geneid | 53343 |
---|---|
ensemblid | ENSG00000170502.13 |
hgncid | 8056 |
symbol | NUDT9 |
name | nudix hydrolase 9 |
refseq_nuc | NM_024047.5 |
refseq_prot | NP_076952.1 |
ensembl_nuc | ENST00000302174.9 |
ensembl_prot | ENSP00000303575.4 |
mane_status | MANE Select |
chr | chr4 |
start | 87422573 |
end | 87459455 |
strand | + |
ver | v1.2 |
region | chr4:87422573-87459455 |
region5000 | chr4:87417573-87464455 |
regionname0 | NUDT9_chr4_87422573_87459455 |
regionname5000 | NUDT9_chr4_87417573_87464455 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 350 | 386 | 89 | 52 | 196 | 16 | 31 | 150 | NUDT9_chr4_87417573_87464455 | NUDT9 | copy fasta | chr4 | 87417573 | 87464455 |
a0002 | 0/0 | 350 | 12 | 11 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | copy fasta | chr4 | 87417573 | 87464455 |
a0003 | 0/0 | 350 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | copy fasta | chr4 | 87417573 | 87464455 |
a0004 | 0/0 | 350 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | copy fasta | chr4 | 87417573 | 87464455 |
a0005 | 0/0 | 57 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | copy fasta | chr4 | 87417573 | 87464455 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1053 | 352 | 56 | 51 | 196 | 16 | 31 | NUDT9_chr4_87417573_87464455 | NUDT9 | copy fasta | chr4 | 87417573 | 87464455 |
c0002 | 0/0 | 1053 | 33 | 32 | 1 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | copy fasta | chr4 | 87417573 | 87464455 |
c0003 | 0/0 | 1053 | 10 | 9 | 1 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | copy fasta | chr4 | 87417573 | 87464455 |
c0004 | 0/0 | 1053 | 2 | 0 | 2 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | copy fasta | chr4 | 87417573 | 87464455 |
c0005 | 0/0 | 1053 | 2 | 2 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | copy fasta | chr4 | 87417573 | 87464455 |
c0006 | 0/0 | 1053 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | copy fasta | chr4 | 87417573 | 87464455 |
c0007 | 0/0 | 1053 | 1 | 0 | 0 | 0 | 0 | 1 | NUDT9_chr4_87417573_87464455 | NUDT9 | copy fasta | chr4 | 87417573 | 87464455 |
c0008 | 0/0 | 371 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | copy fasta | chr4 | 87417573 | 87464455 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 1768 | 270 | 41 | 39 | 148 | 12 | 28 | NUDT9_chr4_87417573_87464455 | NUDT9 | copy fasta | chr4 | 87417573 | 87464455 |
t0002 | 0/0 | 1755 | 71 | 18 | 8 | 42 | 1 | 2 | NUDT9_chr4_87417573_87464455 | NUDT9 | copy fasta | chr4 | 87417573 | 87464455 |
t0003 | 0/0 | 1768 | 18 | 9 | 6 | 0 | 2 | 1 | NUDT9_chr4_87417573_87464455 | NUDT9 | copy fasta | chr4 | 87417573 | 87464455 |
t0004 | 0/0 | 1755 | 16 | 15 | 1 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | copy fasta | chr4 | 87417573 | 87464455 |
t0005 | 0/0 | 1768 | 5 | 0 | 0 | 5 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | copy fasta | chr4 | 87417573 | 87464455 |
t0006 | 0/0 | 1768 | 4 | 4 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | copy fasta | chr4 | 87417573 | 87464455 |
t0007 | 0/0 | 1768 | 4 | 4 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | copy fasta | chr4 | 87417573 | 87464455 |
t0008 | 0/0 | 1755 | 2 | 2 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | copy fasta | chr4 | 87417573 | 87464455 |
t0009 | 0/0 | 1768 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | copy fasta | chr4 | 87417573 | 87464455 |
t0010 | 0/0 | 1768 | 1 | 0 | 0 | 0 | 1 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | copy fasta | chr4 | 87417573 | 87464455 |
t0011 | 0/0 | 1768 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | copy fasta | chr4 | 87417573 | 87464455 |
t0012 | 0/0 | 1768 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | copy fasta | chr4 | 87417573 | 87464455 |
t0013 | 0/0 | 1768 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | copy fasta | chr4 | 87417573 | 87464455 |
t0014 | 0/0 | 1768 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | copy fasta | chr4 | 87417573 | 87464455 |
t0015 | 0/0 | 1768 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | copy fasta | chr4 | 87417573 | 87464455 |
t0016 | 0/0 | 1755 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | copy fasta | chr4 | 87417573 | 87464455 |
t0017 | 0/0 | 1755 | 1 | 0 | 0 | 0 | 0 | 1 | NUDT9_chr4_87417573_87464455 | NUDT9 | copy fasta | chr4 | 87417573 | 87464455 |
t0018 | 0/0 | 1755 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | copy fasta | chr4 | 87417573 | 87464455 |
t0019 | 0/0 | 1755 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | copy fasta | chr4 | 87417573 | 87464455 |
t0020 | 0/0 | 1768 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | copy fasta | chr4 | 87417573 | 87464455 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0002 | 0/0 | 7 | 0 | 1 | 5 | 0 | 1 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0003 | 0/1 | 5 | 1 | 2 | 0 | 1 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0004 | 0/0 | 5 | 0 | 2 | 0 | 2 | 1 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0005 | 1/0 | 5 | 0 | 0 | 2 | 0 | 2 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0006 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0007 | 0/0 | 4 | 1 | 1 | 2 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0009 | 0/0 | 4 | 2 | 1 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0011 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0013 | 0/0 | 3 | 0 | 0 | 0 | 2 | 1 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0018 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0020 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0024 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0025 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0029 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0032 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0034 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0036 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1053 | 352 | 56 | 51 | 196 | 16 | 31 | NUDT9_chr4_87417573_87464455 | NUDT9 | copy fasta | chr4 | 87417573 | 87464455 |
a0001c0002 | 0/0 | 1053 | 33 | 32 | 1 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | copy fasta | chr4 | 87417573 | 87464455 |
a0001c0006 | 0/0 | 1053 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | copy fasta | chr4 | 87417573 | 87464455 |
a0002c0003 | 0/0 | 1053 | 10 | 9 | 1 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | copy fasta | chr4 | 87417573 | 87464455 |
a0002c0005 | 0/0 | 1053 | 2 | 2 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | copy fasta | chr4 | 87417573 | 87464455 |
a0003c0004 | 0/0 | 1053 | 2 | 0 | 2 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | copy fasta | chr4 | 87417573 | 87464455 |
a0004c0007 | 0/0 | 1053 | 1 | 0 | 0 | 0 | 0 | 1 | NUDT9_chr4_87417573_87464455 | NUDT9 | copy fasta | chr4 | 87417573 | 87464455 |
a0005c0008 | 0/0 | 371 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | copy fasta | chr4 | 87417573 | 87464455 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 2820 | 243 | 19 | 35 | 148 | 12 | 27 | NUDT9_chr4_87417573_87464455 | NUDT9 | copy fasta | chr4 | 87417573 | 87464455 |
a0001c0001t0002 | 0/0 | 2807 | 70 | 17 | 8 | 42 | 1 | 2 | NUDT9_chr4_87417573_87464455 | NUDT9 | copy fasta | chr4 | 87417573 | 87464455 |
a0001c0001t0003 | 0/0 | 2820 | 8 | 0 | 5 | 0 | 2 | 1 | NUDT9_chr4_87417573_87464455 | NUDT9 | copy fasta | chr4 | 87417573 | 87464455 |
a0001c0001t0004 | 0/0 | 2807 | 16 | 15 | 1 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | copy fasta | chr4 | 87417573 | 87464455 |
a0001c0001t0005 | 0/0 | 2820 | 5 | 0 | 0 | 5 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | copy fasta | chr4 | 87417573 | 87464455 |
a0001c0001t0008 | 0/0 | 2807 | 2 | 2 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | copy fasta | chr4 | 87417573 | 87464455 |
a0001c0001t0009 | 0/0 | 2820 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | copy fasta | chr4 | 87417573 | 87464455 |
a0001c0001t0010 | 0/0 | 2820 | 1 | 0 | 0 | 0 | 1 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | copy fasta | chr4 | 87417573 | 87464455 |
a0001c0001t0012 | 0/0 | 2820 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | copy fasta | chr4 | 87417573 | 87464455 |
a0001c0001t0013 | 0/0 | 2820 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | copy fasta | chr4 | 87417573 | 87464455 |
a0001c0001t0015 | 0/0 | 2820 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | copy fasta | chr4 | 87417573 | 87464455 |
a0001c0001t0017 | 0/0 | 2807 | 1 | 0 | 0 | 0 | 0 | 1 | NUDT9_chr4_87417573_87464455 | NUDT9 | copy fasta | chr4 | 87417573 | 87464455 |
a0001c0001t0018 | 0/0 | 2807 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | copy fasta | chr4 | 87417573 | 87464455 |
a0001c0001t0019 | 0/0 | 2807 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | copy fasta | chr4 | 87417573 | 87464455 |
a0001c0002t0001 | 0/0 | 2820 | 22 | 21 | 1 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | copy fasta | chr4 | 87417573 | 87464455 |
a0001c0002t0006 | 0/0 | 2820 | 4 | 4 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | copy fasta | chr4 | 87417573 | 87464455 |
a0001c0002t0007 | 0/0 | 2820 | 4 | 4 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | copy fasta | chr4 | 87417573 | 87464455 |
a0001c0002t0011 | 0/0 | 2820 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | copy fasta | chr4 | 87417573 | 87464455 |
a0001c0002t0014 | 0/0 | 2820 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | copy fasta | chr4 | 87417573 | 87464455 |
a0001c0002t0020 | 0/0 | 2820 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | copy fasta | chr4 | 87417573 | 87464455 |
a0001c0006t0001 | 0/0 | 2820 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | copy fasta | chr4 | 87417573 | 87464455 |
a0002c0003t0003 | 0/0 | 2820 | 10 | 9 | 1 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | copy fasta | chr4 | 87417573 | 87464455 |
a0002c0005t0002 | 0/0 | 2807 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | copy fasta | chr4 | 87417573 | 87464455 |
a0002c0005t0016 | 0/0 | 2807 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | copy fasta | chr4 | 87417573 | 87464455 |
a0003c0004t0001 | 0/0 | 2820 | 2 | 0 | 2 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | copy fasta | chr4 | 87417573 | 87464455 |
a0004c0007t0001 | 0/0 | 2820 | 1 | 0 | 0 | 0 | 0 | 1 | NUDT9_chr4_87417573_87464455 | NUDT9 | copy fasta | chr4 | 87417573 | 87464455 |
a0005c0008t0001 | 0/0 | 2138 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | copy fasta | chr4 | 87417573 | 87464455 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0002 | 0/0 | 7 | 0 | 1 | 5 | 0 | 1 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0003 | 0/1 | 5 | 1 | 2 | 0 | 1 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0005 | 1/0 | 5 | 0 | 0 | 2 | 0 | 2 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0007 | 0/0 | 4 | 1 | 1 | 2 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0009 | 0/0 | 4 | 2 | 1 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0011 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0013 | 0/0 | 3 | 0 | 0 | 0 | 2 | 1 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0029 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0002g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0002g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0002g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0002g0036 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0002g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0002g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0002g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0002g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0002g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0002g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0002g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0002g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0002g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0002g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0002g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0002g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0002g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0002g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0002g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0002g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0002g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0002g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0002g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0002g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0002g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0002g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0003g0004 | 0/0 | 5 | 0 | 2 | 0 | 2 | 1 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0003g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0003g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0003g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0004g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0004g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0004g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0004g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0004g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0004g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0004g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0004g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0004g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0004g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0004g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0004g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0004g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0004g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0004g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0005g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0005g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0005g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0008g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0008g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0009g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0010g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0012g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0013g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0015g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0017g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0018g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0001t0019g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0002t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0002t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0002t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0002t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0002t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0002t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0002t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0002t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0002t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0002t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0002t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0002t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0002t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0002t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0002t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0002t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0002t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0002t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0002t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0002t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0002t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0002t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0002t0006g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0002t0006g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0002t0006g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0002t0007g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0002t0007g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0002t0007g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0002t0011g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0002t0014g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0002t0020g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0001c0006t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0002c0003t0003g0006 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0002c0003t0003g0034 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0002c0003t0003g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0002c0003t0003g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0002c0003t0003g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0002c0005t0002g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0002c0005t0016g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0003c0004t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0003c0004t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0004c0007t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
