geneid | 22978 |
---|---|
ensemblid | ENSG00000076685.19 |
hgncid | 8022 |
symbol | NT5C2 |
name | 5'-nucleotidase, cytosolic II |
refseq_nuc | NM_001351169.2 |
refseq_prot | NP_001338098.1 |
ensembl_nuc | ENST00000404739.8 |
ensembl_prot | ENSP00000383960.3 |
mane_status | MANE Select |
chr | chr10 |
start | 103088038 |
end | 103193272 |
strand | - |
ver | v1.2 |
region | chr10:103088038-103193272 |
region5000 | chr10:103083038-103198272 |
regionname0 | NT5C2_chr10_103088038_103193272 |
regionname5000 | NT5C2_chr10_103083038_103198272 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 561 | 308 | 64 | 51 | 143 | 10 | 38 | 113 | NT5C2_chr10_103083038_103198272 | NT5C2 | copy fasta | chr10 | 103083038 | 103198272 |
a0002 | 0/0 | 561 | 31 | 2 | 11 | 16 | 2 | 0 | 11 | NT5C2_chr10_103083038_103198272 | NT5C2 | copy fasta | chr10 | 103083038 | 103198272 |
a0003 | 0/0 | 561 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | copy fasta | chr10 | 103083038 | 103198272 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1686 | 172 | 27 | 33 | 84 | 5 | 21 | NT5C2_chr10_103083038_103198272 | NT5C2 | copy fasta | chr10 | 103083038 | 103198272 |
c0002 | 0/0 | 1686 | 136 | 37 | 18 | 59 | 5 | 17 | NT5C2_chr10_103083038_103198272 | NT5C2 | copy fasta | chr10 | 103083038 | 103198272 |
c0003 | 0/0 | 1686 | 31 | 2 | 11 | 16 | 2 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | copy fasta | chr10 | 103083038 | 103198272 |
c0004 | 0/0 | 1686 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | copy fasta | chr10 | 103083038 | 103198272 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 1840 | 94 | 26 | 17 | 37 | 3 | 11 | NT5C2_chr10_103083038_103198272 | NT5C2 | copy fasta | chr10 | 103083038 | 103198272 |
t0002 | 1/1 | 1840 | 63 | 1 | 12 | 36 | 2 | 10 | NT5C2_chr10_103083038_103198272 | NT5C2 | copy fasta | chr10 | 103083038 | 103198272 |
t0003 | 0/0 | 1840 | 62 | 4 | 9 | 42 | 0 | 7 | NT5C2_chr10_103083038_103198272 | NT5C2 | copy fasta | chr10 | 103083038 | 103198272 |
t0004 | 0/0 | 1840 | 47 | 12 | 13 | 16 | 4 | 2 | NT5C2_chr10_103083038_103198272 | NT5C2 | copy fasta | chr10 | 103083038 | 103198272 |
t0005 | 0/0 | 1840 | 28 | 13 | 5 | 7 | 3 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | copy fasta | chr10 | 103083038 | 103198272 |
t0006 | 0/0 | 1840 | 17 | 0 | 2 | 9 | 0 | 6 | NT5C2_chr10_103083038_103198272 | NT5C2 | copy fasta | chr10 | 103083038 | 103198272 |
t0007 | 0/0 | 1840 | 8 | 0 | 0 | 8 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | copy fasta | chr10 | 103083038 | 103198272 |
t0008 | 0/0 | 1840 | 7 | 7 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | copy fasta | chr10 | 103083038 | 103198272 |
t0009 | 0/0 | 1840 | 3 | 0 | 0 | 3 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | copy fasta | chr10 | 103083038 | 103198272 |
t0010 | 0/0 | 1840 | 2 | 0 | 0 | 0 | 0 | 2 | NT5C2_chr10_103083038_103198272 | NT5C2 | copy fasta | chr10 | 103083038 | 103198272 |
t0011 | 0/0 | 1840 | 2 | 0 | 2 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | copy fasta | chr10 | 103083038 | 103198272 |
t0012 | 0/0 | 1840 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | copy fasta | chr10 | 103083038 | 103198272 |
t0013 | 0/0 | 1840 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | copy fasta | chr10 | 103083038 | 103198272 |
t0014 | 0/0 | 1840 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | copy fasta | chr10 | 103083038 | 103198272 |
t0015 | 0/0 | 1840 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | copy fasta | chr10 | 103083038 | 103198272 |
t0016 | 0/0 | 1840 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | copy fasta | chr10 | 103083038 | 103198272 |
t0017 | 0/0 | 1840 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | copy fasta | chr10 | 103083038 | 103198272 |
t0018 | 0/0 | 1840 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | copy fasta | chr10 | 103083038 | 103198272 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0262 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0289 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0302 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0321 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0331 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0332 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1686 | 172 | 27 | 33 | 84 | 5 | 21 | NT5C2_chr10_103083038_103198272 | NT5C2 | copy fasta | chr10 | 103083038 | 103198272 |
a0001c0002 | 0/0 | 1686 | 136 | 37 | 18 | 59 | 5 | 17 | NT5C2_chr10_103083038_103198272 | NT5C2 | copy fasta | chr10 | 103083038 | 103198272 |
a0002c0003 | 0/0 | 1686 | 31 | 2 | 11 | 16 | 2 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | copy fasta | chr10 | 103083038 | 103198272 |
a0003c0004 | 0/0 | 1686 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | copy fasta | chr10 | 103083038 | 103198272 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 3525 | 94 | 26 | 17 | 37 | 3 | 11 | NT5C2_chr10_103083038_103198272 | NT5C2 | copy fasta | chr10 | 103083038 | 103198272 |
a0001c0001t0002 | 1/1 | 3525 | 63 | 1 | 12 | 36 | 2 | 10 | NT5C2_chr10_103083038_103198272 | NT5C2 | copy fasta | chr10 | 103083038 | 103198272 |
a0001c0001t0005 | 0/0 | 3525 | 2 | 0 | 0 | 2 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | copy fasta | chr10 | 103083038 | 103198272 |
a0001c0001t0007 | 0/0 | 3525 | 8 | 0 | 0 | 8 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | copy fasta | chr10 | 103083038 | 103198272 |
a0001c0001t0011 | 0/0 | 3525 | 2 | 0 | 2 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | copy fasta | chr10 | 103083038 | 103198272 |
a0001c0001t0012 | 0/0 | 3525 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | copy fasta | chr10 | 103083038 | 103198272 |
a0001c0001t0016 | 0/0 | 3525 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | copy fasta | chr10 | 103083038 | 103198272 |
a0001c0001t0018 | 0/0 | 3525 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | copy fasta | chr10 | 103083038 | 103198272 |
a0001c0002t0003 | 0/0 | 3525 | 62 | 4 | 9 | 42 | 0 | 7 | NT5C2_chr10_103083038_103198272 | NT5C2 | copy fasta | chr10 | 103083038 | 103198272 |
a0001c0002t0004 | 0/0 | 3525 | 16 | 10 | 2 | 0 | 2 | 2 | NT5C2_chr10_103083038_103198272 | NT5C2 | copy fasta | chr10 | 103083038 | 103198272 |
a0001c0002t0005 | 0/0 | 3525 | 25 | 13 | 5 | 4 | 3 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | copy fasta | chr10 | 103083038 | 103198272 |
a0001c0002t0006 | 0/0 | 3525 | 17 | 0 | 2 | 9 | 0 | 6 | NT5C2_chr10_103083038_103198272 | NT5C2 | copy fasta | chr10 | 103083038 | 103198272 |
a0001c0002t0008 | 0/0 | 3525 | 7 | 7 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | copy fasta | chr10 | 103083038 | 103198272 |
a0001c0002t0009 | 0/0 | 3525 | 3 | 0 | 0 | 3 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | copy fasta | chr10 | 103083038 | 103198272 |
a0001c0002t0010 | 0/0 | 3525 | 2 | 0 | 0 | 0 | 0 | 2 | NT5C2_chr10_103083038_103198272 | NT5C2 | copy fasta | chr10 | 103083038 | 103198272 |
a0001c0002t0013 | 0/0 | 3525 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | copy fasta | chr10 | 103083038 | 103198272 |
a0001c0002t0014 | 0/0 | 3525 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | copy fasta | chr10 | 103083038 | 103198272 |
a0001c0002t0015 | 0/0 | 3525 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | copy fasta | chr10 | 103083038 | 103198272 |
a0001c0002t0017 | 0/0 | 3525 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | copy fasta | chr10 | 103083038 | 103198272 |
a0002c0003t0004 | 0/0 | 3525 | 31 | 2 | 11 | 16 | 2 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | copy fasta | chr10 | 103083038 | 103198272 |
a0003c0004t0005 | 0/0 | 3525 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | copy fasta | chr10 | 103083038 | 103198272 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0002g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0002g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0002g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0002g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0002g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0002g0262 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0002g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0002g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0002g0289 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0002g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0002g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0002g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0002g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0002g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0002g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0002g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0005g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0005g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0007g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0007g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0007g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0007g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0007g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0007g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0007g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0007g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0011g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0011g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0012g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0016g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0001t0018g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0003g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0003g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0003g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0003g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0003g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0003g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0003g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0003g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0003g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0003g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0003g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0003g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0003g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0003g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0003g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0003g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0003g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0003g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0003g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0003g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0003g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0003g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0003g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0003g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0003g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0003g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0003g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0003g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0003g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0003g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0003g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0003g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0003g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0003g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0003g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0003g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0003g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0003g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0004g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0004g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0004g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0004g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0004g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0004g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0004g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0004g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0004g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0004g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0004g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0004g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0004g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0004g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0004g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0004g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0005g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0005g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0005g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0005g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0005g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0005g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0005g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0005g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0005g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0005g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0005g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0005g0321 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0005g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0005g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0005g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0005g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0005g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0005g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0005g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0005g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0005g0331 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0005g0332 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0005g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0005g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0005g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0006g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0006g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0006g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0006g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0006g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0006g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0006g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0006g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0006g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0006g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0006g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0006g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0006g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0006g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0006g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0006g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0006g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0008g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0008g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0008g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0008g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0008g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0008g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0008g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0009g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0009g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0009g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0010g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0010g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0013g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0014g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0015g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0001c0002t0017g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0002c0003t0004g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0002c0003t0004g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0002c0003t0004g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0002c0003t0004g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0002c0003t0004g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0002c0003t0004g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0002c0003t0004g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0002c0003t0004g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0002c0003t0004g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0002c0003t0004g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0002c0003t0004g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0002c0003t0004g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0002c0003t0004g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0002c0003t0004g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0002c0003t0004g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0002c0003t0004g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0002c0003t0004g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0002c0003t0004g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0002c0003t0004g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0002c0003t0004g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0002c0003t0004g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0002c0003t0004g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0002c0003t0004g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0002c0003t0004g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0002c0003t0004g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0002c0003t0004g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0002c0003t0004g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0002c0003t0004g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0002c0003t0004g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
a0003c0004t0005g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00280 | hp1 | a0001 | c0001 | t0002 | g0302 | EUR | FIN | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0146 | EUR | FIN | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | CHS | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG00408 | hp2 | a0001 | c0002 | t0006 | g0184 | EAS | CHS | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | CHS | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG00544 | hp2 | a0001 | c0002 | t0003 | g0026 | EAS | CHS | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG00558 | hp1 | a0001 | c0001 | t0018 | g0256 | EAS | CHS | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG00558 | hp2 | a0001 | c0001 | t0007 | g0144 | EAS | CHS | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG00597 | hp1 | a0001 | c0001 | t0002 | g0270 | EAS | CHS | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG00597 | hp2 | a0003 | c0004 | t0005 | g0336 | EAS | CHS | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG00609 | hp1 | a0001 | c0002 | t0006 | g0185 | EAS | CHS | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG00609 | hp2 | a0002 | c0003 | t0004 | g0003 | EAS | CHS | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0278 | EAS | CHS | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG00621 | hp2 | a0002 | c0003 | t0004 | g0217 | EAS | CHS | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG00639 | hp1 | a0002 | c0003 | t0004 | g0222 | AMR | PUR | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG00639 | hp2 | a0001 | c0002 | t0005 | g0333 | AMR | PUR | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG00642 | hp1 | a0002 | c0003 | t0004 | g0232 | AMR | PUR | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG00673 | hp1 | a0002 | c0003 | t0004 | g0234 | EAS | CHS | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG00673 | hp2 | a0001 | c0002 | t0005 | g0328 | EAS | CHS | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG00733 | hp1 | a0001 | c0001 | t0011 | g0288 | AMR | PUR | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG00733 | hp2 | a0002 | c0003 | t0004 | g0240 | AMR | PUR | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG00735 | hp1 | a0002 | c0003 | t0004 | g0220 | AMR | PUR | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG00735 | hp2 | a0001 | c0002 | t0004 | g0020 | AMR | PUR | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG00738 | hp1 | a0001 | c0002 | t0005 | g0329 | AMR | PUR | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG01069 | hp1 | a0001 | c0002 | t0003 | g0047 | AMR | PUR | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG01069 | hp2 | a0001 | c0001 | t0002 | g0287 | AMR | PUR | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG01070 | hp2 | a0001 | c0002 | t0006 | g0189 | AMR | PUR | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG01071 | hp1 | a0001 | c0002 | t0006 | g0190 | AMR | PUR | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0254 | AMR | PUR | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0244 | AMR | PUR | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG01081 | hp2 | a0001 | c0001 | t0002 | g0253 | AMR | PUR | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG01099 | hp1 | a0002 | c0003 | t0004 | g0219 | AMR | PUR | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG01099 | hp2 | a0001 | c0001 | t0002 | g0290 | AMR | PUR | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG01106 | hp1 | a0001 | c0001 | t0002 | g0259 | AMR | PUR | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG01106 | hp2 | a0001 | c0001 | t0016 | g0125 | AMR | PUR | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG01109 | hp2 | a0001 | c0002 | t0004 | g0017 | AMR | PUR | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG01167 | hp1 | a0001 | c0002 | t0003 | g0049 | AMR | PUR | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG01169 | hp2 | a0001 | c0002 | t0005 | g0324 | AMR | PUR | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG01243 | hp1 | a0001 | c0002 | t0005 | g0310 | AMR | PUR | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | PUR | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | CLM | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG01255 | hp2 | a0002 | c0003 | t0004 | g0225 | AMR | CLM | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG01257 | hp1 | a0002 | c0003 | t0004 | g0002 | AMR | CLM | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0305 | AMR | CLM | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | CLM | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG01258 | hp2 | a0002 | c0003 | t0004 | g0002 | AMR | CLM | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG01358 | hp1 | a0001 | c0001 | t0002 | g0255 | AMR | CLM | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG01358 | hp2 | a0001 | c0002 | t0003 | g0067 | AMR | CLM | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | CLM | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG01361 | hp2 | a0001 | c0001 | t0002 | g0300 | AMR | CLM | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG01433 | hp1 | a0001 | c0001 | t0011 | g0306 | AMR | CLM | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG01433 | hp2 | a0001 | c0002 | t0003 | g0059 | AMR | CLM | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG01496 | hp1 | a0002 | c0003 | t0004 | g0229 | AMR | CLM | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0303 | AMR | CLM | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG01515 | hp1 | a0001 | c0002 | t0005 | g0331 | EUR | IBS | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG01515 | hp2 | a0001 | c0001 | t0002 | g0291 | EUR | IBS | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG01516 | hp1 | a0001 | c0002 | t0004 | g0019 | EUR | IBS | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0176 | EUR | IBS | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG01517 | hp1 | a0001 | c0002 | t0005 | g0332 | EUR | IBS | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG01517 | hp2 | a0001 | c0002 | t0004 | g0018 | EUR | IBS | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | ACB | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG01884 | hp2 | a0001 | c0002 | t0008 | g0210 | AFR | ACB | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | PEL | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG01928 | hp2 | a0001 | c0001 | t0012 | g0110 | AMR | PEL | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG01943 | hp1 | a0001 | c0002 | t0003 | g0060 | AMR | PEL | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG01943 | hp2 | a0001 | c0001 | t0002 | g0299 | AMR | PEL | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | PEL | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG01952 | hp2 | a0001 | c0002 | t0005 | g0325 | AMR | PEL | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG01978 | hp1 | a0001 | c0001 | t0002 | g0304 | AMR | PEL | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG01978 | hp2 | a0001 | c0002 | t0003 | g0065 | AMR | PEL | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG02004 | hp1 | a0001 | c0001 | t0002 | g0298 | AMR | PEL | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG02004 | hp2 | a0001 | c0002 | t0003 | g0061 | AMR | PEL | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | KHV | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG02027 | hp2 | a0002 | c0003 | t0004 | g0239 | EAS | KHV | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG02040 | hp1 | a0001 | c0002 | t0006 | g0191 | EAS | KHV | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | KHV | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | ACB | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG02055 | hp2 | a0001 | c0002 | t0004 | g0022 | AFR | ACB | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | KHV | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG02071 | hp2 | a0001 | c0002 | t0017 | g0066 | EAS | KHV | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG02074 | hp1 | a0001 | c0001 | t0007 | g0140 | EAS | KHV | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG02074 | hp2 | a0001 | c0002 | t0003 | g0054 | EAS | KHV | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG02083 | hp1 | a0001 | c0002 | t0003 | g0056 | EAS | KHV | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0279 | EAS | KHV | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | KHV | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG02129 | hp2 | a0001 | c0002 | t0003 | g0025 | EAS | KHV | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | KHV | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG02135 | hp2 | a0002 | c0003 | t0004 | g0236 | EAS | KHV | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | ACB | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG02145 | hp2 | a0001 | c0002 | t0008 | g0214 | AFR | ACB | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG02155 | hp1 | a0001 | c0002 | t0003 | g0053 | EAS | CDX | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | CDX | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG02257 | hp1 | a0001 | c0002 | t0008 | g0206 | AFR | ACB | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG02257 | hp2 | a0001 | c0002 | t0003 | g0062 | AFR | ACB | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG02258 | hp1 | a0001 | c0002 | t0005 | g0320 | AFR | ACB | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG02258 | hp2 | a0001 | c0002 | t0015 | g0013 | AFR | ACB | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG02273 | hp1 | a0001 | c0002 | t0003 | g0043 | AMR | PEL | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | PEL | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG02280 | hp1 | a0002 | c0003 | t0004 | g0224 | AFR | ACB | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | ACB | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG02300 | hp1 | a0001 | c0002 | t0003 | g0045 | AMR | PEL | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG02300 | hp2 | a0002 | c0003 | t0004 | g0226 | AMR | PEL | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG02523 | hp1 | a0001 | c0001 | t0007 | g0139 | EAS | KHV | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG02523 | hp2 | a0001 | c0002 | t0006 | g0188 | EAS | KHV | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0257 | SAS | PJL | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0208 | SAS | PJL | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG02622 | hp1 | a0001 | c0002 | t0004 | g0205 | AFR | GWD | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG02622 | hp2 | a0001 | c0002 | t0008 | g0212 | AFR | GWD | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG02647 | hp1 | a0001 | c0002 | t0008 | g0215 | AFR | GWD | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG02647 | hp2 | a0001 | c0002 | t0005 | g0335 | AFR | GWD | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG02683 | hp1 | a0001 | c0002 | t0006 | g0187 | SAS | PJL | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG02683 | hp2 | a0001 | c0001 | t0002 | g0263 | SAS | PJL | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0129 | SAS | PJL | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0145 | SAS | PJL | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | GWD | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG02717 | hp2 | a0001 | c0002 | t0004 | g0021 | AFR | GWD | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG02735 | hp1 | a0001 | c0002 | t0003 | g0069 | SAS | PJL | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG02735 | hp2 | a0001 | c0002 | t0006 | g0198 | SAS | PJL | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG02809 | hp1 | a0001 | c0002 | t0003 | g0050 | AFR | GWD | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG02809 | hp2 | a0001 | c0002 | t0005 | g0322 | AFR | GWD | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | GWD | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG02818 | hp2 | a0001 | c0002 | t0005 | g0319 | AFR | GWD | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG02896 | hp1 | a0001 | c0002 | t0004 | g0203 | AFR | GWD | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | GWD | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | ESN | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG02922 | hp2 | a0001 | c0002 | t0004 | g0202 | AFR | ESN | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG02970 | hp1 | a0001 | c0002 | t0005 | g0316 | AFR | ESN | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | ESN | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG02976 | hp2 | a0001 | c0002 | t0004 | g0011 | AFR | ESN | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG03017 | hp1 | a0001 | c0002 | t0003 | g0070 | SAS | PJL | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG03017 | hp2 | a0001 | c0001 | t0002 | g0269 | SAS | PJL | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | GWD | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG03041 | hp2 | a0001 | c0002 | t0005 | g0312 | AFR | GWD | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | MSL | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG03098 | hp2 | a0001 | c0002 | t0005 | g0311 | AFR | MSL | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG03139 | hp1 | a0001 | c0002 | t0005 | g0318 | AFR | ESN | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | ESN | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | ESN | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG03195 | hp2 | a0001 | c0002 | t0013 | g0195 | AFR | ESN | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | MSL | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | MSL | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG03225 | hp1 | a0001 | c0002 | t0005 | g0309 | AFR | MSL | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG03225 | hp2 | a0001 | c0002 | t0008 | g0211 | AFR | MSL | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0181 | SAS | PJL | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0207 | SAS | PJL | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | MSL | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG03486 | hp2 | a0001 | c0002 | t0005 | g0313 | AFR | MSL | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG03490 | hp1 | a0001 | c0002 | t0004 | g0015 | SAS | PJL | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG03490 | hp2 | a0001 | c0001 | t0002 | g0260 | SAS | PJL | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0264 | SAS | PJL | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG03491 | hp2 | a0001 | c0002 | t0003 | g0068 | SAS | PJL | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG03492 | hp1 | a0001 | c0002 | t0004 | g0016 | SAS | PJL | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0280 | SAS | PJL | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG03516 | hp1 | a0001 | c0002 | t0005 | g0314 | AFR | ESN | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | ESN | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG03540 | hp1 | a0001 | c0002 | t0004 | g0014 | AFR | GWD | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | GWD | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0276 | SAS | PJL | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0156 | SAS | PJL | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0261 | SAS | STU | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG03688 | hp2 | a0001 | c0002 | t0003 | g0036 | SAS | STU | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG03831 | hp1 | a0001 | c0002 | t0006 | g0200 | SAS | BEB | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0248 | SAS | BEB | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG03834 | hp1 | a0001 | c0002 | t0003 | g0046 | SAS | BEB | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0096 | SAS | BEB | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0161 | SAS | BEB | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG03927 | hp2 | a0001 | c0002 | t0003 | g0051 | SAS | BEB | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG03942 | hp1 | a0001 | c0002 | t0010 | g0006 | SAS | BEB | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG03942 | hp2 | a0001 | c0002 | t0006 | g0194 | SAS | BEB | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG04115 | hp1 | a0001 | c0002 | t0006 | g0199 | SAS | STU | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG04115 | hp2 | a0001 | c0002 | t0010 | g0042 | SAS | STU | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG04184 | hp1 | a0001 | c0002 | t0006 | g0197 | SAS | BEB | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0141 | SAS | BEB | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0283 | SAS | STU | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0164 | SAS | STU | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0209 | SAS | STU | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG04228 | hp2 | a0001 | c0002 | t0003 | g0058 | SAS | STU | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA18522 | hp1 | a0001 | c0002 | t0008 | g0213 | AFR | YRI | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | YRI | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA18612 | hp1 | a0001 | c0001 | t0007 | g0138 | EAS | CHB | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA18612 | hp2 | a0001 | c0002 | t0003 | g0035 | EAS | CHB | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA18747 | hp1 | a0001 | c0002 | t0006 | g0201 | EAS | CHB | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA18747 | hp2 | a0001 | c0002 | t0003 | g0048 | EAS | CHB | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA18939 | hp1 | a0001 | c0002 | t0003 | g0037 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA18940 | hp1 | a0001 | c0001 | t0002 | g0247 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA18941 | hp1 | a0001 | c0001 | t0002 | g0292 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA18941 | hp2 | a0002 | c0003 | t0004 | g0218 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA18943 | hp1 | a0001 | c0001 | t0002 | g0294 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0285 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA18947 | hp2 | a0001 | c0002 | t0005 | g0330 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA18950 | hp1 | a0002 | c0003 | t0004 | g0237 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA18950 | hp2 | a0001 | c0001 | t0002 | g0271 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA18951 | hp2 | a0001 | c0002 | t0003 | g0084 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0258 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA18952 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA18953 | hp1 | a0001 | c0001 | t0002 | g0286 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA18954 | hp2 | a0001 | c0002 | t0003 | g0044 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA18957 | hp1 | a0001 | c0002 | t0003 | g0023 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA18957 | hp2 | a0001 | c0001 | t0007 | g0172 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA18960 | hp1 | a0001 | c0001 | t0002 | g0296 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA18960 | hp2 | a0001 | c0002 | t0005 | g0327 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA18961 | hp1 | a0001 | c0002 | t0003 | g0085 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA18961 | hp2 | a0001 | c0001 | t0002 | g0268 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA18962 | hp1 | a0002 | c0003 | t0004 | g0003 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA18962 | hp2 | a0001 | c0002 | t0003 | g0031 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA18963 | hp2 | a0002 | c0003 | t0004 | g0228 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA18965 | hp2 | a0002 | c0003 | t0004 | g0238 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA18968 | hp2 | a0001 | c0002 | t0003 | g0077 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA18971 | hp1 | a0001 | c0001 | t0002 | g0297 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA18971 | hp2 | a0001 | c0002 | t0003 | g0039 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA18973 | hp1 | a0001 | c0001 | t0005 | g0323 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA18975 | hp2 | a0001 | c0002 | t0003 | g0057 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA18977 | hp1 | a0001 | c0002 | t0006 | g0186 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA18978 | hp1 | a0001 | c0002 | t0003 | g0079 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA18978 | hp2 | a0001 | c0001 | t0002 | g0267 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA18981 | hp1 | a0001 | c0002 | t0003 | g0063 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA18981 | hp2 | a0001 | c0001 | t0007 | g0137 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA18982 | hp1 | a0001 | c0002 | t0003 | g0040 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0265 