geneid | 80204 |
---|---|
ensemblid | ENSG00000138081.22 |
hgncid | 13590 |
symbol | FBXO11 |
name | F-box protein 11 |
refseq_nuc | NM_001190274.2 |
refseq_prot | NP_001177203.1 |
ensembl_nuc | ENST00000403359.8 |
ensembl_prot | ENSP00000384823.4 |
mane_status | MANE Select |
chr | chr2 |
start | 47806920 |
end | 47906498 |
strand | - |
ver | v1.2 |
region | chr2:47806920-47906498 |
region5000 | chr2:47801920-47911498 |
regionname0 | FBXO11_chr2_47806920_47906498 |
regionname5000 | FBXO11_chr2_47801920_47911498 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 927 | 307 | 82 | 58 | 117 | 14 | 34 | 91 | FBXO11_chr2_47801920_47911498 | FBXO11 | copy fasta | chr2 | 47801920 | 47911498 |
a0002 | 0/0 | 927 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | copy fasta | chr2 | 47801920 | 47911498 |
a0003 | 0/0 | 928 | 3 | 1 | 1 | 1 | 0 | 0 | 1 | FBXO11_chr2_47801920_47911498 | FBXO11 | copy fasta | chr2 | 47801920 | 47911498 |
a0004 | 0/0 | 922 | 2 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | copy fasta | chr2 | 47801920 | 47911498 |
a0005 | 0/0 | 927 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | copy fasta | chr2 | 47801920 | 47911498 |
a0006 | 0/0 | 927 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | copy fasta | chr2 | 47801920 | 47911498 |
a0007 | 0/0 | 927 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | copy fasta | chr2 | 47801920 | 47911498 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 2784 | 297 | 74 | 56 | 117 | 14 | 34 | FBXO11_chr2_47801920_47911498 | FBXO11 | copy fasta | chr2 | 47801920 | 47911498 |
c0002 | 0/0 | 2784 | 9 | 8 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | copy fasta | chr2 | 47801920 | 47911498 |
c0003 | 0/0 | 2787 | 3 | 1 | 1 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | copy fasta | chr2 | 47801920 | 47911498 |
c0004 | 0/0 | 2784 | 3 | 3 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | copy fasta | chr2 | 47801920 | 47911498 |
c0005 | 0/0 | 2769 | 2 | 1 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | copy fasta | chr2 | 47801920 | 47911498 |
c0006 | 0/0 | 2784 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | copy fasta | chr2 | 47801920 | 47911498 |
c0007 | 0/0 | 2784 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | copy fasta | chr2 | 47801920 | 47911498 |
c0008 | 0/0 | 2784 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | copy fasta | chr2 | 47801920 | 47911498 |
c0009 | 0/0 | 2784 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | copy fasta | chr2 | 47801920 | 47911498 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 1976 | 209 | 53 | 33 | 86 | 12 | 25 | FBXO11_chr2_47801920_47911498 | FBXO11 | copy fasta | chr2 | 47801920 | 47911498 |
t0002 | 1/1 | 1977 | 84 | 23 | 26 | 23 | 2 | 8 | FBXO11_chr2_47801920_47911498 | FBXO11 | copy fasta | chr2 | 47801920 | 47911498 |
t0003 | 0/0 | 1977 | 6 | 6 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | copy fasta | chr2 | 47801920 | 47911498 |
t0004 | 0/0 | 1982 | 3 | 0 | 0 | 3 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | copy fasta | chr2 | 47801920 | 47911498 |
t0005 | 0/0 | 2004 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | copy fasta | chr2 | 47801920 | 47911498 |
t0006 | 0/0 | 1976 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | copy fasta | chr2 | 47801920 | 47911498 |
t0007 | 0/0 | 1976 | 1 | 0 | 0 | 0 | 0 | 1 | FBXO11_chr2_47801920_47911498 | FBXO11 | copy fasta | chr2 | 47801920 | 47911498 |
t0008 | 0/0 | 1976 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | copy fasta | chr2 | 47801920 | 47911498 |
t0009 | 0/0 | 1977 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | copy fasta | chr2 | 47801920 | 47911498 |
t0010 | 0/0 | 1977 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | copy fasta | chr2 | 47801920 | 47911498 |
t0011 | 0/0 | 1976 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | copy fasta | chr2 | 47801920 | 47911498 |
t0012 | 0/0 | 1976 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | copy fasta | chr2 | 47801920 | 47911498 |
t0013 | 0/0 | 1977 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | copy fasta | chr2 | 47801920 | 47911498 |
t0014 | 0/0 | 1977 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | copy fasta | chr2 | 47801920 | 47911498 |
t0015 | 0/0 | 1976 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | copy fasta | chr2 | 47801920 | 47911498 |
t0016 | 0/0 | 1992 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | copy fasta | chr2 | 47801920 | 47911498 |
t0017 | 0/0 | 1976 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | copy fasta | chr2 | 47801920 | 47911498 |
t0018 | 0/0 | 1976 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | copy fasta | chr2 | 47801920 | 47911498 |
t0019 | 0/0 | 1976 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | copy fasta | chr2 | 47801920 | 47911498 |
t0020 | 0/0 | 1977 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | copy fasta | chr2 | 47801920 | 47911498 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0037 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0142 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0287 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2784 | 297 | 74 | 56 | 117 | 14 | 34 | FBXO11_chr2_47801920_47911498 | FBXO11 | copy fasta | chr2 | 47801920 | 47911498 |
a0001c0002 | 0/0 | 2784 | 9 | 8 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | copy fasta | chr2 | 47801920 | 47911498 |
a0001c0007 | 0/0 | 2784 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | copy fasta | chr2 | 47801920 | 47911498 |
a0002c0004 | 0/0 | 2784 | 3 | 3 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | copy fasta | chr2 | 47801920 | 47911498 |
a0003c0003 | 0/0 | 2787 | 3 | 1 | 1 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | copy fasta | chr2 | 47801920 | 47911498 |
a0004c0005 | 0/0 | 2769 | 2 | 1 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | copy fasta | chr2 | 47801920 | 47911498 |
a0005c0009 | 0/0 | 2784 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | copy fasta | chr2 | 47801920 | 47911498 |
a0006c0008 | 0/0 | 2784 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | copy fasta | chr2 | 47801920 | 47911498 |
a0007c0006 | 0/0 | 2784 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | copy fasta | chr2 | 47801920 | 47911498 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 4759 | 203 | 51 | 31 | 84 | 12 | 25 | FBXO11_chr2_47801920_47911498 | FBXO11 | copy fasta | chr2 | 47801920 | 47911498 |
a0001c0001t0002 | 1/1 | 4760 | 69 | 11 | 24 | 22 | 2 | 8 | FBXO11_chr2_47801920_47911498 | FBXO11 | copy fasta | chr2 | 47801920 | 47911498 |
a0001c0001t0003 | 0/0 | 4760 | 6 | 6 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | copy fasta | chr2 | 47801920 | 47911498 |
a0001c0001t0004 | 0/0 | 4765 | 3 | 0 | 0 | 3 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | copy fasta | chr2 | 47801920 | 47911498 |
a0001c0001t0005 | 0/0 | 4787 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | copy fasta | chr2 | 47801920 | 47911498 |
a0001c0001t0006 | 0/0 | 4759 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | copy fasta | chr2 | 47801920 | 47911498 |
a0001c0001t0007 | 0/0 | 4759 | 1 | 0 | 0 | 0 | 0 | 1 | FBXO11_chr2_47801920_47911498 | FBXO11 | copy fasta | chr2 | 47801920 | 47911498 |
a0001c0001t0008 | 0/0 | 4759 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | copy fasta | chr2 | 47801920 | 47911498 |
a0001c0001t0009 | 0/0 | 4760 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | copy fasta | chr2 | 47801920 | 47911498 |
a0001c0001t0010 | 0/0 | 4760 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | copy fasta | chr2 | 47801920 | 47911498 |
a0001c0001t0011 | 0/0 | 4759 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | copy fasta | chr2 | 47801920 | 47911498 |
a0001c0001t0012 | 0/0 | 4759 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | copy fasta | chr2 | 47801920 | 47911498 |
a0001c0001t0013 | 0/0 | 4760 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | copy fasta | chr2 | 47801920 | 47911498 |
a0001c0001t0014 | 0/0 | 4760 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | copy fasta | chr2 | 47801920 | 47911498 |
a0001c0001t0015 | 0/0 | 4759 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | copy fasta | chr2 | 47801920 | 47911498 |
a0001c0001t0016 | 0/0 | 4775 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | copy fasta | chr2 | 47801920 | 47911498 |
a0001c0001t0017 | 0/0 | 4759 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | copy fasta | chr2 | 47801920 | 47911498 |
a0001c0001t0018 | 0/0 | 4759 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | copy fasta | chr2 | 47801920 | 47911498 |
a0001c0001t0019 | 0/0 | 4759 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | copy fasta | chr2 | 47801920 | 47911498 |
a0001c0001t0020 | 0/0 | 4760 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | copy fasta | chr2 | 47801920 | 47911498 |
a0001c0002t0002 | 0/0 | 4760 | 9 | 8 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | copy fasta | chr2 | 47801920 | 47911498 |
a0001c0007t0002 | 0/0 | 4760 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | copy fasta | chr2 | 47801920 | 47911498 |
a0002c0004t0002 | 0/0 | 4760 | 3 | 3 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | copy fasta | chr2 | 47801920 | 47911498 |
a0003c0003t0001 | 0/0 | 4762 | 3 | 1 | 1 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | copy fasta | chr2 | 47801920 | 47911498 |
a0004c0005t0002 | 0/0 | 4745 | 2 | 1 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | copy fasta | chr2 | 47801920 | 47911498 |
a0005c0009t0001 | 0/0 | 4759 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | copy fasta | chr2 | 47801920 | 47911498 |
a0006c0008t0001 | 0/0 | 4759 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | copy fasta | chr2 | 47801920 | 47911498 |
a0007c0006t0001 | 0/0 | 4759 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | copy fasta | chr2 | 47801920 | 47911498 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0002g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0002g0037 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0002g0142 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0002g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0002g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0002g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0002g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0002g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0002g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0002g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0002g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0002g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0002g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0002g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0002g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0002g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0002g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0002g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0002g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0002g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0003g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0003g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0003g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0003g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0003g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0003g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0004g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0004g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0004g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0005g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0006g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0007g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0008g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0009g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0010g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0011g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0012g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0013g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0014g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0015g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0016g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0017g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0018g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0019g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0001t0020g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0002t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0002t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0002t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0002t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0002t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0002t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0002t0002g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0002t0002g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0002t0002g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0001c0007t0002g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0002c0004t0002g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0002c0004t0002g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0002c0004t0002g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0003c0003t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0003c0003t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0003c0003t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0004c0005t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0004c0005t0002g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0005c0009t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0006c0008t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
a0007c0006t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0218 | EUR | GBR | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0217 | EUR | GBR | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG00280 | hp1 | a0001 | c0001 | t0002 | g0166 | EUR | FIN | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0287 | EUR | FIN | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0073 | EUR | FIN | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0184 | EUR | FIN | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | CHS | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | CHS | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | CHS | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | CHS | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | CHS | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | CHS | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | CHS | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | CHS | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | CHS | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | CHS | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0229 | AMR | PUR | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0160 | AMR | PUR | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0286 | AMR | PUR | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG00738 | hp2 | a0001 | c0007 | t0002 | g0168 | AMR | PUR | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0222 | AMR | PUR | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG00741 | hp2 | a0003 | c0003 | t0001 | g0015 | AMR | PUR | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG01069 | hp1 | a0001 | c0001 | t0002 | g0163 | AMR | PUR | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0236 | AMR | PUR | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0264 | AMR | PUR | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | PUR | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0164 | AMR | PUR | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | PUR | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG01074 | hp1 | a0001 | c0001 | t0002 | g0109 | AMR | PUR | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG01074 | hp2 | a0001 | c0001 | t0002 | g0272 | AMR | PUR | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0288 | AMR | PUR | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0230 | AMR | PUR | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0172 | AMR | PUR | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG01109 | hp2 | a0001 | c0002 | t0002 | g0283 | AMR | PUR | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG01168 | hp2 | a0001 | c0001 | t0002 | g0146 | AMR | PUR | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG01169 | hp1 | a0001 | c0001 | t0002 | g0080 | AMR | PUR | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG01169 | hp2 | a0001 | c0001 | t0016 | g0309 | AMR | PUR | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG01175 | hp1 | a0001 | c0001 | t0002 | g0173 | AMR | PUR | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG01175 | hp2 | a0001 | c0001 | t0002 | g0169 | AMR | PUR | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0290 | AMR | CLM | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0170 | AMR | CLM | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG01256 | hp1 | a0001 | c0001 | t0002 | g0136 | AMR | CLM | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | CLM | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG01257 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0289 | AMR | CLM | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | CLM | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0235 | AMR | CLM | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0251 | AMR | CLM | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | CLM | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0144 | AMR | CLM | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG01358 | hp1 | a0001 | c0001 | t0002 | g0148 | AMR | CLM | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0298 | AMR | CLM | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | CLM | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0234 | EUR | IBS | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG01515 | hp2 | a0001 | c0001 | t0002 | g0145 | EUR | IBS | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0216 | EUR | IBS | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0292 | EUR | IBS | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG01884 | hp1 | a0002 | c0004 | t0002 | g0266 | AFR | ACB | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG01884 | hp2 | a0001 | c0002 | t0002 | g0034 | AFR | ACB | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0276 | AFR | ACB | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG01978 | hp1 | a0001 | c0001 | t0002 | g0154 | AMR | PEL | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0101 | AMR | PEL | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG01981 | hp1 | a0001 | c0001 | t0002 | g0301 | AMR | PEL | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG01981 | hp2 | a0001 | c0001 | t0002 | g0133 | AMR | PEL | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | PEL | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG01993 | hp2 | a0007 | c0006 | t0001 | g0108 | AMR | PEL | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0140 | EAS | KHV | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | KHV | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG02055 | hp1 | a0001 | c0001 | t0002 | g0248 | AFR | ACB | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | KHV | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | KHV | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | KHV | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | KHV | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0134 | EAS | KHV | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | KHV | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG02135 | hp1 | a0001 | c0001 | t0011 | g0040 | EAS | KHV | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG02135 | hp2 | a0001 | c0001 | t0004 | g0012 | EAS | KHV | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG02145 | hp1 | a0001 | c0001 | t0003 | g0282 | AFR | ACB | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG02145 | hp2 | a0001 | c0001 | t0020 | g0313 | AFR | ACB | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0303 | EAS | CDX | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | CDX | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0141 | EAS | CDX | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG02165 | hp2 | a0006 | c0008 | t0001 | g0305 | EAS | CDX | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG02257 | hp2 | a0001 | c0001 | t0003 | g0107 | AFR | ACB | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG02258 | hp1 | a0001 | c0001 | t0002 | g0143 | AFR | ACB | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG02258 | hp2 | a0005 | c0009 | t0001 | g0306 | AFR | ACB | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | PEL | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0155 | AMR | PEL | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | ACB | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | ACB | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0226 | AMR | PEL | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PEL | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG02451 | hp1 | a0004 | c0005 | t0002 | g0308 | AFR | ACB | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG02523 | hp1 | a0004 | c0005 | t0002 | g0307 | EAS | KHV | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG02523 | hp2 | a0001 | c0001 | t0004 | g0013 | EAS | KHV | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG02572 | hp1 | a0001 | c0001 | t0002 | g0179 | AFR | GWD | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | GWD | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0213 | AFR | GWD | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | GWD | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | GWD | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0239 | AFR | GWD | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | GWD | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG02717 | hp1 | a0001 | c0001 | t0003 | g0294 | AFR | GWD | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0268 | AFR | GWD | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | GWD | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG02723 | hp2 | a0001 | c0001 | t0014 | g0284 | AFR | GWD | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0092 | SAS | PJL | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0291 | SAS | PJL | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | GWD | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0247 | AFR | GWD | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG02818 | hp2 | a0001 | c0002 | t0002 | g0120 | AFR | GWD | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | GWD | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG02886 | hp2 | a0001 | c0001 | t0006 | g0007 | AFR | GWD | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG02895 | hp1 | a0001 | c0002 | t0002 | g0031 | AFR | GWD | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG02895 | hp2 | a0001 | c0001 | t0002 | g0281 | AFR | GWD | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG02896 | hp1 | a0002 | c0004 | t0002 | g0263 | AFR | GWD | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG02897 | hp1 | a0001 | c0002 | t0002 | g0030 | AFR | GWD | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG02922 | hp1 | a0001 | c0001 | t0002 | g0250 | AFR | ESN | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0271 | AFR | ESN | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | ESN | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0297 | SAS | PJL | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0280 | SAS | PJL | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | GWD | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG03041 | hp2 | a0001 | c0001 | t0002 | g0147 | AFR | GWD | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG03130 | hp1 | a0001 | c0001 | t0003 | g0243 | AFR | ESN | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | ESN | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0267 | AFR | ESN | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | ESN | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG03195 | hp1 | a0001 | c0002 | t0002 | g0302 | AFR | ESN | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0304 | AFR | MSL | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG03209 | hp2 | a0001 | c0001 | t0002 | g0249 | AFR | MSL | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0270 | AFR | MSL | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG03225 | hp2 | a0001 | c0001 | t0003 | g0295 | AFR | MSL | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0279 | SAS | PJL | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0185 | SAS | PJL | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | MSL | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG03453 | hp2 | a0001 | c0001 | t0013 | g0165 | AFR | MSL | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG03486 | hp1 | a0001 | c0001 | t0002 | g0139 | AFR | MSL | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | MSL | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0211 | SAS | PJL | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0296 | SAS | PJL | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0210 | SAS | PJL | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0192 | SAS | PJL | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG03516 | hp1 | a0002 | c0004 | t0002 | g0262 | AFR | ESN | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG03516 | hp2 | a0001 | c0001 | t0002 | g0196 | AFR | ESN | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0265 | AFR | GWD | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG03540 | hp2 | a0001 | c0002 | t0002 | g0032 | AFR | GWD | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG03579 | hp1 | a0001 | c0001 | t0003 | g0293 | AFR | MSL | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0269 | AFR | MSL | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG03669 | hp1 | a0001 | c0001 | t0007 | g0008 | SAS | PJL | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0137 | SAS | STU | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG03688 | hp2 | a0001 | c0001 | t0002 | g0153 | SAS | STU | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0242 | SAS | PJL | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0150 | SAS | PJL | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0135 | SAS | PJL | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0069 | SAS | BEB | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0205 | SAS | BEB | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0299 | SAS | BEB | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0175 | SAS | BEB | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0237 | SAS | STU | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0219 | SAS | STU | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | BEB | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0161 | SAS | BEB | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0097 | SAS | STU | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0063 | SAS | STU | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0159 | SAS | STU | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0076 | SAS | STU | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | YRI | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | YRI | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0158 | EAS | CHB | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | CHB | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
NA18906 | hp1 | a0001 | c0001 | t0010 | g0132 | AFR | YRI | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | YRI | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
NA18942 | hp1 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
NA18952 | hp2 | a0001 | c0001 | t0012 | g0253 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
NA18953 | hp1 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
NA18954 | hp1 | a0001 | c0001 | t0017 | g0310 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
NA18964 | hp1 | a0001 | c0001 | t0009 | g0010 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
NA18965 | hp1 | a0001 | c0001 | t0018 | g0311 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
NA18965 | hp2 | a0001 | c0001 | t0019 | g0312 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
NA18966 | hp1 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
NA18967 | hp1 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
NA18969 | hp2 | a0001 | c0001 | t0008 | g0009 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
NA18974 | hp2 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
NA18982 | hp2 | a0001 | c0001 | t0004 | g0011 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
NA18985 | hp1 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
NA18991 | hp1 | a0001 | c0001 | t0002 | g0225 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
NA18993 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
NA19000 | hp2 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | LWK | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
NA19043 | hp2 | a0001 | c0001 | t0015 | g0130 | AFR | LWK | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
NA19057 | hp1 | a0001 | c0001 | t0005 | g0006 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
NA19057 | hp2 | a0001 | c0001 | t0002 | g0138 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
NA19058 | hp1 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
NA19066 | hp2 | a0001 | c0001 | t0002 | g0162 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
