41-489G>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183127798 | ||||||
chr2:183127835
|
G | C | 42 | a0001c0001t0001g0052a0001c0001t0001g0070a0001c0001t0001g0075others(39): Show | 50 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(47): Show |
intron_variant | MODIFIER | c.41-452G>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183127835 | ||||||
chr2:183127879
|
T | C | 42 | a0001c0001t0001g0052a0001c0001t0001g0070a0001c0001t0001g0075others(39): Show | 50 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(47): Show |
intron_variant | MODIFIER | c.41-408T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183127879 | ||||||
chr2:183127880
|
C | G | 1 | a0001c0001t0001g0026 | 2 | HG02145.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.41-407C>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183127880 | ||||||
chr2:183127884
|
G | C | 42 | a0001c0001t0001g0052a0001c0001t0001g0070a0001c0001t0001g0075others(39): Show | 50 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(47): Show |
intron_variant | MODIFIER | c.41-403G>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183127884 | ||||||
chr2:183127908
|
G | A | 42 | a0001c0001t0001g0052a0001c0001t0001g0070a0001c0001t0001g0075others(39): Show | 50 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(47): Show |
intron_variant | MODIFIER | c.41-379G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183127908 | ||||||
chr2:183127929
|
C | T | 36 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(33): Show | 64 | HG00323.hp2 HG00438.hp1 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.41-358C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183127929 | ||||||
chr2:183127934
|
C | T | 3 | a0001c0002t0001g0019a0001c0002t0001g0049a0001c0002t0001g0050 | 4 | HG02257.hp1 HG02280.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.41-353C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183127934 | ||||||
chr2:183127956
|
C | G | 1 | a0001c0001t0003g0092 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.41-331C>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183127956 | ||||||
chr2:183128073
|
G | GA | 43 | a0001c0001t0001g0052a0001c0001t0001g0070a0001c0001t0001g0075others(40): Show | 51 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(48): Show |
intron_variant | MODIFIER | c.41-201dupA | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 183128073 | |||||
chr2:183128073
|
GA | G | 37 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(34): Show | 65 | HG00323.hp2 HG00438.hp1 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.41-201delA | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 183128073 | |||||
chr2:183128505
|
A | G | 36 | a0001c0001t0001g0078a0001c0001t0002g0014a0001c0001t0002g0038others(33): Show | 43 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(40): Show |
intron_variant | MODIFIER | c.211+48A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 2/8 | chr2 | 183128505 | ||||||
chr2:183128561
|
C | T | 44 | a0001c0001t0001g0005a0001c0001t0001g0023a0001c0001t0001g0024others(41): Show | 50 | HG00099.hp2 HG00597.hp1 HG00741.hp2 others(47): Show |
intron_variant | MODIFIER | c.211+104C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 2/8 | chr2 | 183128561 | ||||||
chr2:183128599
|
TA | T | 99 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(96): Show | 137 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.211+157delA | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 183128599 | |||||
chr2:183128599
|
TAA | T | 32 | a0001c0001t0001g0005a0001c0001t0001g0023a0001c0001t0001g0024others(29): Show | 38 | HG00099.hp2 HG00597.hp1 HG00741.hp2 others(35): Show |
intron_variant | MODIFIER | c.211+156_211+157del others(2): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 183128599 | |||||
chr2:183128628
|
T | G | 45 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(42): Show | 75 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.211+171T>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 2/8 | chr2 | 183128628 | ||||||
chr2:183128713
|
T | C | 4 | a0001c0001t0001g0025a0001c0001t0001g0117a0001c0001t0001g0119others(1): Show | 5 | HG00280.hp2 HG00639.hp2 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.211+256T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 2/8 | chr2 | 183128713 | ||||||
chr2:183128738
|
T | A | 233 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(230): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(300): Show |
intron_variant | MODIFIER | c.211+281T>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 2/8 | chr2 | 183128738 | ||||||
chr2:183128774
|
A | ACATT | 42 | a0001c0001t0001g0052a0001c0001t0001g0070a0001c0001t0001g0075others(39): Show | 50 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(47): Show |
intron_variant | MODIFIER | c.211+318_211+321dup others(4): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 183128774 | |||||
chr2:183128867
|
T | A | 42 | a0001c0001t0001g0052a0001c0001t0001g0070a0001c0001t0001g0075others(39): Show | 50 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(47): Show |
intron_variant | MODIFIER | c.211+410T>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 2/8 | chr2 | 183128867 | ||||||
chr2:183128868
|
C | T | 42 | a0001c0001t0001g0052a0001c0001t0001g0070a0001c0001t0001g0075others(39): Show | 50 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(47): Show |
intron_variant | MODIFIER | c.211+411C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 2/8 | chr2 | 183128868 | ||||||
chr2:183128937
|
A | G | 24 | a0001c0001t0001g0005a0001c0001t0001g0023a0001c0001t0001g0024others(21): Show | 29 | HG00099.hp2 HG00597.hp1 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.211+480A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 2/8 | chr2 | 183128937 | ||||||
chr2:183129039
|
C | T | 42 | a0001c0001t0001g0052a0001c0001t0001g0070a0001c0001t0001g0075others(39): Show | 50 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(47): Show |
intron_variant | MODIFIER | c.211+582C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 2/8 | chr2 | 183129039 | ||||||
chr2:183129054
|
A | G | 6 | a0001c0001t0001g0052a0001c0001t0001g0070a0001c0001t0001g0075others(3): Show | 7 | HG01099.hp1 HG01358.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.211+597A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 2/8 | chr2 | 183129054 | ||||||
chr2:183129090
|
A | G | 3 | a0001c0002t0001g0019a0001c0002t0001g0049a0001c0002t0001g0050 | 4 | HG02257.hp1 HG02280.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.211+633A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 2/8 | chr2 | 183129090 | ||||||
chr2:183129201
|
C | T | 1 | a0001c0001t0001g0105 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.211+744C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 2/8 | chr2 | 183129201 | ||||||
chr2:183129217
|
T | TG | 44 | a0001c0001t0001g0005a0001c0001t0001g0023a0001c0001t0001g0024others(41): Show | 50 | HG00099.hp2 HG00597.hp1 HG00741.hp2 others(47): Show |
intron_variant | MODIFIER | c.211+767dupG | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 183129217 | |||||
chr2:183129217
|
TG | T | 42 | a0001c0001t0001g0052a0001c0001t0001g0070a0001c0001t0001g0075others(39): Show | 50 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(47): Show |
intron_variant | MODIFIER | c.211+767delG | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 183129217 | |||||
chr2:183129282
|
G | A | 131 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(128): Show | 175 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(172): Show |
intron_variant | MODIFIER | c.211+825G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 2/8 | chr2 | 183129282 | ||||||
chr2:183129314
|
C | T | 42 | a0001c0001t0001g0052a0001c0001t0001g0070a0001c0001t0001g0075others(39): Show | 50 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(47): Show |
intron_variant | MODIFIER | c.211+857C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 2/8 | chr2 | 183129314 | ||||||
chr2:183129412
|
A | G | 1 | a0001c0001t0001g0116 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.211+955A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 2/8 | chr2 | 183129412 | ||||||
chr2:183129467
|
T | C | 2 | a0001c0001t0001g0077a0001c0001t0001g0091 | 2 | HG02145.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.212-951T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 2/8 | chr2 | 183129467 | ||||||
chr2:183129623
|
A | G | 36 | a0001c0001t0001g0078a0001c0001t0002g0014a0001c0001t0002g0038others(33): Show | 43 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(40): Show |
intron_variant | MODIFIER | c.212-795A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 2/8 | chr2 | 183129623 | ||||||
chr2:183129726
|
C | T | 44 | a0001c0001t0001g0005a0001c0001t0001g0023a0001c0001t0001g0024others(41): Show | 50 | HG00099.hp2 HG00597.hp1 HG00741.hp2 others(47): Show |
intron_variant | MODIFIER | c.212-692C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 2/8 | chr2 | 183129726 | ||||||
chr2:183129732
|
A | G | 1 | a0001c0001t0001g0251 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.212-686A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 2/8 | chr2 | 183129732 | ||||||
chr2:183129783
|
G | A | 1 | a0001c0001t0001g0126 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.212-635G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 2/8 | chr2 | 183129783 | ||||||
chr2:183129880
|
A | C | 1 | a0001c0001t0001g0190 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.212-538A>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 2/8 | chr2 | 183129880 | ||||||
chr2:183130024
|
G | T | 2 | a0001c0002t0001g0049a0001c0002t0001g0050 | 2 | HG02280.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.212-394G>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 2/8 | chr2 | 183130024 | ||||||
chr2:183130164
|
A | C | 1 | a0001c0001t0001g0195 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.212-254A>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 2/8 | chr2 | 183130164 | ||||||
chr2:183130197
|
T | C | 238 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(235): Show | 308 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(305): Show |
intron_variant | MODIFIER | c.212-221T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 2/8 | chr2 | 183130197 | ||||||
chr2:183130217
|
C | G | 6 | a0001c0001t0001g0052a0001c0001t0001g0070a0001c0001t0001g0075others(3): Show | 7 | HG01099.hp1 HG01358.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.212-201C>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 2/8 | chr2 | 183130217 | ||||||
chr2:183130317
|
T | C | 12 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0107others(9): Show | 12 | HG01255.hp1 HG01261.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.212-101T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 2/8 | chr2 | 183130317 | ||||||
chr2:183130347
|
A | G | 36 | a0001c0001t0001g0078a0001c0001t0002g0014a0001c0001t0002g0038others(33): Show | 43 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(40): Show |
intron_variant | MODIFIER | c.212-71A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 2/8 | chr2 | 183130347 | ||||||
chr2:183130355
|
A | T | 1 | a0001c0001t0001g0189 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.212-63A>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 2/8 | chr2 | 183130355 | ||||||
chr2:183130357
|
T | C | 1 | a0001c0001t0001g0189 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.212-61T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 2/8 | chr2 | 183130357 | ||||||
chr2:183130359
|
T | A | 1 | a0001c0001t0001g0043 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.212-59T>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 2/8 | chr2 | 183130359 | ||||||
chr2:183130387
|
C | CT | 52 | a0001c0001t0001g0005a0001c0001t0001g0023a0001c0001t0001g0024others(49): Show | 59 | HG00099.hp2 HG00597.hp1 HG00741.hp2 others(56): Show |
intron_variant | MODIFIER | c.212-12dupT | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 183130387 | |||||
chr2:183130387
|
CT | C | 93 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(90): Show | 119 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.212-12delT | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 183130387 | |||||
chr2:183130387
|
CTT | C | 77 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(74): Show | 113 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.212-13_212-12delTT | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 183130387 | |||||
chr2:183130392
|
T | A | 1 | a0001c0003t0002g0118 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.212-26T>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 2/8 | chr2 | 183130392 | ||||||
chr2:183130393
|
T | A | 35 | a0001c0001t0001g0078a0001c0001t0002g0014a0001c0001t0002g0038others(32): Show | 42 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.212-25T>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 2/8 | chr2 | 183130393 | ||||||
chr2:183130414
|
G | T | 36 | a0001c0001t0001g0078a0001c0001t0002g0014a0001c0001t0002g0038others(33): Show | 43 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(40): Show |
splice_region_variant&intron_variant | LOW | c.212-4G>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 2/8 | chr2 | 183130414 | ||||||
chr2:183130614
|
C | G | 1 | a0001c0001t0001g0026 | 2 | HG02145.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.339+69C>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 3/8 | chr2 | 183130614 | ||||||
chr2:183130784
|
G | T | 36 | a0001c0001t0001g0078a0001c0001t0002g0014a0001c0001t0002g0038others(33): Show | 43 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(40): Show |
intron_variant | MODIFIER | c.339+239G>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 3/8 | chr2 | 183130784 | ||||||
chr2:183130808
|
C | T | 24 | a0001c0001t0001g0005a0001c0001t0001g0023a0001c0001t0001g0024others(21): Show | 29 | HG00099.hp2 HG00597.hp1 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.339+263C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 3/8 | chr2 | 183130808 | ||||||
chr2:183130870
|
GTTTAATA | G | 2 | a0001c0001t0001g0027a0001c0001t0001g0127 | 3 | NA18969.hp2 NA18983.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.339+338_339+344del others(7): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 183130870 | |||||
chr2:183130927
|
A | C | 1 | a0001c0001t0001g0078 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.339+382A>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 3/8 | chr2 | 183130927 | ||||||
chr2:183131001
|
C | T | 4 | a0001c0001t0001g0025a0001c0001t0001g0117a0001c0001t0001g0119others(1): Show | 5 | HG00280.hp2 HG00639.hp2 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.339+456C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 3/8 | chr2 | 183131001 | ||||||
chr2:183131014
|
A | C | 236 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(233): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(303): Show |
intron_variant | MODIFIER | c.339+469A>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 3/8 | chr2 | 183131014 | ||||||
chr2:183131146
|
A | AT | 6 | a0001c0001t0001g0052a0001c0001t0001g0070a0001c0001t0001g0075others(3): Show | 7 | HG01099.hp1 HG01358.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.339+610dupT | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 183131146 | |||||
chr2:183131175
|
G | A | 1 | a0001c0001t0001g0293 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.339+630G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 3/8 | chr2 | 183131175 | ||||||
chr2:183131193
|
C | T | 1 | a0001c0001t0001g0184 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.339+648C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 3/8 | chr2 | 183131193 | ||||||
chr2:183131213
|
C | T | 6 | a0001c0001t0001g0052a0001c0001t0001g0070a0001c0001t0001g0075others(3): Show | 7 | HG01099.hp1 HG01358.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.339+668C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 3/8 | chr2 | 183131213 | ||||||
chr2:183131247
|
ACTTTT | A | 8 | a0001c0001t0003g0021a0001c0001t0003g0081a0001c0001t0003g0082others(5): Show | 9 | HG02257.hp2 HG02451.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.339+708_339+712del others(5): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 183131247 | |||||
chr2:183131353
|
G | A | 132 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(129): Show | 177 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(174): Show |
intron_variant | MODIFIER | c.339+808G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 3/8 | chr2 | 183131353 | ||||||
chr2:183131767
|
A | G | 24 | a0001c0001t0001g0005a0001c0001t0001g0023a0001c0001t0001g0024others(21): Show | 29 | HG00099.hp2 HG00597.hp1 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.339+1222A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 3/8 | chr2 | 183131767 | ||||||
chr2:183131847
|
A | G | 3 | a0001c0002t0001g0019a0001c0002t0001g0049a0001c0002t0001g0050 | 4 | HG02257.hp1 HG02280.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.339+1302A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 3/8 | chr2 | 183131847 | ||||||
chr2:183131925
|
T | C | 3 | a0001c0001t0001g0023a0001c0001t0001g0094a0001c0001t0006g0023 | 3 | HG01256.hp1 HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.339+1380T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 3/8 | chr2 | 183131925 | ||||||
chr2:183132088
|
G | C | 42 | a0001c0001t0001g0052a0001c0001t0001g0070a0001c0001t0001g0075others(39): Show | 50 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(47): Show |
intron_variant | MODIFIER | c.340-1478G>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 3/8 | chr2 | 183132088 | ||||||
chr2:183132108
|
C | T | 6 | a0001c0001t0001g0052a0001c0001t0001g0070a0001c0001t0001g0075others(3): Show | 7 | HG01099.hp1 HG01358.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.340-1458C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 3/8 | chr2 | 183132108 | ||||||
chr2:183132332
|
