geneid | 84081 |
---|---|
ensemblid | ENSG00000126653.18 |
hgncid | 25305 |
symbol | NSRP1 |
name | nuclear speckle splicing regulatory protein 1 |
refseq_nuc | NM_032141.4 |
refseq_prot | NP_115517.1 |
ensembl_nuc | ENST00000247026.10 |
ensembl_prot | ENSP00000247026.5 |
mane_status | MANE Select |
chr | chr17 |
start | 30116816 |
end | 30186475 |
strand | + |
ver | v1.2 |
region | chr17:30116816-30186475 |
region5000 | chr17:30111816-30191475 |
regionname0 | NSRP1_chr17_30116816_30186475 |
regionname5000 | NSRP1_chr17_30111816_30191475 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 558 | 258 | 89 | 51 | 67 | 12 | 37 | 56 | NSRP1_chr17_30111816_30191475 | NSRP1 | copy fasta | chr17 | 30111816 | 30191475 |
a0002 | 0/0 | 558 | 7 | 0 | 4 | 3 | 0 | 0 | 2 | NSRP1_chr17_30111816_30191475 | NSRP1 | copy fasta | chr17 | 30111816 | 30191475 |
a0003 | 0/0 | 558 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | copy fasta | chr17 | 30111816 | 30191475 |
a0004 | 0/0 | 558 | 3 | 0 | 2 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | copy fasta | chr17 | 30111816 | 30191475 |
a0005 | 0/0 | 558 | 3 | 0 | 2 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | copy fasta | chr17 | 30111816 | 30191475 |
a0006 | 0/0 | 558 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | NSRP1_chr17_30111816_30191475 | NSRP1 | copy fasta | chr17 | 30111816 | 30191475 |
a0007 | 0/0 | 558 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | copy fasta | chr17 | 30111816 | 30191475 |
a0008 | 0/0 | 558 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | copy fasta | chr17 | 30111816 | 30191475 |
a0009 | 0/0 | 558 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | copy fasta | chr17 | 30111816 | 30191475 |
a0010 | 0/0 | 558 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | copy fasta | chr17 | 30111816 | 30191475 |
a0011 | 0/0 | 558 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | copy fasta | chr17 | 30111816 | 30191475 |
a0012 | 0/0 | 558 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | copy fasta | chr17 | 30111816 | 30191475 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 1677 | 129 | 43 | 30 | 34 | 4 | 18 | NSRP1_chr17_30111816_30191475 | NSRP1 | copy fasta | chr17 | 30111816 | 30191475 |
c0002 | 1/1 | 1677 | 125 | 43 | 21 | 33 | 8 | 18 | NSRP1_chr17_30111816_30191475 | NSRP1 | copy fasta | chr17 | 30111816 | 30191475 |
c0003 | 0/0 | 1677 | 7 | 0 | 4 | 3 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | copy fasta | chr17 | 30111816 | 30191475 |
c0004 | 0/0 | 1677 | 3 | 0 | 2 | 0 | 1 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | copy fasta | chr17 | 30111816 | 30191475 |
c0005 | 0/0 | 1677 | 3 | 3 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | copy fasta | chr17 | 30111816 | 30191475 |
c0006 | 0/0 | 1677 | 3 | 0 | 2 | 0 | 1 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | copy fasta | chr17 | 30111816 | 30191475 |
c0007 | 0/0 | 1677 | 2 | 0 | 0 | 2 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | copy fasta | chr17 | 30111816 | 30191475 |
c0008 | 0/0 | 1677 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | copy fasta | chr17 | 30111816 | 30191475 |
c0009 | 0/0 | 1677 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | copy fasta | chr17 | 30111816 | 30191475 |
c0010 | 0/0 | 1677 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | copy fasta | chr17 | 30111816 | 30191475 |
c0011 | 0/0 | 1677 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | copy fasta | chr17 | 30111816 | 30191475 |
c0012 | 0/0 | 1677 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | copy fasta | chr17 | 30111816 | 30191475 |
c0013 | 0/0 | 1677 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | copy fasta | chr17 | 30111816 | 30191475 |
c0014 | 0/0 | 1677 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | copy fasta | chr17 | 30111816 | 30191475 |
c0015 | 0/0 | 1677 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | copy fasta | chr17 | 30111816 | 30191475 |
c0016 | 0/0 | 1677 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | copy fasta | chr17 | 30111816 | 30191475 |
c0017 | 0/0 | 1677 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | copy fasta | chr17 | 30111816 | 30191475 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 830 | 151 | 58 | 27 | 36 | 10 | 18 | NSRP1_chr17_30111816_30191475 | NSRP1 | copy fasta | chr17 | 30111816 | 30191475 |
t0002 | 0/0 | 830 | 99 | 13 | 25 | 38 | 4 | 19 | NSRP1_chr17_30111816_30191475 | NSRP1 | copy fasta | chr17 | 30111816 | 30191475 |
t0003 | 0/0 | 830 | 19 | 14 | 5 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | copy fasta | chr17 | 30111816 | 30191475 |
t0004 | 0/0 | 830 | 4 | 3 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | copy fasta | chr17 | 30111816 | 30191475 |
t0005 | 0/0 | 830 | 3 | 3 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | copy fasta | chr17 | 30111816 | 30191475 |
t0006 | 0/0 | 830 | 2 | 0 | 2 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | copy fasta | chr17 | 30111816 | 30191475 |
t0007 | 0/0 | 830 | 2 | 2 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | copy fasta | chr17 | 30111816 | 30191475 |
t0008 | 0/0 | 830 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | copy fasta | chr17 | 30111816 | 30191475 |
t0009 | 0/0 | 830 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | copy fasta | chr17 | 30111816 | 30191475 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0043 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0055 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0280 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 1677 | 129 | 43 | 30 | 34 | 4 | 18 | NSRP1_chr17_30111816_30191475 | NSRP1 | copy fasta | chr17 | 30111816 | 30191475 |
a0001c0002 | 1/1 | 1677 | 125 | 43 | 21 | 33 | 8 | 18 | NSRP1_chr17_30111816_30191475 | NSRP1 | copy fasta | chr17 | 30111816 | 30191475 |
a0001c0008 | 0/0 | 1677 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | copy fasta | chr17 | 30111816 | 30191475 |
a0001c0009 | 0/0 | 1677 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | copy fasta | chr17 | 30111816 | 30191475 |
a0001c0011 | 0/0 | 1677 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | copy fasta | chr17 | 30111816 | 30191475 |
a0001c0014 | 0/0 | 1677 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | copy fasta | chr17 | 30111816 | 30191475 |
a0002c0003 | 0/0 | 1677 | 7 | 0 | 4 | 3 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | copy fasta | chr17 | 30111816 | 30191475 |
a0003c0005 | 0/0 | 1677 | 3 | 3 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | copy fasta | chr17 | 30111816 | 30191475 |
a0004c0004 | 0/0 | 1677 | 3 | 0 | 2 | 0 | 1 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | copy fasta | chr17 | 30111816 | 30191475 |
a0005c0006 | 0/0 | 1677 | 3 | 0 | 2 | 0 | 1 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | copy fasta | chr17 | 30111816 | 30191475 |
a0006c0007 | 0/0 | 1677 | 2 | 0 | 0 | 2 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | copy fasta | chr17 | 30111816 | 30191475 |
a0007c0012 | 0/0 | 1677 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | copy fasta | chr17 | 30111816 | 30191475 |
a0008c0013 | 0/0 | 1677 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | copy fasta | chr17 | 30111816 | 30191475 |
a0009c0015 | 0/0 | 1677 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | copy fasta | chr17 | 30111816 | 30191475 |
a0010c0010 | 0/0 | 1677 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | copy fasta | chr17 | 30111816 | 30191475 |
a0011c0016 | 0/0 | 1677 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | copy fasta | chr17 | 30111816 | 30191475 |
a0012c0017 | 0/0 | 1677 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | copy fasta | chr17 | 30111816 | 30191475 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 2506 | 26 | 24 | 2 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | copy fasta | chr17 | 30111816 | 30191475 |
a0001c0001t0002 | 0/0 | 2506 | 94 | 13 | 25 | 34 | 4 | 18 | NSRP1_chr17_30111816_30191475 | NSRP1 | copy fasta | chr17 | 30111816 | 30191475 |
a0001c0001t0004 | 0/0 | 2506 | 4 | 3 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | copy fasta | chr17 | 30111816 | 30191475 |
a0001c0001t0005 | 0/0 | 2506 | 3 | 3 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | copy fasta | chr17 | 30111816 | 30191475 |
a0001c0001t0006 | 0/0 | 2506 | 2 | 0 | 2 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | copy fasta | chr17 | 30111816 | 30191475 |
a0001c0002t0001 | 1/1 | 2506 | 104 | 28 | 16 | 33 | 8 | 17 | NSRP1_chr17_30111816_30191475 | NSRP1 | copy fasta | chr17 | 30111816 | 30191475 |
a0001c0002t0003 | 0/0 | 2506 | 18 | 13 | 5 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | copy fasta | chr17 | 30111816 | 30191475 |
a0001c0002t0007 | 0/0 | 2506 | 2 | 2 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | copy fasta | chr17 | 30111816 | 30191475 |
a0001c0002t0009 | 0/0 | 2506 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | copy fasta | chr17 | 30111816 | 30191475 |
a0001c0008t0001 | 0/0 | 2506 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | copy fasta | chr17 | 30111816 | 30191475 |
a0001c0009t0001 | 0/0 | 2506 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | copy fasta | chr17 | 30111816 | 30191475 |
a0001c0011t0002 | 0/0 | 2506 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | copy fasta | chr17 | 30111816 | 30191475 |
a0001c0014t0008 | 0/0 | 2506 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | copy fasta | chr17 | 30111816 | 30191475 |
a0002c0003t0001 | 0/0 | 2506 | 7 | 0 | 4 | 3 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | copy fasta | chr17 | 30111816 | 30191475 |
a0003c0005t0001 | 0/0 | 2506 | 3 | 3 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | copy fasta | chr17 | 30111816 | 30191475 |
a0004c0004t0001 | 0/0 | 2506 | 3 | 0 | 2 | 0 | 1 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | copy fasta | chr17 | 30111816 | 30191475 |
a0005c0006t0001 | 0/0 | 2506 | 3 | 0 | 2 | 0 | 1 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | copy fasta | chr17 | 30111816 | 30191475 |
a0006c0007t0002 | 0/0 | 2506 | 2 | 0 | 0 | 2 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | copy fasta | chr17 | 30111816 | 30191475 |
a0007c0012t0002 | 0/0 | 2506 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | copy fasta | chr17 | 30111816 | 30191475 |
a0008c0013t0002 | 0/0 | 2506 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | copy fasta | chr17 | 30111816 | 30191475 |
a0009c0015t0001 | 0/0 | 2506 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | copy fasta | chr17 | 30111816 | 30191475 |
a0010c0010t0001 | 0/0 | 2506 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | copy fasta | chr17 | 30111816 | 30191475 |
a0011c0016t0001 | 0/0 | 2506 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | copy fasta | chr17 | 30111816 | 30191475 |
a0012c0017t0003 | 0/0 | 2506 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | copy fasta | chr17 | 30111816 | 30191475 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0002g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0002g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0002g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0002g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0002g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0002g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0002g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0002g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0002g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0002g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0002g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0002g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0002g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0002g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0002g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0004g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0004g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0004g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0004g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0005g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0005g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0005g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0006g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0001t0006g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0001g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0001g0043 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0001g0055 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0003g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0003g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0003g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0003g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0003g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0003g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0003g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0003g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0003g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0003g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0003g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0003g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0003g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0003g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0003g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0003g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0003g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0003g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0007g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0007g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0002t0009g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0008t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0009t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0011t0002g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0001c0014t0008g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0002c0003t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0002c0003t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0002c0003t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0002c0003t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0002c0003t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0002c0003t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0002c0003t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0003c0005t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0003c0005t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0003c0005t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0004c0004t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0004c0004t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0004c0004t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0005c0006t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0005c0006t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0005c0006t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0006c0007t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0006c0007t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0007c0012t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0008c0013t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0009c0015t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0010c0010t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0011c0016t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
a0012c0017t0003g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0005 | c0006 | t0001 | g0118 | EUR | GBR | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0224 | EUR | GBR | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG00140 | hp1 | a0001 | c0002 | t0001 | g0090 | EUR | GBR | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG00140 | hp2 | a0001 | c0002 | t0001 | g0107 | EUR | GBR | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG00280 | hp1 | a0004 | c0004 | t0001 | g0050 | EUR | FIN | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG00280 | hp2 | a0001 | c0001 | t0002 | g0189 | EUR | FIN | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0236 | EUR | FIN | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG00323 | hp2 | a0001 | c0002 | t0001 | g0073 | EUR | FIN | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG00597 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | CHS | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0247 | EAS | CHS | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG00609 | hp1 | a0001 | c0002 | t0001 | g0113 | EAS | CHS | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG00609 | hp2 | a0001 | c0001 | t0002 | g0245 | EAS | CHS | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG00639 | hp1 | a0001 | c0002 | t0001 | g0106 | AMR | PUR | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0193 | AMR | PUR | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0223 | AMR | PUR | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG00642 | hp2 | a0001 | c0002 | t0001 | g0051 | AMR | PUR | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG00733 | hp1 | a0001 | c0001 | t0002 | g0194 | AMR | PUR | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG00733 | hp2 | a0001 | c0002 | t0001 | g0076 | AMR | PUR | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0263 | AMR | PUR | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG00741 | hp2 | a0001 | c0002 | t0001 | g0269 | AMR | PUR | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG01069 | hp1 | a0001 | c0002 | t0003 | g0026 | AMR | PUR | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG01069 | hp2 | a0001 | c0001 | t0002 | g0256 | AMR | PUR | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG01070 | hp1 | a0001 | c0001 | t0002 | g0177 | AMR | PUR | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG01070 | hp2 | a0004 | c0004 | t0001 | g0045 | AMR | PUR | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG01071 | hp1 | a0004 | c0004 | t0001 | g0049 | AMR | PUR | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG01071 | hp2 | a0001 | c0002 | t0003 | g0027 | AMR | PUR | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0216 | AMR | PUR | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG01081 | hp2 | a0001 | c0002 | t0001 | g0093 | AMR | PUR | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG01099 | hp1 | a0001 | c0002 | t0001 | g0016 | AMR | PUR | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG01099 | hp2 | a0001 | c0001 | t0002 | g0178 | AMR | PUR | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG01109 | hp1 | a0001 | c0002 | t0003 | g0034 | AMR | PUR | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG01109 | hp2 | a0001 | c0001 | t0002 | g0211 | AMR | PUR | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG01167 | hp1 | a0001 | c0002 | t0001 | g0018 | AMR | PUR | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG01167 | hp2 | a0001 | c0001 | t0002 | g0200 | AMR | PUR | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG01168 | hp1 | a0009 | c0015 | t0001 | g0052 | AMR | PUR | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG01168 | hp2 | a0001 | c0001 | t0006 | g0241 | AMR | PUR | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG01169 | hp1 | a0001 | c0001 | t0006 | g0242 | AMR | PUR | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG01169 | hp2 | a0001 | c0002 | t0001 | g0013 | AMR | PUR | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG01192 | hp1 | a0001 | c0002 | t0003 | g0109 | AMR | PUR | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG01192 | hp2 | a0001 | c0002 | t0001 | g0065 | AMR | PUR | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG01243 | hp1 | a0001 | c0002 | t0001 | g0282 | AMR | PUR | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0218 | AMR | CLM | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG01255 | hp2 | a0001 | c0002 | t0001 | g0066 | AMR | CLM | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG01261 | hp1 | a0001 | c0002 | t0001 | g0059 | AMR | CLM | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0210 | AMR | CLM | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG01346 | hp1 | a0001 | c0002 | t0003 | g0078 | AMR | CLM | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG01346 | hp2 | a0002 | c0003 | t0001 | g0056 | AMR | CLM | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG01361 | hp1 | a0001 | c0002 | t0001 | g0096 | AMR | CLM | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG01361 | hp2 | a0001 | c0001 | t0002 | g0227 | AMR | CLM | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG01433 | hp1 | a0001 | c0001 | t0004 | g0275 | AMR | CLM | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG01433 | hp2 | a0001 | c0001 | t0002 | g0171 | AMR | CLM | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0212 | AMR | CLM | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG01496 | hp2 | a0005 | c0006 | t0001 | g0041 | AMR | CLM | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG01516 | hp1 | a0001 | c0002 | t0001 | g0017 | EUR | IBS | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG01516 | hp2 | a0001 | c0002 | t0001 | g0279 | EUR | IBS | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG01517 | hp1 | a0001 | c0002 | t0001 | g0061 | EUR | IBS | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG01517 | hp2 | a0001 | c0002 | t0001 | g0280 | EUR | IBS | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | ACB | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG01884 | hp2 | a0001 | c0001 | t0002 | g0270 | AFR | ACB | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | ACB | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | ACB | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG01934 | hp1 | a0001 | c0001 | t0002 | g0187 | AMR | PEL | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | PEL | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG01952 | hp1 | a0001 | c0001 | t0002 | g0197 | AMR | PEL | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG01952 | hp2 | a0001 | c0002 | t0001 | g0117 | AMR | PEL | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG01978 | hp1 | a0001 | c0001 | t0002 | g0204 | AMR | PEL | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG01978 | hp2 | a0002 | c0003 | t0001 | g0062 | AMR | PEL | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0237 | AMR | PEL | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG01993 | hp2 | a0002 | c0003 | t0001 | g0068 | AMR | PEL | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG02004 | hp1 | a0002 | c0003 | t0001 | g0067 | AMR | PEL | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG02004 | hp2 | a0001 | c0001 | t0002 | g0238 | AMR | PEL | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG02055 | hp1 | a0001 | c0002 | t0003 | g0035 | AFR | ACB | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG02055 | hp2 | a0001 | c0009 | t0001 | g0149 | AFR | ACB | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0182 | EAS | KHV | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG02074 | hp2 | a0001 | c0002 | t0001 | g0132 | EAS | KHV | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG02129 | hp1 | a0002 | c0003 | t0001 | g0101 | EAS | KHV | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG02129 | hp2 | a0001 | c0002 | t0001 | g0104 | EAS | KHV | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG02132 | hp1 | a0001 | c0002 | t0001 | g0281 | EAS | KHV | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG02132 | hp2 | a0001 | c0001 | t0002 | g0243 | EAS | KHV | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG02145 | hp1 | a0001 | c0002 | t0001 | g0110 | AFR | ACB | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | ACB | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG02148 | hp1 | a0001 | c0002 | t0001 | g0015 | AMR | PEL | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG02148 | hp2 | a0001 | c0001 | t0002 | g0222 | AMR | PEL | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG02257 | hp1 | a0001 | c0001 | t0002 | g0235 | AFR | ACB | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG02257 | hp2 | a0001 | c0002 | t0003 | g0025 | AFR | ACB | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | ACB | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG02258 | hp2 | a0001 | c0001 | t0002 | g0174 | AFR | ACB | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG02273 | hp1 | a0001 | c0001 | t0002 | g0186 | AMR | PEL | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG02273 | hp2 | a0001 | c0002 | t0001 | g0116 | AMR | PEL | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG02280 | hp1 | a0001 | c0002 | t0003 | g0028 | AFR | ACB | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG02280 | hp2 | a0001 | c0001 | t0002 | g0183 | AFR | ACB | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG02293 | hp1 | a0001 | c0001 | t0002 | g0208 | AMR | PEL | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG02293 | hp2 | a0001 | c0001 | t0002 | g0201 | AMR | PEL | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | ACB | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG02451 | hp2 | a0001 | c0001 | t0002 | g0176 | AFR | ACB | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG02523 | hp1 | a0001 | c0002 | t0001 | g0009 | EAS | KHV | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG02523 | hp2 | a0001 | c0001 | t0002 | g0179 | EAS | KHV | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG02572 | hp1 | a0001 | c0001 | t0002 | g0257 | AFR | GWD | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG02572 | hp2 | a0001 | c0002 | t0001 | g0053 | AFR | GWD | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0199 | SAS | PJL | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0195 | SAS | PJL | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG02615 | hp1 | a0001 | c0001 | t0004 | g0272 | AFR | GWD | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG02615 | hp2 | a0001 | c0002 | t0001 | g0127 | AFR | GWD | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG02622 | hp1 | a0001 | c0002 | t0003 | g0031 | AFR | GWD | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG02622 | hp2 | a0001 | c0002 | t0001 | g0126 | AFR | GWD | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG02630 | hp1 | a0001 | c0001 | t0002 | g0259 | AFR | GWD | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG02630 | hp2 | a0001 | c0002 | t0001 | g0098 | AFR | GWD | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG02647 | hp1 | a0001 | c0001 | t0002 | g0240 | AFR | GWD | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG02647 | hp2 | a0001 | c0002 | t0003 | g0036 | AFR | GWD | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG02683 | hp1 | a0001 | c0001 | t0002 | g0230 | SAS | PJL | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG02683 | hp2 | a0001 | c0002 | t0001 | g0012 | SAS | PJL | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0184 | SAS | PJL | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG02698 | hp2 | a0001 | c0002 | t0001 | g0074 | SAS | PJL | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG02717 | hp1 | a0001 | c0002 | t0001 | g0086 | AFR | GWD | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | GWD | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG02723 | hp1 | a0001 | c0002 | t0001 | g0129 | AFR | GWD | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | GWD | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG02735 | hp1 | a0001 | c0002 | t0001 | g0072 | SAS | PJL | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0214 | SAS | PJL | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0265 | SAS | PJL | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG02738 | hp2 | a0001 | c0002 | t0001 | g0137 | SAS | PJL | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG02809 | hp1 | a0001 | c0002 | t0003 | g0030 | AFR | GWD | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | GWD | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG02818 | hp1 | a0001 | c0002 | t0001 | g0128 | AFR | GWD | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG02818 | hp2 | a0001 | c0002 | t0003 | g0032 | AFR | GWD | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG02886 | hp1 | a0001 | c0002 | t0001 | g0125 | AFR | GWD | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | GWD | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG02895 | hp1 | a0003 | c0005 | t0001 | g0268 | AFR | GWD | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG02896 | hp1 | a0001 | c0002 | t0001 | g0094 | AFR | GWD | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG02922 | hp1 | a0001 | c0001 | t0002 | g0271 | AFR | ESN | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG02922 | hp2 | a0001 | c0001 | t0005 | g0150 | AFR | ESN | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG02965 | hp1 | a0001 | c0002 | t0001 | g0123 | AFR | ESN | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG02965 | hp2 | a0001 | c0002 | t0003 | g0014 | AFR | ESN | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG02976 | hp1 | a0001 | c0008 | t0001 | g0156 | AFR | ESN | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | ESN | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0180 | SAS | PJL | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG03017 | hp2 | a0001 | c0002 | t0009 | g0069 | SAS | PJL | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG03041 | hp1 | a0001 | c0002 | t0001 | g0124 | AFR | GWD | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG03041 | hp2 | a0001 | c0002 | t0001 | g0278 | AFR | GWD | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG03098 | hp1 | a0001 | c0002 | t0001 | g0102 | AFR | MSL | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG03098 | hp2 | a0001 | c0001 | t0002 | g0276 | AFR | MSL | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | ESN | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG03130 | hp2 | a0001 | c0001 | t0002 | g0170 | AFR | ESN | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG03139 | hp1 | a0001 | c0002 | t0001 | g0130 | AFR | ESN | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | ESN | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG03195 | hp1 | a0001 | c0001 | t0005 | g0147 | AFR | ESN | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG03195 | hp2 | a0001 | c0002 | t0001 | g0022 | AFR | ESN | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG03209 | hp1 | a0001 | c0001 | t0004 | g0273 | AFR | MSL | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG03209 | hp2 | a0001 | c0002 | t0001 | g0063 | AFR | MSL | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | MSL | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG03225 | hp2 | a0001 | c0002 | t0001 | g0103 | AFR | MSL | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0209 | SAS | PJL | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG03239 | hp2 | a0001 | c0002 | t0001 | g0038 | SAS | PJL | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG03453 | hp1 | a0001 | c0002 | t0003 | g0079 | AFR | MSL | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | MSL | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG03486 | hp1 | a0010 | c0010 | t0001 | g0141 | AFR | MSL | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG03486 | hp2 | a0001 | c0002 | t0001 | g0277 | AFR | MSL | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG03490 | hp1 | a0001 | c0001 | t0002 | g0226 | SAS | PJL | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG03490 | hp2 | a0001 | c0002 | t0001 | g0099 | SAS | PJL | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG03492 | hp1 | a0001 | c0002 | t0001 | g0100 | SAS | PJL | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG03492 | hp2 | a0001 | c0002 | t0001 | g0054 | SAS | PJL | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG03516 | hp1 | a0001 | c0002 | t0001 | g0134 | AFR | ESN | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG03516 | hp2 | a0001 | c0001 | t0002 | g0175 | AFR | ESN | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG03540 | hp1 | a0001 | c0002 | t0003 | g0029 | AFR | GWD | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG03540 | hp2 | a0001 | c0002 | t0001 | g0042 | AFR | GWD | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG03579 | hp1 | a0012 | c0017 | t0003 | g0077 | AFR | MSL | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG03579 | hp2 | a0001 | c0002 | t0001 | g0131 | AFR | MSL | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0188 | SAS | PJL | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG03669 | hp2 | a0011 | c0016 | t0001 | g0057 | SAS | PJL | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG03704 | hp1 | a0001 | c0011 | t0002 | g0215 | SAS | PJL | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG03704 | hp2 | a0001 | c0002 | t0001 | g0048 | SAS | PJL | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0213 | SAS | BEB | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG03834 | hp2 | a0001 | c0002 | t0001 | g0020 | SAS | BEB | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG03927 | hp1 | a0001 | c0002 | t0001 | g0083 | SAS | BEB | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG03927 | hp2 | a0001 | c0001 | t0002 | g0207 | SAS | BEB | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG03942 | hp1 | a0001 | c0002 | t0001 | g0064 | SAS | BEB | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG03942 | hp2 | a0001 | c0001 | t0002 | g0233 | SAS | BEB | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0255 | SAS | STU | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG04115 | hp2 | a0001 | c0002 | t0001 | g0039 | SAS | STU | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG04199 | hp1 | a0001 | c0002 | t0001 | g0060 | SAS | STU | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG04199 | hp2 | a0001 | c0001 | t0002 | g0239 | SAS | STU | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG04204 | hp1 | a0001 | c0002 | t0001 | g0075 | SAS | STU | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0185 | SAS | STU | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG04228 | hp1 | a0001 | c0002 | t0001 | g0108 | SAS | STU | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0231 | SAS | STU | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