NA19068 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
NA19076 | hp2 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
NA19079 | hp1 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
NA19090 | hp1 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
NA19091 | hp1 | a0003 | c0003 | t0001 | g0014 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | YRI | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0275 | AFR | YRI | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0273 | AFR | ASW | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ASW | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0060 | EUR | TSI | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0223 | EUR | TSI | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0231 | EUR | TSI | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0047 | EUR | TSI | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0129 | SAS | GIH | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0055 | SAS | GIH | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG01123 | hp1 | a0001 | c0001 | t0002 | g0149 | AMR | CLM | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | CLM | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | ACB | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG02109 | hp2 | a0001 | c0002 | t0002 | g0033 | AFR | ACB | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG02559 | hp1 | a0001 | c0001 | t0002 | g0285 | AFR | ACB | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0238 | AFR | MSL | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
HG03471 | hp2 | a0001 | c0002 | t0002 | g0300 | AFR | MSL | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | USA | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
NA20300 | hp2 | a0003 | c0003 | t0001 | g0016 | AFR | USA | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0274 | AFR | LWK | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | LWK | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0142 | REF | REF | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0037 | REF | REF | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:47806922
|
A | G | 1 | a0001 | 1 | HG03453.hp2 | splice_region_variant | LOW | c.*1196T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 23/23 | chr2 | 47806922 | ||||||
chr2:47832769
|
C | T | 1 | a0007 | 1 | HG01993.hp2 | missense_variant&splice_region_variant | MODERATE | c.1153G>A | p.Val385Ile | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 9/23 | 1931/4760 | 1153/2784 | 385/927 | chr2 | 47832769 | ||
chr2:47839485
|
T | A | 1 | a0002 | 3 | HG01884.hp1 HG02896.hp1 HG03516.hp1 |
missense_variant | MODERATE | c.376A>T | p.Thr126Ser | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 3/23 | 1154/4760 | 376/2784 | 126/927 | chr2 | 47839485 | ||
chr2:47905551
|
G | GGCT | 1 | a0003 | 3 | HG00741.hp2 NA19091.hp1 NA20300.hp2 |
conservative_inframe_insertion | MODERATE | c.167_169dupAGC | p.Gln56dup | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/23 | 947/4760 | 169/2784 | 57/927 | chr2 | 47905551 | ||
chr2:47905569
|
T | G | 1 | a0005 | 1 | HG02258.hp2 | missense_variant | MODERATE | c.152A>C | p.Gln51Pro | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/23 | 930/4760 | 152/2784 | 51/927 | chr2 | 47905569 | ||
chr2:47905572
|
T | G | 2 | a0005a0006 | 2 | HG02165.hp2 HG02258.hp2 |
missense_variant | MODERATE | c.149A>C | p.Gln50Pro | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/23 | 927/4760 | 149/2784 | 50/927 | chr2 | 47905572 | ||
chr2:47905586
|
AGGCTGCT others(8): Show |
A | 1 | a0004 | 2 | HG02451.hp1 HG02523.hp1 |
disruptive_inframe_deletion | MODERATE | c.120_134delGCCCCAGC others(7): Show |
p.Pro41_Pro45del | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/23 | 912/4760 | 120/2784 | 40/927 | chr2 | 47905586 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:47823181
|
T | C | 1 | a0001c0002 | 9 | HG01109.hp2 HG01884.hp2 HG02109.hp2 others(6): Show |
synonymous_variant | LOW | c.1578A>G | p.Ala526Ala | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 12/23 | 2356/4760 | 1578/2784 | 526/927 | chr2 | 47823181 | ||
chr2:47823196
|
A | G | 1 | a0001c0007 | 1 | HG00738.hp2 | synonymous_variant | LOW | c.1563T>C | p.Tyr521Tyr | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 12/23 | 2341/4760 | 1563/2784 | 521/927 | chr2 | 47823196 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:47807347
|
G | C | 1 | a0001c0001t0011 | 1 | HG02135.hp1 | 3_prime_UTR_variant | MODIFIER | c.*771C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 23/23 | 771 | chr2 | 47807347 | |||||
chr2:47807549
|
G | A | 1 | a0001c0001t0014 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*569C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 23/23 | 569 | chr2 | 47807549 | |||||
chr2:47807657
|
G | A | 1 | a0001c0001t0012 | 1 | NA18952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*461C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 23/23 | 461 | chr2 | 47807657 | |||||
chr2:47807667
|
TA | T | 17 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(14): Show | 223 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(220): Show |
3_prime_UTR_variant | MODIFIER | c.*450delT | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 23/23 | 450 | chr2 | 47807667 | |||||
chr2:47807682
|
A | C | 1 | a0001c0001t0010 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*436T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 23/23 | 436 | chr2 | 47807682 | |||||
chr2:47807777
|
T | C | 1 | a0001c0001t0015 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*341A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 23/23 | 341 | chr2 | 47807777 | |||||
chr2:47807848
|
T | C | 1 | a0001c0001t0003 | 6 | HG02145.hp1 HG02257.hp2 HG02717.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*270A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 23/23 | 270 | chr2 | 47807848 | |||||
chr2:47905758
|
A | ACACACG | 1 | a0001c0001t0004 | 3 | HG02135.hp2 HG02523.hp2 NA18982.hp2 |
5_prime_UTR_variant | MODIFIER | c.-44_-39dupCGTGTG | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/23 | 39 | chr2 | 47905758 | |||||
chr2:47905786
|
G | A | 1 | a0001c0001t0020 | 1 | HG02145.hp2 | 5_prime_UTR_variant | MODIFIER | c.-66C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/23 | 66 | chr2 | 47905786 | |||||
chr2:47905810
|
T | TGGGAGAG others(9): Show |
1 | a0001c0001t0016 | 1 | HG01169.hp2 | 5_prime_UTR_variant | MODIFIER | c.-106_-91dupTCCTCCC others(9): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/23 | 91 | chr2 | 47905810 | |||||
chr2:47905818
|
G | T | 1 | a0001c0001t0009 | 1 | NA18964.hp1 | 5_prime_UTR_variant | MODIFIER | c.-98C>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/23 | 98 | chr2 | 47905818 | |||||
chr2:47905885
|
G | A | 1 | a0001c0001t0017 | 1 | NA18954.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-165C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/23 | chr2 | 47905885 | ||||||
chr2:47906100
|
G | A | 1 | a0001c0001t0018 | 1 | NA18965.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-380C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/23 | chr2 | 47906100 | ||||||
chr2:47906165
|
G | A | 1 | a0001c0001t0019 | 1 | NA18965.hp2 | 5_prime_UTR_variant | MODIFIER | c.-445C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/23 | 445 | chr2 | 47906165 | |||||
chr2:47906215
|
C | T | 1 | a0001c0001t0008 | 1 | NA18969.hp2 | 5_prime_UTR_variant | MODIFIER | c.-495G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/23 | 495 | chr2 | 47906215 | |||||
chr2:47906314
|
C | G | 1 | a0001c0001t0007 | 1 | HG03669.hp1 | 5_prime_UTR_variant | MODIFIER | c.-594G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/23 | 594 | chr2 | 47906314 | |||||
chr2:47906326
|
C | T | 1 | a0001c0001t0006 | 1 | HG02886.hp2 | 5_prime_UTR_variant | MODIFIER | c.-606G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/23 | 606 | chr2 | 47906326 | |||||
chr2:47906327
|
G | C | 1 | a0001c0001t0020 | 1 | HG02145.hp2 | 5_prime_UTR_variant | MODIFIER | c.-607C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/23 | 607 | chr2 | 47906327 | |||||
chr2:47906331
|
A | AAGGGGAA others(21): Show |
1 | a0001c0001t0005 | 1 | NA19057.hp1 | 5_prime_UTR_variant | MODIFIER | c.-639_-612dupATCTCC others(22): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/23 | 612 | chr2 | 47906331 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:47808492
|
TTTATA | T | 7 | a0001c0001t0001g0264a0001c0001t0001g0287a0001c0001t0001g0288others(4): Show | 7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.2556-70_2556-66del others(5): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 21/22 | chr2 | 47808492 | ||||||
chr2:47808503
|
C | G | 1 | a0001c0001t0001g0068 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.2556-76G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 21/22 | chr2 | 47808503 | ||||||
chr2:47808534
|
A | G | 123 | a0001c0001t0001g0003a0001c0001t0001g0036a0001c0001t0001g0038others(120): Show | 124 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(121): Show |
intron_variant | MODIFIER | c.2556-107T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 21/22 | chr2 | 47808534 | ||||||
chr2:47808679
|
C | G | 6 | a0001c0001t0003g0107a0001c0001t0003g0243a0001c0001t0003g0282others(3): Show | 6 | HG02145.hp1 HG02257.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.2556-252G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 21/22 | chr2 | 47808679 | ||||||
chr2:47808684
|
G | C | 11 | a0001c0001t0001g0264a0001c0001t0001g0287a0001c0001t0001g0288others(8): Show | 11 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(8): Show |
intron_variant | MODIFIER | c.2556-257C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 21/22 | chr2 | 47808684 | ||||||
chr2:47808735
|
A | G | 6 | a0001c0001t0003g0107a0001c0001t0003g0243a0001c0001t0003g0282others(3): Show | 6 | HG02145.hp1 HG02257.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.2556-308T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 21/22 | chr2 | 47808735 | ||||||
chr2:47808744
|
G | GA | 9 | a0001c0002t0002g0030a0001c0002t0002g0031a0001c0002t0002g0032others(6): Show | 9 | HG01109.hp2 HG01884.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.2556-318dupT | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 21/22 | chr2 | 47808744 | ||||||
chr2:47808854
|
T | G | 9 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(6): Show | 9 | HG01346.hp1 HG02615.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.2555+304A>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 21/22 | chr2 | 47808854 | ||||||
chr2:47808860
|
T | C | 1 | a0001c0001t0001g0029 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2555+298A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 21/22 | chr2 | 47808860 | ||||||
chr2:47808943
|
C | G | 1 | a0001c0001t0001g0081 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.2555+215G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 21/22 | chr2 | 47808943 | ||||||
chr2:47808991
|
C | G | 5 | a0001c0001t0002g0281a0001c0001t0002g0285a0001c0001t0002g0286others(2): Show | 5 | HG00738.hp1 HG01109.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.2555+167G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 21/22 | chr2 | 47808991 | ||||||
chr2:47809030
|
A | C | 1 | a0001c0001t0001g0066 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.2555+128T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 21/22 | chr2 | 47809030 | ||||||
chr2:47809048
|
A | G | 1 | a0002c0004t0002g0266 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2555+110T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 21/22 | chr2 | 47809048 | ||||||
chr2:47809105
|
A | G | 3 | a0001c0001t0002g0249a0001c0001t0002g0250a0001c0001t0002g0251 | 3 | HG01261.hp2 HG02922.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2555+53T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 21/22 | chr2 | 47809105 | ||||||
chr2:47809440
|
T | C | 1 | a0001c0001t0001g0038 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2446+160A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 20/22 | chr2 | 47809440 | ||||||
chr2:47809748
|
A | C | 1 | a0001c0001t0001g0219 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2339-41T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 19/22 | chr2 | 47809748 | ||||||
chr2:47809772
|
A | G | 1 | a0001c0001t0001g0288 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2339-65T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 19/22 | chr2 | 47809772 | ||||||
chr2:47809793
|
T | G | 1 | a0002c0004t0002g0263 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2339-86A>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 19/22 | chr2 | 47809793 | ||||||
chr2:47809860
|
C | G | 3 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0005g0006 | 3 | HG00609.hp2 HG02080.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.2339-153G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 19/22 | chr2 | 47809860 | ||||||
chr2:47809903
|
A | C | 2 | a0001c0001t0001g0004a0001c0001t0001g0215 | 3 | HG02055.hp2 NA18522.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2339-196T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 19/22 | chr2 | 47809903 | ||||||
chr2:47809914
|
G | A | 1 | a0001c0001t0001g0231 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2339-207C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 19/22 | chr2 | 47809914 | ||||||
chr2:47809942
|
A | G | 1 | a0001c0001t0001g0209 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2339-235T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 19/22 | chr2 | 47809942 | ||||||
chr2:47810103
|
T | C | 1 | a0001c0001t0017g0310 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.2338+213A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 19/22 | chr2 | 47810103 | ||||||
chr2:47810171
|
C | T | 1 | a0001c0001t0001g0039 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.2338+145G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 19/22 | chr2 | 47810171 | ||||||
chr2:47810454
|
G | A | 7 | a0001c0001t0001g0066a0001c0001t0001g0070a0001c0001t0001g0071others(4): Show | 7 | HG00609.hp2 HG02027.hp2 HG02080.hp2 others(4): Show |
intron_variant | MODIFIER | c.2228-28C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 18/22 | chr2 | 47810454 | ||||||
chr2:47810480
|
C | G | 4 | a0001c0001t0002g0281a0001c0001t0002g0285a0001c0001t0002g0286others(1): Show | 4 | HG00738.hp1 HG02559.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.2228-54G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 18/22 | chr2 | 47810480 | ||||||
chr2:47810650
|
C | T | 1 | a0001c0001t0001g0167 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.2228-224G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 18/22 | chr2 | 47810650 | ||||||
chr2:47810683
|
T | G | 2 | a0001c0001t0002g0112a0001c0001t0002g0180 | 2 | NA19007.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.2228-257A>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 18/22 | chr2 | 47810683 | ||||||
chr2:47810766
|
C | T | 4 | a0001c0001t0002g0281a0001c0001t0002g0285a0001c0001t0002g0286others(1): Show | 4 | HG00738.hp1 HG02559.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.2228-340G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 18/22 | chr2 | 47810766 | ||||||
chr2:47810771
|
A | G | 11 | a0001c0001t0002g0054a0001c0001t0002g0062a0001c0001t0002g0162others(8): Show | 11 | HG00280.hp1 HG00738.hp2 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.2228-345T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 18/22 | chr2 | 47810771 | ||||||
chr2:47810831
|
A | T | 1 | a0001c0001t0001g0123 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2228-405T>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 18/22 | chr2 | 47810831 | ||||||
chr2:47810927
|
T | C | 1 | a0001c0001t0013g0165 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2228-501A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 18/22 | chr2 | 47810927 | ||||||
chr2:47811003
|
A | C | 1 | a0001c0001t0002g0249 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2228-577T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 18/22 | chr2 | 47811003 | ||||||
chr2:47811102
|
C | T | 7 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(4): Show | 7 | NA18971.hp2 NA19010.hp2 NA19066.hp1 others(4): Show |
intron_variant | MODIFIER | c.2228-676G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 18/22 | chr2 | 47811102 | ||||||
chr2:47811143
|
A | G | 1 | a0001c0001t0001g0118 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2228-717T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 18/22 | chr2 | 47811143 | ||||||
chr2:47811144
|
T | A | 1 | a0001c0001t0001g0118 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2228-718A>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 18/22 | chr2 | 47811144 | ||||||
chr2:47811145
|
T | A | 1 | a0001c0001t0001g0118 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2228-719A>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 18/22 | chr2 | 47811145 | ||||||
chr2:47811146
|
A | C | 1 | a0001c0001t0001g0118 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2228-720T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 18/22 | chr2 | 47811146 | ||||||
chr2:47811192
|
G | A | 39 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(36): Show | 42 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.2228-766C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 18/22 | chr2 | 47811192 | ||||||
chr2:47811207
|
G | A | 1 | a0001c0001t0001g0061 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2228-781C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 18/22 | chr2 | 47811207 | ||||||
chr2:47811318
|
G | C | 1 | a0001c0001t0001g0254 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.2228-892C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 18/22 | chr2 | 47811318 | ||||||
chr2:47811640
|
T | C | 11 | a0001c0001t0001g0264a0001c0001t0001g0287a0001c0001t0001g0288others(8): Show | 11 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(8): Show |
intron_variant | MODIFIER | c.2228-1214A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 18/22 | chr2 | 47811640 | ||||||
chr2:47811744
|
C | T | 1 | a0001c0001t0003g0243 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2228-1318G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 18/22 | chr2 | 47811744 | ||||||
chr2:47811798
|
C | A | 2 | a0001c0001t0002g0139a0001c0001t0013g0165 | 2 | HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2228-1372G>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 18/22 | chr2 | 47811798 | ||||||
chr2:47811805
|
A | G | 262 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(259): Show | 267 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(264): Show |
intron_variant | MODIFIER | c.2228-1379T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 18/22 | chr2 | 47811805 | ||||||
chr2:47811809
|
C | T | 11 | a0001c0001t0001g0264a0001c0001t0001g0287a0001c0001t0001g0288others(8): Show | 11 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(8): Show |
intron_variant | MODIFIER | c.2228-1383G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 18/22 | chr2 | 47811809 | ||||||
chr2:47811905
|
T | C | 29 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0044others(26): Show | 29 | HG00280.hp2 HG00639.hp1 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.2227+1329A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 18/22 | chr2 | 47811905 | ||||||
chr2:47811913
|
G | A | 1 | a0001c0001t0001g0003 | 2 | HG02257.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2227+1321C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 18/22 | chr2 | 47811913 | ||||||
chr2:47811945
|
C | T | 4 | a0001c0001t0002g0281a0001c0001t0002g0285a0001c0001t0002g0286others(1): Show | 4 | HG00738.hp1 HG02559.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.2227+1289G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 18/22 | chr2 | 47811945 | ||||||
chr2:47811951
|
C | A | 4 | a0001c0001t0002g0281a0001c0001t0002g0285a0001c0001t0002g0286others(1): Show | 4 | HG00738.hp1 HG02559.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.2227+1283G>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 18/22 | chr2 | 47811951 | ||||||
chr2:47811982
|
T | C | 1 | a0001c0001t0001g0207 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.2227+1252A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 18/22 | chr2 | 47811982 | ||||||
chr2:47812084
|
T | G | 38 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0044others(35): Show | 38 | HG00280.hp2 HG00639.hp1 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.2227+1150A>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 18/22 | chr2 | 47812084 | ||||||
chr2:47812088
|
A | C | 9 | a0001c0002t0002g0030a0001c0002t0002g0031a0001c0002t0002g0032others(6): Show | 9 | HG01109.hp2 HG01884.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.2227+1146T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 18/22 | chr2 | 47812088 | ||||||
chr2:47812112
|
CCT | C | 7 | a0001c0001t0001g0264a0001c0001t0001g0287a0001c0001t0001g0288others(4): Show | 7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.2227+1120_2227+112 others(6): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 18/22 | chr2 | 47812112 | ||||||
chr2:47812173
|
T | C | 1 | a0001c0001t0001g0219 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2227+1061A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 18/22 | chr2 | 47812173 | ||||||
chr2:47812345
|
T | G | 10 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(7): Show | 10 | HG01346.hp1 HG02615.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.2227+889A>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 18/22 | chr2 | 47812345 | ||||||
chr2:47812480
|
A | G | 1 | a0001c0001t0002g0180 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.2227+754T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 18/22 | chr2 | 47812480 | ||||||
chr2:47812543
|
A | T | 2 | a0001c0001t0001g0195a0001c0001t0001g0246 | 2 | NA18953.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.2227+691T>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 18/22 | chr2 | 47812543 | ||||||
chr2:47812605
|
C | T | 36 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0044others(33): Show | 36 | HG00280.hp2 HG00639.hp1 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.2227+629G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 18/22 | chr2 | 47812605 | ||||||
chr2:47812683
|
G | T | 1 | a0001c0001t0001g0087 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.2227+551C>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 18/22 | chr2 | 47812683 | ||||||
chr2:47812789
|
C | T | 1 | a0001c0001t0001g0105 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.2227+445G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 18/22 | chr2 | 47812789 | ||||||
chr2:47812891
|
T | C | 1 | a0001c0001t0002g0160 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2227+343A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 18/22 | chr2 | 47812891 | ||||||
chr2:47813114
|
A | G | 1 | a0001c0001t0001g0287 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2227+120T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 18/22 | chr2 | 47813114 | ||||||
chr2:47813146
|
A | C | 7 | a0001c0001t0001g0063a0001c0001t0001g0087a0001c0001t0001g0111others(4): Show | 7 | HG00323.hp2 HG00438.hp2 HG00642.hp2 others(4): Show |
intron_variant | MODIFIER | c.2227+88T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 18/22 | chr2 | 47813146 | ||||||
chr2:47813425
|
A | ATTT | 7 | a0001c0001t0001g0061a0001c0001t0001g0074a0001c0001t0001g0086others(4): Show | 7 | HG00280.hp1 HG02071.hp1 HG04115.hp2 others(4): Show |
intron_variant | MODIFIER | c.2084-51_2084-49dup others(3): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 17/22 | chr2 | 47813425 | ||||||
chr2:47813425
|
A | ATTTT | 75 | a0001c0001t0001g0038a0001c0001t0001g0043a0001c0001t0001g0044others(72): Show | 76 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.2084-52_2084-49dup others(4): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 17/22 | chr2 | 47813425 | ||||||
chr2:47813425
|
A | ATTTTT | 13 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0052others(10): Show | 13 | HG01109.hp1 HG01346.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.2084-53_2084-49dup others(5): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 17/22 | chr2 | 47813425 | ||||||
chr2:47813425
|
A | ATTTTTTT others(2): Show |
34 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0018others(31): Show | 35 | HG00099.hp1 HG00621.hp1 HG00741.hp1 others(32): Show |
intron_variant | MODIFIER | c.2084-57_2084-49dup others(9): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 17/22 | chr2 | 47813425 | ||||||
chr2:47813425
|
A | ATTTTTTT others(3): Show |
50 | a0001c0001t0001g0001a0001c0001t0001g0023a0001c0001t0001g0039others(47): Show | 51 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(48): Show |
intron_variant | MODIFIER | c.2084-58_2084-49dup others(10): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 17/22 | chr2 | 47813425 | ||||||
chr2:47813425
|
A | ATTTTTTT others(4): Show |
19 | a0001c0001t0001g0021a0001c0001t0001g0026a0001c0001t0001g0036others(16): Show | 19 | HG01070.hp2 HG01071.hp2 HG01258.hp1 others(16): Show |
intron_variant | MODIFIER | c.2084-59_2084-49dup others(11): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 17/22 | chr2 | 47813425 | ||||||
chr2:47813425
|
A | ATTTTTTT others(5): Show |
11 | a0001c0001t0001g0058a0001c0001t0001g0200a0001c0001t0001g0214others(8): Show | 11 | HG00738.hp1 HG01884.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.2084-60_2084-49dup others(12): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 17/22 | chr2 | 47813425 | ||||||
chr2:47813425
|
A | ATTTTTTT others(6): Show |
4 | a0001c0001t0002g0248a0001c0001t0002g0250a0001c0001t0002g0251others(1): Show | 4 | HG01261.hp2 HG02055.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.2084-61_2084-49dup others(13): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 17/22 | chr2 | 47813425 | ||||||
chr2:47813425
|
A | ATTTTTTT others(7): Show |
3 | a0001c0001t0001g0186a0001c0001t0001g0259a0001c0001t0003g0282 | 3 | HG02145.hp1 HG02630.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.2084-62_2084-49dup others(14): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 17/22 | chr2 | 47813425 | ||||||
chr2:47813425
|
A | ATTTTTTT others(8): Show |
6 | a0001c0001t0001g0167a0001c0001t0002g0196a0001c0001t0002g0249others(3): Show | 6 | HG02451.hp1 HG02897.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.2084-63_2084-49dup others(15): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 17/22 | chr2 | 47813425 | ||||||
chr2:47813425
|
A | ATTTTTTT others(9): Show |
5 | a0001c0001t0001g0289a0001c0002t0002g0031a0001c0002t0002g0034others(2): Show | 5 | HG01109.hp2 HG01257.hp2 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.2084-64_2084-49dup others(16): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 17/22 | chr2 | 47813425 | ||||||
chr2:47813425
|
A | ATTTTTTT others(10): Show |
11 | a0001c0001t0001g0003a0001c0001t0001g0239a0001c0001t0001g0264others(8): Show | 12 | HG00280.hp2 HG01070.hp1 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.2084-65_2084-49dup others(17): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 17/22 | chr2 | 47813425 | ||||||
chr2:47813425
|
A | ATTTTTTT others(11): Show |
3 | a0001c0001t0001g0291a0001c0001t0003g0293a0001c0002t0002g0032 | 3 | HG02735.hp2 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2084-66_2084-49dup others(18): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 17/22 | chr2 | 47813425 | ||||||
chr2:47813425
|
A | ATTTTTTT others(13): Show |
1 | a0001c0001t0015g0130 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2084-68_2084-49dup others(20): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 17/22 | chr2 | 47813425 | ||||||
chr2:47813425
|
A | ATTTTTTT others(14): Show |
1 | a0001c0001t0001g0288 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2084-69_2084-49dup others(21): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 17/22 | chr2 | 47813425 | ||||||
chr2:47813425
|
A | ATTTTTTT others(20): Show |
1 | a0001c0001t0003g0243 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2084-49_2084-48ins others(27): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 17/22 | chr2 | 47813425 | ||||||
chr2:47813425
|
ATTTT | A | 7 | a0001c0001t0001g0121a0001c0001t0001g0124a0001c0001t0001g0125others(4): Show | 7 | HG02109.hp1 HG02280.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.2084-52_2084-49del others(4): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 17/22 | chr2 | 47813425 | ||||||
chr2:47813519
|
C | G | 7 | a0001c0001t0001g0264a0001c0001t0001g0287a0001c0001t0001g0288others(4): Show | 7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.2084-142G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 17/22 | chr2 | 47813519 | ||||||
chr2:47813560
|
T | C | 7 | a0001c0001t0001g0264a0001c0001t0001g0287a0001c0001t0001g0288others(4): Show | 7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.2084-183A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 17/22 | chr2 | 47813560 | ||||||
chr2:47813564
|
T | C | 1 | a0001c0001t0001g0304 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2084-187A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 17/22 | chr2 | 47813564 | ||||||
chr2:47813645
|
C | T | 35 | a0001c0001t0001g0058a0001c0001t0001g0064a0001c0001t0001g0065others(32): Show | 35 | HG00438.hp1 HG00544.hp1 HG00597.hp1 others(32): Show |
intron_variant | MODIFIER | c.2083+146G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 17/22 | chr2 | 47813645 | ||||||
chr2:47813667
|