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA18985 | hp1 | a0001 | c0002 | t0003 | g0076 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA18985 | hp2 | a0001 | c0001 | t0002 | g0246 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA18986 | hp2 | a0001 | c0002 | t0003 | g0080 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA18988 | hp1 | a0001 | c0001 | t0002 | g0284 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA18988 | hp2 | a0001 | c0002 | t0003 | g0243 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA18990 | hp1 | a0001 | c0001 | t0002 | g0281 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA18990 | hp2 | a0001 | c0002 | t0009 | g0028 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA18992 | hp1 | a0001 | c0002 | t0003 | g0241 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA18992 | hp2 | a0001 | c0001 | t0002 | g0245 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA18994 | hp1 | a0001 | c0001 | t0007 | g0166 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA18994 | hp2 | a0002 | c0003 | t0004 | g0233 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA18995 | hp1 | a0001 | c0001 | t0002 | g0250 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA18995 | hp2 | a0002 | c0003 | t0004 | g0235 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA19002 | hp2 | a0001 | c0001 | t0002 | g0272 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA19004 | hp1 | a0001 | c0001 | t0002 | g0266 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA19004 | hp2 | a0001 | c0002 | t0003 | g0033 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA19005 | hp1 | a0002 | c0003 | t0004 | g0227 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA19005 | hp2 | a0001 | c0002 | t0003 | g0032 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA19007 | hp2 | a0001 | c0002 | t0006 | g0196 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA19009 | hp1 | a0001 | c0001 | t0007 | g0162 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA19009 | hp2 | a0001 | c0002 | t0003 | g0064 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA19011 | hp1 | a0002 | c0003 | t0004 | g0216 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0308 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA19030 | hp1 | a0001 | c0002 | t0014 | g0086 | AFR | LWK | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA19030 | hp2 | a0001 | c0002 | t0004 | g0204 | AFR | LWK | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | LWK | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA19043 | hp2 | a0001 | c0002 | t0004 | g0010 | AFR | LWK | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA19054 | hp1 | a0001 | c0002 | t0009 | g0029 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA19055 | hp1 | a0001 | c0001 | t0002 | g0293 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA19055 | hp2 | a0001 | c0002 | t0003 | g0055 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA19056 | hp2 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA19057 | hp2 | a0001 | c0002 | t0003 | g0052 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA19058 | hp1 | a0001 | c0001 | t0002 | g0277 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA19058 | hp2 | a0001 | c0002 | t0003 | g0082 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA19060 | hp1 | a0001 | c0001 | t0002 | g0249 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA19060 | hp2 | a0001 | c0002 | t0003 | g0072 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA19064 | hp1 | a0001 | c0002 | t0003 | g0071 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA19065 | hp1 | a0001 | c0002 | t0003 | g0242 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA19065 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA19067 | hp1 | a0001 | c0002 | t0005 | g0315 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA19067 | hp2 | a0001 | c0001 | t0002 | g0275 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA19070 | hp1 | a0001 | c0002 | t0003 | g0073 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA19076 | hp1 | a0001 | c0001 | t0002 | g0273 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA19076 | hp2 | a0001 | c0002 | t0003 | g0007 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA19077 | hp1 | a0001 | c0002 | t0006 | g0193 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA19077 | hp2 | a0001 | c0002 | t0003 | g0081 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA19078 | hp1 | a0001 | c0001 | t0005 | g0317 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA19078 | hp2 | a0001 | c0001 | t0002 | g0301 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA19081 | hp1 | a0001 | c0001 | t0002 | g0282 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA19081 | hp2 | a0001 | c0002 | t0003 | g0038 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA19082 | hp1 | a0001 | c0001 | t0002 | g0307 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA19082 | hp2 | a0001 | c0002 | t0003 | g0074 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA19083 | hp1 | a0002 | c0003 | t0004 | g0009 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA19083 | hp2 | a0001 | c0002 | t0003 | g0034 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA19084 | hp1 | a0001 | c0002 | t0003 | g0041 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA19084 | hp2 | a0001 | c0002 | t0006 | g0192 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA19086 | hp1 | a0001 | c0002 | t0003 | g0024 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA19086 | hp2 | a0002 | c0003 | t0004 | g0005 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA19087 | hp1 | a0001 | c0002 | t0003 | g0083 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA19089 | hp1 | a0001 | c0002 | t0003 | g0027 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA19089 | hp2 | a0001 | c0001 | t0002 | g0295 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA19090 | hp1 | a0001 | c0001 | t0002 | g0252 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA19090 | hp2 | a0001 | c0002 | t0009 | g0030 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | ASW | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA20129 | hp2 | a0001 | c0002 | t0003 | g0078 | AFR | ASW | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA20752 | hp1 | a0002 | c0003 | t0004 | g0221 | EUR | TSI | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0147 | EUR | TSI | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA20805 | hp1 | a0001 | c0002 | t0005 | g0321 | EUR | TSI | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA20805 | hp2 | a0002 | c0003 | t0004 | g0230 | EUR | TSI | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG01123 | hp1 | a0002 | c0003 | t0004 | g0223 | AMR | CLM | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | CLM | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | ACB | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG02109 | hp2 | a0001 | c0002 | t0004 | g0012 | AFR | ACB | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG02486 | hp1 | a0002 | c0003 | t0004 | g0231 | AFR | ACB | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | ACB | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | MSL | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
HG03471 | hp2 | a0001 | c0001 | t0002 | g0274 | AFR | MSL | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA20300 | hp1 | a0001 | c0002 | t0005 | g0326 | AFR | USA | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | USA | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA21309 | hp1 | a0001 | c0002 | t0005 | g0334 | AFR | LWK | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
NA21309 | hp2 | a0001 | c0002 | t0003 | g0075 | AFR | LWK | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0262 | REF | REF | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0289 | REF | REF | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:103093298
|
T | C | 1 | a0003 | 1 | HG00597.hp2 | missense_variant | MODERATE | c.1000A>G | p.Thr334Ala | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 15/19 | 1205/3525 | 1000/1686 | 334/561 | chr10 | 103093298 | ||
chr10:103174952
|
T | C | 1 | a0002 | 31 | HG00609.hp2 HG00621.hp2 HG00639.hp1 others(28): Show |
missense_variant | MODERATE | c.7A>G | p.Thr3Ala | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/19 | 212/3525 | 7/1686 | 3/561 | chr10 | 103174952 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:103089711
|
G | A | 2 | a0001c0002a0002c0003 | 167 | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(164): Show |
synonymous_variant | LOW | c.1647C>T | p.Asp549Asp | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 19/19 | 1852/3525 | 1647/1686 | 549/561 | chr10 | 103089711 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:103088298
|
C | G | 1 | a0001c0001t0018 | 1 | HG00558.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1374G>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 19/19 | 1374 | chr10 | 103088298 | |||||
chr10:103088366
|
G | A | 14 | a0001c0001t0005a0001c0002t0003a0001c0002t0004others(11): Show | 170 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(167): Show |
3_prime_UTR_variant | MODIFIER | c.*1306C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 19/19 | 1306 | chr10 | 103088366 | |||||
chr10:103088502
|
A | G | 1 | a0001c0001t0007 | 8 | HG00558.hp2 HG02074.hp1 HG02523.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1170T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 19/19 | 1170 | chr10 | 103088502 | |||||
chr10:103088661
|
A | T | 1 | a0001c0002t0014 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1011T>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 19/19 | 1011 | chr10 | 103088661 | |||||
chr10:103088673
|
C | T | 4 | a0001c0002t0003a0001c0002t0009a0001c0002t0010others(1): Show | 68 | HG00544.hp2 HG01069.hp1 HG01167.hp1 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*999G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 19/19 | 999 | chr10 | 103088673 | |||||
chr10:103088693
|
T | G | 1 | a0001c0002t0015 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*979A>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 19/19 | 979 | chr10 | 103088693 | |||||
chr10:103088791
|
T | C | 1 | a0001c0002t0017 | 1 | HG02071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*881A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 19/19 | 881 | chr10 | 103088791 | |||||
chr10:103089087
|
A | T | 2 | a0001c0002t0006a0001c0002t0013 | 18 | HG00408.hp2 HG00609.hp1 HG01070.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*585T>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 19/19 | 585 | chr10 | 103089087 | |||||
chr10:103089098
|
A | T | 2 | a0001c0002t0006a0001c0002t0013 | 18 | HG00408.hp2 HG00609.hp1 HG01070.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*574T>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 19/19 | 574 | chr10 | 103089098 | |||||
chr10:103089150
|
A | G | 1 | a0001c0002t0008 | 7 | HG01884.hp2 HG02145.hp2 HG02257.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*522T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 19/19 | 522 | chr10 | 103089150 | |||||
chr10:103089254
|
G | A | 1 | a0001c0002t0013 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*418C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 19/19 | 418 | chr10 | 103089254 | |||||
chr10:103089359
|
G | C | 6 | a0001c0001t0011a0001c0001t0016a0001c0002t0003others(3): Show | 71 | HG00544.hp2 HG00733.hp1 HG01069.hp1 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*313C>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 19/19 | 313 | chr10 | 103089359 | |||||
chr10:103089387
|
A | C | 2 | a0001c0002t0006a0001c0002t0013 | 18 | HG00408.hp2 HG00609.hp1 HG01070.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*285T>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 19/19 | 285 | chr10 | 103089387 | |||||
chr10:103089457
|
C | G | 1 | a0001c0001t0012 | 1 | HG01928.hp2 | 3_prime_UTR_variant | MODIFIER | c.*215G>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 19/19 | 215 | chr10 | 103089457 | |||||
chr10:103089528
|
A | G | 1 | a0001c0002t0009 | 3 | NA18990.hp2 NA19054.hp1 NA19090.hp2 |
3_prime_UTR_variant | MODIFIER | c.*144T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 19/19 | 144 | chr10 | 103089528 | |||||
chr10:103181189
|
T | C | 4 | a0001c0002t0003a0001c0002t0009a0001c0002t0010others(1): Show | 68 | HG00544.hp2 HG01069.hp1 HG01167.hp1 others(65): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-29A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 2/19 | chr10 | 103181189 | ||||||
chr10:103181263
|
C | T | 1 | a0001c0002t0010 | 2 | HG03942.hp1 HG04115.hp2 |
5_prime_UTR_variant | MODIFIER | c.-103G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 2/19 | 6305 | chr10 | 103181263 | |||||
chr10:103193250
|
C | G | 18 | a0001c0001t0001a0001c0001t0005a0001c0001t0007others(15): Show | 274 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(271): Show |
5_prime_UTR_variant | MODIFIER | c.-183G>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/19 | 18292 | chr10 | 103193250 | |||||
chr10:103193264
|
C | A | 3 | a0001c0001t0005a0001c0002t0005a0003c0004t0005 | 28 | HG00597.hp2 HG00639.hp2 HG00673.hp2 others(25): Show |
5_prime_UTR_variant | MODIFIER | c.-197G>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/19 | 18306 | chr10 | 103193264 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:103089948
|
G | A | 3 | a0001c0002t0006g0187a0001c0002t0006g0189a0001c0002t0006g0190 | 3 | HG01070.hp2 HG01071.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.1450-40C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 18/18 | chr10 | 103089948 | ||||||
chr10:103090304
|
A | G | 1 | a0001c0002t0004g0014 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1449+307T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 18/18 | chr10 | 103090304 | ||||||
chr10:103090398
|
T | C | 2 | a0001c0002t0003g0069a0001c0002t0003g0070 | 2 | HG02735.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.1449+213A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 18/18 | chr10 | 103090398 | ||||||
chr10:103090419
|
A | C | 1 | a0001c0002t0003g0078 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1449+192T>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 18/18 | chr10 | 103090419 | ||||||
chr10:103090811
|
T | G | 13 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(10): Show | 13 | HG02135.hp1 HG03834.hp2 NA18940.hp2 others(10): Show |
intron_variant | MODIFIER | c.1273-24A>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 17/18 | chr10 | 103090811 | ||||||
chr10:103090812
|
C | T | 13 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(10): Show | 13 | HG02135.hp1 HG03834.hp2 NA18940.hp2 others(10): Show |
intron_variant | MODIFIER | c.1273-25G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 17/18 | chr10 | 103090812 | ||||||
chr10:103090861
|
C | G | 1 | a0001c0001t0001g0134 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1273-74G>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 17/18 | chr10 | 103090861 | ||||||
chr10:103090863
|
A | C | 13 | a0002c0003t0004g0002a0002c0003t0004g0220a0002c0003t0004g0221others(10): Show | 14 | HG00639.hp1 HG00642.hp1 HG00733.hp2 others(11): Show |
intron_variant | MODIFIER | c.1272+73T>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 17/18 | chr10 | 103090863 | ||||||
chr10:103090864
|
TAATA | T | 12 | a0001c0002t0004g0015a0001c0002t0004g0016a0001c0002t0004g0017others(9): Show | 12 | HG00735.hp2 HG01109.hp2 HG01516.hp1 others(9): Show |
intron_variant | MODIFIER | c.1272+68_1272+71del others(4): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 17/18 | chr10 | 103090864 | ||||||
chr10:103090875
|
G | A | 184 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(181): Show | 186 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(183): Show |
intron_variant | MODIFIER | c.1272+61C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 17/18 | chr10 | 103090875 | ||||||
chr10:103091064
|
T | C | 1 | a0001c0002t0004g0014 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1212-68A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 16/18 | chr10 | 103091064 | ||||||
chr10:103091066
|
A | G | 1 | a0001c0002t0008g0213 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1212-70T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 16/18 | chr10 | 103091066 | ||||||
chr10:103091078
|
A | G | 68 | a0001c0002t0003g0007a0001c0002t0003g0023a0001c0002t0003g0024others(65): Show | 68 | HG00544.hp2 HG01069.hp1 HG01167.hp1 others(65): Show |
intron_variant | MODIFIER | c.1212-82T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 16/18 | chr10 | 103091078 | ||||||
chr10:103091207
|
T | C | 1 | a0001c0001t0002g0269 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1212-211A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 16/18 | chr10 | 103091207 | ||||||
chr10:103091346
|
G | T | 1 | a0001c0002t0006g0191 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1211+218C>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 16/18 | chr10 | 103091346 | ||||||
chr10:103091349
|
C | CT | 68 | a0001c0002t0003g0007a0001c0002t0003g0023a0001c0002t0003g0024others(65): Show | 69 | HG00544.hp2 HG01069.hp1 HG01167.hp1 others(66): Show |
intron_variant | MODIFIER | c.1211+214dupA | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 16/18 | chr10 | 103091349 | ||||||
chr10:103091367
|
C | T | 6 | a0001c0002t0008g0210a0001c0002t0008g0211a0001c0002t0008g0212others(3): Show | 6 | HG01884.hp2 HG02145.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1211+197G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 16/18 | chr10 | 103091367 | ||||||
chr10:103091384
|
C | T | 1 | a0002c0003t0004g0235 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1211+180G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 16/18 | chr10 | 103091384 | ||||||
chr10:103091517
|
G | A | 1 | a0001c0001t0002g0250 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1211+47C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 16/18 | chr10 | 103091517 | ||||||
chr10:103091528
|
G | A | 100 | a0001c0001t0005g0317a0001c0001t0005g0323a0001c0002t0004g0010others(97): Show | 102 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(99): Show |
intron_variant | MODIFIER | c.1211+36C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 16/18 | chr10 | 103091528 | ||||||
chr10:103091544
|
G | T | 68 | a0001c0002t0003g0007a0001c0002t0003g0023a0001c0002t0003g0024others(65): Show | 68 | HG00544.hp2 HG01069.hp1 HG01167.hp1 others(65): Show |
intron_variant | MODIFIER | c.1211+20C>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 16/18 | chr10 | 103091544 | ||||||
chr10:103091639
|
G | T | 100 | a0001c0001t0005g0317a0001c0001t0005g0323a0001c0002t0004g0010others(97): Show | 102 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(99): Show |
intron_variant | MODIFIER | c.1160-24C>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 15/18 | chr10 | 103091639 | ||||||
chr10:103091643
|
G | A | 17 | a0001c0002t0006g0184a0001c0002t0006g0185a0001c0002t0006g0186others(14): Show | 17 | HG00408.hp2 HG00609.hp1 HG01070.hp2 others(14): Show |
intron_variant | MODIFIER | c.1160-28C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 15/18 | chr10 | 103091643 | ||||||
chr10:103091730
|
A | G | 2 | a0001c0001t0002g0304a0001c0001t0002g0305 | 2 | HG01257.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.1160-115T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 15/18 | chr10 | 103091730 | ||||||
chr10:103091787
|
T | A | 4 | a0002c0003t0004g0216a0002c0003t0004g0217a0002c0003t0004g0218others(1): Show | 4 | HG00621.hp2 HG00673.hp1 NA18941.hp2 others(1): Show |
intron_variant | MODIFIER | c.1160-172A>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 15/18 | chr10 | 103091787 | ||||||
chr10:103091853
|
C | A | 1 | a0001c0001t0002g0245 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1160-238G>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 15/18 | chr10 | 103091853 | ||||||
chr10:103091854
|
A | C | 1 | a0001c0001t0002g0245 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1160-239T>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 15/18 | chr10 | 103091854 | ||||||
chr10:103091855
|
C | A | 1 | a0001c0001t0002g0245 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1160-240G>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 15/18 | chr10 | 103091855 | ||||||
chr10:103092132
|
T | C | 68 | a0001c0002t0003g0007a0001c0002t0003g0023a0001c0002t0003g0024others(65): Show | 68 | HG00544.hp2 HG01069.hp1 HG01167.hp1 others(65): Show |
intron_variant | MODIFIER | c.1160-517A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 15/18 | chr10 | 103092132 | ||||||
chr10:103092155
|
C | T | 68 | a0001c0002t0003g0007a0001c0002t0003g0023a0001c0002t0003g0024others(65): Show | 68 | HG00544.hp2 HG01069.hp1 HG01167.hp1 others(65): Show |
intron_variant | MODIFIER | c.1160-540G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 15/18 | chr10 | 103092155 | ||||||
chr10:103092245
|
T | C | 46 | a0001c0001t0002g0246a0001c0001t0002g0248a0001c0001t0002g0249others(43): Show | 46 | HG00280.hp1 HG00597.hp1 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.1160-630A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 15/18 | chr10 | 103092245 | ||||||
chr10:103092342
|
G | T | 1 | a0001c0001t0002g0248 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1160-727C>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 15/18 | chr10 | 103092342 | ||||||
chr10:103092358
|
A | ATGTC | 181 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(178): Show | 183 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(180): Show |
intron_variant | MODIFIER | c.1160-747_1160-744d others(6): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 15/18 | chr10 | 103092358 | ||||||
chr10:103092409
|
T | G | 113 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(110): Show | 115 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.1159+730A>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 15/18 | chr10 | 103092409 | ||||||
chr10:103092453
|
G | A | 1 | a0001c0002t0015g0013 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1159+686C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 15/18 | chr10 | 103092453 | ||||||
chr10:103092496
|
T | C | 1 | a0002c0003t0004g0240 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1159+643A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 15/18 | chr10 | 103092496 | ||||||
chr10:103092560
|
AATG | A | 6 | a0001c0002t0008g0210a0001c0002t0008g0211a0001c0002t0008g0212others(3): Show | 6 | HG01884.hp2 HG02145.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1159+576_1159+578d others(5): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 15/18 | chr10 | 103092560 | ||||||
chr10:103092609
|
G | C | 1 | a0001c0001t0001g0156 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1159+530C>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 15/18 | chr10 | 103092609 | ||||||
chr10:103092662
|
A | G | 113 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(110): Show | 115 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.1159+477T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 15/18 | chr10 | 103092662 | ||||||
chr10:103092749
|
G | C | 7 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0092others(4): Show | 7 | NA18943.hp2 NA18945.hp2 NA18946.hp1 others(4): Show |
intron_variant | MODIFIER | c.1159+390C>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 15/18 | chr10 | 103092749 | ||||||
chr10:103092772
|
G | A | 1 | a0001c0001t0002g0279 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1159+367C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 15/18 | chr10 | 103092772 | ||||||
chr10:103092776
|
T | C | 1 | a0001c0001t0001g0111 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1159+363A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 15/18 | chr10 | 103092776 | ||||||
chr10:103092813
|
G | A | 1 | a0001c0002t0003g0033 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1159+326C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 15/18 | chr10 | 103092813 | ||||||
chr10:103092891
|
G | A | 113 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(110): Show | 115 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.1159+248C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 15/18 | chr10 | 103092891 | ||||||
chr10:103092902
|
A | AAACTT | 112 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(109): Show | 114 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(111): Show |
intron_variant | MODIFIER | c.1159+232_1159+236d others(7): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 15/18 | chr10 | 103092902 | ||||||
chr10:103093001
|
AG | A | 18 | a0001c0002t0006g0184a0001c0002t0006g0185a0001c0002t0006g0186others(15): Show | 18 | HG00408.hp2 HG00609.hp1 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.1159+137delC | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 15/18 | chr10 | 103093001 | ||||||
chr10:103093360
|
C | T | 1 | a0001c0002t0015g0013 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.989-51G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 14/18 | chr10 | 103093360 | ||||||
chr10:103093533
|
A | G | 11 | a0001c0002t0004g0015a0001c0002t0004g0016a0001c0002t0004g0017others(8): Show | 11 | HG00735.hp2 HG01109.hp2 HG01516.hp1 others(8): Show |
intron_variant | MODIFIER | c.989-224T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 14/18 | chr10 | 103093533 | ||||||
chr10:103093536
|
C | G | 1 | a0001c0001t0001g0171 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.989-227G>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 14/18 | chr10 | 103093536 | ||||||
chr10:103093569
|
A | C | 2 | a0002c0003t0004g0237a0002c0003t0004g0238 | 2 | NA18950.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.989-260T>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 14/18 | chr10 | 103093569 | ||||||
chr10:103093650
|
C | T | 2 | a0001c0001t0001g0174a0001c0001t0001g0181 | 2 | HG01192.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.988+322G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 14/18 | chr10 | 103093650 | ||||||
chr10:103093739
|
A | G | 1 | a0001c0002t0014g0086 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.988+233T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 14/18 | chr10 | 103093739 | ||||||
chr10:103093746
|
A | T | 23 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0105others(20): Show | 23 | HG00408.hp1 HG00642.hp2 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.988+226T>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 14/18 | chr10 | 103093746 | ||||||
chr10:103093820
|
T | C | 13 | a0001c0001t0001g0103a0001c0001t0001g0105a0001c0001t0001g0107others(10): Show | 13 | HG01106.hp1 HG01928.hp2 HG01952.hp1 others(10): Show |
intron_variant | MODIFIER | c.988+152A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 14/18 | chr10 | 103093820 | ||||||
chr10:103094145
|
G | A | 3 | a0001c0002t0003g0060a0001c0002t0003g0061a0001c0002t0003g0062 | 3 | HG01943.hp1 HG02004.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.922-107C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 13/18 | chr10 | 103094145 | ||||||
chr10:103094239
|
C | T | 1 | a0001c0001t0001g0155 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.921+109G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 13/18 | chr10 | 103094239 | ||||||
chr10:103094247
|
T | TA | 41 | a0001c0001t0005g0317a0001c0001t0005g0323a0001c0002t0004g0015others(38): Show | 41 | HG00597.hp2 HG00639.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.921+100dupT | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 13/18 | chr10 | 103094247 | ||||||
chr10:103094505
|
G | A | 2 | a0002c0003t0004g0002a0002c0003t0004g0221 | 3 | HG01257.hp1 HG01258.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.814-50C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 12/18 | chr10 | 103094505 | ||||||
chr10:103094599
|
G | A | 1 | a0001c0001t0001g0105 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.814-144C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 12/18 | chr10 | 103094599 | ||||||
chr10:103094605
|
C | T | 1 | a0001c0001t0002g0277 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.814-150G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 12/18 | chr10 | 103094605 | ||||||
chr10:103094687
|
T | G | 1 | a0001c0001t0002g0286 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.814-232A>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 12/18 | chr10 | 103094687 | ||||||
chr10:103094880
|
C | CA | 257 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(254): Show | 260 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(257): Show |
intron_variant | MODIFIER | c.814-426dupT | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 12/18 | chr10 | 103094880 | ||||||
chr10:103094880
|
C | CAA | 52 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0103others(49): Show | 53 | HG00280.hp2 HG00544.hp1 HG00738.hp2 others(50): Show |
intron_variant | MODIFIER | c.814-427_814-426dup others(2): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 12/18 | chr10 | 103094880 | ||||||
chr10:103094880
|
CAAAA | C | 6 | a0001c0001t0001g0120a0001c0002t0008g0210a0001c0002t0008g0211others(3): Show | 6 | HG01884.hp2 HG02145.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.814-429_814-426del others(4): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 12/18 | chr10 | 103094880 | ||||||
chr10:103095012
|
T | TA | 182 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(179): Show | 184 | HG00408.hp2 HG00544.hp2 HG00597.hp1 others(181): Show |
intron_variant | MODIFIER | c.814-558dupT | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 12/18 | chr10 | 103095012 | ||||||
chr10:103095060
|
A | G | 1 | a0001c0001t0002g0300 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.814-605T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 12/18 | chr10 | 103095060 | ||||||
chr10:103095101
|
C | T | 1 | a0001c0002t0014g0086 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.814-646G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 12/18 | chr10 | 103095101 | ||||||
chr10:103095289
|
T | C | 13 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(10): Show | 13 | HG02135.hp1 HG03834.hp2 NA18940.hp2 others(10): Show |
intron_variant | MODIFIER | c.813+650A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 12/18 | chr10 | 103095289 | ||||||
chr10:103095424
|
A | T | 1 | a0001c0002t0008g0206 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.813+515T>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 12/18 | chr10 | 103095424 | ||||||
chr10:103095504
|
T | C | 2 | a0001c0001t0001g0102a0001c0001t0001g0169 | 2 | HG01243.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.813+435A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 12/18 | chr10 | 103095504 | ||||||
chr10:103095510
|
C | T | 5 | a0001c0002t0004g0015a0001c0002t0004g0016a0001c0002t0004g0018others(2): Show | 5 | HG00735.hp2 HG01516.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.813+429G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 12/18 | chr10 | 103095510 | ||||||
chr10:103095521
|
C | T | 53 | a0001c0002t0004g0010a0001c0002t0004g0011a0001c0002t0004g0012others(50): Show | 55 | HG00408.hp2 HG00609.hp1 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.813+418G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 12/18 | chr10 | 103095521 | ||||||
chr10:103095530
|
A | G | 1 | a0001c0001t0001g0208 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.813+409T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 12/18 | chr10 | 103095530 | ||||||
chr10:103095836
|
T | C | 13 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(10): Show | 13 | HG02135.hp1 HG03834.hp2 NA18940.hp2 others(10): Show |
intron_variant | MODIFIER | c.813+103A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 12/18 | chr10 | 103095836 | ||||||
chr10:103095860
|
C | T | 1 | a0001c0002t0004g0014 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.813+79G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 12/18 | chr10 | 103095860 | ||||||
chr10:103095899
|
T | C | 181 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(178): Show | 183 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(180): Show |
intron_variant | MODIFIER | c.813+40A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 12/18 | chr10 | 103095899 | ||||||
chr10:103095913
|
G | A | 100 | a0001c0001t0005g0317a0001c0001t0005g0323a0001c0002t0004g0010others(97): Show | 102 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(99): Show |
intron_variant | MODIFIER | c.813+26C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 12/18 | chr10 | 103095913 | ||||||
chr10:103095920
|
A | G | 1 | a0001c0001t0001g0148 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.813+19T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 12/18 | chr10 | 103095920 | ||||||
chr10:103096304
|
A | G | 1 | a0002c0003t0004g0235 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.772-324T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 11/18 | chr10 | 103096304 | ||||||
chr10:103096343
|
A | C | 4 | a0001c0002t0003g0068a0001c0002t0003g0069a0001c0002t0003g0070others(1): Show | 4 | HG02735.hp1 HG03017.hp1 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.772-363T>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 11/18 | chr10 | 103096343 | ||||||
chr10:103096405
|
G | A | 68 | a0001c0002t0003g0007a0001c0002t0003g0023a0001c0002t0003g0024others(65): Show | 68 | HG00544.hp2 HG01069.hp1 HG01167.hp1 others(65): Show |
intron_variant | MODIFIER | c.772-425C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 11/18 | chr10 | 103096405 | ||||||
chr10:103096525
|
T | C | 1 | a0001c0002t0004g0010 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.772-545A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 11/18 | chr10 | 103096525 | ||||||
chr10:103096794
|
C | T | 1 | a0001c0002t0003g0037 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.771+497G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 11/18 | chr10 | 103096794 | ||||||
chr10:103096845
|
C | CA | 61 | a0001c0001t0001g0100a0001c0001t0001g0103a0001c0001t0001g0106others(58): Show | 62 | HG00408.hp2 HG00609.hp1 HG01070.hp2 others(59): Show |
intron_variant | MODIFIER | c.771+445dupT | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 11/18 | chr10 | 103096845 | ||||||
chr10:103096845
|
C | CAA | 17 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(14): Show | 17 | HG03540.hp1 HG04115.hp1 NA18940.hp1 others(14): Show |
intron_variant | MODIFIER | c.771+444_771+445dup others(2): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 11/18 | chr10 | 103096845 | ||||||
chr10:103096845
|
C | CAAA | 27 | a0001c0001t0001g0093a0001c0001t0001g0096a0001c0001t0001g0097others(24): Show | 29 | HG00609.hp2 HG00639.hp1 HG00733.hp2 others(26): Show |
intron_variant | MODIFIER | c.771+443_771+445dup others(3): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 11/18 | chr10 | 103096845 | ||||||
chr10:103096845
|
C | CAAAA | 8 | a0002c0003t0004g0216a0002c0003t0004g0217a0002c0003t0004g0218others(5): Show | 8 | HG00621.hp2 HG00642.hp1 HG02027.hp2 others(5): Show |
intron_variant | MODIFIER | c.771+442_771+445dup others(4): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 11/18 | chr10 | 103096845 | ||||||
chr10:103096845
|
CA | C | 28 | a0001c0001t0002g0291a0001c0001t0002g0305a0001c0001t0005g0317others(25): Show | 28 | HG00597.hp2 HG00673.hp2 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.771+445delT | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 11/18 | chr10 | 103096845 | ||||||
chr10:103097007
|
CAA | C | 68 | a0001c0002t0003g0007a0001c0002t0003g0023a0001c0002t0003g0024others(65): Show | 68 | HG00544.hp2 HG01069.hp1 HG01167.hp1 others(65): Show |
intron_variant | MODIFIER | c.771+282_771+283del others(2): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 11/18 | chr10 | 103097007 | ||||||
chr10:103097448
|
GA | G | 53 | a0001c0002t0004g0010a0001c0002t0004g0011a0001c0002t0004g0012others(50): Show | 55 | HG00408.hp2 HG00609.hp1 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.688-75delT | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 10/18 | chr10 | 103097448 | ||||||
chr10:103097461
|
A | C | 53 | a0001c0002t0004g0010a0001c0002t0004g0011a0001c0002t0004g0012others(50): Show | 55 | HG00408.hp2 HG00609.hp1 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.688-87T>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 10/18 | chr10 | 103097461 | ||||||
chr10:103097477
|
C | A | 29 | a0002c0003t0004g0002a0002c0003t0004g0003a0002c0003t0004g0005others(26): Show | 31 | HG00609.hp2 HG00621.hp2 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.688-103G>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 10/18 | chr10 | 103097477 | ||||||
chr10:103097555
|
T | A | 1 | a0001c0002t0015g0013 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.688-181A>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 10/18 | chr10 | 103097555 | ||||||
chr10:103097766
|
A | C | 68 | a0001c0002t0003g0007a0001c0002t0003g0023a0001c0002t0003g0024others(65): Show | 68 | HG00544.hp2 HG01069.hp1 HG01167.hp1 others(65): Show |
intron_variant | MODIFIER | c.688-392T>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 10/18 | chr10 | 103097766 | ||||||
chr10:103097869
|
A | C | 2 | a0001c0001t0001g0170a0001c0001t0012g0110 | 2 | HG01928.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.688-495T>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 10/18 | chr10 | 103097869 | ||||||
chr10:103098184
|
T | TA | 18 | a0001c0001t0001g0150a0001c0001t0001g0180a0001c0001t0002g0004others(15): Show | 19 | HG01257.hp2 HG01361.hp1 HG01943.hp2 others(16): Show |
intron_variant | MODIFIER | c.687+746dupT | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 10/18 | chr10 | 103098184 | ||||||
chr10:103098199
|
T | C | 13 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(10): Show | 13 | HG02135.hp1 HG03834.hp2 NA18940.hp2 others(10): Show |
intron_variant | MODIFIER | c.687+732A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 10/18 | chr10 | 103098199 | ||||||
chr10:103098237
|
A | G | 15 | a0001c0001t0005g0317a0001c0001t0005g0323a0001c0002t0005g0309others(12): Show | 15 | HG00597.hp2 HG00673.hp2 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.687+694T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 10/18 | chr10 | 103098237 | ||||||
chr10:103098387
|
G | T | 29 | a0002c0003t0004g0002a0002c0003t0004g0003a0002c0003t0004g0005others(26): Show | 31 | HG00609.hp2 HG00621.hp2 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.687+544C>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 10/18 | chr10 | 103098387 | ||||||
chr10:103098682
|
T | TA | 4 | a0001c0002t0003g0023a0001c0002t0003g0024a0001c0002t0003g0048others(1): Show | 4 | NA18747.hp2 NA18957.hp1 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.687+248dupT | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 10/18 | chr10 | 103098682 | ||||||