NA18522 | hp1 | a0001 | c0002 | t0001 | g0085 | AFR | YRI | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
NA18522 | hp2 | a0001 | c0001 | t0002 | g0244 | AFR | YRI | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | YRI | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
NA18906 | hp2 | a0003 | c0005 | t0001 | g0267 | AFR | YRI | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
NA18940 | hp1 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
NA18940 | hp2 | a0001 | c0002 | t0001 | g0136 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
NA18946 | hp1 | a0001 | c0002 | t0001 | g0133 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
NA18946 | hp2 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
NA18947 | hp1 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
NA18947 | hp2 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
NA18948 | hp1 | a0001 | c0002 | t0001 | g0115 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
NA18948 | hp2 | a0006 | c0007 | t0002 | g0262 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
NA18951 | hp1 | a0001 | c0002 | t0001 | g0121 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
NA18951 | hp2 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
NA18954 | hp1 | a0001 | c0001 | t0002 | g0252 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
NA18954 | hp2 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
NA18961 | hp1 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
NA18961 | hp2 | a0001 | c0002 | t0001 | g0044 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
NA18962 | hp1 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
NA18962 | hp2 | a0001 | c0002 | t0001 | g0021 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
NA18963 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
NA18963 | hp2 | a0001 | c0001 | t0002 | g0172 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
NA18967 | hp1 | a0001 | c0002 | t0001 | g0088 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
NA18967 | hp2 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
NA18969 | hp1 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
NA18969 | hp2 | a0001 | c0001 | t0002 | g0232 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
NA18972 | hp1 | a0001 | c0002 | t0001 | g0112 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
NA18972 | hp2 | a0001 | c0002 | t0001 | g0122 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
NA18978 | hp1 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
NA18978 | hp2 | a0001 | c0002 | t0001 | g0087 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
NA18988 | hp1 | a0001 | c0001 | t0002 | g0225 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
NA18988 | hp2 | a0006 | c0007 | t0002 | g0173 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
NA18993 | hp1 | a0001 | c0001 | t0002 | g0246 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
NA18993 | hp2 | a0002 | c0003 | t0001 | g0058 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
NA18995 | hp1 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
NA18995 | hp2 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
NA18998 | hp1 | a0001 | c0002 | t0001 | g0071 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
NA18998 | hp2 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
NA19001 | hp1 | a0001 | c0002 | t0001 | g0135 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
NA19001 | hp2 | a0001 | c0001 | t0002 | g0248 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
NA19004 | hp1 | a0001 | c0002 | t0001 | g0089 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
NA19004 | hp2 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
NA19006 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
NA19006 | hp2 | a0001 | c0001 | t0002 | g0254 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
NA19011 | hp1 | a0001 | c0002 | t0001 | g0091 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
NA19011 | hp2 | a0008 | c0013 | t0002 | g0196 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
NA19030 | hp1 | a0001 | c0002 | t0001 | g0070 | AFR | LWK | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
NA19030 | hp2 | a0001 | c0002 | t0003 | g0080 | AFR | LWK | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | LWK | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
NA19043 | hp2 | a0001 | c0002 | t0001 | g0097 | AFR | LWK | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
NA19054 | hp1 | a0002 | c0003 | t0001 | g0046 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
NA19054 | hp2 | a0001 | c0001 | t0002 | g0264 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
NA19056 | hp1 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
NA19056 | hp2 | a0001 | c0001 | t0002 | g0250 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
NA19066 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
NA19066 | hp2 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
NA19067 | hp1 | a0007 | c0012 | t0002 | g0258 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
NA19067 | hp2 | a0001 | c0002 | t0001 | g0120 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
NA19070 | hp1 | a0001 | c0002 | t0001 | g0092 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
NA19070 | hp2 | a0001 | c0001 | t0002 | g0249 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
NA19072 | hp1 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
NA19072 | hp2 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
NA19075 | hp1 | a0001 | c0002 | t0001 | g0105 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
NA19075 | hp2 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
NA19080 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
NA19080 | hp2 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
NA19083 | hp1 | a0001 | c0002 | t0001 | g0084 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
NA19083 | hp2 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
NA19240 | hp1 | a0001 | c0002 | t0007 | g0095 | AFR | YRI | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
NA19240 | hp2 | a0001 | c0001 | t0005 | g0146 | AFR | YRI | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
NA20129 | hp1 | a0001 | c0002 | t0001 | g0114 | AFR | ASW | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
NA20129 | hp2 | a0003 | c0005 | t0001 | g0266 | AFR | ASW | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
NA20752 | hp1 | a0001 | c0002 | t0001 | g0047 | EUR | TSI | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0234 | EUR | TSI | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0191 | SAS | GIH | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
NA20905 | hp2 | a0001 | c0002 | t0001 | g0019 | SAS | GIH | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG01123 | hp1 | a0005 | c0006 | t0001 | g0040 | AMR | CLM | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG01123 | hp2 | a0001 | c0001 | t0002 | g0221 | AMR | CLM | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG02109 | hp1 | a0001 | c0002 | t0001 | g0023 | AFR | ACB | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | ACB | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG02486 | hp1 | a0001 | c0002 | t0003 | g0033 | AFR | ACB | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG02486 | hp2 | a0001 | c0001 | t0004 | g0274 | AFR | ACB | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG02559 | hp1 | a0001 | c0014 | t0008 | g0119 | AFR | ACB | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | ACB | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG03471 | hp1 | a0001 | c0002 | t0001 | g0024 | AFR | MSL | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | MSL | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG06807 | hp1 | a0001 | c0002 | t0007 | g0111 | AFR | USA | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | USA | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
NA18955 | hp1 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
NA18955 | hp2 | a0001 | c0001 | t0002 | g0261 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | LWK | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
NA21309 | hp2 | a0001 | c0002 | t0003 | g0037 | AFR | LWK | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0001 | g0043 | REF | REF | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
homoSapiens_grch38 | hp1 | a0001 | c0002 | t0001 | g0055 | REF | REF | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:30178156
|
A | C | 1 | a0005 | 3 | HG00099.hp1 HG01123.hp1 HG01496.hp2 |
missense_variant | MODERATE | c.257A>C | p.Lys86Thr | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 4/7 | 285/2506 | 257/1677 | 86/558 | chr17 | 30178156 | ||
chr17:30178165
|
A | G | 1 | a0012 | 1 | HG03579.hp1 | missense_variant | MODERATE | c.266A>G | p.Asn89Ser | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 4/7 | 294/2506 | 266/1677 | 89/558 | chr17 | 30178165 | ||
chr17:30184866
|
G | A | 1 | a0002 | 7 | HG01346.hp2 HG01978.hp2 HG01993.hp2 others(4): Show |
missense_variant | MODERATE | c.869G>A | p.Arg290Gln | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 7/7 | 897/2506 | 869/1677 | 290/558 | chr17 | 30184866 | ||
chr17:30184978
|
C | G | 1 | a0011 | 1 | HG03669.hp2 | missense_variant | MODERATE | c.981C>G | p.Asp327Glu | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 7/7 | 1009/2506 | 981/1677 | 327/558 | chr17 | 30184978 | ||
chr17:30185021
|
G | A | 1 | a0010 | 1 | HG03486.hp1 | missense_variant | MODERATE | c.1024G>A | p.Asp342Asn | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 7/7 | 1052/2506 | 1024/1677 | 342/558 | chr17 | 30185021 | ||
chr17:30185305
|
T | G | 1 | a0006 | 2 | NA18948.hp2 NA18988.hp2 |
missense_variant | MODERATE | c.1308T>G | p.Asp436Glu | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 7/7 | 1336/2506 | 1308/1677 | 436/558 | chr17 | 30185305 | ||
chr17:30185315
|
C | G | 1 | a0003 | 3 | HG02895.hp1 NA18906.hp2 NA20129.hp2 |
missense_variant | MODERATE | c.1318C>G | p.Arg440Gly | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 7/7 | 1346/2506 | 1318/1677 | 440/558 | chr17 | 30185315 | ||
chr17:30185316
|
G | A | 1 | a0007 | 1 | NA19067.hp1 | missense_variant | MODERATE | c.1319G>A | p.Arg440Gln | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 7/7 | 1347/2506 | 1319/1677 | 440/558 | chr17 | 30185316 | ||
chr17:30185387
|
G | A | 1 | a0004 | 3 | HG00280.hp1 HG01070.hp2 HG01071.hp1 |
missense_variant | MODERATE | c.1390G>A | p.Asp464Asn | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 7/7 | 1418/2506 | 1390/1677 | 464/558 | chr17 | 30185387 | ||
chr17:30185499
|
G | C | 1 | a0009 | 1 | HG01168.hp1 | missense_variant | MODERATE | c.1502G>C | p.Arg501Thr | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 7/7 | 1530/2506 | 1502/1677 | 501/558 | chr17 | 30185499 | ||
chr17:30185631
|
C | T | 1 | a0008 | 1 | NA19011.hp2 | missense_variant | MODERATE | c.1634C>T | p.Ala545Val | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 7/7 | 1662/2506 | 1634/1677 | 545/558 | chr17 | 30185631 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:30184840
|
G | A | 1 | a0001c0008 | 1 | HG02976.hp1 | synonymous_variant | LOW | c.843G>A | p.Lys281Lys | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 7/7 | 871/2506 | 843/1677 | 281/558 | chr17 | 30184840 | ||
chr17:30184909
|
G | A | 1 | a0001c0009 | 1 | HG02055.hp2 | synonymous_variant | LOW | c.912G>A | p.Thr304Thr | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 7/7 | 940/2506 | 912/1677 | 304/558 | chr17 | 30184909 | ||
chr17:30184960
|
G | A | 8 | a0001c0001a0001c0008a0001c0009others(5): Show | 137 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(134): Show |
synonymous_variant | LOW | c.963G>A | p.Gln321Gln | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 7/7 | 991/2506 | 963/1677 | 321/558 | chr17 | 30184960 | ||
chr17:30185098
|
G | A | 1 | a0001c0014 | 1 | HG02559.hp1 | synonymous_variant | LOW | c.1101G>A | p.Ala367Ala | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 7/7 | 1129/2506 | 1101/1677 | 367/558 | chr17 | 30185098 | ||
chr17:30185233
|
G | A | 1 | a0001c0011 | 1 | HG03704.hp1 | synonymous_variant | LOW | c.1236G>A | p.Glu412Glu | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 7/7 | 1264/2506 | 1236/1677 | 412/558 | chr17 | 30185233 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:30116816
|
G | A | 2 | a0001c0002t0003a0012c0017t0003 | 19 | HG01069.hp1 HG01071.hp2 HG01109.hp1 others(16): Show |
5_prime_UTR_variant | MODIFIER | c.-28G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 1/7 | 28 | chr17 | 30116816 | |||||
chr17:30185736
|
C | T | 1 | a0001c0002t0009 | 1 | HG03017.hp2 | 3_prime_UTR_variant | MODIFIER | c.*62C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 7/7 | 62 | chr17 | 30185736 | |||||
chr17:30185745
|
A | G | 1 | a0001c0002t0007 | 2 | HG06807.hp1 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*71A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 7/7 | 71 | chr17 | 30185745 | |||||
chr17:30185839
|
A | G | 1 | a0001c0001t0004 | 4 | HG01433.hp1 HG02486.hp2 HG02615.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*165A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 7/7 | 165 | chr17 | 30185839 | |||||
chr17:30185988
|
G | A | 1 | a0001c0001t0005 | 3 | HG02922.hp2 HG03195.hp1 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*314G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 7/7 | 314 | chr17 | 30185988 | |||||
chr17:30186047
|
A | T | 1 | a0001c0014t0008 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*373A>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 7/7 | 373 | chr17 | 30186047 | |||||
chr17:30186158
|
G | A | 7 | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(4): Show | 105 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(102): Show |
3_prime_UTR_variant | MODIFIER | c.*484G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 7/7 | 484 | chr17 | 30186158 | |||||
chr17:30186430
|
C | T | 1 | a0001c0001t0006 | 2 | HG01168.hp2 HG01169.hp1 |
3_prime_UTR_variant | MODIFIER | c.*756C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 7/7 | 756 | chr17 | 30186430 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:30117165
|
A | C | 113 | a0001c0001t0002g0170a0001c0001t0002g0171a0001c0001t0002g0172others(110): Show | 113 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.20+302A>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 1/6 | chr17 | 30117165 | ||||||
chr17:30117208
|
G | C | 4 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(1): Show | 4 | NA18963.hp1 NA19006.hp1 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.20+345G>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 1/6 | chr17 | 30117208 | ||||||
chr17:30117236
|
T | A | 96 | a0001c0001t0002g0170a0001c0001t0002g0171a0001c0001t0002g0172others(93): Show | 96 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.20+373T>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 1/6 | chr17 | 30117236 | ||||||
chr17:30117756
|
CAT | C | 22 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144others(19): Show | 22 | HG01243.hp2 HG01884.hp1 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.21-323_21-322delAT | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 1/6 | chr17 | 30117756 | ||||||
chr17:30117756
|
CATG | C | 3 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140 | 3 | HG03139.hp2 NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.21-323_21-321delAT others(1): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 1/6 | chr17 | 30117756 | ||||||
chr17:30117757
|
A | G | 7 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0165others(4): Show | 7 | HG01891.hp1 HG01934.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.21-323A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 1/6 | chr17 | 30117757 | ||||||
chr17:30117758
|
TG | T | 7 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0165others(4): Show | 7 | HG01891.hp1 HG01934.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.21-321delG | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 1/6 | chr17 | 30117758 | ||||||
chr17:30117759
|
G | GT | 6 | a0001c0001t0002g0264a0001c0001t0002g0265a0001c0002t0001g0134others(3): Show | 6 | HG02738.hp1 HG02738.hp2 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.21-303dupT | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 30117759 | |||||
chr17:30117759
|
GT | G | 19 | a0001c0001t0002g0170a0001c0001t0002g0171a0001c0001t0002g0172others(16): Show | 19 | HG00597.hp1 HG00741.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.21-303delT | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 30117759 | |||||
chr17:30117760
|
T | G | 3 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140 | 3 | HG03139.hp2 NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.21-320T>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 1/6 | chr17 | 30117760 | ||||||
chr17:30117944
|
A | C | 2 | a0001c0001t0001g0161a0001c0001t0001g0162 | 2 | HG01884.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.21-136A>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 1/6 | chr17 | 30117944 | ||||||
chr17:30117966
|
A | G | 1 | a0001c0002t0001g0133 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.21-114A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 1/6 | chr17 | 30117966 | ||||||
chr17:30118199
|
G | A | 1 | a0001c0001t0002g0174 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.114+26G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30118199 | ||||||
chr17:30118414
|
T | TG | 3 | a0001c0001t0002g0174a0001c0001t0002g0175a0001c0001t0002g0176 | 3 | HG02258.hp2 HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.114+241_114+242ins others(1): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30118414 | ||||||
chr17:30118556
|
C | T | 2 | a0001c0001t0001g0160a0001c0002t0001g0132 | 2 | HG02074.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.114+383C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30118556 | ||||||
chr17:30118713
|
A | G | 3 | a0001c0001t0002g0263a0006c0007t0002g0173a0006c0007t0002g0262 | 3 | HG00741.hp1 NA18948.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.114+540A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30118713 | ||||||
chr17:30118749
|
C | CT | 8 | a0001c0001t0002g0176a0001c0001t0002g0260a0001c0001t0002g0261others(5): Show | 8 | HG02451.hp2 HG02723.hp1 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.114+593dupT | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30118749 | |||||
chr17:30118749
|
CT | C | 13 | a0001c0001t0001g0142a0001c0001t0002g0177a0001c0001t0002g0178others(10): Show | 13 | HG01070.hp1 HG01099.hp1 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.114+593delT | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30118749 | |||||
chr17:30118750
|
T | TC | 7 | a0001c0001t0002g0270a0001c0001t0002g0271a0001c0001t0002g0276others(4): Show | 7 | HG01433.hp1 HG01884.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.114+577_114+578ins others(1): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30118750 | ||||||
chr17:30118751
|
T | C | 4 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(1): Show | 4 | HG03139.hp2 HG03486.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.114+578T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30118751 | ||||||
chr17:30118879
|
G | C | 4 | a0001c0002t0001g0022a0001c0002t0001g0023a0001c0002t0001g0024others(1): Show | 4 | HG02109.hp1 HG03195.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.114+706G>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30118879 | ||||||
chr17:30119119
|
C | T | 1 | a0001c0002t0001g0127 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.114+946C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30119119 | ||||||
chr17:30119208
|
A | G | 6 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0001g0166others(3): Show | 6 | HG01891.hp1 HG01934.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.114+1035A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30119208 | ||||||
chr17:30119401
|
C | T | 1 | a0001c0001t0002g0259 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.114+1228C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30119401 | ||||||
chr17:30119508
|
G | A | 1 | a0001c0001t0002g0180 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.114+1335G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30119508 | ||||||
chr17:30119525
|
T | C | 1 | a0001c0001t0002g0181 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.114+1352T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30119525 | ||||||
chr17:30119583
|
A | T | 1 | a0001c0002t0001g0021 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.114+1410A>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30119583 | ||||||
chr17:30119619
|
C | T | 1 | a0001c0001t0001g0160 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.114+1446C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30119619 | ||||||
chr17:30119785
|
G | T | 1 | a0001c0002t0001g0127 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.114+1612G>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30119785 | ||||||
chr17:30120072
|
C | T | 11 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(8): Show | 11 | HG01243.hp2 HG01884.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.114+1899C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30120072 | ||||||
chr17:30120076
|
C | T | 4 | a0001c0002t0001g0123a0001c0002t0001g0124a0001c0002t0001g0125others(1): Show | 4 | HG02622.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.114+1903C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30120076 | ||||||
chr17:30120082
|
C | T | 9 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0157others(6): Show | 9 | HG01243.hp2 HG01884.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.114+1909C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30120082 | ||||||
chr17:30120085
|
A | G | 7 | a0001c0001t0002g0270a0001c0001t0002g0271a0001c0001t0002g0276others(4): Show | 7 | HG01433.hp1 HG01884.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.114+1912A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30120085 | ||||||
chr17:30120123
|
T | C | 2 | a0001c0002t0001g0128a0001c0002t0001g0129 | 2 | HG02723.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.114+1950T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30120123 | ||||||
chr17:30120235
|
AT | A | 7 | a0001c0001t0002g0270a0001c0001t0002g0271a0001c0001t0002g0276others(4): Show | 7 | HG01433.hp1 HG01884.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.114+2068delT | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30120235 | |||||
chr17:30120320
|
A | C | 3 | a0001c0002t0001g0120a0001c0002t0001g0121a0001c0002t0001g0122 | 3 | NA18951.hp1 NA18972.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.114+2147A>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30120320 | ||||||
chr17:30120347
|
A | G | 2 | a0001c0001t0001g0158a0001c0001t0001g0159 | 2 | HG01243.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.114+2174A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30120347 | ||||||
chr17:30120381
|
C | G | 8 | a0001c0001t0001g0151a0001c0001t0001g0163a0001c0001t0001g0164others(5): Show | 8 | HG01891.hp1 HG01934.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.114+2208C>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30120381 | ||||||
chr17:30120388
|
A | G | 1 | a0001c0014t0008g0119 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.114+2215A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30120388 | ||||||
chr17:30120552
|
T | TA | 8 | a0001c0001t0001g0151a0001c0001t0001g0163a0001c0001t0001g0164others(5): Show | 8 | HG01891.hp1 HG01934.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.114+2380dupA | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30120552 | |||||
chr17:30120664
|
G | A | 3 | a0003c0005t0001g0266a0003c0005t0001g0267a0003c0005t0001g0268 | 3 | HG02895.hp1 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.114+2491G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30120664 | ||||||
chr17:30120872
|
C | T | 1 | a0005c0006t0001g0118 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.114+2699C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30120872 | ||||||
chr17:30121035
|
C | T | 4 | a0001c0002t0001g0114a0001c0002t0001g0115a0001c0002t0001g0116others(1): Show | 4 | HG01952.hp2 HG02273.hp2 NA18948.hp1 others(1): Show |
intron_variant | MODIFIER | c.114+2862C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30121035 | ||||||
chr17:30121094
|
T | C | 1 | a0001c0002t0001g0120 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.114+2921T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30121094 | ||||||
chr17:30121394
|
AG | A | 8 | a0001c0001t0001g0151a0001c0001t0001g0163a0001c0001t0001g0164others(5): Show | 8 | HG01891.hp1 HG01934.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.114+3222delG | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30121394 | ||||||
chr17:30121453
|
C | CT | 14 | a0001c0001t0001g0148a0001c0001t0001g0157a0001c0001t0002g0256others(11): Show | 14 | HG01069.hp2 HG02055.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.114+3296dupT | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30121453 | |||||
chr17:30121570
|
G | GT | 60 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(57): Show | 60 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.114+3412dupT | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30121570 | |||||
chr17:30121570
|
G | GTT | 6 | a0001c0001t0002g0265a0001c0001t0002g0276a0001c0002t0001g0110others(3): Show | 6 | HG00609.hp1 HG02145.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.114+3411_114+3412d others(4): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30121570 | |||||
chr17:30121570
|
GT | G | 20 | a0001c0002t0001g0021a0001c0002t0001g0269a0001c0002t0001g0277others(17): Show | 20 | HG00741.hp2 HG01069.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.114+3412delT | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30121570 | |||||
chr17:30121591
|
G | A | 9 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0157others(6): Show | 9 | HG01243.hp2 HG01884.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.114+3418G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30121591 | ||||||
chr17:30121676
|
TCTC | T | 28 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144others(25): Show | 28 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(25): Show |
intron_variant | MODIFIER | c.114+3506_114+3508d others(5): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30121676 | |||||
chr17:30121819
|
C | T | 6 | a0001c0001t0002g0247a0001c0001t0002g0248a0001c0001t0002g0249others(3): Show | 6 | HG00597.hp2 NA18954.hp1 NA18995.hp2 others(3): Show |
intron_variant | MODIFIER | c.114+3646C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30121819 | ||||||
chr17:30121860
|
G | T | 1 | a0001c0002t0001g0083 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.114+3687G>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30121860 | ||||||
chr17:30122017
|
G | T | 94 | a0001c0001t0002g0081a0001c0001t0002g0082a0001c0001t0002g0171others(91): Show | 94 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.114+3844G>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122017 | ||||||
chr17:30122253
|
T | G | 2 | a0001c0001t0002g0270a0001c0001t0002g0271 | 2 | HG01884.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.114+4080T>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122253 | ||||||
chr17:30122348
|
GTTTCA | G | 6 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0159others(3): Show | 6 | HG01243.hp2 HG01884.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.114+4177_114+4181d others(7): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30122348 | |||||
chr17:30122348
|
GTTTCATA others(4): Show |
G | 1 | a0001c0001t0001g0148 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.114+4177_114+4187d others(13): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30122348 | |||||