T | C | 6 | a0001c0001t0001g0052a0001c0001t0001g0070a0001c0001t0001g0075others(3): Show | 7 | HG01099.hp1 HG01358.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.340-1234T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 3/8 | chr2 | 183132332 | ||||||
chr2:183132399
|
C | CA | 44 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(41): Show | 73 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.340-1156dupA | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 183132399 | |||||
chr2:183132410
|
A | AT | 3 | a0001c0001t0001g0052a0001c0001t0004g0020a0001c0001t0004g0076 | 4 | HG01099.hp1 HG01358.hp1 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.340-1156_340-1155i others(3): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 3/8 | chr2 | 183132410 | ||||||
chr2:183132410
|
A | T | 35 | a0001c0001t0002g0014a0001c0001t0002g0038a0001c0001t0002g0039others(32): Show | 42 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.340-1156A>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 3/8 | chr2 | 183132410 | ||||||
chr2:183132418
|
T | C | 5 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(2): Show | 5 | HG00738.hp2 HG01243.hp1 HG01256.hp2 others(2): Show |
intron_variant | MODIFIER | c.340-1148T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 3/8 | chr2 | 183132418 | ||||||
chr2:183132504
|
G | A | 1 | a0001c0001t0001g0134 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.340-1062G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 3/8 | chr2 | 183132504 | ||||||
chr2:183132513
|
G | A | 2 | a0001c0001t0001g0294a0001c0001t0001g0295 | 2 | HG02630.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.340-1053G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 3/8 | chr2 | 183132513 | ||||||
chr2:183132519
|
C | T | 6 | a0001c0001t0001g0052a0001c0001t0001g0070a0001c0001t0001g0075others(3): Show | 7 | HG01099.hp1 HG01358.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.340-1047C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 3/8 | chr2 | 183132519 | ||||||
chr2:183132556
|
C | T | 1 | a0001c0001t0001g0183 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.340-1010C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 3/8 | chr2 | 183132556 | ||||||
chr2:183132655
|
A | G | 1 | a0001c0001t0001g0182 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.340-911A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 3/8 | chr2 | 183132655 | ||||||
chr2:183132684
|
T | C | 1 | a0001c0001t0001g0135 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.340-882T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 3/8 | chr2 | 183132684 | ||||||
chr2:183132715
|
A | G | 4 | a0001c0001t0001g0025a0001c0001t0001g0117a0001c0001t0001g0119others(1): Show | 5 | HG00280.hp2 HG00639.hp2 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.340-851A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 3/8 | chr2 | 183132715 | ||||||
chr2:183132896
|
T | G | 1 | a0001c0001t0001g0136 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.340-670T>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 3/8 | chr2 | 183132896 | ||||||
chr2:183133024
|
T | A | 1 | a0001c0001t0001g0137 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.340-542T>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 3/8 | chr2 | 183133024 | ||||||
chr2:183133036
|
A | G | 1 | a0001c0001t0001g0301 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.340-530A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 3/8 | chr2 | 183133036 | ||||||
chr2:183133057
|
A | G | 1 | a0001c0002t0001g0050 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.340-509A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 3/8 | chr2 | 183133057 | ||||||
chr2:183133111
|
A | G | 4 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(1): Show | 4 | HG00323.hp2 HG00642.hp2 HG01243.hp2 others(1): Show |
intron_variant | MODIFIER | c.340-455A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 3/8 | chr2 | 183133111 | ||||||
chr2:183133162
|
A | G | 91 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(88): Show | 116 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.340-404A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 3/8 | chr2 | 183133162 | ||||||
chr2:183133207
|
G | A | 2 | a0001c0001t0001g0066a0001c0001t0001g0067 | 2 | HG02886.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.340-359G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 3/8 | chr2 | 183133207 | ||||||
chr2:183133233
|
T | A | 1 | a0001c0001t0001g0138 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.340-333T>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 3/8 | chr2 | 183133233 | ||||||
chr2:183133323
|
C | CT | 7 | a0001c0001t0001g0034a0001c0001t0001g0127a0001c0001t0001g0180others(4): Show | 8 | HG00423.hp2 HG02922.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.340-228dupT | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 183133323 | |||||
chr2:183133323
|
C | CTT | 5 | a0001c0001t0001g0052a0001c0001t0001g0070a0001c0001t0001g0181others(2): Show | 6 | HG01358.hp1 HG01361.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.340-229_340-228dup others(2): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 183133323 | |||||
chr2:183133323
|
CT | C | 22 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0078others(19): Show | 25 | HG00280.hp2 HG00544.hp2 HG00639.hp2 others(22): Show |
intron_variant | MODIFIER | c.340-228delT | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 183133323 | |||||
chr2:183133323
|
CTT | C | 71 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(68): Show | 105 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.340-229_340-228del others(2): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 183133323 | |||||
chr2:183133350
|
A | C | 35 | a0001c0001t0002g0014a0001c0001t0002g0038a0001c0001t0002g0039others(32): Show | 42 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.340-216A>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 3/8 | chr2 | 183133350 | ||||||
chr2:183133469
|
A | G | 1 | a0001c0001t0001g0074 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.340-97A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 3/8 | chr2 | 183133469 | ||||||
chr2:183133509
|
C | T | 41 | a0001c0001t0001g0005a0001c0001t0001g0023a0001c0001t0001g0024others(38): Show | 47 | HG00099.hp2 HG00597.hp1 HG00741.hp2 others(44): Show |
intron_variant | MODIFIER | c.340-57C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 3/8 | chr2 | 183133509 | ||||||
chr2:183133523
|
A | G | 34 | a0001c0001t0002g0014a0001c0001t0002g0038a0001c0001t0002g0039others(31): Show | 41 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.340-43A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 3/8 | chr2 | 183133523 | ||||||
chr2:183133638
|
CT | C | 146 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(143): Show | 179 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.397+32delT | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183133638 | |||||
chr2:183133638
|
CTT | C | 7 | a0001c0001t0001g0029a0001c0001t0001g0094a0001c0001t0001g0140others(4): Show | 8 | HG01517.hp1 HG03491.hp1 HG03710.hp2 others(5): Show |
intron_variant | MODIFIER | c.397+31_397+32delTT | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183133638 | |||||
chr2:183133656
|
A | T | 3 | a0001c0002t0001g0019a0001c0002t0001g0049a0001c0002t0001g0050 | 4 | HG02257.hp1 HG02280.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.397+33A>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183133656 | ||||||
chr2:183133690
|
A | C | 2 | a0001c0001t0001g0108a0001c0001t0001g0109 | 2 | HG02895.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.397+67A>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183133690 | ||||||
chr2:183133809
|
A | C | 1 | a0001c0003t0002g0118 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.397+186A>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183133809 | ||||||
chr2:183133884
|
A | G | 1 | a0001c0001t0001g0114 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.397+261A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183133884 | ||||||
chr2:183133904
|
G | A | 34 | a0001c0001t0002g0014a0001c0001t0002g0038a0001c0001t0002g0039others(31): Show | 41 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.397+281G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183133904 | ||||||
chr2:183134089
|
G | A | 38 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(35): Show | 66 | HG00323.hp2 HG00438.hp1 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.397+466G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183134089 | ||||||
chr2:183134136
|
T | G | 35 | a0001c0001t0002g0014a0001c0001t0002g0038a0001c0001t0002g0039others(32): Show | 42 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.397+513T>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183134136 | ||||||
chr2:183134201
|
A | G | 1 | a0001c0001t0001g0078 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.397+578A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183134201 | ||||||
chr2:183134386
|
T | A | 12 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0107others(9): Show | 12 | HG01255.hp1 HG01261.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.397+763T>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183134386 | ||||||
chr2:183134399
|
G | A | 6 | a0001c0001t0001g0052a0001c0001t0001g0070a0001c0001t0001g0075others(3): Show | 7 | HG01099.hp1 HG01358.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.397+776G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183134399 | ||||||
chr2:183134399
|
G | C | 90 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(87): Show | 126 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.397+776G>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183134399 | ||||||
chr2:183134399
|
G | T | 2 | a0001c0001t0001g0073a0001c0001t0001g0080 | 2 | HG02717.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.397+776G>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183134399 | ||||||
chr2:183134497
|
C | T | 3 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0122 | 3 | HG01975.hp1 HG03942.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.397+874C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183134497 | ||||||
chr2:183134546
|
G | A | 12 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0107others(9): Show | 12 | HG01255.hp1 HG01261.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.397+923G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183134546 | ||||||
chr2:183134553
|
G | A | 44 | a0001c0001t0001g0005a0001c0001t0001g0023a0001c0001t0001g0024others(41): Show | 50 | HG00099.hp2 HG00597.hp1 HG00741.hp2 others(47): Show |
intron_variant | MODIFIER | c.397+930G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183134553 | ||||||
chr2:183134654
|
C | T | 1 | a0001c0001t0001g0250 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.397+1031C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183134654 | ||||||
chr2:183134655
|
G | A | 3 | a0001c0002t0001g0019a0001c0002t0001g0049a0001c0002t0001g0050 | 4 | HG02257.hp1 HG02280.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.397+1032G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183134655 | ||||||
chr2:183134723
|
C | G | 35 | a0001c0001t0002g0014a0001c0001t0002g0038a0001c0001t0002g0039others(32): Show | 42 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.397+1100C>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183134723 | ||||||
chr2:183134764
|
C | T | 1 | a0001c0001t0001g0178 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.397+1141C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183134764 | ||||||
chr2:183134766
|
C | T | 1 | a0001c0001t0001g0075 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.397+1143C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183134766 | ||||||
chr2:183134773
|
G | C | 3 | a0001c0001t0001g0070a0001c0001t0001g0075a0001c0001t0001g0319 | 3 | HG02818.hp2 HG02886.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.397+1150G>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183134773 | ||||||
chr2:183134782
|
A | ATT | 33 | a0001c0001t0002g0014a0001c0001t0002g0038a0001c0001t0002g0039others(30): Show | 40 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(37): Show |
intron_variant | MODIFIER | c.397+1173_397+1174d others(4): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183134782 | |||||
chr2:183134826
|
G | A | 1 | a0001c0001t0001g0066 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.397+1203G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183134826 | ||||||
chr2:183134870
|
C | T | 4 | a0001c0001t0001g0025a0001c0001t0001g0117a0001c0001t0001g0119others(1): Show | 5 | HG00280.hp2 HG00639.hp2 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.397+1247C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183134870 | ||||||
chr2:183134916
|
G | A | 38 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(35): Show | 66 | HG00323.hp2 HG00438.hp1 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.397+1293G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183134916 | ||||||
chr2:183134925
|
G | T | 6 | a0001c0001t0001g0052a0001c0001t0001g0070a0001c0001t0001g0075others(3): Show | 7 | HG01099.hp1 HG01358.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.397+1302G>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183134925 | ||||||
chr2:183134958
|
A | G | 3 | a0001c0002t0001g0019a0001c0002t0001g0049a0001c0002t0001g0050 | 4 | HG02257.hp1 HG02280.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.397+1335A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183134958 | ||||||
chr2:183134971
|
T | C | 41 | a0001c0001t0001g0052a0001c0001t0001g0070a0001c0001t0001g0075others(38): Show | 49 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.397+1348T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183134971 | ||||||
chr2:183135108
|
A | G | 1 | a0001c0001t0001g0210 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.397+1485A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183135108 | ||||||
chr2:183135146
|
G | C | 130 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(127): Show | 174 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.397+1523G>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183135146 | ||||||
chr2:183135229
|
T | C | 3 | a0001c0001t0001g0070a0001c0001t0001g0075a0001c0001t0001g0319 | 3 | HG02818.hp2 HG02886.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.397+1606T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183135229 | ||||||
chr2:183135289
|
C | T | 4 | a0001c0001t0001g0052a0001c0001t0001g0070a0001c0001t0001g0075others(1): Show | 4 | HG02818.hp2 HG02886.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.397+1666C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183135289 | ||||||
chr2:183135415
|
G | A | 129 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(126): Show | 173 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(170): Show |
intron_variant | MODIFIER | c.397+1792G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183135415 | ||||||
chr2:183135436
|
G | T | 1 | a0001c0001t0001g0247 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.397+1813G>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183135436 | ||||||
chr2:183135439
|
G | A | 44 | a0001c0001t0001g0005a0001c0001t0001g0023a0001c0001t0001g0024others(41): Show | 50 | HG00099.hp2 HG00597.hp1 HG00741.hp2 others(47): Show |
intron_variant | MODIFIER | c.397+1816G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183135439 | ||||||
chr2:183135464
|
G | A | 3 | a0001c0001t0001g0052a0001c0001t0004g0020a0001c0001t0004g0076 | 4 | HG01099.hp1 HG01358.hp1 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.397+1841G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183135464 | ||||||
chr2:183135495
|
A | C | 1 | a0001c0001t0001g0177 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.397+1872A>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183135495 | ||||||
chr2:183135633
|
A | C | 44 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(41): Show | 73 | HG00323.hp2 HG00438.hp1 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.397+2010A>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183135633 | ||||||
chr2:183135676
|
A | G | 1 | a0001c0001t0001g0246 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.397+2053A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183135676 | ||||||
chr2:183135768
|
G | A | 2 | a0001c0001t0001g0077a0001c0001t0001g0091 | 2 | HG02145.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.397+2145G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183135768 | ||||||
chr2:183135802
|
T | A | 1 | a0001c0001t0002g0268 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.397+2179T>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183135802 | ||||||
chr2:183135885
|
T | A | 130 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(127): Show | 174 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.397+2262T>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183135885 | ||||||
chr2:183136183
|
A | C | 6 | a0001c0001t0001g0052a0001c0001t0001g0070a0001c0001t0001g0075others(3): Show | 7 | HG01099.hp1 HG01358.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.397+2560A>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183136183 | ||||||
chr2:183136265
|
C | T | 5 | a0001c0001t0001g0037a0001c0001t0001g0209a0001c0001t0001g0244others(2): Show | 6 | NA18946.hp2 NA18951.hp2 NA18957.hp2 others(3): Show |
intron_variant | MODIFIER | c.397+2642C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183136265 | ||||||
chr2:183136300
|
A | G | 1 | a0001c0001t0001g0176 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.397+2677A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183136300 | ||||||
chr2:183136353
|
T | C | 41 | a0001c0001t0001g0052a0001c0001t0001g0070a0001c0001t0001g0075others(38): Show | 49 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.397+2730T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183136353 | ||||||
chr2:183136585
|