chr10:103098793
|
T | C | 1 | a0001c0002t0003g0045 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.687+138A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 10/18 | chr10 | 103098793 | ||||||
chr10:103099073
|
C | T | 2 | a0001c0001t0001g0118a0001c0001t0001g0119 | 2 | HG01884.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.634-89G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 9/18 | chr10 | 103099073 | ||||||
chr10:103099224
|
C | T | 3 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089 | 3 | NA18977.hp2 NA18989.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.634-240G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 9/18 | chr10 | 103099224 | ||||||
chr10:103099230
|
T | G | 1 | a0001c0002t0006g0184 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.634-246A>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 9/18 | chr10 | 103099230 | ||||||
chr10:103099515
|
T | C | 3 | a0001c0002t0003g0056a0001c0002t0003g0057a0001c0002t0003g0077 | 3 | HG02083.hp1 NA18968.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.633+411A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 9/18 | chr10 | 103099515 | ||||||
chr10:103100296
|
T | A | 100 | a0001c0001t0005g0317a0001c0001t0005g0323a0001c0002t0004g0010others(97): Show | 102 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(99): Show |
intron_variant | MODIFIER | c.540-277A>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 8/18 | chr10 | 103100296 | ||||||
chr10:103100369
|
C | T | 1 | a0001c0001t0002g0279 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.540-350G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 8/18 | chr10 | 103100369 | ||||||
chr10:103100637
|
C | T | 1 | a0001c0002t0004g0014 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.539+408G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 8/18 | chr10 | 103100637 | ||||||
chr10:103100638
|
T | G | 326 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0087others(323): Show | 330 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(327): Show |
intron_variant | MODIFIER | c.539+407A>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 8/18 | chr10 | 103100638 | ||||||
chr10:103101444
|
G | A | 2 | a0001c0002t0004g0011a0001c0002t0004g0012 | 2 | HG02109.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.390-118C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 6/18 | chr10 | 103101444 | ||||||
chr10:103101514
|
A | AT | 110 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(107): Show | 112 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(109): Show |
intron_variant | MODIFIER | c.390-189dupA | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 6/18 | chr10 | 103101514 | ||||||
chr10:103101514
|
AT | A | 71 | a0001c0001t0001g0103a0001c0001t0001g0157a0001c0001t0002g0269others(68): Show | 71 | HG00544.hp2 HG01069.hp1 HG01358.hp2 others(68): Show |
intron_variant | MODIFIER | c.390-189delA | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 6/18 | chr10 | 103101514 | ||||||
chr10:103101666
|
T | C | 4 | a0001c0001t0001g0001a0001c0001t0001g0141a0001c0001t0001g0146others(1): Show | 5 | HG00280.hp2 HG01167.hp2 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.390-340A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 6/18 | chr10 | 103101666 | ||||||
chr10:103101706
|
AT | A | 18 | a0001c0002t0006g0184a0001c0002t0006g0185a0001c0002t0006g0186others(15): Show | 18 | HG00408.hp2 HG00609.hp1 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.390-381delA | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 6/18 | chr10 | 103101706 | ||||||
chr10:103101979
|
T | G | 11 | a0001c0002t0004g0015a0001c0002t0004g0016a0001c0002t0004g0017others(8): Show | 11 | HG00735.hp2 HG01109.hp2 HG01516.hp1 others(8): Show |
intron_variant | MODIFIER | c.390-653A>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 6/18 | chr10 | 103101979 | ||||||
chr10:103102045
|
G | A | 2 | a0001c0001t0001g0111a0001c0001t0001g0117 | 2 | HG03209.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.390-719C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 6/18 | chr10 | 103102045 | ||||||
chr10:103102068
|
T | C | 1 | a0001c0001t0001g0089 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.390-742A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 6/18 | chr10 | 103102068 | ||||||
chr10:103102186
|
C | G | 1 | a0001c0001t0002g0283 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.390-860G>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 6/18 | chr10 | 103102186 | ||||||
chr10:103102232
|
G | A | 6 | a0001c0002t0003g0038a0001c0002t0003g0039a0001c0002t0003g0040others(3): Show | 6 | NA18971.hp2 NA18982.hp1 NA18986.hp2 others(3): Show |
intron_variant | MODIFIER | c.390-906C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 6/18 | chr10 | 103102232 | ||||||
chr10:103102345
|
T | C | 1 | a0001c0002t0005g0326 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.390-1019A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 6/18 | chr10 | 103102345 | ||||||
chr10:103102752
|
CTAGA | C | 13 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(10): Show | 13 | HG02135.hp1 HG03834.hp2 NA18940.hp2 others(10): Show |
intron_variant | MODIFIER | c.390-1430_390-1427d others(6): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 6/18 | chr10 | 103102752 | ||||||
chr10:103102756
|
A | G | 1 | a0001c0002t0003g0068 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.390-1430T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 6/18 | chr10 | 103102756 | ||||||
chr10:103102757
|
T | A | 13 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(10): Show | 13 | HG02135.hp1 HG03834.hp2 NA18940.hp2 others(10): Show |
intron_variant | MODIFIER | c.390-1431A>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 6/18 | chr10 | 103102757 | ||||||
chr10:103103083
|
G | A | 2 | a0001c0001t0002g0273a0001c0001t0002g0275 | 2 | NA19067.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.390-1757C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 6/18 | chr10 | 103103083 | ||||||
chr10:103103404
|
G | A | 4 | a0001c0001t0002g0246a0001c0001t0002g0284a0001c0001t0002g0285others(1): Show | 4 | NA18945.hp1 NA18953.hp1 NA18985.hp2 others(1): Show |
intron_variant | MODIFIER | c.390-2078C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 6/18 | chr10 | 103103404 | ||||||
chr10:103103523
|
T | C | 5 | a0001c0002t0005g0318a0001c0002t0005g0319a0001c0002t0005g0320others(2): Show | 5 | HG02258.hp1 HG02647.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.389+2183A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 6/18 | chr10 | 103103523 | ||||||
chr10:103103672
|
G | A | 1 | a0001c0002t0014g0086 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.389+2034C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 6/18 | chr10 | 103103672 | ||||||
chr10:103104040
|
T | C | 1 | a0001c0002t0003g0053 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.389+1666A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 6/18 | chr10 | 103104040 | ||||||
chr10:103104086
|
T | G | 113 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(110): Show | 115 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.389+1620A>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 6/18 | chr10 | 103104086 | ||||||
chr10:103104157
|
TTAACTC | T | 5 | a0001c0002t0008g0210a0001c0002t0008g0211a0001c0002t0008g0212others(2): Show | 5 | HG01884.hp2 HG02145.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.389+1543_389+1548d others(8): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 6/18 | chr10 | 103104157 | ||||||
chr10:103104291
|
G | A | 1 | a0001c0001t0001g0123 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.389+1415C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 6/18 | chr10 | 103104291 | ||||||
chr10:103104331
|
C | T | 1 | a0001c0002t0008g0215 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.389+1375G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 6/18 | chr10 | 103104331 | ||||||
chr10:103104436
|
T | C | 1 | a0001c0001t0001g0208 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.389+1270A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 6/18 | chr10 | 103104436 | ||||||
chr10:103104532
|
G | A | 1 | a0001c0002t0010g0042 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.389+1174C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 6/18 | chr10 | 103104532 | ||||||
chr10:103104857
|
C | G | 68 | a0001c0002t0003g0007a0001c0002t0003g0023a0001c0002t0003g0024others(65): Show | 68 | HG00544.hp2 HG01069.hp1 HG01167.hp1 others(65): Show |
intron_variant | MODIFIER | c.389+849G>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 6/18 | chr10 | 103104857 | ||||||
chr10:103104921
|
G | A | 68 | a0001c0002t0003g0007a0001c0002t0003g0023a0001c0002t0003g0024others(65): Show | 68 | HG00544.hp2 HG01069.hp1 HG01167.hp1 others(65): Show |
intron_variant | MODIFIER | c.389+785C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 6/18 | chr10 | 103104921 | ||||||
chr10:103105048
|
C | T | 335 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0087others(332): Show | 339 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(336): Show |
intron_variant | MODIFIER | c.389+658G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 6/18 | chr10 | 103105048 | ||||||
chr10:103105190
|
C | T | 1 | a0001c0001t0007g0138 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.389+516G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 6/18 | chr10 | 103105190 | ||||||
chr10:103105318
|
T | C | 13 | a0001c0002t0003g0023a0001c0002t0003g0024a0001c0002t0003g0025others(10): Show | 13 | HG01978.hp2 HG02071.hp2 HG02074.hp2 others(10): Show |
intron_variant | MODIFIER | c.389+388A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 6/18 | chr10 | 103105318 | ||||||
chr10:103105390
|
G | C | 6 | a0001c0002t0003g0038a0001c0002t0003g0039a0001c0002t0003g0040others(3): Show | 6 | NA18971.hp2 NA18982.hp1 NA18986.hp2 others(3): Show |
intron_variant | MODIFIER | c.389+316C>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 6/18 | chr10 | 103105390 | ||||||
chr10:103105990
|
T | G | 1 | a0001c0002t0005g0334 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.294-189A>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 5/18 | chr10 | 103105990 | ||||||
chr10:103106122
|
G | C | 1 | a0001c0001t0001g0123 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.294-321C>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 5/18 | chr10 | 103106122 | ||||||
chr10:103106305
|
C | T | 113 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(110): Show | 115 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.293+284G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 5/18 | chr10 | 103106305 | ||||||
chr10:103106929
|
C | T | 13 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(10): Show | 13 | HG02135.hp1 HG03834.hp2 NA18940.hp2 others(10): Show |
intron_variant | MODIFIER | c.176-223G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103106929 | ||||||
chr10:103106956
|
T | C | 1 | a0001c0002t0014g0086 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.176-250A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103106956 | ||||||
chr10:103106989
|
C | T | 1 | a0001c0002t0005g0310 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.176-283G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103106989 | ||||||
chr10:103107058
|
G | A | 13 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(10): Show | 13 | HG02135.hp1 HG03834.hp2 NA18940.hp2 others(10): Show |
intron_variant | MODIFIER | c.176-352C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103107058 | ||||||
chr10:103107106
|
C | T | 174 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(171): Show | 177 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(174): Show |
intron_variant | MODIFIER | c.176-400G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103107106 | ||||||
chr10:103107201
|
A | G | 181 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(178): Show | 183 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(180): Show |
intron_variant | MODIFIER | c.176-495T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103107201 | ||||||
chr10:103107412
|
T | C | 1 | a0001c0001t0002g0307 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.176-706A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103107412 | ||||||
chr10:103107415
|
C | T | 1 | a0001c0001t0001g0155 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.176-709G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103107415 | ||||||
chr10:103107449
|
C | T | 40 | a0001c0001t0005g0317a0001c0001t0005g0323a0001c0002t0004g0015others(37): Show | 40 | HG00597.hp2 HG00639.hp2 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.176-743G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103107449 | ||||||
chr10:103107676
|
A | C | 1 | a0001c0002t0008g0215 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.176-970T>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103107676 | ||||||
chr10:103107882
|
C | T | 2 | a0001c0001t0001g0102a0001c0001t0001g0169 | 2 | HG01243.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.176-1176G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103107882 | ||||||
chr10:103107929
|
C | T | 73 | a0001c0002t0003g0007a0001c0002t0003g0023a0001c0002t0003g0024others(70): Show | 73 | HG00544.hp2 HG01069.hp1 HG01167.hp1 others(70): Show |
intron_variant | MODIFIER | c.176-1223G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103107929 | ||||||
chr10:103107938
|
T | G | 18 | a0001c0002t0006g0184a0001c0002t0006g0185a0001c0002t0006g0186others(15): Show | 18 | HG00408.hp2 HG00609.hp1 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.176-1232A>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103107938 | ||||||
chr10:103107950
|
T | C | 1 | a0001c0002t0003g0078 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.176-1244A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103107950 | ||||||
chr10:103107952
|
C | T | 1 | a0001c0001t0002g0257 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.176-1246G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103107952 | ||||||
chr10:103108189
|
C | T | 13 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(10): Show | 13 | HG02135.hp1 HG03834.hp2 NA18940.hp2 others(10): Show |
intron_variant | MODIFIER | c.176-1483G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103108189 | ||||||
chr10:103108433
|
T | C | 1 | a0001c0001t0001g0164 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.176-1727A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103108433 | ||||||
chr10:103108527
|
A | G | 2 | a0001c0002t0003g0026a0001c0002t0003g0034 | 2 | HG00544.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.176-1821T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103108527 | ||||||
chr10:103108999
|
C | T | 1 | a0001c0002t0003g0049 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.176-2293G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103108999 | ||||||
chr10:103109080
|
C | T | 3 | a0001c0002t0004g0017a0001c0002t0004g0021a0001c0002t0004g0022 | 3 | HG01109.hp2 HG02055.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.176-2374G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103109080 | ||||||
chr10:103109102
|
G | A | 13 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(10): Show | 13 | HG02135.hp1 HG03834.hp2 NA18940.hp2 others(10): Show |
intron_variant | MODIFIER | c.176-2396C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103109102 | ||||||
chr10:103109107
|
C | T | 1 | a0001c0002t0003g0077 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.176-2401G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103109107 | ||||||
chr10:103109174
|
A | G | 1 | a0002c0003t0004g0227 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.176-2468T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103109174 | ||||||
chr10:103109277
|
A | G | 1 | a0001c0001t0001g0098 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.176-2571T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103109277 | ||||||
chr10:103109281
|
T | C | 68 | a0001c0002t0003g0007a0001c0002t0003g0023a0001c0002t0003g0024others(65): Show | 68 | HG00544.hp2 HG01069.hp1 HG01167.hp1 others(65): Show |
intron_variant | MODIFIER | c.176-2575A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103109281 | ||||||
chr10:103109313
|
T | C | 1 | a0001c0001t0002g0298 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.176-2607A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103109313 | ||||||
chr10:103109518
|
T | C | 1 | a0001c0002t0013g0195 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.176-2812A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103109518 | ||||||
chr10:103109694
|
C | T | 113 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(110): Show | 115 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.176-2988G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103109694 | ||||||
chr10:103109774
|
C | G | 49 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0104others(46): Show | 50 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(47): Show |
intron_variant | MODIFIER | c.176-3068G>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103109774 | ||||||
chr10:103110239
|
T | G | 1 | a0001c0002t0005g0316 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.176-3533A>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103110239 | ||||||
chr10:103110461
|
G | A | 113 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(110): Show | 115 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.176-3755C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103110461 | ||||||
chr10:103110518
|
A | AT | 7 | a0001c0001t0001g0134a0001c0001t0001g0151a0001c0001t0001g0161others(4): Show | 7 | HG00738.hp2 HG01070.hp1 HG01123.hp2 others(4): Show |
intron_variant | MODIFIER | c.176-3813dupA | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103110518 | ||||||
chr10:103110580
|
C | A | 1 | a0001c0002t0014g0086 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.176-3874G>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103110580 | ||||||
chr10:103110779
|
AAACTCCT others(8): Show |
A | 1 | a0001c0002t0006g0187 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.176-4088_176-4074d others(17): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103110779 | ||||||
chr10:103110934
|
C | T | 1 | a0001c0001t0001g0155 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.176-4228G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103110934 | ||||||
chr10:103111044
|
T | A | 3 | a0001c0002t0004g0017a0001c0002t0004g0021a0001c0002t0004g0022 | 3 | HG01109.hp2 HG02055.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.176-4338A>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103111044 | ||||||
chr10:103111045
|
A | G | 1 | a0001c0002t0004g0014 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.176-4339T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103111045 | ||||||
chr10:103111438
|
A | G | 4 | a0001c0001t0002g0246a0001c0001t0002g0284a0001c0001t0002g0285others(1): Show | 4 | NA18945.hp1 NA18953.hp1 NA18985.hp2 others(1): Show |
intron_variant | MODIFIER | c.176-4732T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103111438 | ||||||
chr10:103111447
|
A | G | 68 | a0001c0002t0003g0007a0001c0002t0003g0023a0001c0002t0003g0024others(65): Show | 68 | HG00544.hp2 HG01069.hp1 HG01167.hp1 others(65): Show |
intron_variant | MODIFIER | c.176-4741T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103111447 | ||||||
chr10:103111522
|
T | G | 68 | a0001c0002t0003g0007a0001c0002t0003g0023a0001c0002t0003g0024others(65): Show | 68 | HG00544.hp2 HG01069.hp1 HG01167.hp1 others(65): Show |
intron_variant | MODIFIER | c.176-4816A>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103111522 | ||||||
chr10:103111604
|
A | G | 181 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(178): Show | 183 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(180): Show |
intron_variant | MODIFIER | c.176-4898T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103111604 | ||||||
chr10:103112396
|
T | C | 1 | a0001c0001t0007g0140 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.176-5690A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103112396 | ||||||
chr10:103112454
|
C | A | 2 | a0001c0001t0001g0152a0001c0001t0001g0154 | 2 | HG02071.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.176-5748G>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103112454 | ||||||
chr10:103112710
|
C | G | 4 | a0001c0002t0006g0194a0001c0002t0006g0197a0001c0002t0006g0198others(1): Show | 4 | HG02735.hp2 HG03831.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.176-6004G>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103112710 | ||||||
chr10:103112718
|
C | T | 1 | a0001c0002t0004g0012 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.176-6012G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103112718 | ||||||
chr10:103112790
|
A | T | 181 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(178): Show | 183 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(180): Show |
intron_variant | MODIFIER | c.176-6084T>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103112790 | ||||||
chr10:103112906
|
A | C | 1 | a0001c0002t0008g0206 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.176-6200T>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103112906 | ||||||
chr10:103112927
|
A | G | 113 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(110): Show | 115 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.176-6221T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103112927 | ||||||
chr10:103112988
|
TTAAA | T | 8 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0092others(5): Show | 8 | HG03834.hp2 NA18943.hp2 NA18945.hp2 others(5): Show |
intron_variant | MODIFIER | c.176-6286_176-6283d others(6): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103112988 | ||||||
chr10:103113062
|
C | A | 2 | a0001c0002t0003g0026a0001c0002t0003g0034 | 2 | HG00544.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.176-6356G>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103113062 | ||||||
chr10:103113247
|
A | G | 1 | a0001c0002t0014g0086 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.176-6541T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103113247 | ||||||
chr10:103113289
|
GAAT | G | 8 | a0001c0001t0001g0106a0001c0001t0001g0114a0001c0001t0001g0115others(5): Show | 8 | HG01081.hp1 HG01884.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.176-6586_176-6584d others(5): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103113289 | ||||||
chr10:103113374
|
A | G | 3 | a0001c0002t0006g0187a0001c0002t0006g0189a0001c0002t0006g0190 | 3 | HG01070.hp2 HG01071.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.176-6668T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103113374 | ||||||
chr10:103113416
|
T | C | 1 | a0001c0002t0008g0212 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.176-6710A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103113416 | ||||||
chr10:103113495
|
TA | T | 68 | a0001c0002t0003g0007a0001c0002t0003g0023a0001c0002t0003g0024others(65): Show | 68 | HG00544.hp2 HG01069.hp1 HG01167.hp1 others(65): Show |
intron_variant | MODIFIER | c.176-6790delT | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103113495 | ||||||
chr10:103113496
|
A | G | 1 | a0001c0001t0001g0181 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.176-6790T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103113496 | ||||||
chr10:103113500
|
T | G | 1 | a0001c0002t0014g0086 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.176-6794A>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103113500 | ||||||
chr10:103113674
|
G | C | 7 | a0001c0001t0001g0001a0001c0001t0001g0141a0001c0001t0001g0146others(4): Show | 8 | HG00280.hp2 HG01167.hp2 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.176-6968C>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103113674 | ||||||
chr10:103114004
|
G | C | 68 | a0001c0002t0003g0007a0001c0002t0003g0023a0001c0002t0003g0024others(65): Show | 68 | HG00544.hp2 HG01069.hp1 HG01167.hp1 others(65): Show |
intron_variant | MODIFIER | c.176-7298C>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103114004 | ||||||
chr10:103114085
|
C | G | 1 | a0001c0002t0008g0215 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.176-7379G>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103114085 | ||||||
chr10:103114213
|
G | A | 2 | a0001c0001t0001g0111a0001c0001t0001g0117 | 2 | HG03209.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.176-7507C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103114213 | ||||||
chr10:103114302
|
C | T | 1 | a0001c0001t0002g0249 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.176-7596G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103114302 | ||||||
chr10:103114396
|
G | A | 1 | a0001c0002t0003g0033 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.176-7690C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103114396 | ||||||
chr10:103114403
|
T | C | 1 | a0001c0001t0001g0148 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.176-7697A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103114403 | ||||||
chr10:103114532
|
T | C | 1 | a0001c0002t0004g0010 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.176-7826A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103114532 | ||||||
chr10:103114601
|
A | G | 1 | a0001c0001t0001g0118 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.176-7895T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103114601 | ||||||
chr10:103114852
|
A | C | 2 | a0001c0001t0001g0161a0001c0001t0001g0183 | 2 | HG01192.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.176-8146T>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103114852 | ||||||
chr10:103115128
|
C | T | 1 | a0001c0002t0014g0086 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.176-8422G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103115128 | ||||||
chr10:103115158
|
T | C | 1 | a0001c0002t0008g0206 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.176-8452A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103115158 | ||||||
chr10:103115321
|
G | C | 1 | a0001c0002t0004g0014 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.176-8615C>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103115321 | ||||||
chr10:103115327
|
G | A | 32 | a0001c0002t0004g0010a0001c0002t0004g0011a0001c0002t0004g0012others(29): Show | 34 | HG00609.hp2 HG00621.hp2 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.176-8621C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103115327 | ||||||
chr10:103115376
|
T | C | 1 | a0001c0002t0003g0032 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.176-8670A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103115376 | ||||||
chr10:103115379
|
G | A | 2 | a0001c0001t0001g0132a0001c0001t0001g0145 | 2 | HG00642.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.176-8673C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103115379 | ||||||
chr10:103115399
|
C | T | 1 | a0001c0001t0001g0208 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.176-8693G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103115399 | ||||||
chr10:103115442
|
G | A | 2 | a0001c0001t0001g0113a0001c0001t0001g0122 | 2 | HG03098.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.176-8736C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103115442 | ||||||
chr10:103115547
|
A | C | 18 | a0001c0002t0006g0184a0001c0002t0006g0185a0001c0002t0006g0186others(15): Show | 18 | HG00408.hp2 HG00609.hp1 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.176-8841T>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103115547 | ||||||
chr10:103115574
|
A | G | 1 | a0001c0001t0001g0150 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.176-8868T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103115574 | ||||||
chr10:103115683
|
A | G | 2 | a0001c0002t0006g0194a0001c0002t0006g0197 | 2 | HG03942.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.176-8977T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103115683 | ||||||
chr10:103115782
|
T | C | 1 | a0001c0002t0014g0086 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.176-9076A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103115782 | ||||||
chr10:103115853
|
T | C | 1 | a0001c0002t0003g0074 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.176-9147A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103115853 | ||||||
chr10:103116564
|
A | G | 7 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0092others(4): Show | 7 | NA18943.hp2 NA18945.hp2 NA18946.hp1 others(4): Show |
intron_variant | MODIFIER | c.176-9858T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103116564 | ||||||
chr10:103116586
|
T | C | 1 | a0001c0002t0004g0012 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.176-9880A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103116586 | ||||||
chr10:103116587
|
C | CT | 89 | a0001c0001t0001g0178a0001c0001t0005g0317a0001c0001t0005g0323others(86): Show | 91 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(88): Show |
intron_variant | MODIFIER | c.176-9882dupA | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103116587 | ||||||
chr10:103116587
|
C | CTT | 11 | a0001c0002t0005g0309a0001c0002t0005g0310a0001c0002t0005g0311others(8): Show | 11 | HG01243.hp1 HG02258.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.176-9883_176-9882d others(4): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103116587 | ||||||
chr10:103116587
|
C | T | 1 | a0001c0002t0004g0012 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.176-9881G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103116587 | ||||||
chr10:103116822
|
G | A | 3 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0002t0003g0051 | 3 | HG03927.hp2 NA18943.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.176-10116C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103116822 | ||||||
chr10:103116833
|
C | T | 1 | a0001c0002t0015g0013 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.176-10127G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103116833 | ||||||
chr10:103117084
|
C | T | 1 | a0001c0001t0002g0248 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.176-10378G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103117084 | ||||||
chr10:103117109
|
T | C | 1 | a0001c0002t0004g0014 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.176-10403A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103117109 | ||||||
chr10:103117278
|
T | C | 100 | a0001c0001t0005g0317a0001c0001t0005g0323a0001c0002t0004g0010others(97): Show | 102 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(99): Show |
intron_variant | MODIFIER | c.176-10572A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103117278 | ||||||
chr10:103117545
|
T | C | 68 | a0001c0002t0003g0007a0001c0002t0003g0023a0001c0002t0003g0024others(65): Show | 68 | HG00544.hp2 HG01069.hp1 HG01167.hp1 others(65): Show |
intron_variant | MODIFIER | c.176-10839A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103117545 | ||||||
chr10:103117648
|
AAAC | A | 32 | a0001c0002t0004g0010a0001c0002t0004g0011a0001c0002t0004g0012others(29): Show | 34 | HG00609.hp2 HG00621.hp2 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.176-10945_176-1094 others(7): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103117648 | ||||||
chr10:103117845
|
T | C | 7 | a0001c0001t0001g0103a0001c0001t0001g0107a0001c0001t0001g0127others(4): Show | 7 | HG01928.hp2 HG01952.hp1 HG02273.hp2 others(4): Show |
intron_variant | MODIFIER | c.176-11139A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103117845 | ||||||
chr10:103117902
|
T | A | 1 | a0001c0002t0004g0012 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.176-11196A>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103117902 | ||||||
chr10:103118070
|
A | C | 2 | a0001c0001t0001g0113a0001c0001t0001g0122 | 2 | HG03098.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.176-11364T>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103118070 | ||||||
chr10:103118253
|
A | C | 113 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(110): Show | 115 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.176-11547T>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103118253 | ||||||
chr10:103118361
|
C | CT | 14 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(11): Show | 14 | HG02135.hp1 HG03834.hp2 HG04199.hp2 others(11): Show |
intron_variant | MODIFIER | c.176-11656dupA | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103118361 | ||||||
chr10:103118361
|
C | CTT | 96 | a0001c0001t0005g0317a0001c0001t0005g0323a0001c0002t0004g0010others(93): Show | 98 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(95): Show |
intron_variant | MODIFIER | c.176-11657_176-1165 others(6): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103118361 | ||||||
chr10:103118677
|
T | G | 1 | a0001c0002t0006g0198 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.176-11971A>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103118677 | ||||||
chr10:103118697
|
G | A | 41 | a0001c0001t0005g0317a0001c0001t0005g0323a0001c0002t0004g0015others(38): Show | 41 | HG00597.hp2 HG00639.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.176-11991C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103118697 | ||||||
chr10:103118782
|
T | C | 2 | a0001c0002t0004g0018a0001c0002t0004g0019 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.176-12076A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103118782 | ||||||
chr10:103118786
|
C | T | 68 | a0001c0002t0003g0007a0001c0002t0003g0023a0001c0002t0003g0024others(65): Show | 68 | HG00544.hp2 HG01069.hp1 HG01167.hp1 others(65): Show |
intron_variant | MODIFIER | c.176-12080G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103118786 | ||||||
chr10:103118805
|
T | C | 10 | a0001c0002t0003g0023a0001c0002t0003g0024a0001c0002t0003g0027others(7): Show | 10 | HG01978.hp2 NA18747.hp2 NA18957.hp1 others(7): Show |
intron_variant | MODIFIER | c.176-12099A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103118805 | ||||||
chr10:103118937
|
A | C | 13 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(10): Show | 13 | HG02135.hp1 HG03834.hp2 NA18940.hp2 others(10): Show |
intron_variant | MODIFIER | c.176-12231T>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103118937 | ||||||
chr10:103118989
|
T | C | 1 | a0001c0001t0001g0128 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.176-12283A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103118989 | ||||||
chr10:103119085
|
G | A | 2 | a0001c0001t0001g0103a0001c0001t0001g0131 | 2 | NA18973.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.176-12379C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103119085 | ||||||
chr10:103119175
|
G | A | 1 | a0001c0002t0003g0065 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.176-12469C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103119175 | ||||||
chr10:103119292
|
C | T | 100 | a0001c0001t0005g0317a0001c0001t0005g0323a0001c0002t0004g0010others(97): Show | 102 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(99): Show |
intron_variant | MODIFIER | c.176-12586G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103119292 | ||||||
chr10:103119343
|
T | C | 1 | a0001c0002t0005g0334 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.176-12637A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103119343 | ||||||
chr10:103119645
|
G | C | 113 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(110): Show | 115 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.176-12939C>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103119645 | ||||||
chr10:103119804
|
CA | C | 181 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(178): Show | 183 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(180): Show |
intron_variant | MODIFIER | c.176-13099delT | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103119804 | ||||||
chr10:103119862
|
G | C | 3 | a0001c0002t0004g0203a0001c0002t0004g0204a0001c0002t0004g0205 | 3 | HG02622.hp1 HG02896.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.176-13156C>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103119862 | ||||||
chr10:103120041
|
G | A | 4 | a0001c0001t0002g0253a0001c0001t0002g0254a0001c0001t0002g0255others(1): Show | 4 | HG01069.hp2 HG01071.hp2 HG01081.hp2 others(1): Show |
intron_variant | MODIFIER | c.176-13335C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103120041 | ||||||
chr10:103120090
|
C | A | 113 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(110): Show | 115 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.176-13384G>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103120090 | ||||||
chr10:103120098
|
C | CA | 69 | a0001c0002t0003g0007a0001c0002t0003g0023a0001c0002t0003g0024others(66): Show | 69 | HG00544.hp2 HG01069.hp1 HG01167.hp1 others(66): Show |
intron_variant | MODIFIER | c.176-13393dupT | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103120098 | ||||||
chr10:103120099
|
A | G | 18 | a0001c0002t0006g0184a0001c0002t0006g0185a0001c0002t0006g0186others(15): Show | 18 | HG00408.hp2 HG00609.hp1 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.176-13393T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103120099 | ||||||
chr10:103120364
|
A | T | 1 | a0001c0002t0014g0086 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.176-13658T>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103120364 | ||||||
chr10:103120479
|
T | C | 181 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(178): Show | 183 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(180): Show |
intron_variant | MODIFIER | c.176-13773A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103120479 | ||||||
chr10:103120672
|
C | T | 2 | a0001c0001t0001g0100a0001c0001t0001g0101 | 2 | HG01109.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.176-13966G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103120672 | ||||||
chr10:103120856
|
C | A | 1 | a0001c0001t0002g0285 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.176-14150G>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103120856 | ||||||
chr10:103121016
|
A | G | 4 | a0001c0001t0002g0253a0001c0001t0002g0254a0001c0001t0002g0255others(1): Show | 4 | HG01069.hp2 HG01071.hp2 HG01081.hp2 others(1): Show |
intron_variant | MODIFIER | c.176-14310T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103121016 | ||||||
chr10:103121199
|
T | C | 2 | a0001c0001t0002g0264a0001c0001t0002g0280 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.176-14493A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103121199 | ||||||
chr10:103121249
|
G | A | 6 | a0001c0002t0005g0309a0001c0002t0005g0310a0001c0002t0005g0311others(3): Show | 6 | HG01243.hp1 HG03041.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.176-14543C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103121249 | ||||||