a0005c0008t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0013 | EUR | GBR | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0018 | EUR | GBR | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0180 | EUR | GBR | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG00140 | hp2 | a0001 | c0001 | t0003 | g0004 | EUR | GBR | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0194 | EUR | FIN | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | FIN | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG00408 | hp1 | a0001 | c0001 | t0002 | g0255 | EAS | CHS | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG00423 | hp1 | a0001 | c0001 | t0002 | g0276 | EAS | CHS | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | CHS | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | CHS | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | CHS | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | CHS | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | CHS | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | CHS | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | CHS | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | CHS | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | CHS | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | CHS | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0039 | AMR | PUR | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG00639 | hp2 | a0002 | c0003 | t0003 | g0034 | AMR | PUR | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0241 | AMR | PUR | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | CHS | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG00733 | hp1 | a0001 | c0001 | t0002 | g0039 | AMR | PUR | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG00733 | hp2 | a0003 | c0004 | t0001 | g0226 | AMR | PUR | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG00735 | hp2 | a0003 | c0004 | t0001 | g0161 | AMR | PUR | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0040 | AMR | PUR | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG01070 | hp1 | a0001 | c0001 | t0002 | g0281 | AMR | PUR | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG01109 | hp1 | a0001 | c0001 | t0004 | g0135 | AMR | PUR | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG01167 | hp2 | a0001 | c0002 | t0001 | g0237 | AMR | PUR | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG01192 | hp2 | a0001 | c0001 | t0003 | g0152 | AMR | PUR | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG01255 | hp1 | a0001 | c0001 | t0012 | g0167 | AMR | CLM | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | CLM | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG01256 | hp1 | a0001 | c0001 | t0002 | g0040 | AMR | CLM | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG01256 | hp2 | a0001 | c0001 | t0003 | g0126 | AMR | CLM | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG01257 | hp1 | a0001 | c0001 | t0003 | g0131 | AMR | CLM | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG01258 | hp2 | a0001 | c0001 | t0003 | g0004 | AMR | CLM | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG01261 | hp1 | a0001 | c0001 | t0002 | g0036 | AMR | CLM | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | CLM | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0280 | AMR | CLM | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | CLM | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0198 | EUR | IBS | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG01515 | hp2 | a0001 | c0001 | t0003 | g0004 | EUR | IBS | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0219 | EUR | IBS | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0025 | EUR | IBS | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0025 | EUR | IBS | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0199 | EUR | IBS | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG01884 | hp1 | a0002 | c0003 | t0003 | g0234 | AFR | ACB | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG01884 | hp2 | a0001 | c0001 | t0002 | g0270 | AFR | ACB | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG01891 | hp2 | a0001 | c0002 | t0001 | g0316 | AFR | ACB | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG01928 | hp1 | a0001 | c0001 | t0009 | g0216 | AMR | PEL | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG01928 | hp2 | a0005 | c0008 | t0001 | g0211 | AMR | PEL | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PEL | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0208 | AMR | PEL | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0217 | AMR | PEL | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PEL | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PEL | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0230 | AMR | PEL | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | PEL | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | PEL | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | PEL | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | PEL | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | KHV | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG02027 | hp2 | a0001 | c0001 | t0002 | g0287 | EAS | KHV | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG02055 | hp1 | a0001 | c0001 | t0002 | g0254 | AFR | ACB | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG02055 | hp2 | a0001 | c0002 | t0001 | g0309 | AFR | ACB | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | KHV | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | KHV | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG02071 | hp1 | a0001 | c0001 | t0002 | g0277 | EAS | KHV | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | KHV | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0295 | EAS | KHV | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | KHV | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | KHV | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | KHV | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0240 | EAS | KHV | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | KHV | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | KHV | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | KHV | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | KHV | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | ACB | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG02145 | hp2 | a0001 | c0001 | t0018 | g0239 | AFR | ACB | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | PEL | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | PEL | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | CDX | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG02155 | hp2 | a0001 | c0001 | t0002 | g0258 | EAS | CDX | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | CDX | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0041 | EAS | CDX | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | ACB | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG02257 | hp2 | a0002 | c0003 | t0003 | g0034 | AFR | ACB | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG02258 | hp1 | a0001 | c0001 | t0004 | g0140 | AFR | ACB | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG02258 | hp2 | a0001 | c0002 | t0006 | g0042 | AFR | ACB | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG02280 | hp1 | a0001 | c0001 | t0008 | g0262 | AFR | ACB | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG02451 | hp1 | a0001 | c0002 | t0001 | g0315 | AFR | ACB | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG02451 | hp2 | a0001 | c0002 | t0001 | g0236 | AFR | ACB | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | KHV | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG02572 | hp1 | a0001 | c0002 | t0001 | g0301 | AFR | GWD | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | GWD | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0184 | SAS | PJL | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG02615 | hp1 | a0001 | c0002 | t0001 | g0317 | AFR | GWD | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | GWD | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG02622 | hp1 | a0001 | c0001 | t0004 | g0026 | AFR | GWD | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG02630 | hp1 | a0001 | c0001 | t0002 | g0290 | AFR | GWD | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG02630 | hp2 | a0001 | c0002 | t0001 | g0304 | AFR | GWD | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG02647 | hp2 | a0001 | c0001 | t0004 | g0146 | AFR | GWD | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG02717 | hp1 | a0002 | c0003 | t0003 | g0235 | AFR | GWD | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG02717 | hp2 | a0001 | c0001 | t0004 | g0138 | AFR | GWD | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG02723 | hp1 | a0001 | c0001 | t0002 | g0292 | AFR | GWD | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG02723 | hp2 | a0001 | c0002 | t0001 | g0298 | AFR | GWD | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0209 | SAS | PJL | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0119 | SAS | PJL | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG02809 | hp1 | a0001 | c0002 | t0007 | g0043 | AFR | GWD | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG02809 | hp2 | a0001 | c0001 | t0002 | g0037 | AFR | GWD | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG02818 | hp1 | a0001 | c0001 | t0004 | g0154 | AFR | GWD | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG02818 | hp2 | a0001 | c0002 | t0001 | g0320 | AFR | GWD | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG02886 | hp1 | a0001 | c0001 | t0004 | g0137 | AFR | GWD | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG02886 | hp2 | a0001 | c0002 | t0001 | g0303 | AFR | GWD | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG02895 | hp1 | a0001 | c0001 | t0002 | g0266 | AFR | GWD | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG02895 | hp2 | a0001 | c0002 | t0001 | g0311 | AFR | GWD | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG02896 | hp1 | a0001 | c0001 | t0004 | g0141 | AFR | GWD | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG02896 | hp2 | a0001 | c0001 | t0004 | g0143 | AFR | GWD | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG02897 | hp1 | a0001 | c0001 | t0002 | g0267 | AFR | GWD | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG02897 | hp2 | a0001 | c0001 | t0004 | g0145 | AFR | GWD | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG02922 | hp2 | a0001 | c0002 | t0014 | g0305 | AFR | ESN | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG02965 | hp1 | a0001 | c0001 | t0002 | g0245 | AFR | ESN | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG02965 | hp2 | a0001 | c0002 | t0001 | g0318 | AFR | ESN | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG02970 | hp1 | a0001 | c0001 | t0002 | g0037 | AFR | ESN | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG02970 | hp2 | a0001 | c0001 | t0004 | g0144 | AFR | ESN | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG02976 | hp1 | a0001 | c0002 | t0006 | g0042 | AFR | ESN | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | ESN | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG03041 | hp1 | a0001 | c0001 | t0004 | g0136 | AFR | GWD | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG03041 | hp2 | a0002 | c0005 | t0002 | g0294 | AFR | GWD | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG03098 | hp1 | a0001 | c0001 | t0002 | g0268 | AFR | MSL | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | MSL | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG03130 | hp1 | a0001 | c0002 | t0001 | g0321 | AFR | ESN | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG03130 | hp2 | a0001 | c0002 | t0006 | g0296 | AFR | ESN | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG03139 | hp1 | a0002 | c0003 | t0003 | g0233 | AFR | ESN | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG03139 | hp2 | a0002 | c0005 | t0016 | g0293 | AFR | ESN | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG03195 | hp1 | a0001 | c0001 | t0004 | g0142 | AFR | ESN | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG03195 | hp2 | a0001 | c0002 | t0001 | g0313 | AFR | ESN | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG03209 | hp1 | a0002 | c0003 | t0003 | g0006 | AFR | MSL | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG03209 | hp2 | a0001 | c0002 | t0001 | g0310 | AFR | MSL | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG03225 | hp1 | a0001 | c0001 | t0013 | g0155 | AFR | MSL | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG03225 | hp2 | a0001 | c0002 | t0001 | g0308 | AFR | MSL | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0165 | SAS | PJL | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0250 | SAS | PJL | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG03453 | hp1 | a0001 | c0002 | t0001 | g0299 | AFR | MSL | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG03453 | hp2 | a0001 | c0001 | t0004 | g0139 | AFR | MSL | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG03486 | hp1 | a0002 | c0003 | t0003 | g0006 | AFR | MSL | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | MSL | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0169 | SAS | PJL | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG03491 | hp2 | a0001 | c0001 | t0002 | g0279 | SAS | PJL | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | ESN | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG03516 | hp2 | a0001 | c0001 | t0002 | g0253 | AFR | ESN | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG03540 | hp1 | a0002 | c0003 | t0003 | g0006 | AFR | GWD | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG03540 | hp2 | a0001 | c0001 | t0002 | g0269 | AFR | GWD | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG03579 | hp1 | a0001 | c0001 | t0004 | g0153 | AFR | MSL | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG03579 | hp2 | a0001 | c0001 | t0002 | g0288 | AFR | MSL | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG03654 | hp1 | a0001 | c0001 | t0003 | g0004 | SAS | PJL | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0201 | SAS | PJL | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0057 | SAS | PJL | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0173 | SAS | PJL | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0177 | SAS | PJL | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0073 | SAS | PJL | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0220 | SAS | BEB | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG03831 | hp2 | a0004 | c0007 | t0001 | g0032 | SAS | BEB | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0185 | SAS | BEB | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0172 | SAS | BEB | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0150 | SAS | STU | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0083 | SAS | STU | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | BEB | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0055 | SAS | BEB | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0168 | SAS | STU | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG04228 | hp2 | a0001 | c0001 | t0017 | g0289 | SAS | STU | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA18522 | hp1 | a0001 | c0002 | t0001 | g0319 | AFR | YRI | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | YRI | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | CHB | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | CHB | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | CHB | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | CHB | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA18906 | hp1 | a0001 | c0002 | t0001 | g0300 | AFR | YRI | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | YRI | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA18947 | hp2 | a0001 | c0001 | t0002 | g0246 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0257 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA18954 | hp1 | a0001 | c0001 | t0002 | g0275 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA18957 | hp2 | a0001 | c0001 | t0002 | g0244 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA18962 | hp2 | a0001 | c0001 | t0002 | g0248 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA18964 | hp1 | a0001 | c0001 | t0005 | g0008 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA18967 | hp2 | a0001 | c0001 | t0002 | g0285 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA18970 | hp1 | a0001 | c0001 | t0002 | g0256 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA18970 | hp2 | a0001 | c0001 | t0002 | g0264 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA18973 | hp1 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA18973 | hp2 | a0001 | c0001 | t0005 | g0008 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA18974 | hp1 | a0001 | c0001 | t0002 | g0242 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA18978 | hp1 | a0001 | c0001 | t0002 | g0286 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA18979 | hp1 | a0001 | c0001 | t0002 | g0259 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA18980 | hp2 | a0001 | c0001 | t0005 | g0008 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA18981 | hp1 | a0001 | c0001 | t0002 | g0278 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA18984 | hp1 | a0001 | c0001 | t0005 | g0102 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA18990 | hp1 | a0001 | c0001 | t0002 | g0243 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA18993 | hp2 | a0001 | c0001 | t0002 | g0247 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA18995 | hp1 | a0001 | c0001 | t0002 | g0271 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA19001 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA19004 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA19009 | hp2 | a0001 | c0001 | t0002 | g0272 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA19010 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA19030 | hp1 | a0001 | c0002 | t0001 | g0322 | AFR | LWK | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA19030 | hp2 | a0001 | c0001 | t0008 | g0261 | AFR | LWK | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | LWK | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA19043 | hp2 | a0001 | c0002 | t0007 | g0306 | AFR | LWK | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA19057 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA19058 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA19059 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA19059 | hp2 | a0001 | c0001 | t0002 | g0249 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA19060 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA19065 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA19066 | hp1 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA19076 | hp1 | a0001 | c0001 | t0002 | g0283 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA19078 | hp1 | a0001 | c0001 | t0002 | g0273 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA19078 | hp2 | a0001 | c0001 | t0015 | g0095 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA19080 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA19082 | hp2 | a0001 | c0001 | t0005 | g0120 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA19088 | hp1 | a0001 | c0001 | t0002 | g0282 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA19240 | hp1 | a0001 | c0006 | t0001 | g0314 | AFR | YRI | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA19240 | hp2 | a0001 | c0001 | t0002 | g0284 | AFR | YRI | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA20129 | hp1 | a0001 | c0002 | t0006 | g0297 | AFR | ASW | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA20129 | hp2 | a0001 | c0002 | t0007 | g0307 | AFR | ASW | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA20752 | hp1 | a0001 | c0001 | t0010 | g0127 | EUR | TSI | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0263 | EUR | TSI | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0013 | EUR | TSI | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0060 | EUR | TSI | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | GIH | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0117 | SAS | GIH | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG01123 | hp1 | a0001 | c0001 | t0003 | g0004 | AMR | CLM | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | CLM | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG02109 | hp2 | a0001 | c0002 | t0001 | g0323 | AFR | ACB | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG02486 | hp1 | a0001 | c0002 | t0011 | g0302 | AFR | ACB | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG02486 | hp2 | a0001 | c0002 | t0007 | g0043 | AFR | ACB | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG02559 | hp1 | a0001 | c0001 | t0002 | g0274 | AFR | ACB | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG02559 | hp2 | a0001 | c0001 | t0004 | g0026 | AFR | ACB | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG03471 | hp1 | a0001 | c0002 | t0020 | g0312 | AFR | MSL | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG03471 | hp2 | a0002 | c0003 | t0003 | g0006 | AFR | MSL | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG06807 | hp1 | a0001 | c0001 | t0002 | g0265 | AFR | USA | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
HG06807 | hp2 | a0002 | c0003 | t0003 | g0006 | AFR | USA | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA20300 | hp1 | a0001 | c0001 | t0002 | g0291 | AFR | USA | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | USA | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | LWK | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
NA21309 | hp2 | a0001 | c0001 | t0019 | g0252 | AFR | LWK | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0003 | REF | REF | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0005 | REF | REF | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:87431836
|
TCACCATG others(22167): Show |
