geneid | 51617 |
---|---|
ensemblid | ENSG00000170091.11 |
hgncid | 24955 |
symbol | NSG2 |
name | neuronal vesicle trafficking associated 2 |
refseq_nuc | NM_015980.5 |
refseq_prot | NP_057064.1 |
ensembl_nuc | ENST00000303177.8 |
ensembl_prot | ENSP00000307722.3 |
mane_status | MANE Select |
chr | chr5 |
start | 174045706 |
end | 174109179 |
strand | + |
ver | v1.2 |
region | chr5:174045706-174109179 |
region5000 | chr5:174040706-174114179 |
regionname0 | NSG2_chr5_174045706_174109179 |
regionname5000 | NSG2_chr5_174040706_174114179 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 171 | 294 | 92 | 64 | 86 | 10 | 40 | 64 | NSG2_chr5_174040706_174114179 | NSG2 | copy fasta | chr5 | 174040706 | 174114179 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 516 | 256 | 92 | 55 | 62 | 9 | 36 | NSG2_chr5_174040706_174114179 | NSG2 | copy fasta | chr5 | 174040706 | 174114179 |
c0002 | 0/0 | 516 | 21 | 0 | 7 | 10 | 1 | 3 | NSG2_chr5_174040706_174114179 | NSG2 | copy fasta | chr5 | 174040706 | 174114179 |
c0003 | 0/0 | 516 | 16 | 0 | 1 | 14 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | copy fasta | chr5 | 174040706 | 174114179 |
c0004 | 0/0 | 516 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | copy fasta | chr5 | 174040706 | 174114179 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 1835 | 153 | 26 | 39 | 62 | 5 | 19 | NSG2_chr5_174040706_174114179 | NSG2 | copy fasta | chr5 | 174040706 | 174114179 |
t0002 | 0/0 | 1835 | 40 | 21 | 11 | 0 | 1 | 7 | NSG2_chr5_174040706_174114179 | NSG2 | copy fasta | chr5 | 174040706 | 174114179 |
t0003 | 0/0 | 1833 | 39 | 9 | 7 | 16 | 2 | 5 | NSG2_chr5_174040706_174114179 | NSG2 | copy fasta | chr5 | 174040706 | 174114179 |
t0004 | 0/0 | 1835 | 24 | 18 | 3 | 1 | 0 | 2 | NSG2_chr5_174040706_174114179 | NSG2 | copy fasta | chr5 | 174040706 | 174114179 |
t0005 | 0/0 | 1833 | 5 | 5 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | copy fasta | chr5 | 174040706 | 174114179 |
t0006 | 0/0 | 1835 | 5 | 2 | 1 | 0 | 0 | 2 | NSG2_chr5_174040706_174114179 | NSG2 | copy fasta | chr5 | 174040706 | 174114179 |
t0007 | 0/0 | 1835 | 3 | 0 | 1 | 0 | 1 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | copy fasta | chr5 | 174040706 | 174114179 |
t0008 | 0/0 | 1835 | 3 | 0 | 0 | 0 | 1 | 2 | NSG2_chr5_174040706_174114179 | NSG2 | copy fasta | chr5 | 174040706 | 174114179 |
t0009 | 0/0 | 1833 | 3 | 2 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | copy fasta | chr5 | 174040706 | 174114179 |
t0010 | 0/0 | 1835 | 3 | 0 | 0 | 3 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | copy fasta | chr5 | 174040706 | 174114179 |
t0011 | 0/0 | 1835 | 2 | 2 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | copy fasta | chr5 | 174040706 | 174114179 |
t0012 | 0/0 | 1833 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | copy fasta | chr5 | 174040706 | 174114179 |
t0013 | 0/0 | 1835 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | copy fasta | chr5 | 174040706 | 174114179 |
t0014 | 0/0 | 1835 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | copy fasta | chr5 | 174040706 | 174114179 |
t0015 | 0/0 | 1835 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | copy fasta | chr5 | 174040706 | 174114179 |
t0016 | 0/0 | 1835 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | copy fasta | chr5 | 174040706 | 174114179 |
t0017 | 0/0 | 1835 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | copy fasta | chr5 | 174040706 | 174114179 |
t0018 | 0/0 | 1835 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | copy fasta | chr5 | 174040706 | 174114179 |
t0019 | 0/0 | 1835 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | copy fasta | chr5 | 174040706 | 174114179 |
t0020 | 0/0 | 1835 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | copy fasta | chr5 | 174040706 | 174114179 |
t0021 | 0/0 | 1835 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | copy fasta | chr5 | 174040706 | 174114179 |
t0022 | 0/0 | 1835 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | copy fasta | chr5 | 174040706 | 174114179 |
t0023 | 0/0 | 1833 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | copy fasta | chr5 | 174040706 | 174114179 |
t0024 | 0/0 | 1835 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | copy fasta | chr5 | 174040706 | 174114179 |
t0025 | 0/0 | 1835 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | copy fasta | chr5 | 174040706 | 174114179 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0005 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0008 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0010 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0093 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0151 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 516 | 256 | 92 | 55 | 62 | 9 | 36 | NSG2_chr5_174040706_174114179 | NSG2 | copy fasta | chr5 | 174040706 | 174114179 |
a0001c0002 | 0/0 | 516 | 21 | 0 | 7 | 10 | 1 | 3 | NSG2_chr5_174040706_174114179 | NSG2 | copy fasta | chr5 | 174040706 | 174114179 |
a0001c0003 | 0/0 | 516 | 16 | 0 | 1 | 14 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | copy fasta | chr5 | 174040706 | 174114179 |
a0001c0004 | 0/0 | 516 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | copy fasta | chr5 | 174040706 | 174114179 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 2350 | 132 | 26 | 31 | 52 | 4 | 17 | NSG2_chr5_174040706_174114179 | NSG2 | copy fasta | chr5 | 174040706 | 174114179 |
a0001c0001t0002 | 0/0 | 2350 | 39 | 21 | 11 | 0 | 1 | 6 | NSG2_chr5_174040706_174114179 | NSG2 | copy fasta | chr5 | 174040706 | 174114179 |
a0001c0001t0003 | 0/0 | 2348 | 23 | 9 | 6 | 2 | 2 | 4 | NSG2_chr5_174040706_174114179 | NSG2 | copy fasta | chr5 | 174040706 | 174114179 |
a0001c0001t0004 | 0/0 | 2350 | 24 | 18 | 3 | 1 | 0 | 2 | NSG2_chr5_174040706_174114179 | NSG2 | copy fasta | chr5 | 174040706 | 174114179 |
a0001c0001t0005 | 0/0 | 2348 | 5 | 5 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | copy fasta | chr5 | 174040706 | 174114179 |
a0001c0001t0006 | 0/0 | 2350 | 5 | 2 | 1 | 0 | 0 | 2 | NSG2_chr5_174040706_174114179 | NSG2 | copy fasta | chr5 | 174040706 | 174114179 |
a0001c0001t0007 | 0/0 | 2350 | 3 | 0 | 1 | 0 | 1 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | copy fasta | chr5 | 174040706 | 174114179 |
a0001c0001t0008 | 0/0 | 2350 | 3 | 0 | 0 | 0 | 1 | 2 | NSG2_chr5_174040706_174114179 | NSG2 | copy fasta | chr5 | 174040706 | 174114179 |
a0001c0001t0009 | 0/0 | 2348 | 3 | 2 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | copy fasta | chr5 | 174040706 | 174114179 |
a0001c0001t0010 | 0/0 | 2350 | 3 | 0 | 0 | 3 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | copy fasta | chr5 | 174040706 | 174114179 |
a0001c0001t0011 | 0/0 | 2350 | 2 | 2 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | copy fasta | chr5 | 174040706 | 174114179 |
a0001c0001t0012 | 0/0 | 2348 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | copy fasta | chr5 | 174040706 | 174114179 |
a0001c0001t0013 | 0/0 | 2350 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | copy fasta | chr5 | 174040706 | 174114179 |
a0001c0001t0014 | 0/0 | 2350 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | copy fasta | chr5 | 174040706 | 174114179 |
a0001c0001t0015 | 0/0 | 2350 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | copy fasta | chr5 | 174040706 | 174114179 |
a0001c0001t0016 | 0/0 | 2350 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | copy fasta | chr5 | 174040706 | 174114179 |
a0001c0001t0017 | 0/0 | 2350 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | copy fasta | chr5 | 174040706 | 174114179 |
a0001c0001t0018 | 0/0 | 2350 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | copy fasta | chr5 | 174040706 | 174114179 |
a0001c0001t0019 | 0/0 | 2350 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | copy fasta | chr5 | 174040706 | 174114179 |
a0001c0001t0020 | 0/0 | 2350 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | copy fasta | chr5 | 174040706 | 174114179 |
a0001c0001t0021 | 0/0 | 2350 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | copy fasta | chr5 | 174040706 | 174114179 |
a0001c0001t0022 | 0/0 | 2350 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | copy fasta | chr5 | 174040706 | 174114179 |
a0001c0001t0023 | 0/0 | 2348 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | copy fasta | chr5 | 174040706 | 174114179 |
a0001c0001t0024 | 0/0 | 2350 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | copy fasta | chr5 | 174040706 | 174114179 |
a0001c0001t0025 | 0/0 | 2350 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | copy fasta | chr5 | 174040706 | 174114179 |
a0001c0002t0001 | 0/0 | 2350 | 20 | 0 | 7 | 10 | 1 | 2 | NSG2_chr5_174040706_174114179 | NSG2 | copy fasta | chr5 | 174040706 | 174114179 |
a0001c0002t0002 | 0/0 | 2350 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | copy fasta | chr5 | 174040706 | 174114179 |
a0001c0003t0003 | 0/0 | 2348 | 16 | 0 | 1 | 14 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | copy fasta | chr5 | 174040706 | 174114179 |
a0001c0004t0001 | 0/0 | 2350 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | copy fasta | chr5 | 174040706 | 174114179 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0093 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0151 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0002g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0002g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0002g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0002g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0002g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0002g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0002g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0002g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0002g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0002g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0002g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0002g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0002g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0002g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0002g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0002g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0002g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0002g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0002g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0002g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0002g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0002g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0002g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0002g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0002g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0002g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0003g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0003g0005 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0003g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0003g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0003g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0003g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0003g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0003g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0003g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0003g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0003g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0003g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0003g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0003g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0003g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0003g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0003g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0003g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0004g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0004g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0004g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0004g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0004g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0004g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0004g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0004g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0004g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0004g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0004g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0004g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0004g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0004g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0004g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0004g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0004g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0004g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0004g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0004g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0004g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0004g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0005g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0005g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0005g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0005g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0005g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0006g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0006g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0006g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0006g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0006g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0007g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0007g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0007g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0008g0010 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0008g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0009g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0009g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0009g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0010g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0010g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0010g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0011g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0011g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0012g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0013g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0014g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0015g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0016g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0017g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0018g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0019g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0020g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0021g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0022g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0023g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0024g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0001t0025g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0002t0001g0008 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0002t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0002t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0002t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0002t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0002t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0002t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0002t0002g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0003t0003g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0003t0003g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0003t0003g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0003t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0003t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0003t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0003t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0003t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0003t0003g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0003t0003g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0003t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0003t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0003t0003g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0003t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0003t0003g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
a0001c0004t0001g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0003 | g0017 | EUR | GBR | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0039 | EUR | GBR | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG00280 | hp1 | a0001 | c0001 | t0008 | g0010 | EUR | FIN | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0074 | EUR | FIN | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG00323 | hp1 | a0001 | c0001 | t0003 | g0146 | EUR | FIN | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG00323 | hp2 | a0001 | c0001 | t0007 | g0178 | EUR | FIN | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | CHS | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG00408 | hp2 | a0001 | c0003 | t0003 | g0196 | EAS | CHS | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | CHS | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | CHS | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0231 | AMR | PUR | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | CHS | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG00673 | hp2 | a0001 | c0003 | t0003 | g0203 | EAS | CHS | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG00738 | hp1 | a0001 | c0001 | t0003 | g0006 | AMR | PUR | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | PUR | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG01069 | hp1 | a0001 | c0001 | t0002 | g0232 | AMR | PUR | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG01069 | hp2 | a0001 | c0001 | t0003 | g0007 | AMR | PUR | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG01070 | hp1 | a0001 | c0002 | t0001 | g0177 | AMR | PUR | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0233 | AMR | PUR | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG01071 | hp2 | a0001 | c0002 | t0001 | g0176 | AMR | PUR | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG01074 | hp2 | a0001 | c0001 | t0003 | g0007 | AMR | PUR | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0271 | AMR | PUR | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG01106 | hp1 | a0001 | c0002 | t0001 | g0065 | AMR | PUR | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG01109 | hp1 | a0001 | c0001 | t0003 | g0006 | AMR | PUR | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG01109 | hp2 | a0001 | c0001 | t0002 | g0261 | AMR | PUR | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG01167 | hp1 | a0001 | c0001 | t0009 | g0268 | AMR | PUR | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG01167 | hp2 | a0001 | c0001 | t0004 | g0011 | AMR | PUR | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | PUR | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG01169 | hp1 | a0001 | c0001 | t0004 | g0011 | AMR | PUR | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0278 | AMR | PUR | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG01175 | hp2 | a0001 | c0002 | t0001 | g0064 | AMR | PUR | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG01192 | hp1 | a0001 | c0004 | t0001 | g0001 | AMR | PUR | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0241 | AMR | PUR | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | CLM | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | CLM | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | CLM | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG01257 | hp2 | a0001 | c0001 | t0003 | g0013 | AMR | CLM | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG01258 | hp1 | a0001 | c0001 | t0007 | g0180 | AMR | CLM | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | CLM | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG01261 | hp1 | a0001 | c0001 | t0002 | g0281 | AMR | CLM | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | CLM | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG01358 | hp1 | a0001 | c0003 | t0003 | g0193 | AMR | CLM | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | CLM | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG01433 | hp1 | a0001 | c0001 | t0004 | g0225 | AMR | CLM | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG01433 | hp2 | a0001 | c0001 | t0003 | g0040 | AMR | CLM | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | CLM | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | CLM | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0067 | EUR | IBS | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG01515 | hp2 | a0001 | c0002 | t0001 | g0089 | EUR | IBS | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | ACB | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG01884 | hp2 | a0001 | c0001 | t0002 | g0237 | AFR | ACB | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | ACB | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG01891 | hp2 | a0001 | c0001 | t0002 | g0267 | AFR | ACB | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG01928 | hp1 | a0001 | c0001 | t0025 | g0245 | AMR | PEL | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0279 | AMR | PEL | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG01934 | hp1 | a0001 | c0002 | t0001 | g0008 | AMR | PEL | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | PEL | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG01952 | hp1 | a0001 | c0001 | t0002 | g0257 | AMR | PEL | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG01981 | hp1 | a0001 | c0002 | t0001 | g0187 | AMR | PEL | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | PEL | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG02004 | hp1 | a0001 | c0001 | t0002 | g0256 | AMR | PEL | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PEL | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | KHV | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | KHV | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG02040 | hp1 | a0001 | c0003 | t0003 | g0197 | EAS | KHV | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | KHV | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG02055 | hp1 | a0001 | c0001 | t0003 | g0004 | AFR | ACB | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG02055 | hp2 | a0001 | c0001 | t0002 | g0031 | AFR | ACB | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | KHV | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | KHV | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | KHV | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | KHV | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | KHV | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | KHV | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG02145 | hp1 | a0001 | c0001 | t0004 | g0220 | AFR | ACB | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG02145 | hp2 | a0001 | c0001 | t0002 | g0032 | AFR | ACB | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG02155 | hp1 | a0001 | c0003 | t0003 | g0026 | EAS | CDX | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | CDX | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG02257 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | ACB | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG02257 | hp2 | a0001 | c0001 | t0004 | g0016 | AFR | ACB | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG02258 | hp1 | a0001 | c0001 | t0003 | g0079 | AFR | ACB | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG02258 | hp2 | a0001 | c0001 | t0002 | g0266 | AFR | ACB | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PEL | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0244 | AMR | PEL | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG02280 | hp1 | a0001 | c0001 | t0009 | g0270 | AFR | ACB | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | ACB | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG02293 | hp1 | a0001 | c0001 | t0006 | g0251 | AMR | PEL | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0280 | AMR | PEL | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0243 | AMR | PEL | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | PEL | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | ACB | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG02451 | hp2 | a0001 | c0001 | t0011 | g0024 | AFR | ACB | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG02523 | hp1 | a0001 | c0002 | t0001 | g0062 | EAS | KHV | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | KHV | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG02572 | hp1 | a0001 | c0001 | t0002 | g0240 | AFR | GWD | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG02572 | hp2 | a0001 | c0001 | t0017 | g0029 | AFR | GWD | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG02602 | hp1 | a0001 | c0001 | t0004 | g0282 | SAS | PJL | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG02602 | hp2 | a0001 | c0001 | t0003 | g0005 | SAS | PJL | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | GWD | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG02622 | hp2 | a0001 | c0001 | t0002 | g0250 | AFR | GWD | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG02630 | hp1 | a0001 | c0001 | t0004 | g0002 | AFR | GWD | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG02630 | hp2 | a0001 | c0001 | t0003 | g0076 | AFR | GWD | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG02647 | hp1 | a0001 | c0001 | t0002 | g0273 | AFR | GWD | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | GWD | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0165 | SAS | PJL | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG02683 | hp2 | a0001 | c0001 | t0006 | g0247 | SAS | PJL | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0085 | SAS | PJL | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG02698 | hp2 | a0001 | c0001 | t0003 | g0276 | SAS | PJL | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG02717 | hp1 | a0001 | c0001 | t0004 | g0002 | AFR | GWD | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG02717 | hp2 | a0001 | c0001 | t0002 | g0249 | AFR | GWD | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG02723 | hp1 | a0001 | c0001 | t0004 | g0219 | AFR | GWD | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG02723 | hp2 | a0001 | c0001 | t0002 | g0254 | AFR | GWD | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG02735 | hp1 | a0001 | c0001 | t0004 | g0228 | SAS | PJL | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG02809 | hp1 | a0001 | c0001 | t0004 | g0030 | AFR | GWD | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | GWD | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG02886 | hp1 | a0001 | c0001 | t0005 | g0033 | AFR | GWD | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | GWD | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG02895 | hp1 | a0001 | c0001 | t0004 | g0066 | AFR | GWD | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | GWD | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | GWD | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG02897 | hp2 | a0001 | c0001 | t0002 | g0263 | AFR | GWD | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | ESN | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG02922 | hp2 | a0001 | c0001 | t0002 | g0246 | AFR | ESN | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG02965 | hp1 | a0001 | c0001 | t0015 | g0168 | AFR | ESN | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG02965 | hp2 | a0001 | c0001 | t0002 | g0238 | AFR | ESN | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG02970 | hp1 | a0001 | c0001 | t0005 | g0259 | AFR | ESN | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | ESN | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG02976 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | ESN | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | ESN | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG03041 | hp1 | a0001 | c0001 | t0004 | g0227 | AFR | GWD | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG03041 | hp2 | a0001 | c0001 | t0004 | g0027 | AFR | GWD | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG03098 | hp1 | a0001 | c0001 | t0020 | g0172 | AFR | MSL | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG03098 | hp2 | a0001 | c0001 | t0002 | g0262 | AFR | MSL | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG03130 | hp1 | a0001 | c0001 | t0002 | g0265 | AFR | ESN | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG03130 | hp2 | a0001 | c0001 | t0004 | g0042 | AFR | ESN | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG03139 | hp1 | a0001 | c0001 | t0003 | g0012 | AFR | ESN | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ESN | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | ESN | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | ESN | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG03209 | hp1 | a0001 | c0001 | t0002 | g0229 | AFR | MSL | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | MSL | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | MSL | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG03225 | hp2 | a0001 | c0001 | t0002 | g0274 | AFR | MSL | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0081 | SAS | PJL | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0096 | SAS | PJL | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG03453 | hp1 | a0001 | c0001 | t0011 | g0025 | AFR | MSL | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG03453 | hp2 | a0001 | c0001 | t0004 | g0028 | AFR | MSL | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG03486 | hp1 | a0001 | c0001 | t0003 | g0004 | AFR | MSL | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG03486 | hp2 | a0001 | c0001 | t0002 | g0264 | AFR | MSL | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0253 | SAS | PJL | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0252 | SAS | PJL | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG03492 | hp2 | a0001 | c0001 | t0021 | g0087 | SAS | PJL | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG03516 | hp1 | a0001 | c0001 | t0004 | g0047 | AFR | ESN | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | ESN | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG03540 | hp1 | a0001 | c0001 | t0004 | g0044 | AFR | GWD | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG03540 | hp2 | a0001 | c0001 | t0002 | g0236 | AFR | GWD | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG03579 | hp1 | a0001 | c0001 | t0009 | g0269 | AFR | MSL | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG03579 | hp2 | a0001 | c0001 | t0019 | g0223 | AFR | MSL | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG03654 | hp1 | a0001 | c0002 | t0002 | g0235 | SAS | PJL | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0164 | SAS | PJL | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG03704 | hp1 | a0001 | c0003 | t0003 | g0201 | SAS | PJL | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0051 | SAS | PJL | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG03710 | hp2 | a0001 | c0001 | t0003 | g0148 | SAS | PJL | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG03831 | hp1 | a0001 | c0002 | t0001 | g0086 | SAS | BEB | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0258 | SAS | BEB | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0242 | SAS | BEB | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0048 | SAS | BEB | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG03927 | hp1 | a0001 | c0001 | t0008 | g0275 | SAS | BEB | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0126 | SAS | BEB | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG03942 | hp1 | a0001 | c0001 | t0006 | g0239 | SAS | BEB | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG03942 | hp2 | a0001 | c0001 | t0003 | g0147 | SAS | BEB | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | STU | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0134 | SAS | STU | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG04184 | hp1 | a0001 | c0002 | t0001 | g0157 | SAS | BEB | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0248 | SAS | BEB | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0230 | SAS | STU | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0105 | SAS | STU | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG04228 | hp1 | a0001 | c0001 | t0007 | g0175 | SAS | STU | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0179 | SAS | STU | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
NA18522 | hp1 | a0001 | c0001 | t0005 | g0019 | AFR | YRI | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
NA18522 | hp2 | a0001 | c0001 | t0004 | g0046 | AFR | YRI | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | CHB | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | CHB | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
NA18906 | hp1 | a0001 | c0001 | t0006 | g0260 | AFR | YRI | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
NA18906 | hp2 | a0001 | c0001 | t0003 | g0078 | AFR | YRI | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
NA18943 | hp1 | a0001 | c0002 | t0001 | g0185 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
NA18950 | hp1 | a0001 | c0002 | t0001 | g0181 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
NA18951 | hp1 | a0001 | c0002 | t0001 | g0186 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
NA18952 | hp2 | a0001 | c0003 | t0003 | g0199 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
NA18953 | hp1 | a0001 | c0001 | t0012 | g0149 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
NA18953 | hp2 | a0001 | c0001 | t0010 | g0142 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
NA18959 | hp1 | a0001 | c0001 | t0016 | g0071 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
NA18961 | hp2 | a0001 | c0002 | t0001 | g0184 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
NA18964 | hp1 | a0001 | c0003 | t0003 | g0200 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
NA18964 | hp2 | a0001 | c0001 | t0022 | g0094 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
NA18965 | hp1 | a0001 | c0002 | t0001 | g0182 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
NA18965 | hp2 | a0001 | c0001 | t0004 | g0226 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
NA18970 | hp2 | a0001 | c0003 | t0003 | g0209 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
NA18981 | hp1 | a0001 | c0001 | t0003 | g0163 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
NA18984 | hp2 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
NA18999 | hp1 | a0001 | c0003 | t0003 | g0194 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
NA19000 | hp1 | a0001 | c0002 | t0001 | g0183 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
NA19005 | hp2 | a0001 | c0003 | t0003 | g0202 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0222 | AFR | LWK | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | LWK | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
NA19043 | hp1 | a0001 | c0001 | t0013 | g0068 | AFR | LWK | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
NA19043 | hp2 | a0001 | c0001 | t0004 | g0077 | AFR | LWK | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
NA19056 | hp1 | a0001 | c0001 | t0014 | g0213 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
NA19056 | hp2 | a0001 | c0003 | t0003 | g0206 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
NA19058 | hp1 | a0001 | c0001 | t0010 | g0133 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
NA19060 | hp1 | a0001 | c0002 | t0001 | g0061 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
NA19064 | hp2 | a0001 | c0003 | t0003 | g0204 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
NA19070 | hp1 | a0001 | c0003 | t0003 | g0195 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
NA19082 | hp2 | a0001 | c0003 | t0003 | g0009 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
NA19083 | hp1 | a0001 | c0003 | t0003 | g0009 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
NA19084 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
NA19086 | hp1 | a0001 | c0001 | t0010 | g0125 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | YRI | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
NA19240 | hp2 | a0001 | c0001 | t0006 | g0255 | AFR | YRI | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0234 | EUR | TSI | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0090 | EUR | TSI | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
NA20905 | hp1 | a0001 | c0001 | t0018 | g0277 | SAS | GIH | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
NA20905 | hp2 | a0001 | c0001 | t0008 | g0010 | SAS | GIH | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG01123 | hp2 | a0001 | c0002 | t0001 | g0059 | AMR | CLM | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | ACB | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG02109 | hp2 | a0001 | c0001 | t0003 | g0075 | AFR | ACB | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG02486 | hp1 | a0001 | c0001 | t0005 | g0018 | AFR | ACB | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | ACB | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG02559 | hp1 | a0001 | c0001 | t0003 | g0211 | AFR | ACB | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG02559 | hp2 | a0001 | c0001 | t0023 | g0043 | AFR | ACB | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG03471 | hp1 | a0001 | c0001 | t0004 | g0015 | AFR | MSL | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG03471 | hp2 | a0001 | c0001 | t0004 | g0045 | AFR | MSL | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | USA | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
HG06807 | hp2 | a0001 | c0001 | t0005 | g0207 | AFR | USA | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
NA18955 | hp2 | a0001 | c0002 | t0001 | g0188 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | USA | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
NA20300 | hp2 | a0001 | c0001 | t0024 | g0272 | AFR | USA | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
NA21309 | hp1 | a0001 | c0001 | t0003 | g0080 | AFR | LWK | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
NA21309 | hp2 | a0001 | c0001 | t0004 | g0224 | AFR | LWK | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0093 | REF | REF | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0151 | REF | REF | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
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 |
---|
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:174064297
|
G | A | 1 | a0001c0002 | 21 | HG01070.hp1 HG01071.hp2 HG01106.hp1 others(18): Show |
synonymous_variant | LOW | c.195G>A | p.Pro65Pro | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/5 | 355/2350 | 195/516 | 65/171 | chr5 | 174064297 | ||
chr5:174107421
|
G | A | 1 | a0001c0004 | 1 | HG01192.hp1 | synonymous_variant | LOW | c.432G>A | p.Gln144Gln | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 5/5 | 592/2350 | 432/516 | 144/171 | chr5 | 174107421 | ||
chr5:174107445
|
G | A | 1 | a0001c0003 | 16 | HG00408.hp2 HG00673.hp2 HG01358.hp1 others(13): Show |
synonymous_variant | LOW | c.456G>A | p.Pro152Pro | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 5/5 | 616/2350 | 456/516 | 152/171 | chr5 | 174107445 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:174045763
|
C | G | 1 | a0001c0001t0010 | 3 | NA18953.hp2 NA19058.hp1 NA19086.hp1 |
5_prime_UTR_variant | MODIFIER | c.-103C>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 1/5 | 993 | chr5 | 174045763 | |||||
chr5:174045817
|
G | T | 6 | a0001c0001t0002a0001c0001t0006a0001c0001t0009others(3): Show | 50 | HG00642.hp1 HG01069.hp1 HG01071.hp1 others(47): Show |
5_prime_UTR_variant | MODIFIER | c.-49G>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 1/5 | 939 | chr5 | 174045817 | |||||
chr5:174045824
|
C | G | 1 | a0001c0001t0023 | 1 | HG02559.hp2 | 5_prime_UTR_variant | MODIFIER | c.-42C>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 1/5 | 932 | chr5 | 174045824 | |||||
chr5:174107681
|
C | T | 1 | a0001c0001t0022 | 1 | NA18964.hp2 | 3_prime_UTR_variant | MODIFIER | c.*176C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 5/5 | 176 | chr5 | 174107681 | |||||
chr5:174107798
|
CTT | C | 6 | a0001c0001t0003a0001c0001t0005a0001c0001t0009others(3): Show | 49 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*295_*296delTT | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 5/5 | 295 | INFO_REALIGN_3_PRIME | chr5 | 174107798 | ||||
chr5:174107874
|
A | G | 18 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(15): Show | 125 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(122): Show |
3_prime_UTR_variant | MODIFIER | c.*369A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 5/5 | 369 | chr5 | 174107874 | |||||
chr5:174107932
|
C | T | 1 | a0001c0001t0005 | 5 | HG02486.hp1 HG02886.hp1 HG02970.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*427C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 5/5 | 427 | chr5 | 174107932 | |||||
chr5:174107933
|
G | A | 1 | a0001c0001t0017 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*428G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 5/5 | 428 | chr5 | 174107933 | |||||
chr5:174108008
|
G | A | 1 | a0001c0001t0018 | 1 | NA20905.hp1 | 3_prime_UTR_variant | MODIFIER | c.*503G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 5/5 | 503 | chr5 | 174108008 | |||||
chr5:174108041
|
G | A | 16 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(13): Show | 121 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(118): Show |
3_prime_UTR_variant | MODIFIER | c.*536G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 5/5 | 536 | chr5 | 174108041 | |||||
chr5:174108051
|
G | C | 1 | a0001c0001t0013 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*546G>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 5/5 | 546 | chr5 | 174108051 | |||||
chr5:174108084
|
C | T | 16 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(13): Show | 121 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(118): Show |
3_prime_UTR_variant | MODIFIER | c.*579C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 5/5 | 579 | chr5 | 174108084 | |||||
chr5:174108129
|
C | G | 1 | a0001c0001t0020 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*624C>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 5/5 | 624 | chr5 | 174108129 | |||||
chr5:174108213
|
C | T | 2 | a0001c0001t0005a0001c0001t0011 | 7 | HG02451.hp2 HG02486.hp1 HG02886.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*708C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 5/5 | 708 | chr5 | 174108213 | |||||
chr5:174108311
|
C | T | 1 | a0001c0001t0025 | 1 | HG01928.hp1 | 3_prime_UTR_variant | MODIFIER | c.*806C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 5/5 | 806 | chr5 | 174108311 | |||||
chr5:174108325
|
G | C | 1 | a0001c0001t0014 | 1 | NA19056.hp1 | 3_prime_UTR_variant | MODIFIER | c.*820G>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 5/5 | 820 | chr5 | 174108325 | |||||
chr5:174108434
|
T | G | 1 | a0001c0001t0015 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*929T>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 5/5 | 929 | chr5 | 174108434 | |||||
chr5:174108450
|
A | C | 1 | a0001c0001t0016 | 1 | NA18959.hp1 | 3_prime_UTR_variant | MODIFIER | c.*945A>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 5/5 | 945 | chr5 | 174108450 | |||||
chr5:174108482
|
A | G | 1 | a0001c0001t0012 | 1 | NA18953.hp1 | 3_prime_UTR_variant | MODIFIER | c.*977A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 5/5 | 977 | chr5 | 174108482 | |||||
chr5:174108717
|
G | C | 17 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(14): Show | 124 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(121): Show |
3_prime_UTR_variant | MODIFIER | c.*1212G>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 5/5 | 1212 | chr5 | 174108717 | |||||
chr5:174108739
|
A | G | 1 | a0001c0001t0024 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1234A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 5/5 | 1234 | chr5 | 174108739 | |||||
chr5:174108815
|
A | T | 1 | a0001c0001t0008 | 3 | HG00280.hp1 HG03927.hp1 NA20905.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1310A>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 5/5 | 1310 | chr5 | 174108815 | |||||
chr5:174108977
|
C | T | 1 | a0001c0001t0019 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1472C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 5/5 | 1472 | chr5 | 174108977 | |||||
chr5:174109166
|
A | G | 1 | a0001c0001t0007 | 3 | HG00323.hp2 HG01258.hp1 HG04228.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1661A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 5/5 | 1661 | chr5 | 174109166 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:174045893
|
C | T | 1 | a0001c0001t0004g0282 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-23+50C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 1/4 | chr5 | 174045893 | ||||||
chr5:174046092
|
C | CA | 24 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0021others(21): Show | 26 | HG00099.hp1 HG01257.hp2 HG01952.hp2 others(23): Show |
intron_variant | MODIFIER | c.-23+264dupA | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr5 | 174046092 | |||||
chr5:174046092
|
CA | C | 9 | a0001c0001t0001g0278a0001c0001t0001g0279a0001c0001t0001g0280others(6): Show | 11 | HG00280.hp1 HG01167.hp2 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.-23+264delA | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr5 | 174046092 | |||||
chr5:174046143
|
T | C | 5 | a0001c0001t0003g0276a0001c0001t0004g0011a0001c0001t0008g0010others(2): Show | 7 | HG00280.hp1 HG01167.hp2 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.-23+300T>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 1/4 | chr5 | 174046143 | ||||||
chr5:174046155
|
A | G | 5 | a0001c0001t0003g0276a0001c0001t0004g0011a0001c0001t0008g0010others(2): Show | 7 | HG00280.hp1 HG01167.hp2 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.-23+312A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 1/4 | chr5 | 174046155 | ||||||
chr5:174046351
|
A | G | 71 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0002g0003others(68): Show | 75 | HG00280.hp1 HG00642.hp1 HG01069.hp1 others(72): Show |
intron_variant | MODIFIER | c.-22-383A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 1/4 | chr5 | 174046351 | ||||||
chr5:174046354
|
CG | C | 56 | a0001c0001t0002g0003a0001c0001t0002g0031a0001c0001t0002g0032others(53): Show | 59 | HG00280.hp1 HG00642.hp1 HG01069.hp1 others(56): Show |
intron_variant | MODIFIER | c.-22-372delG | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr5 | 174046354 | |||||
chr5:174046355
|
G | C | 4 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0003g0012others(1): Show | 4 | HG01257.hp2 HG02970.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-22-379G>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 1/4 | chr5 | 174046355 | ||||||
chr5:174046359
|
G | C | 2 | a0001c0001t0004g0027a0001c0001t0004g0028 | 2 | HG03041.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-22-375G>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 1/4 | chr5 | 174046359 | ||||||
chr5:174046376
|
C | T | 15 | a0001c0001t0002g0261a0001c0001t0002g0262a0001c0001t0002g0263others(12): Show | 15 | HG01099.hp1 HG01109.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.-22-358C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 1/4 | chr5 | 174046376 | ||||||
chr5:174047099
|
G | C | 1 | a0001c0001t0002g0229 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.129+215G>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174047099 | ||||||
chr5:174047230
|
G | A | 2 | a0001c0001t0001g0036a0001c0001t0001g0037 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.129+346G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174047230 | ||||||
chr5:174047436
|
T | A | 3 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0003g0040 | 3 | HG00099.hp2 HG01099.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.129+552T>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174047436 | ||||||
chr5:174047462
|
A | G | 56 | a0001c0001t0002g0003a0001c0001t0002g0031a0001c0001t0002g0032others(53): Show | 59 | HG00280.hp1 HG00642.hp1 HG01069.hp1 others(56): Show |
intron_variant | MODIFIER | c.129+578A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174047462 | ||||||
chr5:174047627
|
G | A | 1 | a0001c0001t0001g0041 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.129+743G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174047627 | ||||||
chr5:174047728
|
G | A | 3 | a0001c0001t0002g0003a0001c0001t0002g0031a0001c0001t0002g0032 | 4 | HG02055.hp2 HG02145.hp2 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.129+844G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174047728 | ||||||
chr5:174047824
|
T | C | 6 | a0001c0001t0004g0042a0001c0001t0004g0044a0001c0001t0004g0045others(3): Show | 6 | HG02559.hp2 HG03130.hp2 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.129+940T>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174047824 | ||||||
chr5:174047884
|
T | G | 67 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0002g0003others(64): Show | 71 | HG00280.hp1 HG00642.hp1 HG01069.hp1 others(68): Show |
intron_variant | MODIFIER | c.129+1000T>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174047884 | ||||||
chr5:174047890
|
C | T | 1 | a0001c0001t0001g0218 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.129+1006C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174047890 | ||||||
chr5:174048003
|
A | G | 2 | a0001c0001t0005g0033a0001c0001t0005g0259 | 2 | HG02886.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.129+1119A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174048003 | ||||||
chr5:174048073
|
G | A | 1 | a0001c0001t0001g0048 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.129+1189G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174048073 | ||||||
chr5:174048083
|
G | A | 4 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0004g0219others(1): Show | 4 | HG01891.hp1 HG02145.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.129+1199G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174048083 | ||||||
chr5:174048147
|
A | G | 6 | a0001c0001t0001g0212a0001c0001t0001g0214a0001c0001t0001g0215others(3): Show | 6 | HG02083.hp1 NA18979.hp1 NA19011.hp1 others(3): Show |
intron_variant | MODIFIER | c.129+1263A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174048147 | ||||||
chr5:174048375
|
G | A | 1 | a0001c0001t0001g0049 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.129+1491G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174048375 | ||||||
chr5:174048613
|
A | G | 5 | a0001c0001t0003g0276a0001c0001t0004g0011a0001c0001t0008g0010others(2): Show | 7 | HG00280.hp1 HG01167.hp2 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.129+1729A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174048613 | ||||||
chr5:174048698
|
C | A | 1 | a0001c0001t0001g0050 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.129+1814C>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174048698 | ||||||
chr5:174048805
|
C | T | 1 | a0001c0001t0003g0211 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.129+1921C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174048805 | ||||||
chr5:174048922
|
C | T | 49 | a0001c0001t0002g0003a0001c0001t0002g0031a0001c0001t0002g0032others(46): Show | 50 | HG00642.hp1 HG01069.hp1 HG01071.hp1 others(47): Show |
intron_variant | MODIFIER | c.129+2038C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174048922 | ||||||
chr5:174048939
|
G | A | 1 | a0001c0001t0001g0051 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.129+2055G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174048939 | ||||||
chr5:174049078
|