chr10:103121278
|
T | C | 113 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(110): Show | 115 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.176-14572A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103121278 | ||||||
chr10:103121294
|
T | C | 1 | a0001c0001t0001g0105 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.176-14588A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103121294 | ||||||
chr10:103121645
|
T | C | 113 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(110): Show | 115 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.176-14939A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103121645 | ||||||
chr10:103121993
|
A | G | 113 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(110): Show | 115 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.176-15287T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103121993 | ||||||
chr10:103122019
|
C | T | 1 | a0001c0001t0001g0149 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.176-15313G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103122019 | ||||||
chr10:103122080
|
G | A | 1 | a0001c0002t0008g0215 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.176-15374C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103122080 | ||||||
chr10:103122160
|
C | G | 1 | a0001c0002t0004g0202 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.176-15454G>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103122160 | ||||||
chr10:103122350
|
C | T | 4 | a0001c0002t0008g0210a0001c0002t0008g0211a0001c0002t0008g0212others(1): Show | 4 | HG01884.hp2 HG02145.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.176-15644G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103122350 | ||||||
chr10:103122730
|
G | T | 1 | a0001c0002t0004g0010 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.176-16024C>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103122730 | ||||||
chr10:103122972
|
A | G | 1 | a0001c0002t0003g0083 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.176-16266T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103122972 | ||||||
chr10:103123156
|
G | A | 28 | a0001c0001t0005g0317a0001c0001t0005g0323a0001c0002t0005g0309others(25): Show | 28 | HG00597.hp2 HG00639.hp2 HG00673.hp2 others(25): Show |
intron_variant | MODIFIER | c.175+16250C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103123156 | ||||||
chr10:103123267
|
C | A | 1 | a0001c0001t0002g0249 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.175+16139G>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103123267 | ||||||
chr10:103123513
|
C | T | 1 | a0001c0001t0001g0244 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.175+15893G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103123513 | ||||||
chr10:103123529
|
T | C | 1 | a0001c0001t0002g0276 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.175+15877A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103123529 | ||||||
chr10:103123580
|
A | G | 68 | a0001c0002t0003g0007a0001c0002t0003g0023a0001c0002t0003g0024others(65): Show | 68 | HG00544.hp2 HG01069.hp1 HG01167.hp1 others(65): Show |
intron_variant | MODIFIER | c.175+15826T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103123580 | ||||||
chr10:103123702
|
C | G | 1 | a0001c0001t0001g0150 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.175+15704G>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103123702 | ||||||
chr10:103123737
|
C | T | 4 | a0001c0002t0006g0194a0001c0002t0006g0197a0001c0002t0006g0198others(1): Show | 4 | HG02735.hp2 HG03831.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.175+15669G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103123737 | ||||||
chr10:103123847
|
T | TG | 42 | a0001c0001t0002g0248a0001c0001t0005g0317a0001c0001t0005g0323others(39): Show | 42 | HG00597.hp2 HG00639.hp2 HG00673.hp2 others(39): Show |
intron_variant | MODIFIER | c.175+15558dupC | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103123847 | ||||||
chr10:103123855
|
GA | G | 14 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(11): Show | 14 | HG02135.hp1 HG03834.hp2 NA18940.hp2 others(11): Show |
intron_variant | MODIFIER | c.175+15550delT | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103123855 | ||||||
chr10:103123856
|
A | G | 5 | a0001c0002t0004g0011a0001c0002t0004g0202a0001c0002t0005g0335others(2): Show | 5 | HG02647.hp2 HG02922.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.175+15550T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103123856 | ||||||
chr10:103123893
|
A | G | 111 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(108): Show | 113 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(110): Show |
intron_variant | MODIFIER | c.175+15513T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103123893 | ||||||
chr10:103123988
|
C | G | 2 | a0001c0001t0001g0087a0001c0001t0001g0088 | 2 | NA18989.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.175+15418G>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103123988 | ||||||
chr10:103124055
|
C | T | 113 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(110): Show | 115 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.175+15351G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103124055 | ||||||
chr10:103124076
|
CTT | C | 6 | a0001c0002t0008g0210a0001c0002t0008g0211a0001c0002t0008g0212others(3): Show | 6 | HG01884.hp2 HG02145.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.175+15328_175+1532 others(6): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103124076 | ||||||
chr10:103124105
|
C | T | 1 | a0001c0002t0004g0014 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.175+15301G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103124105 | ||||||
chr10:103124185
|
G | T | 1 | a0002c0003t0004g0236 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.175+15221C>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103124185 | ||||||
chr10:103124211
|
AT | A | 116 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(113): Show | 118 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(115): Show |
intron_variant | MODIFIER | c.175+15194delA | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103124211 | ||||||
chr10:103124237
|
G | T | 2 | a0001c0002t0004g0015a0001c0002t0004g0016 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.175+15169C>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103124237 | ||||||
chr10:103124305
|
C | T | 1 | a0001c0002t0014g0086 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.175+15101G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103124305 | ||||||
chr10:103124451
|
T | C | 68 | a0001c0002t0003g0007a0001c0002t0003g0023a0001c0002t0003g0024others(65): Show | 68 | HG00544.hp2 HG01069.hp1 HG01167.hp1 others(65): Show |
intron_variant | MODIFIER | c.175+14955A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103124451 | ||||||
chr10:103124798
|
T | C | 2 | a0001c0002t0003g0044a0001c0002t0003g0064 | 2 | NA18954.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.175+14608A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103124798 | ||||||
chr10:103124872
|
T | TTAA | 181 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(178): Show | 183 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(180): Show |
intron_variant | MODIFIER | c.175+14531_175+1453 others(7): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103124872 | ||||||
chr10:103125005
|
T | C | 1 | a0001c0001t0002g0263 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.175+14401A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103125005 | ||||||
chr10:103125094
|
T | C | 2 | a0001c0002t0004g0015a0001c0002t0004g0016 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.175+14312A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103125094 | ||||||
chr10:103125191
|
TC | T | 3 | a0001c0002t0004g0203a0001c0002t0004g0204a0001c0002t0004g0205 | 3 | HG02622.hp1 HG02896.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.175+14214delG | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103125191 | ||||||
chr10:103125265
|
C | T | 2 | a0001c0002t0004g0011a0001c0002t0004g0012 | 2 | HG02109.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.175+14141G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103125265 | ||||||
chr10:103125296
|
T | TA | 16 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(13): Show | 16 | HG02135.hp1 HG03834.hp2 HG03942.hp2 others(13): Show |
intron_variant | MODIFIER | c.175+14109dupT | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103125296 | ||||||
chr10:103125296
|
TA | T | 7 | a0001c0001t0011g0288a0001c0002t0005g0318a0001c0002t0005g0319others(4): Show | 7 | HG00733.hp1 HG02040.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.175+14109delT | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103125296 | ||||||
chr10:103125573
|
A | G | 113 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(110): Show | 115 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.175+13833T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103125573 | ||||||
chr10:103126061
|
G | A | 6 | a0001c0002t0008g0210a0001c0002t0008g0211a0001c0002t0008g0212others(3): Show | 6 | HG01884.hp2 HG02145.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.175+13345C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103126061 | ||||||
chr10:103126211
|
G | A | 3 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0182 | 3 | HG01109.hp1 HG02976.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.175+13195C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103126211 | ||||||
chr10:103126268
|
G | A | 1 | a0001c0001t0001g0181 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.175+13138C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103126268 | ||||||
chr10:103126431
|
C | G | 181 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(178): Show | 183 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(180): Show |
intron_variant | MODIFIER | c.175+12975G>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103126431 | ||||||
chr10:103126483
|
G | A | 1 | a0002c0003t0004g0220 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.175+12923C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103126483 | ||||||
chr10:103126545
|
C | G | 4 | a0001c0001t0005g0317a0001c0001t0005g0323a0001c0002t0005g0328others(1): Show | 4 | HG00597.hp2 HG00673.hp2 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.175+12861G>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103126545 | ||||||
chr10:103126591
|
C | A | 13 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(10): Show | 13 | HG02135.hp1 HG03834.hp2 NA18940.hp2 others(10): Show |
intron_variant | MODIFIER | c.175+12815G>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103126591 | ||||||
chr10:103126617
|
G | A | 68 | a0001c0002t0003g0007a0001c0002t0003g0023a0001c0002t0003g0024others(65): Show | 68 | HG00544.hp2 HG01069.hp1 HG01167.hp1 others(65): Show |
intron_variant | MODIFIER | c.175+12789C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103126617 | ||||||
chr10:103126655
|
A | G | 1 | a0001c0002t0004g0011 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.175+12751T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103126655 | ||||||
chr10:103126776
|
G | T | 82 | a0001c0001t0005g0317a0001c0001t0005g0323a0001c0002t0004g0010others(79): Show | 84 | HG00597.hp2 HG00609.hp2 HG00621.hp2 others(81): Show |
intron_variant | MODIFIER | c.175+12630C>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103126776 | ||||||
chr10:103126778
|
T | G | 1 | a0001c0001t0001g0178 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.175+12628A>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103126778 | ||||||
chr10:103126792
|
G | A | 1 | a0001c0002t0003g0074 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.175+12614C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103126792 | ||||||
chr10:103126855
|
A | G | 4 | a0001c0001t0001g0124a0001c0001t0001g0128a0001c0001t0001g0171others(1): Show | 4 | HG01106.hp1 NA18954.hp1 NA18965.hp1 others(1): Show |
intron_variant | MODIFIER | c.175+12551T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103126855 | ||||||
chr10:103126864
|
T | A | 1 | a0001c0002t0003g0050 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.175+12542A>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103126864 | ||||||
chr10:103127009
|
T | C | 1 | a0001c0001t0002g0252 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.175+12397A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103127009 | ||||||
chr10:103127085
|
T | C | 1 | a0001c0002t0004g0014 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.175+12321A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103127085 | ||||||
chr10:103127384
|
G | A | 3 | a0001c0002t0003g0060a0001c0002t0003g0061a0001c0002t0003g0062 | 3 | HG01943.hp1 HG02004.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.175+12022C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103127384 | ||||||
chr10:103127406
|
T | C | 2 | a0001c0001t0001g0128a0001c0001t0001g0171 | 2 | NA18965.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.175+12000A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103127406 | ||||||
chr10:103127742
|
G | A | 3 | a0001c0001t0001g0111a0001c0001t0001g0117a0001c0001t0001g0121 | 3 | HG03041.hp1 HG03209.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.175+11664C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103127742 | ||||||
chr10:103127760
|
G | A | 1 | a0001c0002t0014g0086 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.175+11646C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103127760 | ||||||
chr10:103127769
|
G | A | 1 | a0001c0002t0014g0086 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.175+11637C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103127769 | ||||||
chr10:103127777
|
C | T | 1 | a0001c0002t0015g0013 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.175+11629G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103127777 | ||||||
chr10:103127786
|
G | C | 1 | a0001c0002t0004g0202 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.175+11620C>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103127786 | ||||||
chr10:103127819
|
G | A | 1 | a0001c0002t0004g0205 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.175+11587C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103127819 | ||||||
chr10:103127852
|
G | A | 1 | a0001c0001t0001g0098 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.175+11554C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103127852 | ||||||
chr10:103128044
|
T | TCTCTCC | 49 | a0001c0001t0002g0249a0001c0001t0002g0260a0001c0001t0002g0268others(46): Show | 49 | HG01433.hp2 HG01943.hp1 HG01978.hp2 others(46): Show |
intron_variant | MODIFIER | c.175+11356_175+1136 others(10): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103128044 | ||||||
chr10:103128044
|
T | TCTCTCCC others(5): Show |
8 | a0001c0002t0003g0035a0001c0002t0003g0036a0001c0002t0003g0049others(5): Show | 8 | HG01167.hp1 HG02083.hp1 HG03491.hp2 others(5): Show |
intron_variant | MODIFIER | c.175+11350_175+1136 others(16): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103128044 | ||||||
chr10:103128044
|
T | TCTCTCCC others(11): Show |
2 | a0001c0002t0003g0057a0001c0002t0017g0066 | 2 | HG02071.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.175+11344_175+1136 others(22): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103128044 | ||||||
chr10:103128044
|
TCTCTCC | T | 83 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0100others(80): Show | 84 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.175+11356_175+1136 others(10): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103128044 | ||||||
chr10:103128044
|
TCTCTCCC others(5): Show |
T | 87 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(84): Show | 88 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(85): Show |
intron_variant | MODIFIER | c.175+11350_175+1136 others(16): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103128044 | ||||||
chr10:103128044
|
TCTCTCCC others(11): Show |
T | 14 | a0001c0002t0004g0015a0001c0002t0004g0016a0001c0002t0004g0017others(11): Show | 14 | HG00735.hp2 HG01109.hp2 HG01516.hp1 others(11): Show |
intron_variant | MODIFIER | c.175+11344_175+1136 others(22): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103128044 | ||||||
chr10:103128044
|
TCTCTCCC others(17): Show |
T | 1 | a0001c0002t0008g0215 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.175+11338_175+1136 others(28): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103128044 | ||||||
chr10:103128124
|
G | C | 1 | a0002c0003t0004g0227 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.175+11282C>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103128124 | ||||||
chr10:103128134
|
T | C | 3 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0209 | 3 | HG02602.hp2 HG03239.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.175+11272A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103128134 | ||||||
chr10:103128223
|
G | A | 1 | a0001c0001t0002g0267 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.175+11183C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103128223 | ||||||
chr10:103128263
|
C | T | 1 | a0001c0002t0008g0215 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.175+11143G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103128263 | ||||||
chr10:103128280
|
C | T | 13 | a0001c0001t0001g0150a0001c0001t0001g0180a0001c0001t0002g0004others(10): Show | 14 | HG01361.hp1 HG01943.hp2 HG02004.hp1 others(11): Show |
intron_variant | MODIFIER | c.175+11126G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103128280 | ||||||
chr10:103128301
|
G | A | 4 | a0002c0003t0004g0216a0002c0003t0004g0217a0002c0003t0004g0218others(1): Show | 4 | HG00621.hp2 HG00673.hp1 NA18941.hp2 others(1): Show |
intron_variant | MODIFIER | c.175+11105C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103128301 | ||||||
chr10:103128328
|
G | A | 1 | a0001c0002t0006g0188 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.175+11078C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103128328 | ||||||
chr10:103128356
|
C | G | 113 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(110): Show | 115 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.175+11050G>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103128356 | ||||||
chr10:103128407
|
G | A | 1 | a0001c0002t0006g0198 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.175+10999C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103128407 | ||||||
chr10:103128442
|
T | G | 40 | a0001c0001t0005g0317a0001c0001t0005g0323a0001c0002t0004g0015others(37): Show | 40 | HG00597.hp2 HG00639.hp2 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.175+10964A>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103128442 | ||||||
chr10:103128479
|
G | T | 1 | a0001c0001t0001g0156 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.175+10927C>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103128479 | ||||||
chr10:103128483
|
A | G | 113 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(110): Show | 115 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.175+10923T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103128483 | ||||||
chr10:103128486
|
A | AC | 4 | a0001c0001t0005g0317a0001c0002t0003g0076a0001c0002t0005g0324others(1): Show | 4 | HG01169.hp2 HG02622.hp2 NA18985.hp1 others(1): Show |
intron_variant | MODIFIER | c.175+10919dupG | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103128486 | ||||||
chr10:103128570
|
T | G | 18 | a0001c0002t0006g0184a0001c0002t0006g0185a0001c0002t0006g0186others(15): Show | 18 | HG00408.hp2 HG00609.hp1 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.175+10836A>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103128570 | ||||||
chr10:103128577
|
T | G | 113 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(110): Show | 115 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.175+10829A>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103128577 | ||||||
chr10:103128598
|
C | A | 2 | a0001c0001t0001g0113a0001c0001t0001g0122 | 2 | HG03098.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.175+10808G>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103128598 | ||||||
chr10:103128703
|
C | T | 1 | a0001c0002t0005g0330 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.175+10703G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103128703 | ||||||
chr10:103128715
|
G | A | 1 | a0001c0002t0003g0052 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.175+10691C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103128715 | ||||||
chr10:103128717
|
C | T | 93 | a0001c0001t0005g0317a0001c0001t0005g0323a0001c0002t0004g0010others(90): Show | 95 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(92): Show |
intron_variant | MODIFIER | c.175+10689G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103128717 | ||||||
chr10:103128755
|
G | C | 5 | a0001c0002t0008g0210a0001c0002t0008g0211a0001c0002t0008g0212others(2): Show | 5 | HG01884.hp2 HG02145.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.175+10651C>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103128755 | ||||||
chr10:103128810
|
T | G | 68 | a0001c0002t0003g0007a0001c0002t0003g0023a0001c0002t0003g0024others(65): Show | 68 | HG00544.hp2 HG01069.hp1 HG01167.hp1 others(65): Show |
intron_variant | MODIFIER | c.175+10596A>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103128810 | ||||||
chr10:103128859
|
CCTCCGCC others(33): Show |
C | 2 | a0001c0001t0002g0304a0001c0001t0002g0305 | 2 | HG01257.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.175+10507_175+1054 others(44): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103128859 | ||||||
chr10:103128864
|
G | A | 13 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(10): Show | 13 | HG02135.hp1 HG03834.hp2 NA18940.hp2 others(10): Show |
intron_variant | MODIFIER | c.175+10542C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103128864 | ||||||
chr10:103128891
|
G | A | 2 | a0001c0001t0002g0260a0001c0001t0002g0269 | 2 | HG03017.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.175+10515C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103128891 | ||||||
chr10:103128899
|
T | C | 1 | a0001c0002t0003g0061 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.175+10507A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103128899 | ||||||
chr10:103128974
|
T | TG | 19 | a0001c0002t0003g0007a0001c0002t0003g0026a0001c0002t0003g0045others(16): Show | 19 | HG00544.hp2 HG00597.hp2 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.175+10431_175+1043 others(5): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103128974 | ||||||
chr10:103128974
|
TA | T | 13 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(10): Show | 13 | HG02135.hp1 HG03834.hp2 NA18940.hp2 others(10): Show |
intron_variant | MODIFIER | c.175+10431delT | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103128974 | ||||||
chr10:103128975
|
A | G | 168 | a0001c0001t0005g0317a0001c0001t0005g0323a0001c0002t0003g0007others(165): Show | 170 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(167): Show |
intron_variant | MODIFIER | c.175+10431T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103128975 | ||||||
chr10:103129005
|
C | T | 5 | a0001c0002t0008g0210a0001c0002t0008g0211a0001c0002t0008g0212others(2): Show | 5 | HG01884.hp2 HG02145.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.175+10401G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129005 | ||||||
chr10:103129041
|
C | G | 7 | a0001c0002t0008g0206a0001c0002t0008g0210a0001c0002t0008g0211others(4): Show | 7 | HG01884.hp2 HG02145.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.175+10365G>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129041 | ||||||
chr10:103129064
|
G | A | 40 | a0001c0001t0005g0317a0001c0001t0005g0323a0001c0002t0004g0015others(37): Show | 40 | HG00597.hp2 HG00639.hp2 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.175+10342C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129064 | ||||||
chr10:103129085
|
GCCCCCCA others(544): Show |
G | 1 | a0001c0001t0001g0150 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.175+9770_175+10320 others(3): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129085 | ||||||
chr10:103129109
|
G | A | 120 | a0001c0002t0003g0007a0001c0002t0003g0023a0001c0002t0003g0024others(117): Show | 122 | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(119): Show |
intron_variant | MODIFIER | c.175+10297C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129109 | ||||||
chr10:103129185
|
G | A | 1 | a0001c0002t0015g0013 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.175+10221C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129185 | ||||||
chr10:103129221
|
T | C | 181 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(178): Show | 183 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(180): Show |
intron_variant | MODIFIER | c.175+10185A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129221 | ||||||
chr10:103129279
|
G | A | 3 | a0001c0001t0002g0272a0001c0001t0002g0273a0001c0001t0002g0275 | 3 | NA19002.hp2 NA19067.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.175+10127C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129279 | ||||||
chr10:103129288
|
G | A | 1 | a0001c0001t0002g0276 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.175+10118C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129288 | ||||||
chr10:103129315
|
C | T | 18 | a0001c0002t0006g0184a0001c0002t0006g0185a0001c0002t0006g0186others(15): Show | 18 | HG00408.hp2 HG00609.hp1 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.175+10091G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129315 | ||||||
chr10:103129316
|
GCCCGGCC others(170): Show |
G | 1 | a0001c0001t0016g0125 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.175+9913_175+10089 others(3): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129316 | ||||||
chr10:103129347
|
T | TG | 14 | a0001c0001t0001g0100a0001c0001t0001g0111a0001c0001t0001g0122others(11): Show | 14 | HG00408.hp2 HG00597.hp2 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.175+10058dupC | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129347 | ||||||
chr10:103129360
|
T | C | 1 | a0001c0002t0006g0188 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.175+10046A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129360 | ||||||
chr10:103129362
|
T | C | 1 | a0001c0002t0006g0188 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.175+10044A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129362 | ||||||
chr10:103129382
|
G | A | 1 | a0001c0002t0003g0078 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.175+10024C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129382 | ||||||
chr10:103129385
|
T | C | 1 | a0001c0002t0006g0188 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.175+10021A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129385 | ||||||
chr10:103129397
|
G | T | 1 | a0001c0002t0006g0188 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.175+10009C>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129397 | ||||||
chr10:103129399
|
C | G | 1 | a0001c0002t0006g0188 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.175+10007G>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129399 | ||||||
chr10:103129399
|
C | T | 1 | a0001c0001t0001g0164 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.175+10007G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129399 | ||||||
chr10:103129400
|
G | A | 1 | a0001c0002t0005g0329 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.175+10006C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129400 | ||||||
chr10:103129401
|
C | G | 1 | a0001c0002t0006g0188 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.175+10005G>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129401 | ||||||
chr10:103129402
|
C | G | 1 | a0001c0002t0006g0188 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.175+10004G>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129402 | ||||||
chr10:103129404
|
C | G | 1 | a0001c0002t0006g0188 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.175+10002G>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129404 | ||||||
chr10:103129413
|
C | T | 1 | a0001c0002t0005g0320 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.175+9993G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129413 | ||||||
chr10:103129414
|
G | C | 1 | a0001c0002t0006g0188 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.175+9992C>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129414 | ||||||
chr10:103129417
|
CCTACTGG others(18): Show |
C | 1 | a0001c0002t0006g0188 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.175+9964_175+9988d others(27): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129417 | ||||||
chr10:103129440
|
TCAGCCCG others(92): Show |
T | 1 | a0001c0002t0005g0320 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.175+9867_175+9965d others(101): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129440 | ||||||
chr10:103129455
|
A | G | 1 | a0001c0002t0006g0188 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.175+9951T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129455 | ||||||
chr10:103129473
|
A | G | 1 | a0001c0002t0006g0188 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.175+9933T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129473 | ||||||
chr10:103129474
|
T | TG | 10 | a0001c0001t0001g0132a0001c0001t0001g0141a0001c0001t0001g0161others(7): Show | 10 | HG00609.hp1 HG00642.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.175+9931dupC | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129474 | ||||||
chr10:103129480
|
G | T | 2 | a0001c0002t0005g0331a0001c0002t0005g0332 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.175+9926C>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129480 | ||||||
chr10:103129485
|
G | GC | 10 | a0001c0001t0001g0122a0001c0001t0001g0141a0001c0001t0001g0176others(7): Show | 10 | HG00597.hp2 HG01516.hp2 HG03098.hp1 others(7): Show |
intron_variant | MODIFIER | c.175+9920dupG | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129485 | ||||||
chr10:103129492
|
C | T | 1 | a0001c0002t0006g0188 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.175+9914G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129492 | ||||||
chr10:103129493
|
A | G | 1 | a0001c0002t0006g0188 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.175+9913T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129493 | ||||||
chr10:103129505
|
G | GCCCCGTC others(348): Show |
1 | a0001c0001t0002g0245 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.175+9900_175+9901i others(357): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129505 | ||||||
chr10:103129524
|
T | G | 1 | a0001c0002t0006g0188 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.175+9882A>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129524 | ||||||
chr10:103129524
|
T | TG | 10 | a0001c0001t0001g0122a0001c0001t0001g0135a0001c0001t0001g0141others(7): Show | 10 | HG00544.hp1 HG00597.hp1 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.175+9881dupC | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129524 | ||||||
chr10:103129525
|
G | GCGCCTCT others(17): Show |
1 | a0001c0002t0006g0188 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.175+9880_175+9881i others(26): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129525 | ||||||
chr10:103129529
|
G | A | 1 | a0001c0002t0006g0188 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.175+9877C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129529 | ||||||
chr10:103129530
|
G | A | 1 | a0001c0002t0006g0188 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.175+9876C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129530 | ||||||
chr10:103129533
|
C | G | 1 | a0001c0002t0006g0188 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.175+9873G>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129533 | ||||||
chr10:103129534
|
A | G | 1 | a0001c0002t0004g0020 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.175+9872T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129534 | ||||||
chr10:103129539
|
C | T | 1 | a0001c0002t0006g0188 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.175+9867G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129539 | ||||||
chr10:103129541
|
C | CCGCCCGG others(172): Show |
1 | a0001c0002t0005g0324 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.175+9864_175+9865i others(181): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129541 | ||||||
chr10:103129541
|
C | CGCCCGGC others(171): Show |
1 | a0001c0002t0006g0184 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.175+9864_175+9865i others(180): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129541 | ||||||
chr10:103129541
|
C | CGCCCGGC others(173): Show |
1 | a0003c0004t0005g0336 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.175+9864_175+9865i others(182): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129541 | ||||||
chr10:103129541
|
C | CGCCCGGC others(171): Show |
1 | a0001c0002t0014g0086 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.175+9864_175+9865i others(180): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129541 | ||||||
chr10:103129541
|
C | CGCCCGGC others(172): Show |
2 | a0001c0002t0005g0325a0002c0003t0004g0234 | 2 | HG00673.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.175+9864_175+9865i others(181): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129541 | ||||||
chr10:103129541
|
C | CGCCCGGC others(172): Show |
3 | a0001c0002t0004g0022a0001c0002t0005g0335a0001c0002t0006g0200 | 3 | HG02055.hp2 HG02647.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.175+9864_175+9865i others(181): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129541 | ||||||
chr10:103129541
|
C | CGCCCGGC others(171): Show |
79 | a0001c0001t0005g0317a0001c0001t0005g0323a0001c0002t0004g0011others(76): Show | 81 | HG00609.hp1 HG00609.hp2 HG00621.hp2 others(78): Show |
intron_variant | MODIFIER | c.175+9864_175+9865i others(180): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129541 | ||||||
chr10:103129541
|
C | CGCCCGGC others(171): Show |
3 | a0001c0002t0006g0187a0001c0002t0006g0189a0001c0002t0006g0190 | 3 | HG01070.hp2 HG01071.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.175+9864_175+9865i others(180): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129541 | ||||||
chr10:103129541
|
C | CTGCCCGG others(172): Show |
2 | a0002c0003t0004g0225a0002c0003t0004g0232 | 2 | HG00642.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.175+9864_175+9865i others(181): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129541 | ||||||
chr10:103129541
|
C | T | 2 | a0001c0002t0005g0320a0001c0002t0006g0188 | 2 | HG02258.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.175+9865G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129541 | ||||||
chr10:103129547
|
G | GCCAGCCG others(172): Show |
1 | a0002c0003t0004g0009 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.175+9858_175+9859i others(181): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129547 | ||||||
chr10:103129583
|
A | G | 17 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(14): Show | 17 | HG01496.hp1 HG02135.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.175+9823T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129583 | ||||||
chr10:103129603
|
G | A | 13 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(10): Show | 13 | HG02135.hp1 HG03834.hp2 NA18940.hp2 others(10): Show |
intron_variant | MODIFIER | c.175+9803C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129603 | ||||||
chr10:103129611
|
CGGGA | C | 7 | a0001c0001t0001g0001a0001c0001t0001g0141a0001c0001t0001g0146others(4): Show | 8 | HG00280.hp2 HG01167.hp2 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.175+9791_175+9794d others(6): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129611 | ||||||
chr10:103129612
|
G | A | 1 | a0001c0002t0004g0202 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.175+9794C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129612 | ||||||
chr10:103129622
|
T | TG | 40 | a0001c0001t0001g0105a0001c0001t0001g0132a0001c0001t0001g0161others(37): Show | 40 | HG00597.hp1 HG00642.hp2 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.175+9783dupC | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129622 | ||||||
chr10:103129622
|
T | TGG | 19 | a0001c0001t0005g0323a0001c0002t0004g0011a0001c0002t0004g0012others(16): Show | 19 | HG00408.hp2 HG00609.hp1 HG00639.hp2 others(16): Show |
intron_variant | MODIFIER | c.175+9782_175+9783d others(4): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129622 | ||||||
chr10:103129622
|
T | TGGG | 27 | a0001c0001t0005g0317a0001c0002t0004g0202a0001c0002t0004g0203others(24): Show | 28 | HG00597.hp2 HG00639.hp1 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.175+9781_175+9783d others(5): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129622 | ||||||
chr10:103129622
|
T | TGGGG | 17 | a0001c0002t0004g0204a0001c0002t0004g0205a0001c0002t0005g0310others(14): Show | 18 | HG00609.hp2 HG00735.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.175+9780_175+9783d others(6): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129622 | ||||||
chr10:103129622
|
T | TGGGGGGG others(172): Show |
1 | a0001c0002t0015g0013 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.175+9783_175+9784i others(181): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129622 | ||||||
chr10:103129622
|
T | TGGGGGGG others(123): Show |
1 | a0001c0002t0005g0326 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.175+9783_175+9784i others(132): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129622 | ||||||
chr10:103129623
|
GGGGGGGG others(298): Show |
G | 1 | a0001c0002t0003g0079 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.175+9478_175+9782d others(2): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129623 | ||||||
chr10:103129642
|
C | T | 15 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(12): Show | 15 | HG01496.hp1 HG02135.hp1 HG03834.hp2 others(12): Show |
intron_variant | MODIFIER | c.175+9764G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129642 | ||||||
chr10:103129659
|
T | C | 113 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(110): Show | 115 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.175+9747A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129659 | ||||||
chr10:103129691
|
C | T | 33 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(30): Show | 33 | HG00408.hp2 HG00609.hp1 HG01070.hp2 others(30): Show |
intron_variant | MODIFIER | c.175+9715G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129691 | ||||||
chr10:103129711