chr17:30122349
|
T | TGTG | 8 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144others(5): Show | 8 | HG01891.hp1 HG02109.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.114+4176_114+4177i others(5): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122349 | ||||||
chr17:30122349
|
T | TGTGTG | 3 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0164 | 3 | HG01891.hp2 HG02451.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.114+4176_114+4177i others(7): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122349 | ||||||
chr17:30122349
|
T | TGTGTGTG others(14): Show |
1 | a0001c0001t0005g0147 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.114+4176_114+4177i others(23): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122349 | ||||||
chr17:30122349
|
T | TGTGTGTG others(18): Show |
1 | a0001c0001t0005g0146 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.114+4176_114+4177i others(27): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122349 | ||||||
chr17:30122350
|
T | G | 3 | a0001c0001t0001g0151a0001c0001t0001g0154a0001c0001t0001g0168 | 3 | HG02717.hp2 HG02886.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.114+4177T>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122350 | ||||||
chr17:30122351
|
T | A | 3 | a0001c0001t0001g0164a0001c0001t0005g0146a0001c0001t0005g0147 | 3 | HG02723.hp2 HG03195.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.114+4178T>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122351 | ||||||
chr17:30122351
|
T | G | 11 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144others(8): Show | 11 | HG01891.hp1 HG01891.hp2 HG01934.hp2 others(8): Show |
intron_variant | MODIFIER | c.114+4178T>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122351 | ||||||
chr17:30122351
|
TC | T | 6 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(3): Show | 6 | HG02717.hp2 HG02886.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.114+4179delC | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122351 | ||||||
chr17:30122352
|
C | CAT | 5 | a0001c0002t0001g0005a0001c0002t0001g0023a0001c0002t0001g0093others(2): Show | 5 | HG00597.hp1 HG01081.hp2 HG02074.hp2 others(2): Show |
intron_variant | MODIFIER | c.114+4212_114+4213d others(4): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30122352 | |||||
chr17:30122352
|
C | CATATAT | 10 | a0001c0001t0002g0212a0001c0001t0002g0225a0001c0001t0002g0226others(7): Show | 10 | HG01361.hp2 HG01496.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.114+4208_114+4213d others(8): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30122352 | |||||
chr17:30122352
|
C | CATATATA others(1): Show |
5 | a0001c0001t0002g0192a0001c0001t0002g0198a0001c0001t0002g0199others(2): Show | 5 | HG02602.hp1 HG04115.hp1 NA18961.hp1 others(2): Show |
intron_variant | MODIFIER | c.114+4206_114+4213d others(10): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30122352 | |||||
chr17:30122352
|
C | CATATATA others(3): Show |
9 | a0001c0001t0002g0193a0001c0001t0002g0194a0001c0001t0002g0195others(6): Show | 9 | HG00639.hp2 HG00733.hp1 HG01255.hp1 others(6): Show |
intron_variant | MODIFIER | c.114+4204_114+4213d others(12): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30122352 | |||||
chr17:30122352
|
C | CATATATA others(5): Show |
3 | a0001c0001t0002g0189a0001c0001t0002g0209a0001c0001t0002g0253 | 3 | HG00280.hp2 HG03239.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.114+4202_114+4213d others(14): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30122352 | |||||
chr17:30122352
|
C | CATATATA others(7): Show |
3 | a0001c0001t0002g0185a0001c0001t0002g0186a0001c0001t0002g0248 | 3 | HG02273.hp1 HG04204.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.114+4200_114+4213d others(16): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30122352 | |||||
chr17:30122352
|
C | CATATATA others(9): Show |
1 | a0001c0001t0002g0171 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.114+4198_114+4213d others(18): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30122352 | |||||
chr17:30122352
|
C | CATATATA others(11): Show |
1 | a0001c0001t0002g0188 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.114+4196_114+4213d others(20): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30122352 | |||||
chr17:30122352
|
C | CATATATA others(13): Show |
1 | a0001c0001t0002g0184 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.114+4194_114+4213d others(22): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30122352 | |||||
chr17:30122352
|
C | CATATATA others(41): Show |
1 | a0001c0001t0002g0182 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.114+4213_114+4214i others(50): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30122352 | |||||
chr17:30122352
|
C | T | 15 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144others(12): Show | 15 | HG01891.hp1 HG01891.hp2 HG01934.hp2 others(12): Show |
intron_variant | MODIFIER | c.114+4179C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122352 | ||||||
chr17:30122352
|
CAT | C | 5 | a0001c0002t0001g0020a0001c0002t0001g0071a0001c0002t0001g0120others(2): Show | 5 | HG02004.hp1 HG03834.hp2 NA18940.hp2 others(2): Show |
intron_variant | MODIFIER | c.114+4212_114+4213d others(4): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30122352 | |||||
chr17:30122352
|
CATAT | C | 5 | a0001c0001t0002g0244a0001c0002t0001g0070a0001c0002t0001g0106others(2): Show | 5 | HG00639.hp1 HG01993.hp2 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.114+4210_114+4213d others(6): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30122352 | |||||
chr17:30122352
|
CATATAT | C | 3 | a0001c0002t0001g0072a0001c0002t0001g0073a0001c0002t0001g0074 | 3 | HG00323.hp2 HG02698.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.114+4208_114+4213d others(8): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30122352 | |||||
chr17:30122353
|
A | G | 10 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144others(7): Show | 10 | HG01934.hp2 HG02717.hp2 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.114+4180A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122353 | ||||||
chr17:30122355
|
A | G | 15 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144others(12): Show | 15 | HG01243.hp2 HG01884.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.114+4182A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122355 | ||||||
chr17:30122357
|
A | G | 14 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144others(11): Show | 14 | HG01243.hp2 HG01884.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.114+4184A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122357 | ||||||
chr17:30122359
|
A | G | 10 | a0001c0001t0001g0155a0001c0001t0001g0157a0001c0001t0001g0158others(7): Show | 10 | HG01243.hp2 HG01884.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.114+4186A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122359 | ||||||
chr17:30122361
|
A | G | 10 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0157others(7): Show | 10 | HG01243.hp2 HG01884.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.114+4188A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122361 | ||||||
chr17:30122363
|
A | G | 4 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0005g0150others(1): Show | 4 | HG02055.hp2 HG02809.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.114+4190A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122363 | ||||||
chr17:30122365
|
A | G | 2 | a0001c0001t0001g0148a0001c0009t0001g0149 | 2 | HG02055.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.114+4192A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122365 | ||||||
chr17:30122367
|
A | G | 2 | a0001c0001t0001g0148a0001c0009t0001g0149 | 2 | HG02055.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.114+4194A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122367 | ||||||
chr17:30122369
|
A | G | 2 | a0001c0001t0001g0148a0001c0009t0001g0149 | 2 | HG02055.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.114+4196A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122369 | ||||||
chr17:30122369
|
ATATATAT others(13): Show |
A | 1 | a0001c0001t0002g0179 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.114+4198_114+4217d others(22): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30122369 | |||||
chr17:30122369
|
ATATATAT others(26): Show |
A | 1 | a0001c0002t0003g0037 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.114+4198_114+4230d others(35): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30122369 | |||||
chr17:30122371
|
A | G | 1 | a0001c0001t0001g0148 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.114+4198A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122371 | ||||||
chr17:30122371
|
ATATATAT others(25): Show |
A | 18 | a0001c0002t0003g0014a0001c0002t0003g0025a0001c0002t0003g0026others(15): Show | 18 | HG01069.hp1 HG01071.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.114+4200_114+4231d others(34): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30122371 | |||||
chr17:30122373
|
A | G | 1 | a0001c0001t0002g0259 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.114+4200A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122373 | ||||||
chr17:30122373
|
ATATATAT others(23): Show |
A | 1 | a0001c0002t0001g0281 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.114+4202_114+4231d others(32): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30122373 | |||||
chr17:30122373
|
ATATATAT others(24): Show |
A | 6 | a0001c0002t0001g0269a0001c0002t0001g0277a0001c0002t0001g0278others(3): Show | 6 | HG00741.hp2 HG01243.hp1 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.114+4202_114+4232d others(33): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30122373 | |||||
chr17:30122375
|
ATATATAT others(4): Show |
A | 1 | a0001c0001t0004g0275 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.114+4204_114+4214d others(13): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30122375 | |||||
chr17:30122377
|
ATATATAT others(5): Show |
A | 1 | a0001c0002t0001g0108 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.114+4206_114+4217d others(14): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30122377 | |||||
chr17:30122377
|
ATATATAT others(6): Show |
A | 2 | a0001c0001t0002g0245a0001c0001t0002g0246 | 2 | HG00609.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.114+4206_114+4218d others(15): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30122377 | |||||
chr17:30122377
|
ATATATAT others(7): Show |
A | 1 | a0001c0001t0002g0172 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.114+4206_114+4219d others(16): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30122377 | |||||
chr17:30122377
|
ATATATAT others(11): Show |
A | 1 | a0001c0001t0002g0170 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.114+4206_114+4223d others(20): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30122377 | |||||
chr17:30122379
|
ATATATAT others(14): Show |
A | 2 | a0001c0001t0001g0139a0001c0001t0001g0140 | 2 | NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.114+4208_114+4228d others(23): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30122379 | |||||
chr17:30122379
|
ATATATAT others(15): Show |
A | 1 | a0001c0001t0001g0138 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.114+4208_114+4229d others(24): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30122379 | |||||
chr17:30122380
|
TATATA | T | 3 | a0001c0002t0001g0075a0001c0002t0001g0076a0001c0002t0001g0107 | 3 | HG00140.hp2 HG00733.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.114+4208_114+4212d others(7): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122380 | ||||||
chr17:30122383
|
ATATTTT | A | 6 | a0001c0001t0002g0243a0001c0002t0001g0013a0001c0002t0001g0018others(3): Show | 6 | HG01167.hp1 HG01169.hp2 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.114+4212_114+4217d others(8): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30122383 | |||||
chr17:30122385
|
A | ATATATAT others(4): Show |
1 | a0001c0001t0002g0219 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.114+4213_114+4214i others(13): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30122385 | |||||
chr17:30122385
|
A | ATATATAT others(15): Show |
1 | a0001c0001t0002g0181 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.114+4213_114+4214i others(24): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30122385 | |||||
chr17:30122385
|
A | ATATATAT others(6): Show |
1 | a0001c0001t0002g0220 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.114+4213_114+4214i others(15): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30122385 | |||||
chr17:30122385
|
A | T | 2 | a0001c0002t0001g0071a0001c0002t0001g0126 | 2 | HG02622.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.114+4212A>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122385 | ||||||
chr17:30122385
|
AT | A | 15 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144others(12): Show | 15 | HG00323.hp1 HG01891.hp1 HG01934.hp2 others(12): Show |
intron_variant | MODIFIER | c.114+4250delT | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30122385 | |||||
chr17:30122385
|
ATT | A | 9 | a0001c0002t0001g0007a0001c0002t0001g0008a0001c0002t0001g0024others(6): Show | 9 | HG02630.hp2 HG03471.hp1 HG03490.hp2 others(6): Show |
intron_variant | MODIFIER | c.114+4249_114+4250d others(4): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30122385 | |||||
chr17:30122385
|
ATTT | A | 14 | a0001c0001t0001g0151a0001c0002t0001g0001a0001c0002t0001g0042others(11): Show | 14 | HG00642.hp2 HG01168.hp1 HG01361.hp1 others(11): Show |
intron_variant | MODIFIER | c.114+4248_114+4250d others(5): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30122385 | |||||
chr17:30122385
|
ATTTT | A | 11 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0048others(8): Show | 11 | HG00280.hp1 HG01071.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.114+4247_114+4250d others(6): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30122385 | |||||
chr17:30122385
|
ATTTTT | A | 11 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0002g0175others(8): Show | 11 | HG01070.hp2 HG01884.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.114+4246_114+4250d others(7): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30122385 | |||||
chr17:30122385
|
ATTTTTT | A | 7 | a0001c0001t0001g0155a0001c0002t0001g0006a0001c0002t0001g0015others(4): Show | 7 | HG01099.hp1 HG02148.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.114+4245_114+4250d others(8): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30122385 | |||||
chr17:30122385
|
ATTTTTTT others(3): Show |
A | 1 | a0003c0005t0001g0266 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.114+4241_114+4250d others(12): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30122385 | |||||
chr17:30122386
|
T | TA | 9 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0002g0270others(6): Show | 9 | HG00140.hp1 HG01496.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.114+4213_114+4214i others(3): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122386 | ||||||
chr17:30122386
|
T | TATATA | 16 | a0001c0001t0002g0082a0001c0001t0002g0191a0001c0001t0002g0197others(13): Show | 16 | HG00099.hp2 HG00642.hp1 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.114+4213_114+4214i others(7): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122386 | ||||||
chr17:30122386
|
T | TATATATA | 6 | a0001c0001t0002g0213a0001c0001t0002g0214a0001c0001t0002g0230others(3): Show | 6 | HG00597.hp2 HG02683.hp1 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.114+4213_114+4214i others(9): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122386 | ||||||
chr17:30122386
|
T | TATATATA others(2): Show |
8 | a0001c0001t0002g0081a0001c0001t0002g0200a0001c0001t0002g0201others(5): Show | 8 | HG01081.hp1 HG01167.hp2 HG02293.hp2 others(5): Show |
intron_variant | MODIFIER | c.114+4213_114+4214i others(11): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122386 | ||||||
chr17:30122386
|
T | TATATATA others(4): Show |
3 | a0001c0001t0002g0207a0001c0001t0002g0208a0001c0001t0002g0250 | 3 | HG02293.hp1 HG03927.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.114+4213_114+4214i others(13): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122386 | ||||||
chr17:30122386
|
T | TATATATA others(6): Show |
2 | a0001c0001t0002g0190a0001c0001t0002g0260 | 2 | NA18946.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.114+4213_114+4214i others(15): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122386 | ||||||
chr17:30122386
|
T | TATATATA others(8): Show |
1 | a0001c0001t0002g0187 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.114+4213_114+4214i others(17): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122386 | ||||||
chr17:30122386
|
T | TATATATA others(12): Show |
1 | a0001c0001t0002g0264 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.114+4213_114+4214i others(21): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122386 | ||||||
chr17:30122386
|
T | TATATATA others(16): Show |
1 | a0001c0001t0002g0183 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.114+4213_114+4214i others(25): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122386 | ||||||
chr17:30122386
|
T | TATATATA others(18): Show |
1 | a0001c0002t0001g0134 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.114+4213_114+4214i others(27): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122386 | ||||||
chr17:30122387
|
T | A | 48 | a0001c0001t0001g0148a0001c0001t0001g0152a0001c0001t0001g0153others(45): Show | 48 | HG00099.hp1 HG00280.hp2 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.114+4214T>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122387 | ||||||
chr17:30122388
|
T | A | 49 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144others(46): Show | 49 | HG00099.hp2 HG00323.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.114+4215T>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122388 | ||||||
chr17:30122389
|
T | A | 23 | a0001c0001t0001g0168a0001c0001t0002g0182a0001c0001t0002g0185others(20): Show | 23 | HG00280.hp2 HG00597.hp1 HG00639.hp2 others(20): Show |
intron_variant | MODIFIER | c.114+4216T>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122389 | ||||||
chr17:30122390
|
T | A | 31 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144others(28): Show | 31 | HG00323.hp1 HG00597.hp2 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.114+4217T>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122390 | ||||||
chr17:30122391
|
T | A | 12 | a0001c0001t0002g0182a0001c0001t0002g0192a0001c0002t0001g0005others(9): Show | 12 | HG00597.hp1 HG02074.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.114+4218T>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122391 | ||||||
chr17:30122392
|
T | A | 19 | a0001c0001t0001g0151a0001c0001t0001g0163a0001c0001t0001g0164others(16): Show | 19 | HG00597.hp2 HG00741.hp1 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.114+4219T>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122392 | ||||||
chr17:30122393
|
T | A | 4 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0022others(1): Show | 4 | HG00597.hp1 HG02615.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.114+4220T>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122393 | ||||||
chr17:30122394
|
T | A | 11 | a0001c0001t0001g0151a0001c0001t0001g0164a0001c0001t0001g0165others(8): Show | 11 | HG00597.hp2 HG01891.hp1 HG01934.hp2 others(8): Show |
intron_variant | MODIFIER | c.114+4221T>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122394 | ||||||
chr17:30122395
|
T | A | 3 | a0001c0001t0001g0154a0001c0002t0001g0006a0001c0002t0001g0022 | 3 | HG02886.hp2 HG03195.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.114+4222T>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122395 | ||||||
chr17:30122396
|
T | A | 3 | a0001c0002t0001g0043a0003c0005t0001g0267a0003c0005t0001g0268 | 3 | HG02895.hp1 NA18906.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.114+4223T>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122396 | ||||||
chr17:30122397
|
T | A | 1 | a0003c0005t0001g0266 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.114+4224T>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122397 | ||||||
chr17:30122398
|
T | A | 2 | a0003c0005t0001g0267a0003c0005t0001g0268 | 2 | HG02895.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.114+4225T>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122398 | ||||||
chr17:30122399
|
T | A | 1 | a0003c0005t0001g0266 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.114+4226T>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122399 | ||||||
chr17:30122400
|
T | A | 2 | a0003c0005t0001g0267a0003c0005t0001g0268 | 2 | HG02895.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.114+4227T>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122400 | ||||||
chr17:30122401
|
T | A | 1 | a0003c0005t0001g0266 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.114+4228T>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122401 | ||||||
chr17:30122402
|
T | A | 2 | a0003c0005t0001g0267a0003c0005t0001g0268 | 2 | HG02895.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.114+4229T>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122402 | ||||||
chr17:30122403
|
T | A | 1 | a0003c0005t0001g0266 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.114+4230T>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122403 | ||||||
chr17:30122404
|
T | A | 1 | a0003c0005t0001g0268 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.114+4231T>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122404 | ||||||
chr17:30122405
|
T | A | 1 | a0003c0005t0001g0266 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.114+4232T>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122405 | ||||||
chr17:30122429
|
G | A | 32 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(29): Show | 32 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.114+4256G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122429 | ||||||
chr17:30122463
|
G | A | 2 | a0001c0002t0001g0072a0001c0002t0001g0075 | 2 | HG02735.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.114+4290G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122463 | ||||||
chr17:30122544
|
A | G | 1 | a0001c0001t0002g0203 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.114+4371A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122544 | ||||||
chr17:30122549
|
C | A | 2 | a0005c0006t0001g0040a0005c0006t0001g0118 | 2 | HG00099.hp1 HG01123.hp1 |
intron_variant | MODIFIER | c.114+4376C>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122549 | ||||||
chr17:30122686
|
G | C | 2 | a0001c0001t0001g0152a0001c0001t0001g0153 | 2 | HG01891.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.114+4513G>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122686 | ||||||
chr17:30122718
|
G | A | 1 | a0001c0001t0002g0254 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.114+4545G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122718 | ||||||
chr17:30122732
|
C | T | 1 | a0001c0002t0001g0008 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.114+4559C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122732 | ||||||
chr17:30122978
|
T | C | 1 | a0001c0001t0001g0160 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.114+4805T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122978 | ||||||
chr17:30122995
|
G | A | 6 | a0001c0002t0001g0013a0001c0002t0001g0018a0001c0002t0001g0038others(3): Show | 6 | HG01167.hp1 HG01169.hp2 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.114+4822G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122995 | ||||||
chr17:30122997
|
T | C | 137 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(134): Show | 137 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.114+4824T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122997 | ||||||
chr17:30123011
|
C | T | 2 | a0001c0002t0001g0017a0001c0002t0001g0096 | 2 | HG01361.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.114+4838C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30123011 | ||||||
chr17:30123052
|
TGGGACTA others(64): Show |
T | 20 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144others(17): Show | 20 | HG01243.hp2 HG01884.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.114+4881_114+4951d others(73): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30123052 | |||||
chr17:30123131
|
G | A | 1 | a0001c0002t0007g0111 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.114+4958G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30123131 | ||||||
chr17:30123274
|
C | T | 2 | a0001c0001t0002g0248a0001c0001t0002g0251 | 2 | NA18995.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.114+5101C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30123274 | ||||||
chr17:30123871
|
T | G | 9 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144others(6): Show | 9 | HG02055.hp2 HG02895.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.114+5698T>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30123871 | ||||||
chr17:30123877
|
A | G | 1 | a0010c0010t0001g0141 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.114+5704A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30123877 | ||||||
chr17:30124231
|
C | G | 1 | a0001c0002t0001g0005 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.114+6058C>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30124231 | ||||||
chr17:30124316
|
A | T | 1 | a0001c0002t0001g0130 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.114+6143A>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30124316 | ||||||
chr17:30124578
|
G | A | 1 | a0001c0001t0002g0250 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.114+6405G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30124578 | ||||||
chr17:30124651
|
G | A | 2 | a0001c0001t0001g0152a0001c0001t0001g0153 | 2 | HG01891.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.114+6478G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30124651 | ||||||
chr17:30124847
|
T | C | 137 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(134): Show | 137 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.114+6674T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30124847 | ||||||
chr17:30124848
|
G | A | 1 | a0001c0001t0002g0235 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.114+6675G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30124848 | ||||||
chr17:30124919
|
C | T | 1 | a0001c0002t0001g0071 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.114+6746C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30124919 | ||||||
chr17:30124961
|
G | A | 1 | a0001c0001t0002g0198 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.114+6788G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30124961 | ||||||
chr17:30125131
|
G | A | 1 | a0001c0002t0001g0127 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.114+6958G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30125131 | ||||||
chr17:30125217
|
T | A | 1 | a0001c0001t0002g0260 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.114+7044T>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30125217 | ||||||
chr17:30125584
|
G | T | 2 | a0001c0001t0001g0161a0001c0001t0001g0162 | 2 | HG01884.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.114+7411G>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30125584 | ||||||
chr17:30125608
|
C | T | 1 | a0001c0002t0001g0093 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.114+7435C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30125608 | ||||||
chr17:30125635
|
C | T | 9 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144others(6): Show | 9 | HG02055.hp2 HG02895.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.114+7462C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30125635 | ||||||
chr17:30125986
|
A | C | 1 | a0001c0001t0002g0250 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.114+7813A>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30125986 | ||||||
chr17:30126235
|
GC | G | 4 | a0001c0001t0002g0198a0003c0005t0001g0266a0003c0005t0001g0267others(1): Show | 4 | HG02895.hp1 NA18906.hp2 NA19072.hp1 others(1): Show |
intron_variant | MODIFIER | c.114+8066delC | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30126235 | |||||
chr17:30126287
|
A | T | 1 | a0001c0001t0002g0174 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.114+8114A>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30126287 | ||||||
chr17:30126295
|
G | A | 1 | a0001c0001t0002g0245 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.114+8122G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30126295 | ||||||
chr17:30126335
|
G | C | 1 | a0001c0002t0001g0005 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.114+8162G>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30126335 | ||||||
chr17:30126401
|
A | C | 1 | a0001c0002t0003g0036 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.114+8228A>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30126401 | ||||||
chr17:30126544
|
G | A | 1 | a0001c0001t0002g0239 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.114+8371G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30126544 | ||||||
chr17:30126596
|
A | T | 281 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(278): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.114+8423A>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30126596 | ||||||
chr17:30126709
|
T | C | 1 | a0010c0010t0001g0141 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.114+8536T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30126709 | ||||||
chr17:30126735
|
G | A | 95 | a0001c0001t0002g0081a0001c0001t0002g0082a0001c0001t0002g0170others(92): Show | 95 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.114+8562G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30126735 | ||||||
chr17:30126770
|
G | T | 9 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0157others(6): Show | 9 | HG01243.hp2 HG01884.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.114+8597G>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30126770 | ||||||
chr17:30126839
|
C | G | 1 | a0001c0002t0001g0083 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.114+8666C>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30126839 | ||||||
chr17:30127114
|
A | G | 1 | a0001c0001t0004g0273 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.114+8941A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30127114 | ||||||
chr17:30127258
|
C | G | 2 | a0001c0001t0001g0158a0001c0001t0001g0159 | 2 | HG01243.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.114+9085C>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30127258 | ||||||
chr17:30127405
|
G | C | 105 | a0001c0001t0002g0081a0001c0001t0002g0082a0001c0001t0002g0170others(102): Show | 105 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.114+9232G>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30127405 | ||||||
chr17:30127483
|
