geneid | 79501 |
---|---|
ensemblid | ENSG00000186092.7 |
hgncid | 14825 |
symbol | OR4F5 |
name | olfactory receptor family 4 subfamily F member 5 |
refseq_nuc | NM_001005484.2 |
refseq_prot | NP_001005484.2 |
ensembl_nuc | ENST00000641515.2 |
ensembl_prot | ENSP00000493376.2 |
mane_status | MANE Select |
chr | chr1 |
start | 65419 |
end | 71585 |
strand | + |
ver | v1.2 |
region | chr1:65419-71585 |
region5000 | chr1:60419-76585 |
regionname0 | OR4F5_chr1_65419_71585 |
regionname5000 | OR4F5_chr1_60419_76585 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 326 | 105 | 8 | 12 | 76 | 1 | 8 | 69 | OR4F5_chr1_60419_76585 | OR4F5 | copy fasta | chr1 | 60419 | 76585 |
a0002 | 0/0 | 273 | 41 | 1 | 5 | 35 | 0 | 0 | 33 | OR4F5_chr1_60419_76585 | OR4F5 | copy fasta | chr1 | 60419 | 76585 |
a0003 | 0/0 | 326 | 25 | 5 | 3 | 8 | 3 | 6 | 7 | OR4F5_chr1_60419_76585 | OR4F5 | copy fasta | chr1 | 60419 | 76585 |
a0004 | 0/0 | 326 | 19 | 11 | 5 | 0 | 1 | 2 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | copy fasta | chr1 | 60419 | 76585 |
a0005 | 1/0 | 326 | 15 | 12 | 1 | 0 | 1 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | copy fasta | chr1 | 60419 | 76585 |
a0006 | 0/0 | 326 | 3 | 0 | 1 | 0 | 0 | 2 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | copy fasta | chr1 | 60419 | 76585 |
a0007 | 0/0 | 326 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | OR4F5_chr1_60419_76585 | OR4F5 | copy fasta | chr1 | 60419 | 76585 |
a0008 | 0/0 | 326 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | copy fasta | chr1 | 60419 | 76585 |
a0009 | 0/0 | 326 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | copy fasta | chr1 | 60419 | 76585 |
a0010 | 0/0 | 239 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | copy fasta | chr1 | 60419 | 76585 |
a0011 | 0/0 | 273 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | OR4F5_chr1_60419_76585 | OR4F5 | copy fasta | chr1 | 60419 | 76585 |
a0012 | 0/0 | 326 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | copy fasta | chr1 | 60419 | 76585 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 981 | 90 | 6 | 10 | 67 | 1 | 6 | OR4F5_chr1_60419_76585 | OR4F5 | copy fasta | chr1 | 60419 | 76585 |
c0002 | 0/0 | 981 | 41 | 1 | 5 | 35 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | copy fasta | chr1 | 60419 | 76585 |
c0003 | 0/0 | 981 | 18 | 10 | 5 | 0 | 1 | 2 | OR4F5_chr1_60419_76585 | OR4F5 | copy fasta | chr1 | 60419 | 76585 |
c0004 | 0/0 | 981 | 15 | 5 | 3 | 0 | 3 | 4 | OR4F5_chr1_60419_76585 | OR4F5 | copy fasta | chr1 | 60419 | 76585 |
c0005 | 1/0 | 981 | 15 | 12 | 1 | 0 | 1 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | copy fasta | chr1 | 60419 | 76585 |
c0006 | 0/0 | 981 | 10 | 0 | 1 | 7 | 0 | 2 | OR4F5_chr1_60419_76585 | OR4F5 | copy fasta | chr1 | 60419 | 76585 |
c0007 | 0/0 | 981 | 9 | 0 | 0 | 8 | 0 | 1 | OR4F5_chr1_60419_76585 | OR4F5 | copy fasta | chr1 | 60419 | 76585 |
c0008 | 0/0 | 981 | 3 | 0 | 1 | 0 | 0 | 2 | OR4F5_chr1_60419_76585 | OR4F5 | copy fasta | chr1 | 60419 | 76585 |
c0009 | 0/0 | 981 | 2 | 2 | 0 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | copy fasta | chr1 | 60419 | 76585 |
c0010 | 0/0 | 981 | 2 | 0 | 0 | 2 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | copy fasta | chr1 | 60419 | 76585 |
c0011 | 0/0 | 981 | 1 | 1 | 0 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | copy fasta | chr1 | 60419 | 76585 |
c0012 | 0/0 | 981 | 1 | 0 | 1 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | copy fasta | chr1 | 60419 | 76585 |
c0013 | 0/0 | 981 | 1 | 0 | 0 | 0 | 0 | 1 | OR4F5_chr1_60419_76585 | OR4F5 | copy fasta | chr1 | 60419 | 76585 |
c0014 | 0/0 | 981 | 1 | 0 | 1 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | copy fasta | chr1 | 60419 | 76585 |
c0015 | 0/0 | 981 | 1 | 0 | 1 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | copy fasta | chr1 | 60419 | 76585 |
c0016 | 0/0 | 981 | 1 | 0 | 0 | 1 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | copy fasta | chr1 | 60419 | 76585 |
c0017 | 0/0 | 981 | 1 | 1 | 0 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | copy fasta | chr1 | 60419 | 76585 |
c0018 | 0/0 | 981 | 1 | 0 | 0 | 1 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | copy fasta | chr1 | 60419 | 76585 |
c0019 | 0/0 | 981 | 1 | 0 | 0 | 1 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | copy fasta | chr1 | 60419 | 76585 |
c0020 | 0/0 | 981 | 1 | 0 | 1 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | copy fasta | chr1 | 60419 | 76585 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/0 | 1638 | 107 | 18 | 11 | 70 | 1 | 6 | OR4F5_chr1_60419_76585 | OR4F5 | copy fasta | chr1 | 60419 | 76585 |
t0002 | 0/0 | 1638 | 59 | 5 | 9 | 40 | 1 | 4 | OR4F5_chr1_60419_76585 | OR4F5 | copy fasta | chr1 | 60419 | 76585 |
t0003 | 0/0 | 1638 | 25 | 6 | 3 | 8 | 3 | 5 | OR4F5_chr1_60419_76585 | OR4F5 | copy fasta | chr1 | 60419 | 76585 |
t0004 | 0/0 | 1638 | 8 | 6 | 2 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | copy fasta | chr1 | 60419 | 76585 |
t0005 | 0/0 | 1637 | 4 | 0 | 2 | 0 | 0 | 2 | OR4F5_chr1_60419_76585 | OR4F5 | copy fasta | chr1 | 60419 | 76585 |
t0006 | 0/0 | 1638 | 2 | 0 | 0 | 2 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | copy fasta | chr1 | 60419 | 76585 |
t0007 | 0/0 | 1638 | 2 | 0 | 2 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | copy fasta | chr1 | 60419 | 76585 |
t0008 | 0/0 | 1638 | 1 | 1 | 0 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | copy fasta | chr1 | 60419 | 76585 |
t0009 | 0/0 | 1638 | 1 | 1 | 0 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | copy fasta | chr1 | 60419 | 76585 |
t0010 | 0/0 | 1638 | 1 | 1 | 0 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | copy fasta | chr1 | 60419 | 76585 |
t0011 | 0/0 | 1638 | 1 | 0 | 1 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | copy fasta | chr1 | 60419 | 76585 |
t0012 | 0/0 | 1638 | 1 | 0 | 0 | 0 | 1 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | copy fasta | chr1 | 60419 | 76585 |
t0013 | 0/0 | 1637 | 1 | 0 | 0 | 1 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | copy fasta | chr1 | 60419 | 76585 |
t0014 | 0/0 | 1638 | 1 | 0 | 0 | 1 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | copy fasta | chr1 | 60419 | 76585 |
t0015 | 0/0 | 1638 | 1 | 0 | 0 | 0 | 0 | 1 | OR4F5_chr1_60419_76585 | OR4F5 | copy fasta | chr1 | 60419 | 76585 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 74 | 2 | 10 | 55 | 1 | 6 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
g0002 | 0/0 | 33 | 0 | 3 | 30 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
g0003 | 0/0 | 10 | 0 | 1 | 7 | 0 | 2 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
g0004 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
g0005 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
g0006 | 0/0 | 6 | 0 | 2 | 4 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
g0007 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
g0008 | 1/0 | 4 | 3 | 0 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
g0009 | 0/0 | 4 | 2 | 2 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
g0010 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
g0013 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
g0014 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
g0015 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
g0016 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
g0017 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
g0019 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
g0020 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
g0021 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 981 | 90 | 6 | 10 | 67 | 1 | 6 | OR4F5_chr1_60419_76585 | OR4F5 | copy fasta | chr1 | 60419 | 76585 |
a0001c0006 | 0/0 | 981 | 10 | 0 | 1 | 7 | 0 | 2 | OR4F5_chr1_60419_76585 | OR4F5 | copy fasta | chr1 | 60419 | 76585 |
a0001c0009 | 0/0 | 981 | 2 | 2 | 0 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | copy fasta | chr1 | 60419 | 76585 |
a0001c0012 | 0/0 | 981 | 1 | 0 | 1 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | copy fasta | chr1 | 60419 | 76585 |
a0001c0018 | 0/0 | 981 | 1 | 0 | 0 | 1 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | copy fasta | chr1 | 60419 | 76585 |
a0001c0019 | 0/0 | 981 | 1 | 0 | 0 | 1 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | copy fasta | chr1 | 60419 | 76585 |
a0002c0002 | 0/0 | 981 | 41 | 1 | 5 | 35 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | copy fasta | chr1 | 60419 | 76585 |
a0003c0004 | 0/0 | 981 | 15 | 5 | 3 | 0 | 3 | 4 | OR4F5_chr1_60419_76585 | OR4F5 | copy fasta | chr1 | 60419 | 76585 |
a0003c0007 | 0/0 | 981 | 9 | 0 | 0 | 8 | 0 | 1 | OR4F5_chr1_60419_76585 | OR4F5 | copy fasta | chr1 | 60419 | 76585 |
a0003c0013 | 0/0 | 981 | 1 | 0 | 0 | 0 | 0 | 1 | OR4F5_chr1_60419_76585 | OR4F5 | copy fasta | chr1 | 60419 | 76585 |
a0004c0003 | 0/0 | 981 | 18 | 10 | 5 | 0 | 1 | 2 | OR4F5_chr1_60419_76585 | OR4F5 | copy fasta | chr1 | 60419 | 76585 |
a0004c0011 | 0/0 | 981 | 1 | 1 | 0 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | copy fasta | chr1 | 60419 | 76585 |
a0005c0005 | 1/0 | 981 | 15 | 12 | 1 | 0 | 1 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | copy fasta | chr1 | 60419 | 76585 |
a0006c0008 | 0/0 | 981 | 3 | 0 | 1 | 0 | 0 | 2 | OR4F5_chr1_60419_76585 | OR4F5 | copy fasta | chr1 | 60419 | 76585 |
a0007c0010 | 0/0 | 981 | 2 | 0 | 0 | 2 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | copy fasta | chr1 | 60419 | 76585 |
a0008c0017 | 0/0 | 981 | 1 | 1 | 0 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | copy fasta | chr1 | 60419 | 76585 |
a0009c0015 | 0/0 | 981 | 1 | 0 | 1 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | copy fasta | chr1 | 60419 | 76585 |
a0010c0014 | 0/0 | 981 | 1 | 0 | 1 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | copy fasta | chr1 | 60419 | 76585 |
a0011c0016 | 0/0 | 981 | 1 | 0 | 0 | 1 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | copy fasta | chr1 | 60419 | 76585 |