|
G | A | 1 | a0001c0002t0004g0014 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.175+9695C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129711 | ||||||
chr10:103129737
|
CGTCCGGG others(120): Show |
C | 2 | a0001c0001t0001g0123a0001c0001t0007g0162 | 2 | HG02922.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.175+9542_175+9668d others(2): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129737 | ||||||
chr10:103129738
|
G | A | 2 | a0001c0001t0001g0117a0002c0003t0004g0226 | 2 | HG02300.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.175+9668C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129738 | ||||||
chr10:103129742
|
G | A | 1 | a0001c0002t0005g0325 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.175+9664C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129742 | ||||||
chr10:103129763
|
G | GCCCCCCG others(45): Show |
13 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(10): Show | 13 | HG02135.hp1 HG03834.hp2 NA18940.hp2 others(10): Show |
intron_variant | MODIFIER | c.175+9642_175+9643i others(54): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129763 | ||||||
chr10:103129763
|
G | GCCCCCCG others(48): Show |
1 | a0002c0003t0004g0229 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.175+9642_175+9643i others(57): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129763 | ||||||
chr10:103129763
|
G | GCCCCCCG others(47): Show |
1 | a0001c0002t0004g0010 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.175+9642_175+9643i others(56): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129763 | ||||||
chr10:103129864
|
T | C | 286 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0087others(283): Show | 290 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(287): Show |
intron_variant | MODIFIER | c.175+9542A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129864 | ||||||
chr10:103129880
|
GGGGGTGT others(41): Show |
G | 1 | a0001c0002t0003g0041 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.175+9478_175+9525d others(50): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129880 | ||||||
chr10:103129901
|
G | A | 1 | a0001c0001t0002g0261 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.175+9505C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129901 | ||||||
chr10:103129910
|
C | A | 1 | a0001c0001t0001g0102 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.175+9496G>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129910 | ||||||
chr10:103129912
|
C | A | 4 | a0001c0001t0002g0246a0001c0001t0002g0284a0001c0001t0002g0285others(1): Show | 4 | NA18945.hp1 NA18953.hp1 NA18985.hp2 others(1): Show |
intron_variant | MODIFIER | c.175+9494G>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129912 | ||||||
chr10:103129913
|
C | T | 1 | a0001c0001t0001g0136 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.175+9493G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129913 | ||||||
chr10:103129914
|
G | A | 17 | a0001c0002t0006g0184a0001c0002t0006g0185a0001c0002t0006g0186others(14): Show | 17 | HG00408.hp2 HG00609.hp1 HG01070.hp2 others(14): Show |
intron_variant | MODIFIER | c.175+9492C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129914 | ||||||
chr10:103129928
|
T | TG | 82 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(79): Show | 82 | HG00408.hp2 HG00544.hp2 HG01069.hp1 others(79): Show |
intron_variant | MODIFIER | c.175+9477dupC | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129928 | ||||||
chr10:103129940
|
G | GC | 21 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0105others(18): Show | 21 | HG00408.hp1 HG00408.hp2 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.175+9465dupG | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129940 | ||||||
chr10:103129947
|
C | T | 1 | a0001c0001t0001g0109 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.175+9459G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129947 | ||||||
chr10:103129952
|
G | A | 1 | a0001c0001t0002g0278 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.175+9454C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129952 | ||||||
chr10:103130085
|
T | C | 3 | a0001c0002t0004g0203a0001c0002t0004g0204a0001c0002t0004g0205 | 3 | HG02622.hp1 HG02896.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.175+9321A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103130085 | ||||||
chr10:103130116
|
A | G | 1 | a0001c0001t0001g0123 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.175+9290T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103130116 | ||||||
chr10:103130205
|
C | T | 1 | a0001c0001t0001g0105 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.175+9201G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103130205 | ||||||
chr10:103130364
|
G | C | 1 | a0001c0002t0015g0013 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.175+9042C>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103130364 | ||||||
chr10:103130379
|
A | C | 1 | a0001c0002t0015g0013 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.175+9027T>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103130379 | ||||||
chr10:103130565
|
T | A | 1 | a0001c0002t0014g0086 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.175+8841A>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103130565 | ||||||
chr10:103130566
|
A | T | 1 | a0001c0002t0003g0074 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.175+8840T>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103130566 | ||||||
chr10:103130583
|
T | TA | 180 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(177): Show | 181 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(178): Show |
intron_variant | MODIFIER | c.175+8822dupT | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103130583 | ||||||
chr10:103130583
|
TA | T | 78 | a0001c0001t0001g0001a0001c0001t0001g0089a0001c0001t0001g0090others(75): Show | 79 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.175+8822delT | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103130583 | ||||||
chr10:103130583
|
TAA | T | 11 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0094others(8): Show | 11 | HG01952.hp2 HG02040.hp2 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.175+8821_175+8822d others(4): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103130583 | ||||||
chr10:103130635
|
A | G | 1 | a0001c0001t0001g0109 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.175+8771T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103130635 | ||||||
chr10:103130654
|
C | T | 1 | a0001c0002t0003g0027 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.175+8752G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103130654 | ||||||
chr10:103130854
|
C | T | 13 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(10): Show | 13 | HG02135.hp1 HG03834.hp2 NA18940.hp2 others(10): Show |
intron_variant | MODIFIER | c.175+8552G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103130854 | ||||||
chr10:103131256
|
T | C | 4 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(1): Show | 4 | NA18940.hp2 NA18977.hp2 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.175+8150A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103131256 | ||||||
chr10:103131441
|
T | C | 113 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(110): Show | 115 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.175+7965A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103131441 | ||||||
chr10:103131458
|
G | A | 1 | a0001c0002t0005g0334 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.175+7948C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103131458 | ||||||
chr10:103131639
|
C | G | 181 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(178): Show | 183 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(180): Show |
intron_variant | MODIFIER | c.175+7767G>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103131639 | ||||||
chr10:103131786
|
G | A | 3 | a0001c0002t0004g0203a0001c0002t0004g0204a0001c0002t0004g0205 | 3 | HG02622.hp1 HG02896.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.175+7620C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103131786 | ||||||
chr10:103132171
|
C | T | 3 | a0001c0002t0005g0331a0001c0002t0005g0332a0001c0002t0005g0333 | 3 | HG00639.hp2 HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.175+7235G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103132171 | ||||||
chr10:103132218
|
T | C | 181 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(178): Show | 183 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(180): Show |
intron_variant | MODIFIER | c.175+7188A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103132218 | ||||||
chr10:103132242
|
A | G | 1 | a0002c0003t0004g0227 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.175+7164T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103132242 | ||||||
chr10:103132393
|
A | G | 1 | a0001c0001t0001g0126 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.175+7013T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103132393 | ||||||
chr10:103132459
|
T | C | 18 | a0001c0002t0006g0184a0001c0002t0006g0185a0001c0002t0006g0186others(15): Show | 18 | HG00408.hp2 HG00609.hp1 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.175+6947A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103132459 | ||||||
chr10:103132541
|
A | G | 1 | a0001c0001t0007g0138 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.175+6865T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103132541 | ||||||
chr10:103132608
|
C | T | 1 | a0001c0001t0002g0247 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.175+6798G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103132608 | ||||||
chr10:103132686
|
G | A | 1 | a0001c0002t0003g0074 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.175+6720C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103132686 | ||||||
chr10:103132722
|
G | C | 1 | a0001c0002t0004g0014 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.175+6684C>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103132722 | ||||||
chr10:103132726
|
T | A | 5 | a0001c0002t0004g0015a0001c0002t0004g0016a0001c0002t0004g0018others(2): Show | 5 | HG00735.hp2 HG01516.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.175+6680A>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103132726 | ||||||
chr10:103132929
|
G | A | 3 | a0001c0002t0003g0241a0001c0002t0003g0242a0001c0002t0003g0243 | 3 | NA18988.hp2 NA18992.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.175+6477C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103132929 | ||||||
chr10:103133210
|
C | T | 1 | a0001c0002t0005g0334 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.175+6196G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103133210 | ||||||
chr10:103133211
|
C | T | 1 | a0001c0001t0002g0294 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.175+6195G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103133211 | ||||||
chr10:103133273
|
C | CTT | 18 | a0001c0001t0001g0150a0001c0001t0001g0180a0001c0001t0002g0004others(15): Show | 19 | HG00558.hp1 HG01257.hp2 HG01361.hp1 others(16): Show |
intron_variant | MODIFIER | c.175+6131_175+6132d others(4): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103133273 | ||||||
chr10:103133380
|
A | G | 113 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(110): Show | 115 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.175+6026T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103133380 | ||||||
chr10:103133514
|
A | G | 289 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0087others(286): Show | 293 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(290): Show |
intron_variant | MODIFIER | c.175+5892T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103133514 | ||||||
chr10:103133811
|
A | G | 181 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(178): Show | 183 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(180): Show |
intron_variant | MODIFIER | c.175+5595T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103133811 | ||||||
chr10:103133941
|
A | G | 335 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0087others(332): Show | 339 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(336): Show |
intron_variant | MODIFIER | c.175+5465T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103133941 | ||||||
chr10:103133970
|
G | T | 1 | a0001c0002t0005g0311 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.175+5436C>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103133970 | ||||||
chr10:103134318
|
A | G | 3 | a0001c0002t0004g0203a0001c0002t0004g0204a0001c0002t0004g0205 | 3 | HG02622.hp1 HG02896.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.175+5088T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103134318 | ||||||
chr10:103134379
|
G | A | 6 | a0001c0002t0003g0038a0001c0002t0003g0039a0001c0002t0003g0040others(3): Show | 6 | NA18971.hp2 NA18982.hp1 NA18986.hp2 others(3): Show |
intron_variant | MODIFIER | c.175+5027C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103134379 | ||||||
chr10:103134379
|
G | C | 1 | a0001c0001t0002g0263 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.175+5027C>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103134379 | ||||||
chr10:103135076
|
G | A | 1 | a0001c0002t0005g0334 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.175+4330C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103135076 | ||||||
chr10:103135160
|
T | C | 1 | a0001c0002t0004g0203 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.175+4246A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103135160 | ||||||
chr10:103135540
|
C | T | 28 | a0001c0001t0005g0317a0001c0001t0005g0323a0001c0002t0005g0309others(25): Show | 28 | HG00597.hp2 HG00639.hp2 HG00673.hp2 others(25): Show |
intron_variant | MODIFIER | c.175+3866G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103135540 | ||||||
chr10:103135645
|
G | A | 2 | a0001c0001t0001g0179a0001c0002t0004g0205 | 2 | HG02145.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.175+3761C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103135645 | ||||||
chr10:103135664
|
T | C | 13 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(10): Show | 13 | HG02135.hp1 HG03834.hp2 NA18940.hp2 others(10): Show |
intron_variant | MODIFIER | c.175+3742A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103135664 | ||||||
chr10:103135702
|
C | T | 2 | a0001c0001t0001g0128a0001c0001t0001g0171 | 2 | NA18965.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.175+3704G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103135702 | ||||||
chr10:103135704
|
A | C | 2 | a0001c0001t0002g0273a0001c0001t0002g0275 | 2 | NA19067.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.175+3702T>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103135704 | ||||||
chr10:103135712
|
C | T | 2 | a0001c0001t0002g0273a0001c0001t0002g0275 | 2 | NA19067.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.175+3694G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103135712 | ||||||
chr10:103135713
|
A | G | 2 | a0001c0001t0002g0273a0001c0001t0002g0275 | 2 | NA19067.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.175+3693T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103135713 | ||||||
chr10:103135720
|
G | A | 2 | a0001c0001t0002g0273a0001c0001t0002g0275 | 2 | NA19067.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.175+3686C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103135720 | ||||||
chr10:103135736
|
T | A | 3 | a0001c0002t0006g0187a0001c0002t0006g0189a0001c0002t0006g0190 | 3 | HG01070.hp2 HG01071.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.175+3670A>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103135736 | ||||||
chr10:103135779
|
T | C | 113 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(110): Show | 115 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.175+3627A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103135779 | ||||||
chr10:103135811
|
G | T | 29 | a0002c0003t0004g0002a0002c0003t0004g0003a0002c0003t0004g0005others(26): Show | 31 | HG00609.hp2 HG00621.hp2 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.175+3595C>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103135811 | ||||||
chr10:103136029
|
G | T | 13 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(10): Show | 13 | HG02135.hp1 HG03834.hp2 NA18940.hp2 others(10): Show |
intron_variant | MODIFIER | c.175+3377C>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103136029 | ||||||
chr10:103136030
|
T | A | 13 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(10): Show | 13 | HG02135.hp1 HG03834.hp2 NA18940.hp2 others(10): Show |
intron_variant | MODIFIER | c.175+3376A>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103136030 | ||||||
chr10:103136087
|
C | CA | 18 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(15): Show | 18 | HG00544.hp2 HG00733.hp1 HG02135.hp1 others(15): Show |
intron_variant | MODIFIER | c.175+3318dupT | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103136087 | ||||||
chr10:103136321
|
T | A | 113 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(110): Show | 115 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.175+3085A>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103136321 | ||||||
chr10:103136343
|
G | A | 3 | a0001c0002t0004g0018a0001c0002t0004g0019a0001c0002t0004g0020 | 3 | HG00735.hp2 HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.175+3063C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103136343 | ||||||
chr10:103136531
|
C | T | 1 | a0001c0002t0014g0086 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.175+2875G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103136531 | ||||||
chr10:103136626
|
A | AT | 82 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(79): Show | 84 | HG00597.hp2 HG00609.hp2 HG00621.hp2 others(81): Show |
intron_variant | MODIFIER | c.175+2779dupA | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103136626 | ||||||
chr10:103136626
|
AT | A | 67 | a0001c0001t0001g0151a0001c0001t0001g0167a0001c0002t0003g0007others(64): Show | 67 | HG00544.hp2 HG01069.hp1 HG01123.hp2 others(64): Show |
intron_variant | MODIFIER | c.175+2779delA | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103136626 | ||||||
chr10:103136628
|
T | TA | 22 | a0001c0002t0004g0202a0001c0002t0004g0203a0001c0002t0004g0204others(19): Show | 22 | HG00408.hp2 HG00609.hp1 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.175+2777_175+2778i others(3): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103136628 | ||||||
chr10:103136629
|
T | A | 7 | a0001c0001t0002g0293a0001c0002t0006g0193a0001c0002t0008g0210others(4): Show | 7 | HG01884.hp2 HG02145.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.175+2777A>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103136629 | ||||||
chr10:103136729
|
G | A | 181 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(178): Show | 183 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(180): Show |
intron_variant | MODIFIER | c.175+2677C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103136729 | ||||||
chr10:103136806
|
A | G | 272 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0087others(269): Show | 275 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(272): Show |
intron_variant | MODIFIER | c.175+2600T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103136806 | ||||||
chr10:103136908
|
C | T | 1 | a0001c0001t0002g0308 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.175+2498G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103136908 | ||||||
chr10:103136913
|
G | A | 2 | a0001c0002t0010g0006a0001c0002t0010g0042 | 2 | HG03942.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.175+2493C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103136913 | ||||||
chr10:103136994
|
A | T | 11 | a0001c0002t0004g0015a0001c0002t0004g0016a0001c0002t0004g0017others(8): Show | 11 | HG00735.hp2 HG01109.hp2 HG01516.hp1 others(8): Show |
intron_variant | MODIFIER | c.175+2412T>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103136994 | ||||||
chr10:103137059
|
T | C | 113 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(110): Show | 115 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.175+2347A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103137059 | ||||||
chr10:103137220
|
A | AG | 113 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(110): Show | 115 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.175+2185dupC | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103137220 | ||||||
chr10:103137377
|
CAA | C | 3 | a0001c0002t0003g0060a0001c0002t0003g0061a0001c0002t0003g0062 | 3 | HG01943.hp1 HG02004.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.175+2027_175+2028d others(4): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103137377 | ||||||
chr10:103137390
|
G | A | 1 | a0001c0001t0002g0251 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.175+2016C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103137390 | ||||||
chr10:103137486
|
C | T | 1 | a0001c0002t0005g0325 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.175+1920G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103137486 | ||||||
chr10:103137496
|
T | G | 1 | a0001c0001t0001g0136 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.175+1910A>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103137496 | ||||||
chr10:103137497
|
G | T | 181 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(178): Show | 183 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(180): Show |
intron_variant | MODIFIER | c.175+1909C>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103137497 | ||||||
chr10:103137701
|
C | T | 1 | a0001c0001t0001g0117 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.175+1705G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103137701 | ||||||
chr10:103137906
|
A | C | 1 | a0001c0002t0004g0202 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.175+1500T>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103137906 | ||||||
chr10:103137963
|
A | G | 1 | a0001c0001t0002g0250 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.175+1443T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103137963 | ||||||
chr10:103138013
|
C | G | 2 | a0001c0001t0002g0304a0001c0001t0002g0305 | 2 | HG01257.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.175+1393G>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103138013 | ||||||
chr10:103138144
|
T | C | 68 | a0001c0002t0003g0007a0001c0002t0003g0023a0001c0002t0003g0024others(65): Show | 68 | HG00544.hp2 HG01069.hp1 HG01167.hp1 others(65): Show |
intron_variant | MODIFIER | c.175+1262A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103138144 | ||||||
chr10:103138228
|
T | C | 72 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0102others(69): Show | 73 | HG00280.hp2 HG00408.hp1 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.175+1178A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103138228 | ||||||
chr10:103138369
|
C | T | 68 | a0001c0002t0003g0007a0001c0002t0003g0023a0001c0002t0003g0024others(65): Show | 68 | HG00544.hp2 HG01069.hp1 HG01167.hp1 others(65): Show |
intron_variant | MODIFIER | c.175+1037G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103138369 | ||||||
chr10:103138371
|
T | C | 1 | a0001c0002t0004g0202 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.175+1035A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103138371 | ||||||
chr10:103138397
|
G | A | 1 | a0001c0001t0001g0209 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.175+1009C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103138397 | ||||||
chr10:103138460
|
G | A | 1 | a0001c0001t0001g0174 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.175+946C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103138460 | ||||||
chr10:103138580
|
C | T | 68 | a0001c0002t0003g0007a0001c0002t0003g0023a0001c0002t0003g0024others(65): Show | 68 | HG00544.hp2 HG01069.hp1 HG01167.hp1 others(65): Show |
intron_variant | MODIFIER | c.175+826G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103138580 | ||||||
chr10:103138602
|
G | C | 1 | a0001c0001t0002g0270 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.175+804C>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103138602 | ||||||
chr10:103138612
|
C | A | 1 | a0001c0002t0014g0086 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.175+794G>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103138612 | ||||||
chr10:103138620
|
T | C | 1 | a0001c0001t0001g0097 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.175+786A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103138620 | ||||||
chr10:103138665
|
G | A | 3 | a0001c0002t0005g0331a0001c0002t0005g0332a0001c0002t0005g0333 | 3 | HG00639.hp2 HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.175+741C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103138665 | ||||||
chr10:103139007
|
C | CA | 12 | a0001c0001t0011g0288a0001c0002t0004g0010a0001c0002t0004g0011others(9): Show | 12 | HG00733.hp1 HG01884.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.175+398dupT | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103139007 | ||||||
chr10:103140018
|
G | A | 1 | a0001c0002t0003g0076 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.102-539C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103140018 | ||||||
chr10:103140112
|
C | T | 35 | a0001c0002t0004g0010a0001c0002t0004g0011a0001c0002t0004g0012others(32): Show | 37 | HG00609.hp2 HG00621.hp2 HG00639.hp1 others(34): Show |
intron_variant | MODIFIER | c.102-633G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103140112 | ||||||
chr10:103140364
|
A | AT | 18 | a0001c0002t0006g0184a0001c0002t0006g0185a0001c0002t0006g0186others(15): Show | 18 | HG00408.hp2 HG00609.hp1 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.102-886_102-885ins others(1): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103140364 | ||||||
chr10:103140367
|
C | T | 1 | a0001c0002t0003g0060 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.102-888G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103140367 | ||||||
chr10:103140368
|
G | A | 1 | a0001c0001t0001g0123 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.102-889C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103140368 | ||||||
chr10:103140515
|
G | A | 41 | a0001c0001t0005g0317a0001c0001t0005g0323a0001c0002t0004g0015others(38): Show | 41 | HG00597.hp2 HG00639.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.102-1036C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103140515 | ||||||
chr10:103140584
|
A | G | 1 | a0001c0002t0003g0069 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.102-1105T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103140584 | ||||||
chr10:103140908
|
A | G | 1 | a0001c0001t0002g0267 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.102-1429T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103140908 | ||||||
chr10:103141005
|
C | G | 1 | a0001c0001t0002g0274 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.102-1526G>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103141005 | ||||||
chr10:103141084
|
C | T | 17 | a0001c0002t0006g0184a0001c0002t0006g0185a0001c0002t0006g0186others(14): Show | 17 | HG00408.hp2 HG00609.hp1 HG01070.hp2 others(14): Show |
intron_variant | MODIFIER | c.102-1605G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103141084 | ||||||
chr10:103141088
|
A | T | 1 | a0001c0001t0002g0268 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.102-1609T>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103141088 | ||||||
chr10:103141217
|
G | A | 1 | a0001c0001t0001g0109 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.102-1738C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103141217 | ||||||
chr10:103141274
|
A | G | 68 | a0001c0002t0003g0007a0001c0002t0003g0023a0001c0002t0003g0024others(65): Show | 68 | HG00544.hp2 HG01069.hp1 HG01167.hp1 others(65): Show |
intron_variant | MODIFIER | c.102-1795T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103141274 | ||||||
chr10:103141610
|
C | T | 6 | a0001c0002t0008g0210a0001c0002t0008g0211a0001c0002t0008g0212others(3): Show | 6 | HG01884.hp2 HG02145.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.102-2131G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103141610 | ||||||
chr10:103141734
|
T | C | 68 | a0001c0002t0003g0007a0001c0002t0003g0023a0001c0002t0003g0024others(65): Show | 68 | HG00544.hp2 HG01069.hp1 HG01167.hp1 others(65): Show |
intron_variant | MODIFIER | c.102-2255A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103141734 | ||||||
chr10:103141835
|
G | A | 2 | a0001c0001t0001g0113a0001c0001t0001g0122 | 2 | HG03098.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.102-2356C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103141835 | ||||||
chr10:103141862
|
A | G | 6 | a0001c0002t0003g0023a0001c0002t0003g0024a0001c0002t0003g0041others(3): Show | 6 | NA18747.hp2 NA18957.hp1 NA18978.hp1 others(3): Show |
intron_variant | MODIFIER | c.102-2383T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103141862 | ||||||
chr10:103142182
|
G | T | 1 | a0001c0002t0005g0334 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.102-2703C>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103142182 | ||||||
chr10:103142408
|
A | G | 181 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(178): Show | 183 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(180): Show |
intron_variant | MODIFIER | c.102-2929T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103142408 | ||||||
chr10:103142580
|
A | T | 113 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(110): Show | 115 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.102-3101T>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103142580 | ||||||
chr10:103142673
|
G | GA | 67 | a0001c0002t0003g0007a0001c0002t0003g0023a0001c0002t0003g0024others(64): Show | 67 | HG00544.hp2 HG01069.hp1 HG01167.hp1 others(64): Show |
intron_variant | MODIFIER | c.102-3195dupT | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103142673 | ||||||
chr10:103142980
|
T | C | 181 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(178): Show | 183 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(180): Show |
intron_variant | MODIFIER | c.102-3501A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103142980 | ||||||
chr10:103142986
|
C | CA | 25 | a0001c0001t0001g0001a0001c0001t0001g0089a0001c0001t0001g0097others(22): Show | 26 | HG00280.hp2 HG01167.hp2 HG01169.hp1 others(23): Show |
intron_variant | MODIFIER | c.102-3508dupT | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103142986 | ||||||
chr10:103142987
|
A | C | 5 | a0001c0002t0008g0210a0001c0002t0008g0211a0001c0002t0008g0212others(2): Show | 5 | HG01884.hp2 HG02145.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.102-3508T>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103142987 | ||||||
chr10:103143584
|
G | A | 1 | a0001c0002t0006g0196 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.102-4105C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103143584 | ||||||
chr10:103143602
|
A | AT | 8 | a0001c0001t0001g0112a0001c0001t0001g0150a0001c0001t0001g0151others(5): Show | 8 | HG01123.hp2 HG01257.hp2 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.102-4124dupA | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103143602 | ||||||
chr10:103143602
|
A | ATT | 9 | a0001c0001t0001g0133a0001c0001t0002g0269a0001c0001t0002g0292others(6): Show | 9 | HG01943.hp2 HG01978.hp1 HG02004.hp1 others(6): Show |
intron_variant | MODIFIER | c.102-4125_102-4124d others(4): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103143602 | ||||||
chr10:103143602
|
A | ATTT | 5 | a0001c0001t0001g0180a0001c0001t0002g0004a0001c0001t0002g0247others(2): Show | 6 | HG02055.hp1 NA18940.hp1 NA18952.hp2 others(3): Show |
intron_variant | MODIFIER | c.102-4126_102-4124d others(5): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103143602 | ||||||
chr10:103143602
|
AT | A | 114 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0088others(111): Show | 115 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.102-4124delA | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103143602 | ||||||
chr10:103143602
|
ATT | A | 48 | a0001c0001t0001g0102a0001c0001t0001g0105a0001c0001t0001g0109others(45): Show | 50 | HG00408.hp1 HG00597.hp2 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.102-4125_102-4124d others(4): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103143602 | ||||||
chr10:103143602
|
ATTT | A | 38 | a0001c0001t0005g0323a0001c0002t0004g0015a0001c0002t0004g0016others(35): Show | 38 | HG00639.hp2 HG00673.hp2 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.102-4126_102-4124d others(5): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103143602 | ||||||
chr10:103143602
|
ATTTTTTT others(3): Show |
A | 1 | a0001c0001t0002g0257 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.102-4133_102-4124d others(12): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103143602 | ||||||
chr10:103143611
|
T | G | 3 | a0001c0002t0003g0060a0001c0002t0003g0061a0001c0002t0003g0062 | 3 | HG01943.hp1 HG02004.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.102-4132A>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103143611 | ||||||
chr10:103143615
|
T | G | 66 | a0001c0002t0003g0007a0001c0002t0003g0023a0001c0002t0003g0024others(63): Show | 66 | HG00544.hp2 HG01069.hp1 HG01167.hp1 others(63): Show |
intron_variant | MODIFIER | c.102-4136A>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103143615 | ||||||
chr10:103143626
|
T | G | 1 | a0001c0002t0003g0076 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.102-4147A>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103143626 | ||||||
chr10:103143627
|
T | G | 67 | a0001c0002t0003g0007a0001c0002t0003g0023a0001c0002t0003g0024others(64): Show | 67 | HG00544.hp2 HG01069.hp1 HG01167.hp1 others(64): Show |
intron_variant | MODIFIER | c.102-4148A>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103143627 | ||||||
chr10:103143807
|
T | C | 7 | a0001c0002t0008g0206a0001c0002t0008g0210a0001c0002t0008g0211others(4): Show | 7 | HG01884.hp2 HG02145.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.102-4328A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103143807 | ||||||
chr10:103143881
|
A | G | 113 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(110): Show | 115 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.102-4402T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103143881 | ||||||
chr10:103143899
|
G | A | 13 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(10): Show | 13 | HG02135.hp1 HG03834.hp2 NA18940.hp2 others(10): Show |
intron_variant | MODIFIER | c.102-4420C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103143899 | ||||||
chr10:103143909
|
C | T | 32 | a0001c0002t0004g0010a0001c0002t0004g0011a0001c0002t0004g0012others(29): Show | 34 | HG00609.hp2 HG00621.hp2 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.102-4430G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103143909 | ||||||
chr10:103144404
|
A | G | 1 | a0001c0001t0001g0155 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.102-4925T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103144404 | ||||||
chr10:103144865
|
T | C | 7 | a0001c0002t0008g0206a0001c0002t0008g0210a0001c0002t0008g0211others(4): Show | 7 | HG01884.hp2 HG02145.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.102-5386A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103144865 | ||||||
chr10:103145085
|
G | T | 1 | a0001c0002t0004g0014 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.102-5606C>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103145085 | ||||||
chr10:103145352
|
G | A | 1 | a0001c0002t0003g0085 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.102-5873C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103145352 | ||||||
chr10:103145645
|
G | A | 1 | a0001c0002t0005g0320 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.102-6166C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103145645 | ||||||
chr10:103145772
|
G | A | 100 | a0001c0001t0005g0317a0001c0001t0005g0323a0001c0002t0004g0010others(97): Show | 102 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(99): Show |
intron_variant | MODIFIER | c.102-6293C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103145772 | ||||||
chr10:103145847
|
T | C | 113 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(110): Show | 115 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.102-6368A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103145847 | ||||||
chr10:103145895
|
G | A | 1 | a0001c0001t0002g0261 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.102-6416C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103145895 | ||||||
chr10:103146229
|
A | G | 1 | a0001c0002t0006g0196 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.102-6750T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103146229 | ||||||
chr10:103146360
|
A | G | 1 | a0001c0002t0003g0047 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.102-6881T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103146360 | ||||||
chr10:103146454
|
T | C | 67 | a0001c0002t0003g0007a0001c0002t0003g0023a0001c0002t0003g0024others(64): Show | 67 | HG00544.hp2 HG01069.hp1 HG01167.hp1 others(64): Show |
intron_variant | MODIFIER | c.102-6975A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103146454 | ||||||
chr10:103147235
|
T | C | 41 | a0001c0001t0005g0317a0001c0001t0005g0323a0001c0002t0004g0015others(38): Show | 41 | HG00597.hp2 HG00639.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.102-7756A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103147235 | ||||||
chr10:103147276
|
G | A | 2 | a0001c0002t0005g0331a0001c0002t0005g0332 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.102-7797C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103147276 | ||||||
chr10:103147757
|
A | T | 1 | a0001c0002t0005g0330 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.102-8278T>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103147757 | ||||||
chr10:103147914
|
C | T | 5 | a0001c0002t0003g0043a0001c0002t0003g0044a0001c0002t0003g0045others(2): Show | 5 | HG02273.hp1 HG02300.hp1 NA18954.hp2 others(2): Show |
intron_variant | MODIFIER | c.102-8435G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103147914 | ||||||
chr10:103148033
|
A | G | 1 | a0001c0002t0004g0205 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.102-8554T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103148033 | ||||||
chr10:103148331
|
G | A | 2 | a0001c0002t0005g0331a0001c0002t0005g0332 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.102-8852C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103148331 | ||||||
chr10:103148496
|
C | T | 13 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(10): Show | 13 | HG02135.hp1 HG03834.hp2 NA18940.hp2 others(10): Show |