T | 1 | a0005 | 1 | HG01928.hp2 | exon_loss_variant | HIGH | c.108-3136_790-353de others(1): Show |
NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 87431836 | |||||
chr4:87435021
|
G | C | 1 | a0003 | 2 | HG00733.hp2 HG00735.hp2 |
missense_variant | MODERATE | c.148G>C | p.Val50Leu | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/8 | 481/2820 | 148/1053 | 50/350 | chr4 | 87435021 | ||
chr4:87457911
|
A | G | 1 | a0002 | 12 | HG00639.hp2 HG01884.hp1 HG02257.hp2 others(9): Show |
missense_variant | MODERATE | c.943A>G | p.Asn315Asp | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 8/8 | 1276/2820 | 943/1053 | 315/350 | chr4 | 87457911 | ||
chr4:87457989
|
G | A | 1 | a0004 | 1 | HG03831.hp2 | missense_variant | MODERATE | c.1021G>A | p.Glu341Lys | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 8/8 | 1354/2820 | 1021/1053 | 341/350 | chr4 | 87457989 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:87422911
|
G | C | 3 | a0001c0002a0001c0006a0002c0003 | 44 | HG00639.hp2 HG01167.hp2 HG01884.hp1 others(41): Show |
synonymous_variant | LOW | c.6G>C | p.Ala2Ala | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/8 | 339/2820 | 6/1053 | 2/350 | chr4 | 87422911 | ||
chr4:87438304
|
C | T | 1 | a0001c0006 | 1 | NA19240.hp1 | synonymous_variant | LOW | c.375C>T | p.Asn125Asn | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 3/8 | 708/2820 | 375/1053 | 125/350 | chr4 | 87438304 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:87422737
|
A | T | 1 | a0001c0002t0020 | 1 | HG03471.hp1 | 5_prime_UTR_variant | MODIFIER | c.-169A>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/8 | 169 | chr4 | 87422737 | |||||
chr4:87422760
|
AGCTACTC others(6): Show |
A | 8 | a0001c0001t0002a0001c0001t0004a0001c0001t0008others(5): Show | 93 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(90): Show |
5_prime_UTR_variant | MODIFIER | c.-144_-132delCTACTC others(7): Show |
NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/8 | 132 | INFO_REALIGN_3_PRIME | chr4 | 87422760 | ||||
chr4:87422845
|
G | C | 1 | a0001c0001t0009 | 1 | HG01928.hp1 | 5_prime_UTR_variant | MODIFIER | c.-61G>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/8 | 61 | chr4 | 87422845 | |||||
chr4:87458071
|
A | G | 1 | a0001c0001t0005 | 5 | NA18964.hp1 NA18973.hp2 NA18980.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*50A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 8/8 | 50 | chr4 | 87458071 | |||||
chr4:87458107
|
G | A | 1 | a0001c0001t0010 | 1 | NA20752.hp1 | 3_prime_UTR_variant | MODIFIER | c.*86G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 8/8 | 86 | chr4 | 87458107 | |||||
chr4:87458214
|
C | T | 1 | a0001c0001t0019 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*193C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 8/8 | 193 | chr4 | 87458214 | |||||
chr4:87458379
|
G | C | 1 | a0001c0002t0006 | 4 | HG02258.hp2 HG02976.hp1 HG03130.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*358G>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 8/8 | 358 | chr4 | 87458379 | |||||
chr4:87458391
|
G | A | 11 | a0001c0001t0002a0001c0001t0003a0001c0001t0008others(8): Show | 97 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(94): Show |
3_prime_UTR_variant | MODIFIER | c.*370G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 8/8 | 370 | chr4 | 87458391 | |||||
chr4:87458525
|
A | G | 1 | a0001c0001t0015 | 1 | NA19078.hp2 | 3_prime_UTR_variant | MODIFIER | c.*504A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 8/8 | 504 | chr4 | 87458525 | |||||
chr4:87458617
|
A | G | 2 | a0001c0002t0007a0001c0002t0014 | 5 | HG02486.hp2 HG02809.hp1 HG02922.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*596A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 8/8 | 596 | chr4 | 87458617 | |||||
chr4:87458640
|
A | G | 1 | a0001c0001t0018 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*619A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 8/8 | 619 | chr4 | 87458640 | |||||
chr4:87458849
|
G | T | 1 | a0001c0001t0013 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*828G>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 8/8 | 828 | chr4 | 87458849 | |||||
chr4:87458855
|
G | A | 1 | a0002c0005t0016 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*834G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 8/8 | 834 | chr4 | 87458855 | |||||
chr4:87458951
|
G | A | 2 | a0001c0001t0008a0001c0002t0011 | 3 | HG02280.hp1 HG02486.hp1 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*930G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 8/8 | 930 | chr4 | 87458951 | |||||
chr4:87459053
|
A | G | 1 | a0001c0001t0012 | 1 | HG01255.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1032A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 8/8 | 1032 | chr4 | 87459053 | |||||
chr4:87459230
|
G | A | 1 | a0001c0002t0014 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1209G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 8/8 | 1209 | chr4 | 87459230 | |||||
chr4:87459231
|
C | A | 1 | a0001c0002t0014 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1210C>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 8/8 | 1210 | chr4 | 87459231 | |||||
chr4:87459255
|
T | C | 1 | a0001c0001t0017 | 1 | HG04228.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1234T>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 8/8 | 1234 | chr4 | 87459255 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:87423162
|
T | C | 3 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0046 | 3 | HG03486.hp2 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.107+150T>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87423162 | ||||||
chr4:87423349
|
A | G | 30 | a0001c0002t0001g0298a0001c0002t0001g0299a0001c0002t0001g0300others(27): Show | 32 | HG01891.hp2 HG02055.hp2 HG02109.hp2 others(29): Show |
intron_variant | MODIFIER | c.107+337A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87423349 | ||||||
chr4:87423463
|
T | A | 1 | a0001c0001t0001g0047 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.107+451T>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87423463 | ||||||
chr4:87423499
|
A | T | 67 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0035others(64): Show | 78 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.107+487A>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87423499 | ||||||
chr4:87423518
|
CCTT | C | 62 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(59): Show | 80 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.107+509_107+511del others(3): Show |
NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 87423518 | |||||
chr4:87423647
|
C | A | 1 | a0001c0001t0018g0239 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.107+635C>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87423647 | ||||||
chr4:87423664
|
T | G | 1 | a0001c0001t0001g0048 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.107+652T>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87423664 | ||||||
chr4:87423855
|
G | A | 3 | a0001c0002t0006g0042a0001c0002t0006g0296a0001c0002t0006g0297 | 4 | HG02258.hp2 HG02976.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.107+843G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87423855 | ||||||
chr4:87423921
|
A | G | 19 | a0001c0002t0001g0308a0001c0002t0001g0309a0001c0002t0001g0310others(16): Show | 20 | HG01891.hp2 HG02055.hp2 HG02451.hp1 others(17): Show |
intron_variant | MODIFIER | c.107+909A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87423921 | ||||||
chr4:87424096
|
A | G | 1 | a0001c0001t0001g0238 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.107+1084A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87424096 | ||||||
chr4:87424110
|
G | T | 7 | a0001c0002t0001g0236a0001c0002t0001g0237a0002c0003t0003g0006others(4): Show | 12 | HG00639.hp2 HG01167.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.107+1098G>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87424110 | ||||||
chr4:87424147
|
C | T | 1 | a0001c0001t0002g0295 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.107+1135C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87424147 | ||||||
chr4:87424160
|
C | G | 1 | a0001c0001t0001g0232 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.107+1148C>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87424160 | ||||||
chr4:87424245
|
C | T | 1 | a0001c0001t0002g0295 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.107+1233C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87424245 | ||||||
chr4:87424253
|
CGTTTT | C | 5 | a0002c0003t0003g0006a0002c0003t0003g0034a0002c0003t0003g0233others(2): Show | 10 | HG00639.hp2 HG01884.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.107+1242_107+1246d others(7): Show |
NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87424253 | ||||||
chr4:87424254
|
G | GT | 67 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0017others(64): Show | 85 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.107+1265dupT | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 87424254 | |||||
chr4:87424254
|
G | GTT | 55 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0020others(52): Show | 67 | HG00408.hp2 HG00423.hp1 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.107+1264_107+1265d others(4): Show |
NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 87424254 | |||||
chr4:87424254
|
G | GTTT | 18 | a0001c0001t0001g0007a0001c0001t0001g0021a0001c0001t0001g0083others(15): Show | 22 | HG01168.hp2 HG01243.hp1 HG02523.hp1 others(19): Show |
intron_variant | MODIFIER | c.107+1263_107+1265d others(5): Show |
NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 87424254 | |||||
chr4:87424254
|
G | GTTTT | 9 | a0001c0001t0001g0022a0001c0001t0001g0098a0001c0001t0001g0099others(6): Show | 10 | HG02145.hp2 HG02630.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.107+1262_107+1265d others(6): Show |
NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 87424254 | |||||
chr4:87424254
|
G | GTTTTTTT others(7): Show |
4 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(1): Show | 4 | HG02132.hp1 NA18965.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.107+1253_107+1254i others(16): Show |
NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 87424254 | |||||
chr4:87424254
|
G | GTTTTTTT others(8): Show |
3 | a0001c0001t0001g0048a0001c0001t0001g0053a0001c0001t0001g0054 | 3 | NA18979.hp2 NA19066.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.107+1253_107+1254i others(17): Show |
NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 87424254 | |||||
chr4:87424254
|
G | T | 2 | a0002c0005t0002g0294a0002c0005t0016g0293 | 2 | HG03041.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.107+1242G>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87424254 | ||||||
chr4:87424254
|
GT | G | 19 | a0001c0001t0001g0028a0001c0001t0001g0156a0001c0001t0001g0157others(16): Show | 21 | HG01891.hp2 HG02258.hp2 HG02451.hp1 others(18): Show |
intron_variant | MODIFIER | c.107+1265delT | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 87424254 | |||||
chr4:87424254
|
GTT | G | 10 | a0001c0002t0001g0308a0001c0002t0001g0309a0001c0002t0001g0310others(7): Show | 11 | HG02055.hp2 HG02486.hp2 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.107+1264_107+1265d others(4): Show |
NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 87424254 | |||||
chr4:87424254
|
GTTTT | G | 9 | a0001c0001t0001g0027a0001c0001t0001g0147a0001c0001t0001g0148others(6): Show | 10 | HG01123.hp2 HG01192.hp1 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.107+1262_107+1265d others(6): Show |
NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 87424254 | |||||
chr4:87424254
|
GTTTTT | G | 55 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0011others(52): Show | 71 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.107+1261_107+1265d others(7): Show |
NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 87424254 | |||||
chr4:87424258
|
T | A | 2 | a0001c0002t0001g0236a0001c0002t0001g0237 | 2 | HG01167.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.107+1246T>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87424258 | ||||||
chr4:87424259
|
T | A | 5 | a0002c0003t0003g0006a0002c0003t0003g0034a0002c0003t0003g0233others(2): Show | 10 | HG00639.hp2 HG01884.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.107+1247T>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87424259 | ||||||
chr4:87424296
|
G | C | 64 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0011others(61): Show | 81 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.107+1284G>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87424296 | ||||||
chr4:87424367
|
C | T | 1 | a0001c0002t0001g0237 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.107+1355C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87424367 | ||||||
chr4:87424395
|
G | A | 1 | a0001c0001t0002g0240 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.107+1383G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87424395 | ||||||
chr4:87424416
|
C | T | 1 | a0001c0001t0001g0210 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.107+1404C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87424416 | ||||||
chr4:87424474
|
A | G | 1 | a0001c0001t0004g0146 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.107+1462A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87424474 | ||||||
chr4:87424475
|
T | C | 29 | a0001c0002t0001g0298a0001c0002t0001g0299a0001c0002t0001g0300others(26): Show | 31 | HG01891.hp2 HG02055.hp2 HG02258.hp2 others(28): Show |
intron_variant | MODIFIER | c.107+1463T>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87424475 | ||||||
chr4:87424607
|
T | G | 10 | a0001c0001t0002g0266a0001c0001t0002g0267a0001c0001t0002g0268others(7): Show | 10 | HG01884.hp2 HG02630.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.107+1595T>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87424607 | ||||||
chr4:87424711
|
A | G | 4 | a0001c0001t0004g0026a0001c0001t0004g0143a0001c0001t0004g0144others(1): Show | 5 | HG02559.hp2 HG02622.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.107+1699A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87424711 | ||||||
chr4:87424719
|
C | T | 62 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(59): Show | 80 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.107+1707C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87424719 | ||||||
chr4:87424727
|
A | C | 2 | a0001c0001t0001g0208a0001c0001t0001g0209 | 2 | HG01934.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.107+1715A>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87424727 | ||||||
chr4:87424755
|
C | T | 1 | a0001c0001t0001g0052 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.107+1743C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87424755 | ||||||
chr4:87424825
|
A | G | 36 | a0001c0002t0001g0236a0001c0002t0001g0237a0001c0002t0001g0298others(33): Show | 43 | HG00639.hp2 HG01167.hp2 HG01884.hp1 others(40): Show |
intron_variant | MODIFIER | c.107+1813A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87424825 | ||||||
chr4:87425358
|
G | A | 90 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0011others(87): Show | 108 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(105): Show |
intron_variant | MODIFIER | c.107+2346G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87425358 | ||||||
chr4:87425380
|
G | C | 1 | a0001c0006t0001g0314 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.107+2368G>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87425380 | ||||||
chr4:87425391
|
C | CT | 69 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(66): Show | 85 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.107+2399dupT | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 87425391 | |||||
chr4:87425391
|
C | CTT | 20 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0057others(17): Show | 22 | HG00099.hp2 HG01257.hp2 HG01258.hp1 others(19): Show |
intron_variant | MODIFIER | c.107+2398_107+2399d others(4): Show |
NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 87425391 | |||||
chr4:87425391
|
CT | C | 11 | a0001c0001t0002g0266a0001c0001t0002g0267a0001c0001t0002g0268others(8): Show | 11 | HG01884.hp2 HG02630.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.107+2399delT | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 87425391 | |||||
chr4:87425391
|
CTT | C | 64 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0011others(61): Show | 81 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.107+2398_107+2399d others(4): Show |
NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 87425391 | |||||
chr4:87425445
|
A | T | 1 | a0001c0001t0001g0203 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.107+2433A>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87425445 | ||||||
chr4:87425455
|
C | T | 10 | a0001c0001t0002g0266a0001c0001t0002g0267a0001c0001t0002g0268others(7): Show | 10 | HG01884.hp2 HG02630.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.107+2443C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87425455 | ||||||
chr4:87425517
|
C | T | 2 | a0001c0001t0002g0265a0001c0001t0002g0284 | 2 | HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.107+2505C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87425517 | ||||||
chr4:87425544
|
A | G | 1 | a0001c0002t0001g0323 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.107+2532A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87425544 | ||||||
chr4:87425546
|
C | T | 1 | a0001c0001t0002g0292 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.107+2534C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87425546 | ||||||
chr4:87425632
|
C | A | 2 | a0001c0001t0002g0266a0001c0001t0002g0267 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.107+2620C>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87425632 | ||||||
chr4:87425673
|
G | A | 1 | a0001c0001t0018g0239 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.107+2661G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87425673 | ||||||
chr4:87425712
|
G | GA | 7 | a0001c0001t0001g0159a0001c0001t0001g0212a0001c0001t0002g0241others(4): Show | 7 | HG00642.hp2 HG01109.hp1 HG01928.hp2 others(4): Show |
intron_variant | MODIFIER | c.107+2719dupA | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 87425712 | |||||
chr4:87425712
|
G | GAAA | 52 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(49): Show | 70 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.107+2717_107+2719d others(5): Show |
NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 87425712 | |||||
chr4:87425712
|
G | GAAAA | 9 | a0001c0001t0001g0055a0001c0001t0001g0058a0001c0001t0001g0059others(6): Show | 9 | HG01168.hp2 HG04115.hp2 HG04184.hp2 others(6): Show |
intron_variant | MODIFIER | c.107+2716_107+2719d others(6): Show |
NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 87425712 | |||||
chr4:87425712
|
GA | G | 49 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0011others(46): Show | 64 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.107+2719delA | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 87425712 | |||||
chr4:87425713
|
A | G | 9 | a0001c0001t0001g0202a0001c0002t0001g0301a0001c0002t0001g0304others(6): Show | 9 | HG02055.hp2 HG02148.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.107+2701A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87425713 | ||||||
chr4:87425803
|
C | T | 1 | a0001c0001t0001g0084 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.107+2791C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87425803 | ||||||
