geneid | 4908 |
---|---|
ensemblid | ENSG00000185652.12 |
hgncid | 8023 |
symbol | NTF3 |
name | neurotrophin 3 |
refseq_nuc | NM_001102654.2 |
refseq_prot | NP_001096124.1 |
ensembl_nuc | ENST00000423158.4 |
ensembl_prot | ENSP00000397297.2 |
mane_status | MANE Select |
chr | chr12 |
start | 5432108 |
end | 5495299 |
strand | + |
ver | v1.2 |
region | chr12:5432108-5495299 |
region5000 | chr12:5427108-5500299 |
regionname0 | NTF3_chr12_5432108_5495299 |
regionname5000 | NTF3_chr12_5427108_5500299 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 270 | 315 | 74 | 66 | 123 | 16 | 34 | 93 | NTF3_chr12_5427108_5500299 | NTF3 | copy fasta | chr12 | 5427108 | 5500299 |
a0002 | 0/0 | 270 | 53 | 17 | 10 | 25 | 0 | 1 | 21 | NTF3_chr12_5427108_5500299 | NTF3 | copy fasta | chr12 | 5427108 | 5500299 |
a0003 | 0/0 | 270 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | copy fasta | chr12 | 5427108 | 5500299 |
a0004 | 0/0 | 270 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | copy fasta | chr12 | 5427108 | 5500299 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 813 | 155 | 52 | 32 | 57 | 5 | 8 | NTF3_chr12_5427108_5500299 | NTF3 | copy fasta | chr12 | 5427108 | 5500299 |
c0002 | 1/0 | 813 | 132 | 17 | 27 | 60 | 10 | 17 | NTF3_chr12_5427108_5500299 | NTF3 | copy fasta | chr12 | 5427108 | 5500299 |
c0003 | 0/0 | 813 | 49 | 17 | 10 | 21 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | copy fasta | chr12 | 5427108 | 5500299 |
c0004 | 0/0 | 813 | 21 | 4 | 5 | 3 | 1 | 8 | NTF3_chr12_5427108_5500299 | NTF3 | copy fasta | chr12 | 5427108 | 5500299 |
c0005 | 0/0 | 813 | 4 | 0 | 0 | 4 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | copy fasta | chr12 | 5427108 | 5500299 |
c0006 | 0/0 | 813 | 3 | 0 | 2 | 0 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | copy fasta | chr12 | 5427108 | 5500299 |
c0007 | 0/0 | 813 | 2 | 0 | 0 | 2 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | copy fasta | chr12 | 5427108 | 5500299 |
c0008 | 0/0 | 813 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | copy fasta | chr12 | 5427108 | 5500299 |
c0009 | 0/0 | 813 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | copy fasta | chr12 | 5427108 | 5500299 |
c0010 | 0/0 | 813 | 1 | 0 | 0 | 0 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | copy fasta | chr12 | 5427108 | 5500299 |
c0011 | 0/0 | 813 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | copy fasta | chr12 | 5427108 | 5500299 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 529 | 366 | 89 | 75 | 148 | 16 | 36 | NTF3_chr12_5427108_5500299 | NTF3 | copy fasta | chr12 | 5427108 | 5500299 |
t0002 | 0/0 | 529 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | copy fasta | chr12 | 5427108 | 5500299 |
t0003 | 0/0 | 529 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | copy fasta | chr12 | 5427108 | 5500299 |
t0004 | 0/0 | 529 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | copy fasta | chr12 | 5427108 | 5500299 |
t0005 | 0/0 | 529 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | copy fasta | chr12 | 5427108 | 5500299 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0003 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0018 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0277 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0297 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0305 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0338 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
g0358 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 813 | 155 | 52 | 32 | 57 | 5 | 8 | NTF3_chr12_5427108_5500299 | NTF3 | copy fasta | chr12 | 5427108 | 5500299 |
a0001c0002 | 1/0 | 813 | 132 | 17 | 27 | 60 | 10 | 17 | NTF3_chr12_5427108_5500299 | NTF3 | copy fasta | chr12 | 5427108 | 5500299 |
a0001c0004 | 0/0 | 813 | 21 | 4 | 5 | 3 | 1 | 8 | NTF3_chr12_5427108_5500299 | NTF3 | copy fasta | chr12 | 5427108 | 5500299 |
a0001c0006 | 0/0 | 813 | 3 | 0 | 2 | 0 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | copy fasta | chr12 | 5427108 | 5500299 |
a0001c0007 | 0/0 | 813 | 2 | 0 | 0 | 2 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | copy fasta | chr12 | 5427108 | 5500299 |
a0001c0009 | 0/0 | 813 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | copy fasta | chr12 | 5427108 | 5500299 |
a0001c0011 | 0/0 | 813 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | copy fasta | chr12 | 5427108 | 5500299 |
a0002c0003 | 0/0 | 813 | 49 | 17 | 10 | 21 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | copy fasta | chr12 | 5427108 | 5500299 |
a0002c0005 | 0/0 | 813 | 4 | 0 | 0 | 4 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | copy fasta | chr12 | 5427108 | 5500299 |
a0003c0008 | 0/0 | 813 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | copy fasta | chr12 | 5427108 | 5500299 |
a0004c0010 | 0/0 | 813 | 1 | 0 | 0 | 0 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | copy fasta | chr12 | 5427108 | 5500299 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 1341 | 151 | 49 | 31 | 57 | 5 | 8 | NTF3_chr12_5427108_5500299 | NTF3 | copy fasta | chr12 | 5427108 | 5500299 |
a0001c0001t0002 | 0/0 | 1341 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | copy fasta | chr12 | 5427108 | 5500299 |
a0001c0001t0003 | 0/0 | 1341 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | copy fasta | chr12 | 5427108 | 5500299 |
a0001c0001t0004 | 0/0 | 1341 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | copy fasta | chr12 | 5427108 | 5500299 |
a0001c0001t0005 | 0/0 | 1341 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | copy fasta | chr12 | 5427108 | 5500299 |
a0001c0002t0001 | 1/0 | 1341 | 132 | 17 | 27 | 60 | 10 | 17 | NTF3_chr12_5427108_5500299 | NTF3 | copy fasta | chr12 | 5427108 | 5500299 |
a0001c0004t0001 | 0/0 | 1341 | 21 | 4 | 5 | 3 | 1 | 8 | NTF3_chr12_5427108_5500299 | NTF3 | copy fasta | chr12 | 5427108 | 5500299 |
a0001c0006t0001 | 0/0 | 1341 | 3 | 0 | 2 | 0 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | copy fasta | chr12 | 5427108 | 5500299 |
a0001c0007t0001 | 0/0 | 1341 | 2 | 0 | 0 | 2 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | copy fasta | chr12 | 5427108 | 5500299 |
a0001c0009t0001 | 0/0 | 1341 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | copy fasta | chr12 | 5427108 | 5500299 |
a0001c0011t0001 | 0/0 | 1341 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | copy fasta | chr12 | 5427108 | 5500299 |
a0002c0003t0001 | 0/0 | 1341 | 49 | 17 | 10 | 21 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | copy fasta | chr12 | 5427108 | 5500299 |
a0002c0005t0001 | 0/0 | 1341 | 4 | 0 | 0 | 4 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | copy fasta | chr12 | 5427108 | 5500299 |
a0003c0008t0001 | 0/0 | 1341 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | copy fasta | chr12 | 5427108 | 5500299 |
a0004c0010t0001 | 0/0 | 1341 | 1 | 0 | 0 | 0 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | copy fasta | chr12 | 5427108 | 5500299 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0305 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0001g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0002g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0003g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0004g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0001t0005g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0003 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0018 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0002t0001g0358 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0004t0001g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0004t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0004t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0004t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0004t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0004t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0004t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0004t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0004t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0004t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0004t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0004t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0004t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0004t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0004t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0004t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0004t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0004t0001g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0004t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0004t0001g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0006t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0006t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0006t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0007t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0007t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0009t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0001c0011t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0002c0003t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0002c0003t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0002c0003t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0002c0003t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0002c0003t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0002c0003t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0002c0003t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0002c0003t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0002c0003t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0002c0003t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0002c0003t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0002c0003t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0002c0003t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0002c0003t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0002c0003t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0002c0003t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0002c0003t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0002c0003t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0002c0003t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0002c0003t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0002c0003t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0002c0003t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0002c0003t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0002c0003t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0002c0003t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0002c0003t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0002c0003t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0002c0003t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0002c0003t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0002c0003t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0002c0003t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0002c0003t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0002c0003t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0002c0003t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0002c0003t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0002c0003t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0002c0003t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0002c0003t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0002c0003t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0002c0003t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0002c0003t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0002c0003t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0002c0003t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0002c0003t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0002c0003t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0002c0003t0001g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0002c0003t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0002c0003t0001g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0002c0005t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0002c0005t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0002c0005t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0002c0005t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0003c0008t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
a0004c0010t0001g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0002 | t0001 | g0162 | EUR | GBR | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0134 | EUR | GBR | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG00140 | hp1 | a0001 | c0002 | t0001 | g0358 | EUR | GBR | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0338 | EUR | GBR | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0092 | EUR | FIN | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG00280 | hp2 | a0001 | c0002 | t0001 | g0152 | EUR | FIN | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0249 | EUR | FIN | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG00323 | hp2 | a0001 | c0002 | t0001 | g0003 | EUR | FIN | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG00408 | hp1 | a0002 | c0003 | t0001 | g0342 | EAS | CHS | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG00408 | hp2 | a0002 | c0003 | t0001 | g0043 | EAS | CHS | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG00423 | hp1 | a0001 | c0002 | t0001 | g0071 | EAS | CHS | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG00423 | hp2 | a0001 | c0002 | t0001 | g0022 | EAS | CHS | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | CHS | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | CHS | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG00558 | hp1 | a0001 | c0002 | t0001 | g0013 | EAS | CHS | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | CHS | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG00621 | hp1 | a0001 | c0002 | t0001 | g0184 | EAS | CHS | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG00621 | hp2 | a0001 | c0002 | t0001 | g0234 | EAS | CHS | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0307 | AMR | PUR | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG00639 | hp2 | a0001 | c0002 | t0001 | g0291 | AMR | PUR | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG00642 | hp1 | a0001 | c0002 | t0001 | g0175 | AMR | PUR | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0258 | AMR | PUR | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG00673 | hp1 | a0001 | c0002 | t0001 | g0180 | EAS | CHS | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG00673 | hp2 | a0001 | c0009 | t0001 | g0287 | EAS | CHS | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0268 | AMR | PUR | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0225 | AMR | PUR | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0242 | AMR | PUR | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0239 | AMR | PUR | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG00738 | hp1 | a0001 | c0004 | t0001 | g0008 | AMR | PUR | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0329 | AMR | PUR | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG00741 | hp1 | a0001 | c0002 | t0001 | g0312 | AMR | PUR | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG01069 | hp1 | a0001 | c0002 | t0001 | g0288 | AMR | PUR | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG01070 | hp1 | a0001 | c0004 | t0001 | g0008 | AMR | PUR | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG01070 | hp2 | a0001 | c0002 | t0001 | g0124 | AMR | PUR | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG01074 | hp1 | a0001 | c0001 | t0003 | g0024 | AMR | PUR | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0255 | AMR | PUR | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG01081 | hp2 | a0001 | c0002 | t0001 | g0290 | AMR | PUR | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG01099 | hp1 | a0001 | c0002 | t0001 | g0104 | AMR | PUR | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG01099 | hp2 | a0001 | c0002 | t0001 | g0117 | AMR | PUR | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG01106 | hp1 | a0002 | c0003 | t0001 | g0136 | AMR | PUR | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG01168 | hp1 | a0001 | c0006 | t0001 | g0174 | AMR | PUR | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG01168 | hp2 | a0001 | c0002 | t0001 | g0275 | AMR | PUR | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG01169 | hp1 | a0001 | c0002 | t0001 | g0246 | AMR | PUR | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG01169 | hp2 | a0001 | c0006 | t0001 | g0173 | AMR | PUR | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0323 | AMR | PUR | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG01175 | hp2 | a0001 | c0002 | t0001 | g0254 | AMR | PUR | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG01192 | hp1 | a0001 | c0002 | t0001 | g0003 | AMR | PUR | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG01192 | hp2 | a0001 | c0002 | t0001 | g0101 | AMR | PUR | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG01243 | hp2 | a0001 | c0002 | t0001 | g0210 | AMR | PUR | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG01255 | hp1 | a0002 | c0003 | t0001 | g0130 | AMR | CLM | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG01255 | hp2 | a0001 | c0002 | t0001 | g0267 | AMR | CLM | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG01256 | hp1 | a0001 | c0002 | t0001 | g0181 | AMR | CLM | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0250 | AMR | CLM | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG01257 | hp1 | a0002 | c0003 | t0001 | g0066 | AMR | CLM | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG01257 | hp2 | a0001 | c0002 | t0001 | g0241 | AMR | CLM | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG01258 | hp1 | a0001 | c0002 | t0001 | g0182 | AMR | CLM | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG01258 | hp2 | a0001 | c0002 | t0001 | g0240 | AMR | CLM | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | CLM | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG01261 | hp2 | a0001 | c0004 | t0001 | g0280 | AMR | CLM | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | CLM | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | CLM | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | CLM | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | CLM | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG01361 | hp1 | a0002 | c0003 | t0001 | g0075 | AMR | CLM | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0301 | AMR | CLM | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG01433 | hp1 | a0001 | c0002 | t0001 | g0149 | AMR | CLM | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG01433 | hp2 | a0002 | c0003 | t0001 | g0067 | AMR | CLM | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG01516 | hp1 | a0001 | c0002 | t0001 | g0170 | EUR | IBS | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG01516 | hp2 | a0001 | c0002 | t0001 | g0107 | EUR | IBS | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG01517 | hp1 | a0001 | c0002 | t0001 | g0297 | EUR | IBS | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG01517 | hp2 | a0001 | c0004 | t0001 | g0277 | EUR | IBS | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG01884 | hp1 | a0001 | c0001 | t0002 | g0349 | AFR | ACB | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0345 | AFR | ACB | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0283 | AFR | ACB | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG01891 | hp2 | a0002 | c0003 | t0001 | g0164 | AFR | ACB | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG01928 | hp1 | a0002 | c0003 | t0001 | g0328 | AMR | PEL | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG01928 | hp2 | a0001 | c0002 | t0001 | g0316 | AMR | PEL | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG01934 | hp1 | a0002 | c0003 | t0001 | g0132 | AMR | PEL | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG01934 | hp2 | a0001 | c0002 | t0001 | g0125 | AMR | PEL | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0306 | AMR | PEL | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG01943 | hp2 | a0002 | c0003 | t0001 | g0128 | AMR | PEL | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0262 | AMR | PEL | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0351 | AMR | PEL | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG01975 | hp1 | a0002 | c0003 | t0001 | g0269 | AMR | PEL | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0302 | AMR | PEL | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | PEL | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG01978 | hp2 | a0001 | c0002 | t0001 | g0346 | AMR | PEL | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG01993 | hp1 | a0001 | c0004 | t0001 | g0357 | AMR | PEL | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG01993 | hp2 | a0002 | c0003 | t0001 | g0040 | AMR | PEL | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG02027 | hp1 | a0002 | c0003 | t0001 | g0087 | EAS | KHV | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | KHV | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | ACB | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | ACB | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0347 | EAS | KHV | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | KHV | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG02074 | hp2 | a0001 | c0002 | t0001 | g0009 | EAS | KHV | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG02083 | hp1 | a0001 | c0002 | t0001 | g0332 | EAS | KHV | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | KHV | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | KHV | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG02129 | hp2 | a0001 | c0002 | t0001 | g0093 | EAS | KHV | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG02132 | hp1 | a0001 | c0002 | t0001 | g0204 | EAS | KHV | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | KHV | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | KHV | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | ACB | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0289 | AFR | ACB | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG02148 | hp1 | a0001 | c0004 | t0001 | g0247 | AMR | PEL | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG02148 | hp2 | a0001 | c0002 | t0001 | g0160 | AMR | PEL | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | CDX | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG02165 | hp2 | a0001 | c0002 | t0001 | g0188 | EAS | CDX | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG02257 | hp2 | a0001 | c0002 | t0001 | g0252 | AFR | ACB | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0352 | AFR | ACB | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG02273 | hp1 | a0001 | c0002 | t0001 | g0313 | AMR | PEL | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG02273 | hp2 | a0001 | c0002 | t0001 | g0264 | AMR | PEL | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | ACB | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0327 | AMR | PEL | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG02293 | hp2 | a0001 | c0002 | t0001 | g0151 | AMR | PEL | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0260 | AMR | PEL | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0251 | AMR | PEL | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG02451 | hp1 | a0002 | c0003 | t0001 | g0050 | AFR | ACB | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG02451 | hp2 | a0001 | c0002 | t0001 | g0156 | AFR | ACB | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG02523 | hp2 | a0001 | c0002 | t0001 | g0314 | EAS | KHV | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | GWD | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | GWD | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG02602 | hp1 | a0001 | c0004 | t0001 | g0209 | SAS | PJL | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG02602 | hp2 | a0001 | c0002 | t0001 | g0270 | SAS | PJL | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG02615 | hp2 | a0001 | c0002 | t0001 | g0205 | AFR | GWD | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG02622 | hp1 | a0002 | c0003 | t0001 | g0046 | AFR | GWD | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG02622 | hp2 | a0002 | c0003 | t0001 | g0356 | AFR | GWD | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | GWD | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG02630 | hp2 | a0001 | c0004 | t0001 | g0141 | AFR | GWD | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG02647 | hp2 | a0001 | c0002 | t0001 | g0048 | AFR | GWD | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG02683 | hp1 | a0001 | c0002 | t0001 | g0099 | SAS | PJL | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG02683 | hp2 | a0001 | c0002 | t0001 | g0106 | SAS | PJL | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0090 | SAS | PJL | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG02698 | hp2 | a0001 | c0006 | t0001 | g0086 | SAS | PJL | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0348 | AFR | GWD | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG02717 | hp2 | a0002 | c0003 | t0001 | g0196 | AFR | GWD | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG02723 | hp1 | a0001 | c0011 | t0001 | g0293 | AFR | GWD | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG02723 | hp2 | a0002 | c0003 | t0001 | g0168 | AFR | GWD | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG02735 | hp1 | a0001 | c0004 | t0001 | g0245 | SAS | PJL | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG02735 | hp2 | a0001 | c0002 | t0001 | g0281 | SAS | PJL | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0299 | SAS | PJL | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG02738 | hp2 | a0001 | c0002 | t0001 | g0276 | SAS | PJL | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG02809 | hp2 | a0002 | c0003 | t0001 | g0060 | AFR | GWD | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | GWD | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | GWD | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG02895 | hp1 | a0002 | c0003 | t0001 | g0203 | AFR | GWD | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG02895 | hp2 | a0002 | c0003 | t0001 | g0103 | AFR | GWD | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | ESN | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | ESN | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG02965 | hp2 | a0001 | c0002 | t0001 | g0229 | AFR | ESN | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG02970 | hp1 | a0001 | c0002 | t0001 | g0119 | AFR | ESN | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG02970 | hp2 | a0001 | c0002 | t0001 | g0030 | AFR | ESN | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | ESN | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG02976 | hp2 | a0001 | c0004 | t0001 | g0139 | AFR | ESN | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG03017 | hp1 | a0001 | c0002 | t0001 | g0227 | SAS | PJL | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG03017 | hp2 | a0001 | c0004 | t0001 | g0322 | SAS | PJL | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG03098 | hp1 | a0002 | c0003 | t0001 | g0211 | AFR | MSL | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG03098 | hp2 | a0001 | c0002 | t0001 | g0354 | AFR | MSL | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG03130 | hp1 | a0001 | c0002 | t0001 | g0161 | AFR | ESN | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0282 | AFR | ESN | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG03139 | hp1 | a0002 | c0003 | t0001 | g0047 | AFR | ESN | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG03139 | hp2 | a0001 | c0002 | t0001 | g0031 | AFR | ESN | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0294 | AFR | ESN | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | ESN | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | MSL | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | MSL | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG03225 | hp1 | a0002 | c0003 | t0001 | g0159 | AFR | MSL | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | MSL | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG03239 | hp1 | a0001 | c0002 | t0001 | g0108 | SAS | PJL | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG03239 | hp2 | a0001 | c0002 | t0001 | g0198 | SAS | PJL | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0310 | AFR | MSL | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG03453 | hp2 | a0001 | c0004 | t0001 | g0333 | AFR | MSL | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG03486 | hp1 | a0002 | c0003 | t0001 | g0045 | AFR | MSL | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | MSL | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | ESN | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG03540 | hp1 | a0002 | c0003 | t0001 | g0147 | AFR | GWD | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0350 | AFR | GWD | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG03579 | hp1 | a0001 | c0002 | t0001 | g0353 | AFR | MSL | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | MSL | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG03654 | hp1 | a0001 | c0002 | t0001 | g0296 | SAS | PJL | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG03654 | hp2 | a0001 | c0002 | t0001 | g0027 | SAS | PJL | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG03669 | hp1 | a0001 | c0002 | t0001 | g0153 | SAS | PJL | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG03669 | hp2 | a0001 | c0004 | t0001 | g0109 | SAS | PJL | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG03704 | hp1 | a0001 | c0002 | t0001 | g0243 | SAS | PJL | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG03704 | hp2 | a0004 | c0010 | t0001 | g0326 | SAS | PJL | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG03710 | hp1 | a0001 | c0002 | t0001 | g0158 | SAS | PJL | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG03710 | hp2 | a0001 | c0004 | t0001 | g0257 | SAS | PJL | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG03942 | hp1 | a0001 | c0002 | t0001 | g0145 | SAS | BEB | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG03942 | hp2 | a0001 | c0002 | t0001 | g0150 | SAS | BEB | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG04115 | hp1 | a0001 | c0002 | t0001 | g0169 | SAS | STU | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0044 | SAS | STU | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0253 | SAS | BEB | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0096 | SAS | BEB | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0208 | SAS | STU | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG04199 | hp2 | a0002 | c0003 | t0001 | g0256 | SAS | STU | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG04204 | hp1 | a0001 | c0004 | t0001 | g0057 | SAS | STU | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG04204 | hp2 | a0001 | c0004 | t0001 | g0155 | SAS | STU | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG04228 | hp1 | a0001 | c0002 | t0001 | g0187 | SAS | STU | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0135 | SAS | STU | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | YRI | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA18522 | hp2 | a0001 | c0002 | t0001 | g0355 | AFR | YRI | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA18612 | hp1 | a0002 | c0003 | t0001 | g0324 | EAS | CHB | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | CHB | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHB | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA18747 | hp2 | a0001 | c0002 | t0001 | g0244 | EAS | CHB | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA18906 | hp1 | a0003 | c0008 | t0001 | g0034 | AFR | YRI | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | YRI | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA18940 | hp1 | a0002 | c0003 | t0001 | g0083 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA18940 | hp2 | a0001 | c0002 | t0001 | g0058 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA18941 | hp1 | a0001 | c0002 | t0001 | g0097 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA18941 | hp2 | a0002 | c0003 | t0001 | g0076 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA18942 | hp1 | a0001 | c0002 | t0001 | g0137 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA18942 | hp2 | a0002 | c0003 | t0001 | g0191 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA18943 | hp1 | a0001 | c0002 | t0001 | g0179 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA18943 | hp2 | a0001 | c0002 | t0001 | g0038 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA18944 | hp2 | a0002 | c0003 | t0001 | g0005 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA18946 | hp2 | a0002 | c0003 | t0001 | g0005 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA18947 | hp1 | a0001 | c0002 | t0001 | g0065 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA18947 | hp2 | a0001 | c0002 | t0001 | g0176 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA18949 | hp1 | a0001 | c0002 | t0001 | g0189 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA18949 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA18950 | hp2 | a0001 | c0004 | t0001 | g0202 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA18952 | hp1 | a0002 | c0005 | t0001 | g0259 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA18952 | hp2 | a0001 | c0002 | t0001 | g0343 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA18957 | hp1 | a0002 | c0003 | t0001 | g0320 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA18957 | hp2 | a0001 | c0002 | t0001 | g0056 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA18959 | hp1 | a0002 | c0005 | t0001 | g0319 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA18962 | hp1 | a0001 | c0002 | t0001 | g0197 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA18964 | hp1 | a0001 | c0002 | t0001 | g0274 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA18964 | hp2 | a0001 | c0002 | t0001 | g0315 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA18968 | hp1 | a0001 | c0002 | t0001 | g0035 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0340 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA18969 | hp1 | a0001 | c0004 | t0001 | g0309 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0337 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA18970 | hp2 | a0002 | c0005 | t0001 | g0263 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA18971 | hp1 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA18971 | hp2 | a0001 | c0002 | t0001 | g0233 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA18974 | hp1 | a0002 | c0003 | t0001 | g0325 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA18974 | hp2 | a0001 | c0002 | t0001 | g0334 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA18977 | hp1 | a0001 | c0007 | t0001 | g0220 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA18979 | hp1 | a0002 | c0003 | t0001 | g0042 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA18979 | hp2 | a0001 | c0002 | t0001 | g0094 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA18980 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA18980 | hp2 | a0002 | c0003 | t0001 | g0039 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA18981 | hp2 | a0001 | c0002 | t0001 | g0272 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA18983 | hp1 | a0001 | c0002 | t0001 | g0095 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA18983 | hp2 | a0002 | c0003 | t0001 | g0129 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA18984 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA18985 | hp1 | a0002 | c0003 | t0001 | g0006 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA18985 | hp2 | a0001 | c0002 | t0001 | g0303 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA18986 | hp2 | a0001 | c0002 | t0001 | g0023 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA18991 | hp1 | a0001 | c0007 | t0001 | g0054 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA18991 | hp2 | a0002 | c0003 | t0001 | g0194 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA18993 | hp1 | a0002 | c0003 | t0001 | g0041 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA18994 | hp2 | a0001 | c0002 | t0001 | g0185 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA18995 | hp1 | a0001 | c0002 | t0001 | g0037 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA18997 | hp1 | a0001 | c0002 | t0001 | g0344 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA18997 | hp2 | a0001 | c0002 | t0001 | g0192 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0339 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA18998 | hp2 | a0001 | c0002 | t0001 | g0148 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA19000 | hp1 | a0001 | c0002 | t0001 | g0178 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA19000 | hp2 | a0001 | c0002 | t0001 | g0154 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA19002 | hp1 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA19004 | hp1 | a0001 | c0002 | t0001 | g0317 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA19004 | hp2 | a0001 | c0004 | t0001 | g0273 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA19006 | hp1 | a0001 | c0002 | t0001 | g0321 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA19007 | hp2 | a0001 | c0002 | t0001 | g0055 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA19010 | hp1 | a0001 | c0002 | t0001 | g0218 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA19010 | hp2 | a0002 | c0005 | t0001 | g0261 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA19011 | hp1 | a0001 | c0002 | t0001 | g0183 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0336 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA19030 | hp1 | a0001 | c0001 | t0005 | g0223 | AFR | LWK | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | LWK | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA19043 | hp1 | a0002 | c0003 | t0001 | g0285 | AFR | LWK | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | LWK | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA19057 | hp2 | a0001 | c0002 | t0001 | g0232 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA19058 | hp1 | a0001 | c0002 | t0001 | g0098 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0335 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA19067 | hp1 | a0001 | c0002 | t0001 | g0186 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA19067 | hp2 | a0002 | c0003 | t0001 | g0084 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA19074 | hp1 | a0001 | c0002 | t0001 | g0082 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA19074 | hp2 | a0001 | c0002 | t0001 | g0127 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA19077 | hp1 | a0001 | c0002 | t0001 | g0177 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0331 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA19079 | hp1 | a0002 | c0003 | t0001 | g0062 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA19079 | hp2 | a0001 | c0002 | t0001 | g0318 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA19080 | hp2 | a0001 | c0002 | t0001 | g0214 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA19088 | hp1 | a0002 | c0003 | t0001 | g0235 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0341 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | YRI | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | YRI | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA20129 | hp1 | a0001 | c0002 | t0001 | g0206 | AFR | ASW | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA20129 | hp2 | a0002 | c0003 | t0001 | g0201 | AFR | ASW | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA20752 | hp1 | a0001 | c0002 | t0001 | g0089 | EUR | TSI | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA20752 | hp2 | a0001 | c0002 | t0001 | g0236 | EUR | TSI | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA20805 | hp1 | a0001 | c0002 | t0001 | g0126 | EUR | TSI | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0157 | EUR | TSI | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0308 | SAS | GIH | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA20905 | hp2 | a0001 | c0004 | t0001 | g0248 | SAS | GIH | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG02109 | hp1 | a0001 | c0002 | t0001 | g0230 | AFR | ACB | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | ACB | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG02486 | hp1 | a0001 | c0002 | t0001 | g0199 | AFR | ACB | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG02486 | hp2 | a0001 | c0002 | t0001 | g0271 | AFR | ACB | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG02559 | hp1 | a0001 | c0002 | t0001 | g0226 | AFR | ACB | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | ACB | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG03471 | hp1 | a0001 | c0001 | t0004 | g0311 | AFR | MSL | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | MSL | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0295 | AFR | USA | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
HG06807 | hp2 | a0001 | c0004 | t0001 | g0292 | AFR | USA | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA18955 | hp1 | a0001 | c0002 | t0001 | g0284 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA18955 | hp2 | a0001 | c0002 | t0001 | g0215 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA20300 | hp1 | a0002 | c0003 | t0001 | g0212 | AFR | USA | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | USA | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | LWK | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | LWK | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0305 | REF | REF | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
homoSapiens_grch38 | hp1 | a0001 | c0002 | t0001 | g0018 | REF | REF | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:5494440
|
G | A | 1 | a0004 | 1 | HG03704.hp2 | missense_variant | MODERATE | c.265G>A | p.Gly89Arg | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 2/2 | 482/1341 | 265/813 | 89/270 | chr12 | 5494440 | ||
chr12:5494441
|
G | A | 2 | a0002a0003 | 54 | HG00408.hp1 HG00408.hp2 HG01106.hp1 others(51): Show |
missense_variant | MODERATE | c.266G>A | p.Gly89Glu | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 2/2 | 483/1341 | 266/813 | 89/270 | chr12 | 5494441 | ||
chr12:5494563
|
T | G | 1 | a0003 | 1 | NA18906.hp1 | missense_variant | MODERATE | c.388T>G | p.Leu130Val | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 2/2 | 605/1341 | 388/813 | 130/270 | chr12 | 5494563 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:5494436
|
G | C | 4 | a0001c0009a0002c0003a0002c0005others(1): Show | 55 | HG00408.hp1 HG00408.hp2 HG00673.hp2 others(52): Show |
synonymous_variant | LOW | c.261G>C | p.Arg87Arg | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 2/2 | 478/1341 | 261/813 | 87/270 | chr12 | 5494436 | ||
chr12:5494466
|
G | A | 3 | a0001c0001a0001c0004a0001c0011 | 177 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(174): Show |
synonymous_variant | LOW | c.291G>A | p.Pro97Pro | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 2/2 | 508/1341 | 291/813 | 97/270 | chr12 | 5494466 | ||
chr12:5494769
|
C | T | 3 | a0001c0004a0001c0006a0002c0005 | 28 | HG00738.hp1 HG01070.hp1 HG01168.hp1 others(25): Show |
synonymous_variant | LOW | c.594C>T | p.Pro198Pro | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 2/2 | 811/1341 | 594/813 | 198/270 | chr12 | 5494769 | ||
chr12:5494823
|
C | T | 1 | a0001c0007 | 2 | NA18977.hp1 NA18991.hp1 |
synonymous_variant | LOW | c.648C>T | p.Asn216Asn | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 2/2 | 865/1341 | 648/813 | 216/270 | chr12 | 5494823 | ||
chr12:5494901
|
A | G | 1 | a0001c0011 | 1 | HG02723.hp1 | synonymous_variant | LOW | c.726A>G | p.Ser242Ser | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 2/2 | 943/1341 | 726/813 | 242/270 | chr12 | 5494901 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:5432293
|
T | C | 1 | a0001c0001t0002 | 1 | HG01884.hp1 | 5_prime_UTR_variant | MODIFIER | c.-32T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/2 | 32 | chr12 | 5432293 | |||||
chr12:5495031
|
A | G | 1 | a0001c0001t0005 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*43A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 2/2 | 43 | chr12 | 5495031 | |||||
chr12:5495234
|
C | G | 1 | a0001c0001t0004 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*246C>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 2/2 | 246 | chr12 | 5495234 | |||||
chr12:5495254
|
T | G | 1 | a0001c0001t0003 | 1 | HG01074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*266T>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 2/2 | 266 | chr12 | 5495254 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:5432439
|
A | T | 1 | a0001c0002t0001g0358 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.18+97A>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5432439 | ||||||
chr12:5432458
|
C | G | 1 | a0001c0004t0001g0357 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.18+116C>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5432458 | ||||||
chr12:5432540
|
A | T | 4 | a0001c0002t0001g0353a0001c0002t0001g0354a0001c0002t0001g0355others(1): Show | 4 | HG02622.hp2 HG03098.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.18+198A>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5432540 | ||||||
chr12:5432541
|
C | T | 4 | a0001c0002t0001g0353a0001c0002t0001g0354a0001c0002t0001g0355others(1): Show | 4 | HG02622.hp2 HG03098.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.18+199C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5432541 | ||||||
chr12:5432556
|
T | TAC | 4 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(1): Show | 4 | HG02647.hp1 HG02922.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.18+264_18+265dupCA | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5432556 | |||||
chr12:5432556
|
TAC | T | 14 | a0001c0001t0001g0036a0001c0001t0001g0044a0001c0001t0001g0172others(11): Show | 14 | HG00408.hp2 HG01993.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.18+264_18+265delCA | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5432556 | |||||
chr12:5432556
|
TACAC | T | 75 | a0001c0001t0001g0049a0001c0001t0001g0051a0001c0001t0001g0052others(72): Show | 76 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.18+262_18+265delCA others(2): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5432556 | |||||
chr12:5432556
|
TACACAC | T | 56 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(53): Show | 57 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(54): Show |
intron_variant | MODIFIER | c.18+260_18+265delCA others(4): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5432556 | |||||
chr12:5432556
|
TACACACA others(1): Show |
T | 134 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(131): Show | 138 | HG00323.hp1 HG00438.hp1 HG00558.hp1 others(135): Show |
intron_variant | MODIFIER | c.18+258_18+265delCA others(6): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5432556 | |||||
chr12:5432556
|
TACACACA others(3): Show |
T | 36 | a0001c0001t0001g0010a0001c0001t0001g0300a0001c0001t0001g0301others(33): Show | 38 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.18+256_18+265delCA others(8): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5432556 | |||||
chr12:5432556
|
TACACACA others(5): Show |
T | 18 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0335others(15): Show | 20 | HG00140.hp2 HG00408.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.18+254_18+265delCA others(10): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5432556 | |||||
chr12:5432556
|
TACACACA others(7): Show |
T | 2 | a0001c0001t0001g0350a0001c0001t0001g0351 | 2 | HG01952.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.18+252_18+265delCA others(12): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5432556 | |||||
chr12:5432556
|
TACACACA others(11): Show |
T | 1 | a0001c0001t0001g0352 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.18+248_18+265delCA others(16): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5432556 | |||||
chr12:5432580
|
C | A | 1 | a0001c0002t0001g0013 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.18+238C>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5432580 | ||||||
chr12:5432602
|
C | G | 4 | a0001c0001t0001g0118a0001c0001t0001g0172a0001c0002t0001g0119others(1): Show | 4 | HG02055.hp2 HG02559.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.18+260C>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5432602 | ||||||
chr12:5432650
|
G | A | 1 | a0001c0001t0001g0120 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.18+308G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5432650 | ||||||
chr12:5432725
|
A | G | 152 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0017others(149): Show | 155 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.18+383A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5432725 | ||||||
chr12:5432726
|
A | C | 152 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0017others(149): Show | 155 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.18+384A>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5432726 | ||||||
chr12:5432868
|
G | GC | 3 | a0001c0001t0001g0016a0001c0001t0001g0028a0001c0001t0001g0110 | 3 | HG02257.hp1 HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.18+527dupC | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5432868 | |||||
chr12:5432973
|
G | T | 1 | a0001c0004t0001g0109 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.18+631G>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5432973 | ||||||
chr12:5433024
|
G | C | 1 | a0001c0001t0001g0111 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.18+682G>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5433024 | ||||||
chr12:5433141
|
C | G | 65 | a0001c0001t0001g0010a0001c0001t0001g0111a0001c0001t0001g0113others(62): Show | 66 | HG00099.hp1 HG00558.hp1 HG00639.hp2 others(63): Show |
intron_variant | MODIFIER | c.18+799C>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5433141 | ||||||
chr12:5433173
|
TC | T | 3 | a0001c0001t0001g0033a0001c0001t0001g0282a0001c0001t0001g0283 | 3 | HG01891.hp1 HG03130.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.18+833delC | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5433173 | |||||
chr12:5433199
|
C | T | 24 | a0001c0001t0001g0010a0001c0001t0001g0171a0001c0001t0001g0298others(21): Show | 25 | HG00738.hp2 HG01106.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.18+857C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5433199 | ||||||
chr12:5433368
|
T | C | 66 | a0001c0001t0001g0010a0001c0001t0001g0111a0001c0001t0001g0113others(63): Show | 67 | HG00099.hp1 HG00558.hp1 HG00639.hp2 others(64): Show |
intron_variant | MODIFIER | c.18+1026T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5433368 | ||||||
chr12:5433448
|
G | GGAGGGGC | 31 | a0001c0001t0001g0010a0001c0001t0001g0167a0001c0001t0001g0171others(28): Show | 32 | HG00738.hp2 HG01106.hp2 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.18+1112_18+1118dup others(7): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5433448 | |||||
chr12:5433454
|
G | GCGAGGGC | 38 | a0001c0001t0001g0033a0001c0001t0001g0111a0001c0001t0001g0113others(35): Show | 38 | HG00099.hp1 HG00558.hp1 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.18+1120_18+1126dup others(7): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5433454 | |||||
chr12:5433521
|
C | T | 1 | a0001c0002t0001g0281 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.18+1179C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5433521 | ||||||
chr12:5433597
|
CTGAGACC others(2): Show |
C | 17 | a0001c0001t0001g0111a0001c0001t0001g0114a0001c0001t0001g0115others(14): Show | 17 | HG00099.hp1 HG00639.hp2 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.18+1258_18+1266del others(9): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5433597 | |||||
chr12:5433684
|
G | T | 1 | a0002c0003t0001g0168 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.18+1342G>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5433684 | ||||||
chr12:5433704
|
C | G | 1 | a0001c0001t0001g0238 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.18+1362C>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5433704 | ||||||
chr12:5433906
|
G | A | 2 | a0001c0001t0001g0282a0001c0001t0001g0283 | 2 | HG01891.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.18+1564G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5433906 | ||||||
chr12:5433979
|
C | T | 1 | a0001c0001t0001g0237 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.18+1637C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5433979 | ||||||
chr12:5434074
|
T | C | 2 | a0001c0002t0001g0013a0001c0002t0001g0284 | 2 | HG00558.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.18+1732T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5434074 | ||||||
chr12:5434270
|
G | T | 1 | a0001c0002t0001g0290 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.18+1928G>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5434270 | ||||||
chr12:5434440
|
G | A | 2 | a0001c0001t0001g0350a0001c0001t0001g0351 | 2 | HG01952.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.18+2098G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5434440 | ||||||
chr12:5434472
|
A | AGT | 59 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0015others(56): Show | 61 | HG00280.hp2 HG00323.hp2 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.18+2163_18+2164dup others(2): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5434472 | |||||
chr12:5434472
|
A | AGTGT | 25 | a0001c0001t0001g0228a0001c0001t0001g0286a0001c0001t0002g0349others(22): Show | 25 | HG00558.hp1 HG00673.hp2 HG01069.hp1 others(22): Show |
intron_variant | MODIFIER | c.18+2161_18+2164dup others(4): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5434472 | |||||
chr12:5434472
|
A | AGTGTGT | 39 | a0001c0001t0001g0010a0001c0001t0001g0028a0001c0001t0001g0110others(36): Show | 41 | HG00438.hp1 HG00621.hp2 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.18+2159_18+2164dup others(6): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5434472 | |||||
chr12:5434472
|
A | AGTGTGTG others(1): Show |
27 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0029others(24): Show | 27 | HG00099.hp1 HG00738.hp2 HG01099.hp2 others(24): Show |
intron_variant | MODIFIER | c.18+2157_18+2164dup others(8): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5434472 | |||||
chr12:5434472
|
A | AGTGTGTG others(3): Show |
6 | a0001c0001t0001g0166a0001c0001t0001g0295a0001c0001t0001g0330others(3): Show | 6 | HG02970.hp2 HG03453.hp2 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.18+2155_18+2164dup others(10): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5434472 | |||||
chr12:5434472
|
A | AGTGTGTG others(5): Show |
4 | a0001c0001t0001g0033a0001c0001t0001g0167a0001c0002t0001g0031others(1): Show | 4 | HG03139.hp2 HG03195.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.18+2153_18+2164dup others(12): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5434472 | |||||
chr12:5434472
|
A | AGTGTGTG others(7): Show |
3 | a0001c0001t0001g0032a0001c0002t0001g0236a0001c0002t0001g0332 | 3 | HG02083.hp1 HG02809.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.18+2151_18+2164dup others(14): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5434472 | |||||