intron_variant | MODIFIER | c.102-9017G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103148496 | ||||||
chr10:103148561
|
G | A | 2 | a0001c0001t0002g0304a0001c0001t0002g0305 | 2 | HG01257.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.102-9082C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103148561 | ||||||
chr10:103148587
|
G | C | 2 | a0001c0001t0001g0181a0001c0001t0001g0183 | 2 | HG01192.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.102-9108C>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103148587 | ||||||
chr10:103148603
|
CA | C | 163 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(160): Show | 165 | HG00544.hp2 HG00597.hp2 HG00609.hp2 others(162): Show |
intron_variant | MODIFIER | c.102-9125delT | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103148603 | ||||||
chr10:103148650
|
A | G | 1 | a0001c0001t0001g0096 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.102-9171T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103148650 | ||||||
chr10:103148878
|
G | C | 1 | a0001c0001t0001g0244 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.102-9399C>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103148878 | ||||||
chr10:103149466
|
C | T | 6 | a0001c0002t0005g0309a0001c0002t0005g0310a0001c0002t0005g0311others(3): Show | 6 | HG01243.hp1 HG03041.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.102-9987G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103149466 | ||||||
chr10:103149582
|
T | G | 100 | a0001c0001t0005g0317a0001c0001t0005g0323a0001c0002t0004g0010others(97): Show | 102 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(99): Show |
intron_variant | MODIFIER | c.102-10103A>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103149582 | ||||||
chr10:103149678
|
A | C | 4 | a0001c0002t0006g0194a0001c0002t0006g0197a0001c0002t0006g0198others(1): Show | 4 | HG02735.hp2 HG03831.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.102-10199T>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103149678 | ||||||
chr10:103149697
|
T | C | 1 | a0001c0002t0004g0014 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.102-10218A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103149697 | ||||||
chr10:103149803
|
A | G | 1 | a0001c0001t0002g0286 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.102-10324T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103149803 | ||||||
chr10:103149841
|
C | T | 4 | a0001c0002t0003g0041a0001c0002t0009g0028a0001c0002t0009g0029others(1): Show | 4 | NA18990.hp2 NA19054.hp1 NA19084.hp1 others(1): Show |
intron_variant | MODIFIER | c.102-10362G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103149841 | ||||||
chr10:103149989
|
G | GAATATGA others(2): Show |
181 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(178): Show | 183 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(180): Show |
intron_variant | MODIFIER | c.102-10511_102-1051 others(13): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103149989 | ||||||
chr10:103150133
|
A | G | 288 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0087others(285): Show | 292 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(289): Show |
intron_variant | MODIFIER | c.102-10654T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103150133 | ||||||
chr10:103150166
|
G | C | 2 | a0001c0001t0001g0111a0001c0001t0001g0117 | 2 | HG03209.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.102-10687C>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103150166 | ||||||
chr10:103150425
|
G | A | 1 | a0001c0002t0006g0184 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.102-10946C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103150425 | ||||||
chr10:103150626
|
A | G | 1 | a0001c0002t0004g0014 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.102-11147T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103150626 | ||||||
chr10:103151045
|
A | C | 1 | a0002c0003t0004g0009 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.102-11566T>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103151045 | ||||||
chr10:103151202
|
G | A | 67 | a0001c0002t0003g0007a0001c0002t0003g0023a0001c0002t0003g0024others(64): Show | 67 | HG00544.hp2 HG01069.hp1 HG01167.hp1 others(64): Show |
intron_variant | MODIFIER | c.102-11723C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103151202 | ||||||
chr10:103151282
|
T | C | 2 | a0001c0001t0001g0112a0001c0001t0001g0133 | 2 | HG02486.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.102-11803A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103151282 | ||||||
chr10:103151464
|
T | TA | 52 | a0001c0001t0005g0317a0001c0001t0005g0323a0001c0002t0004g0010others(49): Show | 52 | HG00597.hp2 HG00639.hp2 HG00673.hp2 others(49): Show |
intron_variant | MODIFIER | c.102-11986dupT | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103151464 | ||||||
chr10:103151464
|
T | TAA | 41 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(38): Show | 43 | HG00609.hp2 HG00621.hp2 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.102-11987_102-1198 others(6): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103151464 | ||||||
chr10:103151473
|
A | C | 1 | a0001c0001t0001g0121 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.102-11994T>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103151473 | ||||||
chr10:103151477
|
A | AAAC | 16 | a0001c0002t0006g0184a0001c0002t0006g0185a0001c0002t0006g0187others(13): Show | 16 | HG00408.hp2 HG00609.hp1 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.102-12001_102-1199 others(7): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103151477 | ||||||
chr10:103151599
|
A | G | 113 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(110): Show | 115 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.102-12120T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103151599 | ||||||
chr10:103151663
|
C | T | 1 | a0001c0001t0001g0111 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.102-12184G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103151663 | ||||||
chr10:103152024
|
A | G | 1 | a0001c0001t0002g0261 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.102-12545T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103152024 | ||||||
chr10:103152279
|
C | G | 1 | a0001c0002t0005g0334 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.102-12800G>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103152279 | ||||||
chr10:103152492
|
C | G | 1 | a0001c0002t0004g0014 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.102-13013G>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103152492 | ||||||
chr10:103152555
|
A | C | 2 | a0001c0001t0007g0144a0001c0001t0007g0162 | 2 | HG00558.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.102-13076T>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103152555 | ||||||
chr10:103152596
|
G | A | 1 | a0001c0001t0001g0095 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.102-13117C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103152596 | ||||||
chr10:103152607
|
C | T | 5 | a0001c0002t0008g0210a0001c0002t0008g0211a0001c0002t0008g0212others(2): Show | 5 | HG01884.hp2 HG02145.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.102-13128G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103152607 | ||||||
chr10:103153127
|
T | C | 1 | a0001c0001t0001g0180 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.102-13648A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103153127 | ||||||
chr10:103153425
|
A | C | 1 | a0002c0003t0004g0009 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.102-13946T>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103153425 | ||||||
chr10:103153720
|
G | C | 1 | a0001c0001t0001g0097 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.102-14241C>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103153720 | ||||||
chr10:103153895
|
C | T | 1 | a0001c0002t0003g0078 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.102-14416G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103153895 | ||||||
chr10:103153896
|
G | A | 66 | a0001c0002t0003g0007a0001c0002t0003g0023a0001c0002t0003g0024others(63): Show | 66 | HG00544.hp2 HG01069.hp1 HG01167.hp1 others(63): Show |
intron_variant | MODIFIER | c.102-14417C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103153896 | ||||||
chr10:103154113
|
C | T | 180 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(177): Show | 182 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(179): Show |
intron_variant | MODIFIER | c.102-14634G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103154113 | ||||||
chr10:103154183
|
T | C | 68 | a0001c0001t0001g0121a0001c0002t0003g0007a0001c0002t0003g0023others(65): Show | 68 | HG00544.hp2 HG01069.hp1 HG01167.hp1 others(65): Show |
intron_variant | MODIFIER | c.102-14704A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103154183 | ||||||
chr10:103154264
|
G | A | 3 | a0001c0002t0004g0010a0001c0002t0004g0011a0001c0002t0004g0012 | 3 | HG02109.hp2 HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.102-14785C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103154264 | ||||||
chr10:103154348
|
A | G | 1 | a0001c0002t0014g0086 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.102-14869T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103154348 | ||||||
chr10:103154734
|
A | T | 113 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(110): Show | 115 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.102-15255T>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103154734 | ||||||
chr10:103155165
|
T | G | 1 | a0001c0002t0003g0078 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.102-15686A>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103155165 | ||||||
chr10:103155553
|
G | A | 113 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(110): Show | 115 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.102-16074C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103155553 | ||||||
chr10:103155613
|
C | T | 3 | a0001c0002t0005g0309a0001c0002t0005g0312a0001c0002t0005g0313 | 3 | HG03041.hp2 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.102-16134G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103155613 | ||||||
chr10:103155830
|
A | G | 1 | a0001c0002t0014g0086 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.102-16351T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103155830 | ||||||
chr10:103155864
|
T | G | 1 | a0001c0001t0001g0142 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.102-16385A>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103155864 | ||||||
chr10:103156361
|
T | C | 1 | a0001c0001t0001g0163 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.102-16882A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103156361 | ||||||
chr10:103156530
|
G | A | 2 | a0001c0002t0006g0194a0001c0002t0006g0197 | 2 | HG03942.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.102-17051C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103156530 | ||||||
chr10:103156755
|
C | CA | 100 | a0001c0001t0001g0117a0001c0001t0005g0317a0001c0001t0005g0323others(97): Show | 102 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(99): Show |
intron_variant | MODIFIER | c.102-17277dupT | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103156755 | ||||||
chr10:103157100
|
T | C | 52 | a0001c0002t0004g0010a0001c0002t0004g0011a0001c0002t0004g0012others(49): Show | 54 | HG00408.hp2 HG00609.hp1 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.102-17621A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103157100 | ||||||
chr10:103157223
|
T | C | 113 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(110): Show | 115 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.101+17635A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103157223 | ||||||
chr10:103157470
|
A | T | 11 | a0001c0002t0004g0015a0001c0002t0004g0016a0001c0002t0004g0017others(8): Show | 11 | HG00735.hp2 HG01109.hp2 HG01516.hp1 others(8): Show |
intron_variant | MODIFIER | c.101+17388T>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103157470 | ||||||
chr10:103157585
|
C | A | 29 | a0002c0003t0004g0002a0002c0003t0004g0003a0002c0003t0004g0005others(26): Show | 31 | HG00609.hp2 HG00621.hp2 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.101+17273G>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103157585 | ||||||
chr10:103157628
|
A | G | 13 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(10): Show | 13 | HG02135.hp1 HG03834.hp2 NA18940.hp2 others(10): Show |
intron_variant | MODIFIER | c.101+17230T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103157628 | ||||||
chr10:103157687
|
C | T | 13 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(10): Show | 13 | HG02135.hp1 HG03834.hp2 NA18940.hp2 others(10): Show |
intron_variant | MODIFIER | c.101+17171G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103157687 | ||||||
chr10:103157803
|
G | A | 3 | a0001c0002t0004g0010a0001c0002t0004g0011a0001c0002t0004g0012 | 3 | HG02109.hp2 HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.101+17055C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103157803 | ||||||
chr10:103157900
|
C | T | 1 | a0001c0001t0001g0118 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.101+16958G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103157900 | ||||||
chr10:103158063
|
C | T | 13 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(10): Show | 13 | HG02135.hp1 HG03834.hp2 NA18940.hp2 others(10): Show |
intron_variant | MODIFIER | c.101+16795G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103158063 | ||||||
chr10:103158077
|
G | GA | 20 | a0001c0001t0001g0150a0001c0001t0001g0180a0001c0001t0002g0004others(17): Show | 21 | HG00558.hp1 HG01257.hp2 HG01361.hp1 others(18): Show |
intron_variant | MODIFIER | c.101+16780dupT | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103158077 | ||||||
chr10:103158163
|
C | T | 1 | a0001c0001t0001g0123 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.101+16695G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103158163 | ||||||
chr10:103158356
|
A | T | 2 | a0001c0001t0002g0304a0001c0001t0002g0305 | 2 | HG01257.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.101+16502T>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103158356 | ||||||
chr10:103158364
|
A | G | 1 | a0001c0001t0002g0249 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.101+16494T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103158364 | ||||||
chr10:103158401
|
T | C | 1 | a0001c0002t0015g0013 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.101+16457A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103158401 | ||||||
chr10:103158644
|
C | T | 1 | a0001c0001t0001g0121 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.101+16214G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103158644 | ||||||
chr10:103158686
|
G | A | 1 | a0001c0001t0001g0183 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.101+16172C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103158686 | ||||||
chr10:103158817
|
TA | T | 150 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(147): Show | 150 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(147): Show |
intron_variant | MODIFIER | c.101+16040delT | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103158817 | ||||||
chr10:103159048
|
T | C | 1 | a0002c0003t0004g0219 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.101+15810A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103159048 | ||||||
chr10:103159075
|
A | C | 1 | a0001c0002t0005g0310 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.101+15783T>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103159075 | ||||||
chr10:103159110
|
G | C | 1 | a0001c0002t0014g0086 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.101+15748C>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103159110 | ||||||
chr10:103159195
|
T | A | 6 | a0001c0002t0008g0210a0001c0002t0008g0211a0001c0002t0008g0212others(3): Show | 6 | HG01884.hp2 HG02145.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.101+15663A>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103159195 | ||||||
chr10:103159251
|
G | GCA | 51 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(48): Show | 51 | HG00280.hp1 HG00597.hp1 HG00642.hp2 others(48): Show |
intron_variant | MODIFIER | c.101+15605_101+1560 others(6): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103159251 | ||||||
chr10:103159251
|
G | GCACA | 19 | a0001c0001t0001g0001a0001c0001t0001g0126a0001c0001t0001g0135others(16): Show | 20 | HG00280.hp2 HG00408.hp1 HG00544.hp1 others(17): Show |
intron_variant | MODIFIER | c.101+15603_101+1560 others(8): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103159251 | ||||||
chr10:103159251
|
G | GCACACA | 3 | a0001c0001t0001g0008a0001c0001t0001g0143a0001c0001t0001g0173 | 3 | HG02970.hp2 HG03139.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.101+15601_101+1560 others(10): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103159251 | ||||||
chr10:103159251
|
GCA | G | 49 | a0001c0001t0001g0106a0001c0001t0001g0112a0001c0001t0001g0114others(46): Show | 51 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.101+15605_101+1560 others(6): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103159251 | ||||||
chr10:103159251
|
GCACA | G | 85 | a0001c0001t0001g0097a0001c0001t0001g0208a0001c0001t0005g0317others(82): Show | 85 | HG00544.hp2 HG00597.hp2 HG00673.hp2 others(82): Show |
intron_variant | MODIFIER | c.101+15603_101+1560 others(8): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103159251 | ||||||
chr10:103159251
|
GCACACA | G | 28 | a0001c0001t0002g0246a0001c0002t0003g0037a0001c0002t0003g0081others(25): Show | 28 | HG00408.hp2 HG00609.hp1 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.101+15601_101+1560 others(10): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103159251 | ||||||
chr10:103159251
|
GCACACAC others(1): Show |
G | 15 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(12): Show | 15 | HG02257.hp1 HG02922.hp2 HG03041.hp2 others(12): Show |
intron_variant | MODIFIER | c.101+15599_101+1560 others(12): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103159251 | ||||||
chr10:103159251
|
GCACACAC others(5): Show |
G | 2 | a0001c0001t0002g0295a0001c0002t0004g0014 | 2 | HG03540.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.101+15595_101+1560 others(16): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103159251 | ||||||
chr10:103159251
|
GCACACAC others(7): Show |
G | 3 | a0001c0001t0002g0272a0001c0001t0002g0273a0001c0001t0002g0275 | 3 | NA19002.hp2 NA19067.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.101+15593_101+1560 others(18): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103159251 | ||||||
chr10:103159516
|
T | C | 1 | a0001c0001t0001g0169 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.101+15342A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103159516 | ||||||
chr10:103159559
|
G | A | 13 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(10): Show | 13 | HG02135.hp1 HG03834.hp2 NA18940.hp2 others(10): Show |
intron_variant | MODIFIER | c.101+15299C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103159559 | ||||||
chr10:103160179
|
T | C | 3 | a0001c0002t0004g0017a0001c0002t0004g0021a0001c0002t0004g0022 | 3 | HG01109.hp2 HG02055.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.101+14679A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103160179 | ||||||
chr10:103160470
|
A | G | 1 | a0001c0001t0001g0165 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.101+14388T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103160470 | ||||||
chr10:103160475
|
A | G | 181 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(178): Show | 183 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(180): Show |
intron_variant | MODIFIER | c.101+14383T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103160475 | ||||||
chr10:103160584
|
A | G | 113 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(110): Show | 115 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.101+14274T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103160584 | ||||||
chr10:103160743
|
G | A | 1 | a0002c0003t0004g0235 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.101+14115C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103160743 | ||||||
chr10:103160752
|
C | T | 34 | a0001c0002t0004g0010a0001c0002t0004g0011a0001c0002t0004g0012others(31): Show | 36 | HG00609.hp2 HG00621.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.101+14106G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103160752 | ||||||
chr10:103160841
|
T | C | 2 | a0001c0002t0003g0007a0001c0002t0003g0035 | 2 | NA18612.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.101+14017A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103160841 | ||||||
chr10:103161066
|
C | T | 1 | a0001c0002t0014g0086 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.101+13792G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103161066 | ||||||
chr10:103161132
|
T | C | 4 | a0001c0001t0001g0008a0001c0001t0001g0104a0001c0001t0001g0143others(1): Show | 4 | HG01928.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.101+13726A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103161132 | ||||||
chr10:103161411
|
TATG | T | 3 | a0001c0001t0001g0106a0001c0001t0001g0114a0001c0001t0001g0115 | 3 | HG02280.hp2 HG02717.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.101+13444_101+1344 others(7): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103161411 | ||||||
chr10:103161478
|
G | C | 1 | a0001c0001t0001g0164 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.101+13380C>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103161478 | ||||||
chr10:103161886
|
G | A | 13 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(10): Show | 13 | HG02135.hp1 HG03834.hp2 NA18940.hp2 others(10): Show |
intron_variant | MODIFIER | c.101+12972C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103161886 | ||||||
chr10:103162070
|
C | A | 1 | a0002c0003t0004g0229 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.101+12788G>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103162070 | ||||||
chr10:103162102
|
G | A | 13 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(10): Show | 13 | HG02135.hp1 HG03834.hp2 NA18940.hp2 others(10): Show |
intron_variant | MODIFIER | c.101+12756C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103162102 | ||||||
chr10:103162185
|
T | G | 1 | a0001c0001t0001g0174 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.101+12673A>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103162185 | ||||||
chr10:103162282
|
A | G | 180 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(177): Show | 182 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(179): Show |
intron_variant | MODIFIER | c.101+12576T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103162282 | ||||||
chr10:103162305
|
C | T | 1 | a0001c0002t0004g0014 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.101+12553G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103162305 | ||||||
chr10:103162373
|
A | G | 1 | a0001c0001t0001g0123 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.101+12485T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103162373 | ||||||
chr10:103162427
|
T | C | 1 | a0002c0003t0004g0224 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.101+12431A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103162427 | ||||||
chr10:103162638
|
C | T | 1 | a0001c0001t0002g0251 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.101+12220G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103162638 | ||||||
chr10:103162788
|
A | G | 10 | a0001c0002t0003g0031a0001c0002t0003g0032a0001c0002t0003g0033others(7): Show | 10 | NA18951.hp2 NA18962.hp2 NA18990.hp2 others(7): Show |
intron_variant | MODIFIER | c.101+12070T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103162788 | ||||||
chr10:103162789
|
T | C | 1 | a0001c0001t0002g0278 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.101+12069A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103162789 | ||||||
chr10:103162989
|
G | C | 2 | a0001c0001t0001g0181a0001c0001t0001g0183 | 2 | HG01192.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.101+11869C>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103162989 | ||||||
chr10:103163155
|
T | C | 1 | a0001c0001t0001g0096 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.101+11703A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103163155 | ||||||
chr10:103163322
|
T | C | 13 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(10): Show | 13 | HG02135.hp1 HG03834.hp2 NA18940.hp2 others(10): Show |
intron_variant | MODIFIER | c.101+11536A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103163322 | ||||||
chr10:103163331
|
C | G | 1 | a0001c0001t0002g0248 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.101+11527G>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103163331 | ||||||
chr10:103163382
|
T | C | 1 | a0001c0002t0014g0086 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.101+11476A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103163382 | ||||||
chr10:103163655
|
C | T | 1 | a0001c0001t0002g0248 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.101+11203G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103163655 | ||||||
chr10:103163710
|
T | TA | 111 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(108): Show | 113 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(110): Show |
intron_variant | MODIFIER | c.101+11147dupT | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103163710 | ||||||
chr10:103163789
|
G | C | 1 | a0001c0002t0003g0032 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.101+11069C>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103163789 | ||||||
chr10:103163838
|
G | A | 113 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(110): Show | 115 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.101+11020C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103163838 | ||||||
chr10:103163843
|
C | T | 1 | a0001c0001t0001g0001 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.101+11015G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103163843 | ||||||
chr10:103163860
|
C | CAAA | 8 | a0001c0001t0001g0088a0001c0001t0001g0090a0001c0001t0001g0092others(5): Show | 8 | HG03834.hp2 NA18940.hp2 NA18943.hp2 others(5): Show |
intron_variant | MODIFIER | c.101+10995_101+1099 others(7): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103163860 | ||||||
chr10:103163863
|
AAAAAAAA others(1): Show |
A | 29 | a0002c0003t0004g0002a0002c0003t0004g0003a0002c0003t0004g0005others(26): Show | 31 | HG00609.hp2 HG00621.hp2 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.101+10987_101+1099 others(12): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103163863 | ||||||
chr10:103163865
|
A | C | 2 | a0001c0001t0001g0122a0001c0001t0001g0167 | 2 | HG03098.hp1 NA18939.hp2 |
intron_variant | MODIFIER | c.101+10993T>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103163865 | ||||||
chr10:103163870
|
AC | A | 124 | a0001c0001t0005g0317a0001c0001t0005g0323a0001c0002t0003g0007others(121): Show | 124 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(121): Show |
intron_variant | MODIFIER | c.101+10987delG | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103163870 | ||||||
chr10:103163871
|
C | A | 24 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(21): Show | 24 | HG00735.hp2 HG01433.hp2 HG01952.hp2 others(21): Show |
intron_variant | MODIFIER | c.101+10987G>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103163871 | ||||||
chr10:103163876
|
A | C | 1 | a0001c0001t0001g0124 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.101+10982T>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103163876 | ||||||
chr10:103164051
|
C | T | 1 | a0001c0001t0001g0112 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.101+10807G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103164051 | ||||||
chr10:103164282
|
G | A | 18 | a0001c0002t0006g0184a0001c0002t0006g0185a0001c0002t0006g0186others(15): Show | 18 | HG00408.hp2 HG00609.hp1 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.101+10576C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103164282 | ||||||
chr10:103164311
|
G | A | 1 | a0001c0002t0015g0013 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.101+10547C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103164311 | ||||||
chr10:103164599
|
A | G | 1 | a0001c0002t0006g0184 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.101+10259T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103164599 | ||||||
chr10:103164675
|
T | C | 1 | a0001c0002t0005g0316 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.101+10183A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103164675 | ||||||
chr10:103164696
|
A | C | 1 | a0001c0002t0003g0078 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.101+10162T>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103164696 | ||||||
chr10:103164697
|
A | T | 1 | a0001c0002t0003g0078 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.101+10161T>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103164697 | ||||||
chr10:103164698
|
A | C | 1 | a0001c0002t0003g0078 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.101+10160T>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103164698 | ||||||
chr10:103165063
|
G | A | 49 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0104others(46): Show | 50 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(47): Show |
intron_variant | MODIFIER | c.101+9795C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103165063 | ||||||
chr10:103165081
|
G | A | 29 | a0002c0003t0004g0002a0002c0003t0004g0003a0002c0003t0004g0005others(26): Show | 31 | HG00609.hp2 HG00621.hp2 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.101+9777C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103165081 | ||||||
chr10:103165219
|
C | T | 1 | a0001c0002t0003g0053 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.101+9639G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103165219 | ||||||
chr10:103165241
|
C | T | 1 | a0001c0002t0005g0330 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.101+9617G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103165241 | ||||||
chr10:103165301
|
C | T | 1 | a0001c0002t0004g0202 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.101+9557G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103165301 | ||||||
chr10:103165408
|
G | A | 1 | a0001c0001t0002g0307 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.101+9450C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103165408 | ||||||
chr10:103165562
|
T | C | 1 | a0001c0001t0002g0262 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.101+9296A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103165562 | ||||||
chr10:103165574
|
C | CT | 7 | a0001c0001t0002g0247a0001c0001t0002g0248a0001c0001t0002g0252others(4): Show | 7 | HG01978.hp1 HG03831.hp2 NA18940.hp1 others(4): Show |
intron_variant | MODIFIER | c.101+9283dupA | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103165574 | ||||||
chr10:103165574
|
CT | C | 205 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0087others(202): Show | 206 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(203): Show |
intron_variant | MODIFIER | c.101+9283delA | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103165574 | ||||||
chr10:103165574
|
CTT | C | 35 | a0001c0001t0001g0112a0001c0001t0001g0133a0001c0001t0001g0161others(32): Show | 37 | HG00609.hp2 HG00621.hp2 HG00639.hp1 others(34): Show |
intron_variant | MODIFIER | c.101+9282_101+9283d others(4): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103165574 | ||||||
chr10:103165675
|
AT | A | 179 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(176): Show | 181 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(178): Show |
intron_variant | MODIFIER | c.101+9182delA | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103165675 | ||||||
chr10:103165786
|
C | G | 18 | a0001c0002t0006g0184a0001c0002t0006g0185a0001c0002t0006g0186others(15): Show | 18 | HG00408.hp2 HG00609.hp1 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.101+9072G>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103165786 | ||||||
chr10:103165806
|
G | C | 1 | a0001c0002t0005g0334 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.101+9052C>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103165806 | ||||||
chr10:103166028
|
G | A | 5 | a0001c0002t0008g0210a0001c0002t0008g0211a0001c0002t0008g0212others(2): Show | 5 | HG01884.hp2 HG02145.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.101+8830C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103166028 | ||||||
chr10:103166072
|
A | C | 181 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(178): Show | 183 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(180): Show |
intron_variant | MODIFIER | c.101+8786T>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103166072 | ||||||
chr10:103166558
|
C | A | 3 | a0001c0002t0006g0187a0001c0002t0006g0189a0001c0002t0006g0190 | 3 | HG01070.hp2 HG01071.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.101+8300G>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103166558 | ||||||
chr10:103166577
|
T | C | 113 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(110): Show | 115 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.101+8281A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103166577 | ||||||
chr10:103166583
|
A | G | 1 | a0001c0002t0008g0215 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.101+8275T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103166583 | ||||||
chr10:103166600
|
A | C | 8 | a0001c0001t0001g0106a0001c0001t0001g0114a0001c0001t0001g0115others(5): Show | 8 | HG01081.hp1 HG01884.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.101+8258T>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103166600 | ||||||
chr10:103166608
|
AAAAC | A | 42 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(39): Show | 44 | HG00609.hp2 HG00621.hp2 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.101+8246_101+8249d others(6): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103166608 | ||||||
chr10:103166666
|
T | C | 1 | a0001c0002t0003g0078 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.101+8192A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103166666 | ||||||
chr10:103166728
|
T | C | 13 | a0002c0003t0004g0002a0002c0003t0004g0220a0002c0003t0004g0221others(10): Show | 14 | HG00639.hp1 HG00642.hp1 HG00733.hp2 others(11): Show |
intron_variant | MODIFIER | c.101+8130A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103166728 | ||||||
chr10:103166758
|
T | A | 1 | a0002c0003t0004g0226 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.101+8100A>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103166758 | ||||||
chr10:103166851
|
T | C | 1 | a0001c0002t0005g0318 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.101+8007A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103166851 | ||||||
chr10:103167119
|
G | A | 12 | a0001c0002t0005g0315a0001c0002t0005g0316a0001c0002t0005g0321others(9): Show | 12 | HG00639.hp2 HG00738.hp1 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.101+7739C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103167119 | ||||||
chr10:103167176
|
T | C | 113 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(110): Show | 115 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.101+7682A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103167176 | ||||||
chr10:103167383
|
A | T | 2 | a0001c0001t0001g0120a0001c0001t0001g0178 | 2 | HG02896.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.101+7475T>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103167383 | ||||||
chr10:103167441
|
C | T | 1 | a0001c0001t0001g0154 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.101+7417G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103167441 | ||||||
chr10:103167615
|
A | T | 1 | a0001c0001t0001g0164 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.101+7243T>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103167615 | ||||||
chr10:103167748
|
T | TA | 11 | a0001c0002t0004g0015a0001c0002t0004g0016a0001c0002t0004g0017others(8): Show | 11 | HG00735.hp2 HG01109.hp2 HG01516.hp1 others(8): Show |
intron_variant | MODIFIER | c.101+7109dupT | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103167748 | ||||||
chr10:103167877
|
A | G | 181 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(178): Show | 183 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(180): Show |
intron_variant | MODIFIER | c.101+6981T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103167877 | ||||||
chr10:103167939
|
T | A | 1 | a0001c0001t0002g0293 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.101+6919A>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103167939 | ||||||
chr10:103168104
|
T | TA | 41 | a0001c0001t0005g0317a0001c0001t0005g0323a0001c0002t0004g0015others(38): Show | 41 | HG00597.hp2 HG00639.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.101+6753dupT | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103168104 | ||||||
chr10:103168378
|
A | G | 2 | a0001c0001t0001g0008a0001c0001t0001g0173 | 2 | HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.101+6480T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103168378 | ||||||
chr10:103168407
|
G | C | 18 | a0001c0002t0006g0184a0001c0002t0006g0185a0001c0002t0006g0186others(15): Show | 18 | HG00408.hp2 HG00609.hp1 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.101+6451C>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103168407 | ||||||
chr10:103168550
|
G | T | 1 | a0001c0002t0004g0012 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.101+6308C>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103168550 | ||||||
chr10:103168956
|
T | G | 1 | a0001c0002t0015g0013 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.101+5902A>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103168956 | ||||||
chr10:103168967
|
G | C | 1 | a0001c0002t0014g0086 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.101+5891C>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103168967 | ||||||
chr10:103169013
|
T | A | 113 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(110): Show | 115 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.101+5845A>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103169013 | ||||||
chr10:103169014
|
TA | T | 113 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(110): Show | 115 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.101+5843delT | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103169014 | ||||||
chr10:103169072
|
T | A | 1 | a0001c0002t0008g0215 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.101+5786A>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103169072 | ||||||
chr10:103169154