chr4:87425835
|
A | T | 133 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(130): Show | 167 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.107+2823A>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87425835 | ||||||
chr4:87425836
|
A | C | 133 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(130): Show | 167 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.107+2824A>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87425836 | ||||||
chr4:87426124
|
A | G | 1 | a0001c0001t0001g0134 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.107+3112A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87426124 | ||||||
chr4:87426216
|
T | C | 230 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(227): Show | 283 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(280): Show |
intron_variant | MODIFIER | c.107+3204T>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87426216 | ||||||
chr4:87426255
|
AC | A | 62 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(59): Show | 80 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.107+3244delC | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87426255 | ||||||
chr4:87426360
|
A | G | 64 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0011others(61): Show | 81 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.107+3348A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87426360 | ||||||
chr4:87426396
|
GTCTTAAT others(2): Show |
G | 5 | a0001c0001t0004g0135a0001c0001t0004g0139a0001c0001t0004g0140others(2): Show | 5 | HG01109.hp1 HG02258.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.107+3390_107+3398d others(11): Show |
NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 87426396 | |||||
chr4:87426415
|
C | CT | 11 | a0001c0001t0001g0133a0001c0001t0004g0135a0001c0001t0004g0136others(8): Show | 11 | HG01109.hp1 HG02258.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.107+3415dupT | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 87426415 | |||||
chr4:87426500
|
C | G | 5 | a0002c0003t0003g0006a0002c0003t0003g0034a0002c0003t0003g0233others(2): Show | 10 | HG00639.hp2 HG01884.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.107+3488C>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87426500 | ||||||
chr4:87426651
|
C | T | 10 | a0001c0002t0001g0298a0001c0002t0001g0299a0001c0002t0001g0300others(7): Show | 11 | HG02258.hp2 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.107+3639C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87426651 | ||||||
chr4:87426661
|
G | A | 1 | a0001c0001t0002g0269 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.107+3649G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87426661 | ||||||
chr4:87426935
|
CA | C | 60 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(57): Show | 78 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.107+3934delA | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 87426935 | |||||
chr4:87426945
|
A | C | 1 | a0001c0001t0004g0153 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.107+3933A>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87426945 | ||||||
chr4:87426960
|
C | A | 2 | a0001c0001t0004g0136a0001c0001t0004g0146 | 2 | HG02647.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.107+3948C>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87426960 | ||||||
chr4:87426997
|
A | G | 200 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(197): Show | 251 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(248): Show |
intron_variant | MODIFIER | c.107+3985A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87426997 | ||||||
chr4:87427119
|
C | CA | 10 | a0001c0001t0001g0053a0001c0001t0001g0061a0001c0001t0001g0080others(7): Show | 10 | HG00735.hp1 HG00735.hp2 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.107+4123dupA | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 87427119 | |||||
chr4:87427119
|
CA | C | 8 | a0001c0001t0001g0132a0001c0001t0001g0228a0001c0001t0002g0283others(5): Show | 8 | HG02630.hp1 HG02723.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.107+4123delA | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 87427119 | |||||
chr4:87427122
|
AAAAAAAA others(9): Show |
A | 1 | a0001c0001t0001g0104 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.107+4126_107+4141d others(18): Show |
NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 87427122 | |||||
chr4:87427138
|
T | TA | 80 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(77): Show | 99 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(96): Show |
intron_variant | MODIFIER | c.107+4139dupA | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 87427138 | |||||
chr4:87427172
|
G | A | 62 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(59): Show | 80 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.107+4160G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87427172 | ||||||
chr4:87427183
|
G | T | 62 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(59): Show | 80 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.107+4171G>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87427183 | ||||||
chr4:87427187
|
A | G | 1 | a0001c0001t0002g0288 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.107+4175A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87427187 | ||||||
chr4:87427284
|
C | T | 1 | a0002c0005t0016g0293 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.107+4272C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87427284 | ||||||
chr4:87427559
|
C | T | 62 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(59): Show | 80 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.107+4547C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87427559 | ||||||
chr4:87427644
|
T | C | 1 | a0001c0001t0001g0162 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.107+4632T>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87427644 | ||||||
chr4:87427723
|
C | G | 230 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(227): Show | 283 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(280): Show |
intron_variant | MODIFIER | c.107+4711C>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87427723 | ||||||
chr4:87427870
|
G | T | 66 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0035others(63): Show | 77 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.107+4858G>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87427870 | ||||||
chr4:87427956
|
T | G | 2 | a0001c0001t0002g0265a0001c0001t0002g0284 | 2 | HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.107+4944T>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87427956 | ||||||
chr4:87428014
|
A | G | 5 | a0002c0003t0003g0006a0002c0003t0003g0034a0002c0003t0003g0233others(2): Show | 10 | HG00639.hp2 HG01884.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.107+5002A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87428014 | ||||||
chr4:87428048
|
C | T | 62 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(59): Show | 80 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.107+5036C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87428048 | ||||||
chr4:87428086
|
C | T | 1 | a0001c0001t0018g0239 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.107+5074C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87428086 | ||||||
chr4:87428219
|
CAG | C | 5 | a0002c0003t0003g0006a0002c0003t0003g0034a0002c0003t0003g0233others(2): Show | 10 | HG00639.hp2 HG01884.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.107+5210_107+5211d others(4): Show |
NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 87428219 | |||||
chr4:87428233
|
G | A | 1 | a0001c0001t0001g0228 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.107+5221G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87428233 | ||||||
chr4:87428533
|
GATATT | G | 230 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(227): Show | 283 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(280): Show |
intron_variant | MODIFIER | c.107+5529_107+5533d others(7): Show |
NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 87428533 | |||||
chr4:87428669
|
A | G | 229 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(226): Show | 282 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(279): Show |
intron_variant | MODIFIER | c.107+5657A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87428669 | ||||||
chr4:87428698
|
A | T | 1 | a0001c0001t0001g0201 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.107+5686A>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87428698 | ||||||
chr4:87428704
|
T | TG | 6 | a0001c0001t0001g0207a0002c0003t0003g0006a0002c0003t0003g0034others(3): Show | 11 | HG00639.hp2 HG01884.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.107+5696dupG | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 87428704 | |||||
chr4:87428858
|
G | A | 2 | a0001c0001t0001g0134a0001c0001t0001g0148 | 2 | HG02135.hp2 NA18956.hp1 |
intron_variant | MODIFIER | c.107+5846G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87428858 | ||||||
chr4:87428905
|
C | T | 3 | a0001c0001t0001g0060a0001c0001t0001g0080a0001c0001t0001g0084 | 3 | HG01168.hp2 HG01981.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.107+5893C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87428905 | ||||||
chr4:87429035
|
A | G | 62 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(59): Show | 80 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.108-5946A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87429035 | ||||||
chr4:87429040
|
C | T | 1 | a0001c0001t0001g0200 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.108-5941C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87429040 | ||||||
chr4:87429151
|
G | A | 1 | a0001c0001t0001g0207 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.108-5830G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87429151 | ||||||
chr4:87429193
|
C | A | 62 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(59): Show | 80 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.108-5788C>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87429193 | ||||||
chr4:87429314
|
A | G | 229 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(226): Show | 282 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(279): Show |
intron_variant | MODIFIER | c.108-5667A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87429314 | ||||||
chr4:87429395
|
C | G | 1 | a0001c0001t0002g0041 | 2 | HG02165.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.108-5586C>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87429395 | ||||||
chr4:87429438
|
GC | G | 53 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0035others(50): Show | 64 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.108-5541delC | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 87429438 | |||||
chr4:87429473
|
A | G | 1 | a0001c0002t0001g0300 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.108-5508A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87429473 | ||||||
chr4:87429687
|
CG | C | 67 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(64): Show | 87 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.108-5293delG | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87429687 | ||||||
chr4:87429743
|
C | T | 11 | a0001c0002t0001g0313a0001c0002t0001g0315a0001c0002t0001g0316others(8): Show | 11 | HG01891.hp2 HG02451.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.108-5238C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87429743 | ||||||
chr4:87429807
|
T | C | 229 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(226): Show | 282 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(279): Show |
intron_variant | MODIFIER | c.108-5174T>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87429807 | ||||||
chr4:87429886
|
A | G | 11 | a0001c0002t0001g0313a0001c0002t0001g0315a0001c0002t0001g0316others(8): Show | 11 | HG01891.hp2 HG02451.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.108-5095A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87429886 | ||||||
chr4:87429894
|
T | G | 62 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(59): Show | 80 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.108-5087T>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87429894 | ||||||
chr4:87429908
|
G | A | 2 | a0002c0003t0003g0034a0002c0003t0003g0233 | 3 | HG00639.hp2 HG02257.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.108-5073G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87429908 | ||||||
chr4:87430047
|
A | G | 1 | a0001c0001t0001g0079 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.108-4934A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87430047 | ||||||
chr4:87430066
|
C | T | 4 | a0001c0001t0004g0026a0001c0001t0004g0143a0001c0001t0004g0144others(1): Show | 5 | HG02559.hp2 HG02622.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.108-4915C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87430066 | ||||||
chr4:87430129
|
A | G | 3 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0046 | 3 | HG03486.hp2 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.108-4852A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87430129 | ||||||
chr4:87430228
|
G | C | 66 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0035others(63): Show | 77 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.108-4753G>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87430228 | ||||||
chr4:87430452
|
T | C | 66 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0035others(63): Show | 77 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.108-4529T>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87430452 | ||||||
chr4:87430630
|
A | C | 3 | a0001c0002t0001g0236a0001c0002t0001g0237a0001c0002t0001g0323 | 3 | HG01167.hp2 HG02109.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.108-4351A>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87430630 | ||||||
chr4:87430726
|
A | G | 53 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0035others(50): Show | 64 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.108-4255A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87430726 | ||||||
chr4:87430895
|
CTTGA | C | 2 | a0001c0001t0001g0027a0001c0001t0001g0147 | 3 | HG01192.hp1 HG01243.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.108-4082_108-4079d others(6): Show |
NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 87430895 | |||||
chr4:87431178
|
G | T | 1 | a0001c0001t0004g0153 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.108-3803G>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87431178 | ||||||
chr4:87431206
|
C | T | 1 | a0001c0001t0001g0132 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.108-3775C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87431206 | ||||||
chr4:87431273
|
C | G | 1 | a0001c0001t0002g0282 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.108-3708C>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87431273 | ||||||
chr4:87431333
|
G | T | 1 | a0001c0001t0018g0239 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.108-3648G>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87431333 | ||||||
chr4:87431334
|
C | T | 1 | a0001c0002t0001g0237 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.108-3647C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87431334 | ||||||
chr4:87431587
|
A | G | 53 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0035others(50): Show | 64 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.108-3394A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87431587 | ||||||
chr4:87431709
|
T | C | 1 | a0001c0001t0001g0133 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.108-3272T>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87431709 | ||||||
chr4:87431858
|
G | T | 1 | a0001c0001t0001g0093 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.108-3123G>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87431858 | ||||||
chr4:87431860
|
A | T | 1 | a0001c0001t0001g0093 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.108-3121A>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87431860 | ||||||
chr4:87431865
|
T | TTTTTTTT others(613): Show |
1 | a0001c0001t0001g0093 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.108-3116_108-3115i others(622): Show |
NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87431865 | ||||||
chr4:87431882
|
C | T | 7 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0050others(4): Show | 7 | HG02132.hp1 NA18965.hp1 NA18979.hp2 others(4): Show |
intron_variant | MODIFIER | c.108-3099C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87431882 | ||||||
chr4:87431891
|
G | A | 2 | a0001c0002t0001g0298a0001c0002t0001g0299 | 2 | HG02723.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.108-3090G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87431891 | ||||||
chr4:87431916
|
C | G | 1 | a0001c0001t0002g0242 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.108-3065C>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87431916 | ||||||
chr4:87431932
|
A | G | 1 | a0001c0001t0001g0100 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.108-3049A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87431932 | ||||||
chr4:87432108
|
C | T | 1 | a0001c0002t0001g0236 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.108-2873C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87432108 | ||||||
chr4:87432113
|
G | A | 1 | a0001c0001t0001g0214 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.108-2868G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87432113 | ||||||
chr4:87432186
|
G | T | 10 | a0001c0001t0002g0266a0001c0001t0002g0267a0001c0001t0002g0268others(7): Show | 10 | HG01884.hp2 HG02630.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.108-2795G>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87432186 | ||||||
chr4:87432303
|
A | G | 4 | a0001c0002t0007g0043a0001c0002t0007g0306a0001c0002t0007g0307others(1): Show | 5 | HG02486.hp2 HG02809.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.108-2678A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87432303 | ||||||
chr4:87432330
|
T | C | 1 | a0002c0005t0016g0293 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.108-2651T>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87432330 | ||||||
chr4:87432768
|
G | GT | 65 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(62): Show | 83 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(80): Show |
intron_variant | MODIFIER | c.108-2201dupT | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 87432768 | |||||
chr4:87432770
|
T | G | 4 | a0001c0002t0007g0043a0001c0002t0007g0306a0001c0002t0007g0307others(1): Show | 5 | HG02486.hp2 HG02809.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.108-2211T>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87432770 | ||||||
chr4:87432780
|
T | C | 1 | a0001c0001t0001g0105 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.108-2201T>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87432780 | ||||||
chr4:87432868
|
A | G | 1 | a0001c0001t0001g0047 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.108-2113A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87432868 | ||||||
chr4:87432987
|
T | C | 62 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(59): Show | 80 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.108-1994T>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87432987 | ||||||
chr4:87433044
|
C | G | 133 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(130): Show | 167 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.108-1937C>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87433044 | ||||||