C | T | 1 | a0001c0002t0001g0089 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.114+9310C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30127483 | ||||||
chr17:30127551
|
C | T | 1 | a0001c0001t0004g0273 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.114+9378C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30127551 | ||||||
chr17:30127604
|
G | T | 4 | a0001c0001t0002g0202a0001c0001t0002g0206a0001c0001t0002g0229others(1): Show | 4 | NA18947.hp2 NA18967.hp2 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.114+9431G>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30127604 | ||||||
chr17:30127807
|
A | G | 4 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(1): Show | 4 | NA18963.hp1 NA19006.hp1 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.114+9634A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30127807 | ||||||
chr17:30127809
|
A | G | 1 | a0001c0001t0002g0199 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.114+9636A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30127809 | ||||||
chr17:30127835
|
A | T | 1 | a0001c0002t0001g0132 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.114+9662A>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30127835 | ||||||
chr17:30128172
|
T | TTA | 4 | a0001c0001t0002g0202a0001c0001t0002g0206a0001c0001t0002g0229others(1): Show | 4 | NA18947.hp2 NA18967.hp2 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.114+10012_114+1001 others(6): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30128172 | |||||
chr17:30128187
|
A | T | 7 | a0001c0001t0002g0270a0001c0001t0002g0271a0001c0001t0002g0276others(4): Show | 7 | HG01433.hp1 HG01884.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.114+10014A>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30128187 | ||||||
chr17:30128338
|
A | G | 7 | a0001c0001t0002g0270a0001c0001t0002g0271a0001c0001t0002g0276others(4): Show | 7 | HG01433.hp1 HG01884.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.114+10165A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30128338 | ||||||
chr17:30128520
|
T | C | 229 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(226): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.114+10347T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30128520 | ||||||
chr17:30128657
|
GATATA | G | 105 | a0001c0001t0002g0081a0001c0001t0002g0082a0001c0001t0002g0170others(102): Show | 105 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.114+10490_114+1049 others(9): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30128657 | |||||
chr17:30128903
|
A | C | 1 | a0001c0002t0003g0014 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.114+10730A>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30128903 | ||||||
chr17:30128980
|
A | T | 1 | a0001c0002t0001g0043 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.114+10807A>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30128980 | ||||||
chr17:30129026
|
G | A | 2 | a0001c0001t0001g0148a0001c0009t0001g0149 | 2 | HG02055.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.114+10853G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30129026 | ||||||
chr17:30129047
|
C | T | 1 | a0001c0001t0002g0231 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.114+10874C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30129047 | ||||||
chr17:30129057
|
A | G | 20 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144others(17): Show | 20 | HG01243.hp2 HG01884.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.114+10884A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30129057 | ||||||
chr17:30129060
|
AT | A | 9 | a0001c0001t0001g0151a0001c0001t0001g0163a0001c0001t0001g0164others(6): Show | 9 | HG01891.hp1 HG01934.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.114+10898delT | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30129060 | |||||
chr17:30129094
|
A | G | 3 | a0001c0001t0002g0174a0001c0001t0002g0175a0001c0001t0002g0176 | 3 | HG02258.hp2 HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.114+10921A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30129094 | ||||||
chr17:30129134
|
A | G | 1 | a0001c0002t0007g0095 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.114+10961A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30129134 | ||||||
chr17:30129181
|
C | T | 1 | a0001c0001t0004g0272 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.114+11008C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30129181 | ||||||
chr17:30129549
|
A | G | 1 | a0001c0002t0003g0014 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.114+11376A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30129549 | ||||||
chr17:30129586
|
C | G | 1 | a0001c0001t0001g0148 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.114+11413C>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30129586 | ||||||
chr17:30129682
|
C | T | 5 | a0001c0002t0001g0042a0001c0002t0001g0053a0001c0002t0001g0063others(2): Show | 5 | HG02572.hp2 HG03098.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.114+11509C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30129682 | ||||||
chr17:30129719
|
A | C | 2 | a0001c0002t0001g0017a0001c0002t0001g0096 | 2 | HG01361.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.114+11546A>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30129719 | ||||||
chr17:30129740
|
C | T | 140 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(137): Show | 140 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.114+11567C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30129740 | ||||||
chr17:30129793
|
A | G | 1 | a0001c0002t0001g0281 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.114+11620A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30129793 | ||||||
chr17:30129963
|
A | C | 1 | a0001c0001t0004g0275 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.114+11790A>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30129963 | ||||||
chr17:30130031
|
A | G | 20 | a0001c0002t0001g0020a0001c0002t0001g0084a0001c0002t0001g0087others(17): Show | 20 | HG00140.hp1 HG00609.hp1 HG00639.hp1 others(17): Show |
intron_variant | MODIFIER | c.114+11858A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30130031 | ||||||
chr17:30130123
|
G | A | 2 | a0001c0001t0002g0210a0001c0001t0002g0211 | 2 | HG01109.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.114+11950G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30130123 | ||||||
chr17:30130205
|
C | A | 1 | a0001c0001t0001g0151 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.114+12032C>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30130205 | ||||||
chr17:30130289
|
G | C | 1 | a0001c0002t0001g0084 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.114+12116G>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30130289 | ||||||
chr17:30130602
|
A | G | 2 | a0001c0001t0001g0142a0001c0001t0001g0144 | 2 | HG02895.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.114+12429A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30130602 | ||||||
chr17:30130856
|
T | C | 3 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140 | 3 | HG03139.hp2 NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.114+12683T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30130856 | ||||||
chr17:30130967
|
C | G | 7 | a0001c0001t0002g0270a0001c0001t0002g0271a0001c0001t0002g0276others(4): Show | 7 | HG01433.hp1 HG01884.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.114+12794C>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30130967 | ||||||
chr17:30130971
|
A | G | 168 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(165): Show | 168 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.114+12798A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30130971 | ||||||
chr17:30131087
|
A | G | 105 | a0001c0001t0002g0081a0001c0001t0002g0082a0001c0001t0002g0170others(102): Show | 105 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.114+12914A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30131087 | ||||||
chr17:30131259
|
A | G | 1 | a0001c0001t0002g0174 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.114+13086A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30131259 | ||||||
chr17:30131324
|
T | TTATTTTG others(314): Show |
2 | a0001c0001t0002g0175a0001c0001t0002g0176 | 2 | HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.114+13166_114+1316 others(325): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30131324 | |||||
chr17:30131548
|
T | TA | 281 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(278): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.114+13382dupA | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30131548 | |||||
chr17:30131700
|
G | T | 1 | a0001c0001t0004g0272 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.114+13527G>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30131700 | ||||||
chr17:30131969
|
C | T | 1 | a0001c0001t0002g0198 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.114+13796C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30131969 | ||||||
chr17:30131977
|
G | C | 1 | a0001c0001t0002g0213 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.114+13804G>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30131977 | ||||||
chr17:30132097
|
A | C | 1 | a0001c0001t0002g0252 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.114+13924A>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30132097 | ||||||
chr17:30132121
|
G | A | 6 | a0001c0002t0003g0014a0001c0002t0003g0036a0001c0002t0003g0078others(3): Show | 6 | HG01192.hp1 HG01346.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.114+13948G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30132121 | ||||||
chr17:30132123
|
C | CT | 16 | a0001c0001t0002g0183a0001c0001t0002g0197a0001c0001t0002g0200others(13): Show | 16 | HG00099.hp2 HG01167.hp2 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.114+13951dupT | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30132123 | |||||
chr17:30132163
|
G | A | 32 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(29): Show | 32 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.114+13990G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30132163 | ||||||
chr17:30132223
|
G | A | 7 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0165others(4): Show | 7 | HG01891.hp1 HG01934.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.114+14050G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30132223 | ||||||
chr17:30132245
|
C | CA | 23 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(20): Show | 23 | HG01433.hp1 HG01884.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.114+14086dupA | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30132245 | |||||
chr17:30132302
|
C | T | 1 | a0001c0014t0008g0119 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.114+14129C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30132302 | ||||||
chr17:30132336
|
T | G | 1 | a0001c0002t0003g0025 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.114+14163T>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30132336 | ||||||
chr17:30132566
|
C | G | 1 | a0001c0014t0008g0119 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.114+14393C>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30132566 | ||||||
chr17:30132589
|
G | C | 1 | a0001c0002t0001g0127 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.114+14416G>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30132589 | ||||||
chr17:30132689
|
C | T | 2 | a0001c0001t0001g0152a0001c0001t0001g0153 | 2 | HG01891.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.114+14516C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30132689 | ||||||
chr17:30132894
|
A | G | 2 | a0001c0001t0001g0152a0001c0001t0001g0153 | 2 | HG01891.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.114+14721A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30132894 | ||||||
chr17:30132981
|
T | G | 9 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144others(6): Show | 9 | HG02055.hp2 HG02895.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.114+14808T>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30132981 | ||||||
chr17:30132991
|
G | C | 7 | a0001c0001t0002g0270a0001c0001t0002g0271a0001c0001t0002g0276others(4): Show | 7 | HG01433.hp1 HG01884.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.114+14818G>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30132991 | ||||||
chr17:30133109
|
A | AT | 14 | a0001c0002t0001g0004a0001c0002t0001g0006a0001c0002t0001g0008others(11): Show | 14 | HG00741.hp2 HG01167.hp1 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.114+14958dupT | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30133109 | |||||
chr17:30133109
|
AT | A | 59 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(56): Show | 59 | HG01069.hp1 HG01071.hp2 HG01192.hp1 others(56): Show |
intron_variant | MODIFIER | c.114+14958delT | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30133109 | |||||
chr17:30133109
|
ATT | A | 98 | a0001c0001t0002g0081a0001c0001t0002g0082a0001c0001t0002g0170others(95): Show | 98 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.114+14957_114+1495 others(6): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30133109 | |||||
chr17:30133141
|
A | G | 1 | a0001c0002t0009g0069 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.114+14968A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30133141 | ||||||
chr17:30133283
|
G | A | 1 | a0001c0002t0001g0003 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.114+15110G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30133283 | ||||||
chr17:30133339
|
T | A | 1 | a0001c0001t0002g0082 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.114+15166T>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30133339 | ||||||
chr17:30133380
|
C | T | 1 | a0001c0002t0001g0130 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.114+15207C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30133380 | ||||||
chr17:30133549
|
A | G | 1 | a0001c0002t0003g0036 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.114+15376A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30133549 | ||||||
chr17:30133959
|
A | G | 1 | a0001c0001t0002g0179 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.114+15786A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30133959 | ||||||
chr17:30134039
|
C | T | 3 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140 | 3 | HG03139.hp2 NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.114+15866C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30134039 | ||||||
chr17:30134237
|
A | G | 1 | a0001c0002t0001g0074 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.114+16064A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30134237 | ||||||
chr17:30134333
|
A | G | 1 | a0001c0001t0001g0163 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.114+16160A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30134333 | ||||||
chr17:30134669
|
T | C | 138 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(135): Show | 138 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.114+16496T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30134669 | ||||||
chr17:30135001
|
T | TAC | 10 | a0001c0001t0002g0200a0001c0001t0002g0207a0001c0001t0002g0224others(7): Show | 10 | HG00099.hp2 HG01167.hp2 HG01168.hp2 others(7): Show |
intron_variant | MODIFIER | c.114+16829_114+1683 others(6): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30135001 | |||||
chr17:30135010
|
A | T | 1 | a0001c0002t0009g0069 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.114+16837A>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30135010 | ||||||
chr17:30135049
|
T | C | 1 | a0010c0010t0001g0141 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.114+16876T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30135049 | ||||||
chr17:30135113
|
A | C | 32 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(29): Show | 32 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.114+16940A>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30135113 | ||||||
chr17:30135117
|
C | A | 8 | a0001c0001t0002g0175a0001c0001t0002g0176a0001c0002t0001g0013others(5): Show | 8 | HG01069.hp1 HG01071.hp2 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.114+16944C>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30135117 | ||||||
chr17:30135121
|
C | A | 1 | a0001c0001t0002g0199 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.114+16948C>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30135121 | ||||||
chr17:30135492
|
C | G | 137 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(134): Show | 137 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.114+17319C>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30135492 | ||||||
chr17:30135537
|
G | A | 26 | a0001c0002t0001g0269a0001c0002t0001g0277a0001c0002t0001g0278others(23): Show | 26 | HG00741.hp2 HG01069.hp1 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.114+17364G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30135537 | ||||||
chr17:30135642
|
T | G | 26 | a0001c0002t0001g0269a0001c0002t0001g0277a0001c0002t0001g0278others(23): Show | 26 | HG00741.hp2 HG01069.hp1 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.114+17469T>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30135642 | ||||||
chr17:30135721
|
C | T | 32 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(29): Show | 32 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.114+17548C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30135721 | ||||||
chr17:30135749
|
C | T | 12 | a0001c0002t0001g0085a0001c0002t0001g0086a0001c0002t0001g0097others(9): Show | 12 | HG02145.hp1 HG02622.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.114+17576C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30135749 | ||||||
chr17:30135814
|
A | T | 2 | a0001c0001t0001g0152a0001c0001t0001g0153 | 2 | HG01891.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.114+17641A>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30135814 | ||||||
chr17:30135986
|
G | A | 1 | a0001c0014t0008g0119 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.114+17813G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30135986 | ||||||
chr17:30136396
|
G | A | 1 | a0001c0001t0002g0170 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.114+18223G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30136396 | ||||||
chr17:30136548
|
G | A | 1 | a0001c0001t0002g0255 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.114+18375G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30136548 | ||||||
chr17:30136568
|
A | G | 1 | a0001c0001t0002g0260 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.114+18395A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30136568 | ||||||
chr17:30136746
|
C | T | 1 | a0001c0002t0001g0124 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.114+18573C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30136746 | ||||||
chr17:30136817
|
TC | T | 9 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0157others(6): Show | 9 | HG01243.hp2 HG01884.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.114+18645delC | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30136817 | ||||||
chr17:30136857
|
C | T | 1 | a0001c0002t0001g0066 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.114+18684C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30136857 | ||||||
chr17:30136875
|
T | C | 1 | a0001c0001t0002g0174 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.114+18702T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30136875 | ||||||
chr17:30137103
|
G | A | 3 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140 | 3 | HG03139.hp2 NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.114+18930G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30137103 | ||||||
chr17:30137155
|
T | C | 4 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(1): Show | 4 | NA18963.hp1 NA19006.hp1 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.114+18982T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30137155 | ||||||
chr17:30137165
|
A | G | 3 | a0001c0002t0001g0061a0001c0002t0001g0076a0001c0002t0001g0107 | 3 | HG00140.hp2 HG00733.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.114+18992A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30137165 | ||||||
chr17:30137456
|
T | C | 137 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(134): Show | 137 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.114+19283T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30137456 | ||||||
chr17:30137945
|
G | C | 1 | a0001c0002t0001g0005 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.114+19772G>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30137945 | ||||||
chr17:30137988
|
A | G | 3 | a0001c0002t0003g0025a0001c0002t0003g0032a0001c0002t0003g0033 | 3 | HG02257.hp2 HG02486.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.114+19815A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30137988 | ||||||
chr17:30138160
|
G | A | 8 | a0001c0001t0001g0151a0001c0001t0001g0163a0001c0001t0001g0164others(5): Show | 8 | HG01891.hp1 HG01934.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.114+19987G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30138160 | ||||||
chr17:30138258
|
T | C | 3 | a0001c0001t0002g0263a0006c0007t0002g0173a0006c0007t0002g0262 | 3 | HG00741.hp1 NA18948.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.114+20085T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30138258 | ||||||
chr17:30138270
|
T | C | 32 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(29): Show | 32 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.114+20097T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30138270 | ||||||
chr17:30138281
|
A | G | 11 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(8): Show | 11 | HG01243.hp2 HG01884.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.114+20108A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30138281 | ||||||
chr17:30138364
|
G | C | 1 | a0001c0001t0002g0174 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.114+20191G>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30138364 | ||||||
chr17:30138380
|
T | A | 7 | a0001c0001t0002g0270a0001c0001t0002g0271a0001c0001t0002g0276others(4): Show | 7 | HG01433.hp1 HG01884.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.114+20207T>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30138380 | ||||||
chr17:30138662
|
G | A | 1 | a0001c0002t0001g0127 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.114+20489G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30138662 | ||||||
chr17:30138909
|
G | GT | 52 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0151others(49): Show | 52 | HG00140.hp2 HG00280.hp1 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.114+20762dupT | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30138909 | |||||
chr17:30138909
|
G | GTT | 11 | a0001c0001t0001g0140a0001c0001t0001g0158a0001c0001t0002g0170others(8): Show | 11 | HG01168.hp1 HG01243.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.114+20761_114+2076 others(6): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30138909 | |||||
chr17:30138909
|
G | GTTT | 59 | a0001c0001t0001g0159a0001c0001t0002g0081a0001c0001t0002g0082others(56): Show | 59 | HG00099.hp2 HG00597.hp2 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.114+20760_114+2076 others(7): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30138909 | |||||
chr17:30138909
|
G | GTTTT | 40 | a0001c0001t0002g0172a0001c0001t0002g0176a0001c0001t0002g0178others(37): Show | 40 | HG00280.hp2 HG00642.hp1 HG00733.hp1 others(37): Show |
intron_variant | MODIFIER | c.114+20759_114+2076 others(8): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30138909 | |||||
chr17:30138909
|
GT | G | 18 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144others(15): Show | 18 | HG01167.hp1 HG01169.hp2 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.114+20762delT | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30138909 | |||||
chr17:30138920
|
T | G | 1 | a0001c0002t0001g0076 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.114+20747T>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30138920 | ||||||
chr17:30138922
|
T | TG | 6 | a0001c0002t0001g0269a0001c0002t0001g0277a0001c0002t0001g0278others(3): Show | 6 | HG00741.hp2 HG01516.hp2 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.114+20749_114+2075 others(5): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30138922 | ||||||
chr17:30138943
|
A | C | 1 | a0001c0002t0001g0131 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.114+20770A>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30138943 | ||||||
chr17:30138973
|
A | G | 2 | a0001c0001t0002g0228a0001c0001t0002g0232 | 2 | NA18969.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.114+20800A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30138973 | ||||||
chr17:30138996
|
CAAGCTCC others(184): Show |
C | 3 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140 | 3 | HG03139.hp2 NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.114+20825_114+2101 others(4): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30138996 | |||||
chr17:30139098
|
TAGTAGAG others(80): Show |
T | 1 | a0001c0002t0001g0137 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.114+20926_114+2101 others(91): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30139098 | ||||||
chr17:30139108
|
G | A | 1 | a0001c0002t0001g0064 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.114+20935G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30139108 | ||||||
chr17:30139163
|
C | T | 1 | a0001c0001t0002g0228 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.114+20990C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30139163 | ||||||
chr17:30139187
|
G | T | 1 | a0001c0002t0001g0137 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.114+21014G>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30139187 | ||||||
chr17:30139197
|
G | A | 1 | a0001c0002t0001g0127 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.114+21024G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30139197 | ||||||
chr17:30139239
|
G | A | 105 | a0001c0001t0002g0081a0001c0001t0002g0082a0001c0001t0002g0170others(102): Show | 105 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.114+21066G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30139239 | ||||||
chr17:30139722
|
G | C | 26 | a0001c0002t0001g0269a0001c0002t0001g0277a0001c0002t0001g0278others(23): Show | 26 | HG00741.hp2 HG01069.hp1 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.114+21549G>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30139722 | ||||||
chr17:30139798
|
G | A | 105 | a0001c0001t0002g0081a0001c0001t0002g0082a0001c0001t0002g0170others(102): Show | 105 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.114+21625G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30139798 | ||||||
chr17:30139806
|
T | C | 105 | a0001c0001t0002g0081a0001c0001t0002g0082a0001c0001t0002g0170others(102): Show | 105 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.114+21633T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30139806 | ||||||
chr17:30139891
|
G | A | 1 | a0001c0001t0002g0171 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.114+21718G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30139891 | ||||||
chr17:30140425
|
A | G | 3 | a0003c0005t0001g0266a0003c0005t0001g0267a0003c0005t0001g0268 | 3 | HG02895.hp1 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.114+22252A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30140425 | ||||||
chr17:30140520
|
C | CT | 15 | a0001c0001t0002g0270a0001c0001t0002g0271a0001c0001t0002g0276others(12): Show | 15 | HG00609.hp1 HG01884.hp2 HG01978.hp2 others(12): Show |
intron_variant | MODIFIER | c.114+22373dupT | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30140520 | |||||
chr17:30140520
|
CT | C | 117 | a0001c0001t0002g0081a0001c0001t0002g0082a0001c0001t0002g0170others(114): Show | 117 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.114+22373delT | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30140520 | |||||
chr17:30140520
|
CTT | C | 10 | a0001c0001t0002g0190a0001c0001t0002g0229a0001c0001t0002g0238others(7): Show | 10 | HG01069.hp1 HG01069.hp2 HG01168.hp2 others(7): Show |
intron_variant | MODIFIER | c.114+22372_114+2237 others(6): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30140520 | |||||
chr17:30140520
|
CTTTT | C | 31 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(28): Show | 31 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.114+22370_114+2237 others(8): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30140520 | |||||
chr17:30140590
|
G | A | 9 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0157others(6): Show | 9 | HG01243.hp2 HG01884.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.114+22417G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30140590 | ||||||
chr17:30140605
|
T | C | 2 | a0001c0001t0002g0270a0001c0001t0002g0271 | 2 | HG01884.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.114+22432T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30140605 | ||||||
chr17:30140621
|
C | G | 4 | a0001c0002t0001g0128a0001c0002t0001g0129a0001c0002t0001g0130others(1): Show | 4 | HG02723.hp1 HG02818.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.114+22448C>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30140621 | ||||||
chr17:30140731
|
T | C | 1 | a0001c0002t0001g0132 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.114+22558T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30140731 | ||||||
chr17:30140752
|
A | T | 4 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144others(1): Show | 4 | HG02895.hp2 HG02896.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.114+22579A>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30140752 | ||||||
chr17:30140770
|
C | T | 32 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(29): Show | 32 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.114+22597C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30140770 | ||||||
chr17:30140817
|
C | T | 1 | a0001c0002t0001g0038 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.114+22644C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30140817 | ||||||
chr17:30140831
|
G | T | 1 | a0001c0014t0008g0119 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.114+22658G>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30140831 | ||||||
chr17:30140914
|
A | G | 1 | a0001c0014t0008g0119 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.114+22741A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30140914 | ||||||
chr17:30141161
|
CTATTT | C | 3 | a0004c0004t0001g0045a0004c0004t0001g0049a0004c0004t0001g0050 | 3 | HG00280.hp1 HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.114+22993_114+2299 others(9): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30141161 | |||||
chr17:30141189
|
T | C | 7 | a0001c0002t0001g0006a0001c0002t0001g0007a0001c0002t0001g0008others(4): Show | 7 | HG02523.hp1 HG02683.hp2 NA18954.hp2 others(4): Show |
intron_variant | MODIFIER | c.114+23016T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30141189 | ||||||