G | C | 1 | a0001c0001t0017g0029 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.129+2194G>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174049078 | ||||||
chr5:174049114
|
C | T | 3 | a0001c0001t0004g0027a0001c0001t0004g0028a0001c0001t0017g0029 | 3 | HG02572.hp2 HG03041.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.129+2230C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174049114 | ||||||
chr5:174049135
|
C | G | 1 | a0001c0001t0001g0210 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.129+2251C>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174049135 | ||||||
chr5:174049136
|
G | A | 1 | a0001c0001t0001g0014 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.129+2252G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174049136 | ||||||
chr5:174049155
|
C | G | 3 | a0001c0001t0003g0276a0001c0001t0004g0011a0001c0001t0018g0277 | 4 | HG01167.hp2 HG01169.hp1 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.129+2271C>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174049155 | ||||||
chr5:174049165
|
G | C | 56 | a0001c0001t0002g0003a0001c0001t0002g0031a0001c0001t0002g0032others(53): Show | 59 | HG00280.hp1 HG00642.hp1 HG01069.hp1 others(56): Show |
intron_variant | MODIFIER | c.129+2281G>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174049165 | ||||||
chr5:174049204
|
G | A | 1 | a0001c0001t0004g0225 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.129+2320G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174049204 | ||||||
chr5:174049211
|
G | C | 2 | a0001c0001t0005g0033a0001c0001t0005g0259 | 2 | HG02886.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.129+2327G>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174049211 | ||||||
chr5:174049264
|
T | C | 7 | a0001c0001t0003g0276a0001c0001t0004g0011a0001c0001t0005g0033others(4): Show | 9 | HG00280.hp1 HG01167.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.129+2380T>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174049264 | ||||||
chr5:174049340
|
AAAACAAA others(1): Show |
A | 16 | a0001c0001t0001g0001a0001c0001t0001g0038a0001c0001t0001g0039others(13): Show | 17 | HG00099.hp2 HG00621.hp2 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.129+2476_129+2483d others(10): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 174049340 | |||||
chr5:174049432
|
TGCACGC | T | 51 | a0001c0001t0002g0003a0001c0001t0002g0031a0001c0001t0002g0032others(48): Show | 52 | HG00642.hp1 HG01069.hp1 HG01071.hp1 others(49): Show |
intron_variant | MODIFIER | c.129+2554_129+2559d others(8): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 174049432 | |||||
chr5:174049437
|
G | A | 2 | a0001c0002t0001g0061a0001c0002t0001g0062 | 2 | HG02523.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.129+2553G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174049437 | ||||||
chr5:174049443
|
G | A | 6 | a0001c0001t0002g0230a0001c0001t0002g0231a0001c0001t0002g0232others(3): Show | 6 | HG00642.hp1 HG01069.hp1 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.129+2559G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174049443 | ||||||
chr5:174049449
|
A | G | 1 | a0001c0003t0003g0209 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.129+2565A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174049449 | ||||||
chr5:174049647
|
C | G | 1 | a0001c0001t0001g0208 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.129+2763C>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174049647 | ||||||
chr5:174049736
|
G | A | 1 | a0001c0001t0001g0063 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.129+2852G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174049736 | ||||||
chr5:174049936
|
C | G | 6 | a0001c0001t0004g0042a0001c0001t0004g0044a0001c0001t0004g0045others(3): Show | 6 | HG02559.hp2 HG03130.hp2 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.129+3052C>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174049936 | ||||||
chr5:174050032
|
T | C | 2 | a0001c0002t0001g0064a0001c0002t0001g0065 | 2 | HG01106.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.129+3148T>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174050032 | ||||||
chr5:174050070
|
C | T | 1 | a0001c0001t0005g0207 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.129+3186C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174050070 | ||||||
chr5:174050155
|
T | C | 3 | a0001c0001t0004g0015a0001c0001t0004g0016a0001c0001t0004g0066 | 3 | HG02257.hp2 HG02895.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.129+3271T>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174050155 | ||||||
chr5:174050366
|
C | T | 20 | a0001c0001t0001g0198a0001c0001t0001g0205a0001c0001t0004g0015others(17): Show | 21 | HG00408.hp2 HG00673.hp2 HG01358.hp1 others(18): Show |
intron_variant | MODIFIER | c.129+3482C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174050366 | ||||||
chr5:174050400
|
G | T | 10 | a0001c0001t0001g0189a0001c0001t0001g0190a0001c0001t0001g0191others(7): Show | 10 | HG00673.hp1 HG02071.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.129+3516G>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174050400 | ||||||
chr5:174050554
|
C | A | 2 | a0001c0001t0005g0033a0001c0001t0005g0259 | 2 | HG02886.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.129+3670C>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174050554 | ||||||
chr5:174050566
|
C | A | 1 | a0001c0001t0001g0067 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.129+3682C>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174050566 | ||||||
chr5:174050718
|
G | A | 3 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0048 | 3 | HG00099.hp2 HG01099.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.129+3834G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174050718 | ||||||
chr5:174050871
|
G | A | 5 | a0001c0001t0003g0276a0001c0001t0004g0011a0001c0001t0008g0010others(2): Show | 7 | HG00280.hp1 HG01167.hp2 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.129+3987G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174050871 | ||||||
chr5:174050964
|
C | T | 11 | a0001c0002t0001g0008a0001c0002t0001g0061a0001c0002t0001g0062others(8): Show | 12 | HG01934.hp1 HG01981.hp1 HG02523.hp1 others(9): Show |
intron_variant | MODIFIER | c.129+4080C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174050964 | ||||||
chr5:174051022
|
C | T | 2 | a0001c0001t0011g0024a0001c0001t0011g0025 | 2 | HG02451.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.129+4138C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174051022 | ||||||
chr5:174051048
|
G | A | 1 | a0001c0001t0019g0223 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.129+4164G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174051048 | ||||||
chr5:174051168
|
A | T | 1 | a0001c0001t0002g0274 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.129+4284A>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174051168 | ||||||
chr5:174051241
|
G | T | 3 | a0001c0001t0003g0276a0001c0001t0004g0011a0001c0001t0018g0277 | 4 | HG01167.hp2 HG01169.hp1 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.129+4357G>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174051241 | ||||||
chr5:174051255
|
C | T | 3 | a0001c0001t0001g0179a0001c0001t0007g0178a0001c0001t0007g0180 | 3 | HG00323.hp2 HG01258.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.129+4371C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174051255 | ||||||
chr5:174051259
|
T | C | 9 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0004g0002others(6): Show | 10 | HG01891.hp1 HG02145.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.129+4375T>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174051259 | ||||||
chr5:174051575
|
T | TCATC | 21 | a0001c0001t0001g0198a0001c0001t0001g0205a0001c0001t0004g0015others(18): Show | 22 | HG00408.hp2 HG00673.hp2 HG01358.hp1 others(19): Show |
intron_variant | MODIFIER | c.129+4710_129+4713d others(6): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 174051575 | |||||
chr5:174051595
|
C | T | 2 | a0001c0002t0001g0176a0001c0002t0001g0177 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.129+4711C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174051595 | ||||||
chr5:174051656
|
G | A | 1 | a0001c0002t0001g0181 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.129+4772G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174051656 | ||||||
chr5:174051786
|
G | T | 1 | a0001c0001t0007g0175 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.129+4902G>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174051786 | ||||||
chr5:174051935
|
G | T | 51 | a0001c0001t0002g0003a0001c0001t0002g0031a0001c0001t0002g0032others(48): Show | 53 | HG00280.hp1 HG00642.hp1 HG01069.hp1 others(50): Show |
intron_variant | MODIFIER | c.129+5051G>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174051935 | ||||||
chr5:174051979
|
A | T | 71 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0002g0003others(68): Show | 75 | HG00280.hp1 HG00642.hp1 HG01069.hp1 others(72): Show |
intron_variant | MODIFIER | c.129+5095A>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174051979 | ||||||
chr5:174052075
|
G | T | 4 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0001t0001g0279others(1): Show | 4 | HG01928.hp2 HG02074.hp1 HG02155.hp2 others(1): Show |
intron_variant | MODIFIER | c.129+5191G>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174052075 | ||||||
chr5:174052087
|
G | A | 3 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0013g0068 | 3 | HG02809.hp2 HG03195.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.129+5203G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174052087 | ||||||
chr5:174052088
|
G | A | 1 | a0001c0001t0004g0011 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.129+5204G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174052088 | ||||||
chr5:174052123
|
C | T | 5 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(2): Show | 5 | HG02622.hp1 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.129+5239C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174052123 | ||||||
chr5:174052379
|
C | T | 1 | a0001c0003t0003g0206 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.129+5495C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174052379 | ||||||
chr5:174052477
|
C | T | 1 | a0001c0001t0004g0224 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.129+5593C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174052477 | ||||||
chr5:174052564
|
A | C | 1 | a0001c0001t0007g0180 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.129+5680A>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174052564 | ||||||
chr5:174052672
|
C | T | 1 | a0001c0001t0001g0167 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.129+5788C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174052672 | ||||||
chr5:174052806
|
G | A | 1 | a0001c0001t0004g0225 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.129+5922G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174052806 | ||||||
chr5:174052829
|
G | C | 56 | a0001c0001t0002g0003a0001c0001t0002g0031a0001c0001t0002g0032others(53): Show | 59 | HG00280.hp1 HG00642.hp1 HG01069.hp1 others(56): Show |
intron_variant | MODIFIER | c.129+5945G>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174052829 | ||||||
chr5:174052893
|
G | A | 1 | a0001c0001t0016g0071 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.129+6009G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174052893 | ||||||
chr5:174053225
|
G | C | 2 | a0001c0001t0008g0010a0001c0001t0008g0275 | 3 | HG00280.hp1 HG03927.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.129+6341G>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174053225 | ||||||
chr5:174053444
|
A | G | 1 | a0001c0001t0001g0166 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.129+6560A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174053444 | ||||||
chr5:174053503
|
C | T | 51 | a0001c0001t0002g0003a0001c0001t0002g0031a0001c0001t0002g0032others(48): Show | 52 | HG00642.hp1 HG01069.hp1 HG01071.hp1 others(49): Show |
intron_variant | MODIFIER | c.129+6619C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174053503 | ||||||
chr5:174053822
|
C | A | 1 | a0001c0001t0001g0072 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.129+6938C>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174053822 | ||||||
chr5:174053904
|
A | G | 2 | a0001c0001t0001g0221a0001c0001t0001g0222 | 2 | HG01891.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.129+7020A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174053904 | ||||||
chr5:174054066
|
C | T | 2 | a0001c0001t0001g0164a0001c0001t0001g0165 | 2 | HG02683.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.129+7182C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174054066 | ||||||
chr5:174054145
|
C | T | 2 | a0001c0001t0002g0273a0001c0001t0024g0272 | 2 | HG02647.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.129+7261C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174054145 | ||||||
chr5:174054339
|
T | C | 51 | a0001c0001t0002g0003a0001c0001t0002g0031a0001c0001t0002g0032others(48): Show | 52 | HG00642.hp1 HG01069.hp1 HG01071.hp1 others(49): Show |
intron_variant | MODIFIER | c.129+7455T>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174054339 | ||||||
chr5:174054530
|
A | G | 1 | a0001c0001t0001g0060 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.129+7646A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174054530 | ||||||
chr5:174054535
|
A | G | 1 | a0001c0001t0003g0163 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.129+7651A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174054535 | ||||||
chr5:174054539
|
C | T | 2 | a0001c0001t0005g0033a0001c0001t0005g0259 | 2 | HG02886.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.129+7655C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174054539 | ||||||
chr5:174054710
|
A | G | 77 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0002g0003others(74): Show | 81 | HG00280.hp1 HG00642.hp1 HG01069.hp1 others(78): Show |
intron_variant | MODIFIER | c.129+7826A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174054710 | ||||||
chr5:174054936
|
T | C | 1 | a0001c0001t0001g0052 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.129+8052T>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174054936 | ||||||
chr5:174054978
|
A | G | 9 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0004g0002others(6): Show | 10 | HG01891.hp1 HG02145.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.129+8094A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174054978 | ||||||
chr5:174055057
|
C | G | 17 | a0001c0001t0001g0198a0001c0001t0001g0205a0001c0003t0003g0009others(14): Show | 18 | HG00408.hp2 HG00673.hp2 HG01358.hp1 others(15): Show |
intron_variant | MODIFIER | c.129+8173C>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174055057 | ||||||
chr5:174055081
|
G | A | 1 | a0001c0001t0004g0042 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.129+8197G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174055081 | ||||||
chr5:174055132
|
T | C | 71 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0002g0003others(68): Show | 75 | HG00280.hp1 HG00642.hp1 HG01069.hp1 others(72): Show |
intron_variant | MODIFIER | c.129+8248T>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174055132 | ||||||
chr5:174055265
|
C | T | 1 | a0001c0001t0005g0207 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.129+8381C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174055265 | ||||||
chr5:174055310
|
T | G | 1 | a0001c0002t0001g0061 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.129+8426T>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174055310 | ||||||
chr5:174055369
|
G | A | 4 | a0001c0001t0002g0229a0001c0001t0002g0236a0001c0001t0002g0237others(1): Show | 4 | HG01884.hp2 HG02965.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.129+8485G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174055369 | ||||||
chr5:174055409
|
C | G | 2 | a0001c0001t0003g0012a0001c0001t0003g0013 | 2 | HG01257.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.129+8525C>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174055409 | ||||||
chr5:174055411
|
G | C | 1 | a0001c0001t0005g0207 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.129+8527G>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174055411 | ||||||
chr5:174055429
|
TA | T | 77 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0002g0003others(74): Show | 81 | HG00280.hp1 HG00642.hp1 HG01069.hp1 others(78): Show |
intron_variant | MODIFIER | c.129+8555delA | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 174055429 | |||||
chr5:174055467
|
A | G | 46 | a0001c0001t0002g0229a0001c0001t0002g0230a0001c0001t0002g0231others(43): Show | 46 | HG00642.hp1 HG01069.hp1 HG01071.hp1 others(43): Show |
intron_variant | MODIFIER | c.129+8583A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174055467 | ||||||
chr5:174055490
|
C | T | 1 | a0001c0001t0004g0220 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.129+8606C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174055490 | ||||||
chr5:174055578
|
C | T | 49 | a0001c0001t0002g0003a0001c0001t0002g0031a0001c0001t0002g0032others(46): Show | 50 | HG00642.hp1 HG01069.hp1 HG01071.hp1 others(47): Show |
intron_variant | MODIFIER | c.130-8654C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174055578 | ||||||
chr5:174055651
|
G | A | 1 | a0001c0001t0017g0029 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.130-8581G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174055651 | ||||||
chr5:174055925
|
C | G | 51 | a0001c0001t0002g0003a0001c0001t0002g0031a0001c0001t0002g0032others(48): Show | 52 | HG00642.hp1 HG01069.hp1 HG01071.hp1 others(49): Show |
intron_variant | MODIFIER | c.130-8307C>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174055925 | ||||||
chr5:174056117
|
C | T | 3 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0162 | 3 | NA18952.hp1 NA18970.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.130-8115C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174056117 | ||||||
chr5:174056140
|
A | G | 51 | a0001c0001t0002g0003a0001c0001t0002g0031a0001c0001t0002g0032others(48): Show | 52 | HG00642.hp1 HG01069.hp1 HG01071.hp1 others(49): Show |
intron_variant | MODIFIER | c.130-8092A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174056140 | ||||||
chr5:174056171
|
A | T | 1 | a0001c0001t0017g0029 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.130-8061A>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174056171 | ||||||
chr5:174056256
|
CCTT | C | 49 | a0001c0001t0002g0003a0001c0001t0002g0031a0001c0001t0002g0032others(46): Show | 50 | HG00642.hp1 HG01069.hp1 HG01071.hp1 others(47): Show |
intron_variant | MODIFIER | c.130-7975_130-7973d others(5): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174056256 | ||||||
chr5:174056299
|
G | T | 1 | a0001c0001t0001g0159 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.130-7933G>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174056299 | ||||||
chr5:174056450
|
A | G | 1 | a0001c0001t0003g0007 | 2 | HG01069.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.130-7782A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174056450 | ||||||
chr5:174056468
|
G | A | 1 | a0001c0001t0004g0226 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.130-7764G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174056468 | ||||||
chr5:174056608
|
T | C | 56 | a0001c0001t0002g0003a0001c0001t0002g0031a0001c0001t0002g0032others(53): Show | 59 | HG00280.hp1 HG00642.hp1 HG01069.hp1 others(56): Show |
intron_variant | MODIFIER | c.130-7624T>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174056608 | ||||||
chr5:174056615
|
G | A | 1 | a0001c0001t0001g0073 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.130-7617G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174056615 | ||||||
chr5:174056678
|
T | C | 3 | a0001c0001t0004g0015a0001c0001t0004g0016a0001c0001t0004g0066 | 3 | HG02257.hp2 HG02895.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.130-7554T>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174056678 | ||||||
chr5:174056824
|
G | C | 56 | a0001c0001t0002g0003a0001c0001t0002g0031a0001c0001t0002g0032others(53): Show | 59 | HG00280.hp1 HG00642.hp1 HG01069.hp1 others(56): Show |
intron_variant | MODIFIER | c.130-7408G>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174056824 | ||||||
chr5:174056879
|
T | C | 1 | a0001c0001t0011g0024 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.130-7353T>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174056879 | ||||||
chr5:174056886
|
T | C | 51 | a0001c0001t0002g0003a0001c0001t0002g0031a0001c0001t0002g0032others(48): Show | 52 | HG00642.hp1 HG01069.hp1 HG01071.hp1 others(49): Show |
intron_variant | MODIFIER | c.130-7346T>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174056886 | ||||||
chr5:174057027
|
C | T | 2 | a0001c0001t0011g0024a0001c0001t0011g0025 | 2 | HG02451.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.130-7205C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174057027 | ||||||
chr5:174057163
|
G | C | 51 | a0001c0001t0002g0003a0001c0001t0002g0031a0001c0001t0002g0032others(48): Show | 52 | HG00642.hp1 HG01069.hp1 HG01071.hp1 others(49): Show |
intron_variant | MODIFIER | c.130-7069G>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174057163 | ||||||
chr5:174057417
|
A | G | 3 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0020g0172 | 3 | HG02895.hp2 HG02897.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.130-6815A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174057417 | ||||||
chr5:174057490
|
CTA | C | 51 | a0001c0001t0002g0003a0001c0001t0002g0031a0001c0001t0002g0032others(48): Show | 52 | HG00642.hp1 HG01069.hp1 HG01071.hp1 others(49): Show |
intron_variant | MODIFIER | c.130-6741_130-6740d others(4): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174057490 | ||||||
chr5:174057491
|
T | C | 2 | a0001c0001t0011g0024a0001c0001t0011g0025 | 2 | HG02451.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.130-6741T>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174057491 | ||||||
chr5:174057534
|
T | C | 51 | a0001c0001t0002g0003a0001c0001t0002g0031a0001c0001t0002g0032others(48): Show | 52 | HG00642.hp1 HG01069.hp1 HG01071.hp1 others(49): Show |
intron_variant | MODIFIER | c.130-6698T>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174057534 | ||||||
chr5:174057575
|
A | G | 1 | a0001c0001t0001g0158 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.130-6657A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174057575 | ||||||
chr5:174057695
|
C | T | 1 | a0001c0002t0001g0157 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.130-6537C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174057695 | ||||||
chr5:174057722
|
T | C | 2 | a0001c0001t0005g0033a0001c0001t0005g0259 | 2 | HG02886.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.130-6510T>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174057722 | ||||||
chr5:174057808
|
A | G | 1 | a0001c0001t0017g0029 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.130-6424A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174057808 | ||||||
chr5:174057823
|
G | A | 1 | a0001c0001t0004g0042 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.130-6409G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174057823 | ||||||
chr5:174057857
|
C | T | 6 | a0001c0001t0004g0042a0001c0001t0004g0044a0001c0001t0004g0045others(3): Show | 6 | HG02559.hp2 HG03130.hp2 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.130-6375C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174057857 | ||||||
chr5:174057858
|
C | T | 1 | a0001c0001t0001g0156 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.130-6374C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174057858 | ||||||
chr5:174058086
|
A | T | 2 | a0001c0001t0001g0221a0001c0001t0001g0222 | 2 | HG01891.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.130-6146A>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174058086 | ||||||
chr5:174058405
|
T | G | 1 | a0001c0001t0019g0223 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.130-5827T>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174058405 | ||||||
chr5:174058412
|
A | C | 56 | a0001c0001t0002g0003a0001c0001t0002g0031a0001c0001t0002g0032others(53): Show | 59 | HG00280.hp1 HG00642.hp1 HG01069.hp1 others(56): Show |
intron_variant | MODIFIER | c.130-5820A>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174058412 | ||||||
chr5:174058586
|
G | A | 1 | a0001c0001t0004g0282 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.130-5646G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174058586 | ||||||
chr5:174058646
|
G | A | 1 | a0001c0001t0001g0050 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.130-5586G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174058646 | ||||||
chr5:174058809
|
C | T | 1 | a0001c0001t0019g0223 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.130-5423C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174058809 | ||||||
chr5:174059116
|
C | T | 51 | a0001c0001t0002g0003a0001c0001t0002g0031a0001c0001t0002g0032others(48): Show | 52 | HG00642.hp1 HG01069.hp1 HG01071.hp1 others(49): Show |
intron_variant | MODIFIER | c.130-5116C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174059116 | ||||||
chr5:174059280
|
A | G | 2 | a0001c0001t0005g0033a0001c0001t0005g0259 | 2 | HG02886.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.130-4952A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174059280 | ||||||
chr5:174059466
|
G | A | 1 | a0001c0001t0003g0017 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.130-4766G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174059466 | ||||||
chr5:174059486
|
G | A | 6 | a0001c0001t0004g0042a0001c0001t0004g0044a0001c0001t0004g0045others(3): Show | 6 | HG02559.hp2 HG03130.hp2 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.130-4746G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174059486 | ||||||
chr5:174059562
|