chr4:87433063
|
G | A | 5 | a0002c0003t0003g0006a0002c0003t0003g0034a0002c0003t0003g0233others(2): Show | 10 | HG00639.hp2 HG01884.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.108-1918G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87433063 | ||||||
chr4:87433117
|
C | T | 1 | a0001c0002t0001g0236 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.108-1864C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87433117 | ||||||
chr4:87433231
|
A | T | 15 | a0001c0001t0004g0026a0001c0001t0004g0135a0001c0001t0004g0136others(12): Show | 16 | HG01109.hp1 HG02258.hp1 HG02559.hp2 others(13): Show |
intron_variant | MODIFIER | c.108-1750A>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87433231 | ||||||
chr4:87433251
|
C | T | 10 | a0001c0001t0002g0266a0001c0001t0002g0267a0001c0001t0002g0268others(7): Show | 10 | HG01884.hp2 HG02630.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.108-1730C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87433251 | ||||||
chr4:87433450
|
G | A | 2 | a0001c0001t0001g0028a0001c0001t0001g0204 | 3 | HG02572.hp2 NA18522.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.108-1531G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87433450 | ||||||
chr4:87433520
|
G | T | 1 | a0001c0002t0001g0323 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.108-1461G>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87433520 | ||||||
chr4:87433552
|
C | T | 1 | a0001c0002t0001g0237 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.108-1429C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87433552 | ||||||
chr4:87433660
|
T | C | 1 | a0001c0002t0001g0237 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.108-1321T>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87433660 | ||||||
chr4:87433777
|
G | T | 1 | a0001c0001t0001g0197 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.108-1204G>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87433777 | ||||||
chr4:87434030
|
G | A | 59 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0012others(56): Show | 78 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.108-951G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87434030 | ||||||
chr4:87434271
|
T | A | 64 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0011others(61): Show | 81 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.108-710T>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87434271 | ||||||
chr4:87434394
|
A | G | 62 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(59): Show | 80 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.108-587A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87434394 | ||||||
chr4:87434407
|
A | T | 1 | a0001c0001t0001g0078 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.108-574A>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87434407 | ||||||
chr4:87434422
|
C | CT | 295 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(292): Show | 368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.108-543dupT | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 87434422 | |||||
chr4:87434626
|
C | CT | 7 | a0001c0001t0001g0132a0001c0002t0001g0236a0001c0002t0001g0237others(4): Show | 7 | HG01167.hp2 HG02055.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.108-344dupT | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 87434626 | |||||
chr4:87434626
|
CT | C | 64 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(61): Show | 82 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(79): Show |
intron_variant | MODIFIER | c.108-344delT | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 87434626 | |||||
chr4:87434825
|
G | A | 4 | a0001c0002t0007g0043a0001c0002t0007g0306a0001c0002t0007g0307others(1): Show | 5 | HG02486.hp2 HG02809.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.108-156G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87434825 | ||||||
chr4:87434849
|
C | T | 3 | a0001c0002t0006g0042a0001c0002t0006g0296a0001c0002t0006g0297 | 4 | HG02258.hp2 HG02976.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.108-132C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87434849 | ||||||
chr4:87434899
|
G | A | 1 | a0001c0001t0004g0153 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.108-82G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87434899 | ||||||
chr4:87434959
|
T | C | 64 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0011others(61): Show | 81 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.108-22T>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87434959 | ||||||
chr4:87435239
|
G | A | 2 | a0001c0001t0001g0107a0001c0002t0020g0312 | 2 | HG00741.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.347+19G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | chr4 | 87435239 | ||||||
chr4:87435487
|
T | G | 1 | a0001c0001t0001g0215 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.347+267T>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | chr4 | 87435487 | ||||||
chr4:87435594
|
C | T | 5 | a0002c0003t0003g0006a0002c0003t0003g0034a0002c0003t0003g0233others(2): Show | 10 | HG00639.hp2 HG01884.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.347+374C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | chr4 | 87435594 | ||||||
chr4:87435647
|
C | T | 71 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0035others(68): Show | 87 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.347+427C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | chr4 | 87435647 | ||||||
chr4:87435662
|
C | A | 1 | a0001c0001t0002g0243 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.347+442C>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | chr4 | 87435662 | ||||||
chr4:87435740
|
T | C | 1 | a0001c0001t0002g0244 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.347+520T>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | chr4 | 87435740 | ||||||
chr4:87435777
|
A | T | 1 | a0001c0001t0002g0242 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.347+557A>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | chr4 | 87435777 | ||||||
chr4:87435778
|
T | G | 1 | a0001c0001t0002g0242 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.347+558T>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | chr4 | 87435778 | ||||||
chr4:87435779
|
G | T | 1 | a0001c0001t0002g0242 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.347+559G>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | chr4 | 87435779 | ||||||
chr4:87435863
|
A | G | 53 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0035others(50): Show | 64 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.347+643A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | chr4 | 87435863 | ||||||
chr4:87435993
|
A | G | 2 | a0001c0001t0001g0076a0001c0001t0001g0077 | 2 | HG00609.hp2 HG02056.hp2 |
intron_variant | MODIFIER | c.347+773A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | chr4 | 87435993 | ||||||
chr4:87436002
|
A | G | 1 | a0001c0002t0006g0297 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.347+782A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | chr4 | 87436002 | ||||||
chr4:87436017
|
G | GCT | 64 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0011others(61): Show | 81 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.347+808_347+809dup others(2): Show |
NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 87436017 | |||||
chr4:87436049
|
A | T | 5 | a0002c0003t0003g0006a0002c0003t0003g0034a0002c0003t0003g0233others(2): Show | 10 | HG00639.hp2 HG01884.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.347+829A>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | chr4 | 87436049 | ||||||
chr4:87436168
|
T | C | 1 | a0001c0001t0001g0023 | 2 | HG01975.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.347+948T>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | chr4 | 87436168 | ||||||
chr4:87436239
|
C | T | 1 | a0001c0001t0004g0153 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.347+1019C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | chr4 | 87436239 | ||||||
chr4:87436299
|
C | A | 1 | a0002c0005t0002g0294 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.347+1079C>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | chr4 | 87436299 | ||||||
chr4:87436324
|
T | C | 1 | a0001c0001t0001g0185 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.347+1104T>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | chr4 | 87436324 | ||||||
chr4:87436668
|
A | G | 15 | a0001c0001t0004g0026a0001c0001t0004g0135a0001c0001t0004g0136others(12): Show | 16 | HG01109.hp1 HG02258.hp1 HG02559.hp2 others(13): Show |
intron_variant | MODIFIER | c.347+1448A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | chr4 | 87436668 | ||||||
chr4:87436690
|
A | C | 71 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0035others(68): Show | 87 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.347+1470A>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | chr4 | 87436690 | ||||||
chr4:87436706
|
A | G | 1 | a0001c0002t0001g0236 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.347+1486A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | chr4 | 87436706 | ||||||
chr4:87436731
|
G | A | 1 | a0001c0001t0002g0271 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.347+1511G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | chr4 | 87436731 | ||||||
chr4:87436750
|
A | C | 1 | a0001c0002t0007g0307 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.348-1527A>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | chr4 | 87436750 | ||||||
chr4:87436843
|
A | G | 1 | a0001c0001t0001g0092 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.348-1434A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | chr4 | 87436843 | ||||||
chr4:87436853
|
A | G | 1 | a0001c0001t0013g0155 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.348-1424A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | chr4 | 87436853 | ||||||
chr4:87436981
|
G | T | 4 | a0001c0002t0001g0308a0001c0002t0001g0309a0001c0002t0001g0310others(1): Show | 4 | HG02055.hp2 HG02895.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.348-1296G>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | chr4 | 87436981 | ||||||
chr4:87437024
|
G | A | 7 | a0001c0002t0001g0298a0001c0002t0001g0299a0001c0002t0001g0300others(4): Show | 7 | HG02486.hp1 HG02572.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.348-1253G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | chr4 | 87437024 | ||||||
chr4:87437249
|
C | CA | 57 | a0001c0001t0001g0084a0001c0001t0001g0091a0001c0001t0001g0108others(54): Show | 68 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.348-1009dupA | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 87437249 | |||||
chr4:87437249
|
C | CAA | 57 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(54): Show | 75 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.348-1010_348-1009d others(4): Show |
NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 87437249 | |||||
chr4:87437249
|
CA | C | 8 | a0001c0001t0001g0130a0001c0001t0001g0148a0001c0001t0001g0157others(5): Show | 8 | HG01257.hp1 HG01261.hp2 NA18942.hp2 others(5): Show |
intron_variant | MODIFIER | c.348-1009delA | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 87437249 | |||||
chr4:87437275
|
AAG | A | 10 | a0001c0001t0004g0135a0001c0001t0004g0136a0001c0001t0004g0137others(7): Show | 10 | HG01109.hp1 HG02258.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.348-1000_348-999de others(3): Show |
NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 87437275 | |||||
chr4:87437286
|
A | AT | 61 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(58): Show | 79 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.348-983dupT | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 87437286 | |||||
chr4:87437286
|
AT | A | 64 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0011others(61): Show | 81 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.348-983delT | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 87437286 | |||||
chr4:87437318
|
A | C | 5 | a0001c0001t0001g0010a0001c0001t0001g0074a0001c0001t0001g0075others(2): Show | 7 | HG00408.hp2 HG02083.hp1 NA18944.hp1 others(4): Show |
intron_variant | MODIFIER | c.348-959A>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | chr4 | 87437318 | ||||||
chr4:87437379
|
C | A | 2 | a0001c0001t0001g0164a0001c0001t0001g0212 | 2 | NA18965.hp2 NA18972.hp1 |
intron_variant | MODIFIER | c.348-898C>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | chr4 | 87437379 | ||||||
chr4:87437419
|
G | C | 70 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(67): Show | 88 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.348-858G>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | chr4 | 87437419 | ||||||
chr4:87437449
|
T | A | 11 | a0001c0001t0002g0245a0001c0001t0002g0266a0001c0001t0002g0267others(8): Show | 11 | HG01884.hp2 HG02630.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.348-828T>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | chr4 | 87437449 | ||||||
chr4:87437465
|
C | G | 5 | a0002c0003t0003g0006a0002c0003t0003g0034a0002c0003t0003g0233others(2): Show | 10 | HG00639.hp2 HG01884.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.348-812C>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | chr4 | 87437465 | ||||||
chr4:87437465
|
C | T | 1 | a0001c0001t0001g0180 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.348-812C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | chr4 | 87437465 | ||||||
chr4:87437477
|
G | A | 6 | a0002c0003t0003g0006a0002c0003t0003g0034a0002c0003t0003g0233others(3): Show | 11 | HG00639.hp2 HG01884.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.348-800G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | chr4 | 87437477 | ||||||
chr4:87437485
|
T | C | 7 | a0001c0001t0002g0246a0001c0001t0002g0285a0002c0003t0003g0006others(4): Show | 12 | HG00639.hp2 HG01884.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.348-792T>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | chr4 | 87437485 | ||||||
chr4:87437490
|
A | G | 10 | a0001c0001t0002g0290a0001c0001t0002g0291a0001c0001t0002g0292others(7): Show | 15 | HG00639.hp2 HG01884.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.348-787A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | chr4 | 87437490 | ||||||
chr4:87437497
|
T | C | 5 | a0002c0003t0003g0006a0002c0003t0003g0034a0002c0003t0003g0233others(2): Show | 10 | HG00639.hp2 HG01884.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.348-780T>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | chr4 | 87437497 | ||||||
chr4:87437498
|
G | A | 5 | a0002c0003t0003g0006a0002c0003t0003g0034a0002c0003t0003g0233others(2): Show | 10 | HG00639.hp2 HG01884.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.348-779G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | chr4 | 87437498 | ||||||
chr4:87437502
|
A | G | 5 | a0002c0003t0003g0006a0002c0003t0003g0034a0002c0003t0003g0233others(2): Show | 10 | HG00639.hp2 HG01884.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.348-775A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | chr4 | 87437502 | ||||||
chr4:87437515
|
T | A | 5 | a0002c0003t0003g0006a0002c0003t0003g0034a0002c0003t0003g0233others(2): Show | 10 | HG00639.hp2 HG01884.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.348-762T>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | chr4 | 87437515 | ||||||
chr4:87437516
|
ATT | A | 5 | a0001c0002t0001g0298a0001c0002t0001g0299a0001c0002t0001g0300others(2): Show | 5 | HG02109.hp2 HG02723.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.348-755_348-754del others(2): Show |
NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 87437516 | |||||
chr4:87437531
|
A | G | 2 | a0001c0001t0001g0055a0001c0001t0001g0057 | 2 | HG03669.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.348-746A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | chr4 | 87437531 | ||||||
chr4:87437532
|
T | C | 11 | a0001c0002t0001g0298a0001c0002t0001g0299a0001c0002t0001g0301others(8): Show | 16 | HG00639.hp2 HG01884.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.348-745T>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | chr4 | 87437532 | ||||||
chr4:87437539
|
C | T | 9 | a0001c0001t0001g0214a0001c0001t0002g0291a0001c0002t0001g0236others(6): Show | 14 | HG00639.hp2 HG01884.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.348-738C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | chr4 | 87437539 | ||||||
chr4:87437544
|
A | G | 7 | a0001c0001t0001g0128a0001c0001t0001g0133a0002c0003t0003g0006others(4): Show | 12 | HG00639.hp2 HG01884.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.348-733A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | chr4 | 87437544 | ||||||
chr4:87437549
|
A | G | 19 | a0001c0001t0001g0030a0001c0001t0001g0033a0001c0001t0001g0157others(16): Show | 21 | HG01109.hp1 HG02165.hp1 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.348-728A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | chr4 | 87437549 | ||||||
chr4:87437555
|
G | A | 5 | a0002c0003t0003g0006a0002c0003t0003g0034a0002c0003t0003g0233others(2): Show | 10 | HG00639.hp2 HG01884.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.348-722G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | chr4 | 87437555 | ||||||
chr4:87437559
|
G | C | 5 | a0002c0003t0003g0006a0002c0003t0003g0034a0002c0003t0003g0233others(2): Show | 10 | HG00639.hp2 HG01884.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.348-718G>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | chr4 | 87437559 | ||||||
chr4:87437563
|
T | C | 10 | a0001c0001t0001g0210a0001c0001t0002g0035a0001c0001t0002g0247others(7): Show | 16 | HG00639.hp2 HG01884.hp1 HG02071.hp2 others(13): Show |
intron_variant | MODIFIER | c.348-714T>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | chr4 | 87437563 | ||||||
chr4:87437577
|
T | C | 7 | a0001c0001t0001g0165a0001c0001t0001g0210a0002c0003t0003g0006others(4): Show | 12 | HG00639.hp2 HG01884.hp1 HG02071.hp2 others(9): Show |
intron_variant | MODIFIER | c.348-700T>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | chr4 | 87437577 | ||||||
chr4:87437584
|
T | C | 5 | a0002c0003t0003g0006a0002c0003t0003g0034a0002c0003t0003g0233others(2): Show | 10 | HG00639.hp2 HG01884.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.348-693T>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | chr4 | 87437584 | ||||||
chr4:87437622
|
G | A | 3 | a0001c0001t0002g0248a0001c0001t0002g0271a0001c0002t0001g0236 | 3 | HG02451.hp2 NA18962.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.348-655G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | chr4 | 87437622 | ||||||
chr4:87437637
|
T | A | 1 | a0001c0001t0002g0242 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.348-640T>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | chr4 | 87437637 | ||||||
chr4:87437686
|
A | C | 1 | a0001c0002t0001g0323 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.348-591A>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | chr4 | 87437686 | ||||||
chr4:87437801
|
A | G | 1 | a0001c0001t0001g0073 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.348-476A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | chr4 | 87437801 | ||||||
chr4:87437822
|
A | G | 1 | a0001c0002t0001g0310 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.348-455A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | chr4 | 87437822 | ||||||
chr4:87437976
|