a0012c0020 | 0/0 | 981 | 1 | 0 | 1 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | copy fasta | chr1 | 60419 | 76585 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 2618 | 87 | 6 | 8 | 66 | 1 | 6 | OR4F5_chr1_60419_76585 | OR4F5 | copy fasta | chr1 | 60419 | 76585 |
a0001c0001t0007 | 0/0 | 2618 | 2 | 0 | 2 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | copy fasta | chr1 | 60419 | 76585 |
a0001c0001t0014 | 0/0 | 2618 | 1 | 0 | 0 | 1 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | copy fasta | chr1 | 60419 | 76585 |
a0001c0006t0002 | 0/0 | 2618 | 8 | 0 | 1 | 5 | 0 | 2 | OR4F5_chr1_60419_76585 | OR4F5 | copy fasta | chr1 | 60419 | 76585 |
a0001c0006t0006 | 0/0 | 2618 | 2 | 0 | 0 | 2 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | copy fasta | chr1 | 60419 | 76585 |
a0001c0009t0008 | 0/0 | 2618 | 1 | 1 | 0 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | copy fasta | chr1 | 60419 | 76585 |
a0001c0009t0009 | 0/0 | 2618 | 1 | 1 | 0 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | copy fasta | chr1 | 60419 | 76585 |
a0001c0012t0001 | 0/0 | 2618 | 1 | 0 | 1 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | copy fasta | chr1 | 60419 | 76585 |
a0001c0018t0001 | 0/0 | 2618 | 1 | 0 | 0 | 1 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | copy fasta | chr1 | 60419 | 76585 |
a0001c0019t0001 | 0/0 | 2618 | 1 | 0 | 0 | 1 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | copy fasta | chr1 | 60419 | 76585 |
a0002c0002t0002 | 0/0 | 2618 | 40 | 1 | 5 | 34 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | copy fasta | chr1 | 60419 | 76585 |
a0002c0002t0013 | 0/0 | 2617 | 1 | 0 | 0 | 1 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | copy fasta | chr1 | 60419 | 76585 |
a0003c0004t0003 | 0/0 | 2618 | 15 | 5 | 3 | 0 | 3 | 4 | OR4F5_chr1_60419_76585 | OR4F5 | copy fasta | chr1 | 60419 | 76585 |
a0003c0007t0003 | 0/0 | 2618 | 9 | 0 | 0 | 8 | 0 | 1 | OR4F5_chr1_60419_76585 | OR4F5 | copy fasta | chr1 | 60419 | 76585 |
a0003c0013t0015 | 0/0 | 2618 | 1 | 0 | 0 | 0 | 0 | 1 | OR4F5_chr1_60419_76585 | OR4F5 | copy fasta | chr1 | 60419 | 76585 |
a0004c0003t0002 | 0/0 | 2618 | 8 | 3 | 2 | 0 | 1 | 2 | OR4F5_chr1_60419_76585 | OR4F5 | copy fasta | chr1 | 60419 | 76585 |
a0004c0003t0004 | 0/0 | 2618 | 8 | 6 | 2 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | copy fasta | chr1 | 60419 | 76585 |
a0004c0003t0010 | 0/0 | 2618 | 1 | 1 | 0 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | copy fasta | chr1 | 60419 | 76585 |
a0004c0003t0011 | 0/0 | 2618 | 1 | 0 | 1 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | copy fasta | chr1 | 60419 | 76585 |
a0004c0011t0003 | 0/0 | 2618 | 1 | 1 | 0 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | copy fasta | chr1 | 60419 | 76585 |
a0005c0005t0001 | 1/0 | 2618 | 13 | 12 | 0 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | copy fasta | chr1 | 60419 | 76585 |
a0005c0005t0005 | 0/0 | 2617 | 1 | 0 | 1 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | copy fasta | chr1 | 60419 | 76585 |
a0005c0005t0012 | 0/0 | 2618 | 1 | 0 | 0 | 0 | 1 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | copy fasta | chr1 | 60419 | 76585 |
a0006c0008t0005 | 0/0 | 2617 | 3 | 0 | 1 | 0 | 0 | 2 | OR4F5_chr1_60419_76585 | OR4F5 | copy fasta | chr1 | 60419 | 76585 |
a0007c0010t0001 | 0/0 | 2618 | 2 | 0 | 0 | 2 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | copy fasta | chr1 | 60419 | 76585 |
a0008c0017t0002 | 0/0 | 2618 | 1 | 1 | 0 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | copy fasta | chr1 | 60419 | 76585 |
a0009c0015t0001 | 0/0 | 2618 | 1 | 0 | 1 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | copy fasta | chr1 | 60419 | 76585 |
a0010c0014t0002 | 0/0 | 2618 | 1 | 0 | 1 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | copy fasta | chr1 | 60419 | 76585 |
a0011c0016t0002 | 0/0 | 2618 | 1 | 0 | 0 | 1 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | copy fasta | chr1 | 60419 | 76585 |
a0012c0020t0001 | 0/0 | 2618 | 1 | 0 | 1 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | copy fasta | chr1 | 60419 | 76585 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 68 | 2 | 8 | 51 | 1 | 6 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
a0001c0001t0001g0004 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
a0001c0001t0001g0015 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
a0001c0001t0007g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
a0001c0001t0007g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
a0001c0001t0014g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
a0001c0006t0002g0003 | 0/0 | 8 | 0 | 1 | 5 | 0 | 2 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
a0001c0006t0006g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
a0001c0009t0008g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
a0001c0009t0009g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
a0001c0012t0001g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
a0001c0018t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
a0001c0019t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
a0002c0002t0002g0002 | 0/0 | 32 | 0 | 3 | 29 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
a0002c0002t0002g0006 | 0/0 | 6 | 0 | 2 | 4 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
a0002c0002t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
a0002c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
a0002c0002t0013g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
a0003c0004t0003g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
a0003c0004t0003g0019 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
a0003c0004t0003g0020 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
a0003c0004t0003g0021 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
a0003c0004t0003g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
a0003c0004t0003g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
a0003c0004t0003g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
a0003c0004t0003g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
a0003c0004t0003g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
a0003c0004t0003g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
a0003c0004t0003g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
a0003c0007t0003g0007 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
a0003c0007t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
a0003c0007t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
a0003c0007t0003g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
a0003c0013t0015g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
a0004c0003t0002g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
a0004c0003t0002g0013 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
a0004c0003t0002g0017 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
a0004c0003t0002g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
a0004c0003t0002g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
a0004c0003t0004g0009 | 0/0 | 4 | 2 | 2 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
a0004c0003t0004g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
a0004c0003t0004g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
a0004c0003t0004g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
a0004c0003t0010g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
a0004c0003t0011g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
a0004c0011t0003g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
a0005c0005t0001g0005 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
a0005c0005t0001g0008 | 1/0 | 4 | 3 | 0 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
a0005c0005t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
a0005c0005t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
a0005c0005t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
a0005c0005t0005g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
a0005c0005t0012g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
a0006c0008t0005g0016 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
a0006c0008t0005g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
a0007c0010t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
a0008c0017t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
a0009c0015t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
a0010c0014t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
a0011c0016t0002g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
a0012c0020t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0003 | c0004 | t0003 | g0019 | EUR | GBR | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
HG00099 | hp2 | a0005 | c0005 | t0012 | g0014 | EUR | GBR | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
HG00544 | hp1 | a0003 | c0007 | t0003 | g0007 | EAS | CHS | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
HG00639 | hp1 | a0010 | c0014 | t0002 | g0045 | AMR | PUR | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
HG00642 | hp1 | a0005 | c0005 | t0005 | g0010 | AMR | PUR | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
HG00738 | hp1 | a0001 | c0012 | t0001 | g0001 | AMR | PUR | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
HG00741 | hp1 | a0009 | c0015 | t0001 | g0010 | AMR | PUR | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
HG00741 | hp2 | a0003 | c0004 | t0003 | g0052 | AMR | PUR | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
HG01106 | hp1 | a0004 | c0003 | t0002 | g0017 | AMR | PUR | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
HG01106 | hp2 | a0004 | c0003 | t0002 | g0025 | AMR | PUR | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
HG01109 | hp1 | a0001 | c0001 | t0007 | g0001 | AMR | PUR | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
HG01109 | hp2 | a0004 | c0003 | t0004 | g0009 | AMR | PUR | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
HG01167 | hp2 | a0003 | c0004 | t0003 | g0051 | AMR | PUR | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
HG01243 | hp1 | a0001 | c0001 | t0007 | g0028 | AMR | PUR | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
HG01243 | hp2 | a0004 | c0003 | t0011 | g0029 | AMR | PUR | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