G | C | 2 | a0001c0001t0005g0018a0001c0001t0005g0019 | 2 | HG02486.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.130-4670G>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174059562 | ||||||
chr5:174059636
|
C | T | 3 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0013g0068 | 3 | HG02809.hp2 HG03195.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.130-4596C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174059636 | ||||||
chr5:174059695
|
A | G | 2 | a0001c0001t0005g0018a0001c0001t0005g0019 | 2 | HG02486.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.130-4537A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174059695 | ||||||
chr5:174059697
|
G | C | 5 | a0001c0001t0003g0276a0001c0001t0004g0011a0001c0001t0008g0010others(2): Show | 7 | HG00280.hp1 HG01167.hp2 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.130-4535G>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174059697 | ||||||
chr5:174059896
|
C | T | 1 | a0001c0001t0001g0155 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.130-4336C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174059896 | ||||||
chr5:174060065
|
G | A | 3 | a0001c0001t0002g0003a0001c0001t0002g0031a0001c0001t0002g0032 | 4 | HG02055.hp2 HG02145.hp2 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.130-4167G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174060065 | ||||||
chr5:174060109
|
G | A | 15 | a0001c0001t0001g0001a0001c0001t0001g0038a0001c0001t0001g0039others(12): Show | 16 | HG00099.hp2 HG00621.hp2 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.130-4123G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174060109 | ||||||
chr5:174060266
|
G | A | 2 | a0001c0001t0017g0029a0001c0001t0019g0223 | 2 | HG02572.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.130-3966G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174060266 | ||||||
chr5:174060341
|
C | T | 1 | a0001c0001t0019g0223 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.130-3891C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174060341 | ||||||
chr5:174060373
|
AT | A | 9 | a0001c0001t0003g0276a0001c0001t0004g0011a0001c0001t0004g0225others(6): Show | 11 | HG00280.hp1 HG01167.hp2 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.130-3847delT | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 174060373 | |||||
chr5:174060526
|
G | A | 1 | a0001c0001t0001g0074 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.130-3706G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174060526 | ||||||
chr5:174060536
|
G | T | 17 | a0001c0001t0001g0198a0001c0001t0001g0205a0001c0003t0003g0009others(14): Show | 18 | HG00408.hp2 HG00673.hp2 HG01358.hp1 others(15): Show |
intron_variant | MODIFIER | c.130-3696G>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174060536 | ||||||
chr5:174060643
|
AC | A | 111 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0198others(108): Show | 117 | HG00280.hp1 HG00408.hp2 HG00642.hp1 others(114): Show |
intron_variant | MODIFIER | c.130-3587delC | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 174060643 | |||||
chr5:174060685
|
G | A | 1 | a0001c0001t0003g0012 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.130-3547G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174060685 | ||||||
chr5:174060768
|
G | C | 1 | a0001c0001t0019g0223 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.130-3464G>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174060768 | ||||||
chr5:174060779
|
T | A | 7 | a0001c0001t0003g0004a0001c0001t0003g0075a0001c0001t0003g0076others(4): Show | 8 | HG02055.hp1 HG02109.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.130-3453T>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174060779 | ||||||
chr5:174060891
|
C | T | 1 | a0001c0001t0001g0154 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.130-3341C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174060891 | ||||||
chr5:174061116
|
T | C | 1 | a0001c0001t0013g0068 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.130-3116T>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174061116 | ||||||
chr5:174061134
|
T | TAC | 49 | a0001c0001t0002g0003a0001c0001t0002g0031a0001c0001t0002g0032others(46): Show | 50 | HG00642.hp1 HG01069.hp1 HG01071.hp1 others(47): Show |
intron_variant | MODIFIER | c.130-3084_130-3083d others(4): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 174061134 | |||||
chr5:174061244
|
G | C | 1 | a0001c0001t0001g0081 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.130-2988G>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174061244 | ||||||
chr5:174061458
|
G | A | 1 | a0001c0001t0004g0042 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.130-2774G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174061458 | ||||||
chr5:174061628
|
A | G | 5 | a0001c0001t0003g0276a0001c0001t0004g0011a0001c0001t0008g0010others(2): Show | 7 | HG00280.hp1 HG01167.hp2 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.130-2604A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174061628 | ||||||
chr5:174061672
|
T | G | 4 | a0001c0001t0001g0014a0001c0001t0003g0007a0001c0001t0003g0017others(1): Show | 5 | HG00099.hp1 HG01069.hp2 HG01074.hp2 others(2): Show |
intron_variant | MODIFIER | c.130-2560T>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174061672 | ||||||
chr5:174061717
|
C | T | 2 | a0001c0001t0005g0033a0001c0001t0005g0259 | 2 | HG02886.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.130-2515C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174061717 | ||||||
chr5:174061816
|
G | T | 1 | a0001c0001t0002g0271 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.130-2416G>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174061816 | ||||||
chr5:174061883
|
G | A | 3 | a0001c0001t0003g0276a0001c0001t0004g0011a0001c0001t0018g0277 | 4 | HG01167.hp2 HG01169.hp1 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.130-2349G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174061883 | ||||||
chr5:174061897
|
C | T | 1 | a0001c0001t0002g0238 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.130-2335C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174061897 | ||||||
chr5:174061909
|
C | CT | 60 | a0001c0001t0001g0041a0001c0001t0001g0152a0001c0001t0001g0153others(57): Show | 62 | HG00639.hp1 HG00642.hp1 HG01069.hp1 others(59): Show |
intron_variant | MODIFIER | c.130-2301dupT | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 174061909 | |||||
chr5:174061909
|
C | CTT | 11 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0002g0257others(8): Show | 11 | HG01891.hp1 HG01952.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.130-2302_130-2301d others(4): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 174061909 | |||||
chr5:174061909
|
CT | C | 49 | a0001c0001t0001g0036a0001c0001t0001g0051a0001c0001t0001g0067others(46): Show | 51 | HG00323.hp2 HG01070.hp1 HG01070.hp2 others(48): Show |
intron_variant | MODIFIER | c.130-2301delT | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 174061909 | |||||
chr5:174062456
|
T | G | 56 | a0001c0001t0002g0003a0001c0001t0002g0031a0001c0001t0002g0032others(53): Show | 59 | HG00280.hp1 HG00642.hp1 HG01069.hp1 others(56): Show |
intron_variant | MODIFIER | c.130-1776T>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174062456 | ||||||
chr5:174062548
|
G | A | 281 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0020others(278): Show | 292 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.130-1684G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174062548 | ||||||
chr5:174062669
|
G | A | 2 | a0001c0001t0003g0276a0001c0001t0018g0277 | 2 | HG02698.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.130-1563G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174062669 | ||||||
chr5:174062673
|
T | TGG | 5 | a0001c0001t0003g0276a0001c0001t0004g0011a0001c0001t0008g0010others(2): Show | 7 | HG00280.hp1 HG01167.hp2 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.130-1556_130-1555d others(4): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 174062673 | |||||
chr5:174062762
|
C | T | 5 | a0001c0001t0003g0276a0001c0001t0004g0011a0001c0001t0008g0010others(2): Show | 7 | HG00280.hp1 HG01167.hp2 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.130-1470C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174062762 | ||||||
chr5:174062766
|
G | A | 49 | a0001c0001t0002g0003a0001c0001t0002g0031a0001c0001t0002g0032others(46): Show | 50 | HG00642.hp1 HG01069.hp1 HG01071.hp1 others(47): Show |
intron_variant | MODIFIER | c.130-1466G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174062766 | ||||||
chr5:174062779
|
C | G | 1 | a0001c0002t0001g0059 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.130-1453C>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174062779 | ||||||
chr5:174062898
|
C | T | 1 | a0001c0001t0002g0256 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.130-1334C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174062898 | ||||||
chr5:174062917
|
G | A | 1 | a0001c0001t0001g0166 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.130-1315G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174062917 | ||||||
chr5:174062923
|
T | A | 1 | a0001c0001t0019g0223 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.130-1309T>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174062923 | ||||||
chr5:174062946
|
G | A | 56 | a0001c0001t0002g0003a0001c0001t0002g0031a0001c0001t0002g0032others(53): Show | 59 | HG00280.hp1 HG00642.hp1 HG01069.hp1 others(56): Show |
intron_variant | MODIFIER | c.130-1286G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174062946 | ||||||
chr5:174062963
|
A | C | 1 | a0001c0001t0001g0072 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.130-1269A>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174062963 | ||||||
chr5:174062990
|
G | T | 1 | a0001c0001t0019g0223 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.130-1242G>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174062990 | ||||||
chr5:174063107
|
T | C | 1 | a0001c0001t0001g0082 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.130-1125T>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174063107 | ||||||
chr5:174063257
|
C | G | 1 | a0001c0001t0004g0228 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.130-975C>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174063257 | ||||||
chr5:174063446
|
C | T | 51 | a0001c0001t0002g0003a0001c0001t0002g0031a0001c0001t0002g0032others(48): Show | 52 | HG00642.hp1 HG01069.hp1 HG01071.hp1 others(49): Show |
intron_variant | MODIFIER | c.130-786C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174063446 | ||||||
chr5:174063517
|
C | T | 11 | a0001c0001t0001g0014a0001c0001t0003g0005a0001c0001t0003g0006others(8): Show | 14 | HG00099.hp1 HG00323.hp1 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.130-715C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174063517 | ||||||
chr5:174063521
|
C | CTATTT | 10 | a0001c0001t0001g0035a0001c0001t0001g0048a0001c0001t0001g0049others(7): Show | 10 | HG00621.hp2 HG01255.hp2 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.130-665_130-661dup others(5): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 174063521 | |||||
chr5:174063521
|
C | CTATTTTA others(3): Show |
1 | a0001c0001t0004g0227 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.130-670_130-661dup others(10): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 174063521 | |||||
chr5:174063521
|
CTATTT | C | 115 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(112): Show | 116 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.130-665_130-661del others(5): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 174063521 | |||||
chr5:174063521
|
CTATTTTA others(3): Show |
C | 24 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(21): Show | 26 | HG00408.hp2 HG01358.hp1 HG02040.hp1 others(23): Show |
intron_variant | MODIFIER | c.130-670_130-661del others(10): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 174063521 | |||||
chr5:174063521
|
CTATTTTA others(8): Show |
C | 6 | a0001c0001t0001g0083a0001c0001t0001g0278a0001c0001t0003g0075others(3): Show | 6 | HG01168.hp1 HG01169.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.130-675_130-661del others(15): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 174063521 | |||||
chr5:174063521
|
CTATTTTA others(13): Show |
C | 3 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0013g0068 | 3 | HG02809.hp2 HG03195.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.130-680_130-661del others(20): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 174063521 | |||||
chr5:174063543
|
ATTTTATT others(14): Show |
A | 49 | a0001c0001t0002g0003a0001c0001t0002g0031a0001c0001t0002g0032others(46): Show | 50 | HG00642.hp1 HG01069.hp1 HG01071.hp1 others(47): Show |
intron_variant | MODIFIER | c.130-685_130-665del others(21): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 174063543 | |||||
chr5:174063548
|
ATTTTATT others(9): Show |
A | 7 | a0001c0001t0003g0276a0001c0001t0004g0011a0001c0001t0005g0033others(4): Show | 9 | HG00280.hp1 HG01167.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.130-680_130-665del others(16): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 174063548 | |||||
chr5:174063573
|
T | C | 56 | a0001c0001t0002g0003a0001c0001t0002g0031a0001c0001t0002g0032others(53): Show | 59 | HG00280.hp1 HG00642.hp1 HG01069.hp1 others(56): Show |
intron_variant | MODIFIER | c.130-659T>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174063573 | ||||||
chr5:174063574
|
T | A | 56 | a0001c0001t0002g0003a0001c0001t0002g0031a0001c0001t0002g0032others(53): Show | 59 | HG00280.hp1 HG00642.hp1 HG01069.hp1 others(56): Show |
intron_variant | MODIFIER | c.130-658T>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174063574 | ||||||
chr5:174063577
|
C | T | 56 | a0001c0001t0002g0003a0001c0001t0002g0031a0001c0001t0002g0032others(53): Show | 59 | HG00280.hp1 HG00642.hp1 HG01069.hp1 others(56): Show |
intron_variant | MODIFIER | c.130-655C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174063577 | ||||||
chr5:174063578
|
A | T | 56 | a0001c0001t0002g0003a0001c0001t0002g0031a0001c0001t0002g0032others(53): Show | 59 | HG00280.hp1 HG00642.hp1 HG01069.hp1 others(56): Show |
intron_variant | MODIFIER | c.130-654A>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174063578 | ||||||
chr5:174063610
|
G | C | 2 | a0001c0001t0008g0010a0001c0001t0008g0275 | 3 | HG00280.hp1 HG03927.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.130-622G>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174063610 | ||||||
chr5:174063612
|
A | G | 1 | a0001c0001t0005g0207 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.130-620A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174063612 | ||||||
chr5:174063614
|
A | G | 1 | a0001c0001t0001g0128 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.130-618A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174063614 | ||||||
chr5:174064450
|
G | A | 1 | a0001c0001t0004g0219 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.213+135G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174064450 | ||||||
chr5:174064843
|
G | T | 7 | a0001c0001t0003g0004a0001c0001t0003g0075a0001c0001t0003g0076others(4): Show | 8 | HG02055.hp1 HG02109.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.213+528G>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174064843 | ||||||
chr5:174064927
|
A | G | 1 | a0001c0001t0006g0260 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.213+612A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174064927 | ||||||
chr5:174064935
|
T | G | 54 | a0001c0001t0002g0003a0001c0001t0002g0031a0001c0001t0002g0032others(51): Show | 57 | HG00280.hp1 HG00642.hp1 HG01069.hp1 others(54): Show |
intron_variant | MODIFIER | c.213+620T>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174064935 | ||||||
chr5:174064989
|
G | T | 1 | a0001c0001t0020g0172 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.213+674G>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174064989 | ||||||
chr5:174065124
|
C | T | 2 | a0001c0001t0008g0010a0001c0001t0008g0275 | 3 | HG00280.hp1 HG03927.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.213+809C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174065124 | ||||||
chr5:174065282
|
C | G | 1 | a0001c0001t0001g0165 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.213+967C>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174065282 | ||||||
chr5:174065308
|
A | T | 1 | a0001c0001t0001g0127 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.213+993A>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174065308 | ||||||
chr5:174065353
|
G | A | 1 | a0001c0001t0001g0189 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.213+1038G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174065353 | ||||||
chr5:174065382
|
A | C | 1 | a0001c0002t0001g0059 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.213+1067A>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174065382 | ||||||
chr5:174065555
|
A | G | 1 | a0001c0001t0005g0207 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.213+1240A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174065555 | ||||||
chr5:174065822
|
C | T | 4 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0048others(1): Show | 4 | HG00099.hp2 HG01099.hp2 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.213+1507C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174065822 | ||||||
chr5:174065920
|
C | T | 17 | a0001c0001t0001g0198a0001c0001t0001g0205a0001c0003t0003g0009others(14): Show | 18 | HG00408.hp2 HG00673.hp2 HG01358.hp1 others(15): Show |
intron_variant | MODIFIER | c.213+1605C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174065920 | ||||||
chr5:174066011
|
G | A | 5 | a0001c0001t0003g0276a0001c0001t0004g0011a0001c0001t0008g0010others(2): Show | 7 | HG00280.hp1 HG01167.hp2 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.213+1696G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174066011 | ||||||
chr5:174066334
|
C | T | 2 | a0001c0001t0001g0022a0001c0001t0001g0023 | 2 | HG03139.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.213+2019C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174066334 | ||||||
chr5:174066487
|
A | G | 6 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0138others(3): Show | 6 | HG01884.hp1 HG02280.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.213+2172A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174066487 | ||||||
chr5:174066497
|
A | G | 2 | a0001c0001t0005g0018a0001c0001t0005g0019 | 2 | HG02486.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.213+2182A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174066497 | ||||||
chr5:174066694
|
T | TA | 5 | a0001c0001t0001g0189a0001c0001t0001g0190a0001c0001t0001g0191others(2): Show | 6 | HG00280.hp1 HG02071.hp2 HG03927.hp1 others(3): Show |
intron_variant | MODIFIER | c.213+2388dupA | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174066694 | |||||
chr5:174066695
|
A | T | 7 | a0001c0001t0001g0174a0001c0001t0002g0003a0001c0001t0002g0031others(4): Show | 8 | HG01257.hp2 HG02055.hp2 HG02074.hp1 others(5): Show |
intron_variant | MODIFIER | c.213+2380A>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174066695 | ||||||
chr5:174066924
|
A | G | 1 | a0001c0001t0001g0058 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.213+2609A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174066924 | ||||||
chr5:174066938
|
C | T | 1 | a0001c0001t0009g0270 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.213+2623C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174066938 | ||||||
chr5:174066949
|
C | T | 46 | a0001c0001t0002g0229a0001c0001t0002g0230a0001c0001t0002g0231others(43): Show | 46 | HG00642.hp1 HG01069.hp1 HG01071.hp1 others(43): Show |
intron_variant | MODIFIER | c.213+2634C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174066949 | ||||||
chr5:174066984
|
T | C | 112 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0198others(109): Show | 118 | HG00280.hp1 HG00408.hp2 HG00642.hp1 others(115): Show |
intron_variant | MODIFIER | c.213+2669T>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174066984 | ||||||
chr5:174066989
|
C | CA | 97 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0035others(94): Show | 102 | HG00408.hp2 HG00642.hp1 HG00642.hp2 others(99): Show |
intron_variant | MODIFIER | c.213+2701dupA | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174066989 | |||||
chr5:174066989
|
C | CAA | 19 | a0001c0001t0001g0221a0001c0001t0002g0031a0001c0001t0002g0230others(16): Show | 19 | HG01109.hp2 HG01243.hp1 HG01358.hp1 others(16): Show |
intron_variant | MODIFIER | c.213+2700_213+2701d others(4): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174066989 | |||||
chr5:174066989
|
CA | C | 8 | a0001c0001t0001g0091a0001c0001t0001g0098a0001c0001t0001g0128others(5): Show | 8 | HG01123.hp2 HG02735.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.213+2701delA | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174066989 | |||||
chr5:174066989
|
CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0001g0278 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.213+2692_213+2701d others(12): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174066989 | |||||
chr5:174066989
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0001g0092 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.213+2691_213+2701d others(13): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174066989 | |||||
chr5:174066989
|
CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0001g0126 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.213+2690_213+2701d others(14): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174066989 | |||||
chr5:174067035
|
T | G | 2 | a0001c0001t0001g0022a0001c0001t0001g0023 | 2 | HG03139.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.213+2720T>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174067035 | ||||||
chr5:174067057
|
TAAAG | T | 3 | a0001c0001t0003g0276a0001c0001t0004g0011a0001c0001t0018g0277 | 4 | HG01167.hp2 HG01169.hp1 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.213+2744_213+2747d others(6): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174067057 | |||||
chr5:174067182
|
G | T | 1 | a0001c0001t0001g0192 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.213+2867G>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174067182 | ||||||
chr5:174067342
|
CCT | C | 51 | a0001c0001t0002g0003a0001c0001t0002g0031a0001c0001t0002g0032others(48): Show | 52 | HG00642.hp1 HG01069.hp1 HG01071.hp1 others(49): Show |
intron_variant | MODIFIER | c.213+3032_213+3033d others(4): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174067342 | |||||
chr5:174067461
|
G | A | 4 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0004g0219others(1): Show | 4 | HG01891.hp1 HG02145.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.213+3146G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174067461 | ||||||
chr5:174067463
|
G | A | 1 | a0001c0001t0011g0024 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.213+3148G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174067463 | ||||||
chr5:174067549
|
G | A | 2 | a0001c0001t0001g0020a0001c0001t0001g0021 | 2 | NA18943.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.213+3234G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174067549 | ||||||
chr5:174067810
|
G | A | 17 | a0001c0001t0001g0198a0001c0001t0001g0205a0001c0003t0003g0009others(14): Show | 18 | HG00408.hp2 HG00673.hp2 HG01358.hp1 others(15): Show |
intron_variant | MODIFIER | c.213+3495G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174067810 | ||||||
chr5:174067845
|
G | T | 1 | a0001c0001t0002g0031 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.213+3530G>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174067845 | ||||||
chr5:174067913
|
A | T | 2 | a0001c0001t0005g0018a0001c0001t0005g0019 | 2 | HG02486.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.213+3598A>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174067913 | ||||||
chr5:174067983
|
G | A | 1 | a0001c0001t0007g0178 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.213+3668G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174067983 | ||||||
chr5:174068132
|
A | C | 56 | a0001c0001t0002g0003a0001c0001t0002g0031a0001c0001t0002g0032others(53): Show | 59 | HG00280.hp1 HG00642.hp1 HG01069.hp1 others(56): Show |
intron_variant | MODIFIER | c.213+3817A>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174068132 | ||||||
chr5:174068242
|
A | G | 56 | a0001c0001t0002g0003a0001c0001t0002g0031a0001c0001t0002g0032others(53): Show | 59 | HG00280.hp1 HG00642.hp1 HG01069.hp1 others(56): Show |
intron_variant | MODIFIER | c.213+3927A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174068242 | ||||||
chr5:174068541
|
G | GATGTGGA others(13): Show |
56 | a0001c0001t0002g0003a0001c0001t0002g0031a0001c0001t0002g0032others(53): Show | 59 | HG00280.hp1 HG00642.hp1 HG01069.hp1 others(56): Show |
intron_variant | MODIFIER | c.213+4230_213+4231i others(22): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174068541 | |||||
chr5:174068600
|
T | C | 46 | a0001c0001t0002g0229a0001c0001t0002g0230a0001c0001t0002g0231others(43): Show | 46 | HG00642.hp1 HG01069.hp1 HG01071.hp1 others(43): Show |
intron_variant | MODIFIER | c.213+4285T>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174068600 | ||||||
chr5:174068676
|
TCTGGTGC others(46): Show |
T | 257 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0020others(254): Show | 268 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.213+4512_213+4564d others(55): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174068676 | |||||
chr5:174068708
|
AGGTGCTG others(52): Show |
A | 1 | a0001c0001t0001g0097 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.213+4398_213+4456d others(61): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174068708 | |||||
chr5:174068771
|
G | A | 3 | a0001c0001t0003g0276a0001c0001t0004g0011a0001c0001t0018g0277 | 4 | HG01167.hp2 HG01169.hp1 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.213+4456G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174068771 | ||||||