C | T | 1 | a0001c0001t0001g0056 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.397+2962C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183136585 | ||||||
chr2:183136624
|
G | A | 1 | a0001c0001t0001g0077 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.397+3001G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183136624 | ||||||
chr2:183136627
|
G | A | 132 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(129): Show | 176 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(173): Show |
intron_variant | MODIFIER | c.397+3004G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183136627 | ||||||
chr2:183136677
|
T | G | 2 | a0001c0001t0001g0077a0001c0001t0001g0091 | 2 | HG02145.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.397+3054T>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183136677 | ||||||
chr2:183136704
|
A | G | 35 | a0001c0001t0002g0014a0001c0001t0002g0038a0001c0001t0002g0039others(32): Show | 42 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.397+3081A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183136704 | ||||||
chr2:183136755
|
A | G | 4 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0174others(1): Show | 4 | HG00673.hp1 HG02071.hp1 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.397+3132A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183136755 | ||||||
chr2:183136815
|
C | T | 2 | a0001c0001t0002g0260a0001c0001t0002g0265 | 2 | HG02738.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.397+3192C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183136815 | ||||||
chr2:183136816
|
G | A | 67 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(64): Show | 102 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.397+3193G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183136816 | ||||||
chr2:183137017
|
G | A | 1 | a0001c0001t0001g0015 | 3 | HG00438.hp1 NA18944.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.397+3394G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183137017 | ||||||
chr2:183137071
|
T | C | 132 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(129): Show | 176 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(173): Show |
intron_variant | MODIFIER | c.397+3448T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183137071 | ||||||
chr2:183137080
|
A | G | 1 | a0001c0001t0001g0124 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.397+3457A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183137080 | ||||||
chr2:183137126
|
T | C | 35 | a0001c0001t0002g0014a0001c0001t0002g0038a0001c0001t0002g0039others(32): Show | 42 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.397+3503T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183137126 | ||||||
chr2:183137217
|
G | T | 130 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(127): Show | 174 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.397+3594G>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183137217 | ||||||
chr2:183137279
|
G | A | 85 | a0001c0001t0001g0005a0001c0001t0001g0023a0001c0001t0001g0024others(82): Show | 99 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.397+3656G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183137279 | ||||||
chr2:183137345
|
G | A | 1 | a0001c0001t0001g0143 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.397+3722G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183137345 | ||||||
chr2:183137347
|
G | C | 1 | a0002c0005t0001g0311 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.397+3724G>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183137347 | ||||||
chr2:183137398
|
A | T | 6 | a0001c0001t0001g0052a0001c0001t0001g0070a0001c0001t0001g0075others(3): Show | 7 | HG01099.hp1 HG01358.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.397+3775A>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183137398 | ||||||
chr2:183137399
|
G | C | 35 | a0001c0001t0002g0014a0001c0001t0002g0038a0001c0001t0002g0039others(32): Show | 42 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.397+3776G>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183137399 | ||||||
chr2:183137478
|
C | T | 9 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0110others(6): Show | 9 | HG01255.hp1 HG01261.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.397+3855C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183137478 | ||||||
chr2:183137525
|
G | A | 6 | a0001c0001t0001g0052a0001c0001t0001g0070a0001c0001t0001g0075others(3): Show | 7 | HG01099.hp1 HG01358.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.397+3902G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183137525 | ||||||
chr2:183137601
|
T | C | 3 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213 | 3 | HG00735.hp2 HG01257.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.397+3978T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183137601 | ||||||
chr2:183137708
|
G | C | 6 | a0001c0001t0001g0052a0001c0001t0001g0070a0001c0001t0001g0075others(3): Show | 7 | HG01099.hp1 HG01358.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.397+4085G>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183137708 | ||||||
chr2:183137739
|
G | A | 4 | a0001c0001t0002g0014a0001c0001t0002g0264a0001c0001t0002g0267others(1): Show | 6 | HG01069.hp1 HG01071.hp2 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.397+4116G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183137739 | ||||||
chr2:183137789
|
GA | G | 45 | a0001c0001t0002g0014a0001c0001t0002g0038a0001c0001t0002g0039others(42): Show | 53 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(50): Show |
intron_variant | MODIFIER | c.397+4177delA | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183137789 | |||||
chr2:183137841
|
T | C | 238 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(235): Show | 308 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(305): Show |
intron_variant | MODIFIER | c.397+4218T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183137841 | ||||||
chr2:183137842
|
G | T | 1 | a0001c0001t0001g0102 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.397+4219G>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183137842 | ||||||
chr2:183137843
|
G | A | 1 | a0001c0001t0001g0310 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.397+4220G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183137843 | ||||||
chr2:183137860
|
A | G | 35 | a0001c0001t0002g0014a0001c0001t0002g0038a0001c0001t0002g0039others(32): Show | 42 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.397+4237A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183137860 | ||||||
chr2:183137914
|
A | G | 11 | a0001c0001t0001g0195a0001c0001t0001g0234a0001c0001t0001g0235others(8): Show | 11 | HG00323.hp1 HG00597.hp2 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.397+4291A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183137914 | ||||||
chr2:183138031
|
A | G | 1 | a0001c0001t0002g0289 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.397+4408A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183138031 | ||||||
chr2:183138146
|
G | C | 105 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(102): Show | 130 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.397+4523G>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183138146 | ||||||
chr2:183138245
|
C | CTA | 4 | a0001c0001t0001g0073a0001c0001t0001g0207a0001c0001t0001g0244others(1): Show | 4 | HG02717.hp1 HG04228.hp2 NA19086.hp2 others(1): Show |
intron_variant | MODIFIER | c.397+4646_397+4647d others(4): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183138245 | |||||
chr2:183138245
|
C | CTATATAT others(7): Show |
1 | a0001c0001t0001g0108 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.397+4634_397+4647d others(16): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183138245 | |||||
chr2:183138261
|
A | AT | 4 | a0001c0001t0001g0034a0001c0001t0001g0138a0001c0001t0001g0171others(1): Show | 5 | HG02922.hp1 HG02970.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.397+4639dupT | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183138261 | |||||
chr2:183138261
|
ATATATAT others(3): Show |
A | 8 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0043others(5): Show | 13 | HG02055.hp2 HG02572.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.397+4640_397+4649d others(12): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183138261 | |||||
chr2:183138261
|
ATATATAT others(4): Show |
A | 1 | a0001c0001t0001g0051 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.397+4640_397+4650d others(13): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183138261 | |||||
chr2:183138263
|
A | ATT | 6 | a0001c0001t0001g0263a0001c0001t0001g0293a0001c0001t0001g0295others(3): Show | 6 | HG01123.hp2 HG02809.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.397+4641_397+4642i others(4): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183138263 | |||||
chr2:183138263
|
A | T | 4 | a0001c0001t0001g0034a0001c0001t0001g0138a0001c0001t0001g0171others(1): Show | 5 | HG02922.hp1 HG02970.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.397+4640A>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183138263 | ||||||
chr2:183138263
|
ATATATAT others(3): Show |
A | 27 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(24): Show | 48 | HG00323.hp2 HG00438.hp1 HG00609.hp1 others(45): Show |
intron_variant | MODIFIER | c.397+4642_397+4651d others(12): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183138263 | |||||
chr2:183138265
|
A | ATT | 7 | a0001c0001t0001g0106a0001c0001t0001g0131a0001c0001t0001g0146others(4): Show | 7 | HG01069.hp2 HG01515.hp2 HG01975.hp2 others(4): Show |
intron_variant | MODIFIER | c.397+4643_397+4644i others(4): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183138265 | |||||
chr2:183138265
|
A | ATTT | 71 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(68): Show | 94 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.397+4643_397+4644i others(5): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183138265 | |||||
chr2:183138265
|
A | ATTTT | 6 | a0001c0001t0001g0032a0001c0001t0001g0088a0001c0001t0001g0173others(3): Show | 7 | HG00423.hp2 HG00673.hp1 HG02071.hp1 others(4): Show |
intron_variant | MODIFIER | c.397+4643_397+4644i others(6): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183138265 | |||||
chr2:183138265
|
A | T | 11 | a0001c0001t0001g0034a0001c0001t0001g0138a0001c0001t0001g0171others(8): Show | 12 | HG01123.hp2 HG02630.hp2 HG02809.hp1 others(9): Show |
intron_variant | MODIFIER | c.397+4642A>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183138265 | ||||||
chr2:183138267
|
A | ATTT | 3 | a0001c0001t0001g0130a0001c0001t0001g0177a0001c0001t0001g0182 | 3 | HG01256.hp2 HG02630.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.397+4645_397+4646i others(5): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183138267 | |||||
chr2:183138267
|
A | T | 97 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(94): Show | 122 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.397+4644A>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183138267 | ||||||
chr2:183138267
|
ATATTTTT others(6): Show |
A | 1 | a0001c0001t0001g0075 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.397+4646_397+4658d others(15): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183138267 | |||||
chr2:183138269
|
A | ATATATAT others(8): Show |
1 | a0001c0001t0001g0109 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.397+4647_397+4648i others(17): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183138269 | |||||
chr2:183138269
|
A | ATATATAT others(16): Show |
1 | a0001c0001t0001g0111 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.397+4647_397+4648i others(25): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183138269 | |||||
chr2:183138269
|
A | ATATATAT others(20): Show |
1 | a0001c0001t0001g0110 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.397+4647_397+4648i others(29): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183138269 | |||||
chr2:183138269
|
A | ATATATAT others(18): Show |
1 | a0001c0001t0001g0112 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.397+4647_397+4648i others(27): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183138269 | |||||
chr2:183138269
|
A | ATATATAT others(16): Show |
1 | a0001c0001t0001g0114 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.397+4647_397+4648i others(25): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183138269 | |||||
chr2:183138269
|
A | ATATATAT others(14): Show |
2 | a0001c0001t0001g0115a0001c0001t0001g0116 | 2 | HG02258.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.397+4647_397+4648i others(23): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183138269 | |||||
chr2:183138269
|
A | ATATATAT others(16): Show |
1 | a0001c0001t0003g0084 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.397+4647_397+4648i others(25): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183138269 | |||||
chr2:183138269
|
A | ATATATAT others(13): Show |
1 | a0001c0001t0001g0105 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.397+4647_397+4648i others(22): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183138269 | |||||
chr2:183138269
|
A | ATATATAT others(7): Show |
1 | a0001c0001t0003g0092 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.397+4647_397+4648i others(16): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183138269 | |||||
chr2:183138269
|
A | ATATATAT others(8): Show |
3 | a0001c0001t0001g0066a0001c0001t0001g0107a0001c0001t0001g0113 | 3 | HG02970.hp2 HG02976.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.397+4647_397+4648i others(17): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183138269 | |||||
chr2:183138269
|
A | ATATATAT others(9): Show |
1 | a0001c0001t0001g0067 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.397+4647_397+4648i others(18): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183138269 | |||||
chr2:183138269
|
A | ATATATAT others(10): Show |
1 | a0001c0001t0003g0081 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.397+4647_397+4648i others(19): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183138269 | |||||
chr2:183138269
|
A | ATATATAT others(8): Show |
2 | a0001c0001t0003g0021a0001c0001t0003g0085 | 3 | HG02257.hp2 HG03540.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.397+4647_397+4648i others(17): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183138269 | |||||
chr2:183138269
|
A | ATATATAT others(12): Show |
3 | a0001c0001t0002g0038a0001c0001t0002g0270a0001c0001t0002g0271 | 4 | HG03669.hp2 HG03704.hp1 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.397+4647_397+4648i others(21): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183138269 | |||||
chr2:183138269
|
A | ATATATAT others(3): Show |
1 | a0001c0001t0003g0068 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.397+4647_397+4648i others(12): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183138269 | |||||
chr2:183138269
|
A | ATATATAT others(6): Show |
1 | a0001c0001t0003g0086 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.397+4647_397+4648i others(15): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183138269 | |||||
chr2:183138269
|
A | ATATATAT others(8): Show |
3 | a0001c0001t0002g0039a0001c0001t0002g0272a0001c0001t0003g0082 | 4 | HG02080.hp2 HG02135.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.397+4647_397+4648i others(17): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183138269 | |||||
chr2:183138269
|
A | ATATATAT others(9): Show |
1 | a0001c0001t0002g0267 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.397+4647_397+4648i others(18): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183138269 | |||||
chr2:183138269
|
A | ATATATAT others(10): Show |
4 | a0001c0001t0002g0260a0001c0001t0002g0273a0001c0001t0002g0274others(1): Show | 4 | HG02738.hp1 HG03834.hp1 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.397+4647_397+4648i others(19): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183138269 | |||||
chr2:183138269
|
A | ATATATAT others(12): Show |
3 | a0001c0001t0002g0040a0001c0001t0002g0275a0001c0001t0002g0276 | 4 | NA18944.hp2 NA18960.hp1 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.397+4647_397+4648i others(21): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183138269 | |||||
chr2:183138269
|
A | ATATATAT others(6): Show |
1 | a0001c0001t0003g0083 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.397+4647_397+4648i others(15): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183138269 | |||||
chr2:183138269
|
A | ATATATAT others(7): Show |
3 | a0001c0001t0002g0277a0001c0001t0002g0278a0001c0001t0002g0279 | 3 | HG02523.hp1 HG03710.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.397+4647_397+4648i others(16): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183138269 | |||||
chr2:183138269
|
A | ATATATAT others(8): Show |
13 | a0001c0001t0002g0014a0001c0001t0002g0041a0001c0001t0002g0042others(10): Show | 17 | HG00423.hp1 HG01069.hp1 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.397+4647_397+4648i others(17): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183138269 | |||||
chr2:183138269
|
A | ATATATAT others(9): Show |
2 | a0001c0001t0002g0284a0001c0001t0002g0285 | 2 | HG02074.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.397+4647_397+4648i others(18): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183138269 | |||||
chr2:183138269
|
A | ATATATTT others(3): Show |
2 | a0001c0001t0001g0024a0001c0001t0001g0095 | 3 | HG02486.hp2 HG03209.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.397+4647_397+4648i others(12): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183138269 | |||||
chr2:183138269
|
A | ATATATTT others(4): Show |
17 | a0001c0001t0001g0005a0001c0001t0001g0023a0001c0001t0001g0033others(14): Show | 21 | HG00099.hp2 HG00741.hp2 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.397+4647_397+4648i others(13): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183138269 | |||||
chr2:183138269
|
A | ATATATTT others(5): Show |