HG01433 | hp1 | a0006 | c0008 | t0005 | g0038 | AMR | CLM | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
HG01433 | hp2 | a0004 | c0003 | t0004 | g0009 | AMR | CLM | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
HG01496 | hp2 | a0003 | c0004 | t0003 | g0021 | AMR | CLM | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
HG01515 | hp1 | a0004 | c0003 | t0002 | g0017 | EUR | IBS | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
HG01515 | hp2 | a0003 | c0004 | t0003 | g0019 | EUR | IBS | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
HG01891 | hp1 | a0005 | c0005 | t0001 | g0005 | AFR | ACB | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
HG01891 | hp2 | a0003 | c0004 | t0003 | g0018 | AFR | ACB | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
HG01928 | hp1 | a0002 | c0002 | t0002 | g0002 | AMR | PEL | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
HG01928 | hp2 | a0012 | c0020 | t0001 | g0044 | AMR | PEL | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
HG01981 | hp1 | a0002 | c0002 | t0002 | g0006 | AMR | PEL | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
HG01993 | hp1 | a0002 | c0002 | t0002 | g0006 | AMR | PEL | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
HG02083 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | KHV | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | KHV | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | KHV | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
HG02145 | hp1 | a0005 | c0005 | t0001 | g0014 | AFR | ACB | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
HG02145 | hp2 | a0003 | c0004 | t0003 | g0055 | AFR | ACB | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
HG02148 | hp1 | a0001 | c0006 | t0002 | g0003 | AMR | PEL | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
HG02148 | hp2 | a0002 | c0002 | t0002 | g0002 | AMR | PEL | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
HG02257 | hp1 | a0004 | c0011 | t0003 | g0056 | AFR | ACB | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
HG02257 | hp2 | a0005 | c0005 | t0001 | g0005 | AFR | ACB | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
HG02280 | hp1 | a0008 | c0017 | t0002 | g0024 | AFR | ACB | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
HG02293 | hp1 | a0002 | c0002 | t0002 | g0002 | AMR | PEL | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
HG02523 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | KHV | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
HG02572 | hp1 | a0005 | c0005 | t0001 | g0008 | AFR | GWD | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
HG02572 | hp2 | a0003 | c0004 | t0003 | g0021 | AFR | GWD | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
HG02615 | hp1 | a0004 | c0003 | t0010 | g0027 | AFR | GWD | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
HG02615 | hp2 | a0004 | c0003 | t0004 | g0022 | AFR | GWD | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
HG02622 | hp1 | a0005 | c0005 | t0001 | g0005 | AFR | GWD | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
HG02622 | hp2 | a0004 | c0003 | t0004 | g0022 | AFR | GWD | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
HG02630 | hp1 | a0005 | c0005 | t0001 | g0010 | AFR | GWD | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
HG02630 | hp2 | a0005 | c0005 | t0001 | g0005 | AFR | GWD | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
HG02738 | hp1 | a0001 | c0006 | t0002 | g0003 | SAS | PJL | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
HG02738 | hp2 | a0003 | c0004 | t0003 | g0053 | SAS | PJL | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
HG02886 | hp1 | a0002 | c0002 | t0002 | g0026 | AFR | GWD | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
HG02886 | hp2 | a0005 | c0005 | t0001 | g0005 | AFR | GWD | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
HG02976 | hp1 | a0004 | c0003 | t0004 | g0059 | AFR | ESN | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
HG02976 | hp2 | a0004 | c0003 | t0004 | g0009 | AFR | ESN | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
HG03017 | hp2 | a0001 | c0006 | t0002 | g0003 | SAS | PJL | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
HG03098 | hp1 | a0001 | c0009 | t0009 | g0011 | AFR | MSL | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
HG03098 | hp2 | a0004 | c0003 | t0004 | g0009 | AFR | MSL | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
HG03139 | hp1 | a0005 | c0005 | t0001 | g0005 | AFR | ESN | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
HG03139 | hp2 | a0003 | c0004 | t0003 | g0058 | AFR | ESN | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
HG03195 | hp1 | a0004 | c0003 | t0004 | g0060 | AFR | ESN | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
HG03195 | hp2 | a0001 | c0009 | t0008 | g0039 | AFR | ESN | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
HG03239 | hp2 | a0003 | c0004 | t0003 | g0057 | SAS | PJL | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
HG03486 | hp1 | a0005 | c0005 | t0001 | g0008 | AFR | MSL | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | MSL | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
HG03490 | hp1 | a0003 | c0007 | t0003 | g0050 | SAS | PJL | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
HG03490 | hp2 | a0003 | c0004 | t0003 | g0020 | SAS | PJL | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
HG03491 | hp1 | a0006 | c0008 | t0005 | g0016 | SAS | PJL | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
HG03492 | hp1 | a0003 | c0004 | t0003 | g0020 | SAS | PJL | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
HG03492 | hp2 | a0006 | c0008 | t0005 | g0016 | SAS | PJL | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | ESN | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
HG03540 | hp1 | a0004 | c0003 | t0002 | g0012 | AFR | GWD | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
HG03540 | hp2 | a0005 | c0005 | t0001 | g0030 | AFR | GWD | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
HG03579 | hp2 | a0004 | c0003 | t0002 | g0023 | AFR | MSL | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
HG03831 | hp1 | a0004 | c0003 | t0002 | g0013 | SAS | BEB | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
HG04184 | hp2 | a0003 | c0013 | t0015 | g0046 | SAS | BEB | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA18939 | hp1 | a0003 | c0007 | t0003 | g0007 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA18939 | hp2 | a0001 | c0018 | t0001 | g0001 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA18946 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA18952 | hp1 | a0003 | c0007 | t0003 | g0048 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA18956 | hp2 | a0001 | c0001 | t0014 | g0049 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA18957 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA18959 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA18960 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA18962 | hp1 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA18965 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA18966 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA18967 | hp1 | a0002 | c0002 | t0013 | g0042 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA18968 | hp1 | a0007 | c0010 | t0001 | g0001 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA18968 | hp2 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA18970 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA18971 | hp1 | a0001 | c0006 | t0002 | g0003 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA18972 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA18973 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA18974 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA18974 | hp2 | a0001 | c0006 | t0002 | g0003 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA18975 | hp2 | a0001 | c0006 | t0002 | g0003 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA18979 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA18983 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA18985 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA18986 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA18987 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA18987 | hp2 | a0007 | c0010 | t0001 | g0001 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA18988 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA18989 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA18991 | hp1 | a0001 | c0006 | t0006 | g0003 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA18991 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA18998 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA18998 | hp2 | a0001 | c0006 | t0002 | g0003 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA19001 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA19003 | hp1 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA19004 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA19005 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA19007 | hp2 | a0011 | c0016 | t0002 | g0002 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA19011 | hp2 | a0003 | c0007 | t0003 | g0007 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA19043 | hp1 | a0005 | c0005 | t0001 | g0008 | AFR | LWK | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA19043 | hp2 | a0003 | c0004 | t0003 | g0018 | AFR | LWK | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA19062 | hp1 | a0003 | c0007 | t0003 | g0007 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA19065 | hp1 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA19067 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA19070 | hp1 | a0003 | c0007 | t0003 | g0007 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA19072 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA19077 | hp2 | a0001 | c0006 | t0006 | g0003 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA19078 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA19078 | hp2 | a0001 | c0019 | t0001 | g0001 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA19079 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA19081 | hp1 | a0001 | c0006 | t0002 | g0003 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA19082 | hp2 | a0002 | c0002 | t0002 | g0041 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA19083 | hp1 | a0003 | c0007 | t0003 | g0047 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA19085 | hp2 | a0003 | c0007 | t0003 | g0007 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA19091 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA20752 | hp1 | a0003 | c0004 | t0003 | g0054 | EUR | TSI | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA20905 | hp1 | a0004 | c0003 | t0002 | g0013 | SAS | GIH | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