CCTT | C | 5 | a0001c0001t0004g0026a0001c0001t0004g0143a0001c0001t0004g0144others(2): Show | 6 | HG01167.hp2 HG02559.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.348-297_348-295del others(3): Show |
NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 87437976 | |||||
chr4:87438039
|
G | A | 4 | a0001c0002t0007g0043a0001c0002t0007g0306a0001c0002t0007g0307others(1): Show | 5 | HG02486.hp2 HG02809.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.348-238G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | chr4 | 87438039 | ||||||
chr4:87438049
|
TA | T | 5 | a0001c0001t0001g0021a0001c0001t0001g0059a0001c0001t0001g0071others(2): Show | 6 | HG00673.hp1 NA18953.hp1 NA18959.hp2 others(3): Show |
intron_variant | MODIFIER | c.348-226delA | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 87438049 | |||||
chr4:87438138
|
G | GA | 78 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(75): Show | 97 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(94): Show |
intron_variant | MODIFIER | c.348-124dupA | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 87438138 | |||||
chr4:87438138
|
GA | G | 54 | a0001c0001t0001g0027a0001c0001t0001g0147a0001c0001t0002g0015others(51): Show | 70 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(67): Show |
intron_variant | MODIFIER | c.348-124delA | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 87438138 | |||||
chr4:87438140
|
A | G | 1 | a0001c0001t0002g0264 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.348-137A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | chr4 | 87438140 | ||||||
chr4:87438213
|
A | T | 4 | a0001c0002t0001g0308a0001c0002t0001g0309a0001c0002t0001g0310others(1): Show | 4 | HG02055.hp2 HG02895.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.348-64A>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | chr4 | 87438213 | ||||||
chr4:87438262
|
G | A | 1 | a0001c0001t0001g0092 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.348-15G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | chr4 | 87438262 | ||||||
chr4:87438584
|
T | TA | 135 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(132): Show | 167 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.443+213dupA | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 87438584 | |||||
chr4:87438634
|
T | C | 3 | a0001c0001t0001g0217a0001c0001t0009g0216a0001c0001t0012g0167 | 3 | HG01255.hp1 HG01928.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.443+262T>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 3/7 | chr4 | 87438634 | ||||||
chr4:87438733
|
T | C | 1 | a0001c0001t0018g0239 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.443+361T>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 3/7 | chr4 | 87438733 | ||||||
chr4:87438740
|
G | T | 1 | a0001c0001t0001g0178 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.443+368G>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 3/7 | chr4 | 87438740 | ||||||
chr4:87438766
|
C | T | 1 | a0001c0006t0001g0314 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.443+394C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 3/7 | chr4 | 87438766 | ||||||
chr4:87438791
|
A | G | 6 | a0001c0001t0002g0039a0001c0001t0002g0040a0001c0001t0002g0241others(3): Show | 8 | HG00639.hp1 HG00642.hp2 HG00733.hp1 others(5): Show |
intron_variant | MODIFIER | c.443+419A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 3/7 | chr4 | 87438791 | ||||||
chr4:87438799
|
C | T | 240 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(237): Show | 294 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(291): Show |
intron_variant | MODIFIER | c.443+427C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 3/7 | chr4 | 87438799 | ||||||
chr4:87438856
|
T | C | 135 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(132): Show | 167 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.443+484T>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 3/7 | chr4 | 87438856 | ||||||
chr4:87438904
|
C | T | 7 | a0001c0002t0001g0298a0001c0002t0001g0299a0001c0002t0001g0300others(4): Show | 7 | HG02486.hp1 HG02572.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.443+532C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 3/7 | chr4 | 87438904 | ||||||
chr4:87439077
|
G | A | 69 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0035others(66): Show | 84 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.443+705G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 3/7 | chr4 | 87439077 | ||||||
chr4:87439090
|
C | T | 3 | a0001c0001t0001g0189a0001c0001t0001g0190a0001c0001t0001g0191 | 3 | NA18997.hp1 NA19081.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.443+718C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 3/7 | chr4 | 87439090 | ||||||
chr4:87439097
|
C | T | 1 | a0001c0001t0001g0125 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.443+725C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 3/7 | chr4 | 87439097 | ||||||
chr4:87439109
|
T | C | 14 | a0001c0002t0001g0308a0001c0002t0001g0309a0001c0002t0001g0310others(11): Show | 14 | HG01891.hp2 HG02055.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.443+737T>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 3/7 | chr4 | 87439109 | ||||||
chr4:87439131
|
A | G | 7 | a0001c0002t0001g0298a0001c0002t0001g0299a0001c0002t0001g0300others(4): Show | 7 | HG02486.hp1 HG02572.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.443+759A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 3/7 | chr4 | 87439131 | ||||||
chr4:87439140
|
T | C | 2 | a0001c0001t0001g0109a0001c0001t0001g0110 | 2 | NA18952.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.443+768T>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 3/7 | chr4 | 87439140 | ||||||
chr4:87439145
|
G | A | 2 | a0001c0001t0002g0039a0001c0001t0002g0241 | 3 | HG00639.hp1 HG00642.hp2 HG00733.hp1 |
intron_variant | MODIFIER | c.443+773G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 3/7 | chr4 | 87439145 | ||||||
chr4:87439153
|
G | A | 1 | a0001c0002t0011g0302 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.443+781G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 3/7 | chr4 | 87439153 | ||||||
chr4:87439165
|
C | CA | 81 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(78): Show | 105 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(102): Show |
intron_variant | MODIFIER | c.443+804dupA | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 87439165 | |||||
chr4:87439165
|
C | CAA | 67 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0035others(64): Show | 82 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.443+803_443+804dup others(2): Show |
NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 87439165 | |||||
chr4:87439313
|
C | T | 2 | a0002c0005t0002g0294a0002c0005t0016g0293 | 2 | HG03041.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.443+941C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 3/7 | chr4 | 87439313 | ||||||
chr4:87439450
|
G | A | 1 | a0001c0001t0001g0185 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.443+1078G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 3/7 | chr4 | 87439450 | ||||||
chr4:87439517
|
T | A | 241 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(238): Show | 295 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(292): Show |
intron_variant | MODIFIER | c.443+1145T>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 3/7 | chr4 | 87439517 | ||||||
chr4:87439679
|
C | T | 2 | a0001c0001t0001g0027a0001c0001t0001g0147 | 3 | HG01192.hp1 HG01243.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.443+1307C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 3/7 | chr4 | 87439679 | ||||||
chr4:87439873
|
A | G | 5 | a0002c0003t0003g0006a0002c0003t0003g0034a0002c0003t0003g0233others(2): Show | 10 | HG00639.hp2 HG01884.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.443+1501A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 3/7 | chr4 | 87439873 | ||||||
chr4:87440204
|
T | C | 1 | a0001c0001t0013g0155 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.444-1625T>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 3/7 | chr4 | 87440204 | ||||||
chr4:87440281
|
C | A | 76 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0035others(73): Show | 96 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.444-1548C>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 3/7 | chr4 | 87440281 | ||||||
chr4:87440412
|
T | G | 4 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(1): Show | 4 | NA18961.hp1 NA18962.hp1 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.444-1417T>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 3/7 | chr4 | 87440412 | ||||||
chr4:87440512
|
C | T | 2 | a0001c0001t0001g0027a0001c0001t0001g0147 | 3 | HG01192.hp1 HG01243.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.444-1317C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 3/7 | chr4 | 87440512 | ||||||
chr4:87440564
|
C | T | 53 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0035others(50): Show | 64 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.444-1265C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 3/7 | chr4 | 87440564 | ||||||
chr4:87440569
|
C | T | 1 | a0001c0001t0001g0177 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.444-1260C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 3/7 | chr4 | 87440569 | ||||||
chr4:87440586
|
G | A | 76 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0035others(73): Show | 96 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.444-1243G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 3/7 | chr4 | 87440586 | ||||||
chr4:87440845
|
C | CA | 134 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(131): Show | 166 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.444-974dupA | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 87440845 | |||||
chr4:87440856
|
T | A | 1 | a0001c0001t0001g0149 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.444-973T>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 3/7 | chr4 | 87440856 | ||||||
chr4:87441104
|
A | T | 2 | a0001c0001t0001g0159a0001c0001t0001g0220 | 2 | HG03831.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.444-725A>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 3/7 | chr4 | 87441104 | ||||||
chr4:87441143
|
A | G | 1 | a0001c0001t0001g0176 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.444-686A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 3/7 | chr4 | 87441143 | ||||||
chr4:87441215
|
T | A | 1 | a0001c0001t0001g0208 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.444-614T>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 3/7 | chr4 | 87441215 | ||||||
chr4:87441548
|
A | G | 1 | a0001c0001t0001g0110 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.444-281A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 3/7 | chr4 | 87441548 | ||||||
chr4:87441563
|
T | G | 1 | a0001c0001t0001g0232 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.444-266T>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 3/7 | chr4 | 87441563 | ||||||
chr4:87441696
|
A | G | 5 | a0001c0001t0002g0037a0001c0001t0002g0245a0001c0001t0002g0253others(2): Show | 6 | HG02055.hp1 HG02559.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.444-133A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 3/7 | chr4 | 87441696 | ||||||
chr4:87441752
|
C | T | 135 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(132): Show | 167 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.444-77C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 3/7 | chr4 | 87441752 | ||||||
chr4:87441935
|
A | G | 16 | a0001c0001t0001g0011a0001c0001t0001g0023a0001c0001t0001g0108others(13): Show | 19 | HG00544.hp2 HG00673.hp2 HG01952.hp1 others(16): Show |
intron_variant | MODIFIER | c.530+20A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87441935 | ||||||
chr4:87441955
|
A | C | 6 | a0001c0001t0001g0008a0001c0001t0001g0109a0001c0001t0001g0110others(3): Show | 8 | HG02080.hp1 NA18952.hp2 NA18964.hp1 others(5): Show |
intron_variant | MODIFIER | c.530+40A>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87441955 | ||||||
chr4:87442033
|
G | A | 1 | a0001c0001t0001g0159 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.530+118G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87442033 | ||||||
chr4:87442065
|
C | T | 56 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0011others(53): Show | 69 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.530+150C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87442065 | ||||||
chr4:87442279
|
G | A | 15 | a0001c0002t0001g0308a0001c0002t0001g0309a0001c0002t0001g0310others(12): Show | 15 | HG01891.hp2 HG02055.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.530+364G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87442279 | ||||||
chr4:87442323
|
C | T | 1 | a0001c0001t0001g0210 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.530+408C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87442323 | ||||||
chr4:87442330
|
A | G | 1 | a0001c0002t0001g0236 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.530+415A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87442330 | ||||||
chr4:87442613
|
AAC | A | 5 | a0001c0001t0001g0022a0001c0001t0001g0088a0001c0001t0001g0089others(2): Show | 6 | NA18949.hp1 NA18964.hp2 NA18967.hp1 others(3): Show |
intron_variant | MODIFIER | c.530+702_530+703del others(2): Show |
NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 87442613 | |||||
chr4:87442720
|
T | C | 2 | a0002c0005t0002g0294a0002c0005t0016g0293 | 2 | HG03041.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.530+805T>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87442720 | ||||||
chr4:87442828
|
CAG | C | 2 | a0001c0001t0001g0020a0001c0001t0001g0083 | 3 | HG03490.hp2 HG03492.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.530+914_530+915del others(2): Show |
NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87442828 | ||||||
chr4:87442983
|
A | G | 4 | a0001c0002t0007g0043a0001c0002t0007g0306a0001c0002t0007g0307others(1): Show | 5 | HG02486.hp2 HG02809.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.530+1068A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87442983 | ||||||
chr4:87443054
|
T | A | 7 | a0001c0001t0002g0246a0001c0001t0002g0255a0001c0001t0002g0256others(4): Show | 7 | HG00408.hp1 HG00423.hp1 NA18947.hp2 others(4): Show |
intron_variant | MODIFIER | c.530+1139T>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87443054 | ||||||
chr4:87443116
|
G | A | 7 | a0002c0003t0003g0006a0002c0003t0003g0034a0002c0003t0003g0233others(4): Show | 12 | HG00639.hp2 HG01884.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.530+1201G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87443116 | ||||||
chr4:87443179
|
T | C | 53 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0035others(50): Show | 64 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.530+1264T>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87443179 | ||||||
chr4:87443243
|
G | A | 1 | a0001c0001t0004g0136 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.530+1328G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87443243 | ||||||
chr4:87443260
|
CAT | C | 67 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(64): Show | 86 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.530+1346_530+1347d others(4): Show |
NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87443260 | ||||||
chr4:87443352
|
A | G | 2 | a0001c0001t0001g0027a0001c0001t0001g0147 | 3 | HG01192.hp1 HG01243.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.530+1437A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87443352 | ||||||
chr4:87443473
|
A | G | 4 | a0001c0002t0001g0308a0001c0002t0001g0309a0001c0002t0001g0310others(1): Show | 4 | HG02055.hp2 HG02895.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.530+1558A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87443473 | ||||||
chr4:87443605
|
C | T | 2 | a0001c0001t0001g0119a0001c0001t0001g0129 | 2 | HG00642.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.530+1690C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87443605 | ||||||
chr4:87443664
|
A | G | 2 | a0002c0005t0002g0294a0002c0005t0016g0293 | 2 | HG03041.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.530+1749A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87443664 | ||||||
chr4:87443682
|
G | A | 1 | a0001c0001t0018g0239 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.530+1767G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87443682 | ||||||
chr4:87443722
|
C | A | 2 | a0002c0003t0003g0034a0002c0003t0003g0233 | 3 | HG00639.hp2 HG02257.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.530+1807C>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87443722 | ||||||
chr4:87443761
|
A | G | 5 | a0001c0001t0004g0026a0001c0001t0004g0143a0001c0001t0004g0144others(2): Show | 6 | HG01167.hp2 HG02559.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.530+1846A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87443761 | ||||||
chr4:87443895
|
T | C | 1 | a0001c0001t0001g0062 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.530+1980T>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87443895 | ||||||
chr4:87443913
|
G | A | 27 | a0001c0002t0001g0298a0001c0002t0001g0299a0001c0002t0001g0300others(24): Show | 29 | HG01891.hp2 HG02055.hp2 HG02258.hp2 others(26): Show |
intron_variant | MODIFIER | c.530+1998G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87443913 | ||||||
chr4:87443920
|
G | A | 1 | a0001c0001t0004g0153 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.530+2005G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87443920 | ||||||
chr4:87443931
|
C | T | 135 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(132): Show | 167 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.530+2016C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87443931 | ||||||
chr4:87444092
|
T | C | 1 | a0001c0002t0001g0236 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.530+2177T>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87444092 | ||||||
chr4:87444176
|
A | C | 1 | a0001c0002t0020g0312 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.530+2261A>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87444176 | ||||||
chr4:87444296
|
A | G | 22 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0021others(19): Show | 32 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(29): Show |
intron_variant | MODIFIER | c.530+2381A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87444296 | ||||||
chr4:87444335
|
T | A | 213 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(210): Show | 265 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(262): Show |
intron_variant | MODIFIER | c.530+2420T>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87444335 | ||||||
chr4:87444475
|
T | C | 1 | a0002c0005t0016g0293 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.530+2560T>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87444475 | ||||||
chr4:87444607
|
T | G | 1 | a0001c0001t0001g0168 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.530+2692T>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87444607 | ||||||
chr4:87444678
|
G | A | 312 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(309): Show | 385 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(382): Show |
intron_variant | MODIFIER | c.530+2763G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87444678 | ||||||
chr4:87444790
|
C | T | 1 | a0001c0001t0001g0113 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.530+2875C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87444790 | ||||||