chr5:174068778
|
G | A | 4 | a0001c0003t0003g0009a0001c0003t0003g0194a0001c0003t0003g0199others(1): Show | 5 | HG03704.hp1 NA18952.hp2 NA18999.hp1 others(2): Show |
intron_variant | MODIFIER | c.213+4463G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174068778 | ||||||
chr5:174068827
|
ATGGGAAT others(46): Show |
A | 1 | a0001c0001t0013g0068 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.213+4565_213+4617d others(55): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174068827 | |||||
chr5:174068886
|
A | G | 2 | a0001c0001t0005g0033a0001c0001t0005g0259 | 2 | HG02886.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.213+4571A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174068886 | ||||||
chr5:174069114
|
G | A | 1 | a0001c0001t0017g0029 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.213+4799G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174069114 | ||||||
chr5:174069401
|
G | A | 1 | a0001c0001t0004g0224 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.213+5086G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174069401 | ||||||
chr5:174069472
|
C | T | 1 | a0001c0001t0019g0223 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.213+5157C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174069472 | ||||||
chr5:174069498
|
C | T | 1 | a0001c0001t0004g0042 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.213+5183C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174069498 | ||||||
chr5:174069507
|
A | G | 3 | a0001c0001t0003g0276a0001c0001t0004g0011a0001c0001t0018g0277 | 4 | HG01167.hp2 HG01169.hp1 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.213+5192A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174069507 | ||||||
chr5:174069564
|
A | G | 1 | a0001c0001t0001g0212 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.213+5249A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174069564 | ||||||
chr5:174069755
|
G | C | 1 | a0001c0001t0019g0223 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.213+5440G>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174069755 | ||||||
chr5:174069836
|
C | G | 2 | a0001c0001t0005g0033a0001c0001t0005g0259 | 2 | HG02886.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.213+5521C>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174069836 | ||||||
chr5:174069843
|
G | A | 3 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0013g0068 | 3 | HG02809.hp2 HG03195.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.213+5528G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174069843 | ||||||
chr5:174069874
|
A | AT | 60 | a0001c0001t0001g0023a0001c0001t0001g0124a0001c0001t0001g0135others(57): Show | 62 | HG01099.hp1 HG01109.hp2 HG01167.hp1 others(59): Show |
intron_variant | MODIFIER | c.213+5580dupT | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174069874 | |||||
chr5:174069874
|
A | ATT | 8 | a0001c0001t0002g0273a0001c0001t0003g0276a0001c0001t0004g0011others(5): Show | 9 | HG01167.hp2 HG01169.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.213+5579_213+5580d others(4): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174069874 | |||||
chr5:174069874
|
A | T | 1 | a0001c0001t0004g0282 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.213+5559A>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174069874 | ||||||
chr5:174069874
|
AT | A | 31 | a0001c0001t0001g0074a0001c0001t0001g0107a0001c0001t0001g0130others(28): Show | 32 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(29): Show |
intron_variant | MODIFIER | c.213+5580delT | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174069874 | |||||
chr5:174069897
|
A | C | 1 | a0001c0001t0019g0223 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.213+5582A>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174069897 | ||||||
chr5:174069996
|
G | A | 5 | a0001c0001t0001g0205a0001c0003t0003g0009a0001c0003t0003g0194others(2): Show | 6 | HG03704.hp1 NA18952.hp2 NA18999.hp1 others(3): Show |
intron_variant | MODIFIER | c.213+5681G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174069996 | ||||||
chr5:174070003
|
A | G | 56 | a0001c0001t0002g0003a0001c0001t0002g0031a0001c0001t0002g0032others(53): Show | 59 | HG00280.hp1 HG00642.hp1 HG01069.hp1 others(56): Show |
intron_variant | MODIFIER | c.213+5688A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174070003 | ||||||
chr5:174070039
|
G | A | 6 | a0001c0001t0004g0042a0001c0001t0004g0044a0001c0001t0004g0045others(3): Show | 6 | HG02559.hp2 HG03130.hp2 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.213+5724G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174070039 | ||||||
chr5:174070054
|
G | A | 2 | a0001c0001t0011g0024a0001c0001t0011g0025 | 2 | HG02451.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.213+5739G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174070054 | ||||||
chr5:174070140
|
G | A | 1 | a0001c0001t0004g0042 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.213+5825G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174070140 | ||||||
chr5:174070162
|
C | CA | 6 | a0001c0001t0002g0243a0001c0001t0002g0244a0001c0001t0002g0256others(3): Show | 6 | HG01261.hp1 HG01928.hp1 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.213+5848dupA | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174070162 | |||||
chr5:174070184
|
G | A | 4 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0004g0219others(1): Show | 4 | HG01891.hp1 HG02145.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.213+5869G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174070184 | ||||||
chr5:174070189
|
G | C | 49 | a0001c0001t0002g0003a0001c0001t0002g0031a0001c0001t0002g0032others(46): Show | 50 | HG00642.hp1 HG01069.hp1 HG01071.hp1 others(47): Show |
intron_variant | MODIFIER | c.213+5874G>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174070189 | ||||||
chr5:174070389
|
T | C | 51 | a0001c0001t0002g0003a0001c0001t0002g0031a0001c0001t0002g0032others(48): Show | 52 | HG00642.hp1 HG01069.hp1 HG01071.hp1 others(49): Show |
intron_variant | MODIFIER | c.213+6074T>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174070389 | ||||||
chr5:174070391
|
T | A | 9 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0004g0002others(6): Show | 10 | HG01891.hp1 HG02145.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.213+6076T>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174070391 | ||||||
chr5:174070570
|
T | C | 1 | a0001c0002t0001g0184 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.213+6255T>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174070570 | ||||||
chr5:174070653
|
A | G | 2 | a0001c0001t0004g0002a0001c0001t0004g0030 | 3 | HG02630.hp1 HG02717.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.213+6338A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174070653 | ||||||
chr5:174070793
|
C | T | 11 | a0001c0001t0001g0014a0001c0001t0003g0005a0001c0001t0003g0006others(8): Show | 14 | HG00099.hp1 HG00323.hp1 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.213+6478C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174070793 | ||||||
chr5:174070800
|
C | T | 2 | a0001c0001t0005g0033a0001c0001t0005g0259 | 2 | HG02886.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.213+6485C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174070800 | ||||||
chr5:174070889
|
G | A | 1 | a0001c0001t0001g0160 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.213+6574G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174070889 | ||||||
chr5:174070908
|
G | A | 5 | a0001c0001t0004g0044a0001c0001t0004g0045a0001c0001t0004g0046others(2): Show | 5 | HG02559.hp2 HG03471.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.213+6593G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174070908 | ||||||
chr5:174071003
|
G | A | 49 | a0001c0001t0002g0003a0001c0001t0002g0031a0001c0001t0002g0032others(46): Show | 50 | HG00642.hp1 HG01069.hp1 HG01071.hp1 others(47): Show |
intron_variant | MODIFIER | c.213+6688G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174071003 | ||||||
chr5:174071092
|
C | T | 1 | a0001c0001t0003g0017 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.213+6777C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174071092 | ||||||
chr5:174071119
|
A | C | 5 | a0001c0001t0003g0276a0001c0001t0004g0011a0001c0001t0008g0010others(2): Show | 7 | HG00280.hp1 HG01167.hp2 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.213+6804A>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174071119 | ||||||
chr5:174071283
|
C | T | 2 | a0001c0001t0001g0122a0001c0001t0001g0123 | 2 | HG00408.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.213+6968C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174071283 | ||||||
chr5:174071442
|
G | A | 1 | a0001c0001t0002g0246 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.213+7127G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174071442 | ||||||
chr5:174071619
|
G | A | 1 | a0001c0001t0006g0260 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.213+7304G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174071619 | ||||||
chr5:174071625
|
C | T | 3 | a0001c0001t0003g0276a0001c0001t0004g0011a0001c0001t0018g0277 | 4 | HG01167.hp2 HG01169.hp1 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.213+7310C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174071625 | ||||||
chr5:174071683
|
G | A | 4 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0001t0001g0279others(1): Show | 4 | HG01928.hp2 HG02074.hp1 HG02155.hp2 others(1): Show |
intron_variant | MODIFIER | c.213+7368G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174071683 | ||||||
chr5:174071683
|
G | C | 1 | a0001c0001t0004g0220 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.213+7368G>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174071683 | ||||||
chr5:174071691
|
G | T | 1 | a0001c0001t0003g0012 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.213+7376G>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174071691 | ||||||
chr5:174071944
|
G | T | 6 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0048others(3): Show | 6 | HG00099.hp2 HG01099.hp2 HG01168.hp2 others(3): Show |
intron_variant | MODIFIER | c.213+7629G>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174071944 | ||||||
chr5:174071996
|
G | A | 2 | a0001c0001t0008g0010a0001c0001t0008g0275 | 3 | HG00280.hp1 HG03927.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.213+7681G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174071996 | ||||||
chr5:174072022
|
A | G | 2 | a0001c0001t0003g0012a0001c0001t0003g0013 | 2 | HG01257.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.213+7707A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174072022 | ||||||
chr5:174072358
|
G | A | 1 | a0001c0001t0019g0223 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.213+8043G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174072358 | ||||||
chr5:174072431
|
A | G | 6 | a0001c0001t0002g0243a0001c0001t0002g0244a0001c0001t0002g0256others(3): Show | 6 | HG01261.hp1 HG01928.hp1 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.213+8116A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174072431 | ||||||
chr5:174072570
|
G | A | 2 | a0001c0001t0008g0010a0001c0001t0008g0275 | 3 | HG00280.hp1 HG03927.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.213+8255G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174072570 | ||||||
chr5:174072795
|
G | A | 1 | a0001c0001t0004g0220 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.213+8480G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174072795 | ||||||
chr5:174072882
|
G | C | 4 | a0001c0001t0004g0002a0001c0001t0004g0027a0001c0001t0004g0028others(1): Show | 5 | HG02630.hp1 HG02717.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.213+8567G>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174072882 | ||||||
chr5:174072933
|
C | T | 56 | a0001c0001t0002g0003a0001c0001t0002g0031a0001c0001t0002g0032others(53): Show | 59 | HG00280.hp1 HG00642.hp1 HG01069.hp1 others(56): Show |
intron_variant | MODIFIER | c.213+8618C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174072933 | ||||||
chr5:174072983
|
CAAAT | C | 3 | a0001c0001t0004g0225a0001c0001t0004g0226a0001c0001t0004g0227 | 3 | HG01433.hp1 HG03041.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.213+8669_213+8672d others(6): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174072983 | ||||||
chr5:174072984
|
A | AAATGAAT others(1): Show |
2 | a0001c0001t0008g0010a0001c0001t0008g0275 | 3 | HG00280.hp1 HG03927.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.213+8686_213+8693d others(10): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174072984 | |||||
chr5:174072987
|
T | G | 6 | a0001c0002t0001g0008a0001c0002t0001g0182a0001c0002t0001g0183others(3): Show | 7 | HG01934.hp1 HG01981.hp1 NA18943.hp1 others(4): Show |
intron_variant | MODIFIER | c.213+8672T>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174072987 | ||||||
chr5:174073043
|
G | A | 1 | a0001c0001t0001g0058 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.213+8728G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174073043 | ||||||
chr5:174073488
|
G | C | 1 | a0001c0001t0003g0012 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.213+9173G>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174073488 | ||||||
chr5:174073515
|
G | T | 46 | a0001c0001t0002g0229a0001c0001t0002g0230a0001c0001t0002g0231others(43): Show | 46 | HG00642.hp1 HG01069.hp1 HG01071.hp1 others(43): Show |
intron_variant | MODIFIER | c.213+9200G>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174073515 | ||||||
chr5:174073528
|
T | C | 3 | a0001c0001t0003g0276a0001c0001t0004g0011a0001c0001t0018g0277 | 4 | HG01167.hp2 HG01169.hp1 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.213+9213T>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174073528 | ||||||
chr5:174073703
|
T | C | 2 | a0001c0001t0008g0010a0001c0001t0008g0275 | 3 | HG00280.hp1 HG03927.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.213+9388T>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174073703 | ||||||
chr5:174073886
|
G | A | 1 | a0001c0001t0006g0247 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.213+9571G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174073886 | ||||||
chr5:174074046
|
C | T | 2 | a0001c0001t0004g0002a0001c0001t0004g0030 | 3 | HG02630.hp1 HG02717.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.213+9731C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174074046 | ||||||
chr5:174074124
|
C | T | 3 | a0001c0001t0003g0276a0001c0001t0004g0011a0001c0001t0018g0277 | 4 | HG01167.hp2 HG01169.hp1 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.213+9809C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174074124 | ||||||
chr5:174074309
|
G | A | 7 | a0001c0001t0001g0058a0001c0001t0004g0042a0001c0001t0004g0044others(4): Show | 7 | HG01496.hp1 HG02559.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.213+9994G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174074309 | ||||||
chr5:174074375
|
A | G | 2 | a0001c0001t0001g0096a0001c0001t0001g0098 | 2 | HG03239.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.213+10060A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174074375 | ||||||
chr5:174074538
|
A | T | 1 | a0001c0001t0003g0080 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.213+10223A>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174074538 | ||||||
chr5:174074587
|
A | C | 1 | a0001c0001t0001g0041 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.213+10272A>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174074587 | ||||||
chr5:174074640
|
G | A | 4 | a0001c0001t0004g0002a0001c0001t0004g0027a0001c0001t0004g0028others(1): Show | 5 | HG02630.hp1 HG02717.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.213+10325G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174074640 | ||||||
chr5:174074750
|
A | G | 17 | a0001c0001t0001g0198a0001c0001t0001g0205a0001c0003t0003g0009others(14): Show | 18 | HG00408.hp2 HG00673.hp2 HG01358.hp1 others(15): Show |
intron_variant | MODIFIER | c.213+10435A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174074750 | ||||||
chr5:174074863
|
G | T | 2 | a0001c0001t0011g0024a0001c0001t0011g0025 | 2 | HG02451.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.213+10548G>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174074863 | ||||||
chr5:174075281
|
C | G | 2 | a0001c0001t0008g0010a0001c0001t0008g0275 | 3 | HG00280.hp1 HG03927.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.213+10966C>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174075281 | ||||||
chr5:174075288
|
G | A | 2 | a0001c0001t0005g0033a0001c0001t0005g0259 | 2 | HG02886.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.213+10973G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174075288 | ||||||
chr5:174075307
|
C | G | 56 | a0001c0001t0002g0003a0001c0001t0002g0031a0001c0001t0002g0032others(53): Show | 59 | HG00280.hp1 HG00642.hp1 HG01069.hp1 others(56): Show |
intron_variant | MODIFIER | c.213+10992C>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174075307 | ||||||
chr5:174075428
|
C | T | 1 | a0001c0001t0013g0068 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.213+11113C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174075428 | ||||||
chr5:174075441
|
T | G | 1 | a0001c0001t0001g0218 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.213+11126T>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174075441 | ||||||
chr5:174075488
|
G | A | 2 | a0001c0001t0001g0034a0001c0001t0001g0035 | 2 | HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.213+11173G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174075488 | ||||||
chr5:174075508
|
G | A | 49 | a0001c0001t0002g0003a0001c0001t0002g0031a0001c0001t0002g0032others(46): Show | 50 | HG00642.hp1 HG01069.hp1 HG01071.hp1 others(47): Show |
intron_variant | MODIFIER | c.213+11193G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174075508 | ||||||
chr5:174075646
|
C | T | 1 | a0001c0002t0001g0185 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.213+11331C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174075646 | ||||||
chr5:174075749
|
T | C | 2 | a0001c0001t0002g0003a0001c0001t0002g0032 | 3 | HG02145.hp2 HG02257.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.213+11434T>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174075749 | ||||||
chr5:174076085
|
T | G | 9 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0004g0002others(6): Show | 10 | HG01891.hp1 HG02145.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.213+11770T>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174076085 | ||||||
chr5:174076153
|
C | T | 2 | a0001c0001t0008g0010a0001c0001t0008g0275 | 3 | HG00280.hp1 HG03927.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.213+11838C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174076153 | ||||||
chr5:174076233
|
C | G | 1 | a0001c0001t0001g0145 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.213+11918C>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174076233 | ||||||
chr5:174076285
|
A | G | 2 | a0001c0001t0008g0010a0001c0001t0008g0275 | 3 | HG00280.hp1 HG03927.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.213+11970A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174076285 | ||||||
chr5:174076314
|
AG | A | 2 | a0001c0001t0008g0010a0001c0001t0008g0275 | 3 | HG00280.hp1 HG03927.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.213+12001delG | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174076314 | |||||
chr5:174076336
|
AAAG | A | 51 | a0001c0001t0002g0003a0001c0001t0002g0031a0001c0001t0002g0032others(48): Show | 52 | HG00642.hp1 HG01069.hp1 HG01071.hp1 others(49): Show |
intron_variant | MODIFIER | c.213+12022_213+1202 others(7): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174076336 | ||||||
chr5:174076447
|
G | A | 1 | a0001c0001t0001g0038 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.213+12132G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174076447 | ||||||
chr5:174076735
|
G | C | 1 | a0001c0001t0003g0013 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.213+12420G>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174076735 | ||||||
chr5:174076915
|
C | A | 1 | a0001c0003t0003g0206 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.213+12600C>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174076915 | ||||||
chr5:174076932
|
G | A | 1 | a0001c0001t0005g0207 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.213+12617G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174076932 | ||||||
chr5:174076950
|
C | T | 1 | a0001c0001t0002g0246 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.213+12635C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174076950 | ||||||
chr5:174076995
|
T | C | 6 | a0001c0001t0001g0050a0001c0001t0001g0095a0001c0001t0001g0097others(3): Show | 6 | HG02015.hp2 NA18951.hp2 NA18961.hp1 others(3): Show |
intron_variant | MODIFIER | c.213+12680T>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174076995 | ||||||
chr5:174077014
|
A | G | 1 | a0001c0001t0001g0221 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.213+12699A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174077014 | ||||||
chr5:174077125
|
C | T | 3 | a0001c0001t0003g0276a0001c0001t0004g0011a0001c0001t0018g0277 | 4 | HG01167.hp2 HG01169.hp1 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.213+12810C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174077125 | ||||||
chr5:174077519
|
C | T | 231 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(228): Show | 238 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(235): Show |
intron_variant | MODIFIER | c.213+13204C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174077519 | ||||||
chr5:174077713
|
T | C | 46 | a0001c0001t0002g0229a0001c0001t0002g0230a0001c0001t0002g0231others(43): Show | 46 | HG00642.hp1 HG01069.hp1 HG01071.hp1 others(43): Show |
intron_variant | MODIFIER | c.213+13398T>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174077713 | ||||||
chr5:174077747
|
G | GT | 3 | a0001c0001t0004g0015a0001c0001t0004g0016a0001c0001t0004g0066 | 3 | HG02257.hp2 HG02895.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.213+13437dupT | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174077747 | |||||
chr5:174077906
|
T | C | 56 | a0001c0001t0002g0003a0001c0001t0002g0031a0001c0001t0002g0032others(53): Show | 59 | HG00280.hp1 HG00642.hp1 HG01069.hp1 others(56): Show |
intron_variant | MODIFIER | c.213+13591T>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174077906 | ||||||
chr5:174078093
|
C | T | 1 | a0001c0001t0001g0070 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.213+13778C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174078093 | ||||||
chr5:174078247
|
G | A | 9 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0004g0002others(6): Show | 10 | HG01891.hp1 HG02145.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.213+13932G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174078247 | ||||||
chr5:174078276
|
CCA | C | 3 | a0001c0001t0003g0276a0001c0001t0004g0011a0001c0001t0018g0277 | 4 | HG01167.hp2 HG01169.hp1 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.213+13978_213+1397 others(6): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174078276 | |||||
chr5:174078289
|
C | T | 1 | a0001c0003t0003g0209 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.213+13974C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174078289 | ||||||
chr5:174078453
|
G | A | 43 | a0001c0001t0002g0229a0001c0001t0002g0230a0001c0001t0002g0231others(40): Show | 43 | HG00642.hp1 HG01069.hp1 HG01071.hp1 others(40): Show |
intron_variant | MODIFIER | c.213+14138G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174078453 | ||||||
chr5:174078964
|
C | T | 3 | a0001c0001t0003g0276a0001c0001t0004g0011a0001c0001t0018g0277 | 4 | HG01167.hp2 HG01169.hp1 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.213+14649C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174078964 | ||||||
chr5:174079019
|
A | G | 4 | a0001c0001t0004g0225a0001c0001t0004g0226a0001c0001t0004g0227others(1): Show | 4 | HG01433.hp1 HG02735.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.213+14704A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174079019 | ||||||
chr5:174079029
|
C | A | 3 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0013g0068 | 3 | HG02809.hp2 HG03195.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.213+14714C>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174079029 | ||||||
chr5:174079029
|
C | T | 1 | a0001c0001t0001g0127 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.213+14714C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174079029 | ||||||
chr5:174079107
|
C | G | 2 | a0001c0003t0003g0009a0001c0003t0003g0194 | 3 | NA18999.hp1 NA19082.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.213+14792C>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174079107 | ||||||
chr5:174079132
|
C | T | 7 | a0001c0001t0003g0004a0001c0001t0003g0075a0001c0001t0003g0076others(4): Show | 8 | HG02055.hp1 HG02109.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.213+14817C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174079132 | ||||||
chr5:174079247
|
T | TTC | 47 | a0001c0001t0002g0003a0001c0001t0002g0031a0001c0001t0002g0032others(44): Show | 48 | HG00642.hp1 HG01069.hp1 HG01071.hp1 others(45): Show |
intron_variant | MODIFIER | c.213+14948_213+1494 others(6): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174079247 | |||||
chr5:174079247
|
TTCTC | T | 16 | a0001c0001t0001g0198a0001c0001t0001g0205a0001c0003t0003g0009others(13): Show | 17 | HG00408.hp2 HG00673.hp2 HG01358.hp1 others(14): Show |
intron_variant | MODIFIER | c.213+14946_213+1494 others(8): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174079247 | |||||
chr5:174079257
|
C | G | 9 | a0001c0001t0003g0004a0001c0001t0003g0075a0001c0001t0003g0076others(6): Show | 11 | HG00280.hp1 HG02055.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.213+14942C>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174079257 | ||||||