|
A | C | 1 | a0001c0002t0003g0032 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.101+5704T>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103169154 | ||||||
chr10:103169157
|
T | A | 67 | a0001c0002t0003g0007a0001c0002t0003g0023a0001c0002t0003g0024others(64): Show | 67 | HG00544.hp2 HG01069.hp1 HG01167.hp1 others(64): Show |
intron_variant | MODIFIER | c.101+5701A>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103169157 | ||||||
chr10:103169356
|
C | A | 41 | a0001c0001t0005g0317a0001c0001t0005g0323a0001c0002t0004g0015others(38): Show | 41 | HG00597.hp2 HG00639.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.101+5502G>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103169356 | ||||||
chr10:103169367
|
A | G | 100 | a0001c0001t0005g0317a0001c0001t0005g0323a0001c0002t0004g0010others(97): Show | 102 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(99): Show |
intron_variant | MODIFIER | c.101+5491T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103169367 | ||||||
chr10:103169434
|
C | T | 181 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(178): Show | 183 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(180): Show |
intron_variant | MODIFIER | c.101+5424G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103169434 | ||||||
chr10:103169440
|
G | A | 1 | a0001c0001t0001g0126 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.101+5418C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103169440 | ||||||
chr10:103169618
|
CA | C | 69 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0102others(66): Show | 70 | HG00280.hp2 HG00408.hp1 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.101+5239delT | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103169618 | ||||||
chr10:103169687
|
A | G | 1 | a0001c0002t0004g0014 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.101+5171T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103169687 | ||||||
chr10:103169798
|
T | C | 1 | a0001c0001t0001g0097 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.101+5060A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103169798 | ||||||
chr10:103169813
|
T | C | 1 | a0001c0001t0001g0156 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.101+5045A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103169813 | ||||||
chr10:103169959
|
T | C | 68 | a0001c0002t0003g0007a0001c0002t0003g0023a0001c0002t0003g0024others(65): Show | 68 | HG00544.hp2 HG01069.hp1 HG01167.hp1 others(65): Show |
intron_variant | MODIFIER | c.101+4899A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103169959 | ||||||
chr10:103169991
|
G | A | 13 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(10): Show | 13 | HG02135.hp1 HG03834.hp2 NA18940.hp2 others(10): Show |
intron_variant | MODIFIER | c.101+4867C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103169991 | ||||||
chr10:103170377
|
C | A | 5 | a0001c0002t0008g0210a0001c0002t0008g0211a0001c0002t0008g0212others(2): Show | 5 | HG01884.hp2 HG02145.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.101+4481G>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103170377 | ||||||
chr10:103170497
|
ACACACAC others(5): Show |
A | 2 | a0001c0001t0007g0144a0001c0001t0007g0162 | 2 | HG00558.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.101+4349_101+4360d others(14): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103170497 | ||||||
chr10:103170526
|
CT | C | 87 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(84): Show | 87 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.101+4331delA | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103170526 | ||||||
chr10:103170526
|
CTT | C | 98 | a0001c0001t0001g0097a0001c0001t0005g0317a0001c0001t0005g0323others(95): Show | 100 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(97): Show |
intron_variant | MODIFIER | c.101+4330_101+4331d others(4): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103170526 | ||||||
chr10:103170625
|
T | C | 113 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(110): Show | 115 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.101+4233A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103170625 | ||||||
chr10:103170634
|
C | T | 4 | a0001c0001t0001g0001a0001c0001t0001g0141a0001c0001t0001g0146others(1): Show | 5 | HG00280.hp2 HG01167.hp2 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.101+4224G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103170634 | ||||||
chr10:103170697
|
G | GT | 26 | a0001c0001t0001g0095a0001c0001t0001g0100a0001c0001t0001g0101others(23): Show | 26 | HG00408.hp2 HG00609.hp1 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.101+4160dupA | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103170697 | ||||||
chr10:103170729
|
C | T | 334 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0087others(331): Show | 338 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(335): Show |
intron_variant | MODIFIER | c.101+4129G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103170729 | ||||||
chr10:103170770
|
G | A | 2 | a0001c0001t0002g0304a0001c0001t0002g0305 | 2 | HG01257.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.101+4088C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103170770 | ||||||
chr10:103170836
|
T | C | 3 | a0001c0002t0006g0187a0001c0002t0006g0189a0001c0002t0006g0190 | 3 | HG01070.hp2 HG01071.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.101+4022A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103170836 | ||||||
chr10:103170879
|
C | T | 1 | a0001c0002t0013g0195 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.101+3979G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103170879 | ||||||
chr10:103170925
|
C | T | 1 | a0001c0002t0003g0067 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.101+3933G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103170925 | ||||||
chr10:103171294
|
C | T | 113 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(110): Show | 115 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.101+3564G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103171294 | ||||||
chr10:103171474
|
G | A | 13 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(10): Show | 13 | HG02135.hp1 HG03834.hp2 NA18940.hp2 others(10): Show |
intron_variant | MODIFIER | c.101+3384C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103171474 | ||||||
chr10:103171501
|
G | C | 1 | a0001c0001t0007g0140 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.101+3357C>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103171501 | ||||||
chr10:103171827
|
G | C | 68 | a0001c0002t0003g0007a0001c0002t0003g0023a0001c0002t0003g0024others(65): Show | 68 | HG00544.hp2 HG01069.hp1 HG01167.hp1 others(65): Show |
intron_variant | MODIFIER | c.101+3031C>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103171827 | ||||||
chr10:103171914
|
A | T | 2 | a0001c0002t0003g0046a0001c0002t0005g0322 | 2 | HG02809.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.101+2944T>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103171914 | ||||||
chr10:103171932
|
G | A | 1 | a0001c0001t0001g0145 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.101+2926C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103171932 | ||||||
chr10:103172061
|
T | C | 3 | a0002c0003t0004g0225a0002c0003t0004g0226a0002c0003t0004g0232 | 3 | HG00642.hp1 HG01255.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.101+2797A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103172061 | ||||||
chr10:103172082
|
T | G | 1 | a0001c0002t0003g0053 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.101+2776A>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103172082 | ||||||
chr10:103172100
|
C | T | 8 | a0001c0002t0003g0007a0001c0002t0003g0035a0001c0002t0003g0043others(5): Show | 8 | HG02273.hp1 HG02300.hp1 NA18612.hp2 others(5): Show |
intron_variant | MODIFIER | c.101+2758G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103172100 | ||||||
chr10:103172102
|
C | T | 8 | a0001c0001t0002g0246a0001c0001t0002g0258a0001c0001t0002g0265others(5): Show | 8 | NA18945.hp1 NA18952.hp1 NA18953.hp1 others(5): Show |
intron_variant | MODIFIER | c.101+2756G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103172102 | ||||||
chr10:103172118
|
G | A | 1 | a0001c0001t0001g0181 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.101+2740C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103172118 | ||||||
chr10:103172134
|
T | C | 9 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0111others(6): Show | 9 | HG01109.hp1 HG02896.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.101+2724A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103172134 | ||||||
chr10:103172166
|
C | T | 13 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(10): Show | 13 | HG02135.hp1 HG03834.hp2 NA18940.hp2 others(10): Show |
intron_variant | MODIFIER | c.101+2692G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103172166 | ||||||
chr10:103172247
|
A | AT | 92 | a0001c0001t0001g0096a0001c0001t0005g0317a0001c0001t0005g0323others(89): Show | 94 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(91): Show |
intron_variant | MODIFIER | c.101+2610dupA | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103172247 | ||||||
chr10:103172247
|
A | ATT | 6 | a0001c0002t0008g0210a0001c0002t0008g0211a0001c0002t0008g0212others(3): Show | 6 | HG01884.hp2 HG02145.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.101+2609_101+2610d others(4): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103172247 | ||||||
chr10:103172249
|
T | A | 1 | a0001c0001t0001g0136 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.101+2609A>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103172249 | ||||||
chr10:103172305
|
G | A | 12 | a0001c0002t0005g0315a0001c0002t0005g0316a0001c0002t0005g0321others(9): Show | 12 | HG00639.hp2 HG00738.hp1 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.101+2553C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103172305 | ||||||
chr10:103172404
|
A | G | 1 | a0001c0002t0004g0010 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.101+2454T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103172404 | ||||||
chr10:103172410
|
G | A | 13 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(10): Show | 13 | HG02135.hp1 HG03834.hp2 NA18940.hp2 others(10): Show |
intron_variant | MODIFIER | c.101+2448C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103172410 | ||||||
chr10:103172494
|
G | A | 1 | a0001c0001t0007g0139 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.101+2364C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103172494 | ||||||
chr10:103172549
|
T | C | 5 | a0001c0002t0005g0318a0001c0002t0005g0319a0001c0002t0005g0320others(2): Show | 5 | HG02258.hp1 HG02647.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.101+2309A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103172549 | ||||||
chr10:103172558
|
ACTCACGG others(5): Show |
A | 3 | a0001c0002t0004g0203a0001c0002t0004g0204a0001c0002t0004g0205 | 3 | HG02622.hp1 HG02896.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.101+2288_101+2299d others(14): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103172558 | ||||||
chr10:103172604
|
G | A | 4 | a0001c0001t0002g0253a0001c0001t0002g0254a0001c0001t0002g0255others(1): Show | 4 | HG01069.hp2 HG01071.hp2 HG01081.hp2 others(1): Show |
intron_variant | MODIFIER | c.101+2254C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103172604 | ||||||
chr10:103172985
|
G | C | 1 | a0001c0002t0006g0196 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.101+1873C>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103172985 | ||||||
chr10:103172995
|
G | A | 2 | a0001c0001t0001g0092a0001c0001t0001g0093 | 2 | NA18943.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.101+1863C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103172995 | ||||||
chr10:103173482
|
T | G | 1 | a0001c0001t0001g0156 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.101+1376A>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103173482 | ||||||
chr10:103173486
|
G | A | 15 | a0002c0003t0004g0003a0002c0003t0004g0005a0002c0003t0004g0009others(12): Show | 16 | HG00609.hp2 HG00621.hp2 HG00673.hp1 others(13): Show |
intron_variant | MODIFIER | c.101+1372C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103173486 | ||||||
chr10:103173611
|
C | CA | 34 | a0001c0001t0001g0122a0001c0001t0001g0163a0001c0001t0002g0246others(31): Show | 34 | HG00408.hp2 HG00609.hp1 HG00733.hp2 others(31): Show |
intron_variant | MODIFIER | c.101+1246dupT | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103173611 | ||||||
chr10:103173611
|
C | CAA | 14 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(11): Show | 14 | HG02135.hp1 HG02683.hp1 HG03834.hp2 others(11): Show |
intron_variant | MODIFIER | c.101+1245_101+1246d others(4): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103173611 | ||||||
chr10:103173648
|
C | T | 1 | a0001c0001t0001g0207 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.101+1210G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103173648 | ||||||
chr10:103173692
|
C | T | 82 | a0001c0001t0005g0317a0001c0001t0005g0323a0001c0002t0004g0010others(79): Show | 84 | HG00597.hp2 HG00609.hp2 HG00621.hp2 others(81): Show |
intron_variant | MODIFIER | c.101+1166G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103173692 | ||||||
chr10:103173754
|
G | T | 29 | a0002c0003t0004g0002a0002c0003t0004g0003a0002c0003t0004g0005others(26): Show | 31 | HG00609.hp2 HG00621.hp2 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.101+1104C>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103173754 | ||||||
chr10:103173897
|
A | G | 41 | a0001c0001t0005g0317a0001c0001t0005g0323a0001c0002t0004g0015others(38): Show | 41 | HG00597.hp2 HG00639.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.101+961T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103173897 | ||||||
chr10:103173913
|
C | T | 1 | a0001c0001t0002g0278 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.101+945G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103173913 | ||||||
chr10:103173922
|
C | T | 2 | a0001c0001t0001g0001a0001c0001t0001g0146 | 3 | HG00280.hp2 HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.101+936G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103173922 | ||||||
chr10:103173964
|
C | T | 1 | a0001c0001t0001g0098 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.101+894G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103173964 | ||||||
chr10:103174074
|
C | T | 1 | a0001c0002t0003g0071 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.101+784G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103174074 | ||||||
chr10:103174095
|
C | CA | 11 | a0001c0001t0001g0106a0001c0001t0001g0112a0001c0001t0001g0133others(8): Show | 11 | HG01069.hp2 HG01071.hp2 HG02027.hp2 others(8): Show |
intron_variant | MODIFIER | c.101+762dupT | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103174095 | ||||||
chr10:103174095
|
CA | C | 66 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(63): Show | 66 | HG00597.hp2 HG00639.hp2 HG00673.hp2 others(63): Show |
intron_variant | MODIFIER | c.101+762delT | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103174095 | ||||||
chr10:103174164
|
C | T | 113 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(110): Show | 115 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.101+694G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103174164 | ||||||
chr10:103174178
|
G | A | 1 | a0001c0002t0004g0202 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.101+680C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103174178 | ||||||
chr10:103174197
|
A | G | 13 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(10): Show | 13 | HG02135.hp1 HG03834.hp2 NA18940.hp2 others(10): Show |
intron_variant | MODIFIER | c.101+661T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103174197 | ||||||
chr10:103174222
|
C | T | 6 | a0001c0002t0008g0210a0001c0002t0008g0211a0001c0002t0008g0212others(3): Show | 6 | HG01884.hp2 HG02145.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.101+636G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103174222 | ||||||
chr10:103174476
|
C | A | 1 | a0001c0001t0001g0097 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.101+382G>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103174476 | ||||||
chr10:103174544
|
C | G | 1 | a0002c0003t0004g0219 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.101+314G>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103174544 | ||||||
chr10:103174639
|
CAA | C | 82 | a0001c0001t0005g0317a0001c0001t0005g0323a0001c0002t0004g0010others(79): Show | 84 | HG00597.hp2 HG00609.hp2 HG00621.hp2 others(81): Show |
intron_variant | MODIFIER | c.101+217_101+218del others(2): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103174639 | ||||||
chr10:103174732
|
G | A | 1 | a0002c0003t0004g0227 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.101+126C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103174732 | ||||||
chr10:103174806
|
G | A | 4 | a0001c0001t0002g0263a0001c0001t0002g0264a0001c0001t0002g0276others(1): Show | 4 | HG02683.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.101+52C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103174806 | ||||||
chr10:103175081
|
C | T | 3 | a0001c0001t0001g0106a0001c0001t0001g0114a0001c0001t0001g0115 | 3 | HG02280.hp2 HG02717.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-24-99G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 2/18 | chr10 | 103175081 | ||||||
chr10:103175138
|
C | G | 1 | a0001c0001t0001g0174 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-24-156G>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 2/18 | chr10 | 103175138 | ||||||
chr10:103175195
|
C | T | 41 | a0001c0001t0005g0317a0001c0001t0005g0323a0001c0002t0004g0015others(38): Show | 41 | HG00597.hp2 HG00639.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.-24-213G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 2/18 | chr10 | 103175195 | ||||||
chr10:103175400
|
G | A | 1 | a0001c0001t0001g0183 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-24-418C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 2/18 | chr10 | 103175400 | ||||||
chr10:103175415
|
T | C | 1 | a0001c0001t0001g0097 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-24-433A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 2/18 | chr10 | 103175415 | ||||||
chr10:103175517
|
G | A | 13 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(10): Show | 13 | HG02135.hp1 HG03834.hp2 NA18940.hp2 others(10): Show |
intron_variant | MODIFIER | c.-24-535C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 2/18 | chr10 | 103175517 | ||||||
chr10:103175607
|
G | T | 1 | a0001c0002t0013g0195 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-24-625C>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 2/18 | chr10 | 103175607 | ||||||
chr10:103175755
|
A | G | 1 | a0001c0001t0001g0120 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-24-773T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 2/18 | chr10 | 103175755 | ||||||
chr10:103175836
|
G | C | 180 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(177): Show | 182 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(179): Show |
intron_variant | MODIFIER | c.-24-854C>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 2/18 | chr10 | 103175836 | ||||||
chr10:103175929
|
G | A | 1 | a0001c0001t0001g0133 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-24-947C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 2/18 | chr10 | 103175929 | ||||||
chr10:103176038
|
A | T | 1 | a0001c0001t0001g0174 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-24-1056T>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 2/18 | chr10 | 103176038 | ||||||
chr10:103176683
|
C | T | 2 | a0002c0003t0004g0216a0002c0003t0004g0218 | 2 | NA18941.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.-24-1701G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 2/18 | chr10 | 103176683 | ||||||
chr10:103176697
|
C | A | 6 | a0001c0002t0008g0210a0001c0002t0008g0211a0001c0002t0008g0212others(3): Show | 6 | HG01884.hp2 HG02145.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-24-1715G>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 2/18 | chr10 | 103176697 | ||||||
chr10:103176813
|
A | G | 1 | a0001c0002t0006g0184 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-24-1831T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 2/18 | chr10 | 103176813 | ||||||
chr10:103176922
|
T | C | 1 | a0001c0001t0002g0283 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-24-1940A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 2/18 | chr10 | 103176922 | ||||||
chr10:103176946
|
TC | T | 3 | a0001c0002t0006g0194a0001c0002t0006g0197a0001c0002t0006g0200 | 3 | HG03831.hp1 HG03942.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.-24-1965delG | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 2/18 | chr10 | 103176946 | ||||||
chr10:103177051
|
T | C | 1 | a0001c0001t0001g0160 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-24-2069A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 2/18 | chr10 | 103177051 | ||||||
chr10:103177209
|
C | T | 2 | a0001c0002t0004g0011a0001c0002t0004g0012 | 2 | HG02109.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-24-2227G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 2/18 | chr10 | 103177209 | ||||||
chr10:103177232
|
A | G | 1 | a0001c0002t0004g0202 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-24-2250T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 2/18 | chr10 | 103177232 | ||||||
chr10:103177343
|
G | C | 100 | a0001c0001t0005g0317a0001c0001t0005g0323a0001c0002t0004g0010others(97): Show | 102 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(99): Show |
intron_variant | MODIFIER | c.-24-2361C>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 2/18 | chr10 | 103177343 | ||||||
chr10:103177470
|
C | T | 1 | a0002c0003t0004g0219 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-24-2488G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 2/18 | chr10 | 103177470 | ||||||
chr10:103177627
|
TC | T | 54 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0104others(51): Show | 55 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(52): Show |
intron_variant | MODIFIER | c.-24-2646delG | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 2/18 | chr10 | 103177627 | ||||||
chr10:103177646
|
AGAACAGC others(12): Show |
A | 1 | a0001c0001t0001g0207 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-24-2683_-24-2665d others(21): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 2/18 | chr10 | 103177646 | ||||||
chr10:103177778
|
A | T | 1 | a0001c0002t0005g0314 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-24-2796T>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 2/18 | chr10 | 103177778 | ||||||
chr10:103178146
|
G | A | 1 | a0001c0001t0001g0126 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-25+3039C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 2/18 | chr10 | 103178146 | ||||||
chr10:103178283
|
C | T | 1 | a0001c0002t0005g0334 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-25+2902G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 2/18 | chr10 | 103178283 | ||||||
chr10:103178356
|
G | A | 1 | a0001c0002t0005g0316 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-25+2829C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 2/18 | chr10 | 103178356 | ||||||
chr10:103178378
|
C | G | 1 | a0001c0001t0001g0177 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-25+2807G>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 2/18 | chr10 | 103178378 | ||||||
chr10:103178456
|
T | G | 1 | a0001c0002t0005g0322 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-25+2729A>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 2/18 | chr10 | 103178456 | ||||||
chr10:103178833
|
C | CA | 82 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(79): Show | 82 | HG00544.hp2 HG00621.hp2 HG01069.hp1 others(79): Show |
intron_variant | MODIFIER | c.-25+2351dupT | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 2/18 | chr10 | 103178833 | ||||||
chr10:103178849
|
A | AG | 18 | a0001c0002t0006g0184a0001c0002t0006g0185a0001c0002t0006g0186others(15): Show | 18 | HG00408.hp2 HG00609.hp1 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.-25+2335dupC | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 2/18 | chr10 | 103178849 | ||||||
chr10:103178954
|
C | CTTTTTTT | 11 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(8): Show | 11 | HG02135.hp1 HG03834.hp2 NA18943.hp2 others(8): Show |
intron_variant | MODIFIER | c.-25+2224_-25+2230d others(9): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 2/18 | chr10 | 103178954 | ||||||
chr10:103178954
|
C | CTTTTTTT others(1): Show |
95 | a0001c0001t0001g0095a0001c0001t0001g0098a0001c0001t0005g0323others(92): Show | 97 | HG00408.hp2 HG00609.hp1 HG00609.hp2 others(94): Show |
intron_variant | MODIFIER | c.-25+2223_-25+2230d others(10): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 2/18 | chr10 | 103178954 | ||||||
chr10:103178954
|
C | CTTTTTTT others(2): Show |
7 | a0001c0001t0005g0317a0001c0002t0005g0319a0001c0002t0006g0198others(4): Show | 7 | HG00597.hp2 HG02257.hp1 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.-25+2222_-25+2230d others(11): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 2/18 | chr10 | 103178954 | ||||||
chr10:103179105
|
T | A | 1 | a0001c0002t0005g0335 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-25+2080A>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 2/18 | chr10 | 103179105 | ||||||
chr10:103179109
|
C | G | 3 | a0001c0002t0004g0017a0001c0002t0004g0021a0001c0002t0004g0022 | 3 | HG01109.hp2 HG02055.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-25+2076G>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 2/18 | chr10 | 103179109 | ||||||
chr10:103179224
|
G | A | 1 | a0001c0002t0003g0078 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-25+1961C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 2/18 | chr10 | 103179224 | ||||||
chr10:103179295
|
C | T | 18 | a0001c0002t0006g0184a0001c0002t0006g0185a0001c0002t0006g0186others(15): Show | 18 | HG00408.hp2 HG00609.hp1 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.-25+1890G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 2/18 | chr10 | 103179295 | ||||||
chr10:103179425
|
G | A | 113 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(110): Show | 115 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.-25+1760C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 2/18 | chr10 | 103179425 | ||||||
chr10:103179458
|
T | C | 68 | a0001c0002t0003g0007a0001c0002t0003g0023a0001c0002t0003g0024others(65): Show | 68 | HG00544.hp2 HG01069.hp1 HG01167.hp1 others(65): Show |
intron_variant | MODIFIER | c.-25+1727A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 2/18 | chr10 | 103179458 | ||||||
chr10:103179475
|
G | A | 41 | a0001c0001t0005g0317a0001c0001t0005g0323a0001c0002t0004g0015others(38): Show | 41 | HG00597.hp2 HG00639.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.-25+1710C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 2/18 | chr10 | 103179475 | ||||||
chr10:103179526
|
A | G | 113 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(110): Show | 115 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.-25+1659T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 2/18 | chr10 | 103179526 | ||||||
chr10:103179633
|
T | TA | 7 | a0001c0001t0001g0106a0001c0001t0001g0114a0001c0001t0001g0115others(4): Show | 7 | HG01081.hp1 HG01884.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.-25+1551_-25+1552i others(3): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 2/18 | chr10 | 103179633 | ||||||
chr10:103180126
|
C | A | 1 | a0001c0001t0002g0248 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-25+1059G>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 2/18 | chr10 | 103180126 | ||||||
chr10:103180397
|
G | A | 1 | a0001c0002t0003g0078 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-25+788C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 2/18 | chr10 | 103180397 | ||||||
chr10:103180496
|
C | T | 1 | a0001c0002t0003g0058 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-25+689G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 2/18 | chr10 | 103180496 | ||||||
chr10:103180525
|
A | C | 2 | a0001c0002t0004g0015a0001c0002t0004g0016 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-25+660T>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 2/18 | chr10 | 103180525 | ||||||
chr10:103180767
|
T | C | 1 | a0001c0002t0005g0316 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-25+418A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 2/18 | chr10 | 103180767 | ||||||
chr10:103180902
|
C | T | 2 | a0001c0001t0002g0277a0001c0001t0018g0256 | 2 | HG00558.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.-25+283G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 2/18 | chr10 | 103180902 | ||||||
chr10:103180957
|
G | A | 3 | a0001c0002t0003g0023a0001c0002t0003g0024a0001c0002t0003g0079 | 3 | NA18957.hp1 NA18978.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.-25+228C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 2/18 | chr10 | 103180957 | ||||||
chr10:103181038
|
G | A | 4 | a0001c0001t0005g0317a0001c0001t0005g0323a0001c0002t0005g0328others(1): Show | 4 | HG00597.hp2 HG00673.hp2 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.-25+147C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 2/18 | chr10 | 103181038 | ||||||
chr10:103181096
|
C | T | 1 | a0001c0001t0001g0136 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-25+89G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 2/18 | chr10 | 103181096 | ||||||
chr10:103181110
|
A | G | 8 | a0001c0002t0004g0015a0001c0002t0004g0016a0001c0002t0004g0017others(5): Show | 8 | HG00735.hp2 HG01109.hp2 HG01516.hp1 others(5): Show |
intron_variant | MODIFIER | c.-25+75T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 2/18 | chr10 | 103181110 | ||||||
chr10:103181178
|
T | C | 3 | a0001c0002t0003g0025a0001c0002t0003g0054a0001c0002t0017g0066 | 3 | HG02071.hp2 HG02074.hp2 HG02129.hp2 |
splice_region_variant&intron_variant | LOW | c.-25+7A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 2/18 | chr10 | 103181178 | ||||||
chr10:103181335
|
C | CA | 72 | a0001c0001t0001g0179a0001c0001t0002g0255a0001c0001t0005g0323others(69): Show | 74 | HG00597.hp2 HG00609.hp2 HG00621.hp2 others(71): Show |
splice_region_variant&intron_variant | LOW | c.-168-8dupT | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103181335 | ||||||
chr10:103181349
|
AT | A | 3 | a0001c0002t0003g0007a0001c0002t0003g0027a0001c0002t0003g0078 | 3 | NA19076.hp2 NA19089.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-168-22delA | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103181349 | ||||||
chr10:103181350
|
T | A | 180 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(177): Show | 182 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(179): Show |
intron_variant | MODIFIER | c.-168-22A>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103181350 | ||||||
chr10:103181355
|
A | T | 182 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(179): Show | 184 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(181): Show |
intron_variant | MODIFIER | c.-168-27T>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103181355 | ||||||
chr10:103181496
|
T | G | 1 | a0001c0002t0003g0053 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-168-168A>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103181496 | ||||||
chr10:103181563
|
T | C | 1 | a0001c0002t0014g0086 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-168-235A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103181563 | ||||||
chr10:103181678
|
T | C | 1 | a0001c0001t0001g0164 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-168-350A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103181678 | ||||||
chr10:103181782
|
A | G | 1 | a0001c0002t0008g0206 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-168-454T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103181782 | ||||||
chr10:103181832
|
C | T | 182 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(179): Show | 184 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(181): Show |
intron_variant | MODIFIER | c.-168-504G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103181832 | ||||||
chr10:103181992
|
A | C | 1 | a0001c0001t0001g0136 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-168-664T>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103181992 | ||||||
chr10:103182009
|
C | CA | 36 | a0001c0001t0002g0245a0001c0001t0002g0277a0001c0001t0018g0256others(33): Show | 38 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.-168-682dupT | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103182009 | ||||||
chr10:103182099
|
A | G | 1 | a0001c0002t0008g0215 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-168-771T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103182099 | ||||||
chr10:103182206
|
T | C | 6 | a0001c0002t0008g0210a0001c0002t0008g0211a0001c0002t0008g0212others(3): Show | 6 | HG01884.hp2 HG02145.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-168-878A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103182206 | ||||||
chr10:103182209
|
C | G | 1 | a0001c0001t0001g0117 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-168-881G>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103182209 | ||||||
chr10:103182225
|
C | T | 1 | a0001c0002t0003g0041 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-168-897G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103182225 | ||||||
chr10:103182248
|
C | T | 4 | a0001c0002t0003g0031a0001c0002t0009g0028a0001c0002t0009g0029others(1): Show | 4 | NA18962.hp2 NA18990.hp2 NA19054.hp1 others(1): Show |
intron_variant | MODIFIER | c.-168-920G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103182248 | ||||||
chr10:103182454
|
T | C | 3 | a0001c0001t0001g0127a0001c0001t0001g0170a0001c0001t0012g0110 | 3 | HG01928.hp2 HG01952.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.-168-1126A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103182454 | ||||||
chr10:103182486
|
G | A | 18 | a0001c0002t0006g0184a0001c0002t0006g0185a0001c0002t0006g0186others(15): Show | 18 | HG00408.hp2 HG00609.hp1 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.-168-1158C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103182486 | ||||||
chr10:103182487
|
T | G | 67 | a0001c0002t0003g0007a0001c0002t0003g0023a0001c0002t0003g0024others(64): Show | 67 | HG00544.hp2 HG01069.hp1 HG01167.hp1 others(64): Show |
intron_variant | MODIFIER | c.-168-1159A>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103182487 | ||||||
chr10:103182545
|
G | A | 1 | a0001c0001t0001g0244 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-168-1217C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103182545 | ||||||
chr10:103182634
|
C | CA | 9 | a0001c0002t0003g0060a0001c0002t0003g0061a0001c0002t0003g0062others(6): Show | 9 | HG01943.hp1 HG02004.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.-168-1307dupT | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103182634 | ||||||
chr10:103182800
|
T | A | 1 | a0001c0001t0002g0249 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-168-1472A>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103182800 | ||||||
chr10:103183248
|
A | G | 1 | a0001c0002t0004g0014 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-168-1920T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103183248 | ||||||
chr10:103183250
|
A | G | 11 | a0001c0002t0004g0015a0001c0002t0004g0016a0001c0002t0004g0017others(8): Show | 11 | HG00735.hp2 HG01109.hp2 HG01516.hp1 others(8): Show |
intron_variant | MODIFIER | c.-168-1922T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103183250 | ||||||
chr10:103183260
|
G | GATATAT | 3 | a0001c0002t0004g0020a0001c0002t0004g0203a0001c0002t0004g0205 | 3 | HG00735.hp2 HG02622.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.-168-1933_-168-193 others(10): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103183260 | ||||||
chr10:103183260
|
G | GATATATA others(3): Show |
1 | a0001c0002t0004g0019 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-168-1933_-168-193 others(14): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103183260 | ||||||
chr10:103183260
|
G | GATATATA others(5): Show |
1 | a0001c0002t0004g0018 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-168-1933_-168-193 others(16): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103183260 | ||||||
chr10:103183260
|
G | GATATATA others(7): Show |
2 | a0001c0002t0004g0017a0001c0002t0004g0022 | 2 | HG01109.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.-168-1933_-168-193 others(18): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103183260 | ||||||
chr10:103183260
|
G | GATATATA others(11): Show |
2 | a0001c0002t0004g0015a0001c0002t0004g0016 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-168-1933_-168-193 others(22): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103183260 | ||||||
chr10:103183261
|
T | A | 18 | a0001c0001t0002g0276a0001c0002t0003g0038a0001c0002t0003g0039others(15): Show | 18 | HG00735.hp2 HG01109.hp2 HG01516.hp1 others(15): Show |
intron_variant | MODIFIER | c.-168-1933A>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103183261 | ||||||
chr10:103183262
|
G | GAT | 15 | a0001c0001t0002g0272a0001c0001t0002g0273a0001c0001t0002g0274others(12): Show | 15 | HG00408.hp2 HG00609.hp1 HG00735.hp1 others(12): Show |
intron_variant | MODIFIER | c.-168-1936_-168-193 others(6): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103183262 | ||||||
chr10:103183262
|
G | GATAT | 33 | a0001c0001t0001g0103a0001c0001t0001g0107a0001c0001t0001g0129others(30): Show | 33 | HG00597.hp1 HG00642.hp2 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.-168-1938_-168-193 others(8): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103183262 | ||||||
chr10:103183262
|
G | GATATAT | 26 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(23): Show | 26 | HG00597.hp2 HG01069.hp2 HG01070.hp2 others(23): Show |
intron_variant | MODIFIER | c.-168-1940_-168-193 others(10): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103183262 | ||||||
chr10:103183262
|
G | GATATATA others(1): Show |
25 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093others(22): Show | 25 | HG00280.hp1 HG00408.hp1 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.-168-1942_-168-193 others(12): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103183262 | ||||||
chr10:103183262
|
G | GATATATA others(3): Show |
27 | a0001c0001t0001g0090a0001c0001t0001g0098a0001c0001t0001g0100others(24): Show | 27 | HG00280.hp2 HG00621.hp1 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.-168-1944_-168-193 others(14): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103183262 | ||||||