1 | a0001c0001t0001g0093 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.397+4647_397+4648i others(14): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183138269 | |||||
chr2:183138269
|
A | ATATATTT others(8): Show |
3 | a0001c0001t0002g0286a0001c0001t0002g0287a0001c0001t0002g0288 | 3 | HG00621.hp2 HG02056.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.397+4647_397+4648i others(17): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183138269 | |||||
chr2:183138269
|
A | ATATTTTT others(3): Show |
1 | a0001c0001t0001g0091 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.397+4647_397+4648i others(12): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183138269 | |||||
chr2:183138269
|
A | ATATTTTT others(4): Show |
1 | a0001c0001t0001g0101 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.397+4647_397+4648i others(13): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183138269 | |||||
chr2:183138269
|
A | T | 112 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(109): Show | 139 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.397+4646A>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183138269 | ||||||
chr2:183138270
|
T | TATATATA others(16): Show |
1 | a0001c0001t0001g0319 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.397+4647_397+4648i others(25): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183138270 | ||||||
chr2:183138270
|
T | TATATATA others(24): Show |
1 | a0001c0001t0001g0070 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.397+4647_397+4648i others(33): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183138270 | ||||||
chr2:183138271
|
T | A | 18 | a0001c0001t0001g0037a0001c0001t0001g0074a0001c0001t0001g0202others(15): Show | 19 | HG00408.hp2 HG00735.hp2 HG02027.hp2 others(16): Show |
intron_variant | MODIFIER | c.397+4648T>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183138271 | ||||||
chr2:183138272
|
T | A | 3 | a0001c0001t0001g0052a0001c0001t0001g0070a0001c0001t0001g0319 | 3 | HG02818.hp2 HG02886.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.397+4649T>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183138272 | ||||||
chr2:183138273
|
T | A | 1 | a0001c0001t0001g0214 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.397+4650T>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183138273 | ||||||
chr2:183138274
|
T | A | 3 | a0001c0001t0001g0052a0001c0001t0001g0070a0001c0001t0001g0319 | 3 | HG02818.hp2 HG02886.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.397+4651T>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183138274 | ||||||
chr2:183138276
|
T | A | 3 | a0001c0001t0001g0052a0001c0001t0001g0070a0001c0001t0001g0319 | 3 | HG02818.hp2 HG02886.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.397+4653T>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183138276 | ||||||
chr2:183138278
|
T | A | 3 | a0001c0001t0001g0052a0001c0001t0001g0070a0001c0001t0001g0319 | 3 | HG02818.hp2 HG02886.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.397+4655T>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183138278 | ||||||
chr2:183138280
|
T | A | 5 | a0001c0001t0001g0052a0001c0001t0001g0070a0001c0001t0001g0319others(2): Show | 6 | HG01099.hp1 HG01358.hp1 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.397+4657T>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183138280 | ||||||
chr2:183138356
|
G | C | 132 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(129): Show | 176 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(173): Show |
intron_variant | MODIFIER | c.397+4733G>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183138356 | ||||||
chr2:183138440
|
G | A | 6 | a0001c0001t0001g0052a0001c0001t0001g0070a0001c0001t0001g0075others(3): Show | 7 | HG01099.hp1 HG01358.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.397+4817G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183138440 | ||||||
chr2:183138573
|
A | C | 34 | a0001c0001t0002g0014a0001c0001t0002g0038a0001c0001t0002g0039others(31): Show | 41 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.397+4950A>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183138573 | ||||||
chr2:183138611
|
A | T | 1 | a0001c0003t0002g0118 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.397+4988A>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183138611 | ||||||
chr2:183138615
|
G | A | 1 | a0001c0002t0001g0049 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.397+4992G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183138615 | ||||||
chr2:183138617
|
T | G | 12 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0107others(9): Show | 12 | HG01255.hp1 HG01261.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.397+4994T>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183138617 | ||||||
chr2:183138790
|
C | CATT | 126 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(123): Show | 169 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(166): Show |
intron_variant | MODIFIER | c.397+5168_397+5170d others(5): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183138790 | |||||
chr2:183138790
|
C | CGTT | 6 | a0001c0001t0001g0052a0001c0001t0001g0070a0001c0001t0001g0075others(3): Show | 7 | HG01099.hp1 HG01358.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.397+5167_397+5168i others(5): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183138790 | ||||||
chr2:183138890
|
G | A | 1 | a0001c0001t0001g0024 | 2 | HG02486.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.397+5267G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183138890 | ||||||
chr2:183138953
|
A | G | 1 | a0001c0001t0001g0181 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.397+5330A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183138953 | ||||||
chr2:183138971
|
G | GCT | 41 | a0001c0001t0001g0052a0001c0001t0001g0070a0001c0001t0001g0075others(38): Show | 49 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.397+5353_397+5354d others(4): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183138971 | |||||
chr2:183138984
|
C | A | 3 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0102 | 3 | HG01884.hp1 HG02109.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.397+5361C>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183138984 | ||||||
chr2:183138998
|
T | C | 1 | a0001c0001t0001g0074 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.397+5375T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183138998 | ||||||
chr2:183138999
|
A | T | 3 | a0001c0001t0001g0052a0001c0001t0004g0020a0001c0001t0004g0076 | 4 | HG01099.hp1 HG01358.hp1 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.397+5376A>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183138999 | ||||||
chr2:183139137
|
T | C | 1 | a0001c0001t0001g0045 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.397+5514T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183139137 | ||||||
chr2:183139209
|
TTTC | T | 23 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0015others(20): Show | 45 | HG00323.hp2 HG00438.hp1 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.397+5589_397+5591d others(5): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183139209 | |||||
chr2:183139210
|
TTC | T | 24 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0022others(21): Show | 30 | HG01099.hp2 HG01169.hp1 HG01884.hp2 others(27): Show |
intron_variant | MODIFIER | c.397+5589_397+5590d others(4): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183139210 | |||||
chr2:183139211
|
TC | T | 145 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(142): Show | 178 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.397+5589delC | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183139211 | ||||||
chr2:183139212
|
C | CT | 34 | a0001c0001t0002g0014a0001c0001t0002g0038a0001c0001t0002g0039others(31): Show | 41 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.397+5603dupT | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183139212 | |||||
chr2:183139212
|
C | T | 93 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0013others(90): Show | 106 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.397+5589C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183139212 | ||||||
chr2:183139818
|
A | G | 4 | a0001c0001t0001g0025a0001c0001t0001g0117a0001c0001t0001g0119others(1): Show | 5 | HG00280.hp2 HG00639.hp2 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.397+6195A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183139818 | ||||||
chr2:183139821
|
T | C | 6 | a0001c0001t0001g0052a0001c0001t0001g0070a0001c0001t0001g0075others(3): Show | 7 | HG01099.hp1 HG01358.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.397+6198T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183139821 | ||||||
chr2:183139834
|
T | C | 236 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(233): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(302): Show |
intron_variant | MODIFIER | c.397+6211T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183139834 | ||||||
chr2:183139844
|
T | G | 236 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(233): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(303): Show |
intron_variant | MODIFIER | c.397+6221T>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183139844 | ||||||
chr2:183140352
|
C | T | 1 | a0001c0001t0001g0243 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.397+6729C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183140352 | ||||||
chr2:183140382
|
T | C | 6 | a0001c0001t0001g0003a0001c0001t0001g0146a0001c0001t0001g0152others(3): Show | 10 | HG02165.hp1 NA18947.hp2 NA18967.hp2 others(7): Show |
intron_variant | MODIFIER | c.397+6759T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183140382 | ||||||
chr2:183140451
|
G | A | 38 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(35): Show | 66 | HG00323.hp2 HG00438.hp1 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.397+6828G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183140451 | ||||||
chr2:183140531
|
C | T | 2 | a0001c0001t0001g0066a0001c0001t0001g0067 | 2 | HG02886.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.397+6908C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183140531 | ||||||
chr2:183140532
|
A | G | 46 | a0001c0001t0001g0005a0001c0001t0001g0023a0001c0001t0001g0024others(43): Show | 52 | HG00099.hp2 HG00597.hp1 HG00741.hp2 others(49): Show |
intron_variant | MODIFIER | c.397+6909A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183140532 | ||||||
chr2:183140592
|
C | T | 2 | a0001c0002t0001g0049a0001c0002t0001g0050 | 2 | HG02280.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.397+6969C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183140592 | ||||||
chr2:183140593
|
G | A | 44 | a0001c0001t0001g0005a0001c0001t0001g0023a0001c0001t0001g0024others(41): Show | 50 | HG00099.hp2 HG00597.hp1 HG00741.hp2 others(47): Show |
intron_variant | MODIFIER | c.397+6970G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183140593 | ||||||
chr2:183140598
|
G | C | 1 | a0001c0001t0001g0078 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.397+6975G>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183140598 | ||||||
chr2:183140629
|
C | T | 46 | a0001c0001t0001g0005a0001c0001t0001g0023a0001c0001t0001g0024others(43): Show | 52 | HG00099.hp2 HG00597.hp1 HG00741.hp2 others(49): Show |
intron_variant | MODIFIER | c.397+7006C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183140629 | ||||||
chr2:183140804
|
C | T | 1 | a0001c0001t0001g0100 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.397+7181C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183140804 | ||||||
chr2:183140822
|
C | CA | 22 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0022others(19): Show | 28 | HG00642.hp1 HG01081.hp2 HG01516.hp2 others(25): Show |
intron_variant | MODIFIER | c.397+7216dupA | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183140822 | |||||
chr2:183140822
|
C | CAA | 42 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(39): Show | 69 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.397+7215_397+7216d others(4): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183140822 | |||||
chr2:183140822
|
CA | C | 8 | a0001c0001t0001g0052a0001c0001t0001g0075a0001c0001t0001g0139others(5): Show | 9 | HG01099.hp1 HG01358.hp1 HG01361.hp2 others(6): Show |
intron_variant | MODIFIER | c.397+7216delA | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183140822 | |||||
chr2:183140878
|
G | A | 223 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(220): Show | 292 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(289): Show |
intron_variant | MODIFIER | c.397+7255G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183140878 | ||||||
chr2:183140906
|
G | T | 2 | a0001c0001t0001g0170a0001c0001t0001g0178 | 2 | HG01361.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.397+7283G>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183140906 | ||||||
chr2:183140942
|
A | G | 34 | a0001c0001t0002g0014a0001c0001t0002g0038a0001c0001t0002g0039others(31): Show | 41 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.397+7319A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183140942 | ||||||
chr2:183141049
|
G | T | 1 | a0002c0005t0001g0311 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.397+7426G>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183141049 | ||||||
chr2:183141096
|
T | G | 6 | a0001c0001t0001g0052a0001c0001t0001g0070a0001c0001t0001g0075others(3): Show | 7 | HG01099.hp1 HG01358.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.397+7473T>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183141096 | ||||||
chr2:183141113
|
T | A | 4 | a0001c0001t0001g0206a0001c0001t0001g0214a0001c0001t0001g0215others(1): Show | 4 | HG00408.hp2 NA18964.hp1 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.397+7490T>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183141113 | ||||||
chr2:183141119
|
G | GT | 6 | a0001c0001t0001g0070a0001c0001t0001g0075a0001c0001t0001g0312others(3): Show | 7 | HG01099.hp1 HG01358.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.397+7509dupT | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183141119 | |||||
chr2:183141131
|
T | A | 22 | a0001c0001t0001g0005a0001c0001t0001g0023a0001c0001t0001g0024others(19): Show | 27 | HG00099.hp2 HG00597.hp1 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.397+7508T>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183141131 | ||||||
chr2:183141186
|
A | G | 6 | a0001c0001t0001g0052a0001c0001t0001g0070a0001c0001t0001g0075others(3): Show | 7 | HG01099.hp1 HG01358.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.397+7563A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183141186 | ||||||
chr2:183141199
|
C | G | 7 | a0001c0001t0003g0021a0001c0001t0003g0081a0001c0001t0003g0082others(4): Show | 8 | HG02257.hp2 HG02451.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.397+7576C>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183141199 | ||||||
chr2:183141241
|
C | G | 1 | a0001c0001t0001g0316 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.397+7618C>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183141241 | ||||||
chr2:183141241
|
C | T | 9 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0043others(6): Show | 14 | HG02055.hp2 HG02572.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.397+7618C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183141241 | ||||||
chr2:183141270
|
G | A | 22 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0107others(19): Show | 23 | HG01255.hp1 HG01261.hp1 HG02257.hp2 others(20): Show |
intron_variant | MODIFIER | c.397+7647G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183141270 | ||||||
chr2:183141299
|
C | T | 46 | a0001c0001t0001g0005a0001c0001t0001g0023a0001c0001t0001g0024others(43): Show | 52 | HG00099.hp2 HG00597.hp1 HG00741.hp2 others(49): Show |
intron_variant | MODIFIER | c.397+7676C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183141299 | ||||||
chr2:183141833
|
A | G | 12 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0107others(9): Show | 12 | HG01255.hp1 HG01261.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.397+8210A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183141833 | ||||||
chr2:183141996
|
T | A | 1 | a0001c0001t0001g0124 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.397+8373T>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183141996 | ||||||
chr2:183142116
|
T | C | 22 | a0001c0001t0001g0005a0001c0001t0001g0023a0001c0001t0001g0024others(19): Show | 27 | HG00099.hp2 HG00597.hp1 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.397+8493T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183142116 | ||||||
chr2:183142121
|
C | T | 1 | a0001c0001t0001g0101 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.397+8498C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183142121 | ||||||
chr2:183142284
|
A | G | 6 | a0001c0001t0001g0052a0001c0001t0001g0070a0001c0001t0001g0075others(3): Show | 7 | HG01099.hp1 HG01358.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.397+8661A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183142284 | ||||||
chr2:183142405
|
A | G | 4 | a0001c0001t0001g0025a0001c0001t0001g0117a0001c0001t0001g0119others(1): Show | 5 | HG00280.hp2 HG00639.hp2 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.397+8782A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183142405 | ||||||
chr2:183142408
|
T | C | 1 | a0001c0001t0002g0272 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.397+8785T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183142408 | ||||||
chr2:183142415
|
G | A | 1 | a0001c0001t0001g0183 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.397+8792G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183142415 | ||||||
chr2:183142454
|
C | CT | 39 | a0001c0001t0001g0025a0001c0001t0001g0117a0001c0001t0001g0119others(36): Show | 47 | HG00280.hp2 HG00423.hp1 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.397+8842dupT | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183142454 | |||||
chr2:183142468
|