chr5:174079263
|
C | CT | 12 | a0001c0001t0003g0004a0001c0001t0003g0075a0001c0001t0003g0076others(9): Show | 15 | HG00280.hp1 HG01167.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.213+14961dupT | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174079263 | |||||
chr5:174079263
|
C | CTT | 11 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0004g0002others(8): Show | 12 | HG01891.hp1 HG02145.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.213+14960_213+1496 others(6): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174079263 | |||||
chr5:174079269
|
T | A | 2 | a0001c0001t0001g0070a0001c0001t0013g0068 | 2 | HG03195.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.213+14954T>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174079269 | ||||||
chr5:174079331
|
C | G | 2 | a0001c0001t0004g0027a0001c0001t0004g0028 | 2 | HG03041.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.213+15016C>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174079331 | ||||||
chr5:174079360
|
C | T | 17 | a0001c0001t0001g0198a0001c0001t0001g0205a0001c0003t0003g0009others(14): Show | 18 | HG00408.hp2 HG00673.hp2 HG01358.hp1 others(15): Show |
intron_variant | MODIFIER | c.213+15045C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174079360 | ||||||
chr5:174079547
|
T | C | 1 | a0001c0001t0001g0152 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.213+15232T>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174079547 | ||||||
chr5:174079607
|
G | A | 2 | a0001c0001t0005g0033a0001c0001t0005g0259 | 2 | HG02886.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.213+15292G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174079607 | ||||||
chr5:174079658
|
A | C | 7 | a0001c0001t0003g0004a0001c0001t0003g0075a0001c0001t0003g0076others(4): Show | 8 | HG02055.hp1 HG02109.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.213+15343A>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174079658 | ||||||
chr5:174079769
|
G | A | 48 | a0001c0001t0002g0003a0001c0001t0002g0031a0001c0001t0002g0032others(45): Show | 49 | HG00642.hp1 HG01069.hp1 HG01071.hp1 others(46): Show |
intron_variant | MODIFIER | c.213+15454G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174079769 | ||||||
chr5:174079849
|
G | A | 1 | a0001c0001t0001g0161 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.213+15534G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174079849 | ||||||
chr5:174079857
|
T | C | 48 | a0001c0001t0002g0003a0001c0001t0002g0031a0001c0001t0002g0032others(45): Show | 49 | HG00642.hp1 HG01069.hp1 HG01071.hp1 others(46): Show |
intron_variant | MODIFIER | c.213+15542T>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174079857 | ||||||
chr5:174080047
|
T | C | 1 | a0001c0001t0001g0192 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.213+15732T>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174080047 | ||||||
chr5:174080077
|
A | G | 9 | a0001c0001t0003g0004a0001c0001t0003g0075a0001c0001t0003g0076others(6): Show | 11 | HG00280.hp1 HG02055.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.213+15762A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174080077 | ||||||
chr5:174080214
|
A | G | 2 | a0001c0001t0008g0010a0001c0001t0008g0275 | 3 | HG00280.hp1 HG03927.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.213+15899A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174080214 | ||||||
chr5:174080258
|
C | T | 1 | a0001c0001t0001g0049 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.213+15943C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174080258 | ||||||
chr5:174080449
|
G | C | 1 | a0001c0002t0001g0188 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.213+16134G>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174080449 | ||||||
chr5:174080467
|
T | TTTTCTTT others(9): Show |
29 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0221others(26): Show | 30 | HG01167.hp1 HG01257.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.213+16197_213+1621 others(20): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174080467 | |||||
chr5:174080467
|
T | TTTTCTTT others(25): Show |
1 | a0001c0001t0019g0223 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.213+16181_213+1621 others(36): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174080467 | |||||
chr5:174080501
|
TTCTTTCT others(5): Show |
T | 2 | a0001c0001t0001g0215a0001c0001t0004g0011 | 3 | HG01167.hp2 HG01169.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.213+16197_213+1620 others(16): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174080501 | |||||
chr5:174080511
|
CCCTCTTT others(7): Show |
C | 1 | a0001c0001t0001g0121 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.213+16197_213+1621 others(18): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174080511 | ||||||
chr5:174080513
|
CTCTT | C | 14 | a0001c0001t0001g0001a0001c0001t0001g0038a0001c0001t0001g0039others(11): Show | 15 | HG00099.hp2 HG00738.hp2 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.213+16210_213+1621 others(8): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174080513 | |||||
chr5:174080517
|
T | TTCTTTCT others(5): Show |
17 | a0001c0001t0001g0198a0001c0001t0001g0205a0001c0003t0003g0009others(14): Show | 18 | HG00408.hp2 HG00673.hp2 HG01358.hp1 others(15): Show |
intron_variant | MODIFIER | c.213+16212_213+1621 others(16): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174080517 | |||||
chr5:174080521
|
T | C | 2 | a0001c0001t0003g0276a0001c0001t0018g0277 | 2 | HG02698.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.213+16206T>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174080521 | ||||||
chr5:174080525
|
T | C | 3 | a0001c0001t0001g0215a0001c0001t0003g0276a0001c0001t0018g0277 | 3 | HG02083.hp1 HG02698.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.213+16210T>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174080525 | ||||||
chr5:174080525
|
T | TTC | 46 | a0001c0001t0001g0051a0001c0001t0001g0067a0001c0001t0001g0072others(43): Show | 47 | HG00323.hp2 HG00621.hp1 HG01070.hp1 others(44): Show |
intron_variant | MODIFIER | c.213+16234_213+1623 others(6): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174080525 | |||||
chr5:174080525
|
T | TTCCCTCT others(11): Show |
7 | a0001c0001t0003g0004a0001c0001t0003g0075a0001c0001t0003g0076others(4): Show | 8 | HG02055.hp1 HG02109.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.213+16212_213+1621 others(22): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174080525 | |||||
chr5:174080525
|
T | TTCTTTCT others(31): Show |
2 | a0001c0001t0008g0010a0001c0001t0008g0275 | 3 | HG00280.hp1 HG03927.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.213+16213_213+1621 others(42): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174080525 | |||||
chr5:174080525
|
T | TTCTTTCT others(29): Show |
1 | a0001c0001t0002g0231 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.213+16213_213+1621 others(40): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174080525 | |||||
chr5:174080525
|
T | TTCTTTCT others(23): Show |
5 | a0001c0001t0002g0229a0001c0001t0002g0236a0001c0001t0002g0237others(2): Show | 5 | HG01884.hp2 HG02897.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.213+16213_213+1621 others(34): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174080525 | |||||
chr5:174080525
|
T | TTCTTTCT others(27): Show |
25 | a0001c0001t0002g0230a0001c0001t0002g0232a0001c0001t0002g0233others(22): Show | 25 | HG01069.hp1 HG01071.hp1 HG01099.hp1 others(22): Show |
intron_variant | MODIFIER | c.213+16213_213+1621 others(38): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174080525 | |||||
chr5:174080525
|
T | TTCTTTCT others(29): Show |
1 | a0001c0001t0002g0258 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.213+16213_213+1621 others(40): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174080525 | |||||
chr5:174080525
|
T | TTCTTTCT others(31): Show |
8 | a0001c0001t0002g0243a0001c0001t0002g0244a0001c0001t0002g0249others(5): Show | 8 | HG01261.hp1 HG01928.hp1 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.213+16213_213+1621 others(42): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174080525 | |||||
chr5:174080525
|
T | TTCTTTCT others(33): Show |
3 | a0001c0001t0002g0242a0001c0001t0002g0248a0001c0001t0006g0247 | 3 | HG02683.hp2 HG03834.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.213+16213_213+1621 others(44): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174080525 | |||||
chr5:174080525
|
TTCTC | T | 13 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0074others(10): Show | 13 | HG00280.hp2 HG00408.hp1 HG01255.hp2 others(10): Show |
intron_variant | MODIFIER | c.213+16232_213+1623 others(8): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174080525 | |||||
chr5:174080527
|
C | CTT | 3 | a0001c0001t0002g0003a0001c0001t0002g0031a0001c0001t0002g0032 | 4 | HG02055.hp2 HG02145.hp2 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.213+16213_213+1621 others(6): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174080527 | |||||
chr5:174080529
|
C | T | 28 | a0001c0001t0001g0198a0001c0001t0001g0205a0001c0001t0001g0221others(25): Show | 30 | HG00408.hp2 HG00673.hp2 HG01358.hp1 others(27): Show |
intron_variant | MODIFIER | c.213+16214C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174080529 | ||||||
chr5:174080551
|
T | C | 2 | a0001c0001t0001g0215a0001c0001t0004g0011 | 3 | HG01167.hp2 HG01169.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.213+16236T>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174080551 | ||||||
chr5:174080554
|
T | TCTCTCTC others(18): Show |
2 | a0001c0001t0002g0003a0001c0001t0002g0032 | 3 | HG02145.hp2 HG02257.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.213+16239_213+1624 others(29): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174080554 | ||||||
chr5:174080554
|
T | TCTCTCTC others(20): Show |
1 | a0001c0001t0002g0031 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.213+16239_213+1624 others(31): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174080554 | ||||||
chr5:174080556
|
T | C | 4 | a0001c0001t0002g0003a0001c0001t0002g0031a0001c0001t0002g0032others(1): Show | 6 | HG01167.hp2 HG01169.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.213+16241T>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174080556 | ||||||
chr5:174080567
|
CTTTCTTT others(3): Show |
C | 2 | a0001c0001t0003g0276a0001c0001t0018g0277 | 2 | HG02698.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.213+16255_213+1626 others(14): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174080567 | |||||
chr5:174080674
|
G | T | 1 | a0001c0001t0004g0224 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.213+16359G>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174080674 | ||||||
chr5:174080766
|
T | C | 4 | a0001c0001t0004g0225a0001c0001t0004g0226a0001c0001t0004g0227others(1): Show | 4 | HG01433.hp1 HG02735.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.213+16451T>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174080766 | ||||||
chr5:174080805
|
C | T | 7 | a0001c0001t0003g0004a0001c0001t0003g0075a0001c0001t0003g0076others(4): Show | 8 | HG02055.hp1 HG02109.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.213+16490C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174080805 | ||||||
chr5:174080809
|
C | T | 1 | a0001c0001t0004g0042 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.213+16494C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174080809 | ||||||
chr5:174080917
|
A | T | 5 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0009g0268others(2): Show | 5 | HG01167.hp1 HG01257.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.213+16602A>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174080917 | ||||||
chr5:174081388
|
A | G | 2 | a0001c0001t0005g0033a0001c0001t0005g0259 | 2 | HG02886.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.213+17073A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174081388 | ||||||
chr5:174081494
|
C | T | 1 | a0001c0001t0001g0055 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.213+17179C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174081494 | ||||||
chr5:174081523
|
G | A | 2 | a0001c0001t0005g0033a0001c0001t0005g0259 | 2 | HG02886.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.213+17208G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174081523 | ||||||
chr5:174081637
|
G | A | 53 | a0001c0001t0002g0003a0001c0001t0002g0031a0001c0001t0002g0032others(50): Show | 56 | HG00280.hp1 HG00642.hp1 HG01069.hp1 others(53): Show |
intron_variant | MODIFIER | c.213+17322G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174081637 | ||||||
chr5:174081641
|
A | AT | 7 | a0001c0001t0003g0004a0001c0001t0003g0075a0001c0001t0003g0076others(4): Show | 8 | HG02055.hp1 HG02109.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.213+17333dupT | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174081641 | |||||
chr5:174081648
|
T | A | 1 | a0001c0001t0001g0100 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.213+17333T>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174081648 | ||||||
chr5:174081677
|
T | G | 1 | a0001c0001t0001g0137 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.213+17362T>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174081677 | ||||||
chr5:174081882
|
C | T | 3 | a0001c0001t0002g0241a0001c0001t0006g0255a0001c0001t0017g0029 | 3 | HG01243.hp1 HG02572.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.213+17567C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174081882 | ||||||
chr5:174081887
|
C | CA | 8 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0048others(5): Show | 8 | HG00099.hp2 HG01099.hp2 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.213+17593dupA | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174081887 | |||||
chr5:174081887
|
CA | C | 65 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0120others(62): Show | 69 | HG00280.hp1 HG00408.hp2 HG00673.hp2 others(66): Show |
intron_variant | MODIFIER | c.213+17593delA | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174081887 | |||||
chr5:174081887
|
CAA | C | 45 | a0001c0001t0002g0003a0001c0001t0002g0031a0001c0001t0002g0229others(42): Show | 46 | HG00642.hp1 HG01071.hp1 HG01099.hp1 others(43): Show |
intron_variant | MODIFIER | c.213+17592_213+1759 others(6): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174081887 | |||||
chr5:174081907
|
A | G | 3 | a0001c0001t0003g0276a0001c0001t0004g0011a0001c0001t0018g0277 | 4 | HG01167.hp2 HG01169.hp1 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.213+17592A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174081907 | ||||||
chr5:174082099
|
C | G | 3 | a0001c0001t0003g0276a0001c0001t0004g0011a0001c0001t0018g0277 | 4 | HG01167.hp2 HG01169.hp1 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.213+17784C>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174082099 | ||||||
chr5:174082365
|
A | G | 1 | a0001c0001t0003g0012 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.213+18050A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174082365 | ||||||
chr5:174082539
|
G | A | 4 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0101others(1): Show | 4 | HG01192.hp2 HG01243.hp2 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.213+18224G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174082539 | ||||||
chr5:174082565
|
G | A | 1 | a0001c0001t0002g0264 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.213+18250G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174082565 | ||||||
chr5:174082585
|
C | T | 1 | a0001c0001t0001g0123 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.213+18270C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174082585 | ||||||
chr5:174082874
|
C | T | 2 | a0001c0001t0004g0002a0001c0001t0004g0030 | 3 | HG02630.hp1 HG02717.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.213+18559C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174082874 | ||||||
chr5:174082918
|
C | T | 2 | a0001c0001t0005g0033a0001c0001t0005g0259 | 2 | HG02886.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.213+18603C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174082918 | ||||||
chr5:174082928
|
G | A | 9 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0004g0002others(6): Show | 10 | HG01891.hp1 HG02145.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.213+18613G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174082928 | ||||||
chr5:174082936
|
C | A | 55 | a0001c0001t0002g0003a0001c0001t0002g0031a0001c0001t0002g0032others(52): Show | 58 | HG00280.hp1 HG00642.hp1 HG01069.hp1 others(55): Show |
intron_variant | MODIFIER | c.213+18621C>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174082936 | ||||||
chr5:174083018
|
A | G | 2 | a0001c0001t0004g0002a0001c0001t0004g0030 | 3 | HG02630.hp1 HG02717.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.213+18703A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174083018 | ||||||
chr5:174083231
|
C | G | 2 | a0001c0001t0001g0173a0001c0001t0001g0174 | 2 | HG02074.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.213+18916C>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174083231 | ||||||
chr5:174083266
|
A | G | 111 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0198others(108): Show | 117 | HG00280.hp1 HG00408.hp2 HG00642.hp1 others(114): Show |
intron_variant | MODIFIER | c.213+18951A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174083266 | ||||||
chr5:174083542
|
A | G | 53 | a0001c0001t0002g0003a0001c0001t0002g0031a0001c0001t0002g0032others(50): Show | 56 | HG00280.hp1 HG00642.hp1 HG01069.hp1 others(53): Show |
intron_variant | MODIFIER | c.213+19227A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174083542 | ||||||
chr5:174083774
|
T | C | 3 | a0001c0001t0003g0276a0001c0001t0004g0011a0001c0001t0018g0277 | 4 | HG01167.hp2 HG01169.hp1 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.213+19459T>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174083774 | ||||||
chr5:174083807
|
G | A | 6 | a0001c0001t0001g0205a0001c0001t0022g0094a0001c0003t0003g0009others(3): Show | 7 | HG03704.hp1 NA18952.hp2 NA18964.hp2 others(4): Show |
intron_variant | MODIFIER | c.213+19492G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174083807 | ||||||
chr5:174083832
|
G | C | 3 | a0001c0001t0003g0276a0001c0001t0004g0011a0001c0001t0018g0277 | 4 | HG01167.hp2 HG01169.hp1 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.213+19517G>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174083832 | ||||||
chr5:174083834
|
C | T | 4 | a0001c0001t0003g0013a0001c0001t0009g0268a0001c0001t0009g0269others(1): Show | 4 | HG01167.hp1 HG01257.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.213+19519C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174083834 | ||||||
chr5:174083954
|
G | A | 1 | a0001c0001t0001g0107 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.213+19639G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174083954 | ||||||
chr5:174083963
|
G | A | 1 | a0001c0001t0019g0223 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.213+19648G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174083963 | ||||||
chr5:174084000
|
A | C | 1 | a0001c0001t0002g0250 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.213+19685A>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174084000 | ||||||
chr5:174084009
|
G | A | 17 | a0001c0002t0001g0008a0001c0002t0001g0061a0001c0002t0001g0062others(14): Show | 18 | HG01070.hp1 HG01071.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.213+19694G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174084009 | ||||||
chr5:174084093
|
A | C | 53 | a0001c0001t0002g0003a0001c0001t0002g0031a0001c0001t0002g0032others(50): Show | 56 | HG00280.hp1 HG00642.hp1 HG01069.hp1 others(53): Show |
intron_variant | MODIFIER | c.213+19778A>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174084093 | ||||||
chr5:174084454
|
G | A | 6 | a0001c0001t0001g0050a0001c0001t0001g0095a0001c0001t0001g0097others(3): Show | 6 | HG02015.hp2 NA18951.hp2 NA18961.hp1 others(3): Show |
intron_variant | MODIFIER | c.214-19774G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174084454 | ||||||
chr5:174084518
|
G | T | 1 | a0001c0001t0001g0092 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.214-19710G>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174084518 | ||||||
chr5:174084736
|
G | C | 10 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0004g0002others(7): Show | 11 | HG01891.hp1 HG02145.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.214-19492G>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174084736 | ||||||
chr5:174084742
|
G | A | 1 | a0001c0001t0002g0261 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.214-19486G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174084742 | ||||||
chr5:174084816
|
A | G | 1 | a0001c0001t0001g0143 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.214-19412A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174084816 | ||||||
chr5:174085021
|
G | C | 1 | a0001c0001t0017g0029 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.214-19207G>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174085021 | ||||||
chr5:174085313
|
G | A | 1 | a0001c0001t0004g0042 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.214-18915G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174085313 | ||||||
chr5:174085388
|
C | G | 46 | a0001c0001t0002g0003a0001c0001t0002g0031a0001c0001t0002g0032others(43): Show | 47 | HG00642.hp1 HG01069.hp1 HG01071.hp1 others(44): Show |
intron_variant | MODIFIER | c.214-18840C>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174085388 | ||||||
chr5:174085431
|
C | T | 15 | a0001c0001t0001g0001a0001c0001t0001g0038a0001c0001t0001g0039others(12): Show | 16 | HG00099.hp2 HG00621.hp2 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.214-18797C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174085431 | ||||||
chr5:174085432
|
A | G | 3 | a0001c0001t0001g0130a0001c0001t0001g0216a0001c0001t0010g0142 | 3 | NA18953.hp2 NA19058.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.214-18796A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174085432 | ||||||
chr5:174085728
|
C | T | 8 | a0001c0001t0004g0042a0001c0001t0004g0044a0001c0001t0004g0045others(5): Show | 8 | HG02451.hp2 HG02559.hp2 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.214-18500C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174085728 | ||||||
chr5:174085915
|
T | C | 1 | a0001c0001t0001g0074 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.214-18313T>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174085915 | ||||||
chr5:174086068
|
G | T | 1 | a0001c0001t0001g0144 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.214-18160G>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174086068 | ||||||
chr5:174086078
|
C | T | 1 | a0001c0001t0004g0224 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.214-18150C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174086078 | ||||||
chr5:174086157
|
A | C | 1 | a0001c0001t0001g0145 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.214-18071A>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174086157 | ||||||
chr5:174086186
|
A | C | 1 | a0001c0001t0001g0088 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.214-18042A>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174086186 | ||||||
chr5:174086235
|
C | T | 1 | a0001c0001t0001g0099 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.214-17993C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174086235 | ||||||
chr5:174086393
|
T | C | 1 | a0001c0001t0001g0190 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.214-17835T>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174086393 | ||||||
chr5:174086514
|
G | A | 5 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0009g0268others(2): Show | 5 | HG01167.hp1 HG01257.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.214-17714G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174086514 | ||||||
chr5:174086528
|
A | G | 1 | a0001c0001t0001g0127 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.214-17700A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174086528 | ||||||
chr5:174086718
|
C | T | 11 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0004g0002others(8): Show | 12 | HG01891.hp1 HG02145.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.214-17510C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174086718 | ||||||
chr5:174087000
|
C | T | 7 | a0001c0001t0003g0004a0001c0001t0003g0075a0001c0001t0003g0076others(4): Show | 8 | HG02055.hp1 HG02109.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.214-17228C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174087000 | ||||||
chr5:174087070
|
T | C | 11 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0004g0002others(8): Show | 12 | HG01891.hp1 HG02145.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.214-17158T>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174087070 | ||||||
chr5:174087237
|
G | T | 7 | a0001c0001t0003g0004a0001c0001t0003g0075a0001c0001t0003g0076others(4): Show | 8 | HG02055.hp1 HG02109.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.214-16991G>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174087237 | ||||||
chr5:174087518
|
G | T | 3 | a0001c0001t0001g0132a0001c0001t0001g0159a0001c0001t0001g0217 | 3 | NA18966.hp2 NA19060.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.214-16710G>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174087518 | ||||||
chr5:174087704
|
C | A | 7 | a0001c0001t0003g0004a0001c0001t0003g0075a0001c0001t0003g0076others(4): Show | 8 | HG02055.hp1 HG02109.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.214-16524C>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174087704 | ||||||
chr5:174087787
|
CA | C | 9 | a0001c0001t0001g0109a0001c0001t0001g0127a0001c0001t0003g0276others(6): Show | 10 | HG01167.hp2 HG01169.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.214-16427delA | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174087787 | |||||