G | A | 2 | a0001c0001t0001g0059a0001c0001t0001g0104 | 2 | NA18966.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.2083+124C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 17/22 | chr2 | 47813667 | ||||||
chr2:47813728
|
C | A | 7 | a0001c0001t0001g0017a0001c0001t0001g0021a0001c0001t0001g0023others(4): Show | 7 | HG01433.hp1 HG02818.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.2083+63G>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 17/22 | chr2 | 47813728 | ||||||
chr2:47813765
|
G | GA | 287 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(284): Show | 292 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.2083+25dupT | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 17/22 | chr2 | 47813765 | ||||||
chr2:47813914
|
C | T | 1 | a0001c0001t0002g0146 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.2007-47G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 16/22 | chr2 | 47813914 | ||||||
chr2:47814235
|
C | T | 1 | a0001c0001t0001g0192 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.2007-368G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 16/22 | chr2 | 47814235 | ||||||
chr2:47814238
|
A | G | 221 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(218): Show | 226 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.2007-371T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 16/22 | chr2 | 47814238 | ||||||
chr2:47814242
|
A | G | 4 | a0001c0001t0003g0282a0001c0001t0003g0293a0001c0001t0003g0294others(1): Show | 4 | HG02145.hp1 HG02717.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.2007-375T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 16/22 | chr2 | 47814242 | ||||||
chr2:47814247
|
T | C | 12 | a0001c0001t0001g0122a0001c0001t0001g0127a0001c0001t0001g0128others(9): Show | 12 | HG00639.hp2 HG00642.hp1 HG01069.hp2 others(9): Show |
intron_variant | MODIFIER | c.2007-380A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 16/22 | chr2 | 47814247 | ||||||
chr2:47814255
|
C | T | 5 | a0001c0001t0001g0195a0001c0001t0001g0241a0001c0001t0001g0244others(2): Show | 5 | NA18953.hp2 NA18979.hp1 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.2007-388G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 16/22 | chr2 | 47814255 | ||||||
chr2:47814333
|
G | A | 1 | a0001c0001t0001g0304 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2007-466C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 16/22 | chr2 | 47814333 | ||||||
chr2:47814373
|
C | CT | 204 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(201): Show | 208 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.2007-507dupA | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 16/22 | chr2 | 47814373 | ||||||
chr2:47814373
|
C | CTT | 14 | a0001c0001t0001g0204a0001c0001t0001g0208a0001c0001t0001g0209others(11): Show | 14 | HG01346.hp1 HG02155.hp1 HG02165.hp2 others(11): Show |
intron_variant | MODIFIER | c.2007-508_2007-507d others(4): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 16/22 | chr2 | 47814373 | ||||||
chr2:47814411
|
T | A | 1 | a0001c0001t0001g0184 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.2007-544A>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 16/22 | chr2 | 47814411 | ||||||
chr2:47814424
|
C | CTGGAGT | 101 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(98): Show | 104 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.2007-563_2007-558d others(8): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 16/22 | chr2 | 47814424 | ||||||
chr2:47814523
|
T | G | 1 | a0001c0001t0001g0195 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.2007-656A>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 16/22 | chr2 | 47814523 | ||||||
chr2:47814701
|
G | A | 14 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(11): Show | 14 | HG01433.hp1 HG01891.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.2007-834C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 16/22 | chr2 | 47814701 | ||||||
chr2:47814906
|
C | A | 1 | a0001c0001t0001g0118 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2007-1039G>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 16/22 | chr2 | 47814906 | ||||||
chr2:47814909
|
C | G | 1 | a0001c0001t0001g0118 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2007-1042G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 16/22 | chr2 | 47814909 | ||||||
chr2:47814919
|
C | A | 5 | a0001c0001t0001g0217a0001c0001t0001g0220a0001c0001t0001g0221others(2): Show | 5 | HG00099.hp2 HG00741.hp2 HG01070.hp2 others(2): Show |
intron_variant | MODIFIER | c.2007-1052G>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 16/22 | chr2 | 47814919 | ||||||
chr2:47815090
|
T | G | 3 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0187 | 3 | HG01243.hp2 HG02886.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.2007-1223A>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 16/22 | chr2 | 47815090 | ||||||
chr2:47815099
|
A | G | 16 | a0001c0001t0001g0001a0001c0001t0001g0093a0001c0001t0001g0094others(13): Show | 17 | HG03492.hp2 HG03704.hp1 NA18942.hp2 others(14): Show |
intron_variant | MODIFIER | c.2007-1232T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 16/22 | chr2 | 47815099 | ||||||
chr2:47815221
|
T | G | 1 | a0001c0001t0001g0023 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2007-1354A>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 16/22 | chr2 | 47815221 | ||||||
chr2:47815433
|
T | G | 1 | a0001c0001t0001g0043 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2007-1566A>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 16/22 | chr2 | 47815433 | ||||||
chr2:47815641
|
C | G | 1 | a0001c0001t0001g0086 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.2007-1774G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 16/22 | chr2 | 47815641 | ||||||
chr2:47815778
|
T | C | 1 | a0001c0001t0002g0248 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2007-1911A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 16/22 | chr2 | 47815778 | ||||||
chr2:47815908
|
G | C | 7 | a0001c0001t0001g0121a0001c0001t0001g0124a0001c0001t0001g0125others(4): Show | 7 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.2007-2041C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 16/22 | chr2 | 47815908 | ||||||
chr2:47816079
|
C | T | 7 | a0001c0001t0001g0264a0001c0001t0001g0287a0001c0001t0001g0288others(4): Show | 7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.2007-2212G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 16/22 | chr2 | 47816079 | ||||||
chr2:47816218
|
C | T | 3 | a0001c0001t0002g0249a0001c0001t0002g0250a0001c0001t0002g0251 | 3 | HG01261.hp2 HG02922.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2007-2351G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 16/22 | chr2 | 47816218 | ||||||
chr2:47816237
|
T | C | 1 | a0001c0001t0003g0243 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2007-2370A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 16/22 | chr2 | 47816237 | ||||||
chr2:47816468
|
A | G | 10 | a0001c0001t0002g0035a0001c0001t0002g0050a0001c0001t0002g0134others(7): Show | 10 | HG02027.hp1 HG02080.hp1 HG02165.hp1 others(7): Show |
intron_variant | MODIFIER | c.2006+2311T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 16/22 | chr2 | 47816468 | ||||||
chr2:47816589
|
G | A | 2 | a0001c0001t0002g0169a0001c0001t0002g0172 | 2 | HG01099.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.2006+2190C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 16/22 | chr2 | 47816589 | ||||||
chr2:47816598
|
A | G | 5 | a0001c0001t0002g0281a0001c0001t0002g0285a0001c0001t0002g0286others(2): Show | 5 | HG00738.hp1 HG01109.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.2006+2181T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 16/22 | chr2 | 47816598 | ||||||
chr2:47816647
|
C | CCA | 28 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(25): Show | 28 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.2006+2130_2006+213 others(6): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 16/22 | chr2 | 47816647 | ||||||
chr2:47816745
|
G | A | 1 | a0001c0002t0002g0302 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2006+2034C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 16/22 | chr2 | 47816745 | ||||||
chr2:47816772
|
C | A | 1 | a0001c0001t0001g0267 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2006+2007G>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 16/22 | chr2 | 47816772 | ||||||
chr2:47816835
|
T | C | 10 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(7): Show | 10 | HG01346.hp1 HG02615.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.2006+1944A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 16/22 | chr2 | 47816835 | ||||||
chr2:47816842
|
T | G | 8 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0175others(5): Show | 8 | HG00099.hp2 HG00741.hp2 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.2006+1937A>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 16/22 | chr2 | 47816842 | ||||||
chr2:47816906
|
G | C | 1 | a0001c0001t0001g0304 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2006+1873C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 16/22 | chr2 | 47816906 | ||||||
chr2:47817021
|
C | G | 2 | a0001c0001t0001g0194a0001c0001t0001g0206 | 2 | HG00609.hp1 HG02056.hp1 |
intron_variant | MODIFIER | c.2006+1758G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 16/22 | chr2 | 47817021 | ||||||
chr2:47817038
|
G | C | 2 | a0001c0001t0001g0194a0001c0001t0001g0206 | 2 | HG00609.hp1 HG02056.hp1 |
intron_variant | MODIFIER | c.2006+1741C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 16/22 | chr2 | 47817038 | ||||||
chr2:47817292
|
T | C | 1 | a0001c0001t0002g0139 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2006+1487A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 16/22 | chr2 | 47817292 | ||||||
chr2:47817307
|
C | T | 1 | a0001c0001t0001g0208 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2006+1472G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 16/22 | chr2 | 47817307 | ||||||
chr2:47817416
|
G | A | 2 | a0001c0001t0001g0275a0001c0001t0001g0276 | 2 | HG01891.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2006+1363C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 16/22 | chr2 | 47817416 | ||||||
chr2:47817461
|
G | C | 1 | a0001c0001t0001g0218 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2006+1318C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 16/22 | chr2 | 47817461 | ||||||
chr2:47817630
|
C | T | 11 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0095others(8): Show | 11 | NA18946.hp1 NA18953.hp2 NA18965.hp1 others(8): Show |
intron_variant | MODIFIER | c.2006+1149G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 16/22 | chr2 | 47817630 | ||||||
chr2:47817633
|
C | T | 192 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(189): Show | 195 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(192): Show |
intron_variant | MODIFIER | c.2006+1146G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 16/22 | chr2 | 47817633 | ||||||
chr2:47817918
|
C | T | 10 | a0001c0001t0001g0001a0001c0001t0001g0082a0001c0001t0001g0083others(7): Show | 11 | HG00544.hp2 HG00597.hp2 NA18942.hp2 others(8): Show |
intron_variant | MODIFIER | c.2006+861G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 16/22 | chr2 | 47817918 | ||||||
chr2:47818056
|
G | A | 1 | a0001c0001t0002g0138 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.2006+723C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 16/22 | chr2 | 47818056 | ||||||
chr2:47818111
|
G | A | 5 | a0001c0001t0002g0050a0001c0001t0003g0282a0001c0001t0003g0293others(2): Show | 5 | HG02145.hp1 HG02717.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.2006+668C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 16/22 | chr2 | 47818111 | ||||||
chr2:47818151
|
A | G | 1 | a0001c0001t0001g0070 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2006+628T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 16/22 | chr2 | 47818151 | ||||||
chr2:47818167
|
T | C | 1 | a0001c0001t0001g0182 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.2006+612A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 16/22 | chr2 | 47818167 | ||||||
chr2:47818873
|
T | TA | 8 | a0001c0001t0001g0059a0001c0001t0001g0167a0001c0001t0002g0181others(5): Show | 8 | HG00738.hp1 HG01109.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1921-10dupT | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 15/22 | chr2 | 47818873 | ||||||
chr2:47819305
|
C | T | 2 | a0001c0001t0001g0227a0001c0001t0001g0228 | 2 | NA18962.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.1798-227G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 14/22 | chr2 | 47819305 | ||||||
chr2:47819364
|
T | C | 12 | a0001c0001t0001g0264a0001c0001t0001g0287a0001c0001t0001g0288others(9): Show | 12 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.1798-286A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 14/22 | chr2 | 47819364 | ||||||
chr2:47819407
|
C | T | 1 | a0001c0001t0010g0132 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1798-329G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 14/22 | chr2 | 47819407 | ||||||
chr2:47819463
|
G | A | 1 | a0001c0002t0002g0034 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1798-385C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 14/22 | chr2 | 47819463 | ||||||
chr2:47819464
|
T | C | 1 | a0001c0001t0003g0243 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1798-386A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 14/22 | chr2 | 47819464 | ||||||
chr2:47819504
|
G | A | 1 | a0001c0001t0014g0284 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1798-426C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 14/22 | chr2 | 47819504 | ||||||
chr2:47819558
|
A | G | 1 | a0001c0001t0002g0248 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1798-480T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 14/22 | chr2 | 47819558 | ||||||
chr2:47819642
|
G | T | 2 | a0001c0001t0002g0139a0001c0001t0013g0165 | 2 | HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1798-564C>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 14/22 | chr2 | 47819642 | ||||||
chr2:47819668
|
A | G | 7 | a0001c0001t0001g0264a0001c0001t0001g0287a0001c0001t0001g0288others(4): Show | 7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.1798-590T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 14/22 | chr2 | 47819668 | ||||||
chr2:47819732
|
T | C | 3 | a0001c0001t0001g0171a0001c0001t0002g0002a0001c0001t0016g0309 | 4 | HG01168.hp1 HG01169.hp2 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.1797+630A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 14/22 | chr2 | 47819732 | ||||||
chr2:47819746
|
T | C | 1 | a0001c0001t0001g0123 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1797+616A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 14/22 | chr2 | 47819746 | ||||||
chr2:47819861
|
T | C | 3 | a0001c0001t0001g0171a0001c0001t0002g0002a0001c0001t0016g0309 | 4 | HG01168.hp1 HG01169.hp2 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.1797+501A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 14/22 | chr2 | 47819861 | ||||||
chr2:47819880
|
G | T | 1 | a0001c0001t0003g0293 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1797+482C>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 14/22 | chr2 | 47819880 | ||||||
chr2:47820061
|
C | A | 4 | a0001c0001t0002g0196a0001c0001t0002g0249a0001c0001t0002g0250others(1): Show | 4 | HG01261.hp2 HG02922.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1797+301G>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 14/22 | chr2 | 47820061 | ||||||
chr2:47820070
|
A | C | 5 | a0001c0001t0002g0281a0001c0001t0002g0285a0001c0001t0002g0286others(2): Show | 5 | HG00738.hp1 HG01109.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.1797+292T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 14/22 | chr2 | 47820070 | ||||||
chr2:47820196
|
A | G | 9 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(6): Show | 9 | HG01346.hp1 HG02615.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.1797+166T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 14/22 | chr2 | 47820196 | ||||||
chr2:47820244
|
C | G | 1 | a0001c0001t0001g0123 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1797+118G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 14/22 | chr2 | 47820244 | ||||||
chr2:47820572
|
G | A | 4 | a0001c0001t0002g0196a0001c0001t0002g0249a0001c0001t0002g0250others(1): Show | 4 | HG01261.hp2 HG02922.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1703-116C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 13/22 | chr2 | 47820572 | ||||||
chr2:47820654
|
C | T | 93 | a0001c0001t0001g0038a0001c0001t0001g0042a0001c0001t0001g0043others(90): Show | 94 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.1703-198G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 13/22 | chr2 | 47820654 | ||||||
chr2:47820927
|
T | C | 3 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0187 | 3 | HG01243.hp2 HG02886.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1703-471A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 13/22 | chr2 | 47820927 | ||||||
chr2:47821023
|
A | C | 6 | a0001c0001t0001g0110a0001c0001t0001g0274a0001c0001t0001g0275others(3): Show | 6 | HG01074.hp2 HG01891.hp2 NA19043.hp1 others(3): Show |
intron_variant | MODIFIER | c.1703-567T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 13/22 | chr2 | 47821023 | ||||||
chr2:47821145
|
C | G | 12 | a0001c0001t0001g0264a0001c0001t0001g0287a0001c0001t0001g0288others(9): Show | 12 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.1703-689G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 13/22 | chr2 | 47821145 | ||||||
chr2:47821201
|
G | A | 5 | a0001c0001t0003g0107a0001c0001t0003g0282a0001c0001t0003g0293others(2): Show | 5 | HG02145.hp1 HG02257.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1703-745C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 13/22 | chr2 | 47821201 | ||||||
chr2:47821201
|
G | C | 1 | a0001c0001t0001g0123 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1703-745C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 13/22 | chr2 | 47821201 | ||||||
chr2:47821337
|
G | A | 1 | a0001c0001t0001g0018 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1702+881C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 13/22 | chr2 | 47821337 | ||||||
chr2:47821365
|
C | T | 1 | a0001c0001t0001g0089 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1702+853G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 13/22 | chr2 | 47821365 | ||||||
chr2:47821367
|
T | A | 1 | a0001c0001t0001g0049 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1702+851A>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 13/22 | chr2 | 47821367 | ||||||
chr2:47821407
|
G | A | 2 | a0001c0001t0001g0051a0001c0001t0001g0079 | 2 | NA18979.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.1702+811C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 13/22 | chr2 | 47821407 | ||||||
chr2:47821440
|
C | T | 2 | a0001c0001t0001g0265a0001c0001t0001g0268 | 2 | HG02717.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1702+778G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 13/22 | chr2 | 47821440 | ||||||
chr2:47821470
|
C | T | 1 | a0001c0001t0001g0265 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1702+748G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 13/22 | chr2 | 47821470 | ||||||
chr2:47821567
|
G | A | 1 | a0001c0001t0001g0116 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1702+651C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 13/22 | chr2 | 47821567 | ||||||
chr2:47821711
|
G | A | 1 | a0001c0001t0001g0125 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1702+507C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 13/22 | chr2 | 47821711 | ||||||
chr2:47821734
|
G | A | 4 | a0001c0001t0002g0281a0001c0001t0002g0285a0001c0001t0002g0286others(1): Show | 4 | HG00738.hp1 HG02559.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1702+484C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 13/22 | chr2 | 47821734 | ||||||
chr2:47821750
|
A | T | 2 | a0001c0001t0001g0210a0001c0001t0001g0211 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1702+468T>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 13/22 | chr2 | 47821750 | ||||||
chr2:47821990
|
G | C | 7 | a0001c0001t0001g0264a0001c0001t0001g0287a0001c0001t0001g0288others(4): Show | 7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.1702+228C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 13/22 | chr2 | 47821990 | ||||||
chr2:47822136
|
G | C | 1 | a0001c0001t0002g0138 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1702+82C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 13/22 | chr2 | 47822136 | ||||||
chr2:47822423
|
T | C | 6 | a0001c0001t0003g0107a0001c0001t0003g0243a0001c0001t0003g0282others(3): Show | 6 | HG02145.hp1 HG02257.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1617-120A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 12/22 | chr2 | 47822423 | ||||||
chr2:47822576
|
G | A | 1 | a0001c0001t0001g0297 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1617-273C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 12/22 | chr2 | 47822576 | ||||||
chr2:47822651
|
C | T | 7 | a0001c0001t0001g0264a0001c0001t0001g0287a0001c0001t0001g0288others(4): Show | 7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.1617-348G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 12/22 | chr2 | 47822651 | ||||||
chr2:47822685
|
T | C | 1 | a0001c0001t0001g0304 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1617-382A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 12/22 | chr2 | 47822685 | ||||||
chr2:47822761
|
T | C | 1 | a0001c0001t0002g0248 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1616+382A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 12/22 | chr2 | 47822761 | ||||||
chr2:47822805
|
A | G | 10 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(7): Show | 10 | HG01346.hp1 HG02615.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.1616+338T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 12/22 | chr2 | 47822805 | ||||||
chr2:47823057
|
T | C | 7 | a0001c0001t0001g0264a0001c0001t0001g0287a0001c0001t0001g0288others(4): Show | 7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.1616+86A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 12/22 | chr2 | 47823057 | ||||||
chr2:47823088
|
T | A | 2 | a0001c0001t0002g0173a0001c0007t0002g0168 | 2 | HG00738.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.1616+55A>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 12/22 | chr2 | 47823088 | ||||||
chr2:47823466
|
C | CTT | 10 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(7): Show | 10 | HG01346.hp1 HG02615.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.1399-107_1399-106i others(4): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47823466 | ||||||
chr2:47823510
|
C | G | 2 | a0001c0002t0002g0283a0001c0002t0002g0302 | 2 | HG01109.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1399-150G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47823510 | ||||||
chr2:47823547
|
A | G | 17 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(14): Show | 17 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(14): Show |
intron_variant | MODIFIER | c.1399-187T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47823547 | ||||||
chr2:47823702
|
G | A | 2 | a0001c0001t0002g0173a0001c0007t0002g0168 | 2 | HG00738.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.1399-342C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47823702 | ||||||
chr2:47823706
|
T | C | 7 | a0001c0001t0001g0264a0001c0001t0001g0287a0001c0001t0001g0288others(4): Show | 7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.1399-346A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47823706 | ||||||
chr2:47823763
|
T | TA | 7 | a0001c0001t0001g0017a0001c0001t0001g0021a0001c0001t0001g0023others(4): Show | 7 | HG01433.hp1 HG02818.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1399-404dupT | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47823763 | ||||||
chr2:47823764
|
A | T | 3 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184 | 3 | HG00323.hp2 HG00642.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.1399-404T>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47823764 | ||||||
chr2:47823849
|
A | AT | 7 | a0001c0001t0002g0143a0001c0001t0003g0107a0001c0001t0003g0243others(4): Show | 7 | HG02145.hp1 HG02257.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1399-490dupA | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47823849 | ||||||
chr2:47823862
|
T | A | 1 | a0001c0001t0001g0277 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1399-502A>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47823862 | ||||||
chr2:47823904
|
G | T | 7 | a0001c0001t0001g0264a0001c0001t0001g0287a0001c0001t0001g0288others(4): Show | 7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.1399-544C>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47823904 | ||||||
chr2:47824032
|
C | G | 10 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(7): Show | 10 | HG01346.hp1 HG02615.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.1399-672G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47824032 | ||||||
chr2:47824072
|
A | G | 1 | a0001c0001t0009g0010 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1399-712T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47824072 | ||||||
chr2:47824324
|
G | A | 7 | a0001c0001t0001g0264a0001c0001t0001g0287a0001c0001t0001g0288others(4): Show | 7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.1399-964C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47824324 | ||||||
chr2:47824543
|
T | A | 1 | a0001c0001t0001g0209 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1399-1183A>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47824543 | ||||||
chr2:47824610
|
A | T | 1 | a0001c0001t0010g0132 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1399-1250T>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47824610 | ||||||
chr2:47824710
|
G | A | 4 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0199others(1): Show | 4 | NA18971.hp1 NA18993.hp2 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.1399-1350C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47824710 | ||||||
chr2:47824763
|
T | G | 9 | a0001c0002t0002g0030a0001c0002t0002g0031a0001c0002t0002g0032others(6): Show | 9 | HG01109.hp2 HG01884.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1399-1403A>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47824763 | ||||||
chr2:47824840
|
T | C | 1 | a0001c0001t0001g0228 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1399-1480A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47824840 | ||||||
chr2:47824852
|
A | G | 2 | a0001c0001t0001g0192a0001c0001t0001g0242 | 2 | HG03492.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.1399-1492T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47824852 | ||||||
chr2:47824965
|
A | G | 1 | a0001c0001t0011g0040 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1399-1605T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47824965 | ||||||
chr2:47824974
|
C | T | 1 | a0001c0001t0001g0188 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1399-1614G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47824974 | ||||||
chr2:47825026
|
T | C | 12 | a0001c0001t0001g0058a0001c0001t0001g0197a0001c0001t0001g0198others(9): Show | 12 | HG00438.hp1 HG02155.hp2 HG02165.hp2 others(9): Show |
intron_variant | MODIFIER | c.1399-1666A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47825026 | ||||||
chr2:47825057
|
T | C | 7 | a0001c0001t0001g0264a0001c0001t0001g0287a0001c0001t0001g0288others(4): Show | 7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.1399-1697A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47825057 | ||||||
chr2:47825091
|
AT | A | 7 | a0001c0001t0001g0264a0001c0001t0001g0287a0001c0001t0001g0288others(4): Show | 7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.1399-1732delA | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47825091 | ||||||
chr2:47825143
|
T | C | 1 | a0001c0001t0001g0189 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1399-1783A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47825143 | ||||||
chr2:47825230
|
GAAC | G | 4 | a0001c0001t0003g0282a0001c0001t0003g0293a0001c0001t0003g0294others(1): Show | 4 | HG02145.hp1 HG02717.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1399-1873_1399-187 others(7): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47825230 | ||||||
chr2:47825270
|
T | C | 1 | a0001c0001t0001g0111 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1399-1910A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47825270 | ||||||
chr2:47825412
|
T | C | 1 | a0001c0001t0001g0111 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1399-2052A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47825412 | ||||||
chr2:47825513
|
C | G | 4 | a0001c0001t0002g0281a0001c0001t0002g0285a0001c0001t0002g0286others(1): Show | 4 | HG00738.hp1 HG02559.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1399-2153G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47825513 | ||||||
chr2:47825571
|
C | CT | 30 | a0001c0001t0001g0044a0001c0001t0001g0047a0001c0001t0001g0071others(27): Show | 31 | HG01074.hp2 HG01169.hp1 HG01169.hp2 others(28): Show |
intron_variant | MODIFIER | c.1399-2212dupA | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47825571 | ||||||
chr2:47825571
|
CT | C | 17 | a0001c0001t0001g0052a0001c0001t0001g0068a0001c0001t0001g0083others(14): Show | 17 | HG00738.hp1 HG01070.hp1 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.1399-2212delA | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47825571 | ||||||
chr2:47825574
|