chr12:5434472
|
A | AGTGTGTG others(9): Show |
1 | a0001c0001t0001g0171 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.18+2149_18+2164dup others(16): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5434472 | |||||
chr12:5434472
|
AGTGTGTG others(5): Show |
A | 1 | a0002c0003t0001g0285 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.18+2153_18+2164del others(12): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5434472 | |||||
chr12:5434603
|
A | G | 1 | a0001c0002t0001g0344 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.18+2261A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5434603 | ||||||
chr12:5435017
|
C | A | 1 | a0001c0002t0001g0148 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.18+2675C>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5435017 | ||||||
chr12:5435031
|
A | G | 1 | a0001c0001t0003g0024 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.18+2689A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5435031 | ||||||
chr12:5435067
|
A | T | 2 | a0001c0001t0001g0310a0001c0001t0001g0352 | 2 | HG02258.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.18+2725A>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5435067 | ||||||
chr12:5435165
|
T | C | 36 | a0001c0001t0001g0010a0001c0001t0001g0146a0001c0001t0001g0171others(33): Show | 37 | HG00438.hp1 HG00621.hp2 HG00738.hp2 others(34): Show |
intron_variant | MODIFIER | c.18+2823T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5435165 | ||||||
chr12:5435459
|
G | A | 31 | a0001c0001t0001g0010a0001c0001t0001g0146a0001c0001t0001g0171others(28): Show | 32 | HG00438.hp1 HG00621.hp2 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.18+3117G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5435459 | ||||||
chr12:5435559
|
A | C | 1 | a0001c0001t0001g0142 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.18+3217A>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5435559 | ||||||
chr12:5435739
|
A | G | 5 | a0001c0002t0001g0353a0001c0002t0001g0354a0001c0002t0001g0355others(2): Show | 5 | HG02622.hp2 HG03098.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.18+3397A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5435739 | ||||||
chr12:5435788
|
G | A | 1 | a0001c0001t0004g0311 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.18+3446G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5435788 | ||||||
chr12:5435828
|
A | G | 308 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(305): Show | 318 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(315): Show |
intron_variant | MODIFIER | c.18+3486A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5435828 | ||||||
chr12:5435832
|
A | G | 38 | a0001c0001t0001g0010a0001c0001t0001g0146a0001c0001t0001g0157others(35): Show | 39 | HG00438.hp1 HG00621.hp2 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.18+3490A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5435832 | ||||||
chr12:5435853
|
C | G | 1 | a0004c0010t0001g0326 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.18+3511C>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5435853 | ||||||
chr12:5435889
|
C | T | 2 | a0001c0002t0001g0214a0001c0002t0001g0215 | 2 | NA18955.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.18+3547C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5435889 | ||||||
chr12:5436025
|
G | T | 1 | a0001c0001t0001g0120 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.18+3683G>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5436025 | ||||||
chr12:5436074
|
C | T | 2 | a0001c0001t0001g0350a0001c0001t0001g0351 | 2 | HG01952.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.18+3732C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5436074 | ||||||
chr12:5436082
|
G | A | 2 | a0001c0001t0001g0017a0001c0001t0001g0348 | 2 | HG02717.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.18+3740G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5436082 | ||||||
chr12:5436093
|
C | T | 3 | a0001c0001t0001g0213a0002c0003t0001g0211a0002c0003t0001g0212 | 3 | HG02965.hp1 HG03098.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.18+3751C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5436093 | ||||||
chr12:5436142
|
T | C | 1 | a0001c0002t0001g0169 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.18+3800T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5436142 | ||||||
chr12:5436225
|
T | C | 1 | a0001c0001t0001g0115 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.18+3883T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5436225 | ||||||
chr12:5436326
|
T | C | 1 | a0001c0002t0001g0334 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.18+3984T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5436326 | ||||||
chr12:5436334
|
A | G | 1 | a0001c0001t0001g0032 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.18+3992A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5436334 | ||||||
chr12:5436366
|
A | G | 36 | a0001c0001t0001g0010a0001c0001t0001g0146a0001c0001t0001g0171others(33): Show | 37 | HG00438.hp1 HG00621.hp2 HG00738.hp2 others(34): Show |
intron_variant | MODIFIER | c.18+4024A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5436366 | ||||||
chr12:5436809
|
G | T | 1 | a0001c0002t0001g0274 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.18+4467G>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5436809 | ||||||
chr12:5436818
|
T | A | 1 | a0001c0007t0001g0054 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.18+4476T>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5436818 | ||||||
chr12:5436886
|
A | G | 1 | a0001c0004t0001g0257 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.18+4544A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5436886 | ||||||
chr12:5436924
|
A | C | 5 | a0001c0002t0001g0035a0001c0002t0001g0318a0001c0002t0001g0321others(2): Show | 5 | NA18957.hp1 NA18959.hp1 NA18968.hp1 others(2): Show |
intron_variant | MODIFIER | c.18+4582A>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5436924 | ||||||
chr12:5436955
|
G | T | 6 | a0001c0001t0001g0294a0001c0001t0001g0310a0001c0001t0001g0350others(3): Show | 6 | HG01952.hp2 HG02258.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.18+4613G>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5436955 | ||||||
chr12:5437157
|
C | T | 1 | a0001c0001t0001g0015 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.18+4815C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5437157 | ||||||
chr12:5437158
|
C | T | 1 | a0001c0002t0001g0210 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.18+4816C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5437158 | ||||||
chr12:5437300
|
C | T | 2 | a0001c0001t0001g0208a0001c0004t0001g0209 | 2 | HG02602.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.18+4958C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5437300 | ||||||
chr12:5437322
|
A | T | 1 | a0001c0001t0001g0100 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.18+4980A>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5437322 | ||||||
chr12:5437390
|
A | G | 1 | a0001c0002t0001g0099 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.18+5048A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5437390 | ||||||
chr12:5437404
|
G | C | 44 | a0001c0001t0001g0010a0001c0001t0001g0033a0001c0001t0001g0146others(41): Show | 46 | HG00438.hp1 HG00738.hp2 HG00741.hp1 others(43): Show |
intron_variant | MODIFIER | c.18+5062G>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5437404 | ||||||
chr12:5437476
|
G | A | 2 | a0001c0001t0001g0016a0001c0001t0001g0028 | 2 | HG02257.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.18+5134G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5437476 | ||||||
chr12:5437668
|
G | T | 7 | a0001c0001t0001g0014a0001c0001t0001g0019a0001c0001t0001g0053others(4): Show | 7 | HG01109.hp2 HG02055.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.18+5326G>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5437668 | ||||||
chr12:5437687
|
G | T | 12 | a0001c0001t0001g0157a0001c0001t0001g0286a0001c0002t0001g0013others(9): Show | 12 | HG00558.hp1 HG00621.hp2 HG00673.hp2 others(9): Show |
intron_variant | MODIFIER | c.18+5345G>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5437687 | ||||||
chr12:5437745
|
A | T | 32 | a0001c0001t0001g0010a0001c0001t0001g0146a0001c0001t0001g0171others(29): Show | 33 | HG00438.hp1 HG00738.hp2 HG01106.hp2 others(30): Show |
intron_variant | MODIFIER | c.18+5403A>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5437745 | ||||||
chr12:5437798
|
G | A | 2 | a0001c0006t0001g0173a0001c0006t0001g0174 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.18+5456G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5437798 | ||||||
chr12:5437930
|
T | C | 32 | a0001c0001t0001g0010a0001c0001t0001g0146a0001c0001t0001g0171others(29): Show | 33 | HG00438.hp1 HG00738.hp2 HG01106.hp2 others(30): Show |
intron_variant | MODIFIER | c.18+5588T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5437930 | ||||||
chr12:5437978
|
T | G | 2 | a0001c0001t0001g0310a0001c0001t0001g0352 | 2 | HG02258.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.18+5636T>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5437978 | ||||||
chr12:5438021
|
A | C | 35 | a0001c0001t0001g0010a0001c0001t0001g0033a0001c0001t0001g0146others(32): Show | 36 | HG00438.hp1 HG00738.hp2 HG01106.hp2 others(33): Show |
intron_variant | MODIFIER | c.18+5679A>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5438021 | ||||||
chr12:5438067
|
A | C | 4 | a0001c0001t0001g0105a0001c0002t0001g0106a0001c0002t0001g0107others(1): Show | 4 | HG01074.hp2 HG01516.hp2 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.18+5725A>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5438067 | ||||||
chr12:5438227
|
C | T | 1 | a0001c0001t0001g0110 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.18+5885C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5438227 | ||||||
chr12:5438559
|
AT | A | 26 | a0001c0001t0001g0010a0001c0001t0001g0146a0001c0001t0001g0171others(23): Show | 27 | HG00438.hp1 HG00642.hp1 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.18+6226delT | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5438559 | |||||
chr12:5438593
|
G | T | 40 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0028others(37): Show | 41 | HG00438.hp1 HG00738.hp2 HG01106.hp2 others(38): Show |
intron_variant | MODIFIER | c.18+6251G>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5438593 | ||||||
chr12:5438702
|
G | A | 3 | a0001c0001t0001g0015a0001c0001t0001g0025a0001c0001t0001g0026 | 3 | HG02647.hp1 HG03471.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.18+6360G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5438702 | ||||||
chr12:5438705
|
G | A | 1 | a0001c0002t0001g0149 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.18+6363G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5438705 | ||||||
chr12:5438789
|
G | A | 2 | a0001c0001t0001g0310a0001c0001t0001g0352 | 2 | HG02258.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.18+6447G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5438789 | ||||||
chr12:5438998
|
G | A | 2 | a0001c0001t0001g0017a0001c0001t0001g0348 | 2 | HG02717.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.18+6656G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5438998 | ||||||
chr12:5439005
|
A | T | 17 | a0001c0001t0001g0157a0001c0001t0001g0286a0001c0002t0001g0013others(14): Show | 17 | HG00558.hp1 HG00621.hp2 HG00673.hp2 others(14): Show |
intron_variant | MODIFIER | c.18+6663A>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5439005 | ||||||
chr12:5439131
|
T | A | 1 | a0001c0001t0001g0142 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.18+6789T>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5439131 | ||||||
chr12:5439135
|
C | T | 256 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(253): Show | 264 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(261): Show |
intron_variant | MODIFIER | c.18+6793C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5439135 | ||||||
chr12:5439254
|
C | T | 1 | a0001c0001t0001g0213 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.18+6912C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5439254 | ||||||
chr12:5439275
|
T | C | 4 | a0001c0001t0001g0239a0001c0001t0001g0258a0001c0002t0001g0240others(1): Show | 4 | HG00642.hp2 HG00735.hp2 HG01257.hp2 others(1): Show |
intron_variant | MODIFIER | c.18+6933T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5439275 | ||||||
chr12:5439495
|
T | G | 62 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(59): Show | 67 | HG00140.hp2 HG00408.hp1 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.18+7153T>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5439495 | ||||||
chr12:5439502
|
G | A | 8 | a0001c0001t0001g0029a0001c0001t0001g0032a0001c0001t0001g0118others(5): Show | 8 | HG02055.hp2 HG02258.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.18+7160G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5439502 | ||||||
chr12:5439518
|
T | A | 1 | a0001c0002t0001g0055 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.18+7176T>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5439518 | ||||||
chr12:5439649
|
G | A | 1 | a0002c0003t0001g0168 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.18+7307G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5439649 | ||||||
chr12:5439688
|
A | G | 1 | a0001c0002t0001g0189 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.18+7346A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5439688 | ||||||
chr12:5439751
|
A | G | 1 | a0001c0004t0001g0141 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.18+7409A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5439751 | ||||||
chr12:5440037
|
A | G | 34 | a0001c0001t0001g0010a0001c0001t0001g0146a0001c0001t0001g0167others(31): Show | 35 | HG00438.hp1 HG00738.hp2 HG01106.hp2 others(32): Show |
intron_variant | MODIFIER | c.18+7695A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5440037 | ||||||
chr12:5440106
|
C | G | 1 | a0001c0002t0001g0156 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.18+7764C>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5440106 | ||||||
chr12:5440290
|
C | T | 37 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0028others(34): Show | 38 | HG00438.hp1 HG00738.hp2 HG01106.hp2 others(35): Show |
intron_variant | MODIFIER | c.18+7948C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5440290 | ||||||
chr12:5440330
|
T | C | 6 | a0001c0001t0001g0294a0001c0001t0001g0310a0001c0001t0001g0350others(3): Show | 6 | HG01952.hp2 HG02258.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.18+7988T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5440330 | ||||||
chr12:5440406
|
C | G | 36 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0146others(33): Show | 37 | HG00438.hp1 HG00738.hp2 HG01106.hp2 others(34): Show |
intron_variant | MODIFIER | c.18+8064C>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5440406 | ||||||
chr12:5440466
|
G | A | 2 | a0001c0001t0001g0310a0001c0001t0001g0352 | 2 | HG02258.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.18+8124G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5440466 | ||||||
chr12:5440550
|
G | A | 3 | a0001c0001t0001g0112a0001c0001t0001g0242a0001c0004t0001g0257 | 3 | HG00735.hp1 HG01069.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.18+8208G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5440550 | ||||||
chr12:5440697
|
A | G | 36 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0146others(33): Show | 37 | HG00438.hp1 HG00738.hp2 HG01106.hp2 others(34): Show |
intron_variant | MODIFIER | c.18+8355A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5440697 | ||||||
chr12:5441172
|
T | C | 36 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0146others(33): Show | 37 | HG00438.hp1 HG00738.hp2 HG01106.hp2 others(34): Show |
intron_variant | MODIFIER | c.18+8830T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5441172 | ||||||
chr12:5441376
|
C | T | 2 | a0001c0001t0001g0350a0001c0001t0001g0351 | 2 | HG01952.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.18+9034C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5441376 | ||||||
chr12:5441468
|
AT | A | 35 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0146others(32): Show | 36 | HG00438.hp1 HG00738.hp2 HG01106.hp2 others(33): Show |
intron_variant | MODIFIER | c.18+9128delT | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5441468 | |||||
chr12:5441471
|
G | C | 35 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0146others(32): Show | 36 | HG00438.hp1 HG00738.hp2 HG01106.hp2 others(33): Show |
intron_variant | MODIFIER | c.18+9129G>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5441471 | ||||||
chr12:5441475
|
A | C | 35 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0146others(32): Show | 36 | HG00438.hp1 HG00738.hp2 HG01106.hp2 others(33): Show |
intron_variant | MODIFIER | c.18+9133A>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5441475 | ||||||
chr12:5441477
|
CCTGGG | C | 35 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0146others(32): Show | 36 | HG00438.hp1 HG00738.hp2 HG01106.hp2 others(33): Show |
intron_variant | MODIFIER | c.18+9136_18+9140del others(5): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5441477 | ||||||
chr12:5441572
|
G | A | 35 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0146others(32): Show | 36 | HG00438.hp1 HG00738.hp2 HG01106.hp2 others(33): Show |
intron_variant | MODIFIER | c.18+9230G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5441572 | ||||||
chr12:5441652
|
G | A | 2 | a0001c0001t0001g0294a0001c0002t0001g0156 | 2 | HG02451.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.18+9310G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5441652 | ||||||
chr12:5441693
|
C | A | 3 | a0001c0001t0001g0016a0001c0001t0001g0028a0001c0001t0001g0033 | 3 | HG02257.hp1 HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.18+9351C>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5441693 | ||||||
chr12:5441720
|
C | T | 304 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(301): Show | 314 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(311): Show |
intron_variant | MODIFIER | c.18+9378C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5441720 | ||||||
chr12:5441723
|
C | T | 1 | a0002c0003t0001g0168 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.18+9381C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5441723 | ||||||
chr12:5441729
|
G | T | 1 | a0001c0001t0001g0329 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.18+9387G>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5441729 | ||||||
chr12:5441821
|
G | A | 2 | a0001c0001t0001g0016a0001c0001t0001g0028 | 2 | HG02257.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.18+9479G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5441821 | ||||||
chr12:5441821
|
G | T | 259 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(256): Show | 268 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.18+9479G>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5441821 | ||||||
chr12:5441844
|
C | T | 1 | a0002c0003t0001g0060 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.18+9502C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5441844 | ||||||
chr12:5441899
|
A | G | 282 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(279): Show | 291 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(288): Show |
intron_variant | MODIFIER | c.18+9557A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5441899 | ||||||
chr12:5442036
|
A | G | 1 | a0001c0004t0001g0141 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.18+9694A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5442036 | ||||||
chr12:5442286
|
G | A | 337 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(334): Show | 347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.18+9944G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5442286 | ||||||
chr12:5442381
|
G | C | 5 | a0001c0002t0001g0232a0001c0002t0001g0233a0001c0002t0001g0234others(2): Show | 5 | HG00621.hp2 NA18955.hp1 NA18971.hp2 others(2): Show |
intron_variant | MODIFIER | c.18+10039G>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5442381 | ||||||
chr12:5442386
|
G | A | 1 | a0001c0001t0001g0305 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.18+10044G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5442386 | ||||||
chr12:5442466
|
G | A | 183 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(180): Show | 190 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.18+10124G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5442466 | ||||||
chr12:5442467
|
A | C | 1 | a0001c0001t0001g0110 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.18+10125A>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5442467 | ||||||
chr12:5442476
|
T | C | 34 | a0001c0001t0001g0036a0001c0001t0001g0053a0001c0001t0001g0115others(31): Show | 34 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.18+10134T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5442476 | ||||||
chr12:5442579
|
A | G | 1 | a0002c0003t0001g0201 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.18+10237A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5442579 | ||||||
chr12:5442841
|
G | A | 1 | a0001c0002t0001g0290 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.18+10499G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5442841 | ||||||
chr12:5442885
|
C | T | 1 | a0001c0002t0001g0344 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.18+10543C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5442885 | ||||||
chr12:5442886
|
T | G | 1 | a0001c0001t0001g0142 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.18+10544T>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5442886 | ||||||
chr12:5442910
|
C | G | 196 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(193): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(199): Show |
intron_variant | MODIFIER | c.18+10568C>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5442910 | ||||||
chr12:5442946
|
G | A | 3 | a0001c0002t0001g0124a0001c0002t0001g0125a0001c0002t0001g0210 | 3 | HG01070.hp2 HG01243.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.18+10604G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5442946 | ||||||
chr12:5442960
|
A | C | 24 | a0001c0001t0001g0026a0001c0001t0001g0051a0001c0001t0001g0052others(21): Show | 24 | HG00099.hp1 HG00639.hp2 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.18+10618A>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5442960 | ||||||
chr12:5443011
|
T | C | 8 | a0001c0001t0001g0032a0001c0001t0001g0165a0001c0001t0002g0349others(5): Show | 8 | HG01884.hp1 HG02280.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.18+10669T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5443011 | ||||||
chr12:5443058
|
A | G | 3 | a0001c0001t0001g0200a0001c0001t0001g0350a0001c0001t0004g0311 | 3 | HG03209.hp2 HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.18+10716A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5443058 | ||||||
chr12:5443113
|
C | T | 30 | a0001c0001t0001g0085a0001c0001t0001g0146a0001c0001t0001g0171others(27): Show | 30 | HG00438.hp1 HG00558.hp1 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.18+10771C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5443113 | ||||||
chr12:5443115
|
C | T | 240 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(237): Show | 247 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.18+10773C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5443115 | ||||||
chr12:5443132
|
C | T | 1 | a0001c0001t0001g0113 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.18+10790C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5443132 | ||||||
chr12:5443265
|
C | T | 1 | a0001c0002t0001g0343 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.18+10923C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5443265 | ||||||
chr12:5443304
|
T | C | 4 | a0001c0001t0001g0085a0001c0001t0001g0171a0001c0001t0001g0330others(1): Show | 4 | NA18990.hp1 NA19012.hp1 NA19077.hp2 others(1): Show |
intron_variant | MODIFIER | c.18+10962T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5443304 | ||||||
chr12:5443503
|
C | T | 251 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(248): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(255): Show |
intron_variant | MODIFIER | c.18+11161C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5443503 | ||||||
chr12:5443653
|
T | C | 2 | a0001c0002t0001g0176a0001c0002t0001g0177 | 2 | NA18947.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.18+11311T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5443653 | ||||||
chr12:5443689
|
T | G | 1 | a0001c0001t0001g0308 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.18+11347T>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5443689 | ||||||
chr12:5443703
|
A | G | 1 | a0001c0001t0001g0096 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.18+11361A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5443703 | ||||||
chr12:5443740
|
A | T | 1 | a0001c0002t0001g0321 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.18+11398A>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5443740 | ||||||
chr12:5443865
|
G | A | 2 | a0001c0001t0001g0308a0001c0002t0001g0275 | 2 | HG01168.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.18+11523G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5443865 | ||||||
chr12:5443895
|
G | A | 56 | a0001c0001t0001g0105a0001c0001t0001g0112a0001c0001t0001g0157others(53): Show | 57 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.18+11553G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5443895 | ||||||
chr12:5444071
|
TC | T | 56 | a0001c0001t0001g0105a0001c0001t0001g0112a0001c0001t0001g0157others(53): Show | 57 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.18+11732delC | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5444071 | |||||
chr12:5444199
|
C | T | 1 | a0001c0002t0001g0187 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.18+11857C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5444199 | ||||||
chr12:5444321
|
G | A | 1 | a0001c0002t0001g0210 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.18+11979G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5444321 | ||||||
chr12:5444337
|
G | A | 307 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(304): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.18+11995G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5444337 | ||||||
chr12:5444347
|
A | G | 2 | a0001c0001t0001g0015a0001c0001t0001g0025 | 2 | HG02647.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.18+12005A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5444347 | ||||||
chr12:5444355
|
T | C | 1 | a0001c0001t0005g0223 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.18+12013T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5444355 | ||||||
chr12:5444378
|
G | A | 1 | a0001c0001t0001g0029 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.18+12036G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5444378 | ||||||
chr12:5444423
|
C | T | 2 | a0001c0001t0001g0278a0001c0001t0001g0347 | 2 | HG02071.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.18+12081C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5444423 | ||||||
chr12:5444448
|
T | C | 6 | a0001c0001t0001g0017a0001c0001t0001g0033a0001c0001t0001g0172others(3): Show | 6 | HG02055.hp2 HG02572.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.18+12106T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5444448 | ||||||
chr12:5444450
|
G | T | 2 | a0002c0003t0001g0083a0002c0003t0001g0084 | 2 | NA18940.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.18+12108G>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5444450 | ||||||