chr5:174087856
|
A | G | 2 | a0001c0001t0005g0033a0001c0001t0005g0259 | 2 | HG02886.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.214-16372A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174087856 | ||||||
chr5:174087889
|
G | C | 1 | a0001c0001t0001g0096 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.214-16339G>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174087889 | ||||||
chr5:174087890
|
G | A | 2 | a0001c0003t0003g0203a0001c0003t0003g0206 | 2 | HG00673.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.214-16338G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174087890 | ||||||
chr5:174088309
|
C | T | 5 | a0001c0001t0003g0276a0001c0001t0004g0011a0001c0001t0005g0033others(2): Show | 6 | HG01167.hp2 HG01169.hp1 HG02698.hp2 others(3): Show |
intron_variant | MODIFIER | c.214-15919C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174088309 | ||||||
chr5:174088319
|
G | T | 1 | a0001c0001t0001g0179 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.214-15909G>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174088319 | ||||||
chr5:174088346
|
C | T | 5 | a0001c0001t0003g0276a0001c0001t0004g0011a0001c0001t0005g0033others(2): Show | 6 | HG01167.hp2 HG01169.hp1 HG02698.hp2 others(3): Show |
intron_variant | MODIFIER | c.214-15882C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174088346 | ||||||
chr5:174088372
|
G | T | 1 | a0001c0001t0001g0069 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.214-15856G>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174088372 | ||||||
chr5:174088541
|
G | A | 1 | a0001c0001t0011g0024 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.214-15687G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174088541 | ||||||
chr5:174088737
|
G | A | 2 | a0001c0001t0008g0010a0001c0001t0008g0275 | 3 | HG00280.hp1 HG03927.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.214-15491G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174088737 | ||||||
chr5:174088765
|
G | A | 53 | a0001c0001t0002g0003a0001c0001t0002g0031a0001c0001t0002g0032others(50): Show | 56 | HG00280.hp1 HG00642.hp1 HG01069.hp1 others(53): Show |
intron_variant | MODIFIER | c.214-15463G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174088765 | ||||||
chr5:174088957
|
A | C | 1 | a0001c0001t0005g0207 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.214-15271A>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174088957 | ||||||
chr5:174089178
|
G | A | 9 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0004g0002others(6): Show | 10 | HG01891.hp1 HG02145.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.214-15050G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174089178 | ||||||
chr5:174089179
|
C | T | 9 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0004g0002others(6): Show | 10 | HG01891.hp1 HG02145.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.214-15049C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174089179 | ||||||
chr5:174089235
|
C | T | 2 | a0001c0001t0005g0033a0001c0001t0005g0259 | 2 | HG02886.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.214-14993C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174089235 | ||||||
chr5:174089314
|
C | T | 10 | a0001c0001t0001g0135a0001c0001t0001g0156a0001c0001t0001g0189others(7): Show | 10 | HG00673.hp1 HG02071.hp2 HG02083.hp2 others(7): Show |
intron_variant | MODIFIER | c.214-14914C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174089314 | ||||||
chr5:174089367
|
G | A | 4 | a0001c0001t0004g0225a0001c0001t0004g0226a0001c0001t0004g0227others(1): Show | 4 | HG01433.hp1 HG02735.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.214-14861G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174089367 | ||||||
chr5:174089517
|
G | A | 1 | a0001c0001t0004g0011 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.214-14711G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174089517 | ||||||
chr5:174089517
|
G | T | 2 | a0001c0001t0008g0010a0001c0001t0008g0275 | 3 | HG00280.hp1 HG03927.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.214-14711G>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174089517 | ||||||
chr5:174089567
|
T | C | 53 | a0001c0001t0002g0003a0001c0001t0002g0031a0001c0001t0002g0032others(50): Show | 56 | HG00280.hp1 HG00642.hp1 HG01069.hp1 others(53): Show |
intron_variant | MODIFIER | c.214-14661T>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174089567 | ||||||
chr5:174089681
|
A | G | 46 | a0001c0001t0002g0003a0001c0001t0002g0031a0001c0001t0002g0032others(43): Show | 47 | HG00642.hp1 HG01069.hp1 HG01071.hp1 others(44): Show |
intron_variant | MODIFIER | c.214-14547A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174089681 | ||||||
chr5:174089731
|
C | T | 1 | a0001c0001t0004g0282 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.214-14497C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174089731 | ||||||
chr5:174089776
|
G | A | 5 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0009g0268others(2): Show | 5 | HG01167.hp1 HG01257.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.214-14452G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174089776 | ||||||
chr5:174089776
|
G | C | 3 | a0001c0001t0003g0276a0001c0001t0004g0011a0001c0001t0018g0277 | 4 | HG01167.hp2 HG01169.hp1 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.214-14452G>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174089776 | ||||||
chr5:174089786
|
T | C | 17 | a0001c0001t0001g0198a0001c0001t0001g0205a0001c0003t0003g0009others(14): Show | 18 | HG00408.hp2 HG00673.hp2 HG01358.hp1 others(15): Show |
intron_variant | MODIFIER | c.214-14442T>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174089786 | ||||||
chr5:174089798
|
T | G | 2 | a0001c0001t0005g0033a0001c0001t0005g0259 | 2 | HG02886.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.214-14430T>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174089798 | ||||||
chr5:174089811
|
G | C | 1 | a0001c0001t0001g0145 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.214-14417G>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174089811 | ||||||
chr5:174089872
|
C | T | 4 | a0001c0001t0004g0225a0001c0001t0004g0226a0001c0001t0004g0227others(1): Show | 4 | HG01433.hp1 HG02735.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.214-14356C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174089872 | ||||||
chr5:174090032
|
G | A | 5 | a0001c0001t0003g0276a0001c0001t0004g0011a0001c0001t0005g0033others(2): Show | 6 | HG01167.hp2 HG01169.hp1 HG02698.hp2 others(3): Show |
intron_variant | MODIFIER | c.214-14196G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174090032 | ||||||
chr5:174090112
|
C | T | 1 | a0001c0001t0017g0029 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.214-14116C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174090112 | ||||||
chr5:174090263
|
C | T | 3 | a0001c0001t0002g0263a0001c0001t0002g0264a0001c0001t0002g0267 | 3 | HG01891.hp2 HG02897.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.214-13965C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174090263 | ||||||
chr5:174090322
|
C | T | 2 | a0001c0001t0001g0083a0001c0001t0001g0278 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.214-13906C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174090322 | ||||||
chr5:174090341
|
T | C | 4 | a0001c0001t0004g0225a0001c0001t0004g0226a0001c0001t0004g0227others(1): Show | 4 | HG01433.hp1 HG02735.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.214-13887T>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174090341 | ||||||
chr5:174090353
|
G | A | 1 | a0001c0001t0015g0168 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.214-13875G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174090353 | ||||||
chr5:174090620
|
G | A | 4 | a0001c0001t0004g0015a0001c0001t0004g0016a0001c0001t0004g0066others(1): Show | 4 | HG02257.hp2 HG02895.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.214-13608G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174090620 | ||||||
chr5:174090740
|
C | T | 45 | a0001c0001t0002g0003a0001c0001t0002g0031a0001c0001t0002g0032others(42): Show | 47 | HG00280.hp1 HG00642.hp1 HG01069.hp1 others(44): Show |
intron_variant | MODIFIER | c.214-13488C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174090740 | ||||||
chr5:174090801
|
A | G | 39 | a0001c0001t0001g0014a0001c0001t0001g0069a0001c0001t0001g0070others(36): Show | 43 | HG00099.hp1 HG00323.hp1 HG00738.hp1 others(40): Show |
intron_variant | MODIFIER | c.214-13427A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174090801 | ||||||
chr5:174090890
|
G | A | 1 | a0001c0001t0015g0168 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.214-13338G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174090890 | ||||||
chr5:174090920
|
G | A | 1 | a0001c0001t0004g0220 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.214-13308G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174090920 | ||||||
chr5:174090983
|
C | T | 1 | a0001c0001t0004g0224 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.214-13245C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174090983 | ||||||
chr5:174091039
|
C | CT | 81 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0023others(78): Show | 82 | HG00408.hp1 HG00621.hp1 HG00621.hp2 others(79): Show |
intron_variant | MODIFIER | c.214-13169dupT | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174091039 | |||||
chr5:174091039
|
CT | C | 53 | a0001c0001t0001g0014a0001c0001t0001g0034a0001c0001t0001g0035others(50): Show | 57 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(54): Show |
intron_variant | MODIFIER | c.214-13169delT | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174091039 | |||||
chr5:174091088
|
T | G | 1 | a0001c0001t0016g0071 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.214-13140T>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174091088 | ||||||
chr5:174091100
|
A | C | 2 | a0001c0001t0008g0010a0001c0001t0008g0275 | 3 | HG00280.hp1 HG03927.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.214-13128A>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174091100 | ||||||
chr5:174091220
|
A | C | 4 | a0001c0001t0004g0225a0001c0001t0004g0226a0001c0001t0004g0227others(1): Show | 4 | HG01433.hp1 HG02735.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.214-13008A>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174091220 | ||||||
chr5:174091236
|
G | A | 1 | a0001c0001t0001g0128 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.214-12992G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174091236 | ||||||
chr5:174091311
|
A | G | 2 | a0001c0001t0001g0038a0001c0001t0001g0039 | 2 | HG00099.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.214-12917A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174091311 | ||||||
chr5:174091483
|
C | T | 1 | a0001c0003t0003g0197 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.214-12745C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174091483 | ||||||
chr5:174091595
|
G | A | 2 | a0001c0001t0008g0010a0001c0001t0008g0275 | 3 | HG00280.hp1 HG03927.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.214-12633G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174091595 | ||||||
chr5:174091615
|
A | G | 2 | a0001c0001t0001g0057a0001c0001t0001g0218 | 2 | HG01168.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.214-12613A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174091615 | ||||||
chr5:174091644
|
G | GGT | 21 | a0001c0001t0001g0074a0001c0001t0001g0129a0001c0001t0001g0131others(18): Show | 22 | HG00280.hp2 HG00642.hp1 HG01069.hp1 others(19): Show |
intron_variant | MODIFIER | c.214-12543_214-1254 others(6): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174091644 | |||||
chr5:174091644
|
G | GGTGT | 4 | a0001c0001t0001g0088a0001c0001t0001g0110a0001c0001t0001g0169others(1): Show | 4 | HG01074.hp1 HG02622.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.214-12545_214-1254 others(8): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174091644 | |||||
chr5:174091644
|
GGT | G | 128 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0036others(125): Show | 134 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.214-12543_214-1254 others(6): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174091644 | |||||
chr5:174091644
|
GGTGT | G | 75 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(72): Show | 76 | HG00280.hp1 HG00408.hp1 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.214-12545_214-1254 others(8): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174091644 | |||||
chr5:174091644
|
GGTGTGT | G | 7 | a0001c0001t0001g0167a0001c0001t0003g0276a0001c0001t0004g0011others(4): Show | 8 | HG01167.hp2 HG01169.hp1 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.214-12547_214-1254 others(10): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174091644 | |||||
chr5:174091644
|
GGTGTGTG others(5): Show |
G | 3 | a0001c0001t0001g0130a0001c0001t0001g0216a0001c0001t0010g0142 | 3 | NA18953.hp2 NA19058.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.214-12553_214-1254 others(16): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174091644 | |||||
chr5:174091644
|
GGTGTGTG others(13): Show |
G | 1 | a0001c0002t0001g0176 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.214-12561_214-1254 others(24): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174091644 | |||||
chr5:174091819
|
T | C | 1 | a0001c0001t0016g0071 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.214-12409T>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174091819 | ||||||
chr5:174091957
|
A | C | 3 | a0001c0001t0003g0276a0001c0001t0004g0011a0001c0001t0018g0277 | 4 | HG01167.hp2 HG01169.hp1 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.214-12271A>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174091957 | ||||||
chr5:174092059
|
C | A | 3 | a0001c0001t0002g0003a0001c0001t0002g0031a0001c0001t0002g0032 | 4 | HG02055.hp2 HG02145.hp2 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.214-12169C>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174092059 | ||||||
chr5:174092386
|
C | T | 4 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(1): Show | 4 | HG02040.hp2 NA18955.hp1 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.214-11842C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174092386 | ||||||
chr5:174092691
|
A | G | 1 | a0001c0001t0002g0246 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.214-11537A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174092691 | ||||||
chr5:174092719
|
C | T | 4 | a0001c0001t0004g0225a0001c0001t0004g0226a0001c0001t0004g0227others(1): Show | 4 | HG01433.hp1 HG02735.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.214-11509C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174092719 | ||||||
chr5:174092748
|
T | C | 5 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0009g0268others(2): Show | 5 | HG01167.hp1 HG01257.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.214-11480T>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174092748 | ||||||
chr5:174092921
|
G | C | 5 | a0001c0001t0001g0067a0001c0001t0001g0083a0001c0001t0001g0088others(2): Show | 5 | HG01074.hp1 HG01168.hp1 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.214-11307G>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174092921 | ||||||
chr5:174093034
|
C | G | 3 | a0001c0001t0005g0033a0001c0001t0005g0207a0001c0001t0005g0259 | 3 | HG02886.hp1 HG02970.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.214-11194C>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174093034 | ||||||
chr5:174093041
|
G | A | 1 | a0001c0001t0004g0220 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.214-11187G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174093041 | ||||||
chr5:174093185
|
A | G | 45 | a0001c0001t0002g0003a0001c0001t0002g0031a0001c0001t0002g0032others(42): Show | 47 | HG00280.hp1 HG00642.hp1 HG01069.hp1 others(44): Show |
intron_variant | MODIFIER | c.214-11043A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174093185 | ||||||
chr5:174093214
|
C | T | 1 | a0001c0001t0004g0228 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.214-11014C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174093214 | ||||||
chr5:174093226
|
G | A | 1 | a0001c0001t0001g0159 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.214-11002G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174093226 | ||||||
chr5:174093251
|
A | T | 4 | a0001c0001t0004g0225a0001c0001t0004g0226a0001c0001t0004g0227others(1): Show | 4 | HG01433.hp1 HG02735.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.214-10977A>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174093251 | ||||||
chr5:174093348
|
C | T | 4 | a0001c0001t0004g0044a0001c0001t0004g0045a0001c0001t0004g0046others(1): Show | 4 | HG03471.hp2 HG03516.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.214-10880C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174093348 | ||||||
chr5:174093363
|
A | G | 1 | a0001c0003t0003g0196 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.214-10865A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174093363 | ||||||
chr5:174093392
|
C | T | 3 | a0001c0001t0005g0033a0001c0001t0005g0207a0001c0001t0005g0259 | 3 | HG02886.hp1 HG02970.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.214-10836C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174093392 | ||||||
chr5:174093542
|
A | T | 2 | a0001c0002t0001g0183a0001c0002t0001g0185 | 2 | NA18943.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.214-10686A>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174093542 | ||||||
chr5:174093824
|
G | C | 1 | a0001c0001t0001g0070 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.214-10404G>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174093824 | ||||||
chr5:174093826
|
A | T | 4 | a0001c0001t0004g0002a0001c0001t0004g0027a0001c0001t0004g0028others(1): Show | 5 | HG02630.hp1 HG02717.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.214-10402A>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174093826 | ||||||
chr5:174094815
|
C | T | 1 | a0001c0001t0004g0227 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.214-9413C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174094815 | ||||||
chr5:174095009
|
A | G | 3 | a0001c0001t0003g0276a0001c0001t0004g0011a0001c0001t0018g0277 | 4 | HG01167.hp2 HG01169.hp1 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.214-9219A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174095009 | ||||||
chr5:174095054
|
C | T | 9 | a0001c0001t0004g0002a0001c0001t0004g0027a0001c0001t0004g0028others(6): Show | 10 | HG02145.hp1 HG02572.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.214-9174C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174095054 | ||||||
chr5:174095055
|
A | T | 1 | a0001c0001t0001g0070 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.214-9173A>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174095055 | ||||||
chr5:174095093
|
C | T | 1 | a0001c0001t0017g0029 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.214-9135C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174095093 | ||||||
chr5:174095095
|
A | G | 1 | a0001c0001t0001g0091 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.214-9133A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174095095 | ||||||
chr5:174095150
|
G | A | 2 | a0001c0001t0001g0096a0001c0001t0001g0098 | 2 | HG03239.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.214-9078G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174095150 | ||||||
chr5:174095229
|
G | A | 1 | a0001c0001t0022g0094 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.214-8999G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174095229 | ||||||
chr5:174095484
|
C | T | 1 | a0001c0002t0001g0059 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.214-8744C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174095484 | ||||||
chr5:174095485
|
G | A | 2 | a0001c0001t0001g0038a0001c0001t0001g0048 | 2 | HG01099.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.214-8743G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174095485 | ||||||
chr5:174095530
|
T | C | 7 | a0001c0001t0001g0069a0001c0001t0001g0221a0001c0001t0001g0222others(4): Show | 8 | HG01167.hp2 HG01169.hp1 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.214-8698T>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174095530 | ||||||
chr5:174095600
|
A | G | 6 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0138others(3): Show | 6 | HG01884.hp1 HG02280.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.214-8628A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174095600 | ||||||
chr5:174095754
|
C | T | 4 | a0001c0001t0004g0044a0001c0001t0004g0045a0001c0001t0004g0046others(1): Show | 4 | HG03471.hp2 HG03516.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.214-8474C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174095754 | ||||||
chr5:174096061
|
T | G | 1 | a0001c0003t0003g0197 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.214-8167T>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174096061 | ||||||
chr5:174096064
|
T | C | 5 | a0001c0001t0001g0074a0001c0001t0001g0129a0001c0001t0001g0131others(2): Show | 5 | HG00280.hp2 HG01255.hp2 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.214-8164T>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174096064 | ||||||
chr5:174096238
|
A | C | 2 | a0001c0001t0011g0024a0001c0001t0011g0025 | 2 | HG02451.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.214-7990A>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174096238 | ||||||
chr5:174096286
|
C | T | 2 | a0001c0001t0005g0018a0001c0001t0005g0019 | 2 | HG02486.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.214-7942C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174096286 | ||||||
chr5:174096444
|
A | C | 1 | a0001c0001t0005g0207 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.214-7784A>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174096444 | ||||||
chr5:174096537
|
G | A | 49 | a0001c0001t0001g0014a0001c0001t0003g0004a0001c0001t0003g0005others(46): Show | 54 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(51): Show |
intron_variant | MODIFIER | c.214-7691G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174096537 | ||||||
chr5:174096806
|
G | A | 10 | a0001c0001t0001g0069a0001c0001t0001g0221a0001c0001t0001g0222others(7): Show | 10 | HG01891.hp1 HG02451.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.214-7422G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174096806 | ||||||
chr5:174097033
|
A | G | 1 | a0001c0001t0004g0011 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.214-7195A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174097033 | ||||||
chr5:174097089
|
T | C | 45 | a0001c0001t0002g0003a0001c0001t0002g0031a0001c0001t0002g0032others(42): Show | 46 | HG00642.hp1 HG01069.hp1 HG01071.hp1 others(43): Show |
intron_variant | MODIFIER | c.214-7139T>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174097089 | ||||||
chr5:174097159
|
C | A | 1 | a0001c0001t0002g0032 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.214-7069C>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174097159 | ||||||
chr5:174097162
|
G | T | 1 | a0001c0001t0019g0223 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.214-7066G>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174097162 | ||||||
chr5:174097266
|
A | G | 121 | a0001c0001t0001g0014a0001c0001t0001g0069a0001c0001t0001g0221others(118): Show | 130 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(127): Show |
intron_variant | MODIFIER | c.214-6962A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174097266 | ||||||
chr5:174097314
|
G | A | 3 | a0001c0001t0003g0276a0001c0001t0004g0011a0001c0001t0018g0277 | 4 | HG01167.hp2 HG01169.hp1 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.214-6914G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174097314 | ||||||
chr5:174097404
|
C | A | 1 | a0001c0001t0001g0127 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.214-6824C>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174097404 | ||||||
chr5:174097413
|
G | A | 2 | a0001c0001t0005g0018a0001c0001t0005g0019 | 2 | HG02486.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.214-6815G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174097413 | ||||||
chr5:174097453
|
G | A | 26 | a0001c0001t0001g0014a0001c0001t0003g0005a0001c0001t0003g0006others(23): Show | 30 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(27): Show |
intron_variant | MODIFIER | c.214-6775G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174097453 | ||||||
chr5:174097463
|
G | A | 4 | a0001c0001t0001g0069a0001c0001t0001g0221a0001c0001t0001g0222others(1): Show | 4 | HG01891.hp1 HG02809.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.214-6765G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174097463 | ||||||
chr5:174097508
|
T | C | 1 | a0001c0001t0004g0228 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.214-6720T>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174097508 | ||||||
chr5:174097537
|
A | G | 47 | a0001c0001t0002g0003a0001c0001t0002g0031a0001c0001t0002g0032others(44): Show | 49 | HG00280.hp1 HG00642.hp1 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.214-6691A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174097537 | ||||||
chr5:174097557
|
CTG | C | 12 | a0001c0001t0001g0014a0001c0001t0003g0005a0001c0001t0003g0006others(9): Show | 15 | HG00099.hp1 HG00323.hp1 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.214-6663_214-6662d others(4): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174097557 | |||||
chr5:174097581
|
CTG | C | 50 | a0001c0001t0001g0014a0001c0001t0003g0004a0001c0001t0003g0005others(47): Show | 55 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(52): Show |
intron_variant | MODIFIER | c.214-6637_214-6636d others(4): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174097581 | |||||
chr5:174097631
|