T | C | 2 | a0001c0001t0001g0189a0001c0001t0001g0239 | 2 | HG02647.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.1399-2214A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47825574 | ||||||
chr2:47825727
|
G | A | 1 | a0001c0001t0001g0075 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1399-2367C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47825727 | ||||||
chr2:47825735
|
C | G | 1 | a0001c0001t0002g0153 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1399-2375G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47825735 | ||||||
chr2:47825758
|
G | C | 3 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184 | 3 | HG00323.hp2 HG00642.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.1399-2398C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47825758 | ||||||
chr2:47825823
|
C | G | 7 | a0001c0001t0001g0264a0001c0001t0001g0287a0001c0001t0001g0288others(4): Show | 7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.1399-2463G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47825823 | ||||||
chr2:47825840
|
G | A | 1 | a0001c0001t0002g0112 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1399-2480C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47825840 | ||||||
chr2:47825881
|
A | G | 1 | a0001c0001t0002g0303 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1399-2521T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47825881 | ||||||
chr2:47825967
|
C | T | 1 | a0001c0001t0001g0043 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1399-2607G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47825967 | ||||||
chr2:47826035
|
TAA | T | 8 | a0001c0002t0002g0030a0001c0002t0002g0031a0001c0002t0002g0032others(5): Show | 8 | HG01884.hp2 HG02109.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.1399-2677_1399-267 others(6): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47826035 | ||||||
chr2:47826037
|
A | G | 1 | a0001c0001t0001g0268 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1399-2677T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47826037 | ||||||
chr2:47826050
|
C | G | 18 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(15): Show | 18 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.1399-2690G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47826050 | ||||||
chr2:47826068
|
G | C | 1 | a0001c0001t0001g0189 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1399-2708C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47826068 | ||||||
chr2:47826121
|
C | T | 4 | a0001c0001t0002g0196a0001c0001t0002g0249a0001c0001t0002g0250others(1): Show | 4 | HG01261.hp2 HG02922.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1399-2761G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47826121 | ||||||
chr2:47826197
|
T | C | 1 | a0001c0001t0010g0132 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1399-2837A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47826197 | ||||||
chr2:47826206
|
C | T | 1 | a0001c0001t0001g0077 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1399-2846G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47826206 | ||||||
chr2:47826225
|
T | A | 1 | a0001c0001t0001g0189 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1399-2865A>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47826225 | ||||||
chr2:47826225
|
T | G | 1 | a0001c0001t0002g0148 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1399-2865A>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47826225 | ||||||
chr2:47826236
|
T | G | 1 | a0001c0001t0010g0132 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1399-2876A>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47826236 | ||||||
chr2:47826303
|
C | T | 1 | a0001c0001t0002g0159 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1399-2943G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47826303 | ||||||
chr2:47826348
|
C | T | 10 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0021others(7): Show | 10 | HG01433.hp1 HG02451.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.1399-2988G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47826348 | ||||||
chr2:47826495
|
T | G | 1 | a0001c0001t0002g0180 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1399-3135A>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47826495 | ||||||
chr2:47826628
|
G | C | 17 | a0001c0001t0001g0005a0001c0001t0001g0017a0001c0001t0001g0018others(14): Show | 18 | HG01243.hp1 HG01433.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.1399-3268C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47826628 | ||||||
chr2:47826640
|
A | C | 1 | a0001c0001t0002g0181 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1399-3280T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47826640 | ||||||
chr2:47826670
|
T | C | 19 | a0001c0001t0001g0036a0001c0001t0001g0039a0001c0001t0001g0041others(16): Show | 19 | HG00099.hp1 HG00099.hp2 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.1399-3310A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47826670 | ||||||
chr2:47826690
|
A | AT | 7 | a0001c0001t0001g0264a0001c0001t0001g0287a0001c0001t0001g0288others(4): Show | 7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.1399-3331dupA | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47826690 | ||||||
chr2:47826774
|
T | G | 10 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(7): Show | 10 | HG01346.hp1 HG02615.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.1399-3414A>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47826774 | ||||||
chr2:47826786
|
C | G | 19 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(16): Show | 19 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.1399-3426G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47826786 | ||||||
chr2:47826992
|
C | T | 1 | a0001c0001t0001g0052 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1399-3632G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47826992 | ||||||
chr2:47827138
|
A | C | 1 | a0001c0001t0002g0225 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1399-3778T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47827138 | ||||||
chr2:47827305
|
TTTTG | T | 6 | a0001c0001t0001g0059a0001c0001t0001g0104a0001c0001t0002g0281others(3): Show | 6 | HG00738.hp1 HG02559.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1399-3949_1399-394 others(8): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47827305 | ||||||
chr2:47827367
|
C | T | 1 | a0001c0001t0011g0040 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1399-4007G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47827367 | ||||||
chr2:47827375
|
C | T | 1 | a0001c0001t0010g0132 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1399-4015G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47827375 | ||||||
chr2:47827390
|
T | A | 1 | a0001c0001t0001g0240 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1399-4030A>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47827390 | ||||||
chr2:47827393
|
A | G | 10 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(7): Show | 10 | HG01346.hp1 HG02615.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.1399-4033T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47827393 | ||||||
chr2:47827472
|
A | G | 7 | a0001c0001t0001g0264a0001c0001t0001g0287a0001c0001t0001g0288others(4): Show | 7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.1399-4112T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47827472 | ||||||
chr2:47827498
|
G | C | 1 | a0001c0001t0003g0107 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1399-4138C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47827498 | ||||||
chr2:47827508
|
T | C | 1 | a0001c0001t0001g0304 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1399-4148A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47827508 | ||||||
chr2:47827701
|
A | AT | 17 | a0001c0001t0001g0066a0001c0001t0001g0070a0001c0001t0001g0071others(14): Show | 17 | HG00609.hp1 HG00609.hp2 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.1399-4342dupA | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47827701 | ||||||
chr2:47827767
|
G | C | 3 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184 | 3 | HG00323.hp2 HG00642.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.1399-4407C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47827767 | ||||||
chr2:47827866
|
A | G | 2 | a0001c0002t0002g0283a0001c0002t0002g0302 | 2 | HG01109.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1398+4483T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47827866 | ||||||
chr2:47828172
|
A | G | 7 | a0001c0001t0001g0264a0001c0001t0001g0287a0001c0001t0001g0288others(4): Show | 7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.1398+4177T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47828172 | ||||||
chr2:47828216
|
T | C | 1 | a0001c0001t0001g0095 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1398+4133A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47828216 | ||||||
chr2:47828344
|
C | G | 10 | a0001c0001t0001g0264a0001c0001t0001g0287a0001c0001t0001g0288others(7): Show | 10 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.1398+4005G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47828344 | ||||||
chr2:47828419
|
C | A | 7 | a0001c0001t0001g0264a0001c0001t0001g0287a0001c0001t0001g0288others(4): Show | 7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.1398+3930G>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47828419 | ||||||
chr2:47828468
|
C | T | 9 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(6): Show | 9 | HG01346.hp1 HG02615.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.1398+3881G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47828468 | ||||||
chr2:47828521
|
T | C | 1 | a0001c0001t0001g0038 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1398+3828A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47828521 | ||||||
chr2:47828571
|
T | C | 11 | a0001c0001t0001g0122a0001c0001t0001g0127a0001c0001t0001g0128others(8): Show | 11 | HG00639.hp2 HG00642.hp1 HG01069.hp2 others(8): Show |
intron_variant | MODIFIER | c.1398+3778A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47828571 | ||||||
chr2:47828603
|
T | C | 5 | a0001c0001t0001g0274a0001c0001t0001g0275a0001c0001t0001g0276others(2): Show | 5 | HG01074.hp2 HG01891.hp2 NA19240.hp2 others(2): Show |
intron_variant | MODIFIER | c.1398+3746A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47828603 | ||||||
chr2:47828609
|
C | CA | 6 | a0001c0001t0001g0036a0001c0001t0001g0074a0001c0001t0001g0102others(3): Show | 6 | HG00544.hp2 HG02135.hp1 HG02602.hp2 others(3): Show |
intron_variant | MODIFIER | c.1398+3739dupT | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47828609 | ||||||
chr2:47828609
|
CA | C | 7 | a0001c0001t0001g0264a0001c0001t0001g0287a0001c0001t0001g0288others(4): Show | 7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.1398+3739delT | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47828609 | ||||||
chr2:47828821
|
T | C | 2 | a0001c0002t0002g0283a0001c0002t0002g0302 | 2 | HG01109.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1398+3528A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47828821 | ||||||
chr2:47828860
|
CTTA | C | 6 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(3): Show | 6 | NA18971.hp2 NA19066.hp1 NA19074.hp1 others(3): Show |
intron_variant | MODIFIER | c.1398+3486_1398+348 others(7): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47828860 | ||||||
chr2:47828904
|
A | C | 1 | a0001c0001t0001g0025 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1398+3445T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47828904 | ||||||
chr2:47828977
|
T | G | 1 | a0001c0001t0001g0224 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1398+3372A>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47828977 | ||||||
chr2:47829029
|
C | G | 7 | a0001c0001t0001g0264a0001c0001t0001g0287a0001c0001t0001g0288others(4): Show | 7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.1398+3320G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47829029 | ||||||
chr2:47829055
|
G | C | 3 | a0001c0001t0001g0214a0001c0001t0001g0238a0001c0001t0001g0247 | 3 | HG02809.hp2 HG03139.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1398+3294C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47829055 | ||||||
chr2:47829092
|
G | A | 297 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(294): Show | 302 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.1398+3257C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47829092 | ||||||
chr2:47829110
|
G | T | 7 | a0001c0001t0001g0264a0001c0001t0001g0287a0001c0001t0001g0288others(4): Show | 7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.1398+3239C>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47829110 | ||||||
chr2:47829280
|
G | A | 1 | a0001c0001t0001g0092 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1398+3069C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47829280 | ||||||
chr2:47829365
|
C | A | 2 | a0001c0001t0001g0256a0001c0001t0001g0257 | 2 | NA18998.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.1398+2984G>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47829365 | ||||||
chr2:47829834
|
T | G | 6 | a0001c0001t0003g0107a0001c0001t0003g0243a0001c0001t0003g0282others(3): Show | 6 | HG02145.hp1 HG02257.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1398+2515A>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47829834 | ||||||
chr2:47829905
|
T | C | 1 | a0001c0001t0001g0021 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1398+2444A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47829905 | ||||||
chr2:47829968
|
C | A | 1 | a0001c0001t0002g0249 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1398+2381G>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47829968 | ||||||
chr2:47830015
|
A | G | 20 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(17): Show | 20 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.1398+2334T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47830015 | ||||||
chr2:47830149
|
T | A | 9 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(6): Show | 9 | HG01346.hp1 HG02615.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.1398+2200A>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47830149 | ||||||
chr2:47830181
|
G | C | 2 | a0001c0001t0001g0094a0001c0001t0001g0096 | 2 | NA18946.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.1398+2168C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47830181 | ||||||
chr2:47830201
|
A | G | 9 | a0001c0001t0003g0282a0001c0002t0002g0030a0001c0002t0002g0031others(6): Show | 9 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.1398+2148T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47830201 | ||||||
chr2:47830282
|
G | A | 1 | a0001c0001t0001g0190 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1398+2067C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47830282 | ||||||
chr2:47830350
|
C | G | 1 | a0001c0001t0001g0192 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1398+1999G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47830350 | ||||||
chr2:47830371
|
C | T | 1 | a0001c0001t0001g0267 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1398+1978G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47830371 | ||||||
chr2:47830388
|
A | G | 2 | a0001c0001t0001g0092a0001c0001t0002g0137 | 2 | HG02735.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.1398+1961T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47830388 | ||||||
chr2:47830418
|
G | C | 9 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(6): Show | 9 | HG01346.hp1 HG02615.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.1398+1931C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47830418 | ||||||
chr2:47830515
|
A | T | 1 | a0001c0001t0001g0056 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1398+1834T>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47830515 | ||||||
chr2:47830581
|
T | C | 1 | a0001c0001t0001g0265 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1398+1768A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47830581 | ||||||
chr2:47830597
|
A | G | 1 | a0001c0002t0002g0283 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1398+1752T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47830597 | ||||||
chr2:47830668
|
T | A | 2 | a0001c0001t0001g0260a0001c0001t0001g0261 | 2 | NA18957.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.1398+1681A>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47830668 | ||||||
chr2:47830676
|
C | T | 1 | a0001c0001t0001g0255 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1398+1673G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47830676 | ||||||
chr2:47830788
|
G | C | 4 | a0001c0001t0002g0196a0001c0001t0002g0249a0001c0001t0002g0250others(1): Show | 4 | HG01261.hp2 HG02922.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1398+1561C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47830788 | ||||||
chr2:47830921
|
C | T | 4 | a0001c0001t0002g0140a0001c0001t0002g0141a0001c0001t0002g0157others(1): Show | 4 | HG02027.hp1 HG02165.hp1 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.1398+1428G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47830921 | ||||||
chr2:47830948
|
G | A | 1 | a0001c0001t0001g0234 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1398+1401C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47830948 | ||||||
chr2:47831019
|
G | C | 1 | a0001c0001t0001g0237 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1398+1330C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47831019 | ||||||
chr2:47831037
|
G | A | 1 | a0001c0001t0001g0083 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1398+1312C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47831037 | ||||||
chr2:47831083
|
G | A | 1 | a0001c0001t0002g0180 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1398+1266C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47831083 | ||||||
chr2:47831094
|
C | T | 26 | a0001c0001t0001g0047a0001c0001t0001g0092a0001c0001t0001g0122others(23): Show | 26 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.1398+1255G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47831094 | ||||||
chr2:47831142
|
C | T | 17 | a0001c0001t0001g0005a0001c0001t0001g0017a0001c0001t0001g0018others(14): Show | 18 | HG01243.hp1 HG01433.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.1398+1207G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47831142 | ||||||
chr2:47831298
|
C | T | 9 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(6): Show | 9 | HG01346.hp1 HG02615.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.1398+1051G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47831298 | ||||||
chr2:47831427
|
G | GA | 22 | a0001c0001t0001g0061a0001c0001t0001g0079a0001c0001t0001g0086others(19): Show | 22 | HG00280.hp1 HG00544.hp2 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.1398+921dupT | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47831427 | ||||||
chr2:47831427
|
GA | G | 10 | a0001c0001t0001g0051a0001c0001t0001g0058a0001c0001t0001g0065others(7): Show | 10 | HG00280.hp2 HG00621.hp1 HG01070.hp1 others(7): Show |
intron_variant | MODIFIER | c.1398+921delT | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47831427 | ||||||
chr2:47831427
|
GAA | G | 21 | a0001c0001t0001g0072a0001c0001t0001g0208a0001c0001t0001g0209others(18): Show | 21 | HG00621.hp2 HG00738.hp1 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.1398+920_1398+921d others(4): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47831427 | ||||||
chr2:47831452
|
A | C | 25 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(22): Show | 25 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.1398+897T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47831452 | ||||||
chr2:47831503
|
T | C | 7 | a0001c0001t0001g0264a0001c0001t0001g0287a0001c0001t0001g0288others(4): Show | 7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.1398+846A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47831503 | ||||||
chr2:47831785
|
A | C | 7 | a0001c0001t0001g0264a0001c0001t0001g0287a0001c0001t0001g0288others(4): Show | 7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.1398+564T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47831785 | ||||||
chr2:47831838
|
A | C | 3 | a0001c0001t0001g0214a0001c0001t0001g0238a0001c0001t0001g0247 | 3 | HG02809.hp2 HG03139.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1398+511T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47831838 | ||||||
chr2:47831977
|
A | G | 1 | a0001c0001t0001g0212 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1398+372T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47831977 | ||||||
chr2:47831990
|
C | G | 1 | a0001c0001t0001g0005 | 2 | HG02976.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1398+359G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47831990 | ||||||
chr2:47831998
|
TG | T | 9 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(6): Show | 9 | HG01346.hp1 HG02615.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.1398+350delC | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47831998 | ||||||
chr2:47832020
|
T | C | 32 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(29): Show | 32 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(29): Show |
intron_variant | MODIFIER | c.1398+329A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47832020 | ||||||
chr2:47832098
|
G | C | 1 | a0001c0001t0002g0145 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1398+251C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47832098 | ||||||
chr2:47832294
|
T | C | 2 | a0001c0001t0001g0238a0001c0001t0001g0247 | 2 | HG02809.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1398+55A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47832294 | ||||||
chr2:47832330
|
TAAA | T | 3 | a0001c0001t0001g0151a0001c0001t0002g0112a0001c0001t0002g0162 | 3 | NA19066.hp2 NA19079.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.1398+16_1398+18del others(3): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47832330 | ||||||
chr2:47832332
|
AAAAT | A | 44 | a0001c0001t0001g0167a0001c0001t0001g0175a0001c0001t0001g0188others(41): Show | 44 | HG00099.hp1 HG00735.hp1 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.1398+13_1398+16del others(4): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47832332 | ||||||
chr2:47832336
|
T | C | 1 | a0001c0001t0002g0147 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1398+13A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47832336 | ||||||
chr2:47832697
|
T | G | 1 | a0001c0001t0002g0179 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1154-19A>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 9/22 | chr2 | 47832697 | ||||||
chr2:47833130
|
T | A | 1 | a0001c0001t0001g0290 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.935-60A>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 7/22 | chr2 | 47833130 | ||||||
chr2:47833174
|
G | T | 1 | a0001c0001t0001g0287 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.935-104C>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 7/22 | chr2 | 47833174 | ||||||
chr2:47833205
|
C | G | 17 | a0001c0001t0001g0005a0001c0001t0001g0017a0001c0001t0001g0018others(14): Show | 18 | HG01243.hp1 HG01433.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.935-135G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 7/22 | chr2 | 47833205 | ||||||
chr2:47833242
|
T | C | 4 | a0001c0001t0001g0212a0001c0001t0001g0214a0001c0001t0001g0238others(1): Show | 4 | HG02809.hp2 HG03139.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.935-172A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 7/22 | chr2 | 47833242 | ||||||
chr2:47833337
|
G | C | 1 | a0001c0001t0001g0191 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.935-267C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 7/22 | chr2 | 47833337 | ||||||
chr2:47833418
|
T | G | 3 | a0001c0001t0001g0227a0001c0001t0001g0228a0001c0001t0002g0225 | 3 | NA18962.hp2 NA18991.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.935-348A>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 7/22 | chr2 | 47833418 | ||||||
chr2:47833450
|
A | C | 1 | a0001c0001t0002g0035 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.935-380T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 7/22 | chr2 | 47833450 | ||||||
chr2:47833510
|
G | C | 1 | a0001c0001t0001g0104 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.935-440C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 7/22 | chr2 | 47833510 | ||||||
chr2:47833641
|
G | C | 3 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184 | 3 | HG00323.hp2 HG00642.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.935-571C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 7/22 | chr2 | 47833641 | ||||||
chr2:47833737
|
T | C | 14 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(11): Show | 14 | HG01346.hp1 HG02615.hp2 HG02723.hp1 others(11): Show |
intron_variant | MODIFIER | c.935-667A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 7/22 | chr2 | 47833737 | ||||||
chr2:47833794
|
C | T | 1 | a0001c0001t0001g0123 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.935-724G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 7/22 | chr2 | 47833794 | ||||||
chr2:47833808
|
G | A | 10 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0044others(7): Show | 10 | HG00639.hp1 HG01109.hp1 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.935-738C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 7/22 | chr2 | 47833808 | ||||||
chr2:47833978
|
T | G | 2 | a0001c0002t0002g0283a0001c0002t0002g0302 | 2 | HG01109.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.934+601A>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 7/22 | chr2 | 47833978 | ||||||
chr2:47834057
|
G | C | 1 | a0001c0001t0010g0132 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.934+522C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 7/22 | chr2 | 47834057 | ||||||
chr2:47834082
|
G | A | 7 | a0001c0001t0001g0264a0001c0001t0001g0287a0001c0001t0001g0288others(4): Show | 7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.934+497C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 7/22 | chr2 | 47834082 | ||||||
chr2:47834171
|
G | A | 1 | a0001c0001t0020g0313 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.934+408C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 7/22 | chr2 | 47834171 | ||||||
chr2:47834201
|
T | C | 1 | a0004c0005t0002g0308 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.934+378A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 7/22 | chr2 | 47834201 | ||||||
chr2:47834208
|
C | G | 28 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(25): Show | 28 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.934+371G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 7/22 | chr2 | 47834208 | ||||||
chr2:47834289
|
A | G | 28 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(25): Show | 28 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.934+290T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 7/22 | chr2 | 47834289 | ||||||
chr2:47834333
|
T | C | 2 | a0001c0002t0002g0283a0001c0002t0002g0302 | 2 | HG01109.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.934+246A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 7/22 | chr2 | 47834333 | ||||||
chr2:47834395
|
T | C | 1 | a0001c0001t0001g0097 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.934+184A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 7/22 | chr2 | 47834395 | ||||||
chr2:47834472
|
CCAG | C | 5 | a0001c0001t0002g0281a0001c0001t0002g0285a0001c0001t0002g0286others(2): Show | 5 | HG00738.hp1 HG01109.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.934+104_934+106del others(3): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 7/22 | chr2 | 47834472 | ||||||
chr2:47835049
|
C | G | 3 | a0001c0001t0001g0171a0001c0001t0002g0002a0001c0001t0016g0309 | 4 | HG01168.hp1 HG01169.hp2 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.718-178G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 5/22 | chr2 | 47835049 | ||||||
chr2:47835098
|
A | G | 7 | a0001c0001t0001g0264a0001c0001t0001g0287a0001c0001t0001g0288others(4): Show | 7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.718-227T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 5/22 | chr2 | 47835098 | ||||||
chr2:47835207
|
A | G | 5 | a0001c0001t0003g0243a0001c0001t0003g0282a0001c0001t0003g0293others(2): Show | 5 | HG02145.hp1 HG02717.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.718-336T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 5/22 | chr2 | 47835207 | ||||||
chr2:47835230
|
A | T | 1 | a0001c0001t0003g0282 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.718-359T>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 5/22 | chr2 | 47835230 | ||||||
chr2:47835232
|
C | T | 7 | a0001c0001t0001g0264a0001c0001t0001g0287a0001c0001t0001g0288others(4): Show | 7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.718-361G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 5/22 | chr2 | 47835232 | ||||||
chr2:47835363
|
C | T | 1 | a0001c0001t0002g0250 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.718-492G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 5/22 | chr2 | 47835363 | ||||||
chr2:47835371
|
T | C | 6 | a0001c0001t0001g0110a0001c0001t0001g0274a0001c0001t0001g0275others(3): Show | 6 | HG01074.hp2 HG01891.hp2 NA19043.hp1 others(3): Show |
intron_variant | MODIFIER | c.718-500A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 5/22 | chr2 | 47835371 | ||||||
chr2:47835622
|
G | A | 7 | a0001c0001t0001g0264a0001c0001t0001g0287a0001c0001t0001g0288others(4): Show | 7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.717+250C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 5/22 | chr2 | 47835622 | ||||||