T | C | 1 | a0001c0001t0001g0026 | 2 | HG02145.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.397+8845T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183142468 | ||||||
chr2:183142476
|
G | T | 35 | a0001c0001t0002g0014a0001c0001t0002g0038a0001c0001t0002g0039others(32): Show | 42 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.397+8853G>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183142476 | ||||||
chr2:183142543
|
A | G | 41 | a0001c0001t0001g0052a0001c0001t0001g0070a0001c0001t0001g0075others(38): Show | 49 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.397+8920A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183142543 | ||||||
chr2:183142550
|
C | T | 43 | a0001c0001t0001g0005a0001c0001t0001g0023a0001c0001t0001g0024others(40): Show | 49 | HG00099.hp2 HG00597.hp1 HG00741.hp2 others(46): Show |
intron_variant | MODIFIER | c.397+8927C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183142550 | ||||||
chr2:183142640
|
G | T | 6 | a0001c0001t0001g0052a0001c0001t0001g0070a0001c0001t0001g0075others(3): Show | 7 | HG01099.hp1 HG01358.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.398-8868G>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183142640 | ||||||
chr2:183142641
|
G | T | 6 | a0001c0001t0001g0052a0001c0001t0001g0070a0001c0001t0001g0075others(3): Show | 7 | HG01099.hp1 HG01358.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.398-8867G>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183142641 | ||||||
chr2:183142644
|
T | TA | 132 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(129): Show | 176 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(173): Show |
intron_variant | MODIFIER | c.398-8863dupA | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183142644 | |||||
chr2:183142646
|
C | T | 132 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(129): Show | 176 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(173): Show |
intron_variant | MODIFIER | c.398-8862C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183142646 | ||||||
chr2:183142660
|
A | G | 4 | a0001c0001t0001g0025a0001c0001t0001g0117a0001c0001t0001g0119others(1): Show | 5 | HG00280.hp2 HG00639.hp2 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.398-8848A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183142660 | ||||||
chr2:183142670
|
G | A | 7 | a0001c0001t0003g0021a0001c0001t0003g0081a0001c0001t0003g0082others(4): Show | 8 | HG02257.hp2 HG02451.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.398-8838G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183142670 | ||||||
chr2:183142680
|
A | G | 1 | a0001c0001t0001g0205 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.398-8828A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183142680 | ||||||
chr2:183142699
|
T | C | 41 | a0001c0001t0001g0052a0001c0001t0001g0070a0001c0001t0001g0075others(38): Show | 49 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.398-8809T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183142699 | ||||||
chr2:183142702
|
A | G | 4 | a0001c0001t0001g0025a0001c0001t0001g0117a0001c0001t0001g0119others(1): Show | 5 | HG00280.hp2 HG00639.hp2 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.398-8806A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183142702 | ||||||
chr2:183142713
|
C | T | 1 | a0001c0001t0001g0026 | 2 | HG02145.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.398-8795C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183142713 | ||||||
chr2:183142831
|
G | C | 1 | a0002c0005t0001g0311 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.398-8677G>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183142831 | ||||||
chr2:183142885
|
G | T | 1 | a0001c0001t0001g0191 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.398-8623G>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183142885 | ||||||
chr2:183142895
|
G | A | 1 | a0001c0001t0001g0051 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.398-8613G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183142895 | ||||||
chr2:183142934
|
G | A | 41 | a0001c0001t0001g0052a0001c0001t0001g0070a0001c0001t0001g0075others(38): Show | 49 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.398-8574G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183142934 | ||||||
chr2:183142959
|
G | A | 3 | a0001c0002t0001g0019a0001c0002t0001g0049a0001c0002t0001g0050 | 4 | HG02257.hp1 HG02280.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.398-8549G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183142959 | ||||||
chr2:183143015
|
G | A | 12 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0107others(9): Show | 12 | HG01255.hp1 HG01261.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.398-8493G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183143015 | ||||||
chr2:183143117
|
C | T | 1 | a0001c0001t0001g0095 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.398-8391C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183143117 | ||||||
chr2:183143141
|
G | A | 1 | a0001c0001t0001g0026 | 2 | HG02145.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.398-8367G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183143141 | ||||||
chr2:183143142
|
C | T | 1 | a0001c0001t0001g0026 | 2 | HG02145.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.398-8366C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183143142 | ||||||
chr2:183143151
|
A | G | 1 | a0001c0002t0001g0049 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.398-8357A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183143151 | ||||||
chr2:183143155
|
C | CA | 72 | a0001c0001t0001g0005a0001c0001t0001g0023a0001c0001t0001g0024others(69): Show | 85 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(82): Show |
intron_variant | MODIFIER | c.398-8338dupA | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183143155 | |||||
chr2:183143155
|
C | CAA | 48 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0015others(45): Show | 75 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.398-8339_398-8338d others(4): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183143155 | |||||
chr2:183143166
|
A | G | 6 | a0001c0001t0001g0052a0001c0001t0001g0070a0001c0001t0001g0075others(3): Show | 7 | HG01099.hp1 HG01358.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.398-8342A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183143166 | ||||||
chr2:183143175
|
A | G | 2 | a0001c0001t0001g0011a0001c0001t0001g0053 | 4 | NA18969.hp1 NA18972.hp2 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.398-8333A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183143175 | ||||||
chr2:183143176
|
G | A | 2 | a0001c0001t0001g0011a0001c0001t0001g0053 | 4 | NA18969.hp1 NA18972.hp2 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.398-8332G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183143176 | ||||||
chr2:183143178
|
A | T | 19 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0110others(16): Show | 20 | HG01255.hp1 HG01261.hp1 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.398-8330A>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183143178 | ||||||
chr2:183143263
|
G | A | 17 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0110others(14): Show | 18 | HG01255.hp1 HG01261.hp1 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.398-8245G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183143263 | ||||||
chr2:183143293
|
T | TC | 86 | a0001c0001t0001g0005a0001c0001t0001g0022a0001c0001t0001g0023others(83): Show | 101 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(98): Show |
intron_variant | MODIFIER | c.398-8215_398-8214i others(3): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183143293 | ||||||
chr2:183143293
|
T | TTC | 46 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(43): Show | 75 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.398-8215_398-8214i others(4): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183143293 | ||||||
chr2:183143295
|
C | A | 3 | a0001c0002t0001g0019a0001c0002t0001g0049a0001c0002t0001g0050 | 4 | HG02257.hp1 HG02280.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.398-8213C>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183143295 | ||||||
chr2:183143295
|
C | T | 1 | a0001c0001t0003g0069 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.398-8213C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183143295 | ||||||
chr2:183143481
|
G | T | 1 | a0001c0003t0002g0118 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.398-8027G>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183143481 | ||||||
chr2:183143703
|
C | T | 1 | a0001c0001t0001g0125 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.398-7805C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183143703 | ||||||
chr2:183143724
|
A | G | 2 | a0001c0001t0001g0077a0001c0001t0001g0091 | 2 | HG02145.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.398-7784A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183143724 | ||||||
chr2:183143878
|
A | G | 2 | a0001c0001t0001g0195a0001c0001t0001g0241 | 2 | HG00597.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.398-7630A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183143878 | ||||||
chr2:183144002
|
A | G | 45 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(42): Show | 75 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.398-7506A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183144002 | ||||||
chr2:183144080
|
G | T | 12 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0107others(9): Show | 12 | HG01255.hp1 HG01261.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.398-7428G>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183144080 | ||||||
chr2:183144236
|
A | G | 1 | a0001c0001t0001g0026 | 2 | HG02145.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.398-7272A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183144236 | ||||||
chr2:183144334
|
A | G | 35 | a0001c0001t0002g0014a0001c0001t0002g0038a0001c0001t0002g0039others(32): Show | 42 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.398-7174A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183144334 | ||||||
chr2:183144342
|
G | T | 38 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(35): Show | 66 | HG00323.hp2 HG00438.hp1 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.398-7166G>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183144342 | ||||||
chr2:183144400
|
C | G | 1 | a0001c0001t0001g0169 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.398-7108C>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183144400 | ||||||
chr2:183144476
|
G | A | 41 | a0001c0001t0001g0052a0001c0001t0001g0070a0001c0001t0001g0075others(38): Show | 49 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.398-7032G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183144476 | ||||||
chr2:183144588
|
T | TAATAAG | 22 | a0001c0001t0001g0005a0001c0001t0001g0023a0001c0001t0001g0024others(19): Show | 27 | HG00099.hp2 HG00597.hp1 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.398-6919_398-6914d others(8): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183144588 | |||||
chr2:183144673
|
C | T | 1 | a0001c0004t0001g0232 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.398-6835C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183144673 | ||||||
chr2:183144682
|
G | A | 1 | a0001c0001t0001g0207 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.398-6826G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183144682 | ||||||
chr2:183144748
|
T | C | 2 | a0001c0001t0003g0068a0001c0001t0003g0069 | 2 | HG02486.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.398-6760T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183144748 | ||||||
chr2:183144804
|
T | G | 38 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(35): Show | 66 | HG00323.hp2 HG00438.hp1 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.398-6704T>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183144804 | ||||||
chr2:183144948
|
A | G | 24 | a0001c0001t0001g0005a0001c0001t0001g0023a0001c0001t0001g0024others(21): Show | 29 | HG00099.hp2 HG00597.hp1 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.398-6560A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183144948 | ||||||
chr2:183144995
|
A | C | 3 | a0001c0001t0002g0274a0001c0001t0002g0282a0001c0001t0002g0283 | 3 | NA18951.hp1 NA18966.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.398-6513A>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183144995 | ||||||
chr2:183145243
|
C | T | 130 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(127): Show | 174 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.398-6265C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183145243 | ||||||
chr2:183145263
|
A | G | 2 | a0001c0001t0001g0070a0001c0001t0001g0319 | 2 | HG02818.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.398-6245A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183145263 | ||||||
chr2:183145277
|
G | A | 5 | a0001c0001t0001g0013a0001c0001t0001g0210a0001c0001t0001g0222others(2): Show | 6 | HG00438.hp2 HG02040.hp1 HG02135.hp1 others(3): Show |
intron_variant | MODIFIER | c.398-6231G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183145277 | ||||||
chr2:183145307
|
G | C | 37 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(34): Show | 65 | HG00323.hp2 HG00438.hp1 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.398-6201G>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183145307 | ||||||
chr2:183145350
|
T | C | 12 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0107others(9): Show | 12 | HG01255.hp1 HG01261.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.398-6158T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183145350 | ||||||
chr2:183145361
|
T | C | 4 | a0001c0001t0001g0025a0001c0001t0001g0117a0001c0001t0001g0119others(1): Show | 5 | HG00280.hp2 HG00639.hp2 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.398-6147T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183145361 | ||||||
chr2:183145544
|
CACATGTA others(6): Show |
C | 1 | a0001c0001t0001g0072 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.398-5959_398-5947d others(15): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183145544 | |||||
chr2:183145764
|
A | C | 22 | a0001c0001t0001g0005a0001c0001t0001g0023a0001c0001t0001g0024others(19): Show | 27 | HG00099.hp2 HG00597.hp1 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.398-5744A>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183145764 | ||||||
chr2:183145873
|
G | T | 1 | a0001c0001t0001g0168 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.398-5635G>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183145873 | ||||||
chr2:183145931
|
A | G | 1 | a0001c0001t0001g0168 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.398-5577A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183145931 | ||||||
chr2:183145967
|
A | G | 1 | a0001c0001t0001g0298 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.398-5541A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183145967 | ||||||
chr2:183146030
|
G | A | 35 | a0001c0001t0002g0014a0001c0001t0002g0038a0001c0001t0002g0039others(32): Show | 42 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.398-5478G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183146030 | ||||||
chr2:183146033
|
C | T | 1 | a0001c0001t0001g0231 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.398-5475C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183146033 | ||||||
chr2:183146142
|
A | C | 6 | a0001c0001t0001g0052a0001c0001t0001g0070a0001c0001t0001g0075others(3): Show | 7 | HG01099.hp1 HG01358.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.398-5366A>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183146142 | ||||||
chr2:183146150
|
C | T | 4 | a0001c0001t0001g0025a0001c0001t0001g0117a0001c0001t0001g0119others(1): Show | 5 | HG00280.hp2 HG00639.hp2 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.398-5358C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183146150 | ||||||
chr2:183146235
|
C | CA | 8 | a0001c0001t0001g0052a0001c0001t0001g0059a0001c0001t0001g0060others(5): Show | 9 | HG00642.hp2 HG01099.hp1 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.398-5263dupA | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183146235 | |||||
chr2:183146252
|
C | A | 1 | a0001c0003t0002g0118 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.398-5256C>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183146252 | ||||||
chr2:183146257
|
A | G | 4 | a0001c0001t0001g0025a0001c0001t0001g0117a0001c0001t0001g0119others(1): Show | 5 | HG00280.hp2 HG00639.hp2 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.398-5251A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183146257 | ||||||
chr2:183146276
|
G | A | 2 | a0001c0001t0002g0038a0001c0001t0002g0271 | 3 | HG03669.hp2 HG03704.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.398-5232G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183146276 | ||||||
chr2:183146329
|
C | T | 4 | a0001c0001t0001g0087a0001c0001t0001g0151a0001c0001t0001g0169others(1): Show | 4 | HG01081.hp1 HG01884.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.398-5179C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183146329 | ||||||
chr2:183146653
|
G | T | 100 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(97): Show | 125 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.398-4855G>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183146653 | ||||||
chr2:183146660
|
G | A | 45 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(42): Show | 75 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.398-4848G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183146660 | ||||||
chr2:183146679
|
C | T | 101 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(98): Show | 126 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(123): Show |
intron_variant | MODIFIER | c.398-4829C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183146679 | ||||||
chr2:183146782
|
A | G | 1 | a0001c0001t0001g0064 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.398-4726A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183146782 | ||||||