chr12:5444669
|
C | CT | 7 | a0001c0001t0001g0115a0001c0001t0001g0166a0002c0003t0001g0045others(4): Show | 7 | HG01891.hp2 HG02109.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.18+12336dupT | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5444669 | |||||
chr12:5444678
|
T | C | 1 | a0001c0001t0001g0026 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.18+12336T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5444678 | ||||||
chr12:5444748
|
C | T | 2 | a0001c0001t0001g0200a0001c0001t0004g0311 | 2 | HG03209.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.18+12406C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5444748 | ||||||
chr12:5444845
|
C | A | 352 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(349): Show | 362 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(359): Show |
intron_variant | MODIFIER | c.18+12503C>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5444845 | ||||||
chr12:5444855
|
A | T | 1 | a0001c0001t0005g0223 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.18+12513A>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5444855 | ||||||
chr12:5445026
|
C | G | 310 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(307): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.18+12684C>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5445026 | ||||||
chr12:5445078
|
G | T | 1 | a0001c0002t0001g0197 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.18+12736G>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5445078 | ||||||
chr12:5445119
|
A | G | 1 | a0002c0003t0001g0046 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.18+12777A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5445119 | ||||||
chr12:5445274
|
C | A | 1 | a0001c0001t0001g0010 | 2 | HG01106.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.18+12932C>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5445274 | ||||||
chr12:5445275
|
C | A | 1 | a0001c0001t0001g0010 | 2 | HG01106.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.18+12933C>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5445275 | ||||||
chr12:5445276
|
T | A | 1 | a0001c0001t0001g0010 | 2 | HG01106.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.18+12934T>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5445276 | ||||||
chr12:5445276
|
T | TG | 306 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(303): Show | 313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.18+12934_18+12935i others(3): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5445276 | ||||||
chr12:5445287
|
GATGTGTG others(5): Show |
G | 7 | a0001c0001t0001g0085a0001c0001t0001g0146a0001c0001t0001g0171others(4): Show | 7 | HG00438.hp1 NA18966.hp1 NA18990.hp1 others(4): Show |
intron_variant | MODIFIER | c.18+12958_18+12969d others(14): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5445287 | |||||
chr12:5445288
|
A | ATG | 37 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0028others(34): Show | 38 | HG01175.hp1 HG01255.hp1 HG01928.hp2 others(35): Show |
intron_variant | MODIFIER | c.18+12956_18+12957d others(4): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5445288 | |||||
chr12:5445288
|
A | ATGTG | 9 | a0001c0001t0001g0036a0001c0001t0001g0053a0001c0001t0001g0118others(6): Show | 10 | HG02055.hp1 HG02074.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.18+12954_18+12957d others(6): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5445288 | |||||
chr12:5445288
|
A | ATGTGTG | 11 | a0001c0001t0001g0167a0001c0001t0001g0228a0001c0001t0001g0306others(8): Show | 11 | HG00408.hp2 HG00741.hp1 HG01943.hp1 others(8): Show |
intron_variant | MODIFIER | c.18+12952_18+12957d others(8): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5445288 | |||||
chr12:5445288
|
A | ATGTGTGT others(3): Show |
1 | a0001c0001t0001g0213 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.18+12948_18+12957d others(12): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5445288 | |||||
chr12:5445288
|
A | ATGTGTGT others(5): Show |
1 | a0001c0002t0001g0346 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.18+12957_18+12958i others(14): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5445288 | |||||
chr12:5445288
|
ATGTGTGT others(9): Show |
A | 2 | a0001c0002t0001g0082a0001c0004t0001g0141 | 2 | HG02630.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.18+12958_18+12973d others(18): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5445288 | |||||
chr12:5445288
|
ATGTGTGT others(11): Show |
A | 1 | a0001c0002t0001g0198 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.18+12958_18+12975d others(20): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5445288 | |||||
chr12:5445290
|
GTGTGTGT others(3): Show |
G | 9 | a0001c0001t0001g0120a0001c0001t0001g0239a0001c0001t0001g0255others(6): Show | 9 | HG00642.hp2 HG00735.hp2 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.18+12958_18+12967d others(12): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5445290 | |||||
chr12:5445292
|
GTGTGTGT others(1): Show |
G | 90 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(87): Show | 95 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.18+12958_18+12965d others(10): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5445292 | |||||
chr12:5445294
|
GTGTGTA | G | 51 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0032others(48): Show | 51 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.18+12958_18+12963d others(8): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5445294 | |||||
chr12:5445296
|
GTGTA | G | 38 | a0001c0001t0001g0011a0001c0001t0001g0051a0001c0001t0001g0052others(35): Show | 39 | HG00099.hp2 HG00558.hp1 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.18+12958_18+12961d others(6): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5445296 | |||||
chr12:5445298
|
GTA | G | 43 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(40): Show | 44 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(41): Show |
intron_variant | MODIFIER | c.18+12958_18+12959d others(4): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5445298 | |||||
chr12:5445300
|
A | G | 108 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0017others(105): Show | 111 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.18+12958A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5445300 | ||||||
chr12:5445338
|
T | G | 1 | a0002c0005t0001g0259 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.18+12996T>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5445338 | ||||||
chr12:5445382
|
A | T | 74 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(71): Show | 79 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.18+13040A>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5445382 | ||||||
chr12:5445481
|
G | A | 1 | a0004c0010t0001g0326 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.18+13139G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5445481 | ||||||
chr12:5445501
|
C | T | 1 | a0001c0001t0004g0311 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.18+13159C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5445501 | ||||||
chr12:5445512
|
T | G | 308 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(305): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.18+13170T>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5445512 | ||||||
chr12:5445631
|
G | A | 1 | a0001c0001t0002g0349 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.18+13289G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5445631 | ||||||
chr12:5445720
|
C | T | 1 | a0001c0002t0001g0296 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.18+13378C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5445720 | ||||||
chr12:5445721
|
G | A | 2 | a0001c0001t0001g0213a0002c0003t0001g0211 | 2 | HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.18+13379G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5445721 | ||||||
chr12:5445741
|
A | T | 1 | a0001c0001t0001g0096 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.18+13399A>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5445741 | ||||||
chr12:5445778
|
C | T | 7 | a0001c0001t0001g0032a0001c0001t0001g0167a0001c0001t0002g0349others(4): Show | 7 | HG01884.hp1 HG02647.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.18+13436C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5445778 | ||||||
chr12:5445874
|
G | A | 220 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(217): Show | 227 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(224): Show |
intron_variant | MODIFIER | c.18+13532G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5445874 | ||||||
chr12:5445954
|
G | A | 23 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0053others(20): Show | 23 | HG00099.hp1 HG00639.hp2 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.18+13612G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5445954 | ||||||
chr12:5446069
|
A | G | 1 | a0001c0001t0001g0331 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.18+13727A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5446069 | ||||||
chr12:5446076
|
T | C | 4 | a0001c0001t0001g0265a0001c0002t0001g0151a0001c0002t0001g0264others(1): Show | 4 | HG02273.hp2 HG02293.hp2 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.18+13734T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5446076 | ||||||
chr12:5446090
|
T | A | 1 | a0001c0001t0001g0352 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.18+13748T>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5446090 | ||||||
chr12:5446252
|
C | T | 1 | a0001c0001t0001g0352 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.18+13910C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5446252 | ||||||
chr12:5446330
|
A | G | 4 | a0001c0001t0001g0016a0001c0001t0001g0028a0001c0001t0001g0111others(1): Show | 4 | HG01346.hp1 HG02257.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.18+13988A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5446330 | ||||||
chr12:5446352
|
C | T | 6 | a0001c0001t0001g0017a0001c0001t0001g0033a0001c0001t0001g0172others(3): Show | 6 | HG02055.hp2 HG02572.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.18+14010C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5446352 | ||||||
chr12:5446368
|
C | T | 1 | a0001c0001t0001g0295 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.18+14026C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5446368 | ||||||
chr12:5446468
|
A | G | 1 | a0001c0001t0001g0110 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.18+14126A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5446468 | ||||||
chr12:5446923
|
C | T | 4 | a0001c0001t0001g0017a0001c0001t0001g0172a0001c0001t0001g0228others(1): Show | 4 | HG02055.hp2 HG02723.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.18+14581C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5446923 | ||||||
chr12:5447047
|
G | A | 7 | a0001c0001t0001g0017a0001c0001t0001g0033a0001c0001t0001g0172others(4): Show | 7 | HG02055.hp2 HG02572.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.18+14705G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5447047 | ||||||
chr12:5447170
|
A | C | 1 | a0001c0002t0001g0186 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.18+14828A>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5447170 | ||||||
chr12:5447450
|
C | T | 2 | a0001c0002t0001g0205a0001c0002t0001g0229 | 2 | HG02615.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.18+15108C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5447450 | ||||||
chr12:5447472
|
G | A | 1 | a0002c0003t0001g0212 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.18+15130G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5447472 | ||||||
chr12:5447551
|
T | A | 1 | a0001c0001t0001g0352 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.18+15209T>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5447551 | ||||||
chr12:5447650
|
G | T | 1 | a0002c0003t0001g0130 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.18+15308G>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5447650 | ||||||
chr12:5448041
|
G | T | 71 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(68): Show | 76 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.18+15699G>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5448041 | ||||||
chr12:5448296
|
G | T | 1 | a0001c0002t0001g0150 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.18+15954G>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5448296 | ||||||
chr12:5448361
|
G | A | 6 | a0001c0001t0001g0114a0001c0002t0001g0117a0001c0002t0001g0160others(3): Show | 6 | HG00099.hp1 HG00639.hp2 HG00741.hp2 others(3): Show |
intron_variant | MODIFIER | c.18+16019G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5448361 | ||||||
chr12:5448727
|
G | A | 226 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0020others(223): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.18+16385G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5448727 | ||||||
chr12:5449037
|
C | A | 2 | a0001c0002t0001g0188a0001c0009t0001g0287 | 2 | HG00673.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.18+16695C>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5449037 | ||||||
chr12:5449133
|
G | A | 1 | a0001c0001t0001g0200 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.18+16791G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5449133 | ||||||
chr12:5449140
|
G | C | 226 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0020others(223): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.18+16798G>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5449140 | ||||||
chr12:5449192
|
G | A | 1 | a0001c0001t0001g0352 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.18+16850G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5449192 | ||||||
chr12:5449234
|
G | A | 1 | a0001c0001t0001g0044 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.18+16892G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5449234 | ||||||
chr12:5449301
|
C | T | 6 | a0001c0001t0001g0017a0001c0001t0001g0033a0001c0001t0001g0172others(3): Show | 6 | HG02055.hp2 HG02572.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.18+16959C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5449301 | ||||||
chr12:5449352
|
C | T | 226 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0020others(223): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.18+17010C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5449352 | ||||||
chr12:5449532
|
A | G | 1 | a0001c0001t0001g0348 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.18+17190A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5449532 | ||||||
chr12:5449574
|
G | A | 1 | a0001c0001t0001g0348 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.18+17232G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5449574 | ||||||
chr12:5449655
|
G | T | 1 | a0002c0003t0001g0196 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.18+17313G>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5449655 | ||||||
chr12:5449907
|
G | C | 1 | a0001c0001t0005g0223 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.18+17565G>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5449907 | ||||||
chr12:5449922
|
C | G | 1 | a0001c0002t0001g0150 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.18+17580C>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5449922 | ||||||
chr12:5449945
|
A | G | 86 | a0001c0001t0001g0061a0001c0001t0001g0063a0001c0001t0001g0064others(83): Show | 87 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.18+17603A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5449945 | ||||||
chr12:5450214
|
G | A | 352 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(349): Show | 362 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(359): Show |
intron_variant | MODIFIER | c.18+17872G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5450214 | ||||||
chr12:5450246
|
G | A | 1 | a0001c0001t0001g0063 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.18+17904G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5450246 | ||||||
chr12:5450432
|
C | T | 1 | a0001c0001t0001g0026 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.18+18090C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5450432 | ||||||
chr12:5450502
|
A | T | 1 | a0001c0002t0001g0272 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.18+18160A>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5450502 | ||||||
chr12:5450579
|
A | G | 1 | a0001c0001t0001g0279 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.18+18237A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5450579 | ||||||
chr12:5450580
|
T | A | 1 | a0001c0002t0001g0290 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.18+18238T>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5450580 | ||||||
chr12:5450700
|
A | T | 1 | a0001c0001t0001g0294 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.18+18358A>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5450700 | ||||||
chr12:5450728
|
G | T | 358 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(355): Show | 368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.18+18386G>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5450728 | ||||||
chr12:5450851
|
C | T | 226 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0020others(223): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.18+18509C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5450851 | ||||||
chr12:5450855
|
G | A | 226 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0020others(223): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.18+18513G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5450855 | ||||||
chr12:5450856
|
G | T | 352 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(349): Show | 362 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(359): Show |
intron_variant | MODIFIER | c.18+18514G>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5450856 | ||||||
chr12:5450992
|
C | T | 78 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(75): Show | 83 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.18+18650C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5450992 | ||||||
chr12:5451283
|
C | A | 1 | a0001c0001t0001g0352 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.18+18941C>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5451283 | ||||||
chr12:5451284
|
T | G | 1 | a0001c0001t0001g0336 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.18+18942T>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5451284 | ||||||
chr12:5451416
|
C | T | 2 | a0001c0002t0001g0199a0001c0002t0001g0206 | 2 | HG02486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.18+19074C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5451416 | ||||||
chr12:5451459
|
A | G | 6 | a0001c0001t0001g0033a0001c0001t0001g0110a0001c0001t0001g0172others(3): Show | 6 | HG02055.hp2 HG02723.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.18+19117A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5451459 | ||||||
chr12:5451476
|
G | A | 6 | a0001c0001t0001g0033a0001c0001t0001g0110a0001c0001t0001g0172others(3): Show | 6 | HG02055.hp2 HG02723.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.18+19134G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5451476 | ||||||
chr12:5451714
|
A | G | 5 | a0001c0001t0001g0016a0001c0001t0001g0028a0001c0001t0001g0110others(2): Show | 5 | HG01346.hp1 HG02257.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.18+19372A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5451714 | ||||||
chr12:5451732
|
G | C | 342 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(339): Show | 352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.18+19390G>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5451732 | ||||||
chr12:5451813
|
C | T | 4 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0135others(1): Show | 4 | HG00280.hp1 HG01261.hp1 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.18+19471C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5451813 | ||||||
chr12:5451980
|
A | G | 1 | a0001c0002t0001g0246 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.18+19638A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5451980 | ||||||
chr12:5452034
|
T | C | 143 | a0001c0001t0001g0010a0001c0001t0001g0020a0001c0001t0001g0021others(140): Show | 145 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(142): Show |
intron_variant | MODIFIER | c.18+19692T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5452034 | ||||||
chr12:5452096
|
CT | C | 96 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0032others(93): Show | 98 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.18+19771delT | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5452096 | |||||
chr12:5452096
|
CTT | C | 252 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(249): Show | 260 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(257): Show |
intron_variant | MODIFIER | c.18+19770_18+19771d others(4): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5452096 | |||||
chr12:5452119
|
C | T | 5 | a0001c0002t0001g0022a0001c0002t0001g0093a0001c0002t0001g0094others(2): Show | 5 | HG00423.hp2 HG02129.hp2 NA18942.hp1 others(2): Show |
intron_variant | MODIFIER | c.18+19777C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5452119 | ||||||
chr12:5452120
|
G | A | 1 | a0001c0002t0001g0154 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.18+19778G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5452120 | ||||||
chr12:5452139
|
G | A | 2 | a0001c0002t0001g0101a0001c0002t0001g0119 | 2 | HG01192.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.18+19797G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5452139 | ||||||
chr12:5452252
|
C | T | 1 | a0001c0002t0001g0296 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.18+19910C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5452252 | ||||||
chr12:5452253
|
G | A | 3 | a0001c0001t0001g0172a0001c0001t0001g0228a0002c0003t0001g0168 | 3 | HG02055.hp2 HG02723.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.18+19911G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5452253 | ||||||
chr12:5452483
|
G | T | 46 | a0001c0001t0001g0017a0001c0001t0001g0032a0001c0001t0001g0138others(43): Show | 48 | HG00323.hp2 HG00558.hp1 HG00621.hp2 others(45): Show |
intron_variant | MODIFIER | c.18+20141G>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5452483 | ||||||
chr12:5452699
|
G | A | 3 | a0001c0001t0001g0299a0001c0001t0001g0329a0001c0002t0001g0027 | 3 | HG00738.hp2 HG02738.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.18+20357G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5452699 | ||||||
chr12:5452756
|
T | C | 3 | a0001c0001t0001g0172a0001c0001t0001g0228a0002c0003t0001g0168 | 3 | HG02055.hp2 HG02723.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.18+20414T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5452756 | ||||||
chr12:5452771
|
A | C | 1 | a0001c0001t0001g0294 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.18+20429A>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5452771 | ||||||
chr12:5452853
|
G | A | 1 | a0001c0001t0001g0064 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.18+20511G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5452853 | ||||||
chr12:5452938
|
A | C | 3 | a0001c0001t0001g0299a0001c0001t0001g0329a0001c0002t0001g0027 | 3 | HG00738.hp2 HG02738.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.18+20596A>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5452938 | ||||||
chr12:5452956
|
G | A | 25 | a0001c0001t0001g0044a0001c0001t0001g0088a0001c0001t0001g0090others(22): Show | 25 | HG00099.hp2 HG00280.hp1 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.18+20614G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5452956 | ||||||
chr12:5452983
|
C | G | 2 | a0002c0003t0001g0324a0002c0003t0001g0325 | 2 | NA18612.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.18+20641C>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5452983 | ||||||
chr12:5453117
|
T | C | 25 | a0001c0001t0001g0026a0001c0001t0001g0032a0001c0001t0001g0044others(22): Show | 25 | HG00099.hp2 HG00280.hp1 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.18+20775T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5453117 | ||||||
chr12:5453135
|
G | T | 1 | a0004c0010t0001g0326 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.18+20793G>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5453135 | ||||||
chr12:5453178
|
G | A | 45 | a0001c0001t0001g0017a0001c0001t0001g0036a0001c0001t0001g0138others(42): Show | 47 | HG00323.hp2 HG00558.hp1 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.18+20836G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5453178 | ||||||
chr12:5453366
|
C | A | 2 | a0001c0001t0001g0294a0001c0001t0001g0352 | 2 | HG02258.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.18+21024C>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5453366 | ||||||
chr12:5453408
|
T | C | 1 | a0001c0006t0001g0086 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.18+21066T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5453408 | ||||||
chr12:5453521
|
C | T | 1 | a0001c0001t0001g0144 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.18+21179C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5453521 | ||||||
chr12:5453546
|
C | T | 1 | a0001c0006t0001g0086 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.18+21204C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5453546 | ||||||
chr12:5453552
|
G | A | 1 | a0001c0001t0001g0017 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.18+21210G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5453552 | ||||||
chr12:5453659
|
G | A | 2 | a0001c0001t0001g0051a0001c0001t0001g0052 | 2 | HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.18+21317G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5453659 | ||||||
chr12:5453701
|
C | T | 31 | a0001c0001t0001g0017a0001c0001t0001g0032a0001c0001t0001g0110others(28): Show | 33 | HG00323.hp2 HG00408.hp1 HG00558.hp1 others(30): Show |
intron_variant | MODIFIER | c.18+21359C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5453701 | ||||||
chr12:5453895
|
C | T | 7 | a0001c0001t0001g0033a0001c0001t0001g0167a0001c0002t0001g0030others(4): Show | 7 | HG02647.hp2 HG02970.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.18+21553C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5453895 | ||||||
chr12:5453996
|
A | G | 125 | a0001c0001t0001g0036a0001c0001t0001g0063a0001c0001t0001g0064others(122): Show | 126 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.18+21654A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5453996 | ||||||
chr12:5454001
|
G | A | 122 | a0001c0001t0001g0036a0001c0001t0001g0063a0001c0001t0001g0064others(119): Show | 123 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.18+21659G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5454001 | ||||||
chr12:5454061
|
G | C | 4 | a0001c0002t0001g0030a0001c0002t0001g0031a0001c0002t0001g0048others(1): Show | 4 | HG02647.hp2 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.18+21719G>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5454061 | ||||||
chr12:5454199
|
C | CTAGCCTC others(3): Show |
1 | a0001c0001t0001g0116 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.18+21868_18+21877d others(12): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5454199 | |||||
chr12:5454343
|
A | G | 332 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(329): Show | 342 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(339): Show |
intron_variant | MODIFIER | c.18+22001A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5454343 | ||||||
chr12:5454516
|