HG02559 | hp2 | a0004 | c0003 | t0002 | g0012 | AFR | ACB | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
homoSapiens_grch38 | hp1 | a0005 | c0005 | t0001 | g0008 | REF | REF | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:69134
|
A | G | 1 | a0012 | 1 | HG01928.hp2 | missense_variant | MODERATE | c.107A>G | p.Glu36Gly | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 3/3 | 167/2618 | 107/981 | 36/326 | chr1 | 69134 | ||
chr1:69284
|
C | T | 1 | a0008 | 1 | HG02280.hp1 | missense_variant | MODERATE | c.257C>T | p.Ser86Phe | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 3/3 | 317/2618 | 257/981 | 86/326 | chr1 | 69284 | ||
chr1:69355
|
G | T | 1 | a0012 | 1 | HG01928.hp2 | missense_variant | MODERATE | c.328G>T | p.Gly110Cys | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 3/3 | 388/2618 | 328/981 | 110/326 | chr1 | 69355 | ||
chr1:69446
|
T | C | 1 | a0011 | 1 | NA19007.hp2 | missense_variant | MODERATE | c.419T>C | p.Ile140Thr | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 3/3 | 479/2618 | 419/981 | 140/326 | chr1 | 69446 | ||
chr1:69448
|
T | C | 1 | a0011 | 1 | NA19007.hp2 | missense_variant | MODERATE | c.421T>C | p.Cys141Arg | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 3/3 | 481/2618 | 421/981 | 141/326 | chr1 | 69448 | ||
chr1:69451
|
A | G | 1 | a0011 | 1 | NA19007.hp2 | missense_variant | MODERATE | c.424A>G | p.Lys142Glu | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 3/3 | 484/2618 | 424/981 | 142/326 | chr1 | 69451 | ||
chr1:69452
|
A | T | 1 | a0011 | 1 | NA19007.hp2 | missense_variant | MODERATE | c.425A>T | p.Lys142Met | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 3/3 | 485/2618 | 425/981 | 142/326 | chr1 | 69452 | ||
chr1:69454
|
C | T | 1 | a0011 | 1 | NA19007.hp2 | missense_variant | MODERATE | c.427C>T | p.Pro143Ser | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 3/3 | 487/2618 | 427/981 | 143/326 | chr1 | 69454 | ||
chr1:69455
|
C | T | 1 | a0011 | 1 | NA19007.hp2 | missense_variant | MODERATE | c.428C>T | p.Pro143Leu | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 3/3 | 488/2618 | 428/981 | 143/326 | chr1 | 69455 | ||
chr1:69511
|
A | G | 11 | a0001a0002a0003others(8): Show | 200 | HG00099.hp1 HG00544.hp1 HG00544.hp2 others(197): Show |
missense_variant | MODERATE | c.484A>G | p.Thr162Ala | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 3/3 | 544/2618 | 484/981 | 162/326 | chr1 | 69511 | ||
chr1:69569
|
T | C | 6 | a0002a0003a0004others(3): Show | 88 | HG00099.hp1 HG00544.hp1 HG00639.hp1 others(85): Show |
missense_variant | MODERATE | c.542T>C | p.Leu181Pro | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 3/3 | 602/2618 | 542/981 | 181/326 | chr1 | 69569 | ||
chr1:69590
|
T | A | 1 | a0012 | 1 | HG01928.hp2 | missense_variant | MODERATE | c.563T>A | p.Val188Asp | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 3/3 | 623/2618 | 563/981 | 188/326 | chr1 | 69590 | ||
chr1:69610
|
C | T | 1 | a0007 | 2 | NA18968.hp1 NA18987.hp2 |
missense_variant | MODERATE | c.583C>T | p.Leu195Phe | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 3/3 | 643/2618 | 583/981 | 195/326 | chr1 | 69610 | ||
chr1:69745
|
C | T | 1 | a0010 | 1 | HG00639.hp1 | stop_gained | HIGH | c.718C>T | p.Gln240* | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 3/3 | 778/2618 | 718/981 | 240/326 | chr1 | 69745 | ||
chr1:69761
|
A | T | 1 | a0006 | 3 | HG01433.hp1 HG03491.hp1 HG03492.hp2 |
missense_variant | MODERATE | c.734A>T | p.Asp245Val | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 3/3 | 794/2618 | 734/981 | 245/326 | chr1 | 69761 | ||
chr1:69849
|
G | A | 2 | a0002a0011 | 42 | HG01928.hp1 HG01981.hp1 HG01993.hp1 others(39): Show |
stop_gained | HIGH | c.822G>A | p.Trp274* | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 3/3 | 882/2618 | 822/981 | 274/326 | chr1 | 69849 | ||
chr1:69899
|
T | A | 1 | a0009 | 1 | HG00741.hp1 | missense_variant | MODERATE | c.872T>A | p.Val291Glu | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 3/3 | 932/2618 | 872/981 | 291/326 | chr1 | 69899 | ||
chr1:69968
|
A | G | 1 | a0003 | 25 | HG00099.hp1 HG00544.hp1 HG00741.hp2 others(22): Show |
missense_variant | MODERATE | c.941A>G | p.Gln314Arg | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 3/3 | 1001/2618 | 941/981 | 314/326 | chr1 | 69968 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:69063
|
T | C | 3 | a0003c0004a0003c0007a0004c0011 | 25 | HG00099.hp1 HG00544.hp1 HG00741.hp2 others(22): Show |
synonymous_variant | LOW | c.36T>C | p.Asn12Asn | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 3/3 | 96/2618 | 36/981 | 12/326 | chr1 | 69063 | ||
chr1:69081
|
G | C | 1 | a0001c0012 | 1 | HG00738.hp1 | synonymous_variant | LOW | c.54G>C | p.Thr18Thr | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 3/3 | 114/2618 | 54/981 | 18/326 | chr1 | 69081 | ||
chr1:69270
|
A | G | 6 | a0001c0001a0001c0012a0001c0018others(3): Show | 98 | HG00544.hp2 HG00639.hp2 HG00642.hp2 others(95): Show |
synonymous_variant | LOW | c.243A>G | p.Ser81Ser | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 3/3 | 303/2618 | 243/981 | 81/326 | chr1 | 69270 | ||
chr1:69369
|
G | A | 2 | a0003c0004a0004c0011 | 16 | HG00099.hp1 HG00741.hp2 HG01167.hp2 others(13): Show |
synonymous_variant | LOW | c.342G>A | p.Gln114Gln | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 3/3 | 402/2618 | 342/981 | 114/326 | chr1 | 69369 | ||
chr1:69441
|
A | C | 1 | a0011c0016 | 1 | NA19007.hp2 | synonymous_variant | LOW | c.414A>C | p.Ile138Ile | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 3/3 | 474/2618 | 414/981 | 138/326 | chr1 | 69441 | ||
chr1:69450
|
C | T | 1 | a0011c0016 | 1 | NA19007.hp2 | synonymous_variant | LOW | c.423C>T | p.Cys141Cys | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 3/3 | 483/2618 | 423/981 | 141/326 | chr1 | 69450 | ||
chr1:69453
|
G | A | 9 | a0001c0006a0002c0002a0003c0004others(6): Show | 97 | HG00099.hp1 HG00544.hp1 HG00639.hp1 others(94): Show |
synonymous_variant | LOW | c.426G>A | p.Lys142Lys | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 3/3 | 486/2618 | 426/981 | 142/326 | chr1 | 69453 | ||
chr1:69534
|
T | C | 1 | a0001c0018 | 1 | NA18939.hp2 | synonymous_variant | LOW | c.507T>C | p.His169His | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 3/3 | 567/2618 | 507/981 | 169/326 | chr1 | 69534 | ||
chr1:69552
|
G | C | 10 | a0001c0006a0002c0002a0003c0004others(7): Show | 98 | HG00099.hp1 HG00544.hp1 HG00639.hp1 others(95): Show |
synonymous_variant | LOW | c.525G>C | p.Ala175Ala | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 3/3 | 585/2618 | 525/981 | 175/326 | chr1 | 69552 | ||
chr1:69735
|
A | G | 1 | a0003c0007 | 9 | HG00544.hp1 HG03490.hp1 NA18939.hp1 others(6): Show |
synonymous_variant | LOW | c.708A>G | p.Leu236Leu | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 3/3 | 768/2618 | 708/981 | 236/326 | chr1 | 69735 | ||
chr1:69876
|
A | G | 1 | a0001c0019 | 1 | NA19078.hp2 | synonymous_variant | LOW | c.849A>G | p.Lys283Lys | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 3/3 | 909/2618 | 849/981 | 283/326 | chr1 | 69876 | ||
chr1:69897
|
T | C | 7 | a0001c0001a0001c0012a0001c0018others(4): Show | 99 | HG00544.hp2 HG00639.hp2 HG00642.hp2 others(96): Show |
synonymous_variant | LOW | c.870T>C | p.Ser290Ser | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 3/3 | 930/2618 | 870/981 | 290/326 | chr1 | 69897 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:65529
|
C | T | 5 | a0001c0001t0014a0003c0004t0003a0003c0007t0003others(2): Show | 27 | HG00099.hp1 HG00544.hp1 HG00741.hp2 others(24): Show |
5_prime_UTR_variant | MODIFIER | c.-36C>T | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/3 | 36 | chr1 | 65529 | |||||
chr1:65552
|
G | A | 4 | a0001c0001t0014a0003c0004t0003a0003c0007t0003others(1): Show | 26 | HG00099.hp1 HG00544.hp1 HG00741.hp2 others(23): Show |
5_prime_UTR_variant | MODIFIER | c.-13G>A | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/3 | 13 | chr1 | 65552 | |||||
chr1:70246
|
A | G | 1 | a0003c0013t0015 | 1 | HG04184.hp2 | 3_prime_UTR_variant | MODIFIER | c.*238A>G | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 3/3 | 238 | chr1 | 70246 | |||||
chr1:70300
|
C | T | 4 | a0003c0004t0003a0003c0007t0003a0003c0013t0015others(1): Show | 26 | HG00099.hp1 HG00544.hp1 HG00741.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*292C>T | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 3/3 | 292 | chr1 | 70300 | |||||
chr1:70302
|
C | T | 1 | a0003c0013t0015 | 1 | HG04184.hp2 | 3_prime_UTR_variant | MODIFIER | c.*294C>T | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 3/3 | 294 | chr1 | 70302 | |||||
chr1:70317
|
G | A | 1 | a0001c0009t0008 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*309G>A | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 3/3 | 309 | chr1 | 70317 | |||||
chr1:70351
|
TA | T | 3 | a0002c0002t0013a0005c0005t0005a0006c0008t0005 | 5 | HG00642.hp1 HG01433.hp1 HG03491.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*352delA | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 3/3 | 352 | INFO_REALIGN_3_PRIME | chr1 | 70351 | ||||
chr1:70352
|
A | T | 1 | a0001c0001t0007 | 2 | HG01109.hp1 HG01243.hp1 |
3_prime_UTR_variant | MODIFIER | c.*344A>T | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 3/3 | 344 | chr1 | 70352 | |||||
chr1:70499