chr10:103183262
|
G | GATATATA others(5): Show |
15 | a0001c0001t0001g0096a0001c0001t0001g0104a0001c0001t0001g0109others(12): Show | 15 | HG00558.hp2 HG01928.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.-168-1946_-168-193 others(16): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103183262 | ||||||
chr10:103183262
|
G | GATATATA others(7): Show |
10 | a0001c0001t0001g0008a0001c0001t0001g0117a0001c0001t0001g0118others(7): Show | 10 | HG02040.hp2 HG02074.hp1 HG02523.hp1 others(7): Show |
intron_variant | MODIFIER | c.-168-1948_-168-193 others(18): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103183262 | ||||||
chr10:103183262
|
G | GATATATA others(9): Show |
5 | a0001c0001t0001g0097a0001c0001t0001g0116a0001c0001t0001g0165others(2): Show | 5 | HG01258.hp1 HG02135.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.-168-1950_-168-193 others(20): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103183262 | ||||||
chr10:103183262
|
G | GATATATA others(11): Show |
3 | a0001c0001t0001g0115a0001c0001t0001g0135a0001c0002t0005g0310 | 3 | HG00544.hp1 HG01243.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-168-1952_-168-193 others(22): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103183262 | ||||||
chr10:103183262
|
G | GATATATA others(13): Show |
4 | a0001c0001t0001g0106a0001c0001t0001g0114a0001c0001t0001g0208others(1): Show | 4 | HG02280.hp2 HG02602.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.-168-1954_-168-193 others(24): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103183262 | ||||||
chr10:103183262
|
G | GATATATA others(15): Show |
4 | a0001c0002t0005g0309a0001c0002t0005g0311a0001c0002t0005g0312others(1): Show | 4 | HG03041.hp2 HG03098.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-168-1956_-168-193 others(26): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103183262 | ||||||
chr10:103183262
|
G | GATATATA others(17): Show |
1 | a0001c0001t0007g0172 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-168-1958_-168-193 others(28): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103183262 | ||||||
chr10:103183262
|
G | GATATATA others(23): Show |
1 | a0001c0001t0001g0169 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-168-1964_-168-193 others(34): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103183262 | ||||||
chr10:103183262
|
G | GTGAT | 6 | a0001c0001t0001g0113a0001c0001t0001g0122a0001c0002t0005g0315others(3): Show | 6 | HG02970.hp1 HG03098.hp1 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.-168-1935_-168-193 others(8): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103183262 | ||||||
chr10:103183262
|
G | GTGATAT | 5 | a0001c0002t0005g0324a0001c0002t0005g0325a0001c0002t0005g0331others(2): Show | 5 | HG00639.hp2 HG01169.hp2 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.-168-1935_-168-193 others(10): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103183262 | ||||||
chr10:103183262
|
G | GTGATATA others(5): Show |
1 | a0001c0002t0005g0321 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-168-1935_-168-193 others(16): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103183262 | ||||||
chr10:103183262
|
G | GTGATATA others(9): Show |
1 | a0001c0002t0005g0330 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-168-1935_-168-193 others(20): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103183262 | ||||||
chr10:103183262
|
G | T | 18 | a0001c0001t0002g0276a0001c0002t0003g0038a0001c0002t0003g0039others(15): Show | 18 | HG00735.hp2 HG01109.hp2 HG01516.hp1 others(15): Show |
intron_variant | MODIFIER | c.-168-1934C>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103183262 | ||||||
chr10:103183262
|
GAT | G | 20 | a0001c0001t0001g0001a0001c0001t0001g0133a0001c0001t0001g0181others(17): Show | 22 | HG00609.hp2 HG00621.hp2 HG00642.hp1 others(19): Show |
intron_variant | MODIFIER | c.-168-1936_-168-193 others(6): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103183262 | ||||||
chr10:103183262
|
GATAT | G | 7 | a0001c0001t0001g0134a0001c0001t0001g0176a0001c0002t0004g0010others(4): Show | 7 | HG00738.hp1 HG01070.hp1 HG01516.hp2 others(4): Show |
intron_variant | MODIFIER | c.-168-1938_-168-193 others(8): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103183262 | ||||||
chr10:103183262
|
GATATATA others(7): Show |
G | 17 | a0001c0001t0002g0004a0001c0001t0002g0245a0001c0001t0002g0247others(14): Show | 18 | HG00558.hp1 HG01257.hp2 HG01361.hp2 others(15): Show |
intron_variant | MODIFIER | c.-168-1948_-168-193 others(18): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103183262 | ||||||
chr10:103183267
|
A | T | 1 | a0001c0002t0005g0329 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-168-1939T>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103183267 | ||||||
chr10:103183268
|
T | G | 1 | a0001c0002t0005g0329 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-168-1940A>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103183268 | ||||||
chr10:103183275
|
A | AATATATA others(22): Show |
1 | a0001c0002t0003g0076 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-168-1948_-168-194 others(33): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103183275 | ||||||
chr10:103183275
|
A | ATATATAT others(24): Show |
1 | a0001c0002t0003g0074 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.-168-1948_-168-194 others(35): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103183275 | ||||||
chr10:103183275
|
A | ATATATAT others(23): Show |
41 | a0001c0002t0003g0007a0001c0002t0003g0023a0001c0002t0003g0024others(38): Show | 41 | HG01069.hp1 HG01167.hp1 HG01943.hp1 others(38): Show |
intron_variant | MODIFIER | c.-168-1948_-168-194 others(34): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103183275 | ||||||
chr10:103183275
|
A | ATATATAT others(21): Show |
17 | a0001c0002t0003g0033a0001c0002t0003g0038a0001c0002t0003g0039others(14): Show | 17 | HG01358.hp2 HG02083.hp1 HG02735.hp1 others(14): Show |
intron_variant | MODIFIER | c.-168-1948_-168-194 others(32): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103183275 | ||||||
chr10:103183275
|
A | ATATATAT others(19): Show |
2 | a0001c0002t0003g0058a0001c0002t0003g0059 | 2 | HG01433.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.-168-1948_-168-194 others(30): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103183275 | ||||||
chr10:103183275
|
A | ATATATAT others(21): Show |
1 | a0001c0002t0003g0078 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-168-1948_-168-194 others(32): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103183275 | ||||||
chr10:103183276
|
T | TATATATA others(21): Show |
1 | a0001c0002t0003g0035 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-168-1949_-168-194 others(32): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103183276 | ||||||
chr10:103183291
|
A | ATTTTATA others(27): Show |
2 | a0001c0002t0003g0026a0001c0002t0003g0063 | 2 | HG00544.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.-168-1964_-168-196 others(38): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103183291 | ||||||
chr10:103183291
|
A | C | 64 | a0001c0002t0003g0007a0001c0002t0003g0023a0001c0002t0003g0024others(61): Show | 64 | HG01069.hp1 HG01167.hp1 HG01358.hp2 others(61): Show |
intron_variant | MODIFIER | c.-168-1963T>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103183291 | ||||||
chr10:103183334
|
C | CT | 7 | a0001c0002t0004g0010a0001c0002t0004g0011a0001c0002t0004g0012others(4): Show | 7 | HG01243.hp1 HG02109.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.-168-2007dupA | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103183334 | ||||||
chr10:103183334
|
CT | C | 220 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0100others(217): Show | 222 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(219): Show |
intron_variant | MODIFIER | c.-168-2007delA | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103183334 | ||||||
chr10:103183366
|
C | T | 1 | a0001c0002t0005g0309 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-168-2038G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103183366 | ||||||
chr10:103183367
|
C | A | 1 | a0001c0001t0002g0291 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-168-2039G>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103183367 | ||||||
chr10:103183508
|
C | CT | 29 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(26): Show | 29 | HG00639.hp2 HG01081.hp2 HG01515.hp1 others(26): Show |
intron_variant | MODIFIER | c.-168-2181dupA | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103183508 | ||||||
chr10:103183508
|
CT | C | 12 | a0001c0001t0001g0108a0001c0001t0001g0123a0001c0001t0001g0171others(9): Show | 12 | HG01081.hp1 HG01496.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.-168-2181delA | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103183508 | ||||||
chr10:103183585
|
A | G | 181 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(178): Show | 183 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(180): Show |
intron_variant | MODIFIER | c.-168-2257T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103183585 | ||||||
chr10:103183625
|
T | C | 1 | a0001c0001t0001g0096 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-168-2297A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103183625 | ||||||
chr10:103183633
|
T | C | 22 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0105others(19): Show | 22 | HG00408.hp1 HG00642.hp2 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.-168-2305A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103183633 | ||||||
chr10:103183661
|
C | T | 1 | a0001c0002t0014g0086 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-168-2333G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103183661 | ||||||
chr10:103183705
|
G | C | 1 | a0001c0001t0002g0247 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-168-2377C>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103183705 | ||||||
chr10:103183735
|
T | C | 1 | a0001c0002t0005g0330 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-168-2407A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103183735 | ||||||
chr10:103183773
|
C | T | 13 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(10): Show | 13 | HG02135.hp1 HG03834.hp2 NA18940.hp2 others(10): Show |
intron_variant | MODIFIER | c.-168-2445G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103183773 | ||||||
chr10:103183865
|
G | T | 4 | a0001c0002t0003g0038a0001c0002t0003g0039a0001c0002t0003g0040others(1): Show | 4 | NA18971.hp2 NA18982.hp1 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.-168-2537C>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103183865 | ||||||
chr10:103183946
|
G | GT | 7 | a0001c0001t0001g0112a0001c0001t0001g0161a0001c0001t0002g0283others(4): Show | 7 | HG02027.hp2 HG02486.hp2 HG03927.hp1 others(4): Show |
intron_variant | MODIFIER | c.-168-2619dupA | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103183946 | ||||||
chr10:103183950
|
T | G | 2 | a0001c0001t0002g0304a0001c0001t0002g0305 | 2 | HG01257.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.-168-2622A>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103183950 | ||||||
chr10:103184127
|
T | C | 1 | a0001c0001t0001g0207 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-168-2799A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103184127 | ||||||
chr10:103184134
|
T | C | 13 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(10): Show | 13 | HG02135.hp1 HG03834.hp2 NA18940.hp2 others(10): Show |
intron_variant | MODIFIER | c.-168-2806A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103184134 | ||||||
chr10:103184229
|
T | A | 181 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(178): Show | 183 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(180): Show |
intron_variant | MODIFIER | c.-168-2901A>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103184229 | ||||||
chr10:103184236
|
G | A | 90 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0100others(87): Show | 91 | HG00280.hp2 HG00408.hp1 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.-168-2908C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103184236 | ||||||
chr10:103184244
|
C | T | 29 | a0002c0003t0004g0002a0002c0003t0004g0003a0002c0003t0004g0005others(26): Show | 31 | HG00609.hp2 HG00621.hp2 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.-168-2916G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103184244 | ||||||
chr10:103184246
|
T | C | 1 | a0001c0002t0003g0075 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-168-2918A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103184246 | ||||||
chr10:103184530
|
G | A | 3 | a0001c0002t0003g0060a0001c0002t0003g0061a0001c0002t0003g0062 | 3 | HG01943.hp1 HG02004.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.-168-3202C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103184530 | ||||||
chr10:103184963
|
A | G | 29 | a0002c0003t0004g0002a0002c0003t0004g0003a0002c0003t0004g0005others(26): Show | 31 | HG00609.hp2 HG00621.hp2 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.-168-3635T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103184963 | ||||||
chr10:103184987
|
C | G | 180 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(177): Show | 182 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(179): Show |
intron_variant | MODIFIER | c.-168-3659G>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103184987 | ||||||
chr10:103185010
|
C | CTG | 180 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(177): Show | 182 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(179): Show |
intron_variant | MODIFIER | c.-168-3683_-168-368 others(6): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103185010 | ||||||
chr10:103185180
|
G | C | 1 | a0001c0001t0001g0178 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-168-3852C>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103185180 | ||||||
chr10:103185182
|
A | C | 1 | a0001c0001t0001g0106 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-168-3854T>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103185182 | ||||||
chr10:103185271
|
C | A | 100 | a0001c0001t0005g0317a0001c0001t0005g0323a0001c0002t0004g0010others(97): Show | 102 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(99): Show |
intron_variant | MODIFIER | c.-168-3943G>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103185271 | ||||||
chr10:103185344
|
T | TA | 80 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0104others(77): Show | 83 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(80): Show |
intron_variant | MODIFIER | c.-168-4017dupT | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103185344 | ||||||
chr10:103185456
|
A | G | 180 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(177): Show | 182 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(179): Show |
intron_variant | MODIFIER | c.-168-4128T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103185456 | ||||||
chr10:103185550
|
A | G | 2 | a0001c0001t0002g0304a0001c0001t0002g0305 | 2 | HG01257.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.-168-4222T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103185550 | ||||||
chr10:103185579
|
C | T | 1 | a0001c0002t0008g0215 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-168-4251G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103185579 | ||||||
chr10:103185649
|
C | CA | 25 | a0001c0001t0001g0089a0001c0001t0001g0111a0001c0001t0005g0317others(22): Show | 25 | HG00597.hp2 HG00673.hp2 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.-168-4322dupT | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103185649 | ||||||
chr10:103185649
|
C | CAA | 11 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0090others(8): Show | 11 | HG03834.hp2 NA18940.hp2 NA18943.hp2 others(8): Show |
intron_variant | MODIFIER | c.-168-4323_-168-432 others(6): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103185649 | ||||||
chr10:103185663
|
A | AAG | 10 | a0001c0002t0003g0076a0001c0002t0005g0309a0001c0002t0005g0310others(7): Show | 10 | HG01243.hp1 HG01515.hp1 HG01517.hp1 others(7): Show |
intron_variant | MODIFIER | c.-168-4336_-168-433 others(6): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103185663 | ||||||
chr10:103185664
|
G | A | 1 | a0001c0001t0001g0089 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-168-4336C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103185664 | ||||||
chr10:103185665
|
G | A | 11 | a0001c0002t0003g0076a0001c0002t0005g0309a0001c0002t0005g0310others(8): Show | 11 | HG00639.hp2 HG01243.hp1 HG01515.hp1 others(8): Show |
intron_variant | MODIFIER | c.-168-4337C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103185665 | ||||||
chr10:103185665
|
G | GA | 22 | a0001c0001t0001g0104a0001c0001t0001g0161a0001c0001t0001g0163others(19): Show | 22 | HG00621.hp1 HG00642.hp1 HG00733.hp2 others(19): Show |
intron_variant | MODIFIER | c.-168-4338dupT | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103185665 | ||||||
chr10:103185666
|
A | G | 1 | a0001c0001t0001g0089 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-168-4338T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103185666 | ||||||
chr10:103185706
|
G | A | 180 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(177): Show | 182 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(179): Show |
intron_variant | MODIFIER | c.-168-4378C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103185706 | ||||||
chr10:103185856
|
A | C | 1 | a0001c0001t0001g0111 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-168-4528T>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103185856 | ||||||
chr10:103185918
|
T | C | 1 | a0001c0002t0008g0206 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-168-4590A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103185918 | ||||||
chr10:103185977
|
T | C | 13 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(10): Show | 13 | HG02135.hp1 HG03834.hp2 NA18940.hp2 others(10): Show |
intron_variant | MODIFIER | c.-168-4649A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103185977 | ||||||
chr10:103185994
|
C | T | 180 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(177): Show | 182 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(179): Show |
intron_variant | MODIFIER | c.-168-4666G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103185994 | ||||||
chr10:103186032
|
C | T | 1 | a0001c0002t0003g0036 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-168-4704G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103186032 | ||||||
chr10:103186066
|
G | A | 67 | a0001c0002t0003g0007a0001c0002t0003g0023a0001c0002t0003g0024others(64): Show | 67 | HG00544.hp2 HG01069.hp1 HG01167.hp1 others(64): Show |
intron_variant | MODIFIER | c.-168-4738C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103186066 | ||||||
chr10:103186099
|
T | G | 1 | a0001c0001t0001g0096 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-168-4771A>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103186099 | ||||||
chr10:103186157
|
C | T | 1 | a0001c0001t0012g0110 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-168-4829G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103186157 | ||||||
chr10:103186288
|
G | T | 3 | a0001c0002t0004g0010a0001c0002t0004g0011a0001c0002t0004g0012 | 3 | HG02109.hp2 HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-168-4960C>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103186288 | ||||||
chr10:103186469
|
C | T | 2 | a0001c0002t0003g0007a0001c0002t0003g0035 | 2 | NA18612.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.-168-5141G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103186469 | ||||||
chr10:103186568
|
T | A | 1 | a0001c0002t0003g0067 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-168-5240A>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103186568 | ||||||
chr10:103186633
|
G | T | 1 | a0001c0002t0003g0034 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-168-5305C>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103186633 | ||||||
chr10:103186653
|
G | A | 1 | a0002c0003t0004g0219 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-168-5325C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103186653 | ||||||
chr10:103186912
|
CA | C | 120 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(117): Show | 122 | HG00544.hp2 HG00609.hp2 HG00621.hp2 others(119): Show |
intron_variant | MODIFIER | c.-168-5585delT | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103186912 | ||||||
chr10:103186929
|
A | G | 1 | a0001c0002t0003g0076 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-168-5601T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103186929 | ||||||
chr10:103186970
|
G | T | 6 | a0001c0002t0003g0031a0001c0002t0003g0032a0001c0002t0003g0033others(3): Show | 6 | NA18962.hp2 NA18990.hp2 NA19004.hp2 others(3): Show |
intron_variant | MODIFIER | c.-168-5642C>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103186970 | ||||||
chr10:103186979
|
G | A | 1 | a0001c0002t0003g0078 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-168-5651C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103186979 | ||||||
chr10:103186982
|
G | C | 1 | a0001c0001t0001g0164 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-168-5654C>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103186982 | ||||||
chr10:103187068
|
G | A | 1 | a0001c0002t0006g0201 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-168-5740C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103187068 | ||||||
chr10:103187241
|
C | G | 1 | a0001c0002t0003g0074 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.-168-5913G>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103187241 | ||||||
chr10:103187242
|
T | A | 1 | a0001c0002t0003g0074 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.-168-5914A>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103187242 | ||||||
chr10:103187547
|
A | T | 1 | a0001c0001t0002g0250 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-169+5689T>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103187547 | ||||||
chr10:103187551
|
T | TA | 34 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(31): Show | 34 | HG00408.hp2 HG01070.hp2 HG01071.hp1 others(31): Show |
intron_variant | MODIFIER | c.-169+5684dupT | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103187551 | ||||||
chr10:103187551
|
TA | T | 9 | a0001c0001t0001g0167a0001c0001t0001g0178a0001c0001t0001g0181others(6): Show | 9 | HG01099.hp1 HG01433.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.-169+5684delT | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103187551 | ||||||
chr10:103187736
|
C | G | 100 | a0001c0001t0005g0317a0001c0001t0005g0323a0001c0002t0004g0010others(97): Show | 102 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(99): Show |
intron_variant | MODIFIER | c.-169+5500G>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103187736 | ||||||
chr10:103187823
|
G | A | 1 | a0001c0002t0005g0334 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-169+5413C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103187823 | ||||||
chr10:103188153
|
G | A | 1 | a0001c0002t0004g0014 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-169+5083C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103188153 | ||||||
chr10:103188163
|
T | C | 3 | a0001c0002t0004g0010a0001c0002t0004g0011a0001c0002t0004g0012 | 3 | HG02109.hp2 HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-169+5073A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103188163 | ||||||
chr10:103188219
|
A | T | 1 | a0001c0002t0008g0206 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-169+5017T>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103188219 | ||||||
chr10:103188666
|
C | T | 4 | a0002c0003t0004g0216a0002c0003t0004g0217a0002c0003t0004g0218others(1): Show | 4 | HG00621.hp2 HG00673.hp1 NA18941.hp2 others(1): Show |
intron_variant | MODIFIER | c.-169+4570G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103188666 | ||||||
chr10:103188705
|
T | A | 1 | a0001c0001t0002g0279 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-169+4531A>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103188705 | ||||||
chr10:103188712
|
C | T | 2 | a0001c0002t0004g0015a0001c0002t0004g0016 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-169+4524G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103188712 | ||||||
chr10:103188858
|
C | T | 41 | a0001c0001t0005g0317a0001c0001t0005g0323a0001c0002t0004g0015others(38): Show | 41 | HG00597.hp2 HG00639.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.-169+4378G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103188858 | ||||||
chr10:103188955
|
T | C | 100 | a0001c0001t0005g0317a0001c0001t0005g0323a0001c0002t0004g0010others(97): Show | 102 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(99): Show |
intron_variant | MODIFIER | c.-169+4281A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103188955 | ||||||
chr10:103188963
|
G | C | 4 | a0001c0002t0003g0068a0001c0002t0003g0069a0001c0002t0003g0070others(1): Show | 4 | HG02735.hp1 HG03017.hp1 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.-169+4273C>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103188963 | ||||||
chr10:103188997
|
G | C | 5 | a0002c0003t0004g0003a0002c0003t0004g0005a0002c0003t0004g0233others(2): Show | 6 | HG00609.hp2 NA18950.hp1 NA18962.hp1 others(3): Show |
intron_variant | MODIFIER | c.-169+4239C>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103188997 | ||||||
chr10:103189038
|
TTGTACTA | T | 100 | a0001c0001t0005g0317a0001c0001t0005g0323a0001c0002t0004g0010others(97): Show | 102 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(99): Show |
intron_variant | MODIFIER | c.-169+4191_-169+419 others(11): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103189038 | ||||||
chr10:103189163
|
T | C | 3 | a0001c0002t0004g0203a0001c0002t0004g0204a0001c0002t0004g0205 | 3 | HG02622.hp1 HG02896.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-169+4073A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103189163 | ||||||
chr10:103189359
|
G | A | 180 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(177): Show | 182 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(179): Show |
intron_variant | MODIFIER | c.-169+3877C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103189359 | ||||||
chr10:103189561
|
G | A | 3 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0177 | 3 | HG02027.hp1 HG02129.hp1 NA18939.hp2 |
intron_variant | MODIFIER | c.-169+3675C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103189561 | ||||||
chr10:103189584
|
G | A | 1 | a0001c0001t0001g0106 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-169+3652C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103189584 | ||||||
chr10:103189604
|
C | CA | 50 | a0001c0001t0001g0087a0001c0001t0001g0097a0001c0001t0001g0098others(47): Show | 50 | HG00597.hp2 HG00673.hp1 HG00738.hp2 others(47): Show |
intron_variant | MODIFIER | c.-169+3631dupT | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103189604 | ||||||
chr10:103189617
|
G | GA | 8 | a0001c0001t0001g0087a0001c0001t0001g0178a0001c0001t0001g0179others(5): Show | 8 | HG00544.hp2 HG02109.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.-169+3618dupT | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103189617 | ||||||
chr10:103189817
|
C | T | 1 | a0001c0002t0005g0316 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-169+3419G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103189817 | ||||||
chr10:103189952
|
G | A | 100 | a0001c0001t0005g0317a0001c0001t0005g0323a0001c0002t0004g0010others(97): Show | 102 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(99): Show |
intron_variant | MODIFIER | c.-169+3284C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103189952 | ||||||
chr10:103189960
|
G | A | 4 | a0001c0001t0002g0246a0001c0001t0002g0284a0001c0001t0002g0285others(1): Show | 4 | NA18945.hp1 NA18953.hp1 NA18985.hp2 others(1): Show |
intron_variant | MODIFIER | c.-169+3276C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103189960 | ||||||
chr10:103189970
|
G | A | 6 | a0001c0002t0008g0210a0001c0002t0008g0211a0001c0002t0008g0212others(3): Show | 6 | HG01884.hp2 HG02145.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-169+3266C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103189970 | ||||||
chr10:103189977
|
C | T | 4 | a0001c0001t0002g0253a0001c0001t0002g0254a0001c0001t0002g0255others(1): Show | 4 | HG01069.hp2 HG01071.hp2 HG01081.hp2 others(1): Show |
intron_variant | MODIFIER | c.-169+3259G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103189977 | ||||||
chr10:103189997
|
C | CT | 101 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0087others(98): Show | 102 | HG00280.hp2 HG00408.hp1 HG00544.hp1 others(99): Show |
intron_variant | MODIFIER | c.-169+3238dupA | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103189997 | ||||||
chr10:103189997
|
C | CTT | 23 | a0001c0001t0001g0088a0001c0001t0001g0100a0001c0001t0001g0101others(20): Show | 24 | HG01109.hp1 HG01255.hp1 HG01928.hp1 others(21): Show |
intron_variant | MODIFIER | c.-169+3237_-169+323 others(6): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103189997 | ||||||
chr10:103189997
|
CT | C | 7 | a0001c0001t0002g0246a0001c0001t0002g0287a0001c0001t0011g0288others(4): Show | 7 | HG00733.hp1 HG01069.hp2 NA18950.hp1 others(4): Show |
intron_variant | MODIFIER | c.-169+3238delA | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103189997 | ||||||
chr10:103190000
|
T | TC | 4 | a0001c0002t0004g0010a0001c0002t0004g0011a0001c0002t0004g0012others(1): Show | 4 | HG02109.hp2 HG02976.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.-169+3235_-169+323 others(5): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103190000 | ||||||
chr10:103190001
|
T | C | 88 | a0001c0001t0005g0317a0001c0001t0005g0323a0001c0002t0004g0014others(85): Show | 90 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(87): Show |
intron_variant | MODIFIER | c.-169+3235A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103190001 | ||||||
chr10:103190002
|
T | C | 2 | a0002c0003t0004g0237a0002c0003t0004g0238 | 2 | NA18950.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.-169+3234A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103190002 | ||||||
chr10:103190024
|
A | G | 333 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0087others(330): Show | 337 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(334): Show |
intron_variant | MODIFIER | c.-169+3212T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103190024 | ||||||
chr10:103190143
|
G | C | 13 | a0001c0001t0001g0180a0001c0001t0002g0004a0001c0001t0002g0247others(10): Show | 14 | HG01361.hp2 HG01943.hp2 HG02004.hp1 others(11): Show |
intron_variant | MODIFIER | c.-169+3093C>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103190143 | ||||||
chr10:103190195
|
T | C | 1 | a0001c0002t0004g0014 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-169+3041A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103190195 | ||||||
chr10:103190406
|
C | T | 1 | a0001c0001t0002g0249 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-169+2830G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103190406 | ||||||
chr10:103190440
|
C | T | 180 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(177): Show | 182 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(179): Show |
intron_variant | MODIFIER | c.-169+2796G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103190440 | ||||||
chr10:103190711
|
T | C | 1 | a0002c0003t0004g0239 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-169+2525A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103190711 | ||||||
chr10:103190716
|
GC | G | 6 | a0001c0002t0008g0210a0001c0002t0008g0211a0001c0002t0008g0212others(3): Show | 6 | HG01884.hp2 HG02145.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-169+2519delG | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103190716 | ||||||
chr10:103190870
|
A | G | 3 | a0001c0002t0003g0023a0001c0002t0003g0024a0001c0002t0003g0079 | 3 | NA18957.hp1 NA18978.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.-169+2366T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103190870 | ||||||
chr10:103191382
|
C | CA | 7 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0183others(4): Show | 7 | HG00280.hp1 HG01192.hp1 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.-169+1853dupT | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103191382 | ||||||
chr10:103191393
|
AAAAAAGA others(1): Show |
A | 6 | a0001c0002t0008g0210a0001c0002t0008g0211a0001c0002t0008g0212others(3): Show | 6 | HG01884.hp2 HG02145.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-169+1835_-169+184 others(12): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103191393 | ||||||
chr10:103191395
|
AAAAG | A | 17 | a0001c0002t0006g0185a0001c0002t0006g0186a0001c0002t0006g0187others(14): Show | 17 | HG00609.hp1 HG01070.hp2 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.-169+1837_-169+184 others(8): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103191395 | ||||||
chr10:103191397
|
A | G | 1 | a0001c0001t0002g0248 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-169+1839T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103191397 | ||||||
chr10:103191397
|
AAGAG | A | 75 | a0001c0001t0005g0317a0001c0001t0005g0323a0001c0002t0004g0010others(72): Show | 77 | HG00597.hp2 HG00609.hp2 HG00621.hp2 others(74): Show |
intron_variant | MODIFIER | c.-169+1835_-169+183 others(8): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103191397 | ||||||
chr10:103191581
|
G | T | 1 | a0001c0001t0001g0087 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-169+1655C>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103191581 | ||||||
chr10:103191709
|
AC | A | 104 | a0001c0001t0005g0317a0001c0001t0005g0323a0001c0002t0003g0081others(101): Show | 106 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(103): Show |
intron_variant | MODIFIER | c.-169+1526delG | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103191709 | ||||||
chr10:103191726
|
C | T | 6 | a0001c0002t0008g0210a0001c0002t0008g0211a0001c0002t0008g0212others(3): Show | 6 | HG01884.hp2 HG02145.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-169+1510G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103191726 | ||||||
chr10:103191731
|
C | T | 6 | a0001c0002t0005g0309a0001c0002t0005g0310a0001c0002t0005g0311others(3): Show | 6 | HG01243.hp1 HG03041.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.-169+1505G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103191731 | ||||||
chr10:103191867
|
A | C | 1 | a0001c0002t0014g0086 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-169+1369T>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103191867 | ||||||
chr10:103191932
|
T | C | 1 | a0001c0002t0008g0215 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-169+1304A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103191932 | ||||||
chr10:103191982
|
C | A | 1 | a0001c0002t0008g0206 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-169+1254G>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103191982 | ||||||
chr10:103192035
|
T | C | 1 | a0002c0003t0004g0240 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-169+1201A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103192035 | ||||||
chr10:103192075
|
G | A | 1 | a0001c0002t0003g0085 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-169+1161C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103192075 | ||||||
chr10:103192188
|
T | C | 3 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0209 | 3 | HG02602.hp2 HG03239.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.-169+1048A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103192188 | ||||||
chr10:103192742
|
C | T | 69 | a0001c0001t0002g0248a0001c0002t0003g0007a0001c0002t0003g0023others(66): Show | 69 | HG00544.hp2 HG01069.hp1 HG01167.hp1 others(66): Show |
intron_variant | MODIFIER | c.-169+494G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103192742 | ||||||
chr10:103192822
|
G | A | 2 | a0001c0001t0002g0304a0001c0001t0002g0305 | 2 | HG01257.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.-169+414C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103192822 | ||||||
chr10:103192830
|
C | G | 8 | a0001c0002t0004g0015a0001c0002t0004g0016a0001c0002t0004g0017others(5): Show | 8 | HG00735.hp2 HG01109.hp2 HG01516.hp1 others(5): Show |
intron_variant | MODIFIER | c.-169+406G>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103192830 | ||||||
chr10:103192839
|
G | A | 1 | a0001c0001t0011g0306 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-169+397C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103192839 | ||||||
chr10:103192867
|
G | C | 6 | a0001c0002t0008g0210a0001c0002t0008g0211a0001c0002t0008g0212others(3): Show | 6 | HG01884.hp2 HG02145.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-169+369C>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103192867 | ||||||
chr10:103192868
|
G | T | 34 | a0001c0002t0004g0010a0001c0002t0004g0011a0001c0002t0004g0012others(31): Show | 36 | HG00609.hp2 HG00621.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.-169+368C>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103192868 | ||||||
chr10:103192875
|
G | A | 29 | a0002c0003t0004g0002a0002c0003t0004g0003a0002c0003t0004g0005others(26): Show | 31 | HG00609.hp2 HG00621.hp2 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.-169+361C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103192875 | ||||||
chr10:103192898
|
C | G | 1 | a0002c0003t0004g0005 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-169+338G>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103192898 | ||||||
chr10:103192916
|
C | CG | 7 | a0001c0001t0001g0008a0001c0001t0002g0246a0001c0001t0002g0247others(4): Show | 7 | HG02970.hp2 HG03942.hp1 NA18940.hp1 others(4): Show |
intron_variant | MODIFIER | c.-169+319dupC | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103192916 | ||||||
chr10:103193036
|
G | A | 2 | a0001c0001t0002g0307a0001c0001t0002g0308 | 2 | NA19011.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.-169+200C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103193036 | ||||||
chr10:103193120
|
G | A | 3 | a0001c0002t0003g0241a0001c0002t0003g0242a0001c0002t0003g0243 | 3 | NA18988.hp2 NA18992.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.-169+116C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103193120 | ||||||
chr10:103193191
|
T | TCGCCCGC others(12): Show |
1 | a0001c0001t0001g0244 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-169+26_-169+44dup others(19): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103193191 | ||||||
chr10:103193213
|
C | T | 1 | a0001c0001t0002g0245 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.-169+23G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103193213 |