G | A | 1 | a0001c0001t0001g0339 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.18+22174G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5454516 | ||||||
chr12:5454725
|
C | A | 1 | a0001c0001t0001g0352 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.18+22383C>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5454725 | ||||||
chr12:5454779
|
C | T | 1 | a0001c0001t0001g0033 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.18+22437C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5454779 | ||||||
chr12:5454806
|
T | G | 1 | a0002c0003t0001g0168 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.18+22464T>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5454806 | ||||||
chr12:5455022
|
A | T | 1 | a0001c0001t0001g0143 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.18+22680A>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5455022 | ||||||
chr12:5455114
|
C | A | 2 | a0001c0001t0001g0193a0002c0003t0001g0103 | 2 | HG02895.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.18+22772C>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5455114 | ||||||
chr12:5455227
|
G | A | 1 | a0001c0001t0001g0330 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.18+22885G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5455227 | ||||||
chr12:5455291
|
A | C | 2 | a0001c0001t0001g0140a0001c0001t0001g0190 | 2 | HG02922.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.18+22949A>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5455291 | ||||||
chr12:5455375
|
G | T | 71 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(68): Show | 76 | HG00140.hp2 HG00423.hp2 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.18+23033G>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5455375 | ||||||
chr12:5455528
|
TCCCCAAC others(3): Show |
T | 1 | a0001c0002t0001g0297 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.18+23188_18+23197d others(12): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5455528 | |||||
chr12:5455533
|
A | AAC | 10 | a0001c0001t0001g0091a0001c0001t0001g0120a0001c0001t0001g0121others(7): Show | 10 | HG00099.hp2 HG00735.hp2 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.18+23241_18+23242d others(4): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5455533 | |||||
chr12:5455533
|
A | AACAC | 3 | a0001c0001t0001g0225a0001c0002t0001g0288a0002c0003t0001g0342 | 3 | HG00408.hp1 HG00733.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.18+23239_18+23242d others(6): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5455533 | |||||
chr12:5455533
|
A | AACACAC | 3 | a0001c0001t0001g0032a0001c0001t0001g0351a0001c0002t0001g0030 | 3 | HG01952.hp2 HG02809.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.18+23237_18+23242d others(8): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5455533 | |||||
chr12:5455533
|
A | AACACACA others(1): Show |
11 | a0001c0001t0001g0033a0001c0001t0001g0306a0001c0002t0001g0003others(8): Show | 12 | HG00323.hp2 HG00621.hp2 HG01192.hp1 others(9): Show |
intron_variant | MODIFIER | c.18+23235_18+23242d others(10): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5455533 | |||||
chr12:5455533
|
A | AACACACA others(3): Show |
12 | a0001c0001t0001g0017a0001c0001t0001g0110a0001c0001t0001g0294others(9): Show | 12 | HG00558.hp1 HG00673.hp2 HG00741.hp1 others(9): Show |
intron_variant | MODIFIER | c.18+23233_18+23242d others(12): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5455533 | |||||
chr12:5455533
|
A | AACACACA others(5): Show |
6 | a0001c0002t0001g0009a0001c0002t0001g0106a0001c0002t0001g0226others(3): Show | 7 | HG01978.hp2 HG02074.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.18+23231_18+23242d others(14): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5455533 | |||||
chr12:5455533
|
A | AACACACA others(7): Show |
5 | a0001c0001t0001g0142a0001c0001t0001g0167a0001c0002t0001g0104others(2): Show | 5 | HG01099.hp1 HG02523.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.18+23229_18+23242d others(16): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5455533 | |||||
chr12:5455533
|
A | AACACACA others(9): Show |
1 | a0001c0002t0001g0038 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.18+23227_18+23242d others(18): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5455533 | |||||
chr12:5455533
|
AAC | A | 7 | a0001c0001t0001g0092a0001c0001t0001g0096a0001c0002t0001g0099others(4): Show | 7 | HG00280.hp1 HG01168.hp1 HG02148.hp1 others(4): Show |
intron_variant | MODIFIER | c.18+23241_18+23242d others(4): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5455533 | |||||
chr12:5455533
|
AACAC | A | 16 | a0001c0001t0001g0012a0001c0001t0001g0016a0001c0001t0001g0019others(13): Show | 17 | HG00323.hp1 HG01109.hp2 HG01192.hp2 others(14): Show |
intron_variant | MODIFIER | c.18+23239_18+23242d others(6): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5455533 | |||||
chr12:5455533
|
AACACAC | A | 19 | a0001c0001t0001g0015a0001c0001t0001g0025a0001c0001t0001g0172others(16): Show | 19 | HG00423.hp2 HG00642.hp1 HG01070.hp2 others(16): Show |
intron_variant | MODIFIER | c.18+23237_18+23242d others(8): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5455533 | |||||
chr12:5455533
|
AACACACA others(1): Show |
A | 62 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(59): Show | 67 | HG00140.hp2 HG00621.hp1 HG00639.hp1 others(64): Show |
intron_variant | MODIFIER | c.18+23235_18+23242d others(10): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5455533 | |||||
chr12:5455533
|
AACACACA others(3): Show |
A | 1 | a0001c0004t0001g0155 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.18+23233_18+23242d others(12): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5455533 | |||||
chr12:5455533
|
AACACACA others(5): Show |
A | 6 | a0001c0001t0001g0258a0001c0002t0001g0215a0001c0002t0001g0240others(3): Show | 6 | HG00642.hp2 HG01257.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.18+23231_18+23242d others(14): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5455533 | |||||
chr12:5455555
|
C | A | 1 | a0001c0004t0001g0109 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.18+23213C>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5455555 | ||||||
chr12:5455567
|
CACACACA others(11): Show |
C | 1 | a0002c0003t0001g0168 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.18+23227_18+23244d others(20): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5455567 | |||||
chr12:5455571
|
CACACACA others(7): Show |
C | 2 | a0001c0001t0004g0311a0001c0002t0001g0170 | 2 | HG01516.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.18+23231_18+23244d others(16): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5455571 | |||||
chr12:5455573
|
CACACACA others(5): Show |
C | 26 | a0001c0001t0001g0029a0001c0001t0001g0157a0001c0001t0001g0265others(23): Show | 27 | HG00280.hp2 HG00733.hp1 HG01168.hp2 others(24): Show |
intron_variant | MODIFIER | c.18+23233_18+23244d others(14): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5455573 | |||||
chr12:5455575
|
CACACACA others(3): Show |
C | 43 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0061others(40): Show | 43 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(40): Show |
intron_variant | MODIFIER | c.18+23235_18+23244d others(12): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5455575 | |||||
chr12:5455577
|
CACACACA others(1): Show |
C | 27 | a0001c0001t0001g0010a0001c0001t0001g0036a0001c0001t0001g0118others(24): Show | 28 | HG01106.hp2 HG01109.hp1 HG01255.hp2 others(25): Show |
intron_variant | MODIFIER | c.18+23237_18+23244d others(10): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5455577 | |||||
chr12:5455579
|
CACACAT | C | 30 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074others(27): Show | 30 | HG00423.hp1 HG01255.hp1 HG01257.hp1 others(27): Show |
intron_variant | MODIFIER | c.18+23239_18+23244d others(8): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5455579 | |||||
chr12:5455581
|
CACAT | C | 37 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0063others(34): Show | 37 | HG00099.hp1 HG00438.hp2 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.18+23241_18+23244d others(6): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5455581 | |||||
chr12:5455583
|
CAT | C | 10 | a0001c0001t0001g0026a0001c0001t0001g0069a0001c0001t0001g0078others(7): Show | 10 | HG00558.hp2 HG02630.hp1 HG03209.hp2 others(7): Show |
intron_variant | MODIFIER | c.18+23243_18+23244d others(4): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5455583 | |||||
chr12:5455585
|
T | C | 53 | a0001c0001t0001g0017a0001c0001t0001g0032a0001c0001t0001g0033others(50): Show | 55 | HG00323.hp2 HG00408.hp1 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.18+23243T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5455585 | ||||||
chr12:5455743
|
A | G | 332 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(329): Show | 342 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(339): Show |
intron_variant | MODIFIER | c.18+23401A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5455743 | ||||||
chr12:5456138
|
G | A | 1 | a0001c0002t0001g0246 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.18+23796G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5456138 | ||||||
chr12:5456199
|
G | A | 1 | a0001c0002t0001g0154 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.18+23857G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5456199 | ||||||
chr12:5456349
|
C | A | 1 | a0001c0004t0001g0109 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.18+24007C>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5456349 | ||||||
chr12:5456394
|
C | T | 1 | a0002c0003t0001g0168 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.18+24052C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5456394 | ||||||
chr12:5456487
|
C | A | 5 | a0001c0001t0001g0213a0001c0004t0001g0139a0001c0004t0001g0333others(2): Show | 5 | HG02965.hp1 HG02976.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.18+24145C>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5456487 | ||||||
chr12:5456524
|
C | T | 5 | a0002c0003t0001g0040a0002c0003t0001g0067a0002c0003t0001g0075others(2): Show | 5 | HG01361.hp1 HG01433.hp2 HG01934.hp1 others(2): Show |
intron_variant | MODIFIER | c.18+24182C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5456524 | ||||||
chr12:5456602
|
C | T | 1 | a0002c0003t0001g0212 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.18+24260C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5456602 | ||||||
chr12:5456620
|
C | A | 2 | a0001c0001t0001g0017a0001c0001t0001g0142 | 2 | HG02976.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.18+24278C>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5456620 | ||||||
chr12:5456648
|
G | C | 1 | a0001c0001t0001g0250 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.18+24306G>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5456648 | ||||||
chr12:5456708
|
C | T | 1 | a0001c0001t0001g0348 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.18+24366C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5456708 | ||||||
chr12:5456941
|
G | A | 1 | a0001c0001t0001g0251 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.18+24599G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5456941 | ||||||
chr12:5456945
|
C | A | 1 | a0001c0001t0001g0200 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.18+24603C>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5456945 | ||||||
chr12:5456966
|
C | T | 29 | a0001c0001t0001g0157a0001c0001t0001g0265a0001c0001t0001g0268others(26): Show | 30 | HG00280.hp2 HG00733.hp1 HG01168.hp2 others(27): Show |
intron_variant | MODIFIER | c.18+24624C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5456966 | ||||||
chr12:5456974
|
G | A | 2 | a0001c0001t0001g0116a0001c0001t0004g0311 | 2 | HG02886.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.18+24632G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5456974 | ||||||
chr12:5457046
|
A | G | 1 | a0001c0002t0001g0089 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.18+24704A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5457046 | ||||||
chr12:5457355
|
C | T | 2 | a0001c0006t0001g0173a0001c0006t0001g0174 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.18+25013C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5457355 | ||||||
chr12:5457511
|
G | A | 1 | a0001c0002t0001g0117 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.18+25169G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5457511 | ||||||
chr12:5457511
|
G | C | 1 | a0001c0011t0001g0293 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.18+25169G>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5457511 | ||||||
chr12:5457638
|
G | A | 1 | a0001c0002t0001g0218 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.18+25296G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5457638 | ||||||
chr12:5457653
|
C | A | 1 | a0002c0003t0001g0168 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.18+25311C>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5457653 | ||||||
chr12:5457811
|
C | T | 1 | a0001c0001t0001g0352 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.18+25469C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5457811 | ||||||
chr12:5457960
|
C | G | 1 | a0002c0003t0001g0046 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.18+25618C>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5457960 | ||||||
chr12:5457979
|
T | C | 187 | a0001c0001t0001g0010a0001c0001t0001g0020a0001c0001t0001g0021others(184): Show | 190 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(187): Show |
intron_variant | MODIFIER | c.18+25637T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5457979 | ||||||
chr12:5457980
|
G | A | 124 | a0001c0001t0001g0036a0001c0001t0001g0063a0001c0001t0001g0064others(121): Show | 125 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.18+25638G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5457980 | ||||||
chr12:5457997
|
A | G | 1 | a0001c0002t0001g0162 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.18+25655A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5457997 | ||||||
chr12:5458084
|
T | C | 1 | a0001c0001t0001g0014 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.18+25742T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5458084 | ||||||
chr12:5458139
|
G | A | 1 | a0001c0004t0001g0248 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.18+25797G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5458139 | ||||||
chr12:5458215
|
A | C | 331 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(328): Show | 341 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(338): Show |
intron_variant | MODIFIER | c.18+25873A>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5458215 | ||||||
chr12:5458284
|
C | T | 3 | a0001c0001t0001g0092a0001c0001t0001g0114a0001c0001t0001g0135 | 3 | HG00280.hp1 HG00741.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.18+25942C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5458284 | ||||||
chr12:5458299
|
C | T | 1 | a0001c0002t0001g0290 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.18+25957C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5458299 | ||||||
chr12:5458410
|
T | G | 8 | a0001c0002t0001g0071a0002c0003t0001g0041a0002c0003t0001g0062others(5): Show | 8 | HG00423.hp1 HG02027.hp1 NA18940.hp1 others(5): Show |
intron_variant | MODIFIER | c.18+26068T>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5458410 | ||||||
chr12:5458427
|
C | T | 1 | a0001c0001t0001g0032 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.18+26085C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5458427 | ||||||
chr12:5458453
|
A | G | 58 | a0001c0001t0001g0010a0001c0001t0001g0020a0001c0001t0001g0021others(55): Show | 60 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.18+26111A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5458453 | ||||||
chr12:5458505
|
T | C | 1 | a0001c0001t0001g0294 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.18+26163T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5458505 | ||||||
chr12:5458669
|
A | G | 1 | a0001c0001t0001g0167 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.18+26327A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5458669 | ||||||
chr12:5458700
|
A | G | 1 | a0001c0001t0002g0349 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.18+26358A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5458700 | ||||||
chr12:5458759
|
T | C | 3 | a0001c0001t0001g0208a0001c0004t0001g0209a0001c0004t0001g0357 | 3 | HG01993.hp1 HG02602.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.18+26417T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5458759 | ||||||
chr12:5458891
|
G | A | 1 | a0001c0001t0004g0311 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.18+26549G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5458891 | ||||||
chr12:5458937
|
C | A | 35 | a0001c0001t0001g0017a0001c0001t0001g0032a0001c0001t0001g0110others(32): Show | 37 | HG00323.hp2 HG00408.hp1 HG00558.hp1 others(34): Show |
intron_variant | MODIFIER | c.18+26595C>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5458937 | ||||||
chr12:5458967
|
C | G | 1 | a0001c0001t0001g0351 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.18+26625C>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5458967 | ||||||
chr12:5459005
|
C | T | 123 | a0001c0001t0001g0036a0001c0001t0001g0063a0001c0001t0001g0064others(120): Show | 124 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.18+26663C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5459005 | ||||||
chr12:5459054
|
C | G | 121 | a0001c0001t0001g0036a0001c0001t0001g0063a0001c0001t0001g0064others(118): Show | 122 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.18+26712C>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5459054 | ||||||
chr12:5459126
|
G | A | 4 | a0001c0002t0001g0232a0001c0002t0001g0233a0001c0002t0001g0234others(1): Show | 4 | HG00621.hp2 NA18955.hp1 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.18+26784G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5459126 | ||||||
chr12:5459227
|
T | C | 5 | a0001c0002t0001g0030a0001c0002t0001g0031a0001c0002t0001g0048others(2): Show | 5 | HG02647.hp2 HG02970.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.18+26885T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5459227 | ||||||
chr12:5459405
|
C | T | 1 | a0001c0002t0001g0343 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.18+27063C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5459405 | ||||||
chr12:5459432
|
C | T | 1 | a0001c0002t0001g0185 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.18+27090C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5459432 | ||||||
chr12:5459750
|
G | A | 1 | a0002c0003t0001g0128 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.18+27408G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5459750 | ||||||
chr12:5460053
|
A | C | 3 | a0001c0001t0001g0091a0001c0001t0001g0133a0001c0001t0001g0134 | 3 | HG00099.hp2 HG01243.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.18+27711A>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5460053 | ||||||
chr12:5460105
|
C | T | 263 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(260): Show | 271 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(268): Show |
intron_variant | MODIFIER | c.18+27763C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5460105 | ||||||
chr12:5460407
|
C | T | 68 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(65): Show | 73 | HG00140.hp2 HG00423.hp2 HG00621.hp1 others(70): Show |
intron_variant | MODIFIER | c.18+28065C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5460407 | ||||||
chr12:5460505
|
A | G | 1 | a0002c0003t0001g0168 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.18+28163A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5460505 | ||||||
chr12:5460535
|
C | T | 4 | a0001c0001t0001g0015a0001c0001t0001g0025a0001c0001t0001g0172others(1): Show | 4 | HG02055.hp2 HG02647.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.18+28193C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5460535 | ||||||
chr12:5460681
|
A | T | 1 | a0001c0002t0001g0204 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.18+28339A>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5460681 | ||||||
chr12:5460742
|
C | T | 1 | a0001c0001t0001g0323 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.18+28400C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5460742 | ||||||
chr12:5460782
|
G | T | 1 | a0001c0002t0001g0030 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.18+28440G>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5460782 | ||||||
chr12:5460802
|
C | T | 1 | a0001c0001t0001g0200 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.18+28460C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5460802 | ||||||
chr12:5460842
|
A | G | 3 | a0001c0002t0001g0127a0001c0002t0001g0183a0001c0002t0001g0184 | 3 | HG00621.hp1 NA19011.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.18+28500A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5460842 | ||||||
chr12:5461034
|
C | G | 1 | a0001c0006t0001g0086 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.18+28692C>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5461034 | ||||||
chr12:5461036
|
C | T | 9 | a0001c0001t0001g0036a0001c0001t0001g0138a0001c0001t0001g0140others(6): Show | 9 | HG02109.hp1 HG02280.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.18+28694C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5461036 | ||||||
chr12:5461049
|
G | A | 1 | a0001c0001t0001g0102 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.18+28707G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5461049 | ||||||
chr12:5461070
|
G | C | 1 | a0001c0002t0001g0169 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.18+28728G>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5461070 | ||||||
chr12:5461089
|
G | A | 119 | a0001c0001t0001g0036a0001c0001t0001g0063a0001c0001t0001g0064others(116): Show | 120 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.18+28747G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5461089 | ||||||
chr12:5461272
|
C | T | 4 | a0001c0001t0001g0015a0001c0001t0001g0025a0001c0001t0001g0172others(1): Show | 4 | HG02055.hp2 HG02647.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.18+28930C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5461272 | ||||||
chr12:5461455
|
T | C | 16 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0069others(13): Show | 16 | HG00438.hp2 HG00558.hp2 HG02074.hp1 others(13): Show |
intron_variant | MODIFIER | c.18+29113T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5461455 | ||||||
chr12:5461580
|
A | G | 4 | a0001c0001t0001g0016a0001c0001t0001g0028a0001c0001t0001g0111others(1): Show | 4 | HG01346.hp1 HG02257.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.18+29238A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5461580 | ||||||
chr12:5462196
|
ACTCT | A | 121 | a0001c0001t0001g0036a0001c0001t0001g0063a0001c0001t0001g0064others(118): Show | 122 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.18+29860_18+29863d others(6): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5462196 | |||||
chr12:5462282
|
T | G | 68 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(65): Show | 73 | HG00140.hp2 HG00423.hp2 HG00621.hp1 others(70): Show |
intron_variant | MODIFIER | c.18+29940T>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5462282 | ||||||
chr12:5462489
|
T | C | 5 | a0001c0002t0001g0022a0001c0002t0001g0093a0001c0002t0001g0094others(2): Show | 5 | HG00423.hp2 HG02129.hp2 NA18942.hp1 others(2): Show |
intron_variant | MODIFIER | c.18+30147T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5462489 | ||||||
chr12:5462570
|
G | A | 2 | a0001c0001t0001g0200a0001c0002t0001g0148 | 2 | HG03209.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.18+30228G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5462570 | ||||||
chr12:5462679
|
C | A | 120 | a0001c0001t0001g0036a0001c0001t0001g0063a0001c0001t0001g0064others(117): Show | 121 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.18+30337C>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5462679 | ||||||
chr12:5462815
|
T | C | 59 | a0001c0001t0001g0010a0001c0001t0001g0020a0001c0001t0001g0021others(56): Show | 61 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.18+30473T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5462815 | ||||||
chr12:5462972
|
A | G | 1 | a0001c0002t0001g0198 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.18+30630A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5462972 | ||||||
chr12:5463044
|
C | T | 8 | a0001c0001t0001g0112a0001c0001t0001g0242a0001c0001t0001g0253others(5): Show | 9 | HG00735.hp1 HG00738.hp1 HG01069.hp2 others(6): Show |
intron_variant | MODIFIER | c.18+30702C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5463044 | ||||||
chr12:5463089
|
C | T | 1 | a0001c0001t0001g0165 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.18+30747C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5463089 | ||||||
chr12:5463205
|
C | G | 126 | a0001c0001t0001g0016a0001c0001t0001g0028a0001c0001t0001g0036others(123): Show | 127 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(124): Show |
intron_variant | MODIFIER | c.18+30863C>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5463205 | ||||||
chr12:5463316
|
A | G | 1 | a0001c0001t0001g0115 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.19-30878A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5463316 | ||||||
chr12:5463380
|
T | C | 4 | a0001c0001t0001g0116a0001c0001t0001g0348a0001c0001t0001g0351others(1): Show | 4 | HG01952.hp2 HG02717.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.19-30814T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5463380 | ||||||
chr12:5463412
|
A | T | 1 | a0001c0001t0001g0352 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.19-30782A>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5463412 | ||||||
chr12:5463916
|
A | G | 1 | a0001c0001t0001g0352 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.19-30278A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5463916 | ||||||
chr12:5464447
|
A | T | 159 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0020others(156): Show | 161 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(158): Show |
intron_variant | MODIFIER | c.19-29747A>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5464447 | ||||||
chr12:5464544
|
G | T | 1 | a0001c0001t0004g0311 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.19-29650G>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5464544 | ||||||
chr12:5464607
|
G | C | 19 | a0001c0001t0001g0044a0001c0001t0001g0105a0001c0001t0001g0249others(16): Show | 19 | HG00323.hp1 HG00639.hp1 HG00642.hp2 others(16): Show |
intron_variant | MODIFIER | c.19-29587G>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5464607 | ||||||
chr12:5464845
|
G | T | 57 | a0001c0001t0001g0017a0001c0001t0001g0032a0001c0001t0001g0051others(54): Show | 59 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(56): Show |
intron_variant | MODIFIER | c.19-29349G>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5464845 | ||||||
chr12:5465131
|
G | A | 2 | a0001c0002t0001g0252a0001c0002t0001g0272 | 2 | HG02257.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.19-29063G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5465131 | ||||||
chr12:5465254
|
C | T | 1 | a0001c0001t0001g0268 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.19-28940C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5465254 | ||||||
chr12:5465310
|
G | C | 1 | a0001c0001t0001g0200 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.19-28884G>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5465310 | ||||||