CTG | C | 5 | a0001c0001t0005g0018a0001c0001t0005g0019a0001c0001t0005g0033others(2): Show | 5 | HG02486.hp1 HG02886.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.214-6587_214-6586d others(4): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174097631 | |||||
chr5:174097643
|
TTC | T | 11 | a0001c0001t0001g0069a0001c0001t0001g0221a0001c0001t0001g0222others(8): Show | 11 | HG01891.hp1 HG02451.hp2 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.214-6578_214-6577d others(4): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174097643 | |||||
chr5:174097679
|
CTCTG | C | 11 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0003g0276others(8): Show | 13 | HG01167.hp2 HG01169.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.214-6543_214-6540d others(6): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174097679 | |||||
chr5:174097807
|
G | A | 3 | a0001c0001t0003g0276a0001c0001t0004g0011a0001c0001t0018g0277 | 4 | HG01167.hp2 HG01169.hp1 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.214-6421G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174097807 | ||||||
chr5:174097833
|
T | G | 45 | a0001c0001t0002g0003a0001c0001t0002g0031a0001c0001t0002g0032others(42): Show | 46 | HG00642.hp1 HG01069.hp1 HG01071.hp1 others(43): Show |
intron_variant | MODIFIER | c.214-6395T>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174097833 | ||||||
chr5:174097843
|
C | G | 5 | a0001c0001t0005g0018a0001c0001t0005g0019a0001c0001t0005g0033others(2): Show | 5 | HG02486.hp1 HG02886.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.214-6385C>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174097843 | ||||||
chr5:174097843
|
CTG | C | 5 | a0001c0001t0001g0217a0001c0001t0004g0042a0001c0001t0008g0010others(2): Show | 6 | HG00280.hp1 HG03130.hp2 HG03927.hp1 others(3): Show |
intron_variant | MODIFIER | c.214-6365_214-6364d others(4): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174097843 | |||||
chr5:174097947
|
A | G | 1 | a0001c0001t0019g0223 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.214-6281A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174097947 | ||||||
chr5:174098018
|
G | A | 1 | a0001c0001t0019g0223 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.214-6210G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174098018 | ||||||
chr5:174098042
|
G | A | 1 | a0001c0001t0002g0243 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.214-6186G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174098042 | ||||||
chr5:174098069
|
A | T | 1 | a0001c0001t0001g0091 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.214-6159A>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174098069 | ||||||
chr5:174098071
|
C | T | 1 | a0001c0001t0001g0173 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.214-6157C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174098071 | ||||||
chr5:174098208
|
C | T | 11 | a0001c0001t0001g0069a0001c0001t0001g0221a0001c0001t0001g0222others(8): Show | 12 | HG01167.hp2 HG01169.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.214-6020C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174098208 | ||||||
chr5:174098214
|
C | G | 7 | a0001c0003t0003g0026a0001c0003t0003g0200a0001c0003t0003g0202others(4): Show | 7 | HG00673.hp2 HG02155.hp1 NA18964.hp1 others(4): Show |
intron_variant | MODIFIER | c.214-6014C>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174098214 | ||||||
chr5:174098438
|
T | TCTC | 121 | a0001c0001t0001g0014a0001c0001t0001g0069a0001c0001t0001g0221others(118): Show | 130 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(127): Show |
intron_variant | MODIFIER | c.214-5787_214-5785d others(5): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174098438 | |||||
chr5:174098688
|
ACT | A | 15 | a0001c0003t0003g0009a0001c0003t0003g0026a0001c0003t0003g0193others(12): Show | 16 | HG00408.hp2 HG00673.hp2 HG01358.hp1 others(13): Show |
intron_variant | MODIFIER | c.214-5534_214-5533d others(4): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174098688 | |||||
chr5:174098728
|
C | G | 49 | a0001c0001t0001g0014a0001c0001t0003g0004a0001c0001t0003g0005others(46): Show | 54 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(51): Show |
intron_variant | MODIFIER | c.214-5500C>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174098728 | ||||||
chr5:174098732
|
G | A | 2 | a0001c0001t0008g0010a0001c0001t0008g0275 | 3 | HG00280.hp1 HG03927.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.214-5496G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174098732 | ||||||
chr5:174098833
|
G | A | 5 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0005g0033others(2): Show | 5 | HG02886.hp1 HG02970.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.214-5395G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174098833 | ||||||
chr5:174098869
|
G | T | 121 | a0001c0001t0001g0014a0001c0001t0001g0069a0001c0001t0001g0221others(118): Show | 130 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(127): Show |
intron_variant | MODIFIER | c.214-5359G>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174098869 | ||||||
chr5:174098887
|
C | T | 1 | a0001c0001t0022g0094 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.214-5341C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174098887 | ||||||
chr5:174098925
|
G | A | 2 | a0001c0001t0008g0010a0001c0001t0008g0275 | 3 | HG00280.hp1 HG03927.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.214-5303G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174098925 | ||||||
chr5:174099233
|
C | G | 1 | a0001c0001t0001g0127 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.214-4995C>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174099233 | ||||||
chr5:174099241
|
C | T | 2 | a0001c0001t0001g0221a0001c0001t0001g0222 | 2 | HG01891.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.214-4987C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174099241 | ||||||
chr5:174099242
|
G | A | 3 | a0001c0001t0003g0276a0001c0001t0004g0011a0001c0001t0018g0277 | 4 | HG01167.hp2 HG01169.hp1 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.214-4986G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174099242 | ||||||
chr5:174099482
|
T | C | 1 | a0001c0001t0001g0124 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.214-4746T>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174099482 | ||||||
chr5:174099615
|
C | T | 1 | a0001c0001t0002g0237 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.214-4613C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174099615 | ||||||
chr5:174099711
|
T | A | 120 | a0001c0001t0001g0069a0001c0001t0001g0221a0001c0001t0001g0222others(117): Show | 129 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.214-4517T>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174099711 | ||||||
chr5:174099776
|
A | T | 8 | a0001c0001t0002g0229a0001c0001t0002g0236a0001c0001t0002g0237others(5): Show | 8 | HG01243.hp1 HG01884.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.214-4452A>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174099776 | ||||||
chr5:174099798
|
C | A | 4 | a0001c0001t0004g0225a0001c0001t0004g0226a0001c0001t0004g0227others(1): Show | 4 | HG01433.hp1 HG02735.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.214-4430C>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174099798 | ||||||
chr5:174100017
|
T | C | 48 | a0001c0001t0002g0003a0001c0001t0002g0031a0001c0001t0002g0032others(45): Show | 49 | HG00642.hp1 HG01069.hp1 HG01071.hp1 others(46): Show |
intron_variant | MODIFIER | c.214-4211T>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174100017 | ||||||
chr5:174100126
|
T | C | 2 | a0001c0001t0001g0136a0001c0001t0001g0139 | 2 | HG01884.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.214-4102T>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174100126 | ||||||
chr5:174100442
|
G | A | 5 | a0001c0001t0003g0013a0001c0001t0009g0268a0001c0001t0009g0269others(2): Show | 5 | HG01167.hp1 HG01257.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.214-3786G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174100442 | ||||||
chr5:174100679
|
C | T | 1 | a0001c0001t0001g0082 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.214-3549C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174100679 | ||||||
chr5:174100685
|
T | C | 1 | a0001c0001t0004g0047 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.214-3543T>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174100685 | ||||||
chr5:174100802
|
G | C | 1 | a0001c0001t0001g0058 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.214-3426G>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174100802 | ||||||
chr5:174100843
|
T | C | 120 | a0001c0001t0001g0069a0001c0001t0001g0221a0001c0001t0001g0222others(117): Show | 129 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.214-3385T>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174100843 | ||||||
chr5:174101073
|
G | A | 1 | a0001c0001t0003g0012 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.214-3155G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174101073 | ||||||
chr5:174101111
|
C | T | 2 | a0001c0001t0008g0010a0001c0001t0008g0275 | 3 | HG00280.hp1 HG03927.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.214-3117C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174101111 | ||||||
chr5:174101247
|
G | T | 56 | a0001c0001t0002g0003a0001c0001t0002g0031a0001c0001t0002g0032others(53): Show | 58 | HG00642.hp1 HG01069.hp1 HG01071.hp1 others(55): Show |
intron_variant | MODIFIER | c.214-2981G>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174101247 | ||||||
chr5:174101351
|
C | T | 4 | a0001c0001t0004g0015a0001c0001t0004g0016a0001c0001t0004g0066others(1): Show | 4 | HG02257.hp2 HG02895.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.214-2877C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174101351 | ||||||
chr5:174101784
|
T | G | 1 | a0001c0001t0001g0069 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.214-2444T>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174101784 | ||||||
chr5:174101966
|
C | A | 1 | a0001c0001t0011g0025 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.214-2262C>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174101966 | ||||||
chr5:174102204
|
C | T | 1 | a0001c0001t0003g0076 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.214-2024C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174102204 | ||||||
chr5:174102276
|
A | G | 1 | a0001c0001t0001g0127 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.214-1952A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174102276 | ||||||
chr5:174102461
|
T | G | 48 | a0001c0001t0003g0004a0001c0001t0003g0005a0001c0001t0003g0006others(45): Show | 53 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(50): Show |
intron_variant | MODIFIER | c.214-1767T>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174102461 | ||||||
chr5:174102509
|
C | T | 1 | a0001c0001t0021g0087 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.214-1719C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174102509 | ||||||
chr5:174102590
|
TAACC | T | 42 | a0001c0001t0002g0229a0001c0001t0002g0230a0001c0001t0002g0231others(39): Show | 42 | HG00642.hp1 HG01069.hp1 HG01071.hp1 others(39): Show |
intron_variant | MODIFIER | c.214-1635_214-1632d others(6): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174102590 | |||||
chr5:174102625
|
GC | G | 4 | a0001c0001t0001g0074a0001c0001t0001g0129a0001c0001t0001g0131others(1): Show | 4 | HG00280.hp2 HG01255.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.214-1598delC | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174102625 | |||||
chr5:174102632
|
CT | C | 118 | a0001c0001t0001g0069a0001c0001t0001g0221a0001c0001t0001g0222others(115): Show | 126 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.214-1593delT | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174102632 | |||||
chr5:174102730
|
C | A | 7 | a0001c0001t0004g0042a0001c0001t0004g0044a0001c0001t0004g0045others(4): Show | 7 | HG02451.hp2 HG03130.hp2 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.214-1498C>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174102730 | ||||||
chr5:174102749
|
GTTTT | G | 87 | a0001c0001t0002g0003a0001c0001t0002g0032a0001c0001t0002g0229others(84): Show | 94 | HG00099.hp1 HG00323.hp1 HG00642.hp1 others(91): Show |
intron_variant | MODIFIER | c.214-1474_214-1471d others(6): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174102749 | |||||
chr5:174102750
|
TTTTTTTT others(1): Show |
T | 8 | a0001c0001t0001g0069a0001c0001t0001g0221a0001c0001t0001g0222others(5): Show | 8 | HG01891.hp1 HG02809.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.214-1474_214-1467d others(10): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174102750 | |||||
chr5:174102750
|
TTTTTTTT others(5): Show |
T | 2 | a0001c0001t0002g0031a0001c0003t0003g0202 | 2 | HG02055.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.214-1474_214-1463d others(14): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174102750 | |||||
chr5:174102750
|
TTTTTTTT others(9): Show |
T | 2 | a0001c0001t0005g0018a0001c0001t0005g0019 | 2 | HG02486.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.214-1474_214-1459d others(18): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174102750 | |||||
chr5:174102754
|
T | A | 23 | a0001c0001t0001g0014a0001c0001t0001g0084a0001c0001t0001g0095others(20): Show | 24 | HG00408.hp2 HG01167.hp1 HG01257.hp2 others(21): Show |
intron_variant | MODIFIER | c.214-1474T>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174102754 | ||||||
chr5:174102754
|
T | TTTTA | 14 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0041others(11): Show | 14 | HG00408.hp1 HG00639.hp2 HG01981.hp1 others(11): Show |
intron_variant | MODIFIER | c.214-1433_214-1430d others(6): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174102754 | |||||
chr5:174102754
|
TTTTA | T | 9 | a0001c0001t0001g0056a0001c0001t0001g0058a0001c0001t0001g0105others(6): Show | 10 | HG00280.hp1 HG00323.hp2 HG01496.hp1 others(7): Show |
intron_variant | MODIFIER | c.214-1433_214-1430d others(6): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174102754 | |||||
chr5:174102754
|
TTTTATTT others(5): Show |
T | 1 | a0001c0001t0001g0280 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.214-1441_214-1430d others(14): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174102754 | |||||
chr5:174102941
|
C | CTT | 16 | a0001c0001t0001g0069a0001c0001t0001g0221a0001c0001t0001g0222others(13): Show | 18 | HG01433.hp1 HG01891.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.214-1269_214-1268d others(4): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174102941 | |||||
chr5:174102941
|
C | CTTT | 51 | a0001c0001t0002g0031a0001c0001t0002g0229a0001c0001t0002g0230others(48): Show | 52 | HG00642.hp1 HG01069.hp1 HG01071.hp1 others(49): Show |
intron_variant | MODIFIER | c.214-1270_214-1268d others(5): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174102941 | |||||
chr5:174102941
|
CT | C | 26 | a0001c0001t0001g0049a0001c0001t0001g0105a0001c0001t0001g0191others(23): Show | 27 | HG00621.hp2 HG01070.hp1 HG01071.hp2 others(24): Show |
intron_variant | MODIFIER | c.214-1268delT | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174102941 | |||||
chr5:174102941
|
CTT | C | 40 | a0001c0001t0003g0004a0001c0001t0003g0005a0001c0001t0003g0006others(37): Show | 45 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(42): Show |
intron_variant | MODIFIER | c.214-1269_214-1268d others(4): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174102941 | |||||
chr5:174102992
|
T | C | 1 | a0001c0001t0013g0068 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.214-1236T>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174102992 | ||||||
chr5:174103009
|
G | A | 9 | a0001c0001t0001g0100a0001c0001t0001g0104a0001c0001t0001g0106others(6): Show | 9 | HG00639.hp2 HG00642.hp2 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.214-1219G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174103009 | ||||||
chr5:174103130
|
G | A | 4 | a0001c0001t0004g0015a0001c0001t0004g0016a0001c0001t0004g0066others(1): Show | 4 | HG02257.hp2 HG02895.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.214-1098G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174103130 | ||||||
chr5:174103136
|
T | C | 2 | a0001c0001t0001g0102a0001c0001t0001g0205 | 2 | NA18998.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.214-1092T>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174103136 | ||||||
chr5:174103410
|
G | A | 67 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0036others(64): Show | 67 | HG00408.hp1 HG00621.hp1 HG00639.hp1 others(64): Show |
intron_variant | MODIFIER | c.214-818G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174103410 | ||||||
chr5:174103439
|
A | C | 3 | a0001c0001t0005g0033a0001c0001t0005g0207a0001c0001t0005g0259 | 3 | HG02886.hp1 HG02970.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.214-789A>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174103439 | ||||||
chr5:174103439
|
A | G | 109 | a0001c0001t0001g0069a0001c0001t0001g0221a0001c0001t0001g0222others(106): Show | 117 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.214-789A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174103439 | ||||||
chr5:174103465
|
A | T | 7 | a0001c0001t0004g0042a0001c0001t0004g0044a0001c0001t0004g0045others(4): Show | 7 | HG02451.hp2 HG03130.hp2 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.214-763A>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174103465 | ||||||
chr5:174103823
|
G | T | 1 | a0001c0001t0016g0071 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.214-405G>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174103823 | ||||||
chr5:174103905
|
C | T | 2 | a0001c0002t0001g0176a0001c0002t0001g0177 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.214-323C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174103905 | ||||||
chr5:174104007
|
C | A | 8 | a0001c0001t0001g0038a0001c0001t0001g0048a0001c0001t0001g0049others(5): Show | 8 | HG00621.hp2 HG01099.hp2 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.214-221C>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174104007 | ||||||
chr5:174104050
|
G | A | 45 | a0001c0001t0002g0003a0001c0001t0002g0031a0001c0001t0002g0032others(42): Show | 46 | HG00642.hp1 HG01069.hp1 HG01071.hp1 others(43): Show |
intron_variant | MODIFIER | c.214-178G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174104050 | ||||||
chr5:174104078
|
A | G | 15 | a0001c0003t0003g0009a0001c0003t0003g0026a0001c0003t0003g0193others(12): Show | 16 | HG00408.hp2 HG00673.hp2 HG01358.hp1 others(13): Show |
intron_variant | MODIFIER | c.214-150A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174104078 | ||||||
chr5:174104120
|
C | T | 2 | a0001c0001t0004g0002a0001c0001t0004g0030 | 3 | HG02630.hp1 HG02717.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.214-108C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174104120 | ||||||
chr5:174104538
|
A | G | 1 | a0001c0001t0002g0258 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.324+200A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 4/4 | chr5 | 174104538 | ||||||
chr5:174104579
|
G | A | 44 | a0001c0001t0002g0003a0001c0001t0002g0031a0001c0001t0002g0032others(41): Show | 45 | HG00642.hp1 HG01069.hp1 HG01071.hp1 others(42): Show |
intron_variant | MODIFIER | c.324+241G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 4/4 | chr5 | 174104579 | ||||||
chr5:174104657
|
G | A | 63 | a0001c0001t0002g0003a0001c0001t0002g0031a0001c0001t0002g0032others(60): Show | 65 | HG00642.hp1 HG01069.hp1 HG01071.hp1 others(62): Show |
intron_variant | MODIFIER | c.324+319G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 4/4 | chr5 | 174104657 | ||||||
chr5:174104748
|
G | A | 1 | a0001c0003t0003g0202 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.324+410G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 4/4 | chr5 | 174104748 | ||||||
chr5:174104766
|
C | G | 2 | a0001c0001t0008g0010a0001c0001t0008g0275 | 3 | HG00280.hp1 HG03927.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.324+428C>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 4/4 | chr5 | 174104766 | ||||||
chr5:174104777
|
C | A | 12 | a0001c0001t0003g0005a0001c0001t0003g0006a0001c0001t0003g0007others(9): Show | 15 | HG00099.hp1 HG00323.hp1 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.324+439C>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 4/4 | chr5 | 174104777 | ||||||
chr5:174104808
|
G | A | 1 | a0001c0001t0001g0128 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.324+470G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 4/4 | chr5 | 174104808 | ||||||
chr5:174104913
|
C | G | 1 | a0001c0003t0003g0203 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.324+575C>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 4/4 | chr5 | 174104913 | ||||||
chr5:174105027
|
A | ATACTAT | 119 | a0001c0001t0001g0069a0001c0001t0001g0221a0001c0001t0001g0222others(116): Show | 128 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.324+691_324+692ins others(6): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr5 | 174105027 | |||||
chr5:174105110
|
G | A | 41 | a0001c0001t0002g0229a0001c0001t0002g0230a0001c0001t0002g0231others(38): Show | 41 | HG00642.hp1 HG01069.hp1 HG01071.hp1 others(38): Show |
intron_variant | MODIFIER | c.324+772G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 4/4 | chr5 | 174105110 | ||||||
chr5:174105277
|
A | C | 2 | a0001c0001t0008g0010a0001c0001t0008g0275 | 3 | HG00280.hp1 HG03927.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.324+939A>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 4/4 | chr5 | 174105277 | ||||||
chr5:174105556
|
C | T | 6 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0009g0268others(3): Show | 6 | HG01167.hp1 HG01257.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.324+1218C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 4/4 | chr5 | 174105556 | ||||||
chr5:174105718
|
T | G | 2 | a0001c0001t0008g0010a0001c0001t0008g0275 | 3 | HG00280.hp1 HG03927.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.324+1380T>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 4/4 | chr5 | 174105718 | ||||||
chr5:174105788
|
T | G | 3 | a0001c0001t0001g0069a0001c0001t0008g0010a0001c0001t0008g0275 | 4 | HG00280.hp1 HG02809.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.324+1450T>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 4/4 | chr5 | 174105788 | ||||||
chr5:174105894
|
C | T | 31 | a0001c0001t0003g0005a0001c0001t0003g0006a0001c0001t0003g0007others(28): Show | 35 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(32): Show |
intron_variant | MODIFIER | c.325-1420C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 4/4 | chr5 | 174105894 | ||||||
chr5:174106034
|
C | T | 3 | a0001c0001t0004g0002a0001c0001t0004g0030a0001c0001t0004g0077 | 4 | HG02630.hp1 HG02717.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.325-1280C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 4/4 | chr5 | 174106034 | ||||||
chr5:174106283
|
C | A | 119 | a0001c0001t0001g0069a0001c0001t0001g0221a0001c0001t0001g0222others(116): Show | 128 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.325-1031C>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 4/4 | chr5 | 174106283 | ||||||
chr5:174106551
|
C | T | 7 | a0001c0001t0004g0042a0001c0001t0004g0044a0001c0001t0004g0045others(4): Show | 7 | HG02451.hp2 HG03130.hp2 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.325-763C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 4/4 | chr5 | 174106551 | ||||||
chr5:174106583
|
C | CT | 60 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0022others(57): Show | 61 | HG00323.hp2 HG00621.hp1 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.325-702dupT | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr5 | 174106583 | |||||
chr5:174106583
|
CT | C | 32 | a0001c0001t0001g0143a0001c0001t0002g0003a0001c0001t0002g0031others(29): Show | 33 | HG00642.hp1 HG01071.hp1 HG01099.hp1 others(30): Show |
intron_variant | MODIFIER | c.325-702delT | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr5 | 174106583 | |||||
chr5:174106583
|
CTTTTTTT others(5): Show |
C | 2 | a0001c0001t0008g0010a0001c0001t0008g0275 | 3 | HG00280.hp1 HG03927.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.325-713_325-702del others(12): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr5 | 174106583 | |||||
chr5:174106583
|
CTTTTTTT others(9): Show |
C | 48 | a0001c0001t0003g0004a0001c0001t0003g0005a0001c0001t0003g0006others(45): Show | 53 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(50): Show |
intron_variant | MODIFIER | c.325-717_325-702del others(16): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr5 | 174106583 | |||||
chr5:174106639
|
C | T | 2 | a0001c0001t0008g0010a0001c0001t0008g0275 | 3 | HG00280.hp1 HG03927.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.325-675C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 4/4 | chr5 | 174106639 | ||||||
chr5:174106882
|
C | G | 45 | a0001c0001t0002g0003a0001c0001t0002g0031a0001c0001t0002g0032others(42): Show | 46 | HG00642.hp1 HG01069.hp1 HG01071.hp1 others(43): Show |
intron_variant | MODIFIER | c.325-432C>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 4/4 | chr5 | 174106882 | ||||||
chr5:174107023
|
G | A | 111 | a0001c0001t0002g0003a0001c0001t0002g0031a0001c0001t0002g0032others(108): Show | 118 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.325-291G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 4/4 | chr5 | 174107023 | ||||||
chr5:174107220
|
G | A | 1 | a0001c0001t0001g0107 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.325-94G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 4/4 | chr5 | 174107220 | ||||||
chr5:174107280
|
G | A | 10 | a0001c0001t0001g0099a0001c0001t0001g0132a0001c0001t0001g0159others(7): Show | 10 | HG02683.hp1 HG03654.hp2 NA18953.hp2 others(7): Show |
intron_variant | MODIFIER | c.325-34G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 4/4 | chr5 | 174107280 |