chr4:87444987
|
C | T | 1 | a0001c0001t0018g0239 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.530+3072C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87444987 | ||||||
chr4:87445093
|
C | G | 1 | a0001c0001t0001g0118 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.530+3178C>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87445093 | ||||||
chr4:87445180
|
G | C | 1 | a0001c0002t0014g0305 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.530+3265G>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87445180 | ||||||
chr4:87445335
|
T | C | 1 | a0001c0001t0001g0017 | 2 | HG02280.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.530+3420T>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87445335 | ||||||
chr4:87445349
|
C | T | 5 | a0002c0003t0003g0006a0002c0003t0003g0034a0002c0003t0003g0233others(2): Show | 10 | HG00639.hp2 HG01884.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.530+3434C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87445349 | ||||||
chr4:87445474
|
G | A | 4 | a0001c0002t0001g0308a0001c0002t0001g0309a0001c0002t0001g0310others(1): Show | 4 | HG02055.hp2 HG02895.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.530+3559G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87445474 | ||||||
chr4:87445567
|
A | G | 1 | a0001c0002t0001g0236 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.531-3575A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87445567 | ||||||
chr4:87445765
|
A | G | 1 | a0001c0001t0001g0221 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.531-3377A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87445765 | ||||||
chr4:87445853
|
C | T | 1 | a0001c0001t0001g0158 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.531-3289C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87445853 | ||||||
chr4:87445879
|
T | C | 1 | a0001c0001t0001g0205 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.531-3263T>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87445879 | ||||||
chr4:87445896
|
C | T | 1 | a0001c0002t0001g0299 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.531-3246C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87445896 | ||||||
chr4:87445933
|
CT | C | 8 | a0001c0001t0001g0114a0001c0001t0001g0169a0001c0001t0001g0183others(5): Show | 8 | HG01167.hp1 HG01256.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.531-3194delT | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 87445933 | |||||
chr4:87445994
|
T | G | 213 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(210): Show | 265 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(262): Show |
intron_variant | MODIFIER | c.531-3148T>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87445994 | ||||||
chr4:87446015
|
C | T | 77 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0035others(74): Show | 97 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.531-3127C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87446015 | ||||||
chr4:87446079
|
A | G | 1 | a0001c0001t0001g0117 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.531-3063A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87446079 | ||||||
chr4:87446087
|
C | T | 6 | a0001c0001t0003g0004a0001c0001t0003g0126a0001c0001t0003g0131others(3): Show | 10 | HG00140.hp2 HG01123.hp1 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.531-3055C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87446087 | ||||||
chr4:87446091
|
T | G | 1 | a0001c0001t0001g0063 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.531-3051T>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87446091 | ||||||
chr4:87446247
|
C | CT | 76 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0021others(73): Show | 98 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.531-2876dupT | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 87446247 | |||||
chr4:87446247
|
C | CTT | 58 | a0001c0001t0001g0007a0001c0001t0001g0017a0001c0001t0001g0018others(55): Show | 67 | HG00099.hp2 HG00609.hp2 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.531-2877_531-2876d others(4): Show |
NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 87446247 | |||||
chr4:87446247
|
C | CTTT | 71 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0011others(68): Show | 88 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.531-2878_531-2876d others(5): Show |
NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 87446247 | |||||
chr4:87446247
|
C | CTTTT | 6 | a0001c0001t0001g0112a0001c0001t0001g0124a0001c0001t0001g0128others(3): Show | 6 | HG01884.hp1 HG02155.hp1 NA18961.hp1 others(3): Show |
intron_variant | MODIFIER | c.531-2879_531-2876d others(6): Show |
NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 87446247 | |||||
chr4:87446247
|
C | CTTTTT | 4 | a0002c0003t0003g0006a0002c0003t0003g0034a0002c0003t0003g0233others(1): Show | 9 | HG00639.hp2 HG02257.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.531-2880_531-2876d others(7): Show |
NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 87446247 | |||||
chr4:87446317
|
C | T | 56 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0011others(53): Show | 69 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.531-2825C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87446317 | ||||||
chr4:87446355
|
C | T | 1 | a0001c0001t0004g0153 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.531-2787C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87446355 | ||||||
chr4:87446373
|
C | G | 1 | a0001c0001t0018g0239 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.531-2769C>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87446373 | ||||||
chr4:87446411
|
A | G | 5 | a0001c0001t0001g0022a0001c0001t0001g0088a0001c0001t0001g0089others(2): Show | 6 | NA18949.hp1 NA18964.hp2 NA18967.hp1 others(3): Show |
intron_variant | MODIFIER | c.531-2731A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87446411 | ||||||
chr4:87446435
|
A | G | 1 | a0001c0001t0001g0158 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.531-2707A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87446435 | ||||||
chr4:87446589
|
G | A | 3 | a0001c0002t0001g0301a0001c0002t0001g0303a0001c0002t0001g0304 | 3 | HG02572.hp1 HG02630.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.531-2553G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87446589 | ||||||
chr4:87446638
|
A | G | 4 | a0001c0002t0001g0308a0001c0002t0001g0309a0001c0002t0001g0310others(1): Show | 4 | HG02055.hp2 HG02895.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.531-2504A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87446638 | ||||||
chr4:87446724
|
A | G | 1 | a0001c0001t0018g0239 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.531-2418A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87446724 | ||||||
chr4:87446750
|
G | A | 1 | a0001c0001t0001g0056 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.531-2392G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87446750 | ||||||
chr4:87446978
|
A | T | 1 | a0001c0001t0001g0196 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.531-2164A>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87446978 | ||||||
chr4:87446988
|
C | G | 4 | a0001c0002t0007g0043a0001c0002t0007g0306a0001c0002t0007g0307others(1): Show | 5 | HG02486.hp2 HG02809.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.531-2154C>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87446988 | ||||||
chr4:87447003
|
G | A | 1 | a0001c0001t0001g0024 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.531-2139G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87447003 | ||||||
chr4:87447080
|
T | C | 1 | a0001c0002t0001g0236 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.531-2062T>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87447080 | ||||||
chr4:87447167
|
A | G | 1 | a0001c0001t0002g0263 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.531-1975A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87447167 | ||||||
chr4:87447198
|
G | A | 6 | a0001c0002t0001g0298a0001c0002t0001g0299a0001c0002t0001g0300others(3): Show | 6 | HG02572.hp1 HG02630.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.531-1944G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87447198 | ||||||
chr4:87447476
|
GT | G | 78 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0035others(75): Show | 98 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.531-1652delT | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 87447476 | |||||
chr4:87447486
|
T | G | 25 | a0001c0001t0001g0113a0001c0001t0001g0115a0001c0001t0001g0133others(22): Show | 27 | HG00408.hp1 HG00423.hp1 HG01167.hp2 others(24): Show |
intron_variant | MODIFIER | c.531-1656T>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87447486 | ||||||
chr4:87447487
|
T | G | 15 | a0001c0002t0001g0308a0001c0002t0001g0309a0001c0002t0001g0310others(12): Show | 15 | HG01891.hp2 HG02055.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.531-1655T>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87447487 | ||||||
chr4:87447501
|
G | T | 77 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0035others(74): Show | 97 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.531-1641G>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87447501 | ||||||
chr4:87447579
|
G | A | 1 | a0001c0001t0001g0196 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.531-1563G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87447579 | ||||||
chr4:87447591
|
T | C | 2 | a0001c0001t0001g0186a0001c0001t0001g0187 | 2 | HG00558.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.531-1551T>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87447591 | ||||||
chr4:87447678
|
A | G | 135 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(132): Show | 167 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.531-1464A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87447678 | ||||||
chr4:87447760
|
C | T | 1 | a0001c0001t0001g0207 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.531-1382C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87447760 | ||||||
chr4:87447833
|
A | T | 1 | a0001c0001t0001g0196 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.531-1309A>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87447833 | ||||||
chr4:87447935
|
G | A | 1 | a0001c0001t0018g0239 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.531-1207G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87447935 | ||||||
chr4:87448034
|
T | A | 2 | a0001c0001t0001g0048a0001c0001t0013g0155 | 2 | HG03225.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.531-1108T>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87448034 | ||||||
chr4:87448035
|
A | T | 18 | a0001c0001t0001g0031a0001c0001t0001g0094a0001c0001t0001g0175others(15): Show | 19 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(16): Show |
intron_variant | MODIFIER | c.531-1107A>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87448035 | ||||||
chr4:87448036
|
A | T | 9 | a0001c0001t0001g0031a0001c0001t0001g0186a0001c0001t0001g0187others(6): Show | 10 | HG00423.hp2 HG00558.hp1 HG02056.hp1 others(7): Show |
intron_variant | MODIFIER | c.531-1106A>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87448036 | ||||||
chr4:87448040
|
A | C | 1 | a0001c0002t0001g0236 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.531-1102A>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87448040 | ||||||
chr4:87448055
|
T | C | 5 | a0001c0001t0001g0012a0001c0001t0001g0156a0001c0001t0001g0175others(2): Show | 7 | HG00438.hp2 HG02040.hp2 NA18941.hp1 others(4): Show |
intron_variant | MODIFIER | c.531-1087T>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87448055 | ||||||
chr4:87448138
|
A | AT | 31 | a0001c0001t0001g0029a0001c0001t0001g0032a0001c0001t0001g0166others(28): Show | 33 | HG00423.hp1 HG01952.hp2 HG02027.hp2 others(30): Show |
intron_variant | MODIFIER | c.531-980dupT | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 87448138 | |||||
chr4:87448138
|
AT | A | 153 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(150): Show | 191 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(188): Show |
intron_variant | MODIFIER | c.531-980delT | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 87448138 | |||||
chr4:87448138
|
ATT | A | 12 | a0001c0001t0001g0060a0001c0001t0002g0266a0001c0001t0002g0267others(9): Show | 16 | HG00140.hp2 HG01123.hp1 HG01192.hp2 others(13): Show |
intron_variant | MODIFIER | c.531-981_531-980del others(2): Show |
NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 87448138 | |||||
chr4:87448207
|
C | T | 5 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(2): Show | 5 | NA18961.hp1 NA18962.hp1 NA18993.hp1 others(2): Show |
intron_variant | MODIFIER | c.531-935C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87448207 | ||||||
chr4:87448223
|
C | T | 135 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(132): Show | 167 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.531-919C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87448223 | ||||||
chr4:87448411
|
T | G | 1 | a0001c0001t0001g0196 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.531-731T>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87448411 | ||||||
chr4:87448442
|
C | T | 1 | a0001c0001t0001g0160 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.531-700C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87448442 | ||||||
chr4:87448446
|
A | G | 55 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0011others(52): Show | 67 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.531-696A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87448446 | ||||||
chr4:87448521
|
G | A | 1 | a0001c0001t0001g0094 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.531-621G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87448521 | ||||||
chr4:87448634
|
C | T | 54 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0011others(51): Show | 66 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(63): Show |
intron_variant | MODIFIER | c.531-508C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87448634 | ||||||
chr4:87448657
|
T | C | 1 | a0001c0001t0001g0196 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.531-485T>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87448657 | ||||||
chr4:87448723
|
T | A | 9 | a0001c0002t0001g0298a0001c0002t0001g0299a0001c0002t0001g0300others(6): Show | 10 | HG02258.hp2 HG02572.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.531-419T>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87448723 | ||||||
chr4:87448744
|
A | C | 1 | a0001c0001t0019g0252 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.531-398A>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87448744 | ||||||
chr4:87448746
|
T | C | 1 | a0002c0005t0016g0293 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.531-396T>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87448746 | ||||||
chr4:87449453
|
G | A | 1 | a0001c0001t0001g0185 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.642+200G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 5/7 | chr4 | 87449453 | ||||||
chr4:87449530
|
C | T | 1 | a0001c0001t0001g0173 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.642+277C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 5/7 | chr4 | 87449530 | ||||||
chr4:87449590
|
A | G | 1 | a0001c0001t0009g0216 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.642+337A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 5/7 | chr4 | 87449590 | ||||||
chr4:87449737
|
T | A | 1 | a0001c0001t0018g0239 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.642+484T>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 5/7 | chr4 | 87449737 | ||||||
chr4:87449867
|
T | C | 5 | a0001c0001t0004g0026a0001c0001t0004g0143a0001c0001t0004g0144others(2): Show | 6 | HG01167.hp2 HG02559.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.642+614T>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 5/7 | chr4 | 87449867 | ||||||
chr4:87450038
|
A | C | 135 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(132): Show | 167 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.642+785A>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 5/7 | chr4 | 87450038 | ||||||
chr4:87450174
|
C | T | 1 | a0001c0002t0001g0236 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.642+921C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 5/7 | chr4 | 87450174 | ||||||
chr4:87450259
|
C | G | 1 | a0001c0001t0001g0194 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.642+1006C>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 5/7 | chr4 | 87450259 | ||||||
chr4:87450339
|
G | A | 55 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0011others(52): Show | 67 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.642+1086G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 5/7 | chr4 | 87450339 | ||||||
chr4:87450372
|
CTTTTTCT others(5): Show |
C | 1 | a0001c0002t0020g0312 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.642+1125_642+1136d others(14): Show |
NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 87450372 | |||||
chr4:87450378
|
C | CT | 9 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0215others(6): Show | 9 | HG03225.hp1 HG03491.hp2 HG03669.hp2 others(6): Show |
intron_variant | MODIFIER | c.642+1145dupT | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 87450378 | |||||
chr4:87450378
|
CT | C | 140 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(137): Show | 174 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.642+1145delT | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 87450378 | |||||
chr4:87450378
|
CTT | C | 10 | a0001c0001t0001g0024a0001c0001t0001g0070a0001c0001t0003g0126others(7): Show | 16 | HG00639.hp2 HG01256.hp2 HG01257.hp1 others(13): Show |
intron_variant | MODIFIER | c.642+1144_642+1145d others(4): Show |
NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 87450378 | |||||
chr4:87450383
|
T | C | 1 | a0001c0001t0002g0255 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.642+1130T>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 5/7 | chr4 | 87450383 | ||||||
chr4:87450384
|
T | C | 1 | a0001c0001t0018g0239 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.642+1131T>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 5/7 | chr4 | 87450384 | ||||||
chr4:87450412
|
A | T | 1 | a0001c0001t0001g0194 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.642+1159A>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 5/7 | chr4 | 87450412 | ||||||
chr4:87450464
|
C | T | 1 | a0001c0002t0001g0317 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.643-1125C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 5/7 | chr4 | 87450464 | ||||||
chr4:87450487
|
C | G | 4 | a0001c0002t0007g0043a0001c0002t0007g0306a0001c0002t0007g0307others(1): Show | 5 | HG02486.hp2 HG02809.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.643-1102C>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 5/7 | chr4 | 87450487 | ||||||
chr4:87450523
|
C | T | 5 | a0002c0003t0003g0006a0002c0003t0003g0034a0002c0003t0003g0233others(2): Show | 10 | HG00639.hp2 HG01884.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.643-1066C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 5/7 | chr4 | 87450523 | ||||||
chr4:87450666
|
T | C | 212 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(209): Show | 264 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(261): Show |
intron_variant | MODIFIER | c.643-923T>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 5/7 | chr4 | 87450666 | ||||||