chr2:47835644
|
T | C | 242 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(239): Show | 246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.717+228A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 5/22 | chr2 | 47835644 | ||||||
chr2:47835645
|
G | A | 46 | a0001c0001t0001g0051a0001c0001t0001g0053a0001c0001t0001g0059others(43): Show | 46 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(43): Show |
intron_variant | MODIFIER | c.717+227C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 5/22 | chr2 | 47835645 | ||||||
chr2:47835749
|
C | G | 5 | a0001c0001t0003g0243a0001c0001t0003g0282a0001c0001t0003g0293others(2): Show | 5 | HG02145.hp1 HG02717.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.717+123G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 5/22 | chr2 | 47835749 | ||||||
chr2:47836027
|
T | C | 1 | a0001c0001t0003g0243 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.588-26A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 4/22 | chr2 | 47836027 | ||||||
chr2:47836102
|
G | C | 7 | a0001c0001t0001g0264a0001c0001t0001g0287a0001c0001t0001g0288others(4): Show | 7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.588-101C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 4/22 | chr2 | 47836102 | ||||||
chr2:47836110
|
G | A | 2 | a0001c0001t0001g0059a0001c0001t0001g0104 | 2 | NA18966.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.588-109C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 4/22 | chr2 | 47836110 | ||||||
chr2:47836110
|
G | T | 1 | a0001c0001t0001g0219 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.588-109C>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 4/22 | chr2 | 47836110 | ||||||
chr2:47836112
|
A | T | 2 | a0001c0001t0001g0059a0001c0001t0001g0104 | 2 | NA18966.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.588-111T>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 4/22 | chr2 | 47836112 | ||||||
chr2:47836176
|
T | C | 1 | a0001c0001t0003g0282 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.588-175A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 4/22 | chr2 | 47836176 | ||||||
chr2:47836251
|
G | A | 1 | a0001c0001t0001g0200 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.588-250C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 4/22 | chr2 | 47836251 | ||||||
chr2:47836516
|
A | G | 1 | a0001c0001t0002g0185 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.588-515T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 4/22 | chr2 | 47836516 | ||||||
chr2:47836559
|
A | G | 1 | a0001c0001t0003g0107 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.588-558T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 4/22 | chr2 | 47836559 | ||||||
chr2:47836595
|
C | T | 1 | a0001c0001t0002g0248 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.588-594G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 4/22 | chr2 | 47836595 | ||||||
chr2:47836652
|
A | C | 1 | a0001c0001t0001g0175 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.588-651T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 4/22 | chr2 | 47836652 | ||||||
chr2:47837075
|
A | T | 1 | a0001c0001t0001g0175 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.588-1074T>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 4/22 | chr2 | 47837075 | ||||||
chr2:47837176
|
T | C | 2 | a0001c0002t0002g0283a0001c0002t0002g0302 | 2 | HG01109.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.588-1175A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 4/22 | chr2 | 47837176 | ||||||
chr2:47837238
|
A | C | 2 | a0001c0001t0001g0227a0001c0001t0001g0228 | 2 | NA18962.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.588-1237T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 4/22 | chr2 | 47837238 | ||||||
chr2:47837502
|
G | A | 1 | a0001c0001t0010g0132 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.587+1357C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 4/22 | chr2 | 47837502 | ||||||
chr2:47837576
|
T | C | 1 | a0001c0001t0002g0137 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.587+1283A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 4/22 | chr2 | 47837576 | ||||||
chr2:47837776
|
G | A | 1 | a0001c0001t0001g0226 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.587+1083C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 4/22 | chr2 | 47837776 | ||||||
chr2:47837793
|
C | T | 3 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0226 | 3 | HG01070.hp2 HG01071.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.587+1066G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 4/22 | chr2 | 47837793 | ||||||
chr2:47837871
|
C | G | 1 | a0002c0004t0002g0266 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.587+988G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 4/22 | chr2 | 47837871 | ||||||
chr2:47837904
|
C | T | 1 | a0001c0001t0001g0209 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.587+955G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 4/22 | chr2 | 47837904 | ||||||
chr2:47837909
|
T | C | 5 | a0001c0001t0002g0281a0001c0001t0002g0285a0001c0001t0002g0286others(2): Show | 5 | HG00738.hp1 HG01109.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.587+950A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 4/22 | chr2 | 47837909 | ||||||
chr2:47837992
|
G | A | 7 | a0001c0001t0001g0264a0001c0001t0001g0287a0001c0001t0001g0288others(4): Show | 7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.587+867C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 4/22 | chr2 | 47837992 | ||||||
chr2:47838061
|
CA | C | 218 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(215): Show | 222 | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(219): Show |
intron_variant | MODIFIER | c.587+797delT | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 4/22 | chr2 | 47838061 | ||||||
chr2:47838061
|
CAA | C | 18 | a0001c0001t0001g0184a0001c0001t0001g0287a0001c0001t0001g0288others(15): Show | 18 | HG00280.hp2 HG00323.hp2 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.587+796_587+797del others(2): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 4/22 | chr2 | 47838061 | ||||||
chr2:47838104
|
A | G | 2 | a0001c0001t0001g0064a0001c0001t0001g0068 | 2 | HG02071.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.587+755T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 4/22 | chr2 | 47838104 | ||||||
chr2:47838428
|
G | GAATTACT others(22): Show |
14 | a0001c0001t0001g0004a0001c0001t0001g0186a0001c0001t0001g0195others(11): Show | 15 | HG02055.hp2 HG02615.hp1 HG02630.hp2 others(12): Show |
intron_variant | MODIFIER | c.587+402_587+430dup others(29): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 4/22 | chr2 | 47838428 | ||||||
chr2:47838498
|
G | T | 1 | a0001c0001t0002g0172 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.587+361C>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 4/22 | chr2 | 47838498 | ||||||
chr2:47838605
|
C | T | 29 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(26): Show | 29 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.587+254G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 4/22 | chr2 | 47838605 | ||||||
chr2:47839092
|
G | C | 5 | a0001c0001t0003g0107a0001c0001t0003g0282a0001c0001t0003g0293others(2): Show | 5 | HG02145.hp1 HG02257.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.443-89C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 3/22 | chr2 | 47839092 | ||||||
chr2:47839093
|
CT | C | 9 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0044others(6): Show | 9 | HG00639.hp1 HG01109.hp1 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.443-91delA | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 3/22 | chr2 | 47839093 | ||||||
chr2:47839130
|
T | C | 1 | a0001c0001t0001g0241 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.443-127A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 3/22 | chr2 | 47839130 | ||||||
chr2:47839505
|
A | G | 2 | a0001c0001t0001g0088a0001c0001t0001g0118 | 2 | NA18747.hp2 NA18946.hp2 |
splice_region_variant&intron_variant | LOW | c.361-5T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 2/22 | chr2 | 47839505 | ||||||
chr2:47839607
|
A | G | 1 | a0001c0001t0003g0107 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.360+35T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 2/22 | chr2 | 47839607 | ||||||
chr2:47839872
|
G | C | 1 | a0001c0001t0001g0304 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.233-103C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47839872 | ||||||
chr2:47840029
|
C | T | 4 | a0001c0001t0001g0061a0001c0001t0001g0086a0001c0001t0001g0190others(1): Show | 4 | HG02071.hp1 NA18967.hp1 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.233-260G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47840029 | ||||||
chr2:47840093
|
G | A | 4 | a0001c0001t0002g0281a0001c0001t0002g0285a0001c0001t0002g0286others(1): Show | 4 | HG00738.hp1 HG02559.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.233-324C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47840093 | ||||||
chr2:47840128
|
A | G | 7 | a0001c0001t0001g0264a0001c0001t0001g0287a0001c0001t0001g0288others(4): Show | 7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.233-359T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47840128 | ||||||
chr2:47840144
|
C | T | 1 | a0001c0001t0002g0162 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.233-375G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47840144 | ||||||
chr2:47840164
|
TG | T | 3 | a0001c0001t0003g0293a0001c0001t0003g0294a0001c0001t0003g0295 | 3 | HG02717.hp1 HG03225.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.233-396delC | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47840164 | ||||||
chr2:47840195
|
G | A | 1 | a0001c0001t0001g0275 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.233-426C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47840195 | ||||||
chr2:47840273
|
G | C | 1 | a0001c0001t0001g0116 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.233-504C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47840273 | ||||||
chr2:47840451
|
CT | C | 15 | a0001c0001t0001g0228a0001c0001t0001g0264a0001c0001t0002g0135others(12): Show | 15 | HG00735.hp1 HG01070.hp1 HG01255.hp2 others(12): Show |
intron_variant | MODIFIER | c.233-683delA | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47840451 | ||||||
chr2:47840487
|
G | A | 1 | a0001c0001t0002g0248 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.233-718C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47840487 | ||||||
chr2:47840490
|
A | G | 11 | a0001c0001t0001g0264a0001c0001t0001g0287a0001c0001t0001g0288others(8): Show | 11 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.233-721T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47840490 | ||||||
chr2:47840513
|
C | T | 1 | a0001c0001t0002g0035 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.233-744G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47840513 | ||||||
chr2:47840641
|
A | G | 1 | a0001c0002t0002g0032 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.233-872T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47840641 | ||||||
chr2:47840723
|
C | T | 1 | a0001c0001t0009g0010 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.233-954G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47840723 | ||||||
chr2:47840726
|
C | G | 1 | a0001c0001t0001g0200 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.233-957G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47840726 | ||||||
chr2:47840738
|
G | A | 1 | a0001c0001t0001g0073 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.233-969C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47840738 | ||||||
chr2:47840853
|
TA | T | 17 | a0001c0001t0001g0058a0001c0001t0001g0174a0001c0001t0001g0193others(14): Show | 17 | HG00280.hp2 HG01070.hp1 HG01070.hp2 others(14): Show |
intron_variant | MODIFIER | c.233-1085delT | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47840853 | ||||||
chr2:47841142
|
G | A | 2 | a0001c0001t0003g0282a0004c0005t0002g0308 | 2 | HG02145.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.233-1373C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47841142 | ||||||
chr2:47841197
|
C | CA | 7 | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0183others(4): Show | 7 | HG00642.hp2 HG01261.hp2 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.233-1429dupT | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47841197 | ||||||
chr2:47841404
|
C | G | 2 | a0001c0001t0001g0182a0001c0001t0001g0183 | 2 | HG00642.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.233-1635G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47841404 | ||||||
chr2:47841488
|
A | C | 5 | a0001c0001t0001g0193a0001c0001t0001g0254a0001c0001t0001g0255others(2): Show | 5 | HG00544.hp1 NA18952.hp2 NA18965.hp2 others(2): Show |
intron_variant | MODIFIER | c.233-1719T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47841488 | ||||||
chr2:47841508
|
C | T | 28 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(25): Show | 28 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.233-1739G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47841508 | ||||||
chr2:47841846
|
G | T | 1 | a0001c0001t0002g0173 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.233-2077C>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47841846 | ||||||
chr2:47841919
|
G | A | 6 | a0001c0001t0001g0110a0001c0001t0001g0274a0001c0001t0001g0275others(3): Show | 6 | HG01074.hp2 HG01891.hp2 NA19043.hp1 others(3): Show |
intron_variant | MODIFIER | c.233-2150C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47841919 | ||||||
chr2:47841974
|
T | A | 4 | a0001c0001t0002g0281a0001c0001t0002g0285a0001c0001t0002g0286others(1): Show | 4 | HG00738.hp1 HG02559.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.233-2205A>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47841974 | ||||||
chr2:47842021
|
A | AT | 8 | a0001c0001t0001g0241a0001c0001t0001g0264a0001c0001t0001g0287others(5): Show | 8 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.233-2253dupA | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47842021 | ||||||
chr2:47842026
|
T | TA | 5 | a0001c0001t0003g0107a0001c0001t0003g0243a0001c0001t0003g0293others(2): Show | 5 | HG02257.hp2 HG02717.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.233-2258_233-2257i others(3): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47842026 | ||||||
chr2:47842164
|
C | T | 7 | a0001c0001t0001g0264a0001c0001t0001g0287a0001c0001t0001g0288others(4): Show | 7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.233-2395G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47842164 | ||||||
chr2:47842306
|
C | T | 20 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(17): Show | 20 | HG00738.hp1 HG01346.hp1 HG02559.hp1 others(17): Show |
intron_variant | MODIFIER | c.233-2537G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47842306 | ||||||
chr2:47842374
|
T | C | 1 | a0001c0001t0002g0154 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.233-2605A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47842374 | ||||||
chr2:47842399
|
A | C | 4 | a0001c0001t0002g0196a0001c0001t0002g0249a0001c0001t0002g0250others(1): Show | 4 | HG01261.hp2 HG02922.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.233-2630T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47842399 | ||||||
chr2:47842544
|
T | G | 1 | a0001c0001t0001g0047 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.233-2775A>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47842544 | ||||||
chr2:47842553
|
C | T | 24 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(21): Show | 24 | HG01109.hp2 HG01433.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.233-2784G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47842553 | ||||||
chr2:47842604
|
T | TA | 9 | a0001c0001t0001g0003a0001c0001t0001g0041a0001c0001t0001g0121others(6): Show | 10 | HG02109.hp1 HG02257.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.233-2836dupT | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47842604 | ||||||
chr2:47842779
|
TA | T | 71 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(68): Show | 71 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.233-3011delT | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47842779 | ||||||
chr2:47842881
|
A | G | 4 | a0001c0001t0003g0107a0001c0001t0003g0293a0001c0001t0003g0294others(1): Show | 4 | HG02257.hp2 HG02717.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.233-3112T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47842881 | ||||||
chr2:47842905
|
C | T | 1 | a0001c0001t0001g0122 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.233-3136G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47842905 | ||||||
chr2:47843136
|
G | T | 2 | a0001c0001t0002g0054a0001c0001t0002g0181 | 2 | NA18993.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.233-3367C>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47843136 | ||||||
chr2:47843160
|
T | C | 16 | a0001c0001t0001g0001a0001c0001t0001g0093a0001c0001t0001g0094others(13): Show | 17 | HG03492.hp2 HG03704.hp1 NA18942.hp2 others(14): Show |
intron_variant | MODIFIER | c.233-3391A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47843160 | ||||||
chr2:47843431
|
CT | C | 21 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(18): Show | 21 | HG00738.hp1 HG01346.hp1 HG02559.hp1 others(18): Show |
intron_variant | MODIFIER | c.233-3663delA | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47843431 | ||||||
chr2:47843517
|
T | C | 8 | a0001c0001t0001g0003a0001c0001t0001g0121a0001c0001t0001g0124others(5): Show | 9 | HG02109.hp1 HG02257.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.233-3748A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47843517 | ||||||
chr2:47843615
|
C | G | 5 | a0001c0001t0002g0196a0001c0001t0002g0248a0001c0001t0002g0249others(2): Show | 5 | HG01261.hp2 HG02055.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.233-3846G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47843615 | ||||||
chr2:47843678
|
T | A | 14 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(11): Show | 14 | HG01346.hp1 HG02615.hp2 HG02723.hp1 others(11): Show |
intron_variant | MODIFIER | c.233-3909A>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47843678 | ||||||
chr2:47843728
|
G | GCTT | 14 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(11): Show | 14 | HG01346.hp1 HG02615.hp2 HG02723.hp1 others(11): Show |
intron_variant | MODIFIER | c.233-3960_233-3959i others(5): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47843728 | ||||||
chr2:47843728
|
G | GCTTCTTC others(2): Show |
3 | a0001c0001t0002g0281a0001c0001t0002g0285a0001c0001t0002g0286 | 3 | HG00738.hp1 HG02559.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.233-3960_233-3959i others(11): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47843728 | ||||||
chr2:47843728
|
G | GCTTCTTC others(5): Show |
1 | a0001c0001t0014g0284 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.233-3960_233-3959i others(14): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47843728 | ||||||
chr2:47843731
|
G | T | 21 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(18): Show | 21 | HG00738.hp1 HG01346.hp1 HG02559.hp1 others(18): Show |
intron_variant | MODIFIER | c.233-3962C>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47843731 | ||||||
chr2:47843734
|
G | T | 28 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(25): Show | 28 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.233-3965C>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47843734 | ||||||
chr2:47843737
|
T | G | 13 | a0001c0001t0001g0218a0001c0001t0001g0222a0001c0001t0001g0223others(10): Show | 13 | HG00099.hp1 HG00741.hp1 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.233-3968A>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47843737 | ||||||
chr2:47843865
|
C | A | 28 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(25): Show | 28 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.233-4096G>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47843865 | ||||||
chr2:47843898
|
G | A | 1 | a0001c0001t0001g0085 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.233-4129C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47843898 | ||||||
chr2:47843902
|
G | C | 7 | a0001c0001t0001g0264a0001c0001t0001g0287a0001c0001t0001g0288others(4): Show | 7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.233-4133C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47843902 | ||||||
chr2:47844116
|
T | A | 25 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(22): Show | 25 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.233-4347A>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47844116 | ||||||
chr2:47844183
|
A | C | 1 | a0001c0002t0002g0283 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.233-4414T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47844183 | ||||||
chr2:47844379
|
T | A | 2 | a0001c0001t0002g0157a0001c0001t0002g0158 | 2 | NA18747.hp1 NA18953.hp1 |
intron_variant | MODIFIER | c.233-4610A>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47844379 | ||||||
chr2:47844431
|
C | T | 2 | a0002c0004t0002g0262a0002c0004t0002g0266 | 2 | HG01884.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.233-4662G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47844431 | ||||||
chr2:47844511
|
GCTATA | G | 14 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(11): Show | 14 | HG00738.hp1 HG01346.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.233-4747_233-4743d others(7): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47844511 | ||||||
chr2:47844517
|
T | A | 14 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(11): Show | 14 | HG00738.hp1 HG01346.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.233-4748A>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47844517 | ||||||
chr2:47844636
|
T | C | 1 | a0001c0001t0001g0297 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.233-4867A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47844636 | ||||||
chr2:47844720
|
C | T | 3 | a0001c0001t0003g0293a0001c0001t0003g0294a0001c0001t0003g0295 | 3 | HG02717.hp1 HG03225.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.233-4951G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47844720 | ||||||
chr2:47844957
|
G | A | 1 | a0001c0001t0001g0268 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.233-5188C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47844957 | ||||||
chr2:47845007
|
T | C | 1 | a0001c0001t0001g0182 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.233-5238A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47845007 | ||||||
chr2:47845019
|
T | G | 1 | a0001c0001t0001g0106 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.233-5250A>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47845019 | ||||||
chr2:47845052
|
G | C | 2 | a0001c0001t0002g0054a0001c0001t0002g0181 | 2 | NA18993.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.233-5283C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47845052 | ||||||
chr2:47845152
|
C | G | 3 | a0001c0001t0003g0293a0001c0001t0003g0294a0001c0001t0003g0295 | 3 | HG02717.hp1 HG03225.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.233-5383G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47845152 | ||||||
chr2:47845164
|
T | A | 6 | a0001c0001t0001g0121a0001c0001t0001g0124a0001c0001t0001g0125others(3): Show | 6 | HG02109.hp1 HG02280.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.233-5395A>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47845164 | ||||||
chr2:47845498
|
G | A | 1 | a0004c0005t0002g0307 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.233-5729C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47845498 | ||||||
chr2:47845716
|
G | A | 54 | a0001c0001t0001g0156a0001c0001t0001g0167a0001c0001t0001g0171others(51): Show | 55 | HG00280.hp1 HG00735.hp1 HG00738.hp2 others(52): Show |
intron_variant | MODIFIER | c.233-5947C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47845716 | ||||||
chr2:47845872
|
A | C | 11 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(8): Show | 11 | HG01346.hp1 HG02615.hp2 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.233-6103T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47845872 | ||||||
chr2:47845888
|
G | GAA | 7 | a0001c0001t0001g0264a0001c0001t0001g0287a0001c0001t0001g0288others(4): Show | 7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.233-6121_233-6120d others(4): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47845888 | ||||||
chr2:47845978
|
C | T | 25 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(22): Show | 25 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.233-6209G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47845978 | ||||||
chr2:47846220
|
C | G | 1 | a0001c0001t0001g0116 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.233-6451G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47846220 | ||||||
chr2:47846297
|
G | A | 1 | a0001c0001t0002g0286 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.233-6528C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47846297 | ||||||
chr2:47846401
|
C | T | 1 | a0001c0001t0001g0279 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.233-6632G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47846401 | ||||||
chr2:47846529
|
T | A | 8 | a0001c0001t0001g0229a0001c0001t0001g0230a0001c0001t0001g0231others(5): Show | 8 | HG00639.hp2 HG00642.hp1 HG01069.hp2 others(5): Show |
intron_variant | MODIFIER | c.233-6760A>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47846529 | ||||||
chr2:47846532
|
T | C | 4 | a0001c0001t0002g0139a0002c0004t0002g0262a0002c0004t0002g0263others(1): Show | 4 | HG01884.hp1 HG02896.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.233-6763A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47846532 | ||||||
chr2:47846583
|
A | AAT | 7 | a0001c0001t0001g0264a0001c0001t0001g0287a0001c0001t0001g0288others(4): Show | 7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.233-6816_233-6815d others(4): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47846583 | ||||||
chr2:47846602
|
A | C | 1 | a0001c0001t0001g0090 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.233-6833T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47846602 | ||||||
chr2:47846610
|
T | G | 1 | a0001c0001t0001g0116 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.233-6841A>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47846610 | ||||||
chr2:47846676
|
T | C | 10 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(7): Show | 10 | HG01346.hp1 HG02615.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.233-6907A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47846676 | ||||||
chr2:47846738
|
TATATC | T | 15 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(12): Show | 15 | HG00738.hp1 HG01346.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.233-6974_233-6970d others(7): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47846738 | ||||||
chr2:47846834
|
C | T | 3 | a0002c0004t0002g0262a0002c0004t0002g0263a0002c0004t0002g0266 | 3 | HG01884.hp1 HG02896.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.233-7065G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47846834 | ||||||
chr2:47846855
|
C | T | 1 | a0001c0001t0001g0126 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.233-7086G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47846855 | ||||||
chr2:47847194
|
G | A | 7 | a0001c0001t0001g0264a0001c0001t0001g0287a0001c0001t0001g0288others(4): Show | 7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.233-7425C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47847194 | ||||||
chr2:47847275
|
T | C | 1 | a0001c0001t0003g0107 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.233-7506A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47847275 | ||||||
chr2:47847332
|
T | C | 1 | a0001c0001t0001g0289 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.233-7563A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47847332 | ||||||
chr2:47847422
|
A | G | 3 | a0001c0001t0003g0293a0001c0001t0003g0294a0001c0001t0003g0295 | 3 | HG02717.hp1 HG03225.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.233-7653T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47847422 | ||||||
chr2:47847444
|
C | A | 5 | a0001c0001t0002g0281a0001c0001t0002g0285a0001c0001t0002g0286others(2): Show | 5 | HG00738.hp1 HG01109.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.233-7675G>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47847444 | ||||||
chr2:47847450
|
T | C | 1 | a0001c0001t0010g0132 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.233-7681A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47847450 | ||||||
chr2:47847981
|
G | A | 1 | a0001c0001t0001g0297 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.233-8212C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47847981 | ||||||
chr2:47848127
|
A | C | 15 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(12): Show | 15 | HG01433.hp1 HG01891.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.233-8358T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47848127 | ||||||
chr2:47848142
|
AC | A | 13 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(10): Show | 13 | HG00738.hp1 HG01346.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.233-8374delG | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47848142 | ||||||
chr2:47848143
|
C | A | 277 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(274): Show | 282 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.233-8374G>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47848143 | ||||||
chr2:47848143
|