|
C | T | 3 | a0003c0004t0003a0003c0007t0003a0004c0011t0003 | 25 | HG00099.hp1 HG00544.hp1 HG00741.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*491C>T | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 3/3 | 491 | chr1 | 70499 | |||||
chr1:70534
|
T | C | 1 | a0001c0006t0006 | 2 | NA18991.hp1 NA19077.hp2 |
3_prime_UTR_variant | MODIFIER | c.*526T>C | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 3/3 | 526 | chr1 | 70534 | |||||
chr1:70594
|
G | C | 1 | a0001c0009t0009 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*586G>C | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 3/3 | 586 | chr1 | 70594 | |||||
chr1:70604
|
G | A | 15 | a0001c0006t0002a0001c0006t0006a0002c0002t0002others(12): Show | 98 | HG00099.hp1 HG00544.hp1 HG00639.hp1 others(95): Show |
3_prime_UTR_variant | MODIFIER | c.*596G>A | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 3/3 | 596 | chr1 | 70604 | |||||
chr1:70806
|
G | A | 1 | a0004c0003t0010 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*798G>A | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 3/3 | 798 | chr1 | 70806 | |||||
chr1:70917
|
C | T | 2 | a0004c0003t0004a0004c0003t0011 | 9 | HG01109.hp2 HG01243.hp2 HG01433.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*909C>T | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 3/3 | 909 | chr1 | 70917 | |||||
chr1:71192
|
A | G | 1 | a0003c0013t0015 | 1 | HG04184.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1184A>G | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 3/3 | 1184 | chr1 | 71192 | |||||
chr1:71298
|
G | A | 1 | a0005c0005t0012 | 1 | HG00099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1290G>A | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 3/3 | 1290 | chr1 | 71298 | |||||
chr1:71381
|
T | C | 3 | a0003c0004t0003a0003c0007t0003a0004c0011t0003 | 25 | HG00099.hp1 HG00544.hp1 HG00741.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*1373T>C | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 3/3 | 1373 | chr1 | 71381 | |||||
chr1:71449
|
G | C | 1 | a0004c0003t0011 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1441G>C | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 3/3 | 1441 | chr1 | 71449 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:65451
|
A | G | 4 | a0004c0003t0004g0009a0004c0003t0004g0022a0004c0003t0004g0059others(1): Show | 8 | HG01109.hp2 HG01433.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.-46+18A>G | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 1/2 | chr1 | 65451 | ||||||
chr1:65591
|
C | T | 18 | a0001c0001t0014g0049a0003c0004t0003g0018a0003c0004t0003g0019others(15): Show | 27 | HG00099.hp1 HG00544.hp1 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.9+18C>T | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 65591 | ||||||
chr1:65649
|
G | A | 1 | a0003c0013t0015g0046 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.9+76G>A | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 65649 | ||||||
chr1:65745
|
A | G | 18 | a0001c0001t0014g0049a0003c0004t0003g0018a0003c0004t0003g0019others(15): Show | 27 | HG00099.hp1 HG00544.hp1 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.9+172A>G | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 65745 | ||||||
chr1:65797
|
T | C | 18 | a0001c0001t0014g0049a0003c0004t0003g0018a0003c0004t0003g0019others(15): Show | 27 | HG00099.hp1 HG00544.hp1 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.9+224T>C | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 65797 | ||||||
chr1:65872
|
T | G | 1 | a0003c0013t0015g0046 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.9+299T>G | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 65872 | ||||||
chr1:65898
|
T | C | 2 | a0001c0001t0001g0011a0001c0009t0009g0011 | 2 | HG03098.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.9+325T>C | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 65898 | ||||||
chr1:65974
|
A | G | 1 | a0010c0014t0002g0045 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.9+401A>G | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 65974 | ||||||
chr1:66008
|
C | G | 18 | a0001c0001t0014g0049a0003c0004t0003g0018a0003c0004t0003g0019others(15): Show | 27 | HG00099.hp1 HG00544.hp1 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.9+435C>G | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66008 | ||||||
chr1:66131
|
C | G | 1 | a0012c0020t0001g0044 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.9+558C>G | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66131 | ||||||
chr1:66160
|
T | TTA | 1 | a0001c0001t0001g0004 | 7 | NA18962.hp2 NA18979.hp2 NA19005.hp1 others(4): Show |
intron_variant | MODIFIER | c.9+601_9+602dupAT | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 66160 | |||||
chr1:66162
|
A | T | 18 | a0001c0001t0014g0049a0003c0004t0003g0018a0003c0004t0003g0019others(15): Show | 27 | HG00099.hp1 HG00544.hp1 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.9+589A>T | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66162 | ||||||
chr1:66176
|
T | A | 5 | a0004c0003t0002g0012a0004c0003t0002g0023a0004c0003t0002g0025others(2): Show | 6 | HG00639.hp1 HG01106.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.9+603T>A | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66176 | ||||||
chr1:66214
|
A | T | 1 | a0001c0001t0001g0043 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.9+641A>T | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66214 | ||||||
chr1:66217
|
T | C | 1 | a0002c0002t0002g0026 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.9+644T>C | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66217 | ||||||
chr1:66218
|
A | T | 1 | a0002c0002t0002g0026 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.9+645A>T | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66218 | ||||||
chr1:66219
|
A | T | 5 | a0002c0002t0002g0002a0002c0002t0002g0006a0002c0002t0002g0041others(2): Show | 41 | HG01928.hp1 HG01981.hp1 HG01993.hp1 others(38): Show |
intron_variant | MODIFIER | c.9+646A>T | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66219 | ||||||
chr1:66220
|
TATATATT others(37): Show |
T | 1 | a0002c0002t0002g0041 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.9+653_9+696delTTAT others(40): Show |
OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 66220 | |||||
chr1:66221
|
A | AT | 12 | a0003c0004t0003g0018a0003c0004t0003g0019a0003c0004t0003g0020others(9): Show | 16 | HG00099.hp1 HG00741.hp2 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.9+649dupT | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 66221 | |||||
chr1:66221
|
ATATATTA others(49): Show |
A | 1 | a0004c0003t0002g0023 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.9+667_9+722delTTAT others(52): Show |
OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 66221 | |||||
chr1:66222
|
T | TTATATAT others(205): Show |
1 | a0003c0004t0003g0051 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.9+649_9+650insTATA others(208): Show |
OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66222 | ||||||
chr1:66224
|
TATTATAT others(44): Show |
T | 1 | a0004c0003t0002g0017 | 2 | HG01106.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.9+659_9+709delAATA others(47): Show |
OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 66224 | |||||
chr1:66225
|
A | T | 1 | a0002c0002t0002g0026 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.9+652A>T | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66225 | ||||||
chr1:66225
|
AT | A | 17 | a0001c0001t0014g0049a0003c0004t0003g0018a0003c0004t0003g0019others(14): Show | 26 | HG00099.hp1 HG00544.hp1 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.9+654delT | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 66225 | |||||
chr1:66226
|
T | A | 1 | a0004c0003t0010g0027 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.9+653T>A | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66226 | ||||||
chr1:66227
|
T | A | 1 | a0003c0004t0003g0051 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.9+654T>A | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66227 | ||||||
chr1:66231
|
TAATATAT others(34): Show |
T | 2 | a0001c0006t0002g0003a0001c0006t0006g0003 | 10 | HG02148.hp1 HG02738.hp1 HG03017.hp2 others(7): Show |
intron_variant | MODIFIER | c.9+659_9+699delAATA others(37): Show |
OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66231 | ||||||
chr1:66233
|
A | T | 1 | a0002c0002t0002g0026 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.9+660A>T | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66233 | ||||||
chr1:66236
|
T | C | 1 | a0002c0002t0002g0026 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.9+663T>C | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66236 | ||||||
chr1:66238
|
T | A | 1 | a0001c0001t0007g0028 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.9+665T>A | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66238 | ||||||
chr1:66238
|
TATTATAT others(30): Show |
T | 14 | a0002c0002t0002g0002a0002c0002t0002g0006a0002c0002t0013g0042others(11): Show | 56 | HG00639.hp1 HG01106.hp2 HG01109.hp2 others(53): Show |
intron_variant | MODIFIER | c.9+710_9+746delTATA others(33): Show |
OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 66238 | |||||
chr1:66240
|
T | A | 1 | a0012c0020t0001g0044 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.9+667T>A | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66240 | ||||||
chr1:66244
|
AT | A | 2 | a0002c0002t0002g0026a0012c0020t0001g0044 | 2 | HG01928.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.9+673delT | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 66244 | |||||
chr1:66246
|
T | A | 1 | a0012c0020t0001g0044 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.9+673T>A | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66246 | ||||||
chr1:66249
|
A | ATATATAA others(170): Show |
1 | a0003c0007t0003g0048 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.9+678_9+679insTATA others(173): Show |
OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 66249 | |||||
chr1:66249
|
A | ATATATAA others(172): Show |