chr17:30141291
|
G | A | 2 | a0001c0002t0001g0135a0001c0002t0001g0136 | 2 | NA18940.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.114+23118G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30141291 | ||||||
chr17:30141717
|
T | A | 2 | a0003c0005t0001g0266a0003c0005t0001g0267 | 2 | NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.114+23544T>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30141717 | ||||||
chr17:30141811
|
C | A | 1 | a0001c0002t0001g0097 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.114+23638C>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30141811 | ||||||
chr17:30141884
|
G | T | 2 | a0001c0002t0001g0277a0001c0002t0001g0278 | 2 | HG03041.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.114+23711G>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30141884 | ||||||
chr17:30142224
|
A | G | 1 | a0001c0001t0002g0174 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.114+24051A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30142224 | ||||||
chr17:30142311
|
T | A | 32 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(29): Show | 32 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.114+24138T>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30142311 | ||||||
chr17:30142338
|
C | T | 3 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140 | 3 | HG03139.hp2 NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.114+24165C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30142338 | ||||||
chr17:30142483
|
G | T | 2 | a0004c0004t0001g0045a0004c0004t0001g0049 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.114+24310G>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30142483 | ||||||
chr17:30142695
|
G | A | 137 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(134): Show | 137 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.114+24522G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30142695 | ||||||
chr17:30142764
|
T | G | 94 | a0001c0001t0002g0081a0001c0001t0002g0082a0001c0001t0002g0171others(91): Show | 94 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.114+24591T>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30142764 | ||||||
chr17:30142782
|
T | G | 3 | a0001c0002t0003g0025a0001c0002t0003g0032a0001c0002t0003g0033 | 3 | HG02257.hp2 HG02486.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.114+24609T>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30142782 | ||||||
chr17:30142877
|
A | G | 6 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0001g0166others(3): Show | 6 | HG01891.hp1 HG01934.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.114+24704A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30142877 | ||||||
chr17:30142955
|
A | G | 2 | a0001c0001t0001g0158a0001c0001t0001g0159 | 2 | HG01243.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.114+24782A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30142955 | ||||||
chr17:30143042
|
A | G | 1 | a0001c0001t0001g0169 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.114+24869A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30143042 | ||||||
chr17:30143073
|
T | C | 168 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(165): Show | 168 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.114+24900T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30143073 | ||||||
chr17:30143268
|
T | C | 2 | a0001c0002t0001g0128a0001c0002t0001g0129 | 2 | HG02723.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.114+25095T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30143268 | ||||||
chr17:30143446
|
C | A | 168 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(165): Show | 168 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.114+25273C>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30143446 | ||||||
chr17:30143456
|
T | C | 1 | a0001c0001t0002g0177 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.114+25283T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30143456 | ||||||
chr17:30143475
|
A | G | 1 | a0010c0010t0001g0141 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.114+25302A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30143475 | ||||||
chr17:30143587
|
T | C | 2 | a0006c0007t0002g0173a0006c0007t0002g0262 | 2 | NA18948.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.114+25414T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30143587 | ||||||
chr17:30143846
|
A | G | 1 | a0001c0001t0002g0227 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.114+25673A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30143846 | ||||||
chr17:30144165
|
T | G | 32 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(29): Show | 32 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.114+25992T>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30144165 | ||||||
chr17:30144230
|
C | T | 105 | a0001c0001t0002g0081a0001c0001t0002g0082a0001c0001t0002g0170others(102): Show | 105 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.114+26057C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30144230 | ||||||
chr17:30144247
|
T | G | 1 | a0001c0002t0001g0042 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.114+26074T>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30144247 | ||||||
chr17:30144260
|
A | T | 6 | a0001c0001t0001g0151a0001c0001t0002g0081a0001c0001t0002g0226others(3): Show | 6 | HG02559.hp1 HG02717.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.114+26087A>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30144260 | ||||||
chr17:30144263
|
A | T | 72 | a0001c0001t0001g0151a0001c0001t0001g0153a0001c0001t0001g0155others(69): Show | 72 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(69): Show |
intron_variant | MODIFIER | c.114+26090A>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30144263 | ||||||
chr17:30144264
|
T | A | 1 | a0001c0001t0002g0082 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.114+26091T>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30144264 | ||||||
chr17:30144266
|
A | T | 176 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(173): Show | 176 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.114+26093A>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30144266 | ||||||
chr17:30144269
|
A | T | 241 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(238): Show | 241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.114+26096A>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30144269 | ||||||
chr17:30144513
|
G | A | 1 | a0001c0002t0001g0135 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.114+26340G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30144513 | ||||||
chr17:30144596
|
C | T | 2 | a0001c0001t0002g0180a0001c0001t0002g0214 | 2 | HG02735.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.114+26423C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30144596 | ||||||
chr17:30144628
|
T | C | 32 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(29): Show | 32 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.114+26455T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30144628 | ||||||
chr17:30144661
|
A | T | 2 | a0001c0002t0001g0017a0001c0002t0001g0096 | 2 | HG01361.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.114+26488A>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30144661 | ||||||
chr17:30144702
|
T | C | 1 | a0001c0001t0002g0253 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.114+26529T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30144702 | ||||||
chr17:30144722
|
T | C | 1 | a0001c0002t0001g0044 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.114+26549T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30144722 | ||||||
chr17:30144795
|
C | T | 2 | a0001c0001t0001g0161a0001c0001t0001g0162 | 2 | HG01884.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.114+26622C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30144795 | ||||||
chr17:30145125
|
A | C | 1 | a0001c0002t0003g0037 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.114+26952A>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30145125 | ||||||
chr17:30145193
|
A | G | 3 | a0003c0005t0001g0266a0003c0005t0001g0267a0003c0005t0001g0268 | 3 | HG02895.hp1 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.114+27020A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30145193 | ||||||
chr17:30145219
|
C | G | 1 | a0001c0001t0002g0170 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.114+27046C>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30145219 | ||||||
chr17:30145239
|
G | A | 4 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(1): Show | 4 | HG02293.hp2 HG03139.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.114+27066G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30145239 | ||||||
chr17:30145255
|
G | A | 7 | a0001c0001t0002g0270a0001c0001t0002g0271a0001c0001t0002g0276others(4): Show | 7 | HG01433.hp1 HG01884.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.114+27082G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30145255 | ||||||
chr17:30145295
|
C | A | 3 | a0001c0002t0003g0025a0001c0002t0003g0032a0001c0002t0003g0033 | 3 | HG02257.hp2 HG02486.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.114+27122C>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30145295 | ||||||
chr17:30145322
|
CCT | C | 137 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(134): Show | 137 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.114+27154_114+2715 others(6): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30145322 | |||||
chr17:30145342
|
T | A | 3 | a0001c0001t0002g0174a0001c0001t0002g0175a0001c0001t0002g0176 | 3 | HG02258.hp2 HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.114+27169T>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30145342 | ||||||
chr17:30145532
|
G | A | 8 | a0001c0001t0001g0151a0001c0001t0001g0163a0001c0001t0001g0164others(5): Show | 8 | HG01891.hp1 HG01934.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.115-27010G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30145532 | ||||||
chr17:30145569
|
G | A | 1 | a0001c0002t0001g0134 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.115-26973G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30145569 | ||||||
chr17:30145744
|
C | T | 9 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144others(6): Show | 9 | HG02055.hp2 HG02895.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.115-26798C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30145744 | ||||||
chr17:30146002
|
AC | A | 98 | a0001c0001t0002g0081a0001c0001t0002g0082a0001c0001t0002g0170others(95): Show | 98 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.115-26538delC | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30146002 | |||||
chr17:30146216
|
C | A | 4 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0001g0168others(1): Show | 4 | HG01891.hp1 HG01934.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.115-26326C>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30146216 | ||||||
chr17:30146238
|
A | G | 94 | a0001c0001t0002g0081a0001c0001t0002g0082a0001c0001t0002g0171others(91): Show | 94 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.115-26304A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30146238 | ||||||
chr17:30146479
|
T | C | 9 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0157others(6): Show | 9 | HG01243.hp2 HG01884.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.115-26063T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30146479 | ||||||
chr17:30146697
|
G | A | 1 | a0001c0001t0002g0195 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.115-25845G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30146697 | ||||||
chr17:30146748
|
G | A | 1 | a0001c0001t0002g0207 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.115-25794G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30146748 | ||||||
chr17:30146816
|
G | A | 2 | a0001c0001t0002g0210a0001c0001t0002g0211 | 2 | HG01109.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.115-25726G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30146816 | ||||||
chr17:30146889
|
G | A | 1 | a0001c0001t0002g0174 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.115-25653G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30146889 | ||||||
chr17:30147132
|
C | CT | 133 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(130): Show | 133 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.115-25397dupT | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30147132 | |||||
chr17:30147368
|
G | A | 2 | a0001c0001t0002g0256a0001c0001t0002g0257 | 2 | HG01069.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.115-25174G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30147368 | ||||||
chr17:30147541
|
G | A | 4 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(1): Show | 4 | HG03139.hp2 HG03486.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.115-25001G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30147541 | ||||||
chr17:30147568
|
A | G | 4 | a0001c0002t0001g0128a0001c0002t0001g0129a0001c0002t0001g0130others(1): Show | 4 | HG02723.hp1 HG02818.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.115-24974A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30147568 | ||||||
chr17:30147619
|
A | C | 6 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0001g0166others(3): Show | 6 | HG01891.hp1 HG01934.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.115-24923A>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30147619 | ||||||
chr17:30147666
|
T | C | 2 | a0001c0001t0002g0270a0001c0001t0002g0271 | 2 | HG01884.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.115-24876T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30147666 | ||||||
chr17:30147709
|
C | T | 1 | a0001c0002t0001g0005 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.115-24833C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30147709 | ||||||
chr17:30147813
|
C | CT | 7 | a0001c0001t0002g0210a0001c0001t0006g0241a0001c0001t0006g0242others(4): Show | 7 | HG01168.hp2 HG01169.hp1 HG01261.hp2 others(4): Show |
intron_variant | MODIFIER | c.115-24714dupT | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30147813 | |||||
chr17:30147916
|
A | T | 15 | a0001c0001t0002g0183a0001c0001t0002g0197a0001c0001t0002g0200others(12): Show | 15 | HG00099.hp2 HG01167.hp2 HG01168.hp2 others(12): Show |
intron_variant | MODIFIER | c.115-24626A>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30147916 | ||||||
chr17:30148008
|
T | C | 1 | a0001c0014t0008g0119 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.115-24534T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30148008 | ||||||
chr17:30148013
|
A | G | 8 | a0001c0001t0001g0151a0001c0001t0001g0163a0001c0001t0001g0164others(5): Show | 8 | HG01891.hp1 HG01934.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.115-24529A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30148013 | ||||||
chr17:30148033
|
G | A | 1 | a0001c0002t0001g0063 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.115-24509G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30148033 | ||||||
chr17:30148361
|
G | A | 167 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(164): Show | 167 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.115-24181G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30148361 | ||||||
chr17:30148507
|
C | A | 2 | a0001c0001t0002g0270a0001c0001t0002g0271 | 2 | HG01884.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.115-24035C>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30148507 | ||||||
chr17:30148711
|
G | A | 105 | a0001c0001t0002g0081a0001c0001t0002g0082a0001c0001t0002g0170others(102): Show | 105 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.115-23831G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30148711 | ||||||
chr17:30149023
|
T | C | 1 | a0001c0001t0001g0151 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.115-23519T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30149023 | ||||||
chr17:30149259
|
G | A | 1 | a0002c0003t0001g0068 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.115-23283G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30149259 | ||||||
chr17:30149284
|
G | A | 2 | a0001c0002t0001g0021a0001c0002t0001g0044 | 2 | NA18961.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.115-23258G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30149284 | ||||||
chr17:30149393
|
A | C | 4 | a0001c0001t0004g0272a0001c0001t0004g0273a0001c0001t0004g0274others(1): Show | 4 | HG01433.hp1 HG02486.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.115-23149A>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30149393 | ||||||
chr17:30149440
|
T | G | 168 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(165): Show | 168 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.115-23102T>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30149440 | ||||||
chr17:30149604
|
G | A | 4 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(1): Show | 4 | NA18963.hp1 NA19006.hp1 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.115-22938G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30149604 | ||||||
chr17:30149637
|
C | A | 8 | a0001c0001t0001g0151a0001c0001t0001g0163a0001c0001t0001g0164others(5): Show | 8 | HG01891.hp1 HG01934.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.115-22905C>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30149637 | ||||||
chr17:30149748
|
T | G | 1 | a0001c0001t0001g0144 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.115-22794T>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30149748 | ||||||
chr17:30149765
|
G | C | 1 | a0001c0001t0001g0144 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.115-22777G>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30149765 | ||||||
chr17:30149834
|
C | CA | 91 | a0001c0001t0002g0081a0001c0001t0002g0082a0001c0001t0002g0170others(88): Show | 91 | HG00099.hp2 HG00280.hp2 HG00609.hp2 others(88): Show |
intron_variant | MODIFIER | c.115-22688dupA | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30149834 | |||||
chr17:30149834
|
C | CAA | 22 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(19): Show | 22 | HG00323.hp1 HG00597.hp2 HG02074.hp1 others(19): Show |
intron_variant | MODIFIER | c.115-22689_115-2268 others(6): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30149834 | |||||
chr17:30149834
|
C | CAAA | 30 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144others(27): Show | 30 | HG01243.hp2 HG01433.hp1 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.115-22690_115-2268 others(7): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30149834 | |||||
chr17:30149855
|
T | A | 17 | a0001c0002t0003g0014a0001c0002t0003g0026a0001c0002t0003g0027others(14): Show | 17 | HG01069.hp1 HG01071.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.115-22687T>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30149855 | ||||||
chr17:30149979
|
C | G | 98 | a0001c0001t0002g0081a0001c0001t0002g0082a0001c0001t0002g0170others(95): Show | 98 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.115-22563C>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30149979 | ||||||
chr17:30150035
|
C | T | 1 | a0001c0001t0002g0255 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.115-22507C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30150035 | ||||||
chr17:30150069
|
A | G | 2 | a0006c0007t0002g0173a0006c0007t0002g0262 | 2 | NA18948.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.115-22473A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30150069 | ||||||
chr17:30150237
|
T | C | 166 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(163): Show | 166 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.115-22305T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30150237 | ||||||
chr17:30150249
|
T | A | 3 | a0001c0002t0003g0029a0001c0002t0003g0030a0001c0002t0003g0031 | 3 | HG02622.hp1 HG02809.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.115-22293T>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30150249 | ||||||
chr17:30150310
|
A | T | 1 | a0001c0001t0001g0151 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.115-22232A>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30150310 | ||||||
chr17:30150461
|
C | T | 1 | a0001c0002t0001g0127 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.115-22081C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30150461 | ||||||
chr17:30150480
|
T | A | 32 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(29): Show | 32 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.115-22062T>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30150480 | ||||||
chr17:30150543
|
C | T | 1 | a0001c0014t0008g0119 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.115-21999C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30150543 | ||||||
chr17:30150573
|
G | A | 9 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0157others(6): Show | 9 | HG01243.hp2 HG01884.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.115-21969G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30150573 | ||||||
chr17:30150684
|
G | GT | 31 | a0001c0001t0001g0138a0001c0001t0001g0157a0001c0001t0001g0159others(28): Show | 31 | HG01071.hp1 HG01361.hp1 HG01978.hp2 others(28): Show |
intron_variant | MODIFIER | c.115-21832dupT | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30150684 | |||||
chr17:30150684
|
G | GTT | 9 | a0001c0001t0001g0151a0001c0001t0001g0158a0001c0001t0001g0163others(6): Show | 9 | HG01243.hp2 HG01891.hp1 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.115-21833_115-2183 others(6): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30150684 | |||||
chr17:30150684
|
GT | G | 47 | a0001c0001t0002g0170a0001c0001t0002g0175a0001c0001t0002g0176others(44): Show | 47 | HG01069.hp1 HG01071.hp2 HG01109.hp1 others(44): Show |
intron_variant | MODIFIER | c.115-21832delT | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30150684 | |||||
chr17:30150684
|
GTT | G | 78 | a0001c0001t0002g0081a0001c0001t0002g0082a0001c0001t0002g0171others(75): Show | 78 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.115-21833_115-2183 others(6): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30150684 | |||||
chr17:30150700
|
T | G | 2 | a0001c0001t0002g0175a0001c0001t0002g0176 | 2 | HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.115-21842T>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30150700 | ||||||
chr17:30150714
|
A | C | 1 | a0003c0005t0001g0267 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.115-21828A>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30150714 | ||||||
chr17:30150764
|
T | C | 9 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144others(6): Show | 9 | HG02055.hp2 HG02895.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.115-21778T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30150764 | ||||||
chr17:30150768
|
A | G | 1 | a0001c0002t0001g0108 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.115-21774A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30150768 | ||||||
chr17:30150801
|
C | T | 2 | a0001c0002t0001g0001a0001c0002t0001g0003 | 2 | NA18963.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.115-21741C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30150801 | ||||||
chr17:30150805
|
A | G | 1 | a0001c0001t0002g0226 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.115-21737A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30150805 | ||||||
chr17:30150929
|
C | A | 24 | a0001c0002t0001g0019a0001c0002t0001g0020a0001c0002t0001g0084others(21): Show | 24 | HG00140.hp1 HG00609.hp1 HG00639.hp1 others(21): Show |
intron_variant | MODIFIER | c.115-21613C>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30150929 | ||||||
chr17:30150940
|
G | A | 1 | a0001c0002t0003g0034 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.115-21602G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30150940 | ||||||
chr17:30151045
|
C | T | 1 | a0001c0001t0002g0252 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.115-21497C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30151045 | ||||||
chr17:30151126
|
C | T | 1 | a0001c0001t0004g0272 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.115-21416C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30151126 | ||||||
chr17:30151170
|
A | C | 1 | a0001c0001t0002g0239 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.115-21372A>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30151170 | ||||||
chr17:30151311
|
C | G | 168 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(165): Show | 168 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.115-21231C>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30151311 | ||||||
chr17:30151367
|
A | G | 2 | a0001c0001t0002g0182a0001c0001t0002g0190 | 2 | HG02074.hp1 NA18946.hp2 |
intron_variant | MODIFIER | c.115-21175A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30151367 | ||||||
chr17:30151375
|
G | T | 1 | a0001c0001t0001g0154 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.115-21167G>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30151375 | ||||||
chr17:30151524
|
A | G | 3 | a0003c0005t0001g0266a0003c0005t0001g0267a0003c0005t0001g0268 | 3 | HG02895.hp1 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.115-21018A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30151524 | ||||||
chr17:30151645
|
G | A | 1 | a0001c0001t0002g0239 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.115-20897G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30151645 | ||||||
chr17:30151686
|
A | G | 3 | a0001c0001t0002g0181a0001c0001t0002g0188a0001c0001t0002g0192 | 3 | HG03669.hp1 NA18961.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.115-20856A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30151686 | ||||||
chr17:30151717
|
A | G | 11 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(8): Show | 11 | HG01243.hp2 HG01884.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.115-20825A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30151717 | ||||||
chr17:30151774
|
C | CT | 29 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0002g0174others(26): Show | 29 | HG00597.hp2 HG00741.hp1 HG01255.hp1 others(26): Show |
intron_variant | MODIFIER | c.115-20743dupT | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30151774 | |||||
chr17:30151774
|
CT | C | 31 | a0001c0001t0001g0148a0001c0001t0001g0151a0001c0001t0001g0153others(28): Show | 31 | HG00323.hp1 HG01069.hp2 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.115-20743delT | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30151774 | |||||
chr17:30151919
|
G | A | 8 | a0001c0001t0001g0151a0001c0001t0001g0163a0001c0001t0001g0164others(5): Show | 8 | HG01891.hp1 HG01934.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.115-20623G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30151919 | ||||||
chr17:30152069
|
G | A | 1 | a0001c0001t0001g0157 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.115-20473G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30152069 | ||||||
chr17:30152103
|
A | G | 2 | a0001c0001t0002g0228a0001c0001t0002g0232 | 2 | NA18969.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.115-20439A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30152103 | ||||||
chr17:30152226
|
G | A | 1 | a0010c0010t0001g0141 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.115-20316G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30152226 | ||||||
chr17:30152247
|
C | T | 1 | a0001c0001t0004g0272 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.115-20295C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30152247 | ||||||
chr17:30152304
|
G | A | 1 | a0001c0002t0001g0120 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.115-20238G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30152304 | ||||||
chr17:30152325
|
C | T | 2 | a0001c0002t0001g0098a0001c0002t0001g0103 | 2 | HG02630.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.115-20217C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30152325 | ||||||
chr17:30152327
|
C | T | 3 | a0003c0005t0001g0266a0003c0005t0001g0267a0003c0005t0001g0268 | 3 | HG02895.hp1 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.115-20215C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30152327 | ||||||
chr17:30152423
|
A | AT | 47 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144others(44): Show | 47 | HG01168.hp2 HG01243.hp2 HG01433.hp1 others(44): Show |
intron_variant | MODIFIER | c.115-20100dupT | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30152423 | |||||
chr17:30152423
|
A | ATT | 95 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(92): Show | 95 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.115-20101_115-2010 others(6): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30152423 | |||||
chr17:30152586
|
G | A | 7 | a0001c0001t0002g0270a0001c0001t0002g0271a0001c0001t0002g0276others(4): Show | 7 | HG01433.hp1 HG01884.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.115-19956G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30152586 | ||||||
chr17:30152781
|
G | A | 273 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(270): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.115-19761G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30152781 | ||||||
chr17:30152836
|
T | C | 94 | a0001c0001t0002g0081a0001c0001t0002g0082a0001c0001t0002g0171others(91): Show | 94 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.115-19706T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30152836 | ||||||
chr17:30152903
|
C | CT | 21 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0160others(18): Show | 21 | HG01243.hp1 HG01891.hp1 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.115-19616dupT | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30152903 | |||||
chr17:30152903
|
C | CTTTTTTT others(3): Show |
1 | a0001c0002t0001g0060 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.115-19625_115-1961 others(14): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30152903 | |||||
chr17:30152903
|
CT | C | 140 | a0001c0001t0002g0081a0001c0001t0002g0082a0001c0001t0002g0170others(137): Show | 140 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.115-19616delT | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30152903 | |||||
chr17:30152903
|
CTT | C | 7 | a0001c0001t0002g0172a0001c0001t0002g0187a0001c0001t0002g0256others(4): Show | 7 | HG01069.hp2 HG01167.hp1 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.115-19617_115-1961 others(6): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30152903 | |||||
chr17:30153007
|
A | G | 1 | a0001c0001t0002g0229 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.115-19535A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30153007 | ||||||
chr17:30153085
|
T | C | 8 | a0001c0001t0001g0151a0001c0001t0001g0163a0001c0001t0001g0164others(5): Show | 8 | HG01891.hp1 HG01934.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.115-19457T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30153085 | ||||||
chr17:30153106
|