CA | C | 11 | a0001c0001t0001g0264a0001c0001t0001g0287a0001c0001t0001g0288others(8): Show | 11 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.233-8375delT | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47848143 | ||||||
chr2:47848157
|
A | AAC | 7 | a0001c0001t0001g0264a0001c0001t0001g0287a0001c0001t0001g0288others(4): Show | 7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.233-8390_233-8389d others(4): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47848157 | ||||||
chr2:47848212
|
G | C | 1 | a0001c0001t0001g0083 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.233-8443C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47848212 | ||||||
chr2:47848263
|
T | C | 4 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0047others(1): Show | 4 | HG00639.hp1 HG01109.hp1 HG01123.hp2 others(1): Show |
intron_variant | MODIFIER | c.233-8494A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47848263 | ||||||
chr2:47848301
|
C | T | 1 | a0001c0001t0001g0067 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.233-8532G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47848301 | ||||||
chr2:47848312
|
G | C | 7 | a0001c0001t0002g0050a0001c0001t0002g0134a0001c0001t0002g0140others(4): Show | 7 | HG02027.hp1 HG02080.hp1 HG02165.hp1 others(4): Show |
intron_variant | MODIFIER | c.233-8543C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47848312 | ||||||
chr2:47848789
|
A | G | 6 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(3): Show | 6 | HG00621.hp1 HG01993.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.233-9020T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47848789 | ||||||
chr2:47848792
|
A | G | 2 | a0001c0001t0003g0282a0004c0005t0002g0308 | 2 | HG02145.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.233-9023T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47848792 | ||||||
chr2:47848827
|
C | T | 1 | a0001c0001t0001g0049 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.233-9058G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47848827 | ||||||
chr2:47848910
|
A | ACACATTT others(5): Show |
1 | a0001c0001t0001g0190 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.233-9153_233-9142d others(14): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47848910 | ||||||
chr2:47848963
|
G | A | 1 | a0001c0001t0002g0196 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.233-9194C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47848963 | ||||||
chr2:47848993
|
A | G | 4 | a0001c0001t0003g0107a0001c0001t0003g0293a0001c0001t0003g0294others(1): Show | 4 | HG02257.hp2 HG02717.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.233-9224T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47848993 | ||||||
chr2:47849002
|
C | G | 1 | a0001c0001t0001g0271 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.233-9233G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47849002 | ||||||
chr2:47849060
|
G | A | 1 | a0001c0001t0001g0187 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.233-9291C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47849060 | ||||||
chr2:47849149
|
T | C | 10 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(7): Show | 10 | HG01346.hp1 HG02615.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.233-9380A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47849149 | ||||||
chr2:47849156
|
T | TA | 101 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(98): Show | 104 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.233-9388dupT | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47849156 | ||||||
chr2:47849180
|
A | G | 6 | a0001c0001t0002g0281a0001c0001t0002g0285a0001c0001t0002g0286others(3): Show | 6 | HG00738.hp1 HG01109.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.233-9411T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47849180 | ||||||
chr2:47849243
|
G | A | 7 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(4): Show | 7 | NA18971.hp2 NA19010.hp2 NA19066.hp1 others(4): Show |
intron_variant | MODIFIER | c.233-9474C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47849243 | ||||||
chr2:47849409
|
A | G | 2 | a0001c0001t0001g0289a0001c0001t0001g0290 | 2 | HG01255.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.233-9640T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47849409 | ||||||
chr2:47849940
|
G | A | 7 | a0001c0001t0001g0264a0001c0001t0001g0287a0001c0001t0001g0288others(4): Show | 7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.233-10171C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47849940 | ||||||
chr2:47849950
|
G | T | 73 | a0001c0001t0001g0038a0001c0001t0001g0051a0001c0001t0001g0052others(70): Show | 73 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.233-10181C>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47849950 | ||||||
chr2:47850040
|
G | C | 13 | a0001c0001t0001g0264a0001c0001t0001g0287a0001c0001t0001g0288others(10): Show | 13 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.233-10271C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47850040 | ||||||
chr2:47850153
|
G | A | 3 | a0001c0001t0001g0254a0001c0001t0012g0253a0001c0001t0019g0312 | 3 | NA18952.hp2 NA18965.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.233-10384C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47850153 | ||||||
chr2:47850253
|
G | C | 1 | a0001c0001t0001g0049 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.233-10484C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47850253 | ||||||
chr2:47850360
|
A | C | 6 | a0001c0001t0001g0265a0001c0001t0001g0268a0001c0001t0001g0269others(3): Show | 6 | HG02717.hp2 HG02922.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.233-10591T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47850360 | ||||||
chr2:47850449
|
G | A | 1 | a0001c0001t0001g0086 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.233-10680C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47850449 | ||||||
chr2:47850515
|
C | T | 6 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0075others(3): Show | 6 | HG00609.hp2 HG02080.hp2 NA18964.hp1 others(3): Show |
intron_variant | MODIFIER | c.233-10746G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47850515 | ||||||
chr2:47850566
|
A | T | 28 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(25): Show | 28 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.233-10797T>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47850566 | ||||||
chr2:47850653
|
A | G | 1 | a0001c0001t0001g0184 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.233-10884T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47850653 | ||||||
chr2:47850702
|
A | G | 1 | a0001c0001t0001g0072 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.233-10933T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47850702 | ||||||
chr2:47850895
|
A | G | 5 | a0001c0001t0001g0224a0001c0001t0002g0281a0001c0001t0002g0285others(2): Show | 5 | HG00738.hp1 HG02056.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.233-11126T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47850895 | ||||||
chr2:47850919
|
G | A | 4 | a0001c0001t0002g0281a0001c0001t0002g0285a0001c0001t0002g0286others(1): Show | 4 | HG00738.hp1 HG02559.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.233-11150C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47850919 | ||||||
chr2:47851053
|
G | A | 3 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184 | 3 | HG00323.hp2 HG00642.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.233-11284C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47851053 | ||||||
chr2:47851072
|
A | T | 15 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(12): Show | 15 | HG01346.hp1 HG02615.hp2 HG02717.hp1 others(12): Show |
intron_variant | MODIFIER | c.233-11303T>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47851072 | ||||||
chr2:47851154
|
A | AAATTAAC | 28 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(25): Show | 28 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.233-11386_233-1138 others(11): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47851154 | ||||||
chr2:47851188
|
G | A | 4 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0047others(1): Show | 4 | HG00639.hp1 HG01109.hp1 HG01123.hp2 others(1): Show |
intron_variant | MODIFIER | c.233-11419C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47851188 | ||||||
chr2:47851198
|
C | T | 9 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0045others(6): Show | 9 | HG00639.hp1 HG00735.hp2 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.233-11429G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47851198 | ||||||
chr2:47851330
|
G | A | 1 | a0001c0001t0001g0279 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.233-11561C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47851330 | ||||||
chr2:47851454
|
C | T | 1 | a0001c0001t0001g0270 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.233-11685G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47851454 | ||||||
chr2:47851542
|
G | C | 2 | a0001c0001t0002g0140a0001c0001t0002g0141 | 2 | HG02027.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.233-11773C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47851542 | ||||||
chr2:47851699
|
C | T | 201 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(198): Show | 204 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(201): Show |
intron_variant | MODIFIER | c.233-11930G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47851699 | ||||||
chr2:47851874
|
T | G | 8 | a0001c0001t0001g0121a0001c0001t0001g0124a0001c0001t0001g0125others(5): Show | 8 | HG02109.hp1 HG02280.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.233-12105A>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47851874 | ||||||
chr2:47851968
|
A | C | 1 | a0001c0001t0003g0282 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.233-12199T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47851968 | ||||||
chr2:47851989
|
A | AT | 18 | a0001c0001t0001g0089a0001c0001t0001g0102a0001c0001t0001g0114others(15): Show | 18 | HG00544.hp2 HG02145.hp1 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.233-12221dupA | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47851989 | ||||||
chr2:47851989
|
A | ATTT | 7 | a0001c0001t0001g0264a0001c0001t0001g0287a0001c0001t0001g0288others(4): Show | 7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.233-12223_233-1222 others(7): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47851989 | ||||||
chr2:47851989
|
AT | A | 23 | a0001c0001t0001g0069a0001c0001t0001g0075a0001c0001t0001g0103others(20): Show | 23 | HG00099.hp2 HG01099.hp1 HG01169.hp1 others(20): Show |
intron_variant | MODIFIER | c.233-12221delA | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47851989 | ||||||
chr2:47852017
|
A | C | 1 | a0001c0001t0001g0241 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.233-12248T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47852017 | ||||||
chr2:47852062
|
G | T | 1 | a0001c0001t0001g0241 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.233-12293C>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47852062 | ||||||
chr2:47852157
|
T | C | 1 | a0001c0001t0002g0179 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.233-12388A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47852157 | ||||||
chr2:47852187
|
G | A | 1 | a0001c0001t0003g0293 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.233-12418C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47852187 | ||||||
chr2:47852318
|
C | T | 4 | a0001c0001t0001g0207a0001c0001t0001g0277a0001c0001t0001g0278others(1): Show | 4 | HG02135.hp1 NA18977.hp2 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.233-12549G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47852318 | ||||||
chr2:47852347
|
A | C | 1 | a0001c0001t0002g0286 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.233-12578T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47852347 | ||||||
chr2:47852347
|
A | G | 10 | a0001c0001t0001g0264a0001c0001t0001g0287a0001c0001t0001g0288others(7): Show | 10 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.233-12578T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47852347 | ||||||
chr2:47852448
|
A | G | 1 | a0001c0001t0001g0121 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.233-12679T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47852448 | ||||||
chr2:47852549
|
C | T | 1 | a0001c0001t0001g0279 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.233-12780G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47852549 | ||||||
chr2:47852564
|
G | C | 7 | a0001c0001t0002g0050a0001c0001t0002g0134a0001c0001t0002g0140others(4): Show | 7 | HG02027.hp1 HG02080.hp1 HG02165.hp1 others(4): Show |
intron_variant | MODIFIER | c.233-12795C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47852564 | ||||||
chr2:47852710
|
A | C | 3 | a0001c0001t0001g0214a0001c0001t0001g0238a0001c0001t0001g0247 | 3 | HG02809.hp2 HG03139.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.233-12941T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47852710 | ||||||
chr2:47852839
|
T | C | 7 | a0001c0001t0001g0264a0001c0001t0001g0287a0001c0001t0001g0288others(4): Show | 7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.233-13070A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47852839 | ||||||
chr2:47852941
|
C | A | 1 | a0001c0001t0003g0282 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.233-13172G>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47852941 | ||||||
chr2:47852963
|
A | G | 2 | a0001c0001t0001g0059a0001c0001t0001g0104 | 2 | NA18966.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.233-13194T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47852963 | ||||||
chr2:47853075
|
A | AT | 16 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(13): Show | 16 | HG01433.hp1 HG01891.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.233-13307dupA | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47853075 | ||||||
chr2:47853121
|
C | G | 212 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(209): Show | 216 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.233-13352G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47853121 | ||||||
chr2:47853416
|
T | C | 2 | a0001c0001t0002g0054a0001c0001t0002g0181 | 2 | NA18993.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.233-13647A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47853416 | ||||||
chr2:47853424
|
T | C | 1 | a0001c0001t0001g0218 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.233-13655A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47853424 | ||||||
chr2:47853426
|
T | C | 1 | a0007c0006t0001g0108 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.233-13657A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47853426 | ||||||
chr2:47853454
|
C | G | 1 | a0001c0001t0001g0187 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.233-13685G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47853454 | ||||||
chr2:47853506
|
G | A | 7 | a0001c0001t0001g0264a0001c0001t0001g0287a0001c0001t0001g0288others(4): Show | 7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.233-13737C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47853506 | ||||||
chr2:47853533
|
C | A | 1 | a0001c0001t0001g0208 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.233-13764G>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47853533 | ||||||
chr2:47853687
|
C | T | 1 | a0001c0001t0001g0063 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.233-13918G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47853687 | ||||||
chr2:47853762
|
T | C | 5 | a0001c0001t0002g0281a0001c0001t0002g0285a0001c0001t0002g0286others(2): Show | 5 | HG00738.hp1 HG01109.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.233-13993A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47853762 | ||||||
chr2:47853836
|
G | A | 2 | a0001c0002t0002g0300a0001c0002t0002g0302 | 2 | HG03195.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.233-14067C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47853836 | ||||||
chr2:47853881
|
A | T | 1 | a0001c0001t0001g0208 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.233-14112T>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47853881 | ||||||
chr2:47853921
|
A | G | 5 | a0001c0001t0002g0281a0001c0001t0002g0285a0001c0001t0002g0286others(2): Show | 5 | HG00738.hp1 HG01109.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.233-14152T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47853921 | ||||||
chr2:47853927
|
G | A | 1 | a0001c0001t0001g0279 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.233-14158C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47853927 | ||||||
chr2:47854256
|
CT | C | 7 | a0001c0001t0001g0167a0001c0001t0001g0216a0001c0001t0001g0234others(4): Show | 7 | HG00738.hp1 HG01069.hp1 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.233-14488delA | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47854256 | ||||||
chr2:47854343
|
T | TA | 3 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0068 | 3 | HG00621.hp1 HG02071.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.233-14575dupT | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47854343 | ||||||
chr2:47854357
|
C | T | 1 | a0001c0001t0001g0156 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.233-14588G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47854357 | ||||||
chr2:47854368
|
C | T | 2 | a0001c0001t0001g0192a0001c0001t0001g0242 | 2 | HG03492.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.233-14599G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47854368 | ||||||
chr2:47854620
|
C | T | 1 | a0001c0001t0018g0311 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.233-14851G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47854620 | ||||||
chr2:47854660
|
T | C | 1 | a0004c0005t0002g0308 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.233-14891A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47854660 | ||||||
chr2:47854863
|
G | T | 10 | a0001c0001t0001g0039a0001c0001t0001g0270a0001c0001t0002g0281others(7): Show | 10 | HG00738.hp1 HG02300.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.233-15094C>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47854863 | ||||||
chr2:47854863
|
GT | G | 269 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(266): Show | 272 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.233-15095delA | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47854863 | ||||||
chr2:47854864
|
T | G | 10 | a0001c0001t0001g0246a0001c0001t0001g0270a0001c0001t0002g0281others(7): Show | 10 | HG00738.hp1 HG02559.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.233-15095A>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47854864 | ||||||
chr2:47855052
|
G | T | 3 | a0001c0001t0003g0293a0001c0001t0003g0294a0001c0001t0003g0295 | 3 | HG02717.hp1 HG03225.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.233-15283C>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47855052 | ||||||
chr2:47855057
|
T | C | 1 | a0001c0001t0002g0248 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.233-15288A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47855057 | ||||||
chr2:47855073
|
T | C | 1 | a0001c0001t0001g0070 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.233-15304A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47855073 | ||||||
chr2:47855097
|
A | C | 1 | a0001c0001t0001g0121 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.233-15328T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47855097 | ||||||
chr2:47855200
|
A | AT | 13 | a0001c0001t0002g0142a0001c0001t0002g0162a0001c0001t0003g0107others(10): Show | 13 | HG01109.hp2 HG01884.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.233-15432dupA | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47855200 | ||||||
chr2:47855201
|
T | A | 1 | a0001c0001t0001g0167 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.233-15432A>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47855201 | ||||||
chr2:47855227
|
G | T | 1 | a0001c0001t0002g0153 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.233-15458C>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47855227 | ||||||
chr2:47855259
|
G | A | 1 | a0001c0001t0002g0196 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.233-15490C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47855259 | ||||||
chr2:47855261
|
C | A | 1 | a0001c0001t0002g0062 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.233-15492G>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47855261 | ||||||
chr2:47855285
|
C | T | 15 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(12): Show | 15 | HG01433.hp1 HG01891.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.233-15516G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47855285 | ||||||
chr2:47855476
|
G | A | 1 | a0001c0001t0001g0213 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.233-15707C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47855476 | ||||||
chr2:47855508
|
G | C | 3 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0029 | 3 | HG01891.hp1 HG02559.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.233-15739C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47855508 | ||||||
chr2:47855609
|
T | C | 1 | a0001c0001t0001g0204 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.233-15840A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47855609 | ||||||
chr2:47855613
|
C | A | 1 | a0001c0001t0001g0038 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.233-15844G>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47855613 | ||||||
chr2:47855758
|
G | A | 1 | a0001c0001t0002g0181 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.233-15989C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47855758 | ||||||
chr2:47855836
|
C | G | 1 | a0001c0001t0001g0175 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.233-16067G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47855836 | ||||||
chr2:47855841
|
C | CA | 21 | a0001c0001t0001g0082a0001c0001t0001g0085a0001c0001t0001g0212others(18): Show | 21 | HG00280.hp2 HG00597.hp2 HG01070.hp1 others(18): Show |
intron_variant | MODIFIER | c.233-16073dupT | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47855841 | ||||||
chr2:47855841
|
CA | C | 6 | a0001c0001t0001g0058a0001c0001t0001g0064a0001c0001t0001g0065others(3): Show | 6 | HG00621.hp1 HG02071.hp2 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.233-16073delT | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47855841 | ||||||
chr2:47855864
|
C | T | 1 | a0001c0001t0001g0003 | 2 | HG02257.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.233-16095G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47855864 | ||||||
chr2:47855890
|
G | A | 7 | a0001c0001t0001g0264a0001c0001t0001g0287a0001c0001t0001g0288others(4): Show | 7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.233-16121C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47855890 | ||||||
chr2:47856433
|
G | T | 1 | a0001c0001t0001g0003 | 2 | HG02257.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.233-16664C>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47856433 | ||||||
chr2:47856472
|
A | C | 1 | a0001c0001t0002g0248 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.233-16703T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47856472 | ||||||
chr2:47856639
|
G | T | 1 | a0001c0001t0001g0224 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.233-16870C>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47856639 | ||||||
chr2:47856785
|
A | G | 310 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(307): Show | 315 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.233-17016T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47856785 | ||||||
chr2:47857267
|
T | C | 2 | a0001c0001t0001g0056a0001c0001t0001g0057 | 2 | NA18952.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.233-17498A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47857267 | ||||||
chr2:47857282
|
G | A | 7 | a0001c0001t0001g0121a0001c0001t0001g0124a0001c0001t0001g0125others(4): Show | 7 | HG02109.hp1 HG02280.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.233-17513C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47857282 | ||||||
chr2:47857423
|
A | T | 27 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(24): Show | 27 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(24): Show |
intron_variant | MODIFIER | c.233-17654T>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47857423 | ||||||
chr2:47857519
|
C | T | 1 | a0001c0001t0002g0136 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.233-17750G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47857519 | ||||||
chr2:47857533
|
C | T | 2 | a0001c0001t0001g0005a0001c0001t0001g0191 | 3 | HG01243.hp1 HG02976.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.233-17764G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47857533 | ||||||
chr2:47857808
|
T | A | 4 | a0001c0001t0001g0252a0001c0001t0001g0259a0001c0001t0001g0260others(1): Show | 4 | NA18957.hp2 NA19012.hp2 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.233-18039A>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47857808 | ||||||
chr2:47857922
|
C | A | 194 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0017others(191): Show | 197 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.233-18153G>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47857922 | ||||||
chr2:47857948
|
T | TAC | 49 | a0001c0001t0001g0001a0001c0001t0001g0051a0001c0001t0001g0053others(46): Show | 50 | HG00323.hp2 HG00438.hp2 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.233-18181_233-1818 others(6): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47857948 | ||||||
chr2:47858022
|
G | A | 1 | a0001c0001t0001g0059 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.233-18253C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47858022 | ||||||
chr2:47858071
|
G | A | 1 | a0001c0001t0001g0216 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.233-18302C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47858071 | ||||||
chr2:47858261
|
C | T | 4 | a0001c0001t0002g0281a0001c0001t0002g0285a0001c0001t0002g0286others(1): Show | 4 | HG00738.hp1 HG02559.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.233-18492G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47858261 | ||||||
chr2:47858397
|
A | T | 1 | a0003c0003t0001g0015 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.233-18628T>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47858397 | ||||||
chr2:47858422
|
C | G | 1 | a0001c0001t0001g0049 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.233-18653G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47858422 | ||||||
chr2:47858525
|
T | C | 5 | a0001c0001t0002g0281a0001c0001t0002g0285a0001c0001t0002g0286others(2): Show | 5 | HG00738.hp1 HG01109.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.233-18756A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47858525 | ||||||
chr2:47858566
|
C | T | 3 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0068 | 3 | HG00621.hp1 HG02071.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.233-18797G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47858566 | ||||||
chr2:47858577
|
G | C | 1 | a0001c0001t0001g0270 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.233-18808C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47858577 | ||||||
chr2:47858675
|
C | T | 1 | a0001c0001t0002g0179 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.233-18906G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47858675 | ||||||
chr2:47858681
|
C | CA | 35 | a0001c0001t0001g0003a0001c0001t0001g0043a0001c0001t0001g0061others(32): Show | 36 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.233-18913dupT | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47858681 | ||||||
chr2:47858681
|
CA | C | 77 | a0001c0001t0001g0004a0001c0001t0001g0114a0001c0001t0001g0122others(74): Show | 78 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.233-18913delT | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47858681 | ||||||
chr2:47858696
|
A | G | 1 | a0001c0001t0001g0072 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.233-18927T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47858696 | ||||||
chr2:47858771
|
G | A | 1 | a0001c0001t0001g0063 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.233-19002C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47858771 | ||||||
chr2:47859041
|
CA | C | 264 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(261): Show | 267 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.233-19273delT | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47859041 | ||||||
chr2:47859041
|
CAA | C | 9 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0021others(6): Show | 9 | HG02258.hp2 HG02451.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.233-19274_233-1927 others(6): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47859041 | ||||||
chr2:47859124
|
T | G | 1 | a0001c0001t0001g0060 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.233-19355A>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47859124 | ||||||
chr2:47859197
|
T | C | 1 | a0001c0001t0001g0193 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.233-19428A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47859197 | ||||||
chr2:47859379
|
G | A | 1 | a0001c0001t0003g0282 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.233-19610C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47859379 | ||||||
chr2:47859543
|
C | T | 1 | a0001c0001t0001g0057 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.233-19774G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47859543 | ||||||
chr2:47859656
|