chr4:87450765
|
G | A | 1 | a0001c0002t0001g0300 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.643-824G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 5/7 | chr4 | 87450765 | ||||||
chr4:87450789
|
C | A | 54 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0035others(51): Show | 65 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.643-800C>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 5/7 | chr4 | 87450789 | ||||||
chr4:87450804
|
C | T | 1 | a0001c0001t0013g0155 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.643-785C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 5/7 | chr4 | 87450804 | ||||||
chr4:87450887
|
C | G | 1 | a0001c0002t0001g0322 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.643-702C>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 5/7 | chr4 | 87450887 | ||||||
chr4:87450990
|
G | A | 1 | a0001c0001t0001g0158 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.643-599G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 5/7 | chr4 | 87450990 | ||||||
chr4:87451257
|
G | A | 1 | a0001c0001t0001g0017 | 2 | HG02280.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.643-332G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 5/7 | chr4 | 87451257 | ||||||
chr4:87451356
|
G | T | 3 | a0001c0001t0001g0033a0001c0001t0001g0162a0001c0001t0001g0179 | 4 | HG02165.hp1 NA18946.hp1 NA18953.hp2 others(1): Show |
intron_variant | MODIFIER | c.643-233G>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 5/7 | chr4 | 87451356 | ||||||
chr4:87451520
|
ACTC | A | 10 | a0001c0002t0001g0315a0001c0002t0001g0316a0001c0002t0001g0317others(7): Show | 10 | HG01891.hp2 HG02451.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.643-68_643-66delCT others(1): Show |
NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 5/7 | chr4 | 87451520 | ||||||
chr4:87451797
|
T | C | 4 | a0001c0001t0002g0258a0001c0001t0002g0277a0001c0001t0002g0282others(1): Show | 4 | HG02071.hp1 HG02074.hp1 HG02155.hp2 others(1): Show |
intron_variant | MODIFIER | c.789+62T>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 6/7 | chr4 | 87451797 | ||||||
chr4:87451855
|
A | C | 1 | a0001c0002t0001g0236 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.789+120A>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 6/7 | chr4 | 87451855 | ||||||
chr4:87451926
|
T | G | 1 | a0001c0002t0001g0300 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.789+191T>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 6/7 | chr4 | 87451926 | ||||||
chr4:87451960
|
TTC | T | 5 | a0002c0003t0003g0006a0002c0003t0003g0034a0002c0003t0003g0233others(2): Show | 10 | HG00639.hp2 HG01884.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.789+226_789+227del others(2): Show |
NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 6/7 | chr4 | 87451960 | ||||||
chr4:87451973
|
T | A | 1 | a0001c0001t0001g0196 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.789+238T>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 6/7 | chr4 | 87451973 | ||||||
chr4:87451979
|
A | G | 54 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0035others(51): Show | 65 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.789+244A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 6/7 | chr4 | 87451979 | ||||||
chr4:87452163
|
C | T | 1 | a0002c0005t0016g0293 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.789+428C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 6/7 | chr4 | 87452163 | ||||||
chr4:87452300
|
G | T | 1 | a0002c0003t0003g0233 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.789+565G>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 6/7 | chr4 | 87452300 | ||||||
chr4:87452311
|
A | G | 77 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0035others(74): Show | 97 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.789+576A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 6/7 | chr4 | 87452311 | ||||||
chr4:87452516
|
T | G | 1 | a0001c0001t0013g0155 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.789+781T>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 6/7 | chr4 | 87452516 | ||||||
chr4:87452606
|
G | A | 1 | a0001c0001t0001g0121 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.789+871G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 6/7 | chr4 | 87452606 | ||||||
chr4:87452618
|
T | C | 4 | a0002c0003t0003g0006a0002c0003t0003g0034a0002c0003t0003g0233others(1): Show | 9 | HG00639.hp2 HG01884.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.789+883T>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 6/7 | chr4 | 87452618 | ||||||
chr4:87452624
|
G | A | 1 | a0001c0001t0001g0184 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.789+889G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 6/7 | chr4 | 87452624 | ||||||
chr4:87452663
|
C | T | 1 | a0001c0001t0004g0142 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.789+928C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 6/7 | chr4 | 87452663 | ||||||
chr4:87452700
|
C | T | 69 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(66): Show | 88 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.789+965C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 6/7 | chr4 | 87452700 | ||||||
chr4:87452809
|
G | GT | 134 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(131): Show | 167 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.789+1094dupT | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 87452809 | |||||
chr4:87452809
|
G | GTT | 9 | a0001c0001t0001g0055a0001c0001t0001g0085a0001c0001t0001g0096others(6): Show | 9 | HG01167.hp2 HG01981.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.789+1093_789+1094d others(4): Show |
NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 87452809 | |||||
chr4:87452809
|
GT | G | 10 | a0001c0001t0001g0156a0001c0001t0002g0247a0001c0001t0002g0249others(7): Show | 10 | HG02055.hp1 HG02071.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.789+1094delT | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 87452809 | |||||
chr4:87452809
|
GTT | G | 45 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0035others(42): Show | 56 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.789+1093_789+1094d others(4): Show |
NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 87452809 | |||||
chr4:87452993
|
G | A | 10 | a0001c0001t0004g0135a0001c0001t0004g0136a0001c0001t0004g0137others(7): Show | 10 | HG01109.hp1 HG02258.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.789+1258G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 6/7 | chr4 | 87452993 | ||||||
chr4:87453084
|
T | G | 4 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0046others(1): Show | 4 | HG03195.hp2 HG03486.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.790-1287T>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 6/7 | chr4 | 87453084 | ||||||
chr4:87453107
|
C | T | 1 | a0001c0001t0001g0025 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.790-1264C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 6/7 | chr4 | 87453107 | ||||||
chr4:87453223
|
C | T | 3 | a0001c0002t0006g0042a0001c0002t0006g0296a0001c0002t0006g0297 | 4 | HG02258.hp2 HG02976.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.790-1148C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 6/7 | chr4 | 87453223 | ||||||
chr4:87453371
|
T | C | 1 | a0001c0001t0001g0116 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.790-1000T>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 6/7 | chr4 | 87453371 | ||||||
chr4:87453498
|
C | T | 1 | a0001c0001t0001g0134 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.790-873C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 6/7 | chr4 | 87453498 | ||||||
chr4:87453611
|
G | T | 27 | a0001c0002t0001g0298a0001c0002t0001g0299a0001c0002t0001g0300others(24): Show | 29 | HG01891.hp2 HG02055.hp2 HG02258.hp2 others(26): Show |
intron_variant | MODIFIER | c.790-760G>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 6/7 | chr4 | 87453611 | ||||||
chr4:87453780
|
G | A | 1 | a0001c0001t0001g0192 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.790-591G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 6/7 | chr4 | 87453780 | ||||||
chr4:87453813
|
A | G | 3 | a0001c0001t0004g0135a0001c0001t0004g0139a0001c0001t0004g0141 | 3 | HG01109.hp1 HG02896.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.790-558A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 6/7 | chr4 | 87453813 | ||||||
chr4:87453861
|
C | CT | 16 | a0001c0001t0001g0195a0001c0001t0002g0266a0001c0001t0002g0267others(13): Show | 20 | HG00140.hp2 HG01123.hp1 HG01192.hp2 others(17): Show |
intron_variant | MODIFIER | c.790-495dupT | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 87453861 | |||||
chr4:87453861
|
CT | C | 6 | a0001c0001t0001g0093a0001c0001t0001g0210a0001c0001t0002g0245others(3): Show | 6 | HG01070.hp1 HG02071.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.790-495delT | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 87453861 | |||||
chr4:87453928
|
G | T | 5 | a0002c0003t0003g0006a0002c0003t0003g0034a0002c0003t0003g0233others(2): Show | 10 | HG00639.hp2 HG01884.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.790-443G>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 6/7 | chr4 | 87453928 | ||||||
chr4:87453985
|
G | C | 4 | a0001c0002t0001g0308a0001c0002t0001g0309a0001c0002t0001g0310others(1): Show | 4 | HG02055.hp2 HG02895.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.790-386G>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 6/7 | chr4 | 87453985 | ||||||
chr4:87453992
|
C | T | 1 | a0001c0001t0001g0208 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.790-379C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 6/7 | chr4 | 87453992 | ||||||
chr4:87454059
|
C | T | 1 | a0002c0005t0016g0293 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.790-312C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 6/7 | chr4 | 87454059 | ||||||
chr4:87454181
|
A | C | 2 | a0001c0001t0002g0268a0001c0001t0002g0270 | 2 | HG01884.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.790-190A>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 6/7 | chr4 | 87454181 | ||||||
chr4:87454778
|
G | A | 1 | a0001c0001t0001g0203 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.874+323G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 7/7 | chr4 | 87454778 | ||||||
chr4:87455464
|
C | T | 1 | a0001c0001t0001g0020 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.874+1009C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 7/7 | chr4 | 87455464 | ||||||
chr4:87455611
|
A | G | 77 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0035others(74): Show | 97 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.874+1156A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 7/7 | chr4 | 87455611 | ||||||
chr4:87455629
|
CG | C | 3 | a0001c0002t0006g0042a0001c0002t0006g0296a0001c0002t0006g0297 | 4 | HG02258.hp2 HG02976.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.874+1175delG | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 7/7 | chr4 | 87455629 | ||||||
chr4:87455630
|
G | A | 238 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(235): Show | 291 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(288): Show |
intron_variant | MODIFIER | c.874+1175G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 7/7 | chr4 | 87455630 | ||||||
chr4:87455651
|
CTTTTTTC others(9): Show |
C | 1 | a0001c0001t0002g0038 | 2 | NA18948.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.874+1203_874+1218d others(18): Show |
NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 87455651 | |||||
chr4:87455658
|
CT | C | 9 | a0001c0001t0001g0049a0001c0001t0001g0158a0001c0001t0001g0174others(6): Show | 9 | HG01516.hp1 HG02897.hp1 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.874+1218delT | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 87455658 | |||||
chr4:87455812
|
C | T | 1 | a0001c0001t0010g0127 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.874+1357C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 7/7 | chr4 | 87455812 | ||||||
chr4:87455822
|
T | A | 7 | a0002c0003t0003g0006a0002c0003t0003g0034a0002c0003t0003g0233others(4): Show | 12 | HG00639.hp2 HG01884.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.874+1367T>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 7/7 | chr4 | 87455822 | ||||||
chr4:87455852
|
G | A | 1 | a0001c0002t0001g0236 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.874+1397G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 7/7 | chr4 | 87455852 | ||||||
chr4:87455853
|
G | A | 54 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0011others(51): Show | 66 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(63): Show |
intron_variant | MODIFIER | c.874+1398G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 7/7 | chr4 | 87455853 | ||||||
chr4:87455858
|
C | A | 1 | a0001c0001t0001g0160 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.874+1403C>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 7/7 | chr4 | 87455858 | ||||||
chr4:87455894
|
T | G | 1 | a0001c0001t0018g0239 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.874+1439T>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 7/7 | chr4 | 87455894 | ||||||
chr4:87455906
|
C | T | 1 | a0001c0001t0018g0239 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.874+1451C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 7/7 | chr4 | 87455906 | ||||||
chr4:87456018
|
A | T | 1 | a0001c0001t0001g0218 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.874+1563A>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 7/7 | chr4 | 87456018 | ||||||
chr4:87456042
|
T | A | 19 | a0001c0002t0001g0308a0001c0002t0001g0309a0001c0002t0001g0310others(16): Show | 20 | HG01891.hp2 HG02055.hp2 HG02451.hp1 others(17): Show |
intron_variant | MODIFIER | c.874+1587T>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 7/7 | chr4 | 87456042 | ||||||
chr4:87456172
|
G | C | 54 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0011others(51): Show | 66 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(63): Show |
intron_variant | MODIFIER | c.875-1671G>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 7/7 | chr4 | 87456172 | ||||||
chr4:87456430
|
T | C | 4 | a0001c0002t0001g0308a0001c0002t0001g0309a0001c0002t0001g0310others(1): Show | 4 | HG02055.hp2 HG02895.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.875-1413T>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 7/7 | chr4 | 87456430 | ||||||
chr4:87456501
|
G | A | 1 | a0001c0001t0002g0256 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.875-1342G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 7/7 | chr4 | 87456501 | ||||||
chr4:87456582
|
A | G | 1 | a0001c0001t0001g0231 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.875-1261A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 7/7 | chr4 | 87456582 | ||||||
chr4:87456820
|
A | T | 1 | a0001c0001t0002g0282 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.875-1023A>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 7/7 | chr4 | 87456820 | ||||||
chr4:87456824
|
G | A | 3 | a0001c0001t0002g0266a0001c0001t0002g0267a0001c0001t0002g0288 | 3 | HG02895.hp1 HG02897.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.875-1019G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 7/7 | chr4 | 87456824 | ||||||
chr4:87457060
|
C | T | 1 | a0001c0002t0001g0236 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.875-783C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 7/7 | chr4 | 87457060 | ||||||
chr4:87457236
|
A | AT | 72 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0011others(69): Show | 86 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.875-589dupT | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 87457236 | |||||
chr4:87457236
|
AT | A | 75 | a0001c0001t0001g0074a0001c0001t0001g0157a0001c0001t0002g0015others(72): Show | 95 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.875-589delT | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 87457236 | |||||
chr4:87457437
|
A | G | 1 | a0001c0001t0001g0013 | 3 | HG00099.hp1 HG02602.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.875-406A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 7/7 | chr4 | 87457437 | ||||||
chr4:87457455
|
T | A | 1 | a0001c0001t0001g0068 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.875-388T>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 7/7 | chr4 | 87457455 | ||||||
chr4:87457456
|
C | T | 66 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(63): Show | 85 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.875-387C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 7/7 | chr4 | 87457456 | ||||||
chr4:87457461
|
T | G | 1 | a0001c0001t0001g0068 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.875-382T>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 7/7 | chr4 | 87457461 | ||||||
chr4:87457462
|
C | A | 1 | a0001c0001t0001g0068 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.875-381C>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 7/7 | chr4 | 87457462 | ||||||
chr4:87457464
|
T | G | 1 | a0001c0001t0001g0068 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.875-379T>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 7/7 | chr4 | 87457464 | ||||||
chr4:87457465
|
G | A | 1 | a0001c0001t0001g0068 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.875-378G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 7/7 | chr4 | 87457465 | ||||||
chr4:87457466
|
A | T | 1 | a0001c0001t0001g0068 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.875-377A>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 7/7 | chr4 | 87457466 | ||||||
chr4:87457467
|
C | G | 1 | a0001c0001t0001g0068 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.875-376C>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 7/7 | chr4 | 87457467 | ||||||
chr4:87457468
|
C | T | 1 | a0001c0001t0001g0068 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.875-375C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 7/7 | chr4 | 87457468 | ||||||
chr4:87457478
|
C | G | 3 | a0001c0001t0002g0266a0001c0001t0002g0267a0001c0001t0002g0288 | 3 | HG02895.hp1 HG02897.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.875-365C>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 7/7 | chr4 | 87457478 | ||||||
chr4:87457484
|
G | T | 7 | a0002c0003t0003g0006a0002c0003t0003g0034a0002c0003t0003g0233others(4): Show | 12 | HG00639.hp2 HG01884.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.875-359G>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 7/7 | chr4 | 87457484 | ||||||
chr4:87457563
|
G | A | 242 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(239): Show | 296 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(293): Show |
intron_variant | MODIFIER | c.875-280G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 7/7 | chr4 | 87457563 | ||||||
chr4:87457666
|
A | G | 135 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(132): Show | 167 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.875-177A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 7/7 | chr4 | 87457666 | ||||||
chr4:87457667
|
G | T | 1 | a0001c0001t0001g0125 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.875-176G>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 7/7 | chr4 | 87457667 | ||||||
chr4:87457780
|
C | T | 1 | a0002c0005t0002g0294 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.875-63C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 7/7 | chr4 | 87457780 |