G | A | 3 | a0001c0001t0002g0174a0001c0001t0002g0175a0001c0001t0002g0176 | 3 | HG02258.hp2 HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.115-19436G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30153106 | ||||||
chr17:30153207
|
G | T | 32 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(29): Show | 32 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.115-19335G>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30153207 | ||||||
chr17:30153400
|
G | A | 9 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0157others(6): Show | 9 | HG01243.hp2 HG01884.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.115-19142G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30153400 | ||||||
chr17:30153824
|
A | G | 1 | a0011c0016t0001g0057 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.115-18718A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30153824 | ||||||
chr17:30153909
|
C | G | 1 | a0001c0002t0001g0108 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.115-18633C>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30153909 | ||||||
chr17:30154140
|
C | T | 4 | a0001c0001t0004g0272a0001c0001t0004g0273a0001c0001t0004g0274others(1): Show | 4 | HG01433.hp1 HG02486.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.115-18402C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30154140 | ||||||
chr17:30154181
|
T | C | 137 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(134): Show | 137 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.115-18361T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30154181 | ||||||
chr17:30154306
|
G | T | 1 | a0001c0002t0001g0108 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.115-18236G>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30154306 | ||||||
chr17:30154513
|
A | G | 1 | a0011c0016t0001g0057 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.115-18029A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30154513 | ||||||
chr17:30154572
|
G | A | 1 | a0001c0002t0001g0094 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.115-17970G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30154572 | ||||||
chr17:30154667
|
G | A | 1 | a0010c0010t0001g0141 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.115-17875G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30154667 | ||||||
chr17:30154819
|
C | T | 1 | a0001c0001t0002g0170 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.115-17723C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30154819 | ||||||
chr17:30155175
|
G | A | 3 | a0003c0005t0001g0266a0003c0005t0001g0267a0003c0005t0001g0268 | 3 | HG02895.hp1 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.115-17367G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30155175 | ||||||
chr17:30155348
|
T | C | 8 | a0001c0001t0002g0178a0001c0001t0002g0191a0001c0001t0002g0209others(5): Show | 8 | HG00642.hp1 HG01099.hp2 HG01123.hp2 others(5): Show |
intron_variant | MODIFIER | c.115-17194T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30155348 | ||||||
chr17:30155440
|
A | G | 7 | a0001c0001t0002g0270a0001c0001t0002g0271a0001c0001t0002g0276others(4): Show | 7 | HG01433.hp1 HG01884.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.115-17102A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30155440 | ||||||
chr17:30155470
|
A | C | 105 | a0001c0001t0002g0081a0001c0001t0002g0082a0001c0001t0002g0170others(102): Show | 105 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.115-17072A>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30155470 | ||||||
chr17:30155486
|
A | G | 1 | a0001c0002t0001g0047 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.115-17056A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30155486 | ||||||
chr17:30155531
|
C | A | 1 | a0010c0010t0001g0141 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.115-17011C>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30155531 | ||||||
chr17:30155700
|
C | T | 1 | a0001c0002t0001g0106 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.115-16842C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30155700 | ||||||
chr17:30155780
|
T | C | 3 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140 | 3 | HG03139.hp2 NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.115-16762T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30155780 | ||||||
chr17:30156039
|
C | T | 2 | a0001c0001t0001g0152a0001c0001t0001g0153 | 2 | HG01891.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.115-16503C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30156039 | ||||||
chr17:30156078
|
G | C | 1 | a0001c0001t0002g0187 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.115-16464G>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30156078 | ||||||
chr17:30156092
|
G | A | 1 | a0001c0001t0001g0167 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.115-16450G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30156092 | ||||||
chr17:30156135
|
C | T | 3 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140 | 3 | HG03139.hp2 NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.115-16407C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30156135 | ||||||
chr17:30156248
|
G | GCTGTTTA others(807): Show |
1 | a0001c0001t0002g0170 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.115-16292_115-1629 others(818): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30156248 | |||||
chr17:30156248
|
G | GCTGTTTA others(807): Show |
1 | a0001c0001t0001g0160 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.115-16292_115-1629 others(818): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30156248 | |||||
chr17:30156248
|
G | GCTGTTTA others(807): Show |
96 | a0001c0001t0002g0081a0001c0001t0002g0082a0001c0001t0002g0171others(93): Show | 96 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.115-16292_115-1629 others(818): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30156248 | |||||
chr17:30156248
|
G | GCTGTTTA others(807): Show |
27 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144others(24): Show | 27 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.115-16292_115-1629 others(818): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30156248 | |||||
chr17:30156248
|
G | GCTGTTTA others(807): Show |
3 | a0003c0005t0001g0266a0003c0005t0001g0267a0003c0005t0001g0268 | 3 | HG02895.hp1 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.115-16292_115-1629 others(818): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30156248 | |||||
chr17:30156248
|
G | GCTGTTTA others(807): Show |
1 | a0001c0001t0002g0265 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.115-16292_115-1629 others(818): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30156248 | |||||
chr17:30156248
|
G | GCTGTTTA others(807): Show |
7 | a0001c0001t0002g0270a0001c0001t0002g0271a0001c0001t0002g0276others(4): Show | 7 | HG01433.hp1 HG01884.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.115-16292_115-1629 others(818): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30156248 | |||||
chr17:30156248
|
G | GCTGTTTA others(807): Show |
4 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(1): Show | 4 | HG03139.hp2 HG03486.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.115-16292_115-1629 others(818): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30156248 | |||||
chr17:30156429
|
A | G | 4 | a0001c0001t0001g0151a0001c0001t0002g0174a0001c0001t0002g0175others(1): Show | 4 | HG02258.hp2 HG02451.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.115-16113A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30156429 | ||||||
chr17:30156623
|
G | A | 1 | a0001c0001t0002g0239 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.115-15919G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30156623 | ||||||
chr17:30156629
|
C | G | 1 | a0001c0001t0002g0183 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.115-15913C>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30156629 | ||||||
chr17:30156739
|
G | A | 3 | a0001c0001t0002g0174a0001c0001t0002g0175a0001c0001t0002g0176 | 3 | HG02258.hp2 HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.115-15803G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30156739 | ||||||
chr17:30156961
|
A | G | 3 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140 | 3 | HG03139.hp2 NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.115-15581A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30156961 | ||||||
chr17:30157133
|
T | C | 3 | a0003c0005t0001g0266a0003c0005t0001g0267a0003c0005t0001g0268 | 3 | HG02895.hp1 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.115-15409T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30157133 | ||||||
chr17:30157185
|
C | A | 1 | a0001c0002t0001g0090 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.115-15357C>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30157185 | ||||||
chr17:30157216
|
G | T | 168 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(165): Show | 168 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.115-15326G>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30157216 | ||||||
chr17:30157920
|
A | G | 2 | a0001c0001t0001g0164a0001c0001t0001g0167 | 2 | HG02723.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.115-14622A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30157920 | ||||||
chr17:30158215
|
A | G | 94 | a0001c0001t0002g0081a0001c0001t0002g0082a0001c0001t0002g0171others(91): Show | 94 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.115-14327A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30158215 | ||||||
chr17:30158308
|
A | AT | 33 | a0001c0001t0001g0169a0001c0001t0002g0170a0001c0001t0002g0174others(30): Show | 33 | HG00741.hp2 HG01069.hp1 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.115-14219dupT | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30158308 | |||||
chr17:30158308
|
A | ATT | 90 | a0001c0001t0002g0081a0001c0001t0002g0082a0001c0001t0002g0171others(87): Show | 90 | HG00099.hp2 HG00323.hp1 HG00597.hp2 others(87): Show |
intron_variant | MODIFIER | c.115-14220_115-1421 others(6): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30158308 | |||||
chr17:30158394
|
C | T | 1 | a0001c0001t0002g0170 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.115-14148C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30158394 | ||||||
chr17:30158651
|
CAG | C | 98 | a0001c0001t0002g0081a0001c0001t0002g0082a0001c0001t0002g0170others(95): Show | 98 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.115-13890_115-1388 others(6): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30158651 | ||||||
chr17:30158744
|
A | G | 137 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(134): Show | 137 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.115-13798A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30158744 | ||||||
chr17:30159053
|
G | A | 7 | a0001c0001t0002g0270a0001c0001t0002g0271a0001c0001t0002g0276others(4): Show | 7 | HG01433.hp1 HG01884.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.115-13489G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30159053 | ||||||
chr17:30159351
|
G | GT | 5 | a0001c0002t0001g0001a0001c0002t0001g0088a0003c0005t0001g0266others(2): Show | 5 | HG02895.hp1 NA18906.hp2 NA18967.hp1 others(2): Show |
intron_variant | MODIFIER | c.115-13183dupT | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30159351 | |||||
chr17:30159358
|
T | G | 140 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(137): Show | 140 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.115-13184T>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30159358 | ||||||
chr17:30159360
|
G | T | 3 | a0003c0005t0001g0266a0003c0005t0001g0267a0003c0005t0001g0268 | 3 | HG02895.hp1 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.115-13182G>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30159360 | ||||||
chr17:30159368
|
G | T | 1 | a0001c0001t0002g0081 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.115-13174G>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30159368 | ||||||
chr17:30159804
|
A | G | 15 | a0001c0001t0002g0183a0001c0001t0002g0197a0001c0001t0002g0200others(12): Show | 15 | HG00099.hp2 HG01167.hp2 HG01168.hp2 others(12): Show |
intron_variant | MODIFIER | c.115-12738A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30159804 | ||||||
chr17:30159957
|
C | T | 19 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(16): Show | 19 | HG00597.hp1 HG01243.hp2 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.115-12585C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30159957 | ||||||
chr17:30160075
|
T | G | 1 | a0001c0002t0001g0127 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.115-12467T>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30160075 | ||||||
chr17:30160253
|
T | G | 1 | a0001c0001t0004g0273 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.115-12289T>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30160253 | ||||||
chr17:30160315
|
T | G | 2 | a0001c0001t0001g0158a0001c0001t0001g0159 | 2 | HG01243.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.115-12227T>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30160315 | ||||||
chr17:30160344
|
T | G | 1 | a0001c0001t0004g0272 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.115-12198T>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30160344 | ||||||
chr17:30160699
|
G | A | 3 | a0003c0005t0001g0266a0003c0005t0001g0267a0003c0005t0001g0268 | 3 | HG02895.hp1 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.115-11843G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30160699 | ||||||
chr17:30160884
|
C | T | 1 | a0001c0001t0002g0256 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.115-11658C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30160884 | ||||||
chr17:30160917
|
C | T | 2 | a0001c0002t0001g0060a0001c0002t0001g0137 | 2 | HG02738.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.115-11625C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30160917 | ||||||
chr17:30160958
|
C | T | 4 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(1): Show | 4 | HG03139.hp2 HG03486.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.115-11584C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30160958 | ||||||
chr17:30161218
|
A | C | 105 | a0001c0001t0002g0081a0001c0001t0002g0082a0001c0001t0002g0170others(102): Show | 105 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.115-11324A>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30161218 | ||||||
chr17:30161383
|
T | C | 7 | a0001c0001t0002g0270a0001c0001t0002g0271a0001c0001t0002g0276others(4): Show | 7 | HG01433.hp1 HG01884.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.115-11159T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30161383 | ||||||
chr17:30161439
|
A | G | 1 | a0001c0002t0001g0021 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.115-11103A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30161439 | ||||||
chr17:30161773
|
C | T | 229 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(226): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.115-10769C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30161773 | ||||||
chr17:30162024
|
CT | C | 171 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(168): Show | 171 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(168): Show |
intron_variant | MODIFIER | c.115-10503delT | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30162024 | |||||
chr17:30162082
|
C | T | 1 | a0012c0017t0003g0077 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.115-10460C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30162082 | ||||||
chr17:30162086
|
G | T | 3 | a0001c0001t0002g0174a0001c0001t0002g0175a0001c0001t0002g0176 | 3 | HG02258.hp2 HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.115-10456G>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30162086 | ||||||
chr17:30162149
|
C | T | 1 | a0001c0001t0002g0203 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.115-10393C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30162149 | ||||||
chr17:30162652
|
A | G | 98 | a0001c0001t0002g0081a0001c0001t0002g0082a0001c0001t0002g0170others(95): Show | 98 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.115-9890A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30162652 | ||||||
chr17:30162752
|
G | A | 168 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(165): Show | 168 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.115-9790G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30162752 | ||||||
chr17:30162758
|
A | T | 2 | a0001c0001t0002g0210a0001c0001t0002g0211 | 2 | HG01109.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.115-9784A>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30162758 | ||||||
chr17:30162790
|
A | G | 1 | a0010c0010t0001g0141 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.115-9752A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30162790 | ||||||
chr17:30163073
|
C | T | 1 | a0001c0001t0002g0237 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.115-9469C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30163073 | ||||||
chr17:30163149
|
C | T | 3 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140 | 3 | HG03139.hp2 NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.115-9393C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30163149 | ||||||
chr17:30163188
|
TTTGTGTG others(10): Show |
T | 1 | a0001c0001t0002g0178 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.115-9352_115-9336d others(19): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30163188 | |||||
chr17:30163189
|
T | TTG | 22 | a0001c0001t0001g0152a0001c0001t0005g0146a0001c0002t0001g0001others(19): Show | 22 | HG00609.hp1 HG01167.hp1 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.115-9295_115-9294d others(4): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30163189 | |||||
chr17:30163189
|
T | TTGTG | 13 | a0001c0001t0001g0151a0001c0002t0001g0007a0001c0002t0001g0042others(10): Show | 13 | HG00642.hp2 HG01346.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.115-9297_115-9294d others(6): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30163189 | |||||
chr17:30163189
|
T | TTGTGTG | 6 | a0001c0001t0005g0147a0001c0002t0001g0010a0001c0002t0001g0044others(3): Show | 6 | HG03195.hp1 HG03209.hp2 NA18940.hp2 others(3): Show |
intron_variant | MODIFIER | c.115-9299_115-9294d others(8): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30163189 | |||||
chr17:30163189
|
T | TTGTGTGT others(1): Show |
3 | a0001c0002t0001g0005a0001c0002t0001g0133a0003c0005t0001g0268 | 3 | HG00597.hp1 HG02895.hp1 NA18946.hp1 |
intron_variant | MODIFIER | c.115-9301_115-9294d others(10): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30163189 | |||||
chr17:30163189
|
T | TTGTGTGT others(3): Show |
3 | a0001c0002t0001g0120a0001c0002t0007g0111a0003c0005t0001g0267 | 3 | HG06807.hp1 NA18906.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.115-9303_115-9294d others(12): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30163189 | |||||
chr17:30163189
|
TTG | T | 17 | a0001c0001t0001g0167a0001c0001t0005g0150a0001c0002t0001g0048others(14): Show | 17 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.115-9295_115-9294d others(4): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30163189 | |||||
chr17:30163189
|
TTGTG | T | 20 | a0001c0001t0001g0164a0001c0002t0001g0016a0001c0002t0001g0019others(17): Show | 20 | HG00323.hp2 HG01099.hp1 HG01255.hp2 others(17): Show |
intron_variant | MODIFIER | c.115-9297_115-9294d others(6): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30163189 | |||||
chr17:30163189
|
TTGTGTG | T | 16 | a0001c0001t0001g0142a0001c0001t0001g0144a0001c0001t0001g0168others(13): Show | 16 | HG00140.hp2 HG01081.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.115-9299_115-9294d others(8): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30163189 | |||||
chr17:30163189
|
TTGTGTGT others(1): Show |
T | 15 | a0001c0001t0001g0140a0001c0001t0001g0145a0001c0001t0001g0163others(12): Show | 15 | HG01516.hp2 HG01517.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.115-9301_115-9294d others(10): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30163189 | |||||
chr17:30163189
|
TTGTGTGT others(3): Show |
T | 9 | a0001c0001t0001g0165a0001c0001t0002g0170a0001c0001t0002g0176others(6): Show | 9 | HG00741.hp2 HG01192.hp1 HG01346.hp1 others(6): Show |
intron_variant | MODIFIER | c.115-9303_115-9294d others(12): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30163189 | |||||
chr17:30163189
|
TTGTGTGT others(5): Show |
T | 8 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0002g0181others(5): Show | 8 | HG00733.hp2 HG02723.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.115-9305_115-9294d others(14): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30163189 | |||||
chr17:30163189
|
TTGTGTGT others(7): Show |
T | 14 | a0001c0001t0002g0172a0001c0001t0002g0224a0001c0001t0002g0247others(11): Show | 14 | HG00099.hp2 HG00597.hp2 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.115-9307_115-9294d others(16): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30163189 | |||||
chr17:30163189
|
TTGTGTGT others(9): Show |
T | 20 | a0001c0001t0002g0081a0001c0001t0002g0179a0001c0001t0002g0184others(17): Show | 20 | HG00280.hp2 HG00639.hp2 HG00733.hp1 others(17): Show |
intron_variant | MODIFIER | c.115-9309_115-9294d others(18): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30163189 | |||||
chr17:30163189
|
TTGTGTGT others(11): Show |
T | 66 | a0001c0001t0002g0082a0001c0001t0002g0171a0001c0001t0002g0177others(63): Show | 66 | HG00323.hp1 HG00609.hp2 HG00642.hp1 others(63): Show |
intron_variant | MODIFIER | c.115-9311_115-9294d others(20): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30163189 | |||||
chr17:30163189
|
TTGTGTGT others(13): Show |
T | 5 | a0001c0001t0002g0200a0001c0001t0002g0204a0001c0001t0002g0210others(2): Show | 5 | HG01167.hp2 HG01261.hp2 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.115-9313_115-9294d others(22): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30163189 | |||||
chr17:30163189
|
TTGTGTGT others(15): Show |
T | 1 | a0001c0011t0002g0215 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.115-9315_115-9294d others(24): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30163189 | |||||
chr17:30163189
|
TTGTGTGT others(21): Show |
T | 5 | a0001c0002t0003g0026a0001c0002t0003g0027a0001c0002t0003g0028others(2): Show | 5 | HG01069.hp1 HG01071.hp2 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.115-9321_115-9294d others(30): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30163189 | |||||
chr17:30163239
|
GTGTGTGT others(3): Show |
G | 4 | a0001c0001t0001g0155a0001c0001t0001g0158a0001c0001t0001g0159others(1): Show | 4 | HG01243.hp2 HG02145.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.115-9301_115-9292d others(12): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30163239 | |||||
chr17:30163243
|
GTGTGTT | G | 4 | a0001c0001t0001g0154a0001c0001t0001g0162a0001c0002t0003g0025others(1): Show | 4 | HG01884.hp1 HG02257.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.115-9297_115-9292d others(8): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30163243 | |||||
chr17:30163247
|
GTT | G | 3 | a0001c0001t0001g0153a0001c0002t0003g0032a0001c0002t0003g0033 | 3 | HG02451.hp1 HG02486.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.115-9291_115-9290d others(4): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30163247 | |||||
chr17:30163249
|
T | G | 1 | a0001c0001t0001g0152 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.115-9293T>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30163249 | ||||||
chr17:30163311
|
G | A | 26 | a0001c0002t0001g0015a0001c0002t0001g0017a0001c0002t0001g0059others(23): Show | 26 | HG00140.hp2 HG00733.hp2 HG01168.hp1 others(23): Show |
intron_variant | MODIFIER | c.115-9231G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30163311 | ||||||
chr17:30163328
|
C | T | 1 | a0001c0002t0001g0102 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.115-9214C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30163328 | ||||||
chr17:30163541
|
A | G | 2 | a0001c0001t0001g0152a0001c0001t0001g0153 | 2 | HG01891.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.115-9001A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30163541 | ||||||
chr17:30163634
|
A | G | 1 | a0001c0002t0003g0109 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.115-8908A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30163634 | ||||||
chr17:30163668
|
T | C | 1 | a0010c0010t0001g0141 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.115-8874T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30163668 | ||||||
chr17:30163675
|
ACCACT | A | 32 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(29): Show | 32 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.115-8866_115-8862d others(7): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30163675 | ||||||
chr17:30163679
|
C | CT | 84 | a0001c0001t0002g0082a0001c0001t0002g0171a0001c0001t0002g0172others(81): Show | 84 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.115-8841dupT | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30163679 | |||||
chr17:30163679
|
C | CTT | 11 | a0001c0001t0002g0187a0001c0001t0002g0211a0001c0001t0002g0233others(8): Show | 11 | HG00597.hp2 HG01109.hp2 HG01934.hp1 others(8): Show |
intron_variant | MODIFIER | c.115-8842_115-8841d others(4): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30163679 | |||||
chr17:30163679
|
CT | C | 16 | a0001c0001t0002g0213a0001c0001t0002g0270a0001c0001t0002g0271others(13): Show | 16 | HG01069.hp1 HG01099.hp1 HG01361.hp1 others(13): Show |
intron_variant | MODIFIER | c.115-8841delT | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30163679 | |||||
chr17:30163681
|
T | G | 32 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(29): Show | 32 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.115-8861T>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30163681 | ||||||
chr17:30163682
|
T | A | 32 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(29): Show | 32 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.115-8860T>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30163682 | ||||||
chr17:30163684
|
T | A | 32 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(29): Show | 32 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.115-8858T>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30163684 | ||||||
chr17:30163685
|
T | G | 32 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(29): Show | 32 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.115-8857T>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30163685 | ||||||
chr17:30163687
|
T | C | 32 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(29): Show | 32 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.115-8855T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30163687 | ||||||
chr17:30163796
|
C | T | 3 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140 | 3 | HG03139.hp2 NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.115-8746C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30163796 | ||||||
chr17:30163887
|
C | T | 9 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144others(6): Show | 9 | HG02055.hp2 HG02895.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.115-8655C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30163887 | ||||||
chr17:30163913
|
T | C | 1 | a0001c0002t0001g0127 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.115-8629T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30163913 | ||||||
chr17:30163966
|
A | G | 7 | a0001c0001t0002g0270a0001c0001t0002g0271a0001c0001t0002g0276others(4): Show | 7 | HG01433.hp1 HG01884.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.115-8576A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30163966 | ||||||
chr17:30163975
|
C | T | 1 | a0001c0001t0001g0155 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.115-8567C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30163975 | ||||||
chr17:30163982
|
G | A | 3 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140 | 3 | HG03139.hp2 NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.115-8560G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30163982 | ||||||
chr17:30164010
|
A | C | 1 | a0001c0001t0001g0163 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.115-8532A>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30164010 | ||||||
chr17:30164011
|
A | T | 105 | a0001c0001t0002g0081a0001c0001t0002g0082a0001c0001t0002g0170others(102): Show | 105 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.115-8531A>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30164011 | ||||||
chr17:30164020
|
TGTGTGTG others(3): Show |
T | 8 | a0001c0001t0001g0151a0001c0001t0001g0163a0001c0001t0001g0164others(5): Show | 8 | HG01891.hp1 HG01934.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.115-8514_115-8505d others(12): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30164020 | |||||
chr17:30164030
|
C | T | 1 | a0001c0001t0002g0178 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.115-8512C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30164030 | ||||||
chr17:30164210
|
T | C | 1 | a0001c0001t0004g0273 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.115-8332T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30164210 | ||||||
chr17:30164383
|
C | G | 11 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(8): Show | 11 | HG01243.hp2 HG01884.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.115-8159C>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30164383 | ||||||
chr17:30164439
|
G | A | 32 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(29): Show | 32 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.115-8103G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30164439 | ||||||
chr17:30164449
|
G | A | 1 | a0001c0001t0001g0160 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.115-8093G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30164449 | ||||||
chr17:30165015
|
C | T | 2 | a0001c0001t0006g0241a0001c0001t0006g0242 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.115-7527C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30165015 | ||||||
chr17:30165124
|
T | C | 8 | a0001c0001t0001g0151a0001c0001t0001g0163a0001c0001t0001g0164others(5): Show | 8 | HG01891.hp1 HG01934.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.115-7418T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30165124 | ||||||
chr17:30165293
|
A | T | 1 | a0001c0001t0002g0260 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.115-7249A>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30165293 | ||||||
chr17:30165311
|
G | C | 1 | a0001c0002t0001g0085 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.115-7231G>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30165311 | ||||||
chr17:30165333
|
A | T | 3 | a0001c0001t0002g0174a0001c0001t0002g0175a0001c0001t0002g0176 | 3 | HG02258.hp2 HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.115-7209A>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30165333 | ||||||