C | T | 1 | a0001c0001t0001g0042 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.233-19887G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47859656 | ||||||
chr2:47859684
|
C | G | 6 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(3): Show | 6 | HG00621.hp1 HG01993.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.233-19915G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47859684 | ||||||
chr2:47859715
|
T | G | 7 | a0001c0001t0001g0264a0001c0001t0001g0287a0001c0001t0001g0288others(4): Show | 7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.233-19946A>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47859715 | ||||||
chr2:47859737
|
T | G | 1 | a0001c0001t0001g0003 | 2 | HG02257.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.233-19968A>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47859737 | ||||||
chr2:47859868
|
G | A | 1 | a0001c0001t0001g0102 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.233-20099C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47859868 | ||||||
chr2:47859888
|
C | G | 26 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(23): Show | 26 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.233-20119G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47859888 | ||||||
chr2:47860192
|
G | A | 1 | a0001c0001t0001g0102 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.233-20423C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47860192 | ||||||
chr2:47860320
|
G | T | 1 | a0001c0001t0001g0055 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.233-20551C>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47860320 | ||||||
chr2:47860400
|
T | C | 2 | a0001c0001t0003g0107a0001c0001t0003g0282 | 2 | HG02145.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.233-20631A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47860400 | ||||||
chr2:47860410
|
A | AT | 18 | a0001c0001t0001g0041a0001c0001t0001g0053a0001c0001t0001g0060others(15): Show | 18 | HG01993.hp1 HG02145.hp1 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.233-20642dupA | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47860410 | ||||||
chr2:47860410
|
AT | A | 10 | a0001c0001t0001g0234a0001c0001t0001g0239a0001c0001t0001g0264others(7): Show | 10 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.233-20642delA | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47860410 | ||||||
chr2:47860543
|
T | C | 1 | a0001c0001t0001g0081 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.233-20774A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47860543 | ||||||
chr2:47860657
|
T | G | 1 | a0001c0001t0001g0123 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.233-20888A>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47860657 | ||||||
chr2:47860658
|
C | T | 2 | a0001c0001t0003g0294a0001c0001t0003g0295 | 2 | HG02717.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.233-20889G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47860658 | ||||||
chr2:47860687
|
G | A | 1 | a0001c0001t0001g0209 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.233-20918C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47860687 | ||||||
chr2:47860691
|
G | C | 2 | a0001c0001t0002g0136a0001c0001t0002g0148 | 2 | HG01256.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.233-20922C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47860691 | ||||||
chr2:47860814
|
GA | G | 290 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(287): Show | 295 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(292): Show |
intron_variant | MODIFIER | c.233-21046delT | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47860814 | ||||||
chr2:47860843
|
AT | A | 169 | a0001c0001t0001g0005a0001c0001t0001g0017a0001c0001t0001g0018others(166): Show | 171 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.233-21075delA | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47860843 | ||||||
chr2:47860843
|
ATT | A | 8 | a0001c0001t0001g0264a0001c0001t0001g0287a0001c0001t0001g0288others(5): Show | 8 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.233-21076_233-2107 others(6): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47860843 | ||||||
chr2:47860949
|
T | C | 8 | a0001c0001t0001g0264a0001c0001t0001g0287a0001c0001t0001g0288others(5): Show | 8 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.233-21180A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47860949 | ||||||
chr2:47861009
|
T | C | 29 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(26): Show | 29 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.233-21240A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47861009 | ||||||
chr2:47861099
|
C | A | 2 | a0001c0001t0002g0285a0001c0002t0002g0283 | 2 | HG01109.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.233-21330G>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47861099 | ||||||
chr2:47861273
|
A | G | 11 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(8): Show | 11 | HG01346.hp1 HG02615.hp2 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.233-21504T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47861273 | ||||||
chr2:47861294
|
T | G | 7 | a0001c0001t0001g0264a0001c0001t0001g0287a0001c0001t0001g0288others(4): Show | 7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.233-21525A>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47861294 | ||||||
chr2:47861318
|
C | CT | 8 | a0001c0001t0001g0085a0001c0001t0001g0287a0001c0001t0001g0288others(5): Show | 8 | HG00280.hp2 HG01081.hp1 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.233-21550dupA | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47861318 | ||||||
chr2:47861356
|
T | C | 4 | a0001c0001t0001g0212a0001c0001t0001g0214a0001c0001t0001g0238others(1): Show | 4 | HG02809.hp2 HG03139.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.233-21587A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47861356 | ||||||
chr2:47861492
|
A | C | 5 | a0001c0001t0002g0281a0001c0001t0002g0285a0001c0001t0002g0286others(2): Show | 5 | HG00738.hp1 HG01109.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.233-21723T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47861492 | ||||||
chr2:47861495
|
T | A | 10 | a0001c0001t0001g0036a0001c0001t0001g0039a0001c0001t0001g0041others(7): Show | 10 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.233-21726A>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47861495 | ||||||
chr2:47861610
|
C | T | 1 | a0001c0002t0002g0120 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.233-21841G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47861610 | ||||||
chr2:47861677
|
T | C | 1 | a0001c0002t0002g0302 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.233-21908A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47861677 | ||||||
chr2:47861700
|
T | A | 3 | a0001c0001t0003g0293a0001c0001t0003g0294a0001c0001t0003g0295 | 3 | HG02717.hp1 HG03225.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.233-21931A>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47861700 | ||||||
chr2:47861717
|
G | C | 6 | a0001c0001t0001g0110a0001c0001t0001g0274a0001c0001t0001g0275others(3): Show | 6 | HG01074.hp2 HG01891.hp2 NA19043.hp1 others(3): Show |
intron_variant | MODIFIER | c.233-21948C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47861717 | ||||||
chr2:47861725
|
C | G | 1 | a0001c0001t0001g0083 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.233-21956G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47861725 | ||||||
chr2:47861800
|
G | C | 1 | a0001c0001t0002g0148 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.233-22031C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47861800 | ||||||
chr2:47861907
|
G | GT | 12 | a0001c0001t0001g0036a0001c0001t0001g0039a0001c0001t0001g0041others(9): Show | 12 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.233-22139dupA | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47861907 | ||||||
chr2:47861907
|
GT | G | 12 | a0001c0001t0001g0024a0001c0001t0001g0208a0001c0001t0001g0209others(9): Show | 12 | HG01169.hp2 HG01346.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.233-22139delA | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47861907 | ||||||
chr2:47862065
|
A | G | 5 | a0001c0001t0002g0281a0001c0001t0002g0285a0001c0001t0002g0286others(2): Show | 5 | HG00738.hp1 HG01109.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.233-22296T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47862065 | ||||||
chr2:47862307
|
A | C | 1 | a0001c0001t0002g0141 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.233-22538T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47862307 | ||||||
chr2:47862549
|
A | C | 1 | a0001c0001t0002g0178 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.233-22780T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47862549 | ||||||
chr2:47862589
|
G | C | 1 | a0001c0001t0001g0186 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.233-22820C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47862589 | ||||||
chr2:47862985
|
G | A | 1 | a0001c0001t0002g0101 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.233-23216C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47862985 | ||||||
chr2:47863055
|
C | CA | 11 | a0001c0001t0001g0151a0001c0001t0001g0156a0001c0001t0001g0235others(8): Show | 11 | HG01169.hp2 HG01175.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.233-23287dupT | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47863055 | ||||||
chr2:47863055
|
CA | C | 20 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0001g0211others(17): Show | 20 | HG00738.hp1 HG01109.hp2 HG01346.hp1 others(17): Show |
intron_variant | MODIFIER | c.233-23287delT | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47863055 | ||||||
chr2:47863064
|
A | C | 7 | a0001c0001t0001g0264a0001c0001t0001g0287a0001c0001t0001g0288others(4): Show | 7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.233-23295T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47863064 | ||||||
chr2:47863065
|
AAAAAAAC | A | 7 | a0001c0001t0001g0264a0001c0001t0001g0287a0001c0001t0001g0288others(4): Show | 7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.233-23303_233-2329 others(11): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47863065 | ||||||
chr2:47863071
|
A | AAAAAAAA others(3): Show |
1 | a0001c0001t0003g0293 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.233-23303_233-2330 others(14): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47863071 | ||||||
chr2:47863072
|
C | A | 7 | a0001c0001t0002g0134a0001c0001t0002g0140a0001c0001t0002g0141others(4): Show | 7 | HG02027.hp1 HG02080.hp1 HG02165.hp1 others(4): Show |
intron_variant | MODIFIER | c.233-23303G>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47863072 | ||||||
chr2:47863086
|
C | T | 7 | a0001c0001t0001g0264a0001c0001t0001g0287a0001c0001t0001g0288others(4): Show | 7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.233-23317G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47863086 | ||||||
chr2:47863178
|
C | G | 1 | a0001c0001t0001g0076 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.233-23409G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47863178 | ||||||
chr2:47863244
|
T | C | 3 | a0001c0001t0004g0011a0001c0001t0004g0012a0001c0001t0004g0013 | 3 | HG02135.hp2 HG02523.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.233-23475A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47863244 | ||||||
chr2:47863273
|
A | G | 2 | a0001c0001t0001g0186a0001c0001t0002g0179 | 2 | HG02572.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.233-23504T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47863273 | ||||||
chr2:47863346
|
A | G | 1 | a0001c0001t0002g0109 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.233-23577T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47863346 | ||||||
chr2:47863404
|
ACAT | A | 7 | a0001c0001t0001g0121a0001c0001t0001g0124a0001c0001t0001g0125others(4): Show | 7 | HG02109.hp1 HG02280.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.233-23638_233-2363 others(7): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47863404 | ||||||
chr2:47863408
|
G | A | 7 | a0001c0001t0001g0121a0001c0001t0001g0124a0001c0001t0001g0125others(4): Show | 7 | HG02109.hp1 HG02280.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.233-23639C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47863408 | ||||||
chr2:47863410
|
C | A | 7 | a0001c0001t0001g0121a0001c0001t0001g0124a0001c0001t0001g0125others(4): Show | 7 | HG02109.hp1 HG02280.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.233-23641G>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47863410 | ||||||
chr2:47863411
|
T | G | 7 | a0001c0001t0001g0121a0001c0001t0001g0124a0001c0001t0001g0125others(4): Show | 7 | HG02109.hp1 HG02280.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.233-23642A>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47863411 | ||||||
chr2:47863440
|
A | C | 1 | a0001c0001t0001g0188 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.233-23671T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47863440 | ||||||
chr2:47863694
|
A | G | 1 | a0001c0001t0001g0111 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.233-23925T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47863694 | ||||||
chr2:47863832
|
T | C | 1 | a0001c0001t0001g0209 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.233-24063A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47863832 | ||||||
chr2:47863870
|
G | C | 2 | a0001c0001t0003g0282a0004c0005t0002g0308 | 2 | HG02145.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.233-24101C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47863870 | ||||||
chr2:47863954
|
C | T | 6 | a0001c0001t0001g0264a0001c0001t0001g0287a0001c0001t0001g0288others(3): Show | 6 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(3): Show |
intron_variant | MODIFIER | c.233-24185G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47863954 | ||||||
chr2:47864266
|
G | C | 3 | a0001c0001t0003g0293a0001c0001t0003g0294a0001c0001t0003g0295 | 3 | HG02717.hp1 HG03225.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.233-24497C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47864266 | ||||||
chr2:47864269
|
A | T | 100 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0036others(97): Show | 102 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.233-24500T>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47864269 | ||||||
chr2:47864302
|
A | G | 1 | a0001c0001t0002g0170 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.233-24533T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47864302 | ||||||
chr2:47864326
|
G | A | 1 | a0001c0001t0010g0132 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.233-24557C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47864326 | ||||||
chr2:47864327
|
C | T | 1 | a0001c0001t0002g0149 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.233-24558G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47864327 | ||||||
chr2:47864584
|
T | A | 29 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0197others(26): Show | 29 | HG00438.hp1 HG00544.hp1 HG00609.hp1 others(26): Show |
intron_variant | MODIFIER | c.233-24815A>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47864584 | ||||||
chr2:47864588
|
A | T | 1 | a0001c0001t0001g0205 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.233-24819T>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47864588 | ||||||
chr2:47864769
|
T | C | 2 | a0001c0002t0002g0032a0001c0002t0002g0034 | 2 | HG01884.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.233-25000A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47864769 | ||||||
chr2:47864820
|
T | G | 2 | a0001c0001t0001g0056a0001c0001t0001g0057 | 2 | NA18952.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.233-25051A>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47864820 | ||||||
chr2:47865215
|
T | G | 1 | a0001c0001t0003g0107 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.233-25446A>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47865215 | ||||||
chr2:47865291
|
T | G | 1 | a0001c0001t0001g0078 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.233-25522A>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47865291 | ||||||
chr2:47865487
|
C | T | 3 | a0001c0001t0003g0282a0001c0001t0003g0294a0001c0001t0003g0295 | 3 | HG02145.hp1 HG02717.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.233-25718G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47865487 | ||||||
chr2:47865526
|
C | T | 11 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(8): Show | 11 | HG01346.hp1 HG02615.hp2 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.233-25757G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47865526 | ||||||
chr2:47865686
|
T | C | 1 | a0001c0001t0001g0084 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.233-25917A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47865686 | ||||||
chr2:47865702
|
T | C | 3 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0029 | 3 | HG01891.hp1 HG02559.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.233-25933A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47865702 | ||||||
chr2:47865750
|
G | C | 1 | a0001c0001t0003g0282 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.233-25981C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47865750 | ||||||
chr2:47865799
|
T | C | 1 | a0001c0001t0003g0293 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.233-26030A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47865799 | ||||||
chr2:47865823
|
T | C | 1 | a0001c0001t0001g0110 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.233-26054A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47865823 | ||||||
chr2:47866017
|
G | T | 10 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(7): Show | 10 | HG01346.hp1 HG02615.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.233-26248C>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47866017 | ||||||
chr2:47866139
|
G | A | 1 | a0001c0001t0014g0284 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.233-26370C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47866139 | ||||||
chr2:47866245
|
C | CA | 63 | a0001c0001t0001g0049a0001c0001t0001g0070a0001c0001t0001g0071others(60): Show | 63 | HG00438.hp1 HG00544.hp1 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.233-26477dupT | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47866245 | ||||||
chr2:47866245
|
CA | C | 27 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(24): Show | 27 | HG01069.hp2 HG01346.hp1 HG01433.hp1 others(24): Show |
intron_variant | MODIFIER | c.233-26477delT | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47866245 | ||||||
chr2:47866333
|
C | T | 7 | a0001c0001t0001g0264a0001c0001t0001g0287a0001c0001t0001g0288others(4): Show | 7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.233-26564G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47866333 | ||||||
chr2:47866337
|
C | T | 2 | a0001c0001t0001g0210a0001c0001t0001g0211 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.233-26568G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47866337 | ||||||
chr2:47866365
|
C | T | 7 | a0001c0001t0001g0121a0001c0001t0001g0124a0001c0001t0001g0125others(4): Show | 7 | HG02109.hp1 HG02280.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.233-26596G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47866365 | ||||||
chr2:47866425
|
G | C | 5 | a0001c0001t0002g0281a0001c0001t0002g0285a0001c0001t0002g0286others(2): Show | 5 | HG00738.hp1 HG01109.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.233-26656C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47866425 | ||||||
chr2:47866440
|
G | A | 8 | a0001c0002t0002g0030a0001c0002t0002g0031a0001c0002t0002g0032others(5): Show | 8 | HG01884.hp2 HG02109.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.233-26671C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47866440 | ||||||
chr2:47866497
|
C | T | 10 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(7): Show | 10 | HG01346.hp1 HG02615.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.233-26728G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47866497 | ||||||
chr2:47866551
|
G | A | 1 | a0001c0001t0001g0098 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.233-26782C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47866551 | ||||||
chr2:47866577
|
G | A | 2 | a0001c0001t0002g0196a0001c0001t0010g0132 | 2 | HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.233-26808C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47866577 | ||||||
chr2:47866614
|
C | A | 15 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(12): Show | 15 | HG01433.hp1 HG01891.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.233-26845G>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47866614 | ||||||
chr2:47867058
|
T | C | 1 | a0004c0005t0002g0308 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.233-27289A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47867058 | ||||||
chr2:47867141
|
A | G | 1 | a0001c0001t0001g0237 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.233-27372T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47867141 | ||||||
chr2:47867198
|
G | C | 173 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(170): Show | 176 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(173): Show |
intron_variant | MODIFIER | c.233-27429C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47867198 | ||||||
chr2:47867426
|
A | C | 1 | a0001c0001t0001g0277 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.233-27657T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47867426 | ||||||
chr2:47867622
|
T | C | 1 | a0001c0001t0014g0284 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.233-27853A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47867622 | ||||||
chr2:47867722
|
TAAGTCA | T | 7 | a0001c0001t0001g0264a0001c0001t0001g0287a0001c0001t0001g0288others(4): Show | 7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.233-27959_233-2795 others(10): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47867722 | ||||||
chr2:47867746
|
A | G | 1 | a0002c0004t0002g0263 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.233-27977T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47867746 | ||||||
chr2:47867748
|
T | C | 1 | a0001c0001t0002g0112 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.233-27979A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47867748 | ||||||
chr2:47867910
|
T | A | 5 | a0001c0001t0002g0196a0001c0001t0002g0248a0001c0001t0002g0249others(2): Show | 5 | HG01261.hp2 HG02055.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.233-28141A>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47867910 | ||||||
chr2:47867926
|
T | C | 5 | a0001c0001t0002g0281a0001c0001t0002g0285a0001c0001t0002g0286others(2): Show | 5 | HG00738.hp1 HG01109.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.233-28157A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47867926 | ||||||
chr2:47867927
|
T | A | 3 | a0001c0001t0001g0254a0001c0001t0012g0253a0001c0001t0019g0312 | 3 | NA18952.hp2 NA18965.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.233-28158A>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47867927 | ||||||
chr2:47867971
|
A | C | 24 | a0001c0001t0001g0005a0001c0001t0001g0191a0001c0001t0001g0208others(21): Show | 25 | HG00738.hp1 HG01109.hp2 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.233-28202T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47867971 | ||||||
chr2:47868036
|
G | A | 10 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(7): Show | 10 | HG01346.hp1 HG02615.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.233-28267C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47868036 | ||||||
chr2:47868178
|
G | T | 1 | a0001c0001t0001g0122 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.233-28409C>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47868178 | ||||||
chr2:47868200
|
T | C | 1 | a0001c0001t0001g0104 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.233-28431A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47868200 | ||||||
chr2:47868208
|
G | A | 1 | a0001c0001t0016g0309 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.233-28439C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47868208 | ||||||
chr2:47868282
|
C | CA | 61 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0036others(58): Show | 63 | HG00099.hp2 HG00544.hp1 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.233-28514dupT | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47868282 | ||||||
chr2:47868282
|
CAA | C | 18 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(15): Show | 18 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.233-28515_233-2851 others(6): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47868282 | ||||||
chr2:47868436
|
C | T | 36 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(33): Show | 36 | HG00438.hp1 HG00544.hp1 HG00597.hp1 others(33): Show |
intron_variant | MODIFIER | c.233-28667G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47868436 | ||||||
chr2:47868507
|
A | G | 1 | a0001c0001t0001g0038 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.233-28738T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47868507 | ||||||
chr2:47868594
|
T | C | 1 | a0001c0001t0001g0217 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.233-28825A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47868594 | ||||||
chr2:47868715
|
C | A | 1 | a0001c0001t0010g0132 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.233-28946G>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47868715 | ||||||
chr2:47868730
|
C | G | 1 | a0001c0001t0020g0313 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.233-28961G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47868730 | ||||||
chr2:47868748
|
G | A | 10 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(7): Show | 10 | HG01346.hp1 HG02615.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.233-28979C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47868748 | ||||||
chr2:47868827
|
G | A | 4 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0199others(1): Show | 4 | NA18971.hp1 NA18993.hp2 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.233-29058C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47868827 | ||||||
chr2:47868833
|
G | A | 10 | a0001c0001t0001g0055a0001c0001t0001g0076a0001c0001t0001g0093others(7): Show | 10 | HG03669.hp1 HG04184.hp1 HG04204.hp1 others(7): Show |
intron_variant | MODIFIER | c.233-29064C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47868833 | ||||||
chr2:47868891
|
T | C | 1 | a0001c0001t0002g0141 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.233-29122A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47868891 | ||||||
chr2:47869240
|
C | T | 1 | a0001c0001t0001g0076 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.233-29471G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47869240 | ||||||
chr2:47869384
|
T | C | 1 | a0001c0001t0001g0038 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.233-29615A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47869384 | ||||||
chr2:47869386
|
G | C | 10 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(7): Show | 10 | HG01346.hp1 HG02615.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.233-29617C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47869386 | ||||||
chr2:47869721
|
G | T | 3 | a0001c0002t0002g0283a0001c0002t0002g0300a0001c0002t0002g0302 | 3 | HG01109.hp2 HG03195.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.233-29952C>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47869721 | ||||||
chr2:47869805
|
T | C | 1 | a0001c0001t0001g0098 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.233-30036A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47869805 | ||||||
chr2:47870027
|
G | A | 1 | a0001c0001t0001g0217 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.233-30258C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47870027 | ||||||
chr2:47870284
|
C | T | 1 | a0001c0001t0001g0205 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.233-30515G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47870284 | ||||||
chr2:47870318
|
T | C | 10 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(7): Show | 10 | HG01346.hp1 HG02615.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.233-30549A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47870318 | ||||||
chr2:47870406
|
T | C | 10 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(7): Show | 10 | HG01346.hp1 HG02615.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.233-30637A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47870406 | ||||||
chr2:47870578
|
C | T | 6 | a0001c0001t0002g0281a0001c0001t0002g0285a0001c0001t0002g0286others(3): Show | 6 | HG00738.hp1 HG01109.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.233-30809G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47870578 | ||||||
chr2:47870650
|
T | G | 1 | a0001c0001t0001g0175 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.233-30881A>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47870650 | ||||||
chr2:47870688
|
G | T | 7 | a0001c0001t0001g0264a0001c0001t0001g0287a0001c0001t0001g0288others(4): Show | 7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.233-30919C>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47870688 | ||||||
chr2:47871000
|
T | A | 6 | a0001c0001t0002g0281a0001c0001t0002g0285a0001c0001t0002g0286others(3): Show | 6 | HG00738.hp1 HG01109.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.233-31231A>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47871000 | ||||||
chr2:47871038
|
T | C | 3 | a0001c0001t0003g0293a0001c0001t0003g0294a0001c0001t0003g0295 | 3 | HG02717.hp1 HG03225.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.233-31269A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47871038 | ||||||