chr2:183146794
|
G | A | 1 | a0001c0001t0001g0099 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.398-4714G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183146794 | ||||||
chr2:183146887
|
C | T | 2 | a0001c0001t0001g0198a0001c0001t0001g0199 | 2 | NA19062.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.398-4621C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183146887 | ||||||
chr2:183147169
|
G | T | 1 | a0001c0001t0001g0167 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.398-4339G>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183147169 | ||||||
chr2:183147202
|
T | G | 35 | a0001c0001t0002g0014a0001c0001t0002g0038a0001c0001t0002g0039others(32): Show | 42 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.398-4306T>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183147202 | ||||||
chr2:183147251
|
C | T | 22 | a0001c0001t0001g0005a0001c0001t0001g0023a0001c0001t0001g0024others(19): Show | 27 | HG00099.hp2 HG00597.hp1 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.398-4257C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183147251 | ||||||
chr2:183147261
|
T | C | 132 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(129): Show | 176 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(173): Show |
intron_variant | MODIFIER | c.398-4247T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183147261 | ||||||
chr2:183147320
|
T | C | 36 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(33): Show | 63 | HG00323.hp2 HG00438.hp1 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.398-4188T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183147320 | ||||||
chr2:183147383
|
G | C | 3 | a0001c0002t0001g0019a0001c0002t0001g0049a0001c0002t0001g0050 | 4 | HG02257.hp1 HG02280.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.398-4125G>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183147383 | ||||||
chr2:183147408
|
G | A | 3 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0122 | 3 | HG01975.hp1 HG03942.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.398-4100G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183147408 | ||||||
chr2:183147423
|
A | G | 2 | a0001c0001t0001g0070a0001c0001t0001g0319 | 2 | HG02818.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.398-4085A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183147423 | ||||||
chr2:183147583
|
T | C | 24 | a0001c0001t0001g0005a0001c0001t0001g0023a0001c0001t0001g0024others(21): Show | 29 | HG00099.hp2 HG00597.hp1 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.398-3925T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183147583 | ||||||
chr2:183147592
|
A | G | 3 | a0001c0001t0001g0070a0001c0001t0001g0075a0001c0001t0001g0319 | 3 | HG02818.hp2 HG02886.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.398-3916A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183147592 | ||||||
chr2:183147667
|
T | C | 35 | a0001c0001t0002g0014a0001c0001t0002g0038a0001c0001t0002g0039others(32): Show | 42 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.398-3841T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183147667 | ||||||
chr2:183147766
|
T | C | 188 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(185): Show | 225 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(222): Show |
intron_variant | MODIFIER | c.398-3742T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183147766 | ||||||
chr2:183147866
|
T | C | 35 | a0001c0001t0002g0014a0001c0001t0002g0038a0001c0001t0002g0039others(32): Show | 42 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.398-3642T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183147866 | ||||||
chr2:183147915
|
A | AT | 37 | a0001c0001t0001g0026a0001c0001t0001g0114a0001c0001t0002g0014others(34): Show | 45 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.398-3580dupT | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183147915 | |||||
chr2:183147915
|
AT | A | 46 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(43): Show | 76 | HG00323.hp2 HG00438.hp1 HG00609.hp1 others(73): Show |
intron_variant | MODIFIER | c.398-3580delT | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183147915 | |||||
chr2:183148006
|
A | G | 2 | a0001c0001t0001g0077a0001c0001t0001g0091 | 2 | HG02145.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.398-3502A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183148006 | ||||||
chr2:183148007
|
C | G | 1 | a0001c0003t0002g0118 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.398-3501C>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183148007 | ||||||
chr2:183148037
|
C | T | 1 | a0001c0001t0001g0181 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.398-3471C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183148037 | ||||||
chr2:183148204
|
C | G | 48 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(45): Show | 78 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.398-3304C>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183148204 | ||||||
chr2:183148306
|
G | A | 2 | a0001c0001t0001g0016a0001c0001t0001g0304 | 4 | NA18961.hp2 NA18999.hp1 NA19001.hp1 others(1): Show |
intron_variant | MODIFIER | c.398-3202G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183148306 | ||||||
chr2:183148402
|
G | T | 14 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0029others(11): Show | 20 | HG00408.hp1 HG02015.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.398-3106G>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183148402 | ||||||
chr2:183148563
|
T | A | 44 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(41): Show | 73 | HG00323.hp2 HG00438.hp1 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.398-2945T>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183148563 | ||||||
chr2:183148610
|
ATTCATGT others(11): Show |
A | 11 | a0001c0001t0001g0005a0001c0001t0001g0023a0001c0001t0001g0094others(8): Show | 14 | HG00099.hp2 HG00741.hp2 HG01081.hp2 others(11): Show |
intron_variant | MODIFIER | c.398-2894_398-2877d others(20): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183148610 | |||||
chr2:183148634
|
T | G | 48 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(45): Show | 78 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.398-2874T>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183148634 | ||||||
chr2:183148799
|
C | T | 1 | a0001c0001t0001g0319 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.398-2709C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183148799 | ||||||
chr2:183148807
|
C | T | 1 | a0001c0001t0001g0148 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.398-2701C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183148807 | ||||||
chr2:183148815
|
C | T | 1 | a0001c0001t0001g0151 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.398-2693C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183148815 | ||||||
chr2:183148821
|
G | C | 6 | a0001c0001t0001g0052a0001c0001t0001g0070a0001c0001t0001g0075others(3): Show | 7 | HG01099.hp1 HG01358.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.398-2687G>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183148821 | ||||||
chr2:183148890
|
C | T | 190 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(187): Show | 227 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(224): Show |
intron_variant | MODIFIER | c.398-2618C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183148890 | ||||||
chr2:183148905
|
C | T | 34 | a0001c0001t0002g0014a0001c0001t0002g0038a0001c0001t0002g0039others(31): Show | 41 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.398-2603C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183148905 | ||||||
chr2:183148906
|
G | A | 2 | a0001c0001t0001g0211a0001c0001t0001g0212 | 2 | HG00735.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.398-2602G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183148906 | ||||||
chr2:183148910
|
G | A | 6 | a0001c0001t0001g0052a0001c0001t0001g0070a0001c0001t0001g0075others(3): Show | 7 | HG01099.hp1 HG01358.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.398-2598G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183148910 | ||||||
chr2:183148922
|
C | T | 41 | a0001c0001t0001g0052a0001c0001t0001g0070a0001c0001t0001g0075others(38): Show | 49 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.398-2586C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183148922 | ||||||
chr2:183148958
|
A | C | 35 | a0001c0001t0002g0014a0001c0001t0002g0038a0001c0001t0002g0039others(32): Show | 42 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.398-2550A>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183148958 | ||||||
chr2:183148968
|
C | A | 1 | a0001c0001t0001g0059 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.398-2540C>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183148968 | ||||||
chr2:183148978
|
A | G | 98 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0013others(95): Show | 109 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.398-2530A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183148978 | ||||||
chr2:183149193
|
G | A | 190 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(187): Show | 227 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(224): Show |
intron_variant | MODIFIER | c.398-2315G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183149193 | ||||||
chr2:183149203
|
G | A | 1 | a0001c0001t0001g0224 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.398-2305G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183149203 | ||||||
chr2:183149281
|
A | G | 1 | a0001c0001t0001g0125 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.398-2227A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183149281 | ||||||
chr2:183149306
|
CAAAATTT | C | 3 | a0001c0001t0001g0023a0001c0001t0001g0094a0001c0001t0006g0023 | 3 | HG01256.hp1 HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.398-2192_398-2186d others(9): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183149306 | |||||
chr2:183149314
|
A | G | 1 | a0001c0001t0001g0026 | 2 | HG02145.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.398-2194A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183149314 | ||||||
chr2:183149353
|
C | T | 1 | a0001c0001t0001g0175 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.398-2155C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183149353 | ||||||
chr2:183149436
|
G | GT | 41 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(38): Show | 69 | HG00323.hp2 HG00438.hp1 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.398-2068dupT | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183149436 | |||||
chr2:183149469
|
A | C | 4 | a0001c0001t0001g0025a0001c0001t0001g0117a0001c0001t0001g0119others(1): Show | 5 | HG00280.hp2 HG00639.hp2 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.398-2039A>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183149469 | ||||||
chr2:183149510
|
C | G | 2 | a0001c0001t0001g0073a0001c0001t0001g0080 | 2 | HG02717.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.398-1998C>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183149510 | ||||||
chr2:183149529
|
T | C | 1 | a0001c0001t0001g0026 | 2 | HG02145.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.398-1979T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183149529 | ||||||
chr2:183149867
|
C | T | 2 | a0001c0001t0001g0163a0001c0001t0001g0164 | 2 | HG01358.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.398-1641C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183149867 | ||||||
chr2:183149909
|
T | A | 104 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0010others(101): Show | 118 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.398-1599T>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183149909 | ||||||
chr2:183150135
|
G | C | 1 | a0001c0001t0001g0137 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.398-1373G>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183150135 | ||||||
chr2:183150210
|
A | G | 48 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(45): Show | 78 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.398-1298A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183150210 | ||||||
chr2:183150237
|
G | C | 4 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(1): Show | 4 | HG00735.hp2 HG01257.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.398-1271G>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183150237 | ||||||
chr2:183150285
|
C | T | 6 | a0001c0001t0001g0052a0001c0001t0001g0070a0001c0001t0001g0075others(3): Show | 7 | HG01099.hp1 HG01358.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.398-1223C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183150285 | ||||||
chr2:183150361
|
G | T | 298 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(295): Show | 374 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(371): Show |
intron_variant | MODIFIER | c.398-1147G>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183150361 | ||||||
chr2:183150375
|
T | G | 1 | a0001c0001t0001g0117 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.398-1133T>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183150375 | ||||||
chr2:183150383
|
C | G | 1 | a0001c0003t0002g0118 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.398-1125C>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183150383 | ||||||
chr2:183150422
|
A | G | 1 | a0001c0001t0001g0166 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.398-1086A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183150422 | ||||||
chr2:183150486
|
C | T | 3 | a0001c0002t0001g0019a0001c0002t0001g0049a0001c0002t0001g0050 | 4 | HG02257.hp1 HG02280.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.398-1022C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183150486 | ||||||
chr2:183150544
|
A | G | 1 | a0001c0001t0001g0091 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.398-964A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183150544 | ||||||
chr2:183150560
|
A | G | 1 | a0001c0001t0001g0240 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.398-948A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183150560 | ||||||
chr2:183150618
|
CTG | C | 6 | a0001c0001t0001g0052a0001c0001t0001g0070a0001c0001t0001g0075others(3): Show | 7 | HG01099.hp1 HG01358.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.398-888_398-887del others(2): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183150618 | |||||
chr2:183150873
|
A | G | 10 | a0001c0001t0003g0021a0001c0001t0003g0068a0001c0001t0003g0069others(7): Show | 11 | HG02257.hp2 HG02451.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.398-635A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183150873 | ||||||
chr2:183150890
|
A | T | 2 | a0001c0001t0001g0077a0001c0001t0001g0091 | 2 | HG02145.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.398-618A>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183150890 | ||||||
chr2:183151053
|
G | C | 35 | a0001c0001t0002g0014a0001c0001t0002g0038a0001c0001t0002g0039others(32): Show | 42 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.398-455G>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183151053 | ||||||
chr2:183151065
|
T | C | 2 | a0001c0001t0001g0157a0001c0001t0001g0158 | 2 | HG01175.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.398-443T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183151065 | ||||||
chr2:183151115
|
C | T | 1 | a0001c0001t0001g0211 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.398-393C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183151115 | ||||||
chr2:183151291
|
A | C | 35 | a0001c0001t0002g0014a0001c0001t0002g0038a0001c0001t0002g0039others(32): Show | 42 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.398-217A>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183151291 | ||||||
chr2:183151385
|
G | A | 1 | a0001c0001t0001g0072 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.398-123G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183151385 | ||||||
chr2:183151417
|
T | C | 7 | a0001c0001t0003g0021a0001c0001t0003g0081a0001c0001t0003g0082others(4): Show | 8 | HG02257.hp2 HG02451.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.398-91T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183151417 | ||||||
chr2:183151462
|
C | T | 1 | a0001c0001t0001g0104 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.398-46C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183151462 | ||||||
chr2:183151500
|
T | G | 1 | a0001c0001t0001g0131 | 1 | HG01515.hp2 | splice_region_variant&intron_variant | LOW | c.398-8T>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183151500 | ||||||
chr2:183151664
|
C | T | 35 | a0001c0001t0002g0014a0001c0001t0002g0038a0001c0001t0002g0039others(32): Show | 42 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.539+15C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183151664 | ||||||
chr2:183151873
|
C | T | 1 | a0001c0001t0003g0082 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.539+224C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183151873 | ||||||
chr2:183151899
|
A | G | 46 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(43): Show | 76 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.539+250A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183151899 | ||||||
chr2:183151939
|
A | T | 279 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(276): Show | 354 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(351): Show |
intron_variant | MODIFIER | c.539+290A>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183151939 | ||||||
chr2:183152063
|
A | G | 27 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0029others(24): Show | 35 | HG00408.hp1 HG00741.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.539+414A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183152063 | ||||||
chr2:183152068
|
G | A | 1 | a0001c0001t0001g0078 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.539+419G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183152068 | ||||||
chr2:183152110
|