2 | a0001c0001t0014g0049a0003c0007t0003g0007 | 7 | HG00544.hp1 NA18939.hp1 NA18956.hp2 others(4): Show |
intron_variant | MODIFIER | c.9+678_9+679insTATA others(175): Show |
OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 66249 | |||||
chr1:66249
|
A | ATATATAA others(186): Show |
1 | a0003c0007t0003g0050 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.9+678_9+679insTATA others(189): Show |
OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 66249 | |||||
chr1:66249
|
A | ATATATAA others(206): Show |
1 | a0003c0004t0003g0052 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.9+678_9+679insTATA others(209): Show |
OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 66249 | |||||
chr1:66249
|
A | ATATATTA others(188): Show |
1 | a0003c0004t0003g0053 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.9+678_9+679insTATT others(191): Show |
OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 66249 | |||||
chr1:66249
|
A | ATATATTA others(208): Show |
1 | a0003c0004t0003g0018 | 2 | HG01891.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.9+678_9+679insTATT others(211): Show |
OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 66249 | |||||
chr1:66249
|
A | ATATATTA others(205): Show |
1 | a0003c0004t0003g0019 | 2 | HG00099.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.9+678_9+679insTATT others(208): Show |
OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 66249 | |||||
chr1:66249
|
A | ATATATTA others(206): Show |
2 | a0003c0004t0003g0054a0003c0004t0003g0055 | 2 | HG02145.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.9+678_9+679insTATT others(209): Show |
OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 66249 | |||||
chr1:66249
|
A | ATATATTA others(215): Show |
2 | a0003c0004t0003g0020a0004c0011t0003g0056 | 3 | HG02257.hp1 HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.9+678_9+679insTATT others(218): Show |
OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 66249 | |||||
chr1:66249
|
A | ATATATTA others(215): Show |
1 | a0003c0004t0003g0057 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.9+678_9+679insTATT others(218): Show |
OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 66249 | |||||
chr1:66249
|
A | ATATATTA others(224): Show |
1 | a0003c0004t0003g0021 | 2 | HG01496.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.9+678_9+679insTATT others(227): Show |
OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 66249 | |||||
chr1:66249
|
A | ATATATTA others(242): Show |
1 | a0003c0004t0003g0058 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.9+678_9+679insTATT others(245): Show |
OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 66249 | |||||
chr1:66252
|
A | ATATATAT others(168): Show |
1 | a0003c0007t0003g0047 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.9+685_9+686insTATA others(171): Show |
OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 66252 | |||||
chr1:66252
|
A | T | 15 | a0001c0001t0014g0049a0003c0004t0003g0018a0003c0004t0003g0019others(12): Show | 24 | HG00099.hp1 HG00544.hp1 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.9+679A>T | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66252 | ||||||
chr1:66258
|
A | G | 1 | a0003c0004t0003g0051 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.9+685A>G | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66258 | ||||||
chr1:66258
|
A | T | 1 | a0012c0020t0001g0044 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.9+685A>T | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66258 | ||||||
chr1:66258
|
AATATAAA others(50): Show |
A | 1 | a0004c0003t0004g0060 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.9+702_9+758delAATT others(53): Show |
OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 66258 | |||||
chr1:66259
|
A | T | 1 | a0002c0002t0002g0026 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.9+686A>T | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66259 | ||||||
chr1:66264
|
A | ATAT | 16 | a0001c0001t0014g0049a0003c0004t0003g0018a0003c0004t0003g0019others(13): Show | 25 | HG00099.hp1 HG00544.hp1 HG00741.hp2 others(22): Show |
intron_variant | MODIFIER | c.9+691_9+692insTAT | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66264 | ||||||
chr1:66264
|
A | ATATATTA others(243): Show |
1 | a0003c0013t0015g0046 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.9+691_9+692insTATA others(246): Show |
OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66264 | ||||||
chr1:66275
|
A | T | 6 | a0001c0006t0002g0003a0001c0006t0006g0003a0002c0002t0002g0026others(3): Show | 14 | HG01167.hp2 HG01928.hp2 HG02148.hp1 others(11): Show |
intron_variant | MODIFIER | c.9+702A>T | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66275 | ||||||
chr1:66276
|
A | T | 17 | a0001c0001t0014g0049a0003c0004t0003g0018a0003c0004t0003g0019others(14): Show | 26 | HG00099.hp1 HG00544.hp1 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.9+703A>T | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66276 | ||||||
chr1:66277
|
T | A | 17 | a0001c0001t0014g0049a0003c0004t0003g0018a0003c0004t0003g0019others(14): Show | 26 | HG00099.hp1 HG00544.hp1 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.9+704T>A | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66277 | ||||||
chr1:66279
|
A | T | 2 | a0003c0004t0003g0051a0012c0020t0001g0044 | 2 | HG01167.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.9+706A>T | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66279 | ||||||
chr1:66289
|
AT | A | 17 | a0001c0001t0014g0049a0003c0004t0003g0018a0003c0004t0003g0019others(14): Show | 26 | HG00099.hp1 HG00544.hp1 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.9+717delT | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66289 | ||||||
chr1:66294
|
T | A | 2 | a0003c0004t0003g0051a0012c0020t0001g0044 | 2 | HG01167.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.9+721T>A | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66294 | ||||||
chr1:66295
|
A | T | 2 | a0003c0004t0003g0051a0012c0020t0001g0044 | 2 | HG01167.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.9+722A>T | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66295 | ||||||
chr1:66300
|
A | ATAT | 17 | a0001c0001t0014g0049a0003c0004t0003g0018a0003c0004t0003g0019others(14): Show | 26 | HG00099.hp1 HG00544.hp1 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.9+727_9+728insTAT | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66300 | ||||||
chr1:66300
|
A | ATTATATA others(5): Show |
1 | a0012c0020t0001g0044 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.9+727_9+728insTTAT others(8): Show |
OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66300 | ||||||
chr1:66301
|
A | T | 1 | a0003c0007t0003g0050 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.9+728A>T | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66301 | ||||||
chr1:66312
|
A | T | 18 | a0001c0001t0014g0049a0003c0004t0003g0018a0003c0004t0003g0019others(15): Show | 27 | HG00099.hp1 HG00544.hp1 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.9+739A>T | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66312 | ||||||
chr1:66320
|
A | T | 1 | a0001c0001t0001g0040 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.9+747A>T | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66320 | ||||||
chr1:66321
|
A | ATATAATA others(24): Show |
1 | a0001c0001t0001g0040 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.9+748_9+749insTATA others(27): Show |
OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66321 | ||||||
chr1:66325
|
TAATATAT others(95): Show |
T | 2 | a0005c0005t0001g0014a0005c0005t0012g0014 | 2 | HG00099.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.9+763_9+864del | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 66325 | |||||
chr1:66331
|
A | C | 5 | a0004c0003t0002g0012a0004c0003t0002g0023a0004c0003t0002g0025others(2): Show | 6 | HG00639.hp1 HG01106.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.9+758A>C | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66331 | ||||||
chr1:66335
|
T | A | 2 | a0003c0004t0003g0051a0012c0020t0001g0044 | 2 | HG01167.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.9+762T>A | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66335 | ||||||
chr1:66336
|
T | A | 1 | a0003c0004t0003g0051 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.9+763T>A | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66336 | ||||||
chr1:66339
|
T | TAATATAT others(41): Show |
1 | a0003c0004t0003g0051 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.9+766_9+767insAATA others(44): Show |
OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66339 | ||||||
chr1:66339
|
T | TCATATAA others(2): Show |
5 | a0001c0001t0014g0049a0003c0007t0003g0007a0003c0007t0003g0047others(2): Show | 10 | HG00544.hp1 HG03490.hp1 NA18939.hp1 others(7): Show |
intron_variant | MODIFIER | c.9+766_9+767insCATA others(5): Show |
OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66339 | ||||||
chr1:66339
|
T | TCATATAA others(7): Show |
11 | a0003c0004t0003g0018a0003c0004t0003g0019a0003c0004t0003g0020others(8): Show | 15 | HG00099.hp1 HG00741.hp2 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.9+766_9+767insCATA others(10): Show |
OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66339 | ||||||
chr1:66356
|
T | A | 17 | a0001c0001t0014g0049a0003c0004t0003g0018a0003c0004t0003g0019others(14): Show | 26 | HG00099.hp1 HG00544.hp1 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.9+783T>A | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66356 | ||||||
chr1:66356
|
T | TATAATAT others(7): Show |
1 | a0003c0013t0015g0046 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.9+785_9+786insAATA others(10): Show |
OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 66356 | |||||
chr1:66364
|
AAATATAA others(14): Show |
A | 1 | a0004c0003t0002g0017 | 2 | HG01106.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.9+805_9+825delAATT others(17): Show |
OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 66364 | |||||
chr1:66370
|
A | ATTATTAT others(159): Show |