chr12:5465335
|
C | A | 1 | a0001c0001t0001g0262 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.19-28859C>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5465335 | ||||||
chr12:5465445
|
G | A | 8 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0053others(5): Show | 8 | HG01358.hp2 HG02055.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.19-28749G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5465445 | ||||||
chr12:5465611
|
A | G | 17 | a0001c0001t0001g0088a0001c0001t0001g0090a0001c0001t0001g0091others(14): Show | 17 | HG00099.hp2 HG00280.hp1 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.19-28583A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5465611 | ||||||
chr12:5465845
|
A | G | 4 | a0001c0001t0001g0351a0001c0002t0001g0230a0001c0002t0001g0353others(1): Show | 4 | HG01952.hp2 HG02109.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.19-28349A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5465845 | ||||||
chr12:5465861
|
C | T | 56 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0025others(53): Show | 58 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(55): Show |
intron_variant | MODIFIER | c.19-28333C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5465861 | ||||||
chr12:5465944
|
C | G | 2 | a0001c0006t0001g0173a0001c0006t0001g0174 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.19-28250C>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5465944 | ||||||
chr12:5466043
|
G | A | 1 | a0001c0002t0001g0056 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.19-28151G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5466043 | ||||||
chr12:5466272
|
C | T | 1 | a0001c0002t0001g0246 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.19-27922C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5466272 | ||||||
chr12:5466301
|
G | A | 112 | a0001c0001t0001g0036a0001c0001t0001g0063a0001c0001t0001g0064others(109): Show | 113 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.19-27893G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5466301 | ||||||
chr12:5466393
|
G | A | 5 | a0001c0001t0001g0016a0001c0001t0001g0028a0001c0001t0001g0111others(2): Show | 5 | HG01346.hp1 HG02257.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.19-27801G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5466393 | ||||||
chr12:5466473
|
G | A | 2 | a0001c0001t0001g0249a0001c0004t0001g0247 | 2 | HG00323.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.19-27721G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5466473 | ||||||
chr12:5466798
|
G | T | 1 | a0001c0001t0001g0329 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.19-27396G>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5466798 | ||||||
chr12:5466954
|
C | T | 1 | a0001c0001t0005g0223 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.19-27240C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5466954 | ||||||
chr12:5466956
|
G | A | 1 | a0001c0001t0001g0268 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.19-27238G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5466956 | ||||||
chr12:5466961
|
A | C | 1 | a0001c0007t0001g0220 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.19-27233A>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5466961 | ||||||
chr12:5467059
|
G | A | 37 | a0001c0001t0001g0213a0001c0001t0001g0242a0001c0001t0001g0251others(34): Show | 37 | HG00280.hp2 HG00423.hp1 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.19-27135G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5467059 | ||||||
chr12:5467091
|
G | A | 3 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0163 | 3 | HG02886.hp1 HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.19-27103G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5467091 | ||||||
chr12:5467103
|
G | A | 1 | a0002c0003t0001g0201 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.19-27091G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5467103 | ||||||
chr12:5467198
|
C | T | 1 | a0001c0002t0001g0175 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.19-26996C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5467198 | ||||||
chr12:5467200
|
A | G | 4 | a0001c0002t0001g0117a0001c0002t0001g0160a0001c0002t0001g0162others(1): Show | 4 | HG00099.hp1 HG00639.hp2 HG01099.hp2 others(1): Show |
intron_variant | MODIFIER | c.19-26994A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5467200 | ||||||
chr12:5467203
|
T | C | 4 | a0001c0002t0001g0117a0001c0002t0001g0160a0001c0002t0001g0162others(1): Show | 4 | HG00099.hp1 HG00639.hp2 HG01099.hp2 others(1): Show |
intron_variant | MODIFIER | c.19-26991T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5467203 | ||||||
chr12:5467205
|
T | G | 4 | a0001c0002t0001g0117a0001c0002t0001g0160a0001c0002t0001g0162others(1): Show | 4 | HG00099.hp1 HG00639.hp2 HG01099.hp2 others(1): Show |
intron_variant | MODIFIER | c.19-26989T>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5467205 | ||||||
chr12:5467228
|
C | CA | 33 | a0001c0001t0001g0049a0001c0001t0001g0059a0001c0001t0001g0070others(30): Show | 34 | HG00280.hp2 HG00423.hp2 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.19-26931dupA | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5467228 | |||||
chr12:5467228
|
C | CAA | 18 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0208others(15): Show | 20 | HG00621.hp1 HG01175.hp2 HG01978.hp2 others(17): Show |
intron_variant | MODIFIER | c.19-26932_19-26931d others(4): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5467228 | |||||
chr12:5467228
|
C | CAAA | 20 | a0001c0001t0001g0250a0001c0002t0001g0030a0001c0002t0001g0048others(17): Show | 21 | HG00738.hp1 HG00741.hp1 HG01070.hp1 others(18): Show |
intron_variant | MODIFIER | c.19-26933_19-26931d others(5): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5467228 | |||||
chr12:5467228
|
C | CAAAA | 7 | a0001c0001t0001g0112a0001c0001t0001g0253a0001c0001t0001g0307others(4): Show | 7 | HG00639.hp1 HG01069.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.19-26934_19-26931d others(6): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5467228 | |||||
chr12:5467228
|
C | CAAAAA | 12 | a0001c0001t0001g0105a0001c0001t0001g0200a0001c0001t0001g0249others(9): Show | 12 | HG00323.hp1 HG00642.hp2 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.19-26935_19-26931d others(7): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5467228 | |||||
chr12:5467228
|
C | CAAAAAAA others(3): Show |
1 | a0001c0002t0001g0240 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.19-26940_19-26931d others(12): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5467228 | |||||
chr12:5467228
|
C | CAAAAAAA others(4): Show |
1 | a0001c0001t0001g0032 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.19-26941_19-26931d others(13): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5467228 | |||||
chr12:5467228
|
CA | C | 29 | a0001c0001t0001g0044a0001c0001t0001g0078a0001c0001t0001g0134others(26): Show | 29 | HG00099.hp2 HG00423.hp1 HG00735.hp1 others(26): Show |
intron_variant | MODIFIER | c.19-26931delA | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5467228 | |||||
chr12:5467228
|
CAA | C | 54 | a0001c0001t0001g0064a0001c0001t0001g0072a0001c0001t0001g0080others(51): Show | 54 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.19-26932_19-26931d others(4): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5467228 | |||||
chr12:5467228
|
CAAA | C | 34 | a0001c0001t0001g0033a0001c0001t0001g0063a0001c0001t0001g0069others(31): Show | 35 | HG00558.hp2 HG00733.hp1 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.19-26933_19-26931d others(5): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5467228 | |||||
chr12:5467228
|
CAAAA | C | 15 | a0001c0001t0001g0015a0001c0001t0001g0025a0001c0001t0001g0036others(12): Show | 15 | HG01891.hp1 HG02055.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.19-26934_19-26931d others(6): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5467228 | |||||
chr12:5467228
|
CAAAAA | C | 7 | a0001c0001t0001g0052a0001c0001t0001g0113a0001c0001t0001g0138others(4): Show | 7 | HG01169.hp1 HG01358.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.19-26935_19-26931d others(7): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5467228 | |||||
chr12:5467228
|
CAAAAAA | C | 11 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0163others(8): Show | 11 | HG01099.hp2 HG01891.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.19-26936_19-26931d others(8): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5467228 | |||||
chr12:5467228
|
CAAAAAAA others(3): Show |
C | 30 | a0001c0001t0001g0017a0001c0001t0001g0142a0001c0001t0001g0221others(27): Show | 31 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(28): Show |
intron_variant | MODIFIER | c.19-26940_19-26931d others(12): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5467228 | |||||
chr12:5467228
|
CAAAAAAA others(4): Show |
C | 47 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(44): Show | 50 | HG00140.hp1 HG00140.hp2 HG00738.hp2 others(47): Show |
intron_variant | MODIFIER | c.19-26941_19-26931d others(13): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5467228 | |||||
chr12:5467228
|
CAAAAAAA others(7): Show |
C | 1 | a0001c0001t0001g0029 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.19-26944_19-26931d others(16): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5467228 | |||||
chr12:5467228
|
CAAAAAAA others(8): Show |
C | 1 | a0002c0003t0001g0168 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.19-26945_19-26931d others(17): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5467228 | |||||
chr12:5467272
|
CTTGCCAA others(10): Show |
C | 6 | a0001c0002t0001g0013a0001c0002t0001g0232a0001c0002t0001g0233others(3): Show | 6 | HG00558.hp1 HG00621.hp2 NA18955.hp1 others(3): Show |
intron_variant | MODIFIER | c.19-26920_19-26904d others(19): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5467272 | |||||
chr12:5467304
|
G | A | 29 | a0001c0001t0001g0017a0001c0001t0001g0142a0001c0001t0001g0167others(26): Show | 30 | HG00323.hp2 HG00408.hp1 HG00558.hp1 others(27): Show |
intron_variant | MODIFIER | c.19-26890G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5467304 | ||||||
chr12:5467332
|
C | A | 3 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0195 | 3 | NA18969.hp2 NA18982.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.19-26862C>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5467332 | ||||||
chr12:5467428
|
C | T | 232 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(229): Show | 238 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(235): Show |
intron_variant | MODIFIER | c.19-26766C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5467428 | ||||||
chr12:5467657
|
T | C | 1 | a0001c0001t0001g0207 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.19-26537T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5467657 | ||||||
chr12:5467777
|
G | A | 46 | a0001c0001t0001g0059a0001c0001t0001g0208a0001c0002t0001g0001others(43): Show | 48 | HG00423.hp2 HG00621.hp1 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.19-26417G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5467777 | ||||||
chr12:5467943
|
A | T | 3 | a0001c0001t0001g0028a0001c0001t0001g0111a0001c0001t0001g0345 | 3 | HG01346.hp1 HG01884.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.19-26251A>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5467943 | ||||||
chr12:5467998
|
C | A | 2 | a0001c0002t0001g0192a0001c0002t0001g0343 | 2 | NA18952.hp2 NA18997.hp2 |
intron_variant | MODIFIER | c.19-26196C>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5467998 | ||||||
chr12:5468119
|
C | T | 2 | a0001c0001t0001g0351a0001c0001t0001g0352 | 2 | HG01952.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.19-26075C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5468119 | ||||||
chr12:5468294
|
C | T | 1 | a0002c0003t0001g0168 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.19-25900C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5468294 | ||||||
chr12:5468325
|
T | A | 2 | a0001c0002t0001g0198a0001c0002t0001g0281 | 2 | HG02735.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.19-25869T>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5468325 | ||||||
chr12:5468393
|
A | G | 31 | a0001c0001t0001g0032a0001c0001t0001g0105a0001c0001t0001g0112others(28): Show | 32 | HG00323.hp1 HG00639.hp1 HG00642.hp2 others(29): Show |
intron_variant | MODIFIER | c.19-25801A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5468393 | ||||||
chr12:5468453
|
C | T | 2 | a0001c0001t0001g0289a0002c0003t0001g0285 | 2 | HG02145.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.19-25741C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5468453 | ||||||
chr12:5468504
|
G | A | 1 | a0002c0005t0001g0261 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.19-25690G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5468504 | ||||||
chr12:5468610
|
A | G | 1 | a0002c0003t0001g0194 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.19-25584A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5468610 | ||||||
chr12:5468701
|
A | G | 79 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(76): Show | 83 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.19-25493A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5468701 | ||||||
chr12:5468784
|
C | G | 2 | a0001c0002t0001g0089a0001c0002t0001g0358 | 2 | HG00140.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.19-25410C>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5468784 | ||||||
chr12:5468901
|
G | T | 1 | a0001c0001t0001g0260 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.19-25293G>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5468901 | ||||||
chr12:5469153
|
G | A | 1 | a0001c0002t0001g0117 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.19-25041G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5469153 | ||||||
chr12:5469318
|
C | T | 6 | a0001c0001t0001g0032a0001c0001t0001g0294a0001c0001t0001g0351others(3): Show | 6 | HG01192.hp2 HG01952.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.19-24876C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5469318 | ||||||
chr12:5469489
|
G | A | 78 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(75): Show | 82 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.19-24705G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5469489 | ||||||
chr12:5469673
|
G | A | 4 | a0001c0001t0001g0032a0001c0001t0001g0294a0001c0002t0001g0101others(1): Show | 4 | HG01192.hp2 HG02809.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.19-24521G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5469673 | ||||||
chr12:5470018
|
G | A | 1 | a0002c0003t0001g0168 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.19-24176G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5470018 | ||||||
chr12:5470039
|
C | G | 1 | a0001c0004t0001g0155 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.19-24155C>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5470039 | ||||||
chr12:5470074
|
G | A | 3 | a0001c0001t0001g0193a0002c0003t0001g0045a0002c0003t0001g0103 | 3 | HG02895.hp2 HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.19-24120G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5470074 | ||||||
chr12:5470204
|
G | A | 6 | a0001c0001t0001g0032a0001c0001t0001g0294a0001c0001t0001g0351others(3): Show | 6 | HG01192.hp2 HG01952.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.19-23990G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5470204 | ||||||
chr12:5470310
|
A | C | 1 | a0001c0001t0001g0029 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.19-23884A>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5470310 | ||||||
chr12:5470337
|
C | T | 1 | a0001c0002t0001g0013 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.19-23857C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5470337 | ||||||
chr12:5470454
|
T | C | 1 | a0001c0001t0001g0085 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.19-23740T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5470454 | ||||||
chr12:5470465
|
A | G | 250 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(247): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.19-23729A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5470465 | ||||||
chr12:5470473
|
A | G | 1 | a0001c0001t0001g0032 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.19-23721A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5470473 | ||||||
chr12:5470475
|
G | A | 1 | a0001c0001t0001g0114 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.19-23719G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5470475 | ||||||
chr12:5470531
|
C | T | 1 | a0002c0003t0001g0212 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.19-23663C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5470531 | ||||||
chr12:5470989
|
C | A | 2 | a0001c0002t0001g0101a0001c0002t0001g0119 | 2 | HG01192.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.19-23205C>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5470989 | ||||||
chr12:5471132
|
C | G | 2 | a0001c0001t0001g0072a0001c0001t0001g0073 | 2 | NA18986.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.19-23062C>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5471132 | ||||||
chr12:5471211
|
G | A | 2 | a0002c0003t0001g0324a0002c0003t0001g0325 | 2 | NA18612.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.19-22983G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5471211 | ||||||
chr12:5471313
|
G | A | 1 | a0001c0001t0001g0033 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.19-22881G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5471313 | ||||||
chr12:5471382
|
G | A | 1 | a0001c0002t0001g0099 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.19-22812G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5471382 | ||||||
chr12:5471519
|
A | T | 1 | a0002c0003t0001g0211 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.19-22675A>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5471519 | ||||||
chr12:5471520
|
C | T | 6 | a0001c0001t0001g0036a0001c0001t0001g0138a0001c0001t0001g0140others(3): Show | 6 | HG02280.hp1 HG02630.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.19-22674C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5471520 | ||||||
chr12:5471636
|
G | A | 1 | a0002c0003t0001g0087 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.19-22558G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5471636 | ||||||
chr12:5471694
|
C | A | 1 | a0001c0001t0001g0213 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.19-22500C>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5471694 | ||||||
chr12:5471713
|
T | A | 1 | a0001c0002t0001g0264 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.19-22481T>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5471713 | ||||||
chr12:5471720
|
T | C | 1 | a0001c0001t0001g0033 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.19-22474T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5471720 | ||||||
chr12:5471739
|
C | A | 1 | a0001c0001t0002g0349 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.19-22455C>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5471739 | ||||||
chr12:5471812
|
T | A | 1 | a0001c0004t0001g0322 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.19-22382T>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5471812 | ||||||
chr12:5471867
|
G | T | 1 | a0001c0001t0001g0348 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.19-22327G>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5471867 | ||||||
chr12:5471992
|
G | A | 6 | a0001c0002t0001g0013a0001c0002t0001g0232a0001c0002t0001g0233others(3): Show | 6 | HG00558.hp1 HG00621.hp2 NA18955.hp1 others(3): Show |
intron_variant | MODIFIER | c.19-22202G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5471992 | ||||||
chr12:5472188
|
A | T | 10 | a0001c0001t0001g0015a0001c0001t0001g0025a0001c0001t0001g0110others(7): Show | 10 | HG01169.hp1 HG01891.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.19-22006A>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5472188 | ||||||
chr12:5472242
|
C | T | 2 | a0001c0001t0001g0021a0002c0003t0001g0320 | 2 | NA18957.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.19-21952C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5472242 | ||||||
chr12:5472271
|
G | A | 1 | a0001c0001t0004g0311 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.19-21923G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5472271 | ||||||
chr12:5472308
|
A | G | 1 | a0002c0003t0001g0168 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.19-21886A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5472308 | ||||||
chr12:5472506
|
G | A | 2 | a0001c0001t0001g0033a0001c0001t0001g0351 | 2 | HG01952.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.19-21688G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5472506 | ||||||
chr12:5472534
|
C | A | 1 | a0002c0003t0001g0328 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.19-21660C>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5472534 | ||||||
chr12:5472953
|
T | C | 40 | a0001c0001t0001g0032a0001c0001t0001g0036a0001c0001t0001g0105others(37): Show | 41 | HG00323.hp1 HG00639.hp1 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.19-21241T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5472953 | ||||||
chr12:5473032
|
G | A | 1 | a0001c0002t0001g0210 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.19-21162G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5473032 | ||||||
chr12:5473063
|
C | T | 6 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0028others(3): Show | 6 | HG01346.hp1 HG01884.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.19-21131C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5473063 | ||||||
chr12:5473202
|
T | C | 1 | a0002c0003t0001g0168 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.19-20992T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5473202 | ||||||
chr12:5473387
|
C | A | 1 | a0001c0002t0001g0071 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.19-20807C>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5473387 | ||||||
chr12:5473394
|
A | G | 38 | a0001c0001t0001g0032a0001c0001t0001g0036a0001c0001t0001g0105others(35): Show | 39 | HG00323.hp1 HG00639.hp1 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.19-20800A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5473394 | ||||||
chr12:5473406
|
G | A | 1 | a0001c0002t0001g0244 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.19-20788G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5473406 | ||||||
chr12:5473416
|
G | A | 5 | a0001c0001t0001g0019a0001c0001t0001g0049a0001c0001t0001g0102others(2): Show | 5 | HG01109.hp2 HG02145.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.19-20778G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5473416 | ||||||
chr12:5473685
|
A | G | 4 | a0001c0002t0001g0030a0001c0002t0001g0031a0001c0002t0001g0048others(1): Show | 4 | HG02647.hp2 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.19-20509A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5473685 | ||||||
chr12:5473727
|
G | A | 1 | a0001c0002t0001g0229 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.19-20467G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5473727 | ||||||
chr12:5473855
|
C | T | 51 | a0001c0001t0001g0059a0001c0001t0005g0223a0001c0002t0001g0001others(48): Show | 53 | HG00423.hp2 HG00621.hp1 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.19-20339C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5473855 | ||||||
chr12:5473856
|
A | G | 127 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0015others(124): Show | 131 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.19-20338A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5473856 | ||||||
chr12:5474001
|
T | C | 2 | a0002c0003t0001g0046a0002c0003t0001g0356 | 2 | HG02622.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.19-20193T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5474001 | ||||||
chr12:5474077
|
G | A | 1 | a0001c0001t0001g0033 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.19-20117G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5474077 | ||||||
chr12:5474408
|
G | A | 1 | a0001c0002t0001g0288 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.19-19786G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5474408 | ||||||
chr12:5474439
|
C | A | 4 | a0001c0001t0001g0012a0001c0001t0001g0336a0001c0001t0001g0337others(1): Show | 5 | HG02071.hp1 HG02523.hp1 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.19-19755C>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5474439 | ||||||
chr12:5474454
|
G | A | 1 | a0001c0001t0001g0219 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.19-19740G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5474454 | ||||||
chr12:5474577
|
A | G | 1 | a0001c0001t0001g0112 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.19-19617A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5474577 | ||||||
chr12:5474671
|
G | A | 1 | a0001c0002t0001g0150 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.19-19523G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5474671 | ||||||
chr12:5474773
|
G | A | 254 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(251): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.19-19421G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5474773 | ||||||
chr12:5474978
|
A | T | 1 | a0001c0002t0001g0187 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.19-19216A>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5474978 | ||||||
chr12:5474989
|
T | C | 2 | a0001c0001t0001g0282a0001c0001t0001g0283 | 2 | HG01891.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.19-19205T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5474989 | ||||||
chr12:5475214
|
G | A | 4 | a0002c0005t0001g0259a0002c0005t0001g0261a0002c0005t0001g0263others(1): Show | 4 | NA18952.hp1 NA18959.hp1 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.19-18980G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5475214 | ||||||
chr12:5475479
|
A | G | 2 | a0001c0004t0001g0139a0001c0004t0001g0333 | 2 | HG02976.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.19-18715A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5475479 | ||||||
chr12:5475565
|
TG | T | 8 | a0001c0001t0005g0223a0001c0002t0001g0030a0001c0002t0001g0031others(5): Show | 8 | HG02451.hp2 HG02647.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.19-18627delG | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5475565 | |||||
chr12:5475728
|
G | C | 1 | a0001c0001t0001g0351 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.19-18466G>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5475728 | ||||||
chr12:5475854
|
A | AAG | 78 | a0001c0001t0001g0032a0001c0001t0001g0036a0001c0001t0001g0059others(75): Show | 81 | HG00323.hp1 HG00423.hp2 HG00621.hp1 others(78): Show |
intron_variant | MODIFIER | c.19-18318_19-18317d others(4): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5475854 | |||||
chr12:5475854
|
A | AAGAG | 3 | a0001c0001t0001g0352a0001c0002t0001g0252a0001c0002t0001g0296 | 3 | HG02257.hp2 HG02258.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.19-18320_19-18317d others(6): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5475854 | |||||
chr12:5475854
|
AAG | A | 5 | a0001c0002t0001g0126a0001c0002t0001g0175a0001c0002t0001g0181others(2): Show | 5 | HG00642.hp1 HG01256.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.19-18318_19-18317d others(4): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5475854 | |||||
chr12:5475854
|
AAGAG | A | 9 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0028others(6): Show | 9 | HG01346.hp1 HG01884.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.19-18320_19-18317d others(6): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5475854 | |||||