chr17:30165787
|
C | T | 94 | a0001c0001t0002g0081a0001c0001t0002g0082a0001c0001t0002g0171others(91): Show | 94 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.115-6755C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30165787 | ||||||
chr17:30165886
|
A | G | 9 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0157others(6): Show | 9 | HG01243.hp2 HG01884.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.115-6656A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30165886 | ||||||
chr17:30165912
|
A | G | 1 | a0001c0001t0002g0226 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.115-6630A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30165912 | ||||||
chr17:30166217
|
T | G | 1 | a0001c0001t0002g0260 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.115-6325T>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30166217 | ||||||
chr17:30166382
|
G | A | 2 | a0001c0001t0002g0270a0001c0001t0002g0271 | 2 | HG01884.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.115-6160G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30166382 | ||||||
chr17:30166503
|
A | G | 9 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0157others(6): Show | 9 | HG01243.hp2 HG01884.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.115-6039A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30166503 | ||||||
chr17:30166520
|
A | T | 3 | a0003c0005t0001g0266a0003c0005t0001g0267a0003c0005t0001g0268 | 3 | HG02895.hp1 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.115-6022A>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30166520 | ||||||
chr17:30166563
|
A | T | 1 | a0001c0001t0002g0260 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.115-5979A>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30166563 | ||||||
chr17:30166787
|
A | G | 136 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(133): Show | 136 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.115-5755A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30166787 | ||||||
chr17:30166814
|
T | C | 1 | a0001c0014t0008g0119 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.115-5728T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30166814 | ||||||
chr17:30166843
|
T | G | 2 | a0001c0001t0002g0270a0001c0001t0002g0271 | 2 | HG01884.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.115-5699T>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30166843 | ||||||
chr17:30166911
|
G | A | 1 | a0001c0002t0001g0106 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.115-5631G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30166911 | ||||||
chr17:30166985
|
A | G | 1 | a0001c0014t0008g0119 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.115-5557A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30166985 | ||||||
chr17:30167132
|
A | G | 26 | a0001c0002t0001g0269a0001c0002t0001g0277a0001c0002t0001g0278others(23): Show | 26 | HG00741.hp2 HG01069.hp1 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.115-5410A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30167132 | ||||||
chr17:30167135
|
C | T | 32 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(29): Show | 32 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.115-5407C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30167135 | ||||||
chr17:30167164
|
T | G | 3 | a0001c0001t0005g0146a0001c0001t0005g0147a0001c0001t0005g0150 | 3 | HG02922.hp2 HG03195.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.115-5378T>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30167164 | ||||||
chr17:30167168
|
C | T | 1 | a0001c0014t0008g0119 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.115-5374C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30167168 | ||||||
chr17:30167294
|
C | T | 1 | a0001c0002t0001g0133 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.115-5248C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30167294 | ||||||
chr17:30167469
|
C | T | 1 | a0001c0001t0002g0216 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.115-5073C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30167469 | ||||||
chr17:30167611
|
A | G | 1 | a0001c0001t0001g0155 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.115-4931A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30167611 | ||||||
chr17:30167664
|
C | T | 1 | a0001c0001t0002g0209 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.115-4878C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30167664 | ||||||
chr17:30167746
|
G | A | 1 | a0001c0002t0001g0019 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.115-4796G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30167746 | ||||||
chr17:30167836
|
TA | T | 5 | a0001c0001t0002g0186a0001c0001t0002g0187a0001c0001t0002g0204others(2): Show | 5 | HG01255.hp1 HG01934.hp1 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.115-4704delA | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30167836 | |||||
chr17:30167841
|
A | C | 3 | a0003c0005t0001g0266a0003c0005t0001g0267a0003c0005t0001g0268 | 3 | HG02895.hp1 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.115-4701A>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30167841 | ||||||
chr17:30167975
|
T | C | 1 | a0001c0002t0003g0037 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.115-4567T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30167975 | ||||||
chr17:30168003
|
G | A | 105 | a0001c0001t0002g0081a0001c0001t0002g0082a0001c0001t0002g0170others(102): Show | 105 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.115-4539G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30168003 | ||||||
chr17:30168048
|
G | A | 1 | a0001c0002t0001g0121 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.115-4494G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30168048 | ||||||
chr17:30168068
|
G | A | 28 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144others(25): Show | 28 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(25): Show |
intron_variant | MODIFIER | c.115-4474G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30168068 | ||||||
chr17:30168094
|
A | G | 168 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(165): Show | 168 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.115-4448A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30168094 | ||||||
chr17:30168428
|
A | T | 1 | a0001c0002t0001g0094 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.115-4114A>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30168428 | ||||||
chr17:30168537
|
A | G | 1 | a0001c0002t0001g0039 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.115-4005A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30168537 | ||||||
chr17:30168574
|
T | TATA | 15 | a0001c0001t0002g0183a0001c0001t0002g0197a0001c0001t0002g0200others(12): Show | 15 | HG00099.hp2 HG01167.hp2 HG01168.hp2 others(12): Show |
intron_variant | MODIFIER | c.115-3952_115-3950d others(5): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30168574 | |||||
chr17:30168590
|
ATAG | A | 3 | a0001c0002t0003g0025a0001c0002t0003g0032a0001c0002t0003g0033 | 3 | HG02257.hp2 HG02486.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.115-3949_115-3947d others(5): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30168590 | |||||
chr17:30168593
|
G | GTAA | 6 | a0001c0002t0003g0014a0001c0002t0003g0036a0001c0002t0003g0078others(3): Show | 6 | HG01192.hp1 HG01346.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.115-3933_115-3931d others(5): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30168593 | |||||
chr17:30168622
|
A | G | 4 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(1): Show | 4 | HG03139.hp2 HG03486.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.115-3920A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30168622 | ||||||
chr17:30168654
|
T | G | 94 | a0001c0001t0002g0081a0001c0001t0002g0082a0001c0001t0002g0171others(91): Show | 94 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.115-3888T>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30168654 | ||||||
chr17:30168751
|
A | G | 1 | a0001c0002t0001g0281 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.115-3791A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30168751 | ||||||
chr17:30168755
|
C | A | 3 | a0003c0005t0001g0266a0003c0005t0001g0267a0003c0005t0001g0268 | 3 | HG02895.hp1 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.115-3787C>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30168755 | ||||||
chr17:30168775
|
A | G | 2 | a0001c0001t0002g0175a0001c0001t0002g0176 | 2 | HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.115-3767A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30168775 | ||||||
chr17:30168831
|
G | A | 2 | a0001c0001t0002g0270a0001c0001t0002g0271 | 2 | HG01884.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.115-3711G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30168831 | ||||||
chr17:30169028
|
T | A | 1 | a0001c0002t0001g0122 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.115-3514T>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30169028 | ||||||
chr17:30169173
|
T | A | 2 | a0001c0001t0004g0273a0001c0001t0004g0274 | 2 | HG02486.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.115-3369T>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30169173 | ||||||
chr17:30169195
|
A | G | 6 | a0001c0002t0001g0013a0001c0002t0001g0018a0001c0002t0001g0038others(3): Show | 6 | HG01167.hp1 HG01169.hp2 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.115-3347A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30169195 | ||||||
chr17:30169402
|
T | C | 11 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(8): Show | 11 | HG01243.hp2 HG01884.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.115-3140T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30169402 | ||||||
chr17:30169412
|
A | T | 105 | a0001c0001t0002g0081a0001c0001t0002g0082a0001c0001t0002g0170others(102): Show | 105 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.115-3130A>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30169412 | ||||||
chr17:30169762
|
T | A | 105 | a0001c0001t0002g0081a0001c0001t0002g0082a0001c0001t0002g0170others(102): Show | 105 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.115-2780T>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30169762 | ||||||
chr17:30169846
|
GA | G | 10 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144others(7): Show | 10 | HG02055.hp2 HG02895.hp2 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.115-2685delA | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30169846 | |||||
chr17:30169853
|
A | C | 3 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140 | 3 | HG03139.hp2 NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.115-2689A>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30169853 | ||||||
chr17:30169989
|
A | G | 9 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144others(6): Show | 9 | HG02055.hp2 HG02895.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.115-2553A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30169989 | ||||||
chr17:30170241
|
T | C | 32 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(29): Show | 32 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.115-2301T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30170241 | ||||||
chr17:30170350
|
G | A | 1 | a0001c0002t0001g0132 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.115-2192G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30170350 | ||||||
chr17:30170390
|
C | T | 6 | a0001c0002t0001g0013a0001c0002t0001g0018a0001c0002t0001g0038others(3): Show | 6 | HG01167.hp1 HG01169.hp2 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.115-2152C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30170390 | ||||||
chr17:30170530
|
A | G | 1 | a0001c0001t0002g0276 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.115-2012A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30170530 | ||||||
chr17:30170594
|
A | ATTGTGGC others(40): Show |
1 | a0001c0001t0002g0082 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.115-1947_115-1901d others(49): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30170594 | |||||
chr17:30170706
|
A | G | 2 | a0001c0001t0002g0177a0001c0001t0002g0208 | 2 | HG01070.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.115-1836A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30170706 | ||||||
chr17:30170737
|
A | G | 1 | a0001c0001t0002g0170 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.115-1805A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30170737 | ||||||
chr17:30170929
|
G | A | 1 | a0001c0001t0002g0209 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.115-1613G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30170929 | ||||||
chr17:30171011
|
C | T | 32 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(29): Show | 32 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.115-1531C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30171011 | ||||||
chr17:30171217
|
A | C | 1 | a0001c0001t0002g0170 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.115-1325A>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30171217 | ||||||
chr17:30171303
|
CT | C | 143 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(140): Show | 143 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.115-1219delT | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30171303 | |||||
chr17:30171303
|
CTT | C | 11 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(8): Show | 11 | HG02055.hp2 HG02615.hp2 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.115-1220_115-1219d others(4): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30171303 | |||||
chr17:30171336
|
G | C | 32 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(29): Show | 32 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.115-1206G>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30171336 | ||||||
chr17:30171394
|
C | T | 2 | a0001c0002t0001g0006a0001c0002t0001g0009 | 2 | HG02523.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.115-1148C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30171394 | ||||||
chr17:30171597
|
G | A | 1 | a0001c0001t0002g0225 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.115-945G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30171597 | ||||||
chr17:30171609
|
A | G | 1 | a0001c0001t0004g0272 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.115-933A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30171609 | ||||||
chr17:30171717
|
T | G | 1 | a0001c0002t0001g0121 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.115-825T>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30171717 | ||||||
chr17:30171807
|
C | A | 3 | a0001c0001t0002g0236a0001c0001t0002g0237a0001c0001t0002g0259 | 3 | HG00323.hp1 HG01993.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.115-735C>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30171807 | ||||||
chr17:30171934
|
T | A | 1 | a0001c0001t0001g0155 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.115-608T>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30171934 | ||||||
chr17:30171934
|
T | TCA | 31 | a0001c0001t0001g0148a0001c0001t0002g0082a0001c0001t0002g0180others(28): Show | 31 | HG00140.hp2 HG00733.hp2 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.115-570_115-569dup others(2): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30171934 | |||||
chr17:30171934
|
T | TCACA | 8 | a0001c0002t0001g0015a0001c0002t0001g0097a0001c0002t0001g0130others(5): Show | 8 | HG00741.hp2 HG01243.hp1 HG01516.hp2 others(5): Show |
intron_variant | MODIFIER | c.115-572_115-569dup others(4): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30171934 | |||||
chr17:30171934
|
T | TCACACA | 5 | a0001c0002t0001g0128a0001c0002t0001g0129a0001c0002t0003g0078others(2): Show | 5 | HG01346.hp1 HG02723.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.115-574_115-569dup others(6): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30171934 | |||||
chr17:30171934
|
T | TCACACAC others(1): Show |
3 | a0001c0001t0005g0150a0001c0002t0001g0131a0001c0002t0003g0014 | 3 | HG02922.hp2 HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.115-576_115-569dup others(8): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30171934 | |||||
chr17:30171934
|
T | TCACACAC others(3): Show |
1 | a0001c0002t0003g0036 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.115-578_115-569dup others(10): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30171934 | |||||
chr17:30171934
|
TCA | T | 16 | a0001c0001t0001g0142a0001c0001t0001g0144a0001c0001t0001g0152others(13): Show | 16 | HG01070.hp1 HG01361.hp1 HG01433.hp1 others(13): Show |
intron_variant | MODIFIER | c.115-570_115-569del others(2): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30171934 | |||||
chr17:30171934
|
TCACA | T | 5 | a0001c0001t0002g0270a0001c0001t0002g0271a0001c0001t0002g0276others(2): Show | 5 | HG01884.hp2 HG02615.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.115-572_115-569del others(4): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30171934 | |||||
chr17:30171958
|
A | C | 1 | a0001c0002t0001g0127 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.115-584A>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30171958 | ||||||
chr17:30171960
|
A | T | 1 | a0001c0002t0001g0127 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.115-582A>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30171960 | ||||||
chr17:30171962
|
A | T | 1 | a0001c0002t0001g0127 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.115-580A>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30171962 | ||||||
chr17:30171964
|
A | T | 1 | a0001c0002t0001g0127 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.115-578A>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30171964 | ||||||
chr17:30171966
|
A | T | 2 | a0001c0001t0002g0229a0001c0002t0001g0127 | 2 | HG02615.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.115-576A>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30171966 | ||||||
chr17:30171966
|
ACACACAC others(7): Show |
A | 1 | a0001c0008t0001g0156 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.115-574_115-561del others(14): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30171966 | |||||
chr17:30171968
|
A | C | 1 | a0001c0001t0002g0229 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.115-574A>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30171968 | ||||||
chr17:30171968
|
A | T | 3 | a0001c0002t0001g0053a0001c0002t0001g0127a0001c0011t0002g0215 | 3 | HG02572.hp2 HG02615.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.115-574A>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30171968 | ||||||
chr17:30171970
|
A | ACTCCCTC others(5): Show |
2 | a0001c0001t0002g0187a0001c0001t0002g0255 | 2 | HG01934.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.115-571_115-570ins others(12): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30171970 | |||||
chr17:30171970
|
A | C | 2 | a0001c0002t0001g0053a0001c0011t0002g0215 | 2 | HG02572.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.115-572A>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30171970 | ||||||
chr17:30171970
|
A | T | 4 | a0001c0001t0001g0155a0001c0001t0002g0188a0001c0001t0002g0229others(1): Show | 4 | HG02615.hp2 HG02809.hp2 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.115-572A>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30171970 | ||||||
chr17:30171972
|
A | ACACACAC others(3): Show |
1 | a0001c0002t0007g0111 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.115-569_115-568ins others(10): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30171972 | |||||
chr17:30171972
|
A | ACACACAC others(5): Show |
3 | a0001c0002t0001g0070a0001c0002t0007g0095a0004c0004t0001g0045 | 3 | HG01070.hp2 NA19030.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.115-569_115-568ins others(12): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30171972 | |||||
chr17:30171972
|
A | ACACACTC others(1): Show |
3 | a0001c0002t0001g0064a0001c0002t0001g0090a0001c0002t0001g0132 | 3 | HG00140.hp1 HG02074.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.115-569_115-568ins others(8): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30171972 | |||||
chr17:30171972
|
A | ACACACTC others(3): Show |
2 | a0001c0002t0001g0110a0004c0004t0001g0049 | 2 | HG01071.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.115-569_115-568ins others(10): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30171972 | |||||
chr17:30171972
|
A | ACACACTC others(5): Show |
1 | a0004c0004t0001g0050 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.115-569_115-568ins others(12): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30171972 | |||||
chr17:30171972
|
A | ACACACTC others(7): Show |
1 | a0001c0002t0001g0066 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.115-569_115-568ins others(14): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30171972 | |||||
chr17:30171972
|
A | ACACACTC others(9): Show |
2 | a0001c0002t0001g0051a0001c0002t0001g0083 | 2 | HG00642.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.115-569_115-568ins others(16): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30171972 | |||||
chr17:30171972
|
A | ACACTCC | 11 | a0001c0002t0001g0016a0001c0002t0001g0020a0001c0002t0001g0047others(8): Show | 11 | HG00609.hp1 HG01099.hp1 HG02129.hp2 others(8): Show |
intron_variant | MODIFIER | c.115-569_115-568ins others(6): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30171972 | |||||
chr17:30171972
|
A | ACACTCCC others(1): Show |
6 | a0001c0002t0001g0004a0001c0002t0001g0042a0001c0002t0001g0063others(3): Show | 6 | HG02622.hp2 HG03209.hp2 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.115-569_115-568ins others(8): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30171972 | |||||
chr17:30171972
|
A | ACACTCCC others(3): Show |
2 | a0001c0002t0001g0102a0003c0005t0001g0267 | 2 | HG03098.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.115-569_115-568ins others(10): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30171972 | |||||
chr17:30171972
|
A | ACACTCCC others(5): Show |
4 | a0001c0001t0002g0175a0001c0002t0001g0038a0001c0002t0001g0073others(1): Show | 4 | HG00099.hp1 HG00323.hp2 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.115-569_115-568ins others(12): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30171972 | |||||
chr17:30171972
|
A | ACACTCCC others(7): Show |
2 | a0001c0002t0001g0048a0005c0006t0001g0041 | 2 | HG01496.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.115-569_115-568ins others(14): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30171972 | |||||
chr17:30171972
|
A | ACACTCCC others(9): Show |
1 | a0001c0002t0001g0074 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.115-569_115-568ins others(16): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30171972 | |||||
chr17:30171972
|
A | ACACTCCC others(11): Show |
1 | a0001c0001t0002g0176 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.115-569_115-568ins others(18): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30171972 | |||||
chr17:30171972
|
A | ACACTCCC others(17): Show |
1 | a0001c0002t0001g0134 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.115-569_115-568ins others(24): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30171972 | |||||
chr17:30171972
|
A | ACACTCCT others(8): Show |
1 | a0001c0002t0001g0054 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.115-569_115-568ins others(15): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30171972 | |||||
chr17:30171972
|
A | ACTCTCCT others(4): Show |
1 | a0001c0002t0001g0065 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.115-567_115-566ins others(11): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30171972 | |||||
chr17:30171972
|
A | C | 2 | a0001c0001t0001g0155a0001c0001t0002g0188 | 2 | HG02809.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.115-570A>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30171972 | ||||||
chr17:30171972
|
A | T | 77 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0002g0081others(74): Show | 77 | HG00099.hp2 HG00323.hp1 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.115-570A>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30171972 | ||||||
chr17:30171972
|
ACT | A | 3 | a0001c0002t0001g0071a0001c0002t0001g0115a0010c0010t0001g0141 | 3 | HG03486.hp1 NA18948.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.115-568_115-567del others(2): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30171972 | |||||
chr17:30171972
|
ACTCCCT | A | 5 | a0001c0001t0001g0151a0001c0001t0001g0164a0001c0001t0001g0166others(2): Show | 5 | HG01891.hp1 HG01934.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.115-566_115-561del others(6): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30171972 | |||||
chr17:30171974
|
T | A | 26 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(23): Show | 26 | HG00741.hp2 HG01192.hp1 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.115-568T>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30171974 | ||||||
chr17:30171974
|
T | C | 65 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0002g0081others(62): Show | 65 | HG00099.hp2 HG00323.hp1 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.115-568T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30171974 | ||||||
chr17:30171976
|
C | A | 10 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(7): Show | 10 | HG01192.hp1 HG02055.hp2 HG03139.hp2 others(7): Show |
intron_variant | MODIFIER | c.115-566C>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30171976 | ||||||
chr17:30171976
|
C | CCT | 18 | a0001c0001t0001g0160a0001c0002t0001g0002a0001c0002t0001g0005others(15): Show | 18 | HG00597.hp1 HG01978.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.115-528_115-527dup others(2): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30171976 | |||||
chr17:30171976
|
C | CCTCT | 3 | a0001c0002t0001g0136a0001c0002t0003g0030a0001c0002t0003g0032 | 3 | HG02809.hp1 HG02818.hp2 NA18940.hp2 |
intron_variant | MODIFIER | c.115-530_115-527dup others(4): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30171976 | |||||
chr17:30171976
|
C | CCTCTCTC others(1): Show |
3 | a0001c0002t0001g0043a0001c0002t0003g0033a0003c0005t0001g0268 | 3 | HG02486.hp1 HG02895.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.115-534_115-527dup others(8): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30171976 | |||||
chr17:30171976
|
C | CCTCTCTC others(3): Show |
1 | a0001c0002t0001g0018 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.115-536_115-527dup others(10): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30171976 | |||||
chr17:30171976
|
C | CCTCTCTC others(5): Show |
1 | a0001c0002t0001g0013 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.115-538_115-527dup others(12): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30171976 | |||||
chr17:30171976
|
C | T | 141 | a0001c0001t0001g0155a0001c0001t0001g0158a0001c0001t0001g0159others(138): Show | 141 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(138): Show |
intron_variant | MODIFIER | c.115-566C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30171976 | ||||||
chr17:30171976
|
CCT | C | 7 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0157others(4): Show | 7 | HG01884.hp1 HG01891.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.115-528_115-527del others(2): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30171976 | |||||
chr17:30171978
|
T | A | 2 | a0001c0001t0001g0168a0001c0002t0003g0109 | 2 | HG01192.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.115-564T>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30171978 | ||||||
chr17:30171978
|
T | C | 19 | a0001c0002t0001g0084a0001c0002t0001g0085a0001c0002t0001g0086others(16): Show | 19 | HG00741.hp2 HG01243.hp1 HG01346.hp1 others(16): Show |
intron_variant | MODIFIER | c.115-564T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30171978 | ||||||
chr17:30171980
|
T | A | 1 | a0001c0001t0001g0151 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.115-562T>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30171980 | ||||||
chr17:30171980
|
T | C | 8 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(5): Show | 8 | HG02055.hp2 HG03139.hp2 HG03486.hp1 others(5): Show |
intron_variant | MODIFIER | c.115-562T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30171980 | ||||||
chr17:30171982
|
T | C | 2 | a0001c0002t0001g0019a0001c0002t0003g0109 | 2 | HG01192.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.115-560T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30171982 | ||||||
chr17:30171984
|
T | C | 1 | a0001c0008t0001g0156 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.115-558T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30171984 | ||||||
chr17:30171988
|
T | TCTCTCTC others(4): Show |
1 | a0005c0006t0001g0040 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.115-553_115-543dup others(11): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30171988 | |||||
chr17:30172012
|
T | A | 3 | a0001c0001t0002g0170a0001c0001t0002g0201a0001c0011t0002g0215 | 3 | HG02293.hp2 HG03130.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.115-530T>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30172012 | ||||||
chr17:30172014
|
T | A | 7 | a0001c0001t0002g0170a0001c0001t0002g0187a0001c0001t0002g0188others(4): Show | 7 | HG01934.hp1 HG02293.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.115-528T>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30172014 | ||||||
chr17:30172014
|
T | TCACA | 8 | a0001c0001t0002g0171a0001c0001t0002g0177a0001c0001t0002g0185others(5): Show | 8 | HG01070.hp1 HG01123.hp2 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.115-527_115-524dup others(4): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30172014 | |||||
chr17:30172014
|
T | TCACACA | 4 | a0001c0001t0002g0240a0001c0001t0002g0247a0001c0001t0002g0249others(1): Show | 4 | HG00597.hp2 HG02647.hp1 NA18995.hp2 others(1): Show |
intron_variant | MODIFIER | c.115-524_115-523ins others(6): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30172014 | |||||
chr17:30172014
|
T | TCTCACA | 8 | a0001c0001t0002g0081a0001c0001t0002g0183a0001c0001t0002g0226others(5): Show | 8 | HG02004.hp2 HG02280.hp2 HG03490.hp1 others(5): Show |
intron_variant | MODIFIER | c.115-527_115-526ins others(6): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30172014 | |||||
chr17:30172014
|
T | TCTCTCAC others(1): Show |
17 | a0001c0001t0002g0172a0001c0001t0002g0181a0001c0001t0002g0182others(14): Show | 17 | HG00099.hp2 HG01069.hp2 HG01109.hp2 others(14): Show |
intron_variant | MODIFIER | c.115-527_115-526ins others(8): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30172014 | |||||
chr17:30172014
|
T | TCTCTCAC others(3): Show |
1 | a0001c0001t0002g0244 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.115-527_115-526ins others(10): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30172014 | |||||
chr17:30172014
|
T | TCTCTCTC others(3): Show |