1 | a0012c0020t0001g0044 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.9+797_9+798insTTAT others(162): Show |
OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66370 | ||||||
chr1:66377
|
A | ATTT | 18 | a0001c0001t0014g0049a0003c0004t0003g0018a0003c0004t0003g0019others(15): Show | 27 | HG00099.hp1 HG00544.hp1 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.9+804_9+805insTTT | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66377 | ||||||
chr1:66378
|
A | T | 19 | a0001c0001t0014g0049a0003c0004t0003g0018a0003c0004t0003g0019others(16): Show | 28 | HG00099.hp1 HG00544.hp1 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.9+805A>T | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66378 | ||||||
chr1:66381
|
T | A | 5 | a0004c0003t0004g0009a0004c0003t0004g0022a0004c0003t0004g0059others(2): Show | 9 | HG01109.hp2 HG01243.hp2 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.9+808T>A | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66381 | ||||||
chr1:66381
|
TATATA | T | 3 | a0001c0001t0001g0011a0001c0009t0009g0011a0004c0003t0002g0025 | 3 | HG01106.hp2 HG03098.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.9+819_9+823delATAT others(1): Show |
OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 66381 | |||||
chr1:66430
|
T | A | 1 | a0005c0005t0001g0030 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.9+857T>A | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66430 | ||||||
chr1:66434
|
T | A | 1 | a0001c0001t0001g0031 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.9+861T>A | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66434 | ||||||
chr1:66435
|
A | T | 1 | a0001c0001t0001g0031 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.9+862A>T | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66435 | ||||||
chr1:66435
|
ATT | A | 5 | a0004c0003t0002g0012a0004c0003t0002g0023a0004c0003t0002g0025others(2): Show | 6 | HG00639.hp1 HG01106.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.9+863_9+864delTT | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66435 | ||||||
chr1:66436
|
T | A | 1 | a0001c0001t0001g0031 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.9+863T>A | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66436 | ||||||
chr1:66438
|
ATATTATA others(12): Show |
A | 1 | a0001c0001t0001g0032 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.9+884_9+902delTTAT others(15): Show |
OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 66438 | |||||
chr1:66442
|
T | A | 1 | a0012c0020t0001g0044 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.9+869T>A | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66442 | ||||||
chr1:66442
|
T | TCTATATA | 18 | a0001c0001t0014g0049a0003c0004t0003g0018a0003c0004t0003g0019others(15): Show | 27 | HG00099.hp1 HG00544.hp1 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.9+869_9+870insCTAT others(3): Show |
OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66442 | ||||||
chr1:66457
|
T | A | 5 | a0004c0003t0004g0009a0004c0003t0004g0022a0004c0003t0004g0059others(2): Show | 9 | HG01109.hp2 HG01243.hp2 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.9+884T>A | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66457 | ||||||
chr1:66461
|
T | A | 1 | a0001c0001t0001g0033 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.9+888T>A | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66461 | ||||||
chr1:66461
|
T | TATATAAT others(39): Show |
1 | a0001c0001t0001g0037 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.9+933_9+934insAATA others(42): Show |
OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 66461 | |||||
chr1:66466
|
A | G | 2 | a0001c0001t0001g0011a0001c0009t0009g0011 | 2 | HG03098.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.9+893A>G | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66466 | ||||||
chr1:66479
|
TATTTATA others(1): Show |
T | 2 | a0004c0003t0002g0013a0004c0003t0010g0027 | 3 | HG02615.hp1 HG03831.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.9+908_9+915delTTTA others(4): Show |
OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 66479 | |||||
chr1:66480
|
AT | A | 5 | a0001c0001t0014g0049a0003c0007t0003g0007a0003c0007t0003g0047others(2): Show | 10 | HG00544.hp1 HG03490.hp1 NA18939.hp1 others(7): Show |
intron_variant | MODIFIER | c.9+910delT | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 66480 | |||||
chr1:66481
|
T | TTATAGAA others(75): Show |
1 | a0012c0020t0001g0044 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.9+909_9+910insATAG others(78): Show |
OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 66481 | |||||
chr1:66488
|
A | T | 2 | a0004c0003t0002g0013a0004c0003t0010g0027 | 3 | HG02615.hp1 HG03831.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.9+915A>T | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66488 | ||||||
chr1:66502
|
T | G | 1 | a0004c0003t0010g0027 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.9+929T>G | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66502 | ||||||
chr1:66507
|
T | A | 18 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0015others(15): Show | 93 | HG00544.hp2 HG00639.hp2 HG00642.hp2 others(90): Show |
intron_variant | MODIFIER | c.9+934T>A | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66507 | ||||||
chr1:66521
|
T | TATATA | 18 | a0001c0001t0014g0049a0003c0004t0003g0018a0003c0004t0003g0019others(15): Show | 27 | HG00099.hp1 HG00544.hp1 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.9+954_9+958dupATAT others(1): Show |
OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 66521 | |||||
chr1:66525
|
T | A | 1 | a0001c0001t0001g0015 | 2 | HG02280.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.9+952T>A | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66525 | ||||||
chr1:66572
|
G | GTACTATA others(5): Show |
17 | a0001c0001t0014g0049a0003c0004t0003g0018a0003c0004t0003g0020others(14): Show | 25 | HG00544.hp1 HG00741.hp2 HG01167.hp2 others(22): Show |
intron_variant | MODIFIER | c.9+1001_9+1002insCT others(10): Show |
OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 66572 | |||||
chr1:66572
|
GTA | G | 1 | a0003c0004t0003g0019 | 2 | HG00099.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.9+1002_9+1003delTA | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 66572 | |||||
chr1:66577
|
A | AATATATT | 17 | a0001c0001t0014g0049a0003c0004t0003g0018a0003c0004t0003g0020others(14): Show | 25 | HG00544.hp1 HG00741.hp2 HG01167.hp2 others(22): Show |
intron_variant | MODIFIER | c.9+1004_9+1005insAT others(5): Show |
OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66577 | ||||||
chr1:66577
|
A | C | 1 | a0003c0004t0003g0019 | 2 | HG00099.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.9+1004A>C | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66577 | ||||||
chr1:66598
|
T | A | 1 | a0006c0008t0005g0038 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.9+1025T>A | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66598 | ||||||
chr1:66598
|
T | TTATATAT others(10): Show |
1 | a0008c0017t0002g0024 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.9+1039_9+1055dupAA others(15): Show |
OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 66598 | |||||
chr1:66605
|
T | A | 5 | a0001c0001t0014g0049a0003c0007t0003g0007a0003c0007t0003g0047others(2): Show | 10 | HG00544.hp1 HG03490.hp1 NA18939.hp1 others(7): Show |
intron_variant | MODIFIER | c.9+1032T>A | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66605 | ||||||
chr1:66667
|
T | C | 1 | a0002c0002t0013g0042 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.9+1094T>C | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66667 | ||||||
chr1:66668
|
G | A | 1 | a0002c0002t0013g0042 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.9+1095G>A | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66668 | ||||||
chr1:66669
|
A | C | 1 | a0002c0002t0013g0042 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.9+1096A>C | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66669 | ||||||
chr1:66670
|
A | T | 1 | a0002c0002t0013g0042 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.9+1097A>T | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66670 | ||||||
chr1:66675
|
T | G | 1 | a0002c0002t0013g0042 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.9+1102T>G | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66675 | ||||||
chr1:66677
|
T | G | 1 | a0002c0002t0013g0042 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.9+1104T>G | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66677 | ||||||
chr1:66678
|
A | T | 1 | a0002c0002t0013g0042 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.9+1105A>T | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66678 | ||||||
chr1:66679
|
C | T | 1 | a0002c0002t0013g0042 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.9+1106C>T | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66679 | ||||||
chr1:66737
|
G | A | 1 | a0012c0020t0001g0044 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.9+1164G>A | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66737 | ||||||
chr1:66795
|
T | A | 17 | a0001c0001t0014g0049a0003c0004t0003g0018a0003c0004t0003g0019others(14): Show | 26 | HG00099.hp1 HG00544.hp1 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.9+1222T>A | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66795 | ||||||
chr1:66814
|
A | G | 18 | a0001c0001t0014g0049a0003c0004t0003g0018a0003c0004t0003g0019others(15): Show | 27 | HG00099.hp1 HG00544.hp1 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.9+1241A>G | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66814 | ||||||
chr1:66861
|
C | T | 5 | a0004c0003t0002g0012a0004c0003t0002g0023a0004c0003t0002g0025others(2): Show | 6 | HG00639.hp1 HG01106.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.9+1288C>T | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66861 | ||||||
chr1:66876
|
T | G | 8 | a0002c0002t0002g0002a0002c0002t0002g0006a0002c0002t0002g0026others(5): Show | 45 | HG01928.hp1 HG01981.hp1 HG01993.hp1 others(42): Show |