A | AAC | 26 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0034others(23): Show | 32 | HG00140.hp2 HG00323.hp1 HG02074.hp1 others(29): Show |
intron_variant | MODIFIER | c.539+505_539+506dup others(2): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 183152110 | |||||
chr2:183152110
|
A | AACAC | 28 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0077others(25): Show | 31 | HG01069.hp2 HG01255.hp2 HG01257.hp1 others(28): Show |
intron_variant | MODIFIER | c.539+503_539+506dup others(4): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 183152110 | |||||
chr2:183152110
|
A | AACACAC | 24 | a0001c0001t0001g0010a0001c0001t0001g0030a0001c0001t0001g0066others(21): Show | 28 | HG00741.hp1 HG01071.hp1 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.539+501_539+506dup others(6): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 183152110 | |||||
chr2:183152110
|
A | AACACACA others(1): Show |
21 | a0001c0001t0001g0013a0001c0001t0001g0035a0001c0001t0001g0036others(18): Show | 24 | HG00438.hp2 HG00544.hp2 HG00597.hp2 others(21): Show |
intron_variant | MODIFIER | c.539+499_539+506dup others(8): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 183152110 | |||||
chr2:183152110
|
A | AACACACA others(3): Show |
18 | a0001c0001t0001g0004a0001c0001t0001g0037a0001c0001t0001g0067others(15): Show | 23 | HG00408.hp2 HG02015.hp1 HG02056.hp2 others(20): Show |
intron_variant | MODIFIER | c.539+497_539+506dup others(10): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 183152110 | |||||
chr2:183152110
|
A | AACACACA others(5): Show |
6 | a0001c0001t0001g0202a0001c0001t0001g0209a0001c0001t0001g0226others(3): Show | 6 | HG01928.hp1 HG02698.hp1 NA18957.hp2 others(3): Show |
intron_variant | MODIFIER | c.539+495_539+506dup others(12): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 183152110 | |||||
chr2:183152110
|
A | AACACACA others(7): Show |
9 | a0001c0001t0001g0065a0001c0001t0001g0192a0001c0001t0001g0195others(6): Show | 9 | HG00140.hp1 HG00609.hp2 HG00673.hp2 others(6): Show |
intron_variant | MODIFIER | c.539+493_539+506dup others(14): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 183152110 | |||||
chr2:183152110
|
A | AACACACA others(9): Show |
5 | a0001c0001t0001g0220a0001c0001t0001g0234a0001c0001t0001g0236others(2): Show | 5 | HG00558.hp1 HG02300.hp2 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.539+491_539+506dup others(16): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 183152110 | |||||
chr2:183152110
|
A | AACACACA others(11): Show |
2 | a0001c0001t0001g0235a0001c0001t0001g0250 | 2 | HG02132.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.539+489_539+506dup others(18): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 183152110 | |||||
chr2:183152110
|
A | ACACACAC others(4): Show |
1 | a0001c0001t0001g0230 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.539+461_539+462ins others(11): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183152110 | ||||||
chr2:183152110
|
A | ACACACAC others(8): Show |
1 | a0001c0001t0001g0240 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.539+461_539+462ins others(15): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183152110 | ||||||
chr2:183152110
|
AAC | A | 44 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0024others(41): Show | 54 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.539+505_539+506del others(2): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 183152110 | |||||
chr2:183152110
|
AACAC | A | 27 | a0001c0001t0001g0005a0001c0001t0001g0023a0001c0001t0001g0094others(24): Show | 30 | HG00099.hp2 HG00597.hp1 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.539+503_539+506del others(4): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 183152110 | |||||
chr2:183152110
|
AACACAC | A | 3 | a0001c0001t0001g0093a0001c0001t0001g0111a0001c0001t0001g0193 | 3 | HG01255.hp1 HG02622.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.539+501_539+506del others(6): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 183152110 | |||||
chr2:183152110
|
AACACACA others(3): Show |
A | 1 | a0001c0001t0003g0082 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.539+497_539+506del others(10): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 183152110 | |||||
chr2:183152110
|
AACACACA others(7): Show |
A | 1 | a0001c0001t0001g0126 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.539+493_539+506del others(14): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 183152110 | |||||
chr2:183152110
|
AACACACA others(9): Show |
A | 4 | a0001c0001t0001g0025a0001c0001t0001g0117a0001c0001t0001g0119others(1): Show | 5 | HG00280.hp2 HG00639.hp2 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.539+491_539+506del others(16): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 183152110 | |||||
chr2:183152110
|
AACACACA others(11): Show |
A | 4 | a0001c0001t0001g0177a0001c0002t0001g0019a0001c0002t0001g0049others(1): Show | 5 | HG02257.hp1 HG02280.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.539+489_539+506del others(18): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 183152110 | |||||
chr2:183152110
|
AACACACA others(13): Show |
A | 41 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(38): Show | 69 | HG00323.hp2 HG00438.hp1 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.539+487_539+506del others(20): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 183152110 | |||||
chr2:183152143
|
A | G | 1 | a0001c0001t0001g0304 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.539+494A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183152143 | ||||||
chr2:183152156
|
A | G | 190 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(187): Show | 227 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(224): Show |
intron_variant | MODIFIER | c.539+507A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183152156 | ||||||
chr2:183152189
|
G | A | 296 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(293): Show | 372 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(369): Show |
intron_variant | MODIFIER | c.539+540G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183152189 | ||||||
chr2:183152193
|
T | C | 1 | a0001c0001t0001g0298 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.539+544T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183152193 | ||||||
chr2:183152209
|
C | CAG | 278 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(275): Show | 353 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(350): Show |
intron_variant | MODIFIER | c.539+561_539+562dup others(2): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 183152209 | |||||
chr2:183152272
|
C | G | 50 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(47): Show | 80 | HG00323.hp2 HG00438.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.539+623C>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183152272 | ||||||
chr2:183152281
|
A | T | 1 | a0001c0001t0001g0113 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.539+632A>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183152281 | ||||||
chr2:183152347
|
T | G | 1 | a0001c0001t0001g0127 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.539+698T>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183152347 | ||||||
chr2:183152382
|
T | C | 102 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(99): Show | 127 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.539+733T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183152382 | ||||||
chr2:183152396
|
G | T | 298 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(295): Show | 374 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(371): Show |
intron_variant | MODIFIER | c.539+747G>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183152396 | ||||||
chr2:183152451
|
C | T | 35 | a0001c0001t0002g0014a0001c0001t0002g0038a0001c0001t0002g0039others(32): Show | 42 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.539+802C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183152451 | ||||||
chr2:183152769
|
A | T | 2 | a0001c0001t0004g0020a0001c0001t0004g0076 | 3 | HG01099.hp1 HG01358.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.539+1120A>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183152769 | ||||||
chr2:183152796
|
T | C | 1 | a0001c0001t0001g0045 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.539+1147T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183152796 | ||||||
chr2:183152849
|
A | G | 41 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(38): Show | 69 | HG00323.hp2 HG00438.hp1 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.539+1200A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183152849 | ||||||
chr2:183152862
|
AT | A | 4 | a0001c0001t0001g0025a0001c0001t0001g0117a0001c0001t0001g0119others(1): Show | 5 | HG00280.hp2 HG00639.hp2 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.539+1214delT | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183152862 | ||||||
chr2:183152878
|
A | G | 3 | a0001c0001t0001g0012a0001c0001t0001g0139a0001c0001t0001g0166 | 5 | NA18965.hp1 NA18993.hp2 NA19002.hp1 others(2): Show |
intron_variant | MODIFIER | c.539+1229A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183152878 | ||||||
chr2:183153027
|
A | G | 35 | a0001c0001t0002g0014a0001c0001t0002g0038a0001c0001t0002g0039others(32): Show | 42 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.539+1378A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183153027 | ||||||
chr2:183153068
|
A | G | 1 | a0001c0001t0001g0162 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.539+1419A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183153068 | ||||||
chr2:183153164
|
G | A | 4 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074others(1): Show | 4 | HG02109.hp1 HG02280.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.539+1515G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183153164 | ||||||
chr2:183153192
|
C | T | 1 | a0001c0001t0001g0078 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.539+1543C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183153192 | ||||||
chr2:183153250
|
A | G | 276 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(273): Show | 350 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(347): Show |
intron_variant | MODIFIER | c.539+1601A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183153250 | ||||||
chr2:183153281
|
C | T | 47 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(44): Show | 77 | HG00323.hp2 HG00438.hp1 HG00609.hp1 others(74): Show |
intron_variant | MODIFIER | c.539+1632C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183153281 | ||||||
chr2:183153448
|
A | G | 191 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(188): Show | 228 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.539+1799A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183153448 | ||||||
chr2:183153466
|
C | A | 4 | a0001c0001t0001g0025a0001c0001t0001g0117a0001c0001t0001g0119others(1): Show | 5 | HG00280.hp2 HG00639.hp2 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.539+1817C>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183153466 | ||||||
chr2:183153602
|
C | T | 1 | a0001c0003t0002g0118 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.539+1953C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183153602 | ||||||
chr2:183153623
|
C | T | 1 | a0001c0001t0002g0284 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.539+1974C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183153623 | ||||||
chr2:183153677
|
C | A | 3 | a0001c0002t0001g0019a0001c0002t0001g0049a0001c0002t0001g0050 | 4 | HG02257.hp1 HG02280.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.539+2028C>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183153677 | ||||||
chr2:183153801
|
A | C | 5 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0236others(2): Show | 5 | HG02132.hp2 NA18982.hp2 NA19002.hp2 others(2): Show |
intron_variant | MODIFIER | c.539+2152A>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183153801 | ||||||
chr2:183153890
|
C | T | 47 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(44): Show | 77 | HG00323.hp2 HG00438.hp1 HG00609.hp1 others(74): Show |
intron_variant | MODIFIER | c.539+2241C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183153890 | ||||||
chr2:183153931
|
A | G | 2 | a0001c0001t0001g0077a0001c0001t0001g0091 | 2 | HG02145.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.539+2282A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183153931 | ||||||
chr2:183154019
|
A | G | 1 | a0001c0001t0001g0026 | 2 | HG02145.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.539+2370A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183154019 | ||||||
chr2:183154067
|
T | TC | 191 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(188): Show | 228 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.539+2422dupC | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 183154067 | |||||
chr2:183154084
|
C | T | 1 | a0001c0001t0002g0284 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.539+2435C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183154084 | ||||||
chr2:183154098
|
A | G | 191 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(188): Show | 228 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.539+2449A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183154098 | ||||||
chr2:183154116
|
C | T | 4 | a0001c0001t0001g0110a0001c0001t0001g0112a0001c0001t0001g0115others(1): Show | 4 | HG01261.hp1 HG02258.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.539+2467C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183154116 | ||||||
chr2:183154152
|
C | G | 1 | a0001c0001t0001g0111 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.539+2503C>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183154152 | ||||||
chr2:183154199
|
T | G | 1 | a0001c0001t0001g0056 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.539+2550T>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183154199 | ||||||
chr2:183154239
|
T | C | 2 | a0001c0002t0001g0049a0001c0002t0001g0050 | 2 | HG02280.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.539+2590T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183154239 | ||||||
chr2:183154342
|
C | T | 1 | a0001c0002t0001g0019 | 2 | HG02257.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.539+2693C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183154342 | ||||||
chr2:183154426
|
T | C | 1 | a0001c0001t0001g0197 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.539+2777T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183154426 | ||||||
chr2:183154434
|
C | T | 4 | a0001c0001t0001g0025a0001c0001t0001g0117a0001c0001t0001g0119others(1): Show | 5 | HG00280.hp2 HG00639.hp2 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.539+2785C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183154434 | ||||||
chr2:183154550
|
C | G | 188 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(185): Show | 225 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(222): Show |
intron_variant | MODIFIER | c.540-2894C>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183154550 | ||||||
chr2:183154577
|
A | G | 3 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0109 | 3 | HG02895.hp1 HG03540.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.540-2867A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183154577 | ||||||
chr2:183154618
|
C | T | 90 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(87): Show | 115 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.540-2826C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183154618 | ||||||
chr2:183154715
|
C | T | 1 | a0001c0001t0001g0079 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.540-2729C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183154715 | ||||||
chr2:183154737
|
G | C | 41 | a0001c0001t0001g0052a0001c0001t0001g0070a0001c0001t0001g0075others(38): Show | 49 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.540-2707G>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183154737 | ||||||
chr2:183154948
|
C | T | 34 | a0001c0001t0002g0014a0001c0001t0002g0038a0001c0001t0002g0039others(31): Show | 41 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.540-2496C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183154948 | ||||||
chr2:183154993
|
G | C | 278 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(275): Show | 352 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(349): Show |
intron_variant | MODIFIER | c.540-2451G>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183154993 | ||||||
chr2:183155010
|
A | C | 1 | a0001c0004t0001g0232 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.540-2434A>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183155010 | ||||||
chr2:183155013
|
TACTC | T | 35 | a0001c0001t0002g0014a0001c0001t0002g0038a0001c0001t0002g0039others(32): Show | 42 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.540-2427_540-2424d others(6): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 183155013 | |||||
chr2:183155218
|
C | G | 34 | a0001c0001t0002g0014a0001c0001t0002g0038a0001c0001t0002g0039others(31): Show | 41 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.540-2226C>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183155218 | ||||||
chr2:183155322
|
A | G | 3 | a0001c0002t0001g0019a0001c0002t0001g0049a0001c0002t0001g0050 | 4 | HG02257.hp1 HG02280.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.540-2122A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183155322 | ||||||
chr2:183155344
|
T | C | 5 | a0001c0001t0001g0052a0001c0001t0001g0070a0001c0001t0001g0319others(2): Show | 6 | HG01099.hp1 HG01358.hp1 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.540-2100T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183155344 | ||||||
chr2:183155579
|
C | CT | 226 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(223): Show | 289 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(286): Show |
intron_variant | MODIFIER | c.540-1851dupT | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 183155579 | |||||
chr2:183155579
|