27 | a0001c0001t0002g0178a0001c0001t0002g0179a0001c0001t0002g0180others(24): Show | 27 | HG00280.hp2 HG00323.hp1 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.115-527_115-526ins others(10): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30172014 | |||||
chr17:30172014
|
T | TCTCTCTC others(5): Show |
1 | a0001c0001t0002g0198 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.115-527_115-526ins others(12): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30172014 | |||||
chr17:30172014
|
T | TCTCTCTC others(5): Show |
14 | a0001c0001t0002g0082a0001c0001t0002g0193a0001c0001t0002g0194others(11): Show | 14 | HG00639.hp2 HG00733.hp1 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.115-527_115-526ins others(12): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30172014 | |||||
chr17:30172014
|
T | TCTCTCTC others(7): Show |
6 | a0001c0001t0002g0184a0001c0001t0002g0197a0001c0001t0002g0203others(3): Show | 6 | HG00609.hp2 HG01952.hp1 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.115-527_115-526ins others(14): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30172014 | |||||
chr17:30172014
|
T | TCTCTCTC others(9): Show |
1 | a0001c0001t0002g0191 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.115-527_115-526ins others(16): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30172014 | |||||
chr17:30172265
|
A | G | 1 | a0010c0010t0001g0141 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.115-277A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30172265 | ||||||
chr17:30172386
|
T | C | 4 | a0001c0001t0002g0186a0001c0001t0002g0187a0001c0001t0002g0204others(1): Show | 4 | HG01255.hp1 HG01934.hp1 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.115-156T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30172386 | ||||||
chr17:30172456
|
C | T | 1 | a0008c0013t0002g0196 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.115-86C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30172456 | ||||||
chr17:30172481
|
T | A | 20 | a0001c0002t0001g0020a0001c0002t0001g0084a0001c0002t0001g0087others(17): Show | 20 | HG00140.hp1 HG00609.hp1 HG00639.hp1 others(17): Show |
intron_variant | MODIFIER | c.115-61T>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30172481 | ||||||
chr17:30172522
|
A | G | 1 | a0001c0002t0007g0111 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.115-20A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30172522 | ||||||
chr17:30173195
|
C | T | 7 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0165others(4): Show | 7 | HG01891.hp1 HG01934.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.171+597C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 3/6 | chr17 | 30173195 | ||||||
chr17:30173206
|
C | T | 4 | a0001c0001t0002g0186a0001c0001t0002g0187a0001c0001t0002g0204others(1): Show | 4 | HG01255.hp1 HG01934.hp1 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.171+608C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 3/6 | chr17 | 30173206 | ||||||
chr17:30173229
|
G | T | 1 | a0001c0001t0001g0155 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.171+631G>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 3/6 | chr17 | 30173229 | ||||||
chr17:30173281
|
C | T | 15 | a0001c0002t0003g0014a0001c0002t0003g0026a0001c0002t0003g0027others(12): Show | 15 | HG01069.hp1 HG01071.hp2 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.171+683C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 3/6 | chr17 | 30173281 | ||||||
chr17:30173337
|
T | A | 32 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(29): Show | 32 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.171+739T>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 3/6 | chr17 | 30173337 | ||||||
chr17:30173388
|
C | T | 1 | a0001c0002t0001g0066 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.171+790C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 3/6 | chr17 | 30173388 | ||||||
chr17:30173439
|
T | G | 1 | a0001c0002t0001g0127 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.171+841T>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 3/6 | chr17 | 30173439 | ||||||
chr17:30173447
|
A | G | 98 | a0001c0001t0002g0081a0001c0001t0002g0082a0001c0001t0002g0170others(95): Show | 98 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.171+849A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 3/6 | chr17 | 30173447 | ||||||
chr17:30173463
|
T | C | 1 | a0001c0001t0002g0170 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.171+865T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 3/6 | chr17 | 30173463 | ||||||
chr17:30173532
|
ATTAT | A | 9 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0157others(6): Show | 9 | HG01243.hp2 HG01884.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.171+939_171+942del others(4): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr17 | 30173532 | |||||
chr17:30174053
|
T | G | 3 | a0001c0002t0001g0112a0001c0002t0001g0120a0001c0002t0001g0121 | 3 | NA18951.hp1 NA18972.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.171+1455T>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 3/6 | chr17 | 30174053 | ||||||
chr17:30174088
|
A | G | 3 | a0001c0001t0002g0270a0001c0001t0002g0271a0001c0001t0002g0276 | 3 | HG01884.hp2 HG02922.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.171+1490A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 3/6 | chr17 | 30174088 | ||||||
chr17:30174392
|
C | G | 1 | a0005c0006t0001g0041 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.171+1794C>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 3/6 | chr17 | 30174392 | ||||||
chr17:30174606
|
A | G | 1 | a0001c0001t0001g0169 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.171+2008A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 3/6 | chr17 | 30174606 | ||||||
chr17:30174660
|
T | A | 2 | a0001c0001t0001g0164a0001c0001t0001g0167 | 2 | HG02723.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.171+2062T>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 3/6 | chr17 | 30174660 | ||||||
chr17:30174757
|
T | C | 1 | a0001c0002t0001g0112 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.171+2159T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 3/6 | chr17 | 30174757 | ||||||
chr17:30174792
|
G | A | 1 | a0001c0001t0002g0178 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.171+2194G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 3/6 | chr17 | 30174792 | ||||||
chr17:30174797
|
T | A | 1 | a0005c0006t0001g0040 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.171+2199T>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 3/6 | chr17 | 30174797 | ||||||
chr17:30175012
|
A | G | 1 | a0001c0014t0008g0119 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.171+2414A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 3/6 | chr17 | 30175012 | ||||||
chr17:30175022
|
A | T | 1 | a0001c0001t0001g0151 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.171+2424A>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 3/6 | chr17 | 30175022 | ||||||
chr17:30175200
|
C | G | 1 | a0001c0001t0002g0239 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.171+2602C>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 3/6 | chr17 | 30175200 | ||||||
chr17:30175349
|
C | G | 1 | a0001c0002t0001g0015 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.172-2722C>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 3/6 | chr17 | 30175349 | ||||||
chr17:30175624
|
C | A | 137 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(134): Show | 137 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.172-2447C>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 3/6 | chr17 | 30175624 | ||||||
chr17:30175633
|
C | G | 137 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(134): Show | 137 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.172-2438C>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 3/6 | chr17 | 30175633 | ||||||
chr17:30175950
|
C | T | 3 | a0001c0001t0002g0201a0001c0001t0002g0212a0001c0001t0002g0238 | 3 | HG01496.hp1 HG02004.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.172-2121C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 3/6 | chr17 | 30175950 | ||||||
chr17:30176000
|
ACC | A | 137 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(134): Show | 137 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.172-2062_172-2061d others(4): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr17 | 30176000 | |||||
chr17:30176092
|
T | A | 1 | a0001c0002t0001g0127 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.172-1979T>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 3/6 | chr17 | 30176092 | ||||||
chr17:30176092
|
T | G | 1 | a0001c0002t0001g0070 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.172-1979T>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 3/6 | chr17 | 30176092 | ||||||
chr17:30176095
|
G | T | 2 | a0001c0002t0001g0112a0003c0005t0001g0266 | 2 | NA18972.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.172-1976G>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 3/6 | chr17 | 30176095 | ||||||
chr17:30176104
|
GTTGTT | G | 168 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(165): Show | 168 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.172-1942_172-1938d others(7): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr17 | 30176104 | |||||
chr17:30176181
|
G | A | 8 | a0001c0001t0001g0151a0001c0001t0001g0163a0001c0001t0001g0164others(5): Show | 8 | HG01891.hp1 HG01934.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.172-1890G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 3/6 | chr17 | 30176181 | ||||||
chr17:30176351
|
A | G | 1 | a0001c0001t0002g0190 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.172-1720A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 3/6 | chr17 | 30176351 | ||||||
chr17:30176525
|
G | A | 1 | a0001c0001t0002g0276 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.172-1546G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 3/6 | chr17 | 30176525 | ||||||
chr17:30176606
|
T | TC | 19 | a0001c0002t0001g0006a0001c0002t0001g0022a0001c0002t0001g0024others(16): Show | 19 | HG01192.hp2 HG01346.hp1 HG01346.hp2 others(16): Show |
intron_variant | MODIFIER | c.172-1453dupC | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr17 | 30176606 | |||||
chr17:30176606
|
TC | T | 24 | a0001c0001t0001g0160a0001c0002t0001g0070a0001c0002t0001g0104others(21): Show | 24 | HG00741.hp2 HG01069.hp1 HG01071.hp2 others(21): Show |
intron_variant | MODIFIER | c.172-1453delC | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr17 | 30176606 | |||||
chr17:30176612
|
C | G | 3 | a0001c0002t0001g0039a0001c0002t0001g0064a0001c0002t0001g0133 | 3 | HG03942.hp1 HG04115.hp2 NA18946.hp1 |
intron_variant | MODIFIER | c.172-1459C>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 3/6 | chr17 | 30176612 | ||||||
chr17:30176613
|
C | T | 1 | a0001c0002t0001g0114 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.172-1458C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 3/6 | chr17 | 30176613 | ||||||
chr17:30176618
|
C | A | 31 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(28): Show | 31 | HG01243.hp2 HG01884.hp1 HG01884.hp2 others(28): Show |
intron_variant | MODIFIER | c.172-1453C>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 3/6 | chr17 | 30176618 | ||||||
chr17:30176618
|
C | CA | 81 | a0001c0001t0001g0151a0001c0001t0001g0155a0001c0001t0001g0164others(78): Show | 81 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.172-1443dupA | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr17 | 30176618 | |||||
chr17:30176618
|
C | CCA | 27 | a0001c0001t0001g0163a0001c0001t0002g0170a0001c0001t0002g0171others(24): Show | 27 | HG00597.hp2 HG00609.hp2 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.172-1453_172-1452i others(4): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 3/6 | chr17 | 30176618 | ||||||
chr17:30176619
|
A | C | 1 | a0001c0002t0001g0010 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.172-1452A>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 3/6 | chr17 | 30176619 | ||||||
chr17:30176745
|
C | T | 1 | a0001c0001t0002g0174 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.172-1326C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 3/6 | chr17 | 30176745 | ||||||
chr17:30177198
|
C | T | 3 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140 | 3 | HG03139.hp2 NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.172-873C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 3/6 | chr17 | 30177198 | ||||||
chr17:30177298
|
G | T | 9 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144others(6): Show | 9 | HG02055.hp2 HG02895.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.172-773G>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 3/6 | chr17 | 30177298 | ||||||
chr17:30177312
|
C | T | 2 | a0001c0001t0002g0175a0001c0001t0002g0176 | 2 | HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.172-759C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 3/6 | chr17 | 30177312 | ||||||
chr17:30177371
|
G | T | 137 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(134): Show | 137 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.172-700G>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 3/6 | chr17 | 30177371 | ||||||
chr17:30177375
|
T | TA | 135 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(132): Show | 135 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.172-682dupA | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr17 | 30177375 | |||||
chr17:30177410
|
A | G | 2 | a0001c0001t0002g0228a0001c0001t0002g0232 | 2 | NA18969.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.172-661A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 3/6 | chr17 | 30177410 | ||||||
chr17:30177436
|
A | G | 9 | a0001c0002t0003g0026a0001c0002t0003g0027a0001c0002t0003g0028others(6): Show | 9 | HG01069.hp1 HG01071.hp2 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.172-635A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 3/6 | chr17 | 30177436 | ||||||
chr17:30177491
|
G | C | 1 | a0001c0014t0008g0119 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.172-580G>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 3/6 | chr17 | 30177491 | ||||||
chr17:30177698
|
T | C | 1 | a0005c0006t0001g0041 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.172-373T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 3/6 | chr17 | 30177698 | ||||||
chr17:30177745
|
T | C | 1 | a0001c0002t0001g0016 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.172-326T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 3/6 | chr17 | 30177745 | ||||||
chr17:30178002
|
A | G | 1 | a0001c0002t0001g0127 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.172-69A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 3/6 | chr17 | 30178002 | ||||||
chr17:30178006
|
G | A | 137 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(134): Show | 137 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.172-65G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 3/6 | chr17 | 30178006 | ||||||
chr17:30178278
|
A | T | 1 | a0001c0002t0001g0059 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.300+79A>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 4/6 | chr17 | 30178278 | ||||||
chr17:30178280
|
C | A | 1 | a0001c0002t0001g0059 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.300+81C>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 4/6 | chr17 | 30178280 | ||||||
chr17:30178282
|
G | C | 1 | a0001c0002t0001g0059 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.300+83G>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 4/6 | chr17 | 30178282 | ||||||
chr17:30178374
|
T | G | 26 | a0001c0002t0001g0269a0001c0002t0001g0277a0001c0002t0001g0278others(23): Show | 26 | HG00741.hp2 HG01069.hp1 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.300+175T>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 4/6 | chr17 | 30178374 | ||||||
chr17:30178465
|
A | G | 3 | a0001c0001t0002g0236a0001c0001t0002g0237a0001c0001t0002g0259 | 3 | HG00323.hp1 HG01993.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.300+266A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 4/6 | chr17 | 30178465 | ||||||
chr17:30178878
|
A | C | 1 | a0001c0001t0001g0155 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.301-212A>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 4/6 | chr17 | 30178878 | ||||||
chr17:30179011
|
A | G | 7 | a0001c0001t0002g0270a0001c0001t0002g0271a0001c0001t0002g0276others(4): Show | 7 | HG01433.hp1 HG01884.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.301-79A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 4/6 | chr17 | 30179011 | ||||||
chr17:30180003
|
C | A | 105 | a0001c0001t0002g0081a0001c0001t0002g0082a0001c0001t0002g0170others(102): Show | 105 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.508+706C>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 5/6 | chr17 | 30180003 | ||||||
chr17:30180045
|
G | A | 225 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(222): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(222): Show |
intron_variant | MODIFIER | c.508+748G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 5/6 | chr17 | 30180045 | ||||||
chr17:30180225
|
T | C | 1 | a0001c0001t0002g0207 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.509-683T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 5/6 | chr17 | 30180225 | ||||||
chr17:30180398
|
C | T | 104 | a0001c0001t0002g0081a0001c0001t0002g0082a0001c0001t0002g0170others(101): Show | 104 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.509-510C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 5/6 | chr17 | 30180398 | ||||||
chr17:30180489
|
A | G | 7 | a0001c0001t0002g0270a0001c0001t0002g0271a0001c0001t0002g0276others(4): Show | 7 | HG01433.hp1 HG01884.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.509-419A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 5/6 | chr17 | 30180489 | ||||||
chr17:30180514
|
A | G | 11 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(8): Show | 11 | HG01243.hp2 HG01884.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.509-394A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 5/6 | chr17 | 30180514 | ||||||
chr17:30180569
|
G | C | 32 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(29): Show | 32 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.509-339G>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 5/6 | chr17 | 30180569 | ||||||
chr17:30180675
|
G | A | 94 | a0001c0001t0002g0081a0001c0001t0002g0082a0001c0001t0002g0171others(91): Show | 94 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.509-233G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 5/6 | chr17 | 30180675 | ||||||
chr17:30180735
|
T | C | 1 | a0001c0002t0001g0133 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.509-173T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 5/6 | chr17 | 30180735 | ||||||
chr17:30180807
|
C | T | 1 | a0001c0001t0002g0235 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.509-101C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 5/6 | chr17 | 30180807 | ||||||
chr17:30180836
|
C | T | 4 | a0001c0001t0004g0272a0001c0001t0004g0273a0001c0001t0004g0274others(1): Show | 4 | HG01433.hp1 HG02486.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.509-72C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 5/6 | chr17 | 30180836 | ||||||
chr17:30180837
|
T | A | 4 | a0001c0001t0004g0272a0001c0001t0004g0273a0001c0001t0004g0274others(1): Show | 4 | HG01433.hp1 HG02486.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.509-71T>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 5/6 | chr17 | 30180837 | ||||||
chr17:30180839
|
T | A | 4 | a0001c0001t0004g0272a0001c0001t0004g0273a0001c0001t0004g0274others(1): Show | 4 | HG01433.hp1 HG02486.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.509-69T>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 5/6 | chr17 | 30180839 | ||||||
chr17:30180840
|
ATGTC | A | 26 | a0001c0002t0001g0269a0001c0002t0001g0277a0001c0002t0001g0278others(23): Show | 26 | HG00741.hp2 HG01069.hp1 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.509-64_509-61delCT others(2): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 30180840 | |||||
chr17:30180840
|
ATGTCTGT others(22): Show |
A | 4 | a0001c0001t0004g0272a0001c0001t0004g0273a0001c0001t0004g0274others(1): Show | 4 | HG01433.hp1 HG02486.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.509-66_509-38delGT others(27): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 30180840 | |||||
chr17:30180870
|
T | A | 4 | a0001c0001t0004g0272a0001c0001t0004g0273a0001c0001t0004g0274others(1): Show | 4 | HG01433.hp1 HG02486.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.509-38T>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 5/6 | chr17 | 30180870 | ||||||
chr17:30181027
|
G | A | 1 | a0001c0014t0008g0119 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.617+11G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 6/6 | chr17 | 30181027 | ||||||
chr17:30181089
|
C | G | 6 | a0001c0002t0001g0013a0001c0002t0001g0018a0001c0002t0001g0038others(3): Show | 6 | HG01167.hp1 HG01169.hp2 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.617+73C>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 6/6 | chr17 | 30181089 | ||||||
chr17:30181280
|
C | G | 1 | a0001c0001t0002g0202 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.617+264C>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 6/6 | chr17 | 30181280 | ||||||
chr17:30181380
|
T | G | 26 | a0001c0002t0001g0269a0001c0002t0001g0277a0001c0002t0001g0278others(23): Show | 26 | HG00741.hp2 HG01069.hp1 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.617+364T>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 6/6 | chr17 | 30181380 | ||||||
chr17:30181398
|
CT | C | 157 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144others(154): Show | 157 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(154): Show |
intron_variant | MODIFIER | c.617+400delT | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr17 | 30181398 | |||||
chr17:30181398
|
CTT | C | 12 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(9): Show | 12 | HG01433.hp1 HG01884.hp2 HG01993.hp1 others(9): Show |
intron_variant | MODIFIER | c.617+399_617+400del others(2): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr17 | 30181398 | |||||
chr17:30181405
|
T | C | 1 | a0001c0001t0002g0170 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.617+389T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 6/6 | chr17 | 30181405 | ||||||
chr17:30181416
|
T | G | 7 | a0001c0001t0002g0270a0001c0001t0002g0271a0001c0001t0002g0276others(4): Show | 7 | HG01433.hp1 HG01884.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.617+400T>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 6/6 | chr17 | 30181416 | ||||||
chr17:30181438
|
G | A | 2 | a0001c0002t0003g0032a0001c0002t0003g0033 | 2 | HG02486.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.617+422G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 6/6 | chr17 | 30181438 | ||||||
chr17:30181478
|
C | T | 1 | a0001c0002t0001g0011 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.617+462C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 6/6 | chr17 | 30181478 | ||||||
chr17:30181524
|
G | A | 1 | a0001c0002t0001g0016 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.617+508G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 6/6 | chr17 | 30181524 | ||||||
chr17:30181597
|
G | GT | 95 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(92): Show | 95 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.617+593dupT | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr17 | 30181597 | |||||
chr17:30181597
|
G | T | 1 | a0001c0002t0001g0134 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.617+581G>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 6/6 | chr17 | 30181597 | ||||||
chr17:30181597
|
GT | G | 7 | a0001c0001t0002g0270a0001c0001t0002g0271a0001c0001t0002g0276others(4): Show | 7 | HG01433.hp1 HG01884.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.617+593delT | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr17 | 30181597 | |||||
chr17:30181604
|
T | G | 2 | a0001c0001t0002g0175a0001c0001t0002g0176 | 2 | HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.617+588T>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 6/6 | chr17 | 30181604 | ||||||
chr17:30181605
|
T | TG | 3 | a0001c0001t0002g0263a0006c0007t0002g0173a0006c0007t0002g0262 | 3 | HG00741.hp1 NA18948.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.617+589_617+590ins others(1): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 6/6 | chr17 | 30181605 | ||||||
chr17:30181607
|
T | G | 1 | a0001c0002t0003g0032 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.617+591T>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 6/6 | chr17 | 30181607 | ||||||
chr17:30181610
|
G | T | 1 | a0001c0002t0001g0120 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.617+594G>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 6/6 | chr17 | 30181610 | ||||||
chr17:30181616
|
T | G | 98 | a0001c0001t0002g0081a0001c0001t0002g0082a0001c0001t0002g0170others(95): Show | 98 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.617+600T>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 6/6 | chr17 | 30181616 | ||||||
chr17:30181721
|
G | A | 2 | a0001c0001t0002g0270a0001c0001t0002g0271 | 2 | HG01884.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.617+705G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 6/6 | chr17 | 30181721 | ||||||
chr17:30181842
|
T | G | 9 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0157others(6): Show | 9 | HG01243.hp2 HG01884.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.617+826T>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 6/6 | chr17 | 30181842 | ||||||
chr17:30181890
|
A | G | 140 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(137): Show | 140 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.617+874A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 6/6 | chr17 | 30181890 | ||||||
chr17:30181901
|
C | T | 3 | a0001c0001t0002g0174a0001c0001t0002g0175a0001c0001t0002g0176 | 3 | HG02258.hp2 HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.617+885C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 6/6 | chr17 | 30181901 | ||||||
chr17:30182048
|
C | CT | 15 | a0001c0002t0001g0020a0001c0002t0001g0084a0001c0002t0001g0088others(12): Show | 15 | HG00609.hp1 HG00639.hp1 HG02129.hp2 others(12): Show |
intron_variant | MODIFIER | c.617+1056dupT | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr17 | 30182048 | |||||
chr17:30182048
|
CT | C | 88 | a0001c0001t0002g0170a0001c0001t0002g0204a0001c0001t0002g0207others(85): Show | 88 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.617+1056delT | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr17 | 30182048 | |||||
chr17:30182048
|
CTT | C | 117 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144others(114): Show | 117 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.617+1055_617+1056d others(4): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr17 | 30182048 | |||||
chr17:30182048
|
CTTT | C | 16 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(13): Show | 16 | HG01884.hp1 HG01891.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.617+1054_617+1056d others(5): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr17 | 30182048 | |||||
chr17:30182072
|
T | A | 1 | a0002c0003t0001g0067 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.617+1056T>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 6/6 | chr17 | 30182072 | ||||||
chr17:30182584
|
G | T | 98 | a0001c0001t0002g0081a0001c0001t0002g0082a0001c0001t0002g0170others(95): Show | 98 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.617+1568G>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 6/6 | chr17 | 30182584 | ||||||
chr17:30182599
|
G | A | 2 | a0001c0002t0001g0021a0001c0002t0001g0044 | 2 | NA18961.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.617+1583G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 6/6 | chr17 | 30182599 | ||||||
chr17:30182646
|
A | C | 6 | a0001c0002t0003g0014a0001c0002t0003g0036a0001c0002t0003g0078others(3): Show | 6 | HG01192.hp1 HG01346.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.617+1630A>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 6/6 | chr17 | 30182646 | ||||||
chr17:30182795
|
G | A | 3 | a0001c0001t0002g0180a0001c0001t0002g0214a0001c0002t0001g0059 | 3 | HG01261.hp1 HG02735.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.617+1779G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 6/6 | chr17 | 30182795 | ||||||
chr17:30182987
|
T | G | 2 | a0001c0001t0002g0270a0001c0001t0002g0271 | 2 | HG01884.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.618-1628T>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 6/6 | chr17 | 30182987 | ||||||
chr17:30183017
|
C | T | 2 | a0001c0001t0002g0256a0001c0001t0002g0257 | 2 | HG01069.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.618-1598C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 6/6 | chr17 | 30183017 | ||||||
chr17:30183087
|
G | C | 1 | a0001c0002t0001g0106 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.618-1528G>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 6/6 | chr17 | 30183087 | ||||||
chr17:30183135
|
G | T | 1 | a0001c0001t0001g0151 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.618-1480G>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 6/6 | chr17 | 30183135 | ||||||
chr17:30183231
|
A | AG | 94 | a0001c0001t0002g0081a0001c0001t0002g0082a0001c0001t0002g0171others(91): Show | 94 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.618-1384_618-1383i others(3): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 6/6 | chr17 | 30183231 | ||||||
chr17:30183320
|
G | A | 1 | a0001c0002t0001g0016 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.618-1295G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 6/6 | chr17 | 30183320 | ||||||
chr17:30183356
|
G | T | 9 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144others(6): Show | 9 | HG02055.hp2 HG02895.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.618-1259G>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 6/6 | chr17 | 30183356 | ||||||
chr17:30183462
|
A | G | 2 | a0001c0002t0001g0021a0001c0002t0001g0044 | 2 | NA18961.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.618-1153A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 6/6 | chr17 | 30183462 | ||||||
chr17:30183638
|
T | G | 1 | a0001c0001t0002g0081 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.618-977T>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 6/6 | chr17 | 30183638 | ||||||
chr17:30183990
|
T | C | 2 | a0001c0001t0001g0158a0001c0001t0001g0159 | 2 | HG01243.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.618-625T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 6/6 | chr17 | 30183990 | ||||||
chr17:30184495
|
A | G | 1 | a0001c0002t0001g0059 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.618-120A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 6/6 | chr17 | 30184495 |