intron_variant | MODIFIER | c.9+1303T>G | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66876 | ||||||
chr1:67181
|
A | G | 5 | a0004c0003t0002g0012a0004c0003t0002g0023a0004c0003t0002g0025others(2): Show | 6 | HG00639.hp1 HG01106.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.9+1608A>G | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 67181 | ||||||
chr1:67184
|
G | A | 2 | a0003c0013t0015g0046a0012c0020t0001g0044 | 2 | HG01928.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.9+1611G>A | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 67184 | ||||||
chr1:67223
|
C | A | 1 | a0012c0020t0001g0044 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.9+1650C>A | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 67223 | ||||||
chr1:67224
|
G | A | 1 | a0004c0003t0004g0022 | 2 | HG02615.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.9+1651G>A | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 67224 | ||||||
chr1:67242
|
A | C | 19 | a0001c0001t0014g0049a0003c0004t0003g0018a0003c0004t0003g0019others(16): Show | 28 | HG00099.hp1 HG00544.hp1 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.9+1669A>C | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 67242 | ||||||
chr1:67314
|
A | C | 1 | a0003c0013t0015g0046 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.10-1723A>C | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 67314 | ||||||
chr1:67400
|
G | A | 1 | a0003c0013t0015g0046 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.10-1637G>A | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 67400 | ||||||
chr1:67437
|
A | T | 1 | a0001c0001t0001g0036 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.10-1600A>T | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 67437 | ||||||
chr1:67448
|
T | A | 17 | a0001c0001t0014g0049a0003c0004t0003g0018a0003c0004t0003g0019others(14): Show | 26 | HG00099.hp1 HG00544.hp1 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.10-1589T>A | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 67448 | ||||||
chr1:67598
|
G | A | 1 | a0001c0001t0001g0034 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.10-1439G>A | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 67598 | ||||||
chr1:67605
|
T | C | 19 | a0001c0001t0014g0049a0003c0004t0003g0018a0003c0004t0003g0019others(16): Show | 28 | HG00099.hp1 HG00544.hp1 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.10-1432T>C | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 67605 | ||||||
chr1:67631
|
G | C | 1 | a0004c0003t0002g0025 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.10-1406G>C | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 67631 | ||||||
chr1:67711
|
C | T | 2 | a0005c0005t0001g0005a0005c0005t0001g0030 | 7 | HG01891.hp1 HG02257.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.10-1326C>T | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 67711 | ||||||
chr1:67744
|
G | A | 4 | a0003c0004t0003g0019a0003c0004t0003g0051a0003c0004t0003g0052others(1): Show | 5 | HG00099.hp1 HG00741.hp2 HG01167.hp2 others(2): Show |
intron_variant | MODIFIER | c.10-1293G>A | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 67744 | ||||||
chr1:67861
|
G | A | 2 | a0003c0004t0003g0018a0003c0004t0003g0054 | 3 | HG01891.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.10-1176G>A | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 67861 | ||||||
chr1:67897
|
GAGTTAAA others(429): Show |
G | 1 | a0003c0013t0015g0046 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.10-1139_10-704del | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 67897 | ||||||
chr1:67942
|
A | C | 2 | a0001c0001t0001g0011a0001c0009t0009g0011 | 2 | HG03098.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.10-1095A>C | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 67942 | ||||||
chr1:68082
|
T | C | 2 | a0006c0008t0005g0016a0006c0008t0005g0038 | 3 | HG01433.hp1 HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.10-955T>C | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 68082 | ||||||
chr1:68120
|
G | T | 1 | a0001c0001t0001g0035 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.10-917G>T | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 68120 | ||||||
chr1:68179
|
A | T | 6 | a0002c0002t0002g0002a0002c0002t0002g0006a0002c0002t0002g0026others(3): Show | 42 | HG01928.hp1 HG01981.hp1 HG01993.hp1 others(39): Show |
intron_variant | MODIFIER | c.10-858A>T | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 68179 | ||||||
chr1:68306
|
C | T | 17 | a0003c0004t0003g0018a0003c0004t0003g0019a0003c0004t0003g0020others(14): Show | 26 | HG00099.hp1 HG00544.hp1 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.10-731C>T | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 68306 | ||||||
chr1:68316
|
T | C | 1 | a0012c0020t0001g0044 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.10-721T>C | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 68316 | ||||||
chr1:68334
|
T | C | 1 | a0003c0013t0015g0046 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.10-703T>C | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 68334 | ||||||
chr1:68336
|
A | C | 1 | a0003c0013t0015g0046 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.10-701A>C | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 68336 | ||||||
chr1:68338
|
T | C | 1 | a0003c0013t0015g0046 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.10-699T>C | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 68338 | ||||||
chr1:68340
|
G | C | 1 | a0003c0013t0015g0046 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.10-697G>C | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 68340 | ||||||
chr1:68341
|
G | C | 1 | a0003c0013t0015g0046 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.10-696G>C | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 68341 | ||||||
chr1:68347
|
T | A | 1 | a0003c0013t0015g0046 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.10-690T>A | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 68347 | ||||||
chr1:68387
|
G | C | 16 | a0003c0004t0003g0018a0003c0004t0003g0019a0003c0004t0003g0020others(13): Show | 25 | HG00099.hp1 HG00544.hp1 HG00741.hp2 others(22): Show |
intron_variant | MODIFIER | c.10-650G>C | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 68387 | ||||||
chr1:68407
|
A | G | 16 | a0003c0004t0003g0018a0003c0004t0003g0019a0003c0004t0003g0020others(13): Show | 25 | HG00099.hp1 HG00544.hp1 HG00741.hp2 others(22): Show |
intron_variant | MODIFIER | c.10-630A>G | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 68407 | ||||||
chr1:68547
|
T | C | 17 | a0003c0004t0003g0018a0003c0004t0003g0019a0003c0004t0003g0020others(14): Show | 26 | HG00099.hp1 HG00544.hp1 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.10-490T>C | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 68547 | ||||||
chr1:68555
|
T | C | 4 | a0003c0004t0003g0019a0003c0004t0003g0051a0003c0004t0003g0052others(1): Show | 5 | HG00099.hp1 HG00741.hp2 HG01167.hp2 others(2): Show |
intron_variant | MODIFIER | c.10-482T>C | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 68555 | ||||||
chr1:68562
|
T | G | 2 | a0003c0004t0003g0020a0003c0004t0003g0057 | 3 | HG03239.hp2 HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.10-475T>G | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 68562 | ||||||
chr1:68596
|
T | C | 1 | a0004c0003t0002g0023 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.10-441T>C | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 68596 | ||||||
chr1:68596
|
T | G | 1 | a0002c0002t0002g0006 | 6 | HG01981.hp1 HG01993.hp1 NA18962.hp1 others(3): Show |
intron_variant | MODIFIER | c.10-441T>G | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 68596 | ||||||
chr1:68616
|
T | C | 1 | a0003c0013t0015g0046 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.10-421T>C | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 68616 | ||||||
chr1:68635
|
A | G | 1 | a0001c0001t0001g0035 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.10-402A>G | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 68635 | ||||||
chr1:68749
|
A | G | 1 | a0004c0003t0004g0059 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.10-288A>G | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 68749 | ||||||
chr1:68777
|
C | T | 1 | a0010c0014t0002g0045 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.10-260C>T | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 68777 | ||||||
chr1:68849
|
C | T | 1 | a0003c0013t0015g0046 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.10-188C>T | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 68849 | ||||||
chr1:68889
|
C | T | 1 | a0001c0009t0008g0039 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.10-148C>T | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 68889 | ||||||
chr1:68894
|
T | C | 1 | a0003c0013t0015g0046 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.10-143T>C | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 68894 | ||||||
chr1:68896
|
G | A | 70 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(67): Show | 211 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(208): Show |
intron_variant | MODIFIER | c.10-141G>A | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 68896 | ||||||
chr1:68905
|
T | A | 4 | a0003c0007t0003g0007a0003c0007t0003g0047a0003c0007t0003g0048others(1): Show | 9 | HG00544.hp1 HG03490.hp1 NA18939.hp1 others(6): Show |
intron_variant | MODIFIER | c.10-132T>A | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 68905 | ||||||
chr1:68934
|
A | C | 16 | a0003c0004t0003g0018a0003c0004t0003g0019a0003c0004t0003g0020others(13): Show | 25 | HG00099.hp1 HG00544.hp1 HG00741.hp2 others(22): Show |
intron_variant | MODIFIER | c.10-103A>C | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 68934 | ||||||
chr1:68945
|
A | T | 1 | a0003c0013t0015g0046 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.10-92A>T | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 68945 | ||||||
chr1:69008
|
C | A | 1 | a0012c0020t0001g0044 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.10-29C>A | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 69008 |