C | CTT | 13 | a0001c0001t0001g0052a0001c0001t0001g0070a0001c0001t0001g0077others(10): Show | 14 | HG00408.hp2 HG01099.hp1 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.540-1852_540-1851d others(4): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 183155579 | |||||
chr2:183155579
|
CT | C | 7 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0111others(4): Show | 7 | HG00621.hp2 HG01255.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.540-1851delT | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 183155579 | |||||
chr2:183155682
|
C | G | 4 | a0001c0001t0001g0025a0001c0001t0001g0117a0001c0001t0001g0119others(1): Show | 5 | HG00280.hp2 HG00639.hp2 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.540-1762C>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183155682 | ||||||
chr2:183155703
|
T | C | 2 | a0001c0001t0001g0077a0001c0001t0001g0091 | 2 | HG02145.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.540-1741T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183155703 | ||||||
chr2:183155758
|
C | T | 1 | a0001c0001t0001g0140 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.540-1686C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183155758 | ||||||
chr2:183155776
|
A | G | 2 | a0001c0001t0001g0097a0001c0001t0001g0102 | 2 | HG02109.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.540-1668A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183155776 | ||||||
chr2:183155862
|
G | C | 2 | a0001c0001t0001g0255a0001c0001t0001g0258 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.540-1582G>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183155862 | ||||||
chr2:183155874
|
C | G | 44 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(41): Show | 73 | HG00323.hp2 HG00438.hp1 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.540-1570C>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183155874 | ||||||
chr2:183155907
|
A | T | 3 | a0001c0001t0001g0070a0001c0001t0001g0075a0001c0001t0001g0319 | 3 | HG02818.hp2 HG02886.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.540-1537A>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183155907 | ||||||
chr2:183155913
|
C | G | 35 | a0001c0001t0002g0014a0001c0001t0002g0038a0001c0001t0002g0039others(32): Show | 42 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.540-1531C>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183155913 | ||||||
chr2:183156093
|
A | G | 35 | a0001c0001t0002g0014a0001c0001t0002g0038a0001c0001t0002g0039others(32): Show | 42 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.540-1351A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183156093 | ||||||
chr2:183156162
|
A | C | 3 | a0001c0002t0001g0019a0001c0002t0001g0049a0001c0002t0001g0050 | 4 | HG02257.hp1 HG02280.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.540-1282A>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183156162 | ||||||
chr2:183156219
|
C | T | 189 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(186): Show | 226 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(223): Show |
intron_variant | MODIFIER | c.540-1225C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183156219 | ||||||
chr2:183156347
|
T | A | 4 | a0001c0001t0001g0025a0001c0001t0001g0117a0001c0001t0001g0119others(1): Show | 5 | HG00280.hp2 HG00639.hp2 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.540-1097T>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183156347 | ||||||
chr2:183156406
|
C | A | 1 | a0001c0001t0001g0207 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.540-1038C>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183156406 | ||||||
chr2:183156443
|
G | T | 1 | a0001c0001t0001g0137 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.540-1001G>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183156443 | ||||||
chr2:183156484
|
T | C | 85 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(82): Show | 122 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.540-960T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183156484 | ||||||
chr2:183156520
|
T | C | 3 | a0001c0001t0001g0070a0001c0001t0001g0075a0001c0001t0001g0319 | 3 | HG02818.hp2 HG02886.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.540-924T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183156520 | ||||||
chr2:183156607
|
C | T | 1 | a0001c0001t0001g0207 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.540-837C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183156607 | ||||||
chr2:183156634
|
C | T | 4 | a0001c0001t0003g0021a0001c0001t0003g0081a0001c0001t0003g0085others(1): Show | 5 | HG02257.hp2 HG02559.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.540-810C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183156634 | ||||||
chr2:183156695
|
A | AT | 89 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(86): Show | 127 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(124): Show |
intron_variant | MODIFIER | c.540-738dupT | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 183156695 | |||||
chr2:183156753
|
A | G | 1 | a0001c0003t0002g0118 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.540-691A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183156753 | ||||||
chr2:183156763
|
G | T | 297 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(294): Show | 373 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(370): Show |
intron_variant | MODIFIER | c.540-681G>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183156763 | ||||||
chr2:183156773
|
G | A | 35 | a0001c0001t0002g0014a0001c0001t0002g0038a0001c0001t0002g0039others(32): Show | 42 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.540-671G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183156773 | ||||||
chr2:183156810
|
A | G | 6 | a0001c0001t0001g0263a0001c0001t0001g0293a0001c0001t0001g0294others(3): Show | 6 | HG01123.hp2 HG02630.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.540-634A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183156810 | ||||||
chr2:183156813
|
C | G | 3 | a0001c0002t0001g0019a0001c0002t0001g0049a0001c0002t0001g0050 | 4 | HG02257.hp1 HG02280.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.540-631C>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183156813 | ||||||
chr2:183156940
|
T | G | 1 | a0001c0003t0002g0118 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.540-504T>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183156940 | ||||||
chr2:183157052
|
A | G | 46 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(43): Show | 75 | HG00323.hp2 HG00438.hp1 HG00609.hp1 others(72): Show |
intron_variant | MODIFIER | c.540-392A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183157052 | ||||||
chr2:183157179
|
C | T | 35 | a0001c0001t0002g0014a0001c0001t0002g0038a0001c0001t0002g0039others(32): Show | 42 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.540-265C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183157179 | ||||||
chr2:183157287
|
G | C | 191 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(188): Show | 228 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.540-157G>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183157287 | ||||||
chr2:183157384
|
A | G | 6 | a0001c0001t0001g0052a0001c0001t0001g0070a0001c0001t0001g0075others(3): Show | 7 | HG01099.hp1 HG01358.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.540-60A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183157384 | ||||||
chr2:183157590
|
A | C | 1 | a0001c0001t0001g0150 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.609+77A>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 6/8 | chr2 | 183157590 | ||||||
chr2:183157665
|
G | A | 6 | a0001c0001t0001g0052a0001c0001t0001g0070a0001c0001t0001g0075others(3): Show | 7 | HG01099.hp1 HG01358.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.609+152G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 6/8 | chr2 | 183157665 | ||||||
chr2:183157717
|
T | G | 299 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(296): Show | 375 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(372): Show |
intron_variant | MODIFIER | c.609+204T>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 6/8 | chr2 | 183157717 | ||||||
chr2:183157726
|
T | A | 2 | a0001c0001t0001g0313a0001c0001t0001g0316 | 2 | NA18962.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.609+213T>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 6/8 | chr2 | 183157726 | ||||||
chr2:183157760
|
C | T | 41 | a0001c0001t0001g0052a0001c0001t0001g0070a0001c0001t0001g0075others(38): Show | 49 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.609+247C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 6/8 | chr2 | 183157760 | ||||||
chr2:183158011
|
T | G | 15 | a0001c0001t0001g0013a0001c0001t0001g0206a0001c0001t0001g0207others(12): Show | 16 | HG00408.hp2 HG00438.hp2 HG02027.hp2 others(13): Show |
intron_variant | MODIFIER | c.610-272T>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 6/8 | chr2 | 183158011 | ||||||
chr2:183158048
|
C | CATT | 280 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(277): Show | 355 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(352): Show |
intron_variant | MODIFIER | c.610-233_610-232ins others(3): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 183158048 | |||||
chr2:183158207
|
CCTATTTT others(15): Show |
C | 1 | a0001c0001t0001g0091 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.610-75_610-54delCT others(20): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 6/8 | chr2 | 183158207 | ||||||
chr2:183158423
|
G | A | 35 | a0001c0001t0002g0014a0001c0001t0002g0038a0001c0001t0002g0039others(32): Show | 42 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.738+12G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 7/8 | chr2 | 183158423 | ||||||
chr2:183158567
|
G | A | 90 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(87): Show | 115 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.738+156G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 7/8 | chr2 | 183158567 | ||||||
chr2:183158649
|
C | A | 1 | a0001c0001t0001g0026 | 2 | HG02145.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.738+238C>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 7/8 | chr2 | 183158649 | ||||||
chr2:183158870
|
T | C | 1 | a0001c0001t0002g0264 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.738+459T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 7/8 | chr2 | 183158870 | ||||||
chr2:183158876
|
T | C | 1 | a0001c0001t0001g0096 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.738+465T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 7/8 | chr2 | 183158876 | ||||||
chr2:183158922
|
G | C | 1 | a0001c0001t0003g0092 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.738+511G>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 7/8 | chr2 | 183158922 | ||||||
chr2:183159014
|
A | T | 3 | a0001c0001t0001g0052a0001c0001t0004g0020a0001c0001t0004g0076 | 4 | HG01099.hp1 HG01358.hp1 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.739-474A>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 7/8 | chr2 | 183159014 | ||||||
chr2:183159156
|
C | T | 278 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(275): Show | 353 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(350): Show |
intron_variant | MODIFIER | c.739-332C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 7/8 | chr2 | 183159156 | ||||||
chr2:183159227
|
T | C | 1 | a0001c0001t0001g0088 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.739-261T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 7/8 | chr2 | 183159227 | ||||||
chr2:183159238
|
T | A | 35 | a0001c0001t0002g0014a0001c0001t0002g0038a0001c0001t0002g0039others(32): Show | 42 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.739-250T>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 7/8 | chr2 | 183159238 | ||||||
chr2:183159298
|
T | G | 299 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(296): Show | 375 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(372): Show |
intron_variant | MODIFIER | c.739-190T>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 7/8 | chr2 | 183159298 | ||||||
chr2:183159415
|
T | C | 97 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0013others(94): Show | 108 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.739-73T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 7/8 | chr2 | 183159415 | ||||||
chr2:183159462
|
A | G | 50 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(47): Show | 80 | HG00323.hp2 HG00438.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.739-26A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 7/8 | chr2 | 183159462 | ||||||
chr2:183159734
|
G | A | 6 | a0001c0001t0001g0052a0001c0001t0001g0070a0001c0001t0001g0075others(3): Show | 7 | HG01099.hp1 HG01358.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.903+82G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 8/8 | chr2 | 183159734 | ||||||
chr2:183159783
|
T | C | 41 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(38): Show | 69 | HG00323.hp2 HG00438.hp1 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.903+131T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 8/8 | chr2 | 183159783 | ||||||
chr2:183159858
|
A | T | 263 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(260): Show | 332 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(329): Show |
intron_variant | MODIFIER | c.903+206A>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 8/8 | chr2 | 183159858 | ||||||
chr2:183159962
|
C | T | 35 | a0001c0001t0002g0014a0001c0001t0002g0038a0001c0001t0002g0039others(32): Show | 42 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.903+310C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 8/8 | chr2 | 183159962 | ||||||
chr2:183159965
|
ATTAAAAC others(3): Show |
A | 1 | a0001c0001t0001g0194 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.903+314_903+323del others(10): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 8/8 | chr2 | 183159965 | ||||||
chr2:183159974
|
T | C | 280 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(277): Show | 355 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(352): Show |
intron_variant | MODIFIER | c.903+322T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 8/8 | chr2 | 183159974 | ||||||
chr2:183160011
|
G | A | 1 | a0001c0001t0001g0257 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.903+359G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 8/8 | chr2 | 183160011 | ||||||
chr2:183160042
|
T | C | 1 | a0001c0001t0001g0237 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.903+390T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 8/8 | chr2 | 183160042 | ||||||
chr2:183160053
|
A | T | 1 | a0001c0001t0001g0078 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.903+401A>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 8/8 | chr2 | 183160053 | ||||||
chr2:183160094
|
A | G | 1 | a0001c0001t0001g0060 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.903+442A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 8/8 | chr2 | 183160094 | ||||||
chr2:183160315
|
G | C | 4 | a0001c0001t0001g0025a0001c0001t0001g0117a0001c0001t0001g0119others(1): Show | 5 | HG00280.hp2 HG00639.hp2 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.903+663G>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 8/8 | chr2 | 183160315 | ||||||
chr2:183160410
|
C | T | 6 | a0001c0001t0001g0052a0001c0001t0001g0070a0001c0001t0001g0075others(3): Show | 7 | HG01099.hp1 HG01358.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.904-644C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 8/8 | chr2 | 183160410 | ||||||
chr2:183160447
|
G | A | 3 | a0001c0002t0001g0019a0001c0002t0001g0049a0001c0002t0001g0050 | 4 | HG02257.hp1 HG02280.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.904-607G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 8/8 | chr2 | 183160447 | ||||||
chr2:183160550
|
T | C | 188 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(185): Show | 224 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.904-504T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 8/8 | chr2 | 183160550 | ||||||
chr2:183160670
|
C | T | 3 | a0001c0001t0001g0052a0001c0001t0004g0020a0001c0001t0004g0076 | 4 | HG01099.hp1 HG01358.hp1 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.904-384C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 8/8 | chr2 | 183160670 | ||||||
chr2:183160804
|
C | A | 1 | a0001c0001t0001g0110 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.904-250C>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 8/8 | chr2 | 183160804 | ||||||
chr2:183160805
|
G | A | 1 | a0001c0001t0001g0160 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.904-249G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 8/8 | chr2 | 183160805 | ||||||
chr2:183160848
|
C | T | 189 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(186): Show | 226 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(223): Show |
intron_variant | MODIFIER | c.904-206C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 8/8 | chr2 | 183160848 | ||||||
chr2:183160995
|
G | A | 3 | a0001c0001t0001g0052a0001c0001t0004g0020a0001c0001t0004g0076 | 4 | HG01099.hp1 HG01358.hp1 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.904-59G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 8/8 | chr2 | 183160995 | ||||||
chr2:183160999
|
A | G | 1 | a0001c0001t0001g0047 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.904-55A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 8/8 | chr2 | 183160999 | ||||||
chr2:183161022
|
TA | T | 4 | a0001c0001t0001g0025a0001c0001t0001g0117a0001c0001t0001g0119others(1): Show | 5 | HG00280.hp2 HG00639.hp2 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.904-30delA | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 183161022 | |||||
chr2:183161027
|
G | GT | 7 | a0001c0001t0001g0077a0001c0001t0001g0155a0001c0001t0001g0227others(4): Show | 7 | HG00423.hp1 HG00621.hp1 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.904-19dupT | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 183161027 |