chr12:5475898
|
G | GAGAA | 8 | a0001c0001t0005g0223a0001c0002t0001g0030a0001c0002t0001g0031others(5): Show | 8 | HG02451.hp2 HG02647.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.19-18280_19-18277d others(6): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5475898 | |||||
chr12:5475898
|
GAGAA | G | 6 | a0001c0001t0001g0019a0001c0001t0001g0049a0001c0001t0001g0102others(3): Show | 6 | HG01109.hp2 HG02145.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.19-18280_19-18277d others(6): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5475898 | |||||
chr12:5475915
|
AGAG | A | 81 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(78): Show | 85 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.19-18278_19-18276d others(5): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5475915 | ||||||
chr12:5475924
|
GAGAGAAA others(5): Show |
G | 6 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0028others(3): Show | 6 | HG01346.hp1 HG01884.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.19-18261_19-18250d others(14): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5475924 | |||||
chr12:5475985
|
A | G | 255 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(252): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.19-18209A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5475985 | ||||||
chr12:5476036
|
G | A | 10 | a0001c0001t0001g0015a0001c0001t0001g0025a0001c0001t0001g0110others(7): Show | 10 | HG01169.hp1 HG01891.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.19-18158G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5476036 | ||||||
chr12:5476071
|
G | A | 1 | a0001c0001t0005g0223 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.19-18123G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5476071 | ||||||
chr12:5476149
|
G | C | 1 | a0001c0001t0001g0207 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.19-18045G>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5476149 | ||||||
chr12:5476489
|
T | C | 2 | a0001c0001t0001g0006a0002c0003t0001g0006 | 2 | NA18981.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.19-17705T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5476489 | ||||||
chr12:5476560
|
T | A | 1 | a0001c0001t0001g0014 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.19-17634T>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5476560 | ||||||
chr12:5476692
|
A | C | 1 | a0001c0001t0001g0294 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.19-17502A>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5476692 | ||||||
chr12:5476882
|
T | C | 1 | a0001c0002t0001g0281 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.19-17312T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5476882 | ||||||
chr12:5477085
|
T | G | 1 | a0001c0001t0001g0200 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.19-17109T>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5477085 | ||||||
chr12:5477139
|
T | A | 81 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0015others(78): Show | 83 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(80): Show |
intron_variant | MODIFIER | c.19-17055T>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5477139 | ||||||
chr12:5477378
|
A | G | 1 | a0001c0001t0001g0294 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.19-16816A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5477378 | ||||||
chr12:5477509
|
C | T | 3 | a0001c0001t0001g0059a0001c0001t0001g0092a0001c0001t0001g0114 | 3 | HG00280.hp1 HG00741.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.19-16685C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5477509 | ||||||
chr12:5477686
|
G | C | 1 | a0001c0002t0001g0030 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.19-16508G>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5477686 | ||||||
chr12:5477744
|
T | C | 2 | a0001c0006t0001g0173a0001c0006t0001g0174 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.19-16450T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5477744 | ||||||
chr12:5477819
|
G | A | 2 | a0001c0001t0001g0301a0001c0001t0001g0302 | 2 | HG01361.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.19-16375G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5477819 | ||||||
chr12:5477986
|
T | G | 81 | a0001c0001t0001g0032a0001c0001t0001g0036a0001c0001t0001g0059others(78): Show | 84 | HG00323.hp1 HG00423.hp2 HG00621.hp1 others(81): Show |
intron_variant | MODIFIER | c.19-16208T>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5477986 | ||||||
chr12:5478050
|
A | C | 1 | a0002c0003t0001g0168 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.19-16144A>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5478050 | ||||||
chr12:5478151
|
A | T | 51 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(48): Show | 54 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.19-16043A>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5478151 | ||||||
chr12:5478173
|
C | T | 2 | a0001c0002t0001g0181a0001c0002t0001g0182 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.19-16021C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5478173 | ||||||
chr12:5478317
|
T | G | 83 | a0001c0001t0001g0032a0001c0001t0001g0036a0001c0001t0001g0059others(80): Show | 86 | HG00323.hp1 HG00423.hp2 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.19-15877T>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5478317 | ||||||
chr12:5478424
|
C | A | 2 | a0002c0003t0001g0042a0002c0003t0001g0043 | 2 | HG00408.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.19-15770C>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5478424 | ||||||
chr12:5478476
|
TC | T | 81 | a0001c0001t0001g0032a0001c0001t0001g0036a0001c0001t0001g0059others(78): Show | 84 | HG00323.hp1 HG00423.hp2 HG00621.hp1 others(81): Show |
intron_variant | MODIFIER | c.19-15714delC | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5478476 | |||||
chr12:5478517
|
G | A | 8 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0028others(5): Show | 8 | HG01346.hp1 HG01884.hp2 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.19-15677G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5478517 | ||||||
chr12:5478586
|
T | C | 1 | a0001c0002t0001g0252 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.19-15608T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5478586 | ||||||
chr12:5478587
|
C | T | 83 | a0001c0001t0001g0032a0001c0001t0001g0036a0001c0001t0001g0059others(80): Show | 86 | HG00323.hp1 HG00423.hp2 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.19-15607C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5478587 | ||||||
chr12:5478588
|
A | G | 83 | a0001c0001t0001g0032a0001c0001t0001g0036a0001c0001t0001g0059others(80): Show | 86 | HG00323.hp1 HG00423.hp2 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.19-15606A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5478588 | ||||||
chr12:5478761
|
G | A | 1 | a0001c0001t0001g0026 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.19-15433G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5478761 | ||||||
chr12:5478764
|
C | T | 2 | a0001c0004t0001g0277a0001c0004t0001g0280 | 2 | HG01261.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.19-15430C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5478764 | ||||||
chr12:5478852
|
G | A | 83 | a0001c0001t0001g0032a0001c0001t0001g0036a0001c0001t0001g0059others(80): Show | 86 | HG00323.hp1 HG00423.hp2 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.19-15342G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5478852 | ||||||
chr12:5478891
|
A | C | 3 | a0001c0001t0001g0193a0002c0003t0001g0045a0002c0003t0001g0103 | 3 | HG02895.hp2 HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.19-15303A>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5478891 | ||||||
chr12:5478963
|
C | T | 22 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0053others(19): Show | 22 | HG00099.hp1 HG00639.hp2 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.19-15231C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5478963 | ||||||
chr12:5479148
|
C | T | 1 | a0001c0001t0001g0268 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.19-15046C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5479148 | ||||||
chr12:5479188
|
G | A | 1 | a0001c0001t0001g0163 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.19-15006G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5479188 | ||||||
chr12:5479220
|
G | C | 1 | a0001c0001t0001g0255 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.19-14974G>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5479220 | ||||||
chr12:5479375
|
G | A | 1 | a0001c0002t0001g0252 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.19-14819G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5479375 | ||||||
chr12:5479426
|
T | G | 85 | a0001c0001t0001g0029a0001c0001t0001g0032a0001c0001t0001g0036others(82): Show | 88 | HG00323.hp1 HG00423.hp2 HG00621.hp1 others(85): Show |
intron_variant | MODIFIER | c.19-14768T>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5479426 | ||||||
chr12:5479506
|
G | A | 29 | a0001c0001t0001g0017a0001c0001t0001g0142a0001c0001t0001g0167others(26): Show | 30 | HG00323.hp2 HG00408.hp1 HG00558.hp1 others(27): Show |
intron_variant | MODIFIER | c.19-14688G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5479506 | ||||||
chr12:5479785
|
C | T | 172 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(169): Show | 179 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.19-14409C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5479785 | ||||||
chr12:5479805
|
A | C | 75 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0015others(72): Show | 77 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.19-14389A>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5479805 | ||||||
chr12:5479833
|
T | C | 247 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(244): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.19-14361T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5479833 | ||||||
chr12:5479839
|
T | G | 1 | a0001c0001t0001g0144 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.19-14355T>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5479839 | ||||||
chr12:5479863
|
A | G | 1 | a0001c0001t0001g0063 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.19-14331A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5479863 | ||||||
chr12:5480106
|
C | G | 41 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0019others(38): Show | 43 | HG00099.hp2 HG00280.hp1 HG00733.hp1 others(40): Show |
intron_variant | MODIFIER | c.19-14088C>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5480106 | ||||||
chr12:5480125
|
C | T | 182 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(179): Show | 189 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.19-14069C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5480125 | ||||||
chr12:5480243
|
A | G | 153 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(150): Show | 159 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.19-13951A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5480243 | ||||||
chr12:5480487
|
C | T | 1 | a0001c0001t0001g0131 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.19-13707C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5480487 | ||||||
chr12:5480528
|
G | T | 2 | a0002c0003t0001g0083a0002c0003t0001g0084 | 2 | NA18940.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.19-13666G>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5480528 | ||||||
chr12:5480530
|
A | G | 1 | a0002c0003t0001g0168 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.19-13664A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5480530 | ||||||
chr12:5480649
|
A | G | 1 | a0001c0001t0001g0029 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.19-13545A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5480649 | ||||||
chr12:5480658
|
G | A | 3 | a0001c0002t0001g0027a0001c0002t0001g0089a0001c0002t0001g0358 | 3 | HG00140.hp1 HG03654.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.19-13536G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5480658 | ||||||
chr12:5480727
|
C | G | 42 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0019others(39): Show | 44 | HG00099.hp2 HG00280.hp1 HG00733.hp1 others(41): Show |
intron_variant | MODIFIER | c.19-13467C>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5480727 | ||||||
chr12:5480748
|
G | A | 1 | a0001c0001t0001g0294 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.19-13446G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5480748 | ||||||
chr12:5480862
|
A | C | 1 | a0001c0001t0001g0294 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.19-13332A>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5480862 | ||||||
chr12:5480904
|
A | C | 1 | a0001c0001t0004g0311 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.19-13290A>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5480904 | ||||||
chr12:5481049
|
A | G | 1 | a0001c0002t0001g0290 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.19-13145A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5481049 | ||||||
chr12:5481347
|
C | T | 1 | a0001c0001t0001g0295 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.19-12847C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5481347 | ||||||
chr12:5481478
|
T | C | 169 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(166): Show | 175 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.19-12716T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5481478 | ||||||
chr12:5481483
|
G | GCACATAC others(568): Show |
2 | a0001c0001t0001g0110a0001c0002t0001g0246 | 2 | HG01169.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.19-12707_19-12706i others(577): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5481483 | |||||
chr12:5481483
|
G | GCACATAC others(564): Show |
2 | a0001c0001t0001g0351a0001c0001t0001g0352 | 2 | HG01952.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.19-12707_19-12706i others(573): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5481483 | |||||
chr12:5481483
|
G | GCACATAC others(568): Show |
1 | a0001c0001t0001g0033 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.19-12707_19-12706i others(577): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5481483 | |||||
chr12:5481483
|
G | GCACATAC others(568): Show |
158 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0015others(155): Show | 161 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.19-12707_19-12706i others(577): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5481483 | |||||
chr12:5481483
|
G | GCACATAC others(568): Show |
5 | a0001c0001t0001g0016a0001c0001t0001g0028a0001c0001t0001g0111others(2): Show | 5 | HG01346.hp1 HG01884.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.19-12707_19-12706i others(577): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5481483 | |||||
chr12:5481483
|
G | GCACATAC others(568): Show |
14 | a0001c0001t0001g0091a0001c0001t0001g0113a0001c0001t0001g0133others(11): Show | 14 | HG00099.hp2 HG01243.hp1 HG01358.hp1 others(11): Show |
intron_variant | MODIFIER | c.19-12707_19-12706i others(577): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5481483 | |||||
chr12:5481483
|
G | GCACATAC others(549): Show |
1 | a0001c0001t0001g0348 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.19-12707_19-12706i others(558): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5481483 | |||||
chr12:5481483
|
G | GCACATAC others(518): Show |
2 | a0002c0003t0001g0042a0002c0003t0001g0043 | 2 | HG00408.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.19-12707_19-12706i others(527): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5481483 | |||||
chr12:5481483
|
G | GCACATAC others(568): Show |
1 | a0001c0001t0001g0239 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.19-12707_19-12706i others(577): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5481483 | |||||
chr12:5481483
|
G | GCACATAC others(568): Show |
2 | a0001c0001t0001g0014a0001c0001t0001g0350 | 2 | HG03516.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.19-12707_19-12706i others(577): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5481483 | |||||
chr12:5481483
|
G | GCACATAC others(566): Show |
1 | a0001c0002t0001g0296 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.19-12707_19-12706i others(575): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5481483 | |||||
chr12:5481483
|
G | GCACATAC others(566): Show |
1 | a0001c0001t0004g0311 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.19-12707_19-12706i others(575): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5481483 | |||||
chr12:5481483
|
G | GCACATAC others(547): Show |
1 | a0002c0003t0001g0168 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.19-12707_19-12706i others(556): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5481483 | |||||
chr12:5481483
|
G | GCACATAC others(566): Show |
138 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(135): Show | 144 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(141): Show |
intron_variant | MODIFIER | c.19-12707_19-12706i others(575): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5481483 | |||||
chr12:5481483
|
G | GCACATAC others(566): Show |
1 | a0001c0001t0001g0053 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.19-12707_19-12706i others(575): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5481483 | |||||
chr12:5481483
|
G | GCACATAC others(450): Show |
1 | a0001c0002t0001g0188 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.19-12707_19-12706i others(459): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5481483 | |||||
chr12:5481483
|
G | GCACATAC others(450): Show |
28 | a0001c0001t0001g0017a0001c0001t0001g0142a0001c0001t0001g0225others(25): Show | 29 | HG00323.hp2 HG00408.hp1 HG00558.hp1 others(26): Show |
intron_variant | MODIFIER | c.19-12707_19-12706i others(459): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5481483 | |||||
chr12:5481506
|
C | G | 61 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(58): Show | 64 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.19-12688C>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5481506 | ||||||
chr12:5481507
|
C | G | 2 | a0001c0001t0001g0351a0001c0001t0001g0352 | 2 | HG01952.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.19-12687C>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5481507 | ||||||
chr12:5481576
|
C | T | 143 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(140): Show | 149 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.19-12618C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5481576 | ||||||
chr12:5481626
|
T | C | 2 | a0001c0001t0001g0348a0002c0003t0001g0168 | 2 | HG02717.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.19-12568T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5481626 | ||||||
chr12:5481637
|
A | ACACATAC others(16): Show |
2 | a0001c0001t0001g0348a0002c0003t0001g0168 | 2 | HG02717.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.19-12557_19-12556i others(25): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5481637 | ||||||
chr12:5481637
|
A | ACACT | 169 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(166): Show | 175 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.19-12557_19-12556i others(6): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5481637 | ||||||
chr12:5481638
|
T | C | 171 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(168): Show | 177 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.19-12556T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5481638 | ||||||
chr12:5481638
|
T | TACTC | 52 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0015others(49): Show | 54 | HG00099.hp2 HG00280.hp1 HG00733.hp1 others(51): Show |
intron_variant | MODIFIER | c.19-12554_19-12553i others(6): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5481638 | |||||
chr12:5481662
|
A | T | 2 | a0001c0001t0001g0348a0002c0003t0001g0168 | 2 | HG02717.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.19-12532A>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5481662 | ||||||
chr12:5481713
|
C | T | 2 | a0001c0001t0001g0348a0002c0003t0001g0168 | 2 | HG02717.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.19-12481C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5481713 | ||||||
chr12:5481754
|
A | T | 3 | a0001c0001t0001g0294a0001c0001t0001g0351a0001c0001t0001g0352 | 3 | HG01952.hp2 HG02258.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.19-12440A>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5481754 | ||||||
chr12:5481809
|
G | C | 7 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0224others(4): Show | 9 | HG02071.hp1 HG02523.hp1 NA18962.hp2 others(6): Show |
intron_variant | MODIFIER | c.19-12385G>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5481809 | ||||||
chr12:5481860
|
A | AACAT | 171 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(168): Show | 177 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.19-12330_19-12327d others(6): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5481860 | |||||
chr12:5481872
|
C | T | 2 | a0001c0001t0001g0348a0002c0003t0001g0168 | 2 | HG02717.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.19-12322C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5481872 | ||||||
chr12:5481940
|
G | A | 1 | a0002c0003t0001g0168 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.19-12254G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5481940 | ||||||
chr12:5481962
|
C | A | 1 | a0002c0003t0001g0168 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.19-12232C>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5481962 | ||||||
chr12:5481990
|
G | GGCATACA others(5): Show |
1 | a0001c0001t0001g0338 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.19-12196_19-12185d others(14): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5481990 | |||||
chr12:5482099
|
T | C | 2 | a0001c0001t0001g0348a0002c0003t0001g0168 | 2 | HG02717.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.19-12095T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5482099 | ||||||
chr12:5482109
|
C | T | 1 | a0001c0001t0005g0223 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.19-12085C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5482109 | ||||||
chr12:5482159
|
C | T | 27 | a0001c0001t0001g0225a0001c0002t0001g0003a0001c0002t0001g0013others(24): Show | 28 | HG00323.hp2 HG00408.hp1 HG00558.hp1 others(25): Show |
intron_variant | MODIFIER | c.19-12035C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5482159 | ||||||
chr12:5482174
|
G | A | 2 | a0001c0002t0001g0233a0002c0003t0001g0325 | 2 | NA18971.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.19-12020G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5482174 | ||||||
chr12:5482175
|
C | T | 1 | a0001c0001t0005g0223 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.19-12019C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5482175 | ||||||
chr12:5482213
|
C | T | 1 | a0001c0001t0001g0338 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.19-11981C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5482213 | ||||||
chr12:5482265
|
G | C | 1 | a0001c0001t0001g0165 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.19-11929G>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5482265 | ||||||
chr12:5482313
|
G | A | 1 | a0001c0001t0001g0350 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.19-11881G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5482313 | ||||||
chr12:5482436
|
G | A | 1 | a0001c0002t0001g0275 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.19-11758G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5482436 | ||||||
chr12:5482561
|
G | A | 1 | a0001c0001t0001g0026 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.19-11633G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5482561 | ||||||
chr12:5482653
|
A | G | 163 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(160): Show | 169 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(166): Show |
intron_variant | MODIFIER | c.19-11541A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5482653 | ||||||
chr12:5482763
|
G | C | 2 | a0001c0001t0001g0348a0002c0003t0001g0168 | 2 | HG02717.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.19-11431G>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5482763 | ||||||
chr12:5482941
|
G | A | 1 | a0001c0002t0001g0169 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.19-11253G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5482941 | ||||||
chr12:5483087
|
ATC | A | 3 | a0001c0001t0001g0258a0001c0002t0001g0240a0001c0002t0001g0241 | 3 | HG00642.hp2 HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.19-11098_19-11097d others(4): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5483087 | |||||
chr12:5483180
|
T | G | 2 | a0001c0001t0001g0351a0001c0001t0001g0352 | 2 | HG01952.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.19-11014T>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5483180 | ||||||
chr12:5483199
|
A | ATC | 48 | a0001c0001t0001g0059a0001c0001t0001g0308a0001c0002t0001g0001others(45): Show | 50 | HG00423.hp2 HG00621.hp1 HG00741.hp1 others(47): Show |
intron_variant | MODIFIER | c.19-10973_19-10972d others(4): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5483199 | |||||
chr12:5483199
|
A | ATCTCTCT others(3): Show |
1 | a0002c0003t0001g0168 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.19-10981_19-10972d others(12): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5483199 | |||||
chr12:5483307
|
G | A | 2 | a0001c0001t0001g0348a0002c0003t0001g0168 | 2 | HG02717.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.19-10887G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5483307 | ||||||
chr12:5483370
|
C | T | 2 | a0001c0001t0001g0348a0002c0003t0001g0168 | 2 | HG02717.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.19-10824C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5483370 | ||||||
chr12:5483540
|
G | A | 1 | a0001c0001t0001g0294 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.19-10654G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5483540 | ||||||
chr12:5483556
|
G | T | 2 | a0001c0001t0001g0348a0002c0003t0001g0168 | 2 | HG02717.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.19-10638G>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5483556 | ||||||
chr12:5483689
|
A | G | 2 | a0001c0001t0001g0348a0002c0003t0001g0168 | 2 | HG02717.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.19-10505A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5483689 | ||||||
chr12:5483828
|
G | C | 1 | a0002c0003t0001g0043 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.19-10366G>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5483828 | ||||||
chr12:5483962
|
C | T | 2 | a0001c0001t0001g0348a0002c0003t0001g0168 | 2 | HG02717.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.19-10232C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5483962 | ||||||
chr12:5484002
|
A | G | 2 | a0001c0001t0001g0348a0002c0003t0001g0168 | 2 | HG02717.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.19-10192A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5484002 | ||||||
chr12:5484035
|
T | C | 2 | a0001c0001t0001g0348a0002c0003t0001g0168 | 2 | HG02717.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.19-10159T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5484035 | ||||||
chr12:5484155
|
G | A | 1 | a0001c0001t0005g0223 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.19-10039G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5484155 | ||||||
chr12:5484198
|
G | T | 2 | a0001c0001t0001g0348a0002c0003t0001g0168 | 2 | HG02717.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.19-9996G>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5484198 | ||||||
chr12:5484239
|
T | C | 1 | a0001c0001t0001g0348 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.19-9955T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5484239 | ||||||
chr12:5484355
|
C | T | 2 | a0001c0001t0001g0110a0001c0002t0001g0246 | 2 | HG01169.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.19-9839C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5484355 | ||||||
chr12:5484515
|
A | T | 1 | a0001c0001t0001g0222 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.19-9679A>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5484515 | ||||||
chr12:5484561
|
G | C | 60 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(57): Show | 63 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(60): Show |
intron_variant | MODIFIER | c.19-9633G>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5484561 | ||||||
chr12:5484586
|
A | G | 1 | a0001c0001t0001g0323 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.19-9608A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5484586 | ||||||
chr12:5484598
|
A | G | 21 | a0001c0001t0001g0113a0001c0001t0001g0115a0001c0001t0001g0116others(18): Show | 21 | HG01358.hp2 HG01891.hp2 HG01952.hp2 others(18): Show |
intron_variant | MODIFIER | c.19-9596A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5484598 | ||||||
chr12:5484676
|
C | A | 1 | a0002c0003t0001g0168 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.19-9518C>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5484676 | ||||||
chr12:5484753
|
T | C | 1 | a0001c0001t0004g0311 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.19-9441T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5484753 | ||||||
chr12:5484842
|
C | A | 2 | a0001c0001t0001g0351a0001c0001t0001g0352 | 2 | HG01952.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.19-9352C>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5484842 | ||||||
chr12:5484937
|
A | G | 158 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(155): Show | 164 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(161): Show |
intron_variant | MODIFIER | c.19-9257A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5484937 | ||||||
chr12:5484993
|
C | T | 1 | a0001c0001t0001g0063 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.19-9201C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5484993 | ||||||
chr12:5485097
|
G | T | 3 | a0001c0002t0001g0152a0001c0002t0001g0254a0001c0002t0001g0271 | 3 | HG00280.hp2 HG01175.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.19-9097G>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5485097 | ||||||
chr12:5485145
|
T | G | 9 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0053others(6): Show | 9 | HG02055.hp1 HG02572.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.19-9049T>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5485145 | ||||||
chr12:5485159
|
C | A | 159 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(156): Show | 165 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.19-9035C>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5485159 | ||||||
chr12:5485237
|
C | T | 159 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(156): Show | 165 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.19-8957C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5485237 | ||||||
chr12:5485323
|
G | A | 1 | a0001c0001t0001g0294 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.19-8871G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5485323 | ||||||
chr12:5485340
|
T | C | 2 | a0001c0001t0001g0113a0001c0001t0005g0223 | 2 | HG01358.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.19-8854T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5485340 | ||||||
chr12:5485427
|
T | C | 159 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(156): Show | 165 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.19-8767T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5485427 | ||||||
chr12:5485432
|
C | T | 152 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(149): Show | 158 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(155): Show |
intron_variant | MODIFIER | c.19-8762C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5485432 | ||||||
chr12:5485461
|
C | T | 152 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(149): Show | 158 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(155): Show |
intron_variant | MODIFIER | c.19-8733C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5485461 | ||||||
chr12:5485556
|
G | A | 141 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(138): Show | 147 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.19-8638G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5485556 | ||||||
chr12:5485714
|
C | T | 1 | a0001c0001t0001g0228 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.19-8480C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5485714 | ||||||
chr12:5485794
|
G | A | 1 | a0001c0001t0001g0294 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.19-8400G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5485794 | ||||||
chr12:5485822
|
A | C | 3 | a0001c0001t0001g0249a0001c0004t0001g0247a0001c0004t0001g0292 | 3 | HG00323.hp1 HG02148.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.19-8372A>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5485822 | ||||||
chr12:5485827
|
C | T | 141 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(138): Show | 147 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.19-8367C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5485827 | ||||||
chr12:5486269
|
A | G | 160 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(157): Show | 166 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.19-7925A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5486269 | ||||||
chr12:5486287
|
C | T | 9 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0053others(6): Show | 9 | HG02055.hp1 HG02572.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.19-7907C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5486287 | ||||||
chr12:5486508
|
C | T | 7 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0166others(4): Show | 7 | HG01891.hp2 HG02109.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.19-7686C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5486508 | ||||||
chr12:5486539
|
A | G | 4 | a0002c0003t0001g0005a0002c0003t0001g0129a0002c0003t0001g0194others(1): Show | 5 | NA18944.hp2 NA18946.hp2 NA18957.hp1 others(2): Show |
intron_variant | MODIFIER | c.19-7655A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5486539 | ||||||
chr12:5486581
|
G | A | 160 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(157): Show | 166 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.19-7613G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5486581 | ||||||
chr12:5486779
|
G | A | 1 | a0001c0002t0001g0344 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.19-7415G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5486779 | ||||||
chr12:5486832
|
T | A | 2 | a0001c0001t0001g0032a0001c0001t0001g0167 | 2 | HG02809.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.19-7362T>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5486832 | ||||||
chr12:5486880
|
G | GGT | 26 | a0001c0001t0001g0017a0001c0001t0001g0077a0001c0001t0001g0090others(23): Show | 27 | HG00280.hp1 HG00323.hp2 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.19-7275_19-7274dup others(2): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5486880 | |||||
chr12:5486880
|
G | GGTGT | 31 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0019others(28): Show | 33 | HG00099.hp2 HG00639.hp2 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.19-7277_19-7274dup others(4): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5486880 | |||||
chr12:5486880
|
G | GGTGTGT | 4 | a0001c0001t0001g0096a0001c0006t0001g0173a0001c0006t0001g0174others(1): Show | 4 | HG01168.hp1 HG01169.hp2 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.19-7279_19-7274dup others(6): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5486880 | |||||
chr12:5486880
|
G | GGTGTGTG others(3): Show |
1 | a0001c0001t0001g0091 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.19-7283_19-7274dup others(10): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5486880 | |||||
chr12:5486880
|
GGT | G | 9 | a0001c0001t0001g0063a0001c0001t0001g0078a0001c0001t0001g0352others(6): Show | 9 | HG01070.hp2 HG02258.hp2 NA18942.hp2 others(6): Show |
intron_variant | MODIFIER | c.19-7275_19-7274del others(2): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5486880 | |||||
chr12:5486880
|
GGTGT | G | 29 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0025others(26): Show | 30 | HG00733.hp2 HG01081.hp2 HG01346.hp1 others(27): Show |
intron_variant | MODIFIER | c.19-7277_19-7274del others(4): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5486880 | |||||
chr12:5486880
|
GGTGTGT | G | 73 | a0001c0001t0001g0014a0001c0001t0001g0032a0001c0001t0001g0036others(70): Show | 75 | HG00423.hp2 HG00621.hp1 HG00642.hp1 others(72): Show |
intron_variant | MODIFIER | c.19-7279_19-7274del others(6): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5486880 | |||||
chr12:5486880
|
GGTGTGTG others(1): Show |
G | 83 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(80): Show | 87 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.19-7281_19-7274del others(8): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5486880 | |||||
chr12:5486880
|
GGTGTGTG others(3): Show |
G | 3 | a0001c0001t0001g0020a0001c0001t0005g0223a0001c0002t0001g0230 | 3 | HG02109.hp1 NA19030.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.19-7283_19-7274del others(10): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5486880 | |||||
chr12:5486969
|
G | A | 5 | a0001c0001t0001g0016a0001c0001t0001g0028a0001c0001t0001g0111others(2): Show | 5 | HG01346.hp1 HG01884.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.19-7225G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5486969 | ||||||
chr12:5486975
|
G | A | 160 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(157): Show | 166 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.19-7219G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5486975 | ||||||
chr12:5487136
|
T | G | 1 | a0001c0001t0001g0029 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.19-7058T>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5487136 | ||||||
chr12:5487180
|
T | C | 160 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(157): Show | 166 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.19-7014T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5487180 | ||||||
chr12:5487249
|
G | A | 60 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(57): Show | 63 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(60): Show |
intron_variant | MODIFIER | c.19-6945G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5487249 | ||||||
chr12:5487288
|
C | T | 141 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(138): Show | 147 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.19-6906C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5487288 | ||||||
chr12:5487412
|
G | A | 1 | a0001c0001t0001g0096 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.19-6782G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5487412 | ||||||
chr12:5487544
|
T | G | 10 | a0001c0001t0001g0113a0001c0001t0005g0223a0001c0002t0001g0030others(7): Show | 10 | HG01358.hp2 HG02451.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.19-6650T>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5487544 | ||||||
chr12:5487640
|
G | A | 7 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0166others(4): Show | 7 | HG01891.hp2 HG02109.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.19-6554G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5487640 | ||||||
chr12:5487646
|
T | C | 160 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(157): Show | 166 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.19-6548T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5487646 | ||||||
chr12:5487673
|
G | A | 1 | a0001c0002t0001g0150 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.19-6521G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5487673 | ||||||
chr12:5487773
|
C | T | 1 | a0001c0001t0001g0033 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.19-6421C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5487773 | ||||||
chr12:5487827
|
T | C | 160 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(157): Show | 166 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.19-6367T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5487827 | ||||||
chr12:5487851
|
A | G | 160 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(157): Show | 166 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.19-6343A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5487851 | ||||||
chr12:5487868
|
C | T | 1 | a0001c0001t0001g0217 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.19-6326C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5487868 | ||||||
chr12:5487918
|
G | A | 2 | a0001c0001t0001g0351a0001c0001t0001g0352 | 2 | HG01952.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.19-6276G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5487918 | ||||||
chr12:5487925
|
G | T | 160 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(157): Show | 166 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.19-6269G>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5487925 | ||||||
chr12:5488039
|
T | A | 160 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(157): Show | 166 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.19-6155T>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5488039 | ||||||
chr12:5488074
|
C | T | 1 | a0001c0001t0001g0295 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.19-6120C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5488074 | ||||||
chr12:5488075
|
A | G | 1 | a0001c0001t0001g0352 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.19-6119A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5488075 | ||||||
chr12:5488175
|
C | T | 7 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0166others(4): Show | 7 | HG01891.hp2 HG02109.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.19-6019C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5488175 | ||||||
chr12:5488215
|
T | C | 165 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(162): Show | 171 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.19-5979T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5488215 | ||||||
chr12:5488357
|
G | C | 4 | a0001c0001t0001g0059a0001c0002t0001g0037a0001c0002t0001g0189others(1): Show | 4 | HG02135.hp1 NA18949.hp1 NA18985.hp2 others(1): Show |
intron_variant | MODIFIER | c.19-5837G>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5488357 | ||||||
chr12:5488728
|
G | C | 7 | a0001c0001t0001g0016a0001c0001t0001g0028a0001c0001t0001g0033others(4): Show | 7 | HG01346.hp1 HG01884.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.19-5466G>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5488728 | ||||||
chr12:5488833
|
G | T | 1 | a0001c0001t0001g0113 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.19-5361G>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5488833 | ||||||
chr12:5488881
|
T | C | 1 | a0001c0002t0001g0095 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.19-5313T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5488881 | ||||||
chr12:5489066
|
A | G | 1 | a0001c0001t0001g0348 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.19-5128A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5489066 | ||||||
chr12:5489129
|
G | A | 7 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0166others(4): Show | 7 | HG01891.hp2 HG02109.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.19-5065G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5489129 | ||||||
chr12:5489215
|
A | T | 2 | a0001c0001t0001g0033a0001c0001t0001g0295 | 2 | HG03195.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.19-4979A>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5489215 | ||||||
chr12:5489387
|
C | T | 9 | a0001c0001t0001g0113a0001c0001t0005g0223a0001c0002t0001g0030others(6): Show | 9 | HG01358.hp2 HG02451.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.19-4807C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5489387 | ||||||
chr12:5489415
|
T | C | 2 | a0001c0006t0001g0173a0001c0006t0001g0174 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.19-4779T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5489415 | ||||||
chr12:5489437
|
AG | A | 7 | a0001c0002t0001g0030a0001c0002t0001g0031a0001c0002t0001g0048others(4): Show | 7 | HG02451.hp2 HG02647.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.19-4755delG | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5489437 | |||||
chr12:5489629
|
A | C | 7 | a0001c0001t0001g0112a0001c0001t0001g0253a0001c0002t0001g0243others(4): Show | 8 | HG00738.hp1 HG01069.hp2 HG01070.hp1 others(5): Show |
intron_variant | MODIFIER | c.19-4565A>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5489629 | ||||||
chr12:5489676
|
T | C | 1 | a0001c0001t0001g0348 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.19-4518T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5489676 | ||||||
chr12:5489716
|
G | A | 1 | a0001c0002t0001g0355 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.19-4478G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5489716 | ||||||
chr12:5489799
|
A | G | 1 | a0001c0001t0001g0348 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.19-4395A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5489799 | ||||||
chr12:5489851
|
A | G | 1 | a0001c0001t0001g0348 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.19-4343A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5489851 | ||||||
chr12:5489924
|
G | A | 6 | a0002c0003t0001g0040a0002c0003t0001g0066a0002c0003t0001g0067others(3): Show | 6 | HG01257.hp1 HG01361.hp1 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.19-4270G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5489924 | ||||||
chr12:5490141
|
T | C | 2 | a0001c0002t0001g0240a0001c0002t0001g0241 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.19-4053T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5490141 | ||||||
chr12:5490231
|
G | A | 2 | a0001c0001t0001g0157a0001c0001t0001g0305 | 2 | NA20805.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.19-3963G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5490231 | ||||||
chr12:5490272
|
G | A | 1 | a0001c0001t0001g0295 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.19-3922G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5490272 | ||||||
chr12:5490480
|
T | C | 148 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(145): Show | 154 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.19-3714T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5490480 | ||||||
chr12:5490501
|
C | T | 1 | a0001c0002t0001g0272 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.19-3693C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5490501 | ||||||
chr12:5490590
|
C | T | 2 | a0001c0001t0001g0249a0001c0004t0001g0292 | 2 | HG00323.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.19-3604C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5490590 | ||||||
chr12:5490736
|
G | C | 146 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(143): Show | 152 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.19-3458G>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5490736 | ||||||
chr12:5490904
|
G | A | 1 | a0001c0002t0001g0126 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.19-3290G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5490904 | ||||||
chr12:5491159
|
C | T | 2 | a0001c0002t0001g0158a0001c0002t0001g0270 | 2 | HG02602.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.19-3035C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5491159 | ||||||
chr12:5491173
|
C | T | 1 | a0001c0001t0001g0110 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.19-3021C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5491173 | ||||||
chr12:5491174
|
G | A | 1 | a0001c0001t0001g0014 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.19-3020G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5491174 | ||||||
chr12:5491300
|
T | G | 67 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(64): Show | 70 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.19-2894T>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5491300 | ||||||
chr12:5491569
|
C | T | 68 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0069others(65): Show | 69 | HG00408.hp2 HG00438.hp2 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.19-2625C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5491569 | ||||||
chr12:5491685
|
C | T | 1 | a0001c0001t0001g0258 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.19-2509C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5491685 | ||||||
chr12:5491716
|
C | CT | 88 | a0001c0001t0001g0015a0001c0001t0001g0025a0001c0001t0001g0059others(85): Show | 91 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.19-2457dupT | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5491716 | |||||
chr12:5491716
|
C | CTT | 6 | a0001c0002t0001g0169a0001c0002t0001g0182a0001c0002t0001g0185others(3): Show | 6 | HG00621.hp2 HG01258.hp1 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.19-2458_19-2457dup others(2): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5491716 | |||||
chr12:5491716
|
CT | C | 125 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(122): Show | 131 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(128): Show |
intron_variant | MODIFIER | c.19-2457delT | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5491716 | |||||
chr12:5491719
|
T | C | 1 | a0001c0001t0001g0143 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.19-2475T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5491719 | ||||||
chr12:5491740
|
A | G | 349 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(346): Show | 359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.19-2454A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5491740 | ||||||
chr12:5491780
|
C | T | 1 | a0001c0002t0001g0281 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.19-2414C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5491780 | ||||||
chr12:5491798
|
T | C | 1 | a0001c0001t0001g0351 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.19-2396T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5491798 | ||||||
chr12:5491845
|
G | A | 5 | a0001c0002t0001g0022a0001c0002t0001g0093a0001c0002t0001g0094others(2): Show | 5 | HG00423.hp2 HG02129.hp2 NA18942.hp1 others(2): Show |
intron_variant | MODIFIER | c.19-2349G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5491845 | ||||||
chr12:5491916
|
T | G | 1 | a0001c0001t0001g0061 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.19-2278T>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5491916 | ||||||
chr12:5491975
|
A | G | 2 | a0001c0001t0001g0351a0001c0001t0001g0352 | 2 | HG01952.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.19-2219A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5491975 | ||||||
chr12:5491984
|
G | T | 1 | a0001c0002t0001g0227 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.19-2210G>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5491984 | ||||||
chr12:5491994
|
A | G | 1 | a0001c0001t0001g0348 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.19-2200A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5491994 | ||||||
chr12:5491996
|
A | G | 353 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(350): Show | 363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.19-2198A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5491996 | ||||||
chr12:5492098
|
A | G | 1 | a0001c0002t0001g0197 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.19-2096A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5492098 | ||||||
chr12:5492190
|
T | C | 6 | a0001c0002t0001g0192a0001c0002t0001g0343a0002c0003t0001g0128others(3): Show | 6 | HG01106.hp1 HG01255.hp1 HG01928.hp1 others(3): Show |
intron_variant | MODIFIER | c.19-2004T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5492190 | ||||||
chr12:5492233
|
A | G | 1 | a0001c0001t0001g0165 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.19-1961A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5492233 | ||||||
chr12:5492379
|
C | T | 2 | a0001c0001t0001g0014a0001c0001t0001g0294 | 2 | HG03195.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.19-1815C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5492379 | ||||||
chr12:5492413
|
T | C | 1 | a0001c0004t0001g0292 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.19-1781T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5492413 | ||||||
chr12:5492530
|
A | G | 1 | a0001c0001t0004g0311 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.19-1664A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5492530 | ||||||
chr12:5492670
|
A | G | 1 | a0001c0001t0005g0223 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.19-1524A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5492670 | ||||||
chr12:5492693
|
T | G | 4 | a0001c0001t0001g0014a0001c0001t0001g0033a0001c0001t0001g0294others(1): Show | 4 | HG03195.hp1 HG03195.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.19-1501T>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5492693 | ||||||
chr12:5492763
|
G | A | 286 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(283): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.19-1431G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5492763 | ||||||
chr12:5492931
|
C | T | 5 | a0001c0002t0001g0035a0001c0002t0001g0056a0001c0002t0001g0317others(2): Show | 5 | NA18957.hp2 NA18968.hp1 NA19004.hp1 others(2): Show |
intron_variant | MODIFIER | c.19-1263C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5492931 | ||||||
chr12:5492963
|
T | C | 1 | a0001c0002t0001g0303 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.19-1231T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5492963 | ||||||
chr12:5493234
|
C | T | 5 | a0001c0001t0001g0016a0001c0001t0001g0028a0001c0001t0001g0111others(2): Show | 5 | HG01346.hp1 HG01884.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.19-960C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5493234 | ||||||
chr12:5493352
|
A | T | 4 | a0002c0003t0001g0005a0002c0003t0001g0129a0002c0003t0001g0194others(1): Show | 5 | NA18944.hp2 NA18946.hp2 NA18957.hp1 others(2): Show |
intron_variant | MODIFIER | c.19-842A>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5493352 | ||||||
chr12:5493484
|
G | A | 1 | a0001c0001t0001g0250 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.19-710G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5493484 | ||||||
chr12:5493653
|
A | T | 1 | a0001c0001t0001g0348 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.19-541A>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5493653 | ||||||
chr12:5493826
|
T | C | 1 | a0001c0004t0001g0008 | 2 | HG00738.hp1 HG01070.hp1 |
intron_variant | MODIFIER | c.19-368T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5493826 | ||||||
chr12:5493905
|
C | T | 1 | a0001c0002t0001g0154 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.19-289C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5493905 | ||||||
chr12:5493926
|
GACCGCAG others(28): Show |
G | 1 | a0001c0001t0001g0329 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.19-264_19-230delGC others(33): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5493926 |