chr2:47871140
|
A | G | 7 | a0001c0001t0002g0050a0001c0001t0002g0134a0001c0001t0002g0140others(4): Show | 7 | HG02027.hp1 HG02080.hp1 HG02165.hp1 others(4): Show |
intron_variant | MODIFIER | c.233-31371T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47871140 | ||||||
chr2:47871144
|
T | G | 10 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(7): Show | 10 | HG01346.hp1 HG02615.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.233-31375A>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47871144 | ||||||
chr2:47871185
|
G | C | 1 | a0001c0001t0001g0100 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.233-31416C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47871185 | ||||||
chr2:47871230
|
G | A | 1 | a0001c0001t0001g0129 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.233-31461C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47871230 | ||||||
chr2:47871434
|
T | C | 1 | a0001c0001t0009g0010 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.233-31665A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47871434 | ||||||
chr2:47871484
|
T | C | 6 | a0001c0001t0003g0107a0001c0001t0003g0243a0001c0001t0003g0282others(3): Show | 6 | HG02145.hp1 HG02257.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.233-31715A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47871484 | ||||||
chr2:47871505
|
T | C | 6 | a0001c0001t0003g0107a0001c0001t0003g0243a0001c0001t0003g0282others(3): Show | 6 | HG02145.hp1 HG02257.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.233-31736A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47871505 | ||||||
chr2:47871513
|
C | T | 7 | a0001c0001t0001g0264a0001c0001t0001g0287a0001c0001t0001g0288others(4): Show | 7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.233-31744G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47871513 | ||||||
chr2:47871569
|
C | T | 49 | a0001c0001t0001g0156a0001c0001t0001g0167a0001c0001t0001g0171others(46): Show | 50 | HG00280.hp1 HG00735.hp1 HG00738.hp2 others(47): Show |
intron_variant | MODIFIER | c.233-31800G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47871569 | ||||||
chr2:47871657
|
A | G | 3 | a0001c0001t0001g0171a0001c0001t0002g0146a0001c0001t0002g0170 | 3 | HG01168.hp1 HG01168.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.233-31888T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47871657 | ||||||
chr2:47871824
|
C | T | 1 | a0001c0001t0010g0132 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.233-32055G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47871824 | ||||||
chr2:47871923
|
T | C | 1 | a0001c0001t0001g0208 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.233-32154A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47871923 | ||||||
chr2:47871962
|
T | C | 10 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(7): Show | 10 | HG01346.hp1 HG02615.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.233-32193A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47871962 | ||||||
chr2:47872359
|
C | T | 11 | a0001c0001t0001g0264a0001c0001t0001g0287a0001c0001t0001g0288others(8): Show | 11 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.233-32590G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47872359 | ||||||
chr2:47872487
|
C | T | 1 | a0001c0001t0003g0293 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.233-32718G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47872487 | ||||||
chr2:47872576
|
G | A | 1 | a0001c0002t0002g0032 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.233-32807C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47872576 | ||||||
chr2:47872666
|
G | T | 1 | a0001c0001t0001g0186 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.232+32823C>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47872666 | ||||||
chr2:47872917
|
T | A | 1 | a0001c0001t0001g0280 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.232+32572A>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47872917 | ||||||
chr2:47873002
|
T | C | 6 | a0001c0001t0002g0281a0001c0001t0002g0285a0001c0001t0002g0286others(3): Show | 6 | HG00738.hp1 HG01109.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.232+32487A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47873002 | ||||||
chr2:47873040
|
T | G | 1 | a0001c0001t0002g0054 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.232+32449A>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47873040 | ||||||
chr2:47873067
|
A | C | 1 | a0001c0001t0011g0040 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.232+32422T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47873067 | ||||||
chr2:47873278
|
T | C | 1 | a0001c0001t0001g0240 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.232+32211A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47873278 | ||||||
chr2:47873776
|
A | G | 40 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(37): Show | 40 | HG00438.hp1 HG00544.hp1 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.232+31713T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47873776 | ||||||
chr2:47873915
|
T | A | 4 | a0001c0001t0001g0238a0001c0001t0001g0247a0001c0001t0002g0157others(1): Show | 4 | HG02809.hp2 HG03471.hp1 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.232+31574A>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47873915 | ||||||
chr2:47873916
|
A | T | 2 | a0001c0001t0001g0276a0001c0001t0003g0282 | 2 | HG01891.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.232+31573T>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47873916 | ||||||
chr2:47874030
|
T | C | 1 | a0001c0001t0002g0155 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.232+31459A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47874030 | ||||||
chr2:47874145
|
C | T | 1 | a0001c0001t0002g0142 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.232+31344G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47874145 | ||||||
chr2:47874150
|
C | A | 1 | a0001c0001t0001g0267 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.232+31339G>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47874150 | ||||||
chr2:47874160
|
G | C | 1 | a0001c0001t0001g0074 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.232+31329C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47874160 | ||||||
chr2:47874161
|
C | T | 1 | a0001c0001t0001g0074 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.232+31328G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47874161 | ||||||
chr2:47874221
|
TAATA | T | 3 | a0001c0001t0001g0227a0001c0001t0001g0228a0001c0001t0002g0225 | 3 | NA18962.hp2 NA18991.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.232+31264_232+3126 others(8): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47874221 | ||||||
chr2:47874489
|
C | G | 1 | a0001c0001t0010g0132 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.232+31000G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47874489 | ||||||
chr2:47874534
|
T | A | 1 | a0001c0001t0001g0001 | 2 | NA18942.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.232+30955A>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47874534 | ||||||
chr2:47874542
|
A | G | 1 | a0001c0001t0001g0195 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.232+30947T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47874542 | ||||||
chr2:47874669
|
G | A | 1 | a0001c0001t0002g0109 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.232+30820C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47874669 | ||||||
chr2:47874681
|
T | C | 1 | a0001c0001t0001g0129 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.232+30808A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47874681 | ||||||
chr2:47874771
|
G | T | 4 | a0001c0001t0003g0107a0001c0001t0003g0282a0001c0001t0003g0294others(1): Show | 4 | HG02145.hp1 HG02257.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.232+30718C>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47874771 | ||||||
chr2:47874773
|
G | A | 1 | a0001c0001t0001g0100 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.232+30716C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47874773 | ||||||
chr2:47874867
|
C | CT | 101 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0036others(98): Show | 103 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.232+30621dupA | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47874867 | ||||||
chr2:47874867
|
C | CTT | 32 | a0001c0001t0001g0192a0001c0001t0001g0209a0001c0001t0001g0210others(29): Show | 32 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(29): Show |
intron_variant | MODIFIER | c.232+30620_232+3062 others(6): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47874867 | ||||||
chr2:47874867
|
CT | C | 7 | a0001c0001t0001g0003a0001c0001t0001g0184a0001c0001t0001g0189others(4): Show | 8 | HG00323.hp2 HG01069.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.232+30621delA | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47874867 | ||||||
chr2:47874887
|
T | A | 1 | a0001c0001t0001g0063 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.232+30602A>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47874887 | ||||||
chr2:47875025
|
T | C | 41 | a0001c0001t0001g0078a0001c0001t0001g0093a0001c0001t0001g0094others(38): Show | 41 | HG00438.hp1 HG00544.hp1 HG00597.hp1 others(38): Show |
intron_variant | MODIFIER | c.232+30464A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47875025 | ||||||
chr2:47875042
|
A | G | 1 | a0001c0001t0002g0166 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.232+30447T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47875042 | ||||||
chr2:47875091
|
T | C | 5 | a0001c0001t0003g0107a0001c0001t0003g0243a0001c0001t0003g0282others(2): Show | 5 | HG02145.hp1 HG02257.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.232+30398A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47875091 | ||||||
chr2:47875092
|
G | A | 26 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(23): Show | 26 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.232+30397C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47875092 | ||||||
chr2:47875139
|
G | A | 4 | a0001c0001t0003g0107a0001c0001t0003g0282a0001c0001t0003g0294others(1): Show | 4 | HG02145.hp1 HG02257.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.232+30350C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47875139 | ||||||
chr2:47875173
|
G | A | 1 | a0001c0001t0010g0132 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.232+30316C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47875173 | ||||||
chr2:47875306
|
C | T | 3 | a0001c0001t0002g0035a0001c0001t0002g0138a0001c0001t0002g0152 | 3 | NA18942.hp1 NA19000.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.232+30183G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47875306 | ||||||
chr2:47875310
|
T | C | 3 | a0001c0001t0001g0005a0001c0001t0001g0191a0001c0001t0010g0132 | 4 | HG01243.hp1 HG02976.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.232+30179A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47875310 | ||||||
chr2:47875450
|
T | C | 1 | a0001c0001t0001g0129 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.232+30039A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47875450 | ||||||
chr2:47875496
|
G | A | 5 | a0001c0001t0002g0281a0001c0001t0002g0285a0001c0001t0002g0286others(2): Show | 5 | HG00738.hp1 HG01109.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.232+29993C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47875496 | ||||||
chr2:47875498
|
CT | C | 190 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0017others(187): Show | 193 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.232+29990delA | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47875498 | ||||||
chr2:47875709
|
C | CT | 5 | a0001c0001t0003g0107a0001c0001t0003g0243a0001c0001t0003g0282others(2): Show | 5 | HG02145.hp1 HG02257.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.232+29779dupA | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47875709 | ||||||
chr2:47875951
|
A | C | 3 | a0001c0001t0001g0227a0001c0001t0001g0228a0001c0001t0002g0225 | 3 | NA18962.hp2 NA18991.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.232+29538T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47875951 | ||||||
chr2:47875955
|
C | T | 1 | a0001c0001t0001g0218 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.232+29534G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47875955 | ||||||
chr2:47875956
|
T | C | 7 | a0001c0001t0001g0121a0001c0001t0001g0124a0001c0001t0001g0125others(4): Show | 7 | HG02109.hp1 HG02280.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.232+29533A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47875956 | ||||||
chr2:47876082
|
A | G | 7 | a0001c0001t0001g0264a0001c0001t0001g0287a0001c0001t0001g0288others(4): Show | 7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.232+29407T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47876082 | ||||||
chr2:47876188
|
TCTTTTTG others(5): Show |
T | 7 | a0001c0001t0001g0264a0001c0001t0001g0287a0001c0001t0001g0288others(4): Show | 7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.232+29289_232+2930 others(16): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47876188 | ||||||
chr2:47876189
|
C | G | 1 | a0001c0001t0001g0097 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.232+29300G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47876189 | ||||||
chr2:47876366
|
A | C | 154 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0064others(151): Show | 156 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.232+29123T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47876366 | ||||||
chr2:47876372
|
T | C | 41 | a0001c0001t0001g0004a0001c0001t0001g0092a0001c0001t0001g0103others(38): Show | 42 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.232+29117A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47876372 | ||||||
chr2:47876392
|
G | T | 1 | a0001c0001t0001g0053 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.232+29097C>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47876392 | ||||||
chr2:47876559
|
C | T | 2 | a0001c0001t0001g0048a0001c0001t0001g0056 | 2 | HG00639.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.232+28930G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47876559 | ||||||
chr2:47876577
|
T | C | 1 | a0003c0003t0001g0015 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.232+28912A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47876577 | ||||||
chr2:47876678
|
T | A | 5 | a0001c0001t0002g0281a0001c0001t0002g0285a0001c0001t0002g0286others(2): Show | 5 | HG00738.hp1 HG01109.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.232+28811A>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47876678 | ||||||
chr2:47876759
|
A | G | 1 | a0001c0001t0010g0132 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.232+28730T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47876759 | ||||||
chr2:47876875
|
T | C | 1 | a0001c0001t0010g0132 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.232+28614A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47876875 | ||||||
chr2:47876905
|
G | A | 19 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(16): Show | 19 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.232+28584C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47876905 | ||||||
chr2:47876916
|
AT | A | 30 | a0001c0001t0001g0074a0001c0001t0001g0208a0001c0001t0001g0209others(27): Show | 30 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.232+28572delA | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47876916 | ||||||
chr2:47876991
|
T | C | 2 | a0001c0001t0001g0094a0001c0001t0001g0096 | 2 | NA18946.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.232+28498A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47876991 | ||||||
chr2:47877007
|
T | C | 7 | a0001c0001t0001g0264a0001c0001t0001g0287a0001c0001t0001g0288others(4): Show | 7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.232+28482A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47877007 | ||||||
chr2:47877020
|
A | C | 1 | a0001c0001t0001g0298 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.232+28469T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47877020 | ||||||
chr2:47877042
|
G | GT | 17 | a0001c0001t0001g0045a0001c0001t0001g0048a0001c0001t0001g0116others(14): Show | 17 | HG00280.hp2 HG00639.hp1 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.232+28446dupA | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47877042 | ||||||
chr2:47877129
|
C | G | 1 | a0001c0001t0001g0097 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.232+28360G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47877129 | ||||||
chr2:47877299
|
A | C | 12 | a0001c0001t0001g0171a0001c0001t0002g0135a0001c0001t0002g0142others(9): Show | 12 | HG00735.hp1 HG01168.hp1 HG01168.hp2 others(9): Show |
intron_variant | MODIFIER | c.232+28190T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47877299 | ||||||
chr2:47877356
|
A | G | 15 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(12): Show | 15 | HG01433.hp1 HG01891.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.232+28133T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47877356 | ||||||
chr2:47877384
|
A | G | 1 | a0001c0001t0002g0139 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.232+28105T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47877384 | ||||||
chr2:47877423
|
T | C | 3 | a0001c0001t0001g0036a0001c0001t0001g0039a0001c0001t0001g0041 | 3 | HG02280.hp2 HG02300.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.232+28066A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47877423 | ||||||
chr2:47877619
|
C | G | 1 | a0001c0001t0014g0284 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.232+27870G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47877619 | ||||||
chr2:47877788
|
G | A | 3 | a0001c0001t0003g0282a0001c0001t0003g0294a0001c0001t0003g0295 | 3 | HG02145.hp1 HG02717.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.232+27701C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47877788 | ||||||
chr2:47877830
|
G | T | 8 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(5): Show | 8 | HG01346.hp1 HG02615.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.232+27659C>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47877830 | ||||||
chr2:47877881
|
T | C | 1 | a0001c0001t0001g0038 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.232+27608A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47877881 | ||||||
chr2:47877938
|
C | G | 1 | a0001c0001t0001g0290 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.232+27551G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47877938 | ||||||
chr2:47878050
|
G | T | 1 | a0001c0001t0010g0132 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.232+27439C>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47878050 | ||||||
chr2:47878051
|
T | A | 1 | a0001c0001t0001g0052 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.232+27438A>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47878051 | ||||||
chr2:47878317
|
T | C | 3 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184 | 3 | HG00323.hp2 HG00642.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.232+27172A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47878317 | ||||||
chr2:47878355
|
T | C | 1 | a0001c0001t0001g0123 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.232+27134A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47878355 | ||||||
chr2:47878479
|
C | T | 1 | a0004c0005t0002g0308 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.232+27010G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47878479 | ||||||
chr2:47878510
|
C | A | 1 | a0001c0001t0002g0135 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.232+26979G>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47878510 | ||||||
chr2:47878517
|
G | C | 18 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(15): Show | 18 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.232+26972C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47878517 | ||||||
chr2:47878661
|
AT | A | 26 | a0001c0001t0001g0110a0001c0001t0001g0209a0001c0001t0001g0210others(23): Show | 26 | HG00280.hp2 HG00639.hp2 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.232+26827delA | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47878661 | ||||||
chr2:47878706
|
G | A | 8 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(5): Show | 8 | HG01346.hp1 HG02615.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.232+26783C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47878706 | ||||||
chr2:47878749
|
A | G | 2 | a0001c0001t0001g0227a0001c0001t0001g0228 | 2 | NA18962.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.232+26740T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47878749 | ||||||
chr2:47878911
|
A | G | 25 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(22): Show | 25 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.232+26578T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47878911 | ||||||
chr2:47878964
|
T | TCAAAACA others(3): Show |
11 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(8): Show | 11 | HG01346.hp1 HG02145.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.232+26515_232+2652 others(14): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47878964 | ||||||
chr2:47879179
|
C | A | 2 | a0001c0001t0001g0174a0001c0001t0002g0180 | 2 | NA18957.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.232+26310G>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47879179 | ||||||
chr2:47879243
|
T | A | 8 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(5): Show | 8 | HG01346.hp1 HG02615.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.232+26246A>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47879243 | ||||||
chr2:47879251
|
A | G | 3 | a0001c0001t0002g0142a0001c0001t0002g0160a0001c0001t0002g0301 | 3 | HG00735.hp1 HG01981.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.232+26238T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47879251 | ||||||
chr2:47879380
|
G | C | 1 | a0001c0001t0001g0063 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.232+26109C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47879380 | ||||||
chr2:47879557
|
C | T | 3 | a0001c0001t0001g0254a0001c0001t0012g0253a0001c0001t0019g0312 | 3 | NA18952.hp2 NA18965.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.232+25932G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47879557 | ||||||
chr2:47879631
|
T | C | 1 | a0001c0001t0001g0103 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.232+25858A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47879631 | ||||||
chr2:47879641
|
G | T | 1 | a0001c0001t0001g0252 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.232+25848C>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47879641 | ||||||
chr2:47879676
|
T | C | 1 | a0001c0001t0001g0216 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.232+25813A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47879676 | ||||||
chr2:47879838
|
A | G | 8 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(5): Show | 8 | HG01346.hp1 HG02615.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.232+25651T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47879838 | ||||||
chr2:47879920
|
C | T | 1 | a0001c0001t0001g0106 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.232+25569G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47879920 | ||||||
chr2:47879940
|
C | T | 23 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(20): Show | 23 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.232+25549G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47879940 | ||||||
chr2:47879962
|
T | C | 1 | a0001c0001t0003g0293 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.232+25527A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47879962 | ||||||
chr2:47880000
|
GT | G | 8 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(5): Show | 8 | HG01346.hp1 HG02615.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.232+25488delA | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47880000 | ||||||
chr2:47880304
|
C | A | 29 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0197others(26): Show | 29 | HG00438.hp1 HG00544.hp1 HG00609.hp1 others(26): Show |
intron_variant | MODIFIER | c.232+25185G>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47880304 | ||||||
chr2:47880469
|
G | C | 1 | a0001c0001t0002g0109 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.232+25020C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47880469 | ||||||
chr2:47880664
|
C | T | 5 | a0001c0001t0003g0243a0001c0001t0003g0282a0001c0001t0003g0293others(2): Show | 5 | HG02145.hp1 HG02717.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.232+24825G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47880664 | ||||||
chr2:47880705
|
T | C | 1 | a0001c0001t0002g0050 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.232+24784A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47880705 | ||||||
chr2:47880754
|
G | C | 7 | a0001c0001t0001g0264a0001c0001t0001g0287a0001c0001t0001g0288others(4): Show | 7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.232+24735C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47880754 | ||||||
chr2:47880810
|
C | T | 1 | a0001c0001t0001g0104 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.232+24679G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47880810 | ||||||
chr2:47880923
|
CTAAAGGT others(25): Show |
C | 1 | a0001c0001t0001g0041 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.232+24534_232+2456 others(36): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47880923 | ||||||
chr2:47880943
|
T | C | 4 | a0001c0001t0002g0281a0001c0001t0002g0285a0001c0001t0002g0286others(1): Show | 4 | HG00738.hp1 HG02559.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.232+24546A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47880943 | ||||||
chr2:47881006
|
G | C | 5 | a0001c0001t0003g0243a0001c0001t0003g0282a0001c0001t0003g0293others(2): Show | 5 | HG02145.hp1 HG02717.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.232+24483C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47881006 | ||||||
chr2:47881011
|
T | G | 1 | a0001c0001t0001g0187 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.232+24478A>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47881011 | ||||||
chr2:47881047
|
G | A | 8 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(5): Show | 8 | HG01346.hp1 HG02615.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.232+24442C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47881047 | ||||||
chr2:47881079
|
C | T | 1 | a0001c0001t0002g0301 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.232+24410G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47881079 | ||||||
chr2:47881108
|
C | T | 1 | a0001c0001t0014g0284 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.232+24381G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47881108 | ||||||
chr2:47881169
|
T | C | 2 | a0001c0001t0001g0005a0001c0001t0001g0191 | 3 | HG01243.hp1 HG02976.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.232+24320A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47881169 | ||||||
chr2:47881178
|
G | C | 4 | a0001c0001t0002g0281a0001c0001t0002g0285a0001c0001t0002g0286others(1): Show | 4 | HG00738.hp1 HG02559.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.232+24311C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47881178 | ||||||
chr2:47881205
|
T | C | 1 | a0001c0001t0001g0129 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.232+24284A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47881205 | ||||||
chr2:47881221
|
C | T | 4 | a0001c0001t0002g0281a0001c0001t0002g0285a0001c0001t0002g0286others(1): Show | 4 | HG00738.hp1 HG02559.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.232+24268G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47881221 | ||||||
chr2:47881263
|
G | C | 1 | a0001c0001t0001g0063 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.232+24226C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47881263 | ||||||
chr2:47881322
|
G | T | 4 | a0001c0001t0002g0281a0001c0001t0002g0285a0001c0001t0002g0286others(1): Show | 4 | HG00738.hp1 HG02559.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.232+24167C>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47881322 | ||||||
chr2:47881490
|
C | A | 1 | a0001c0001t0001g0116 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.232+23999G>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47881490 | ||||||
chr2:47881647
|
C | T | 1 | a0001c0001t0001g0213 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.232+23842G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47881647 | ||||||
chr2:47881704
|
G | A | 1 | a0001c0001t0001g0116 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.232+23785C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47881704 | ||||||
chr2:47881705
|
T | C | 2 | a0001c0001t0001g0074a0001c0001t0001g0084 | 2 | NA19011.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.232+23784A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47881705 | ||||||
chr2:47881754
|
C | CT | 126 | a0001c0001t0001g0004a0001c0001t0001g0036a0001c0001t0001g0039others(123): Show | 127 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.232+23734dupA | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47881754 | ||||||
chr2:47881801
|
A | G | 1 | a0001c0001t0001g0123 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.232+23688T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47881801 | ||||||
chr2:47881858
|
G | C | 15 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(12): Show | 15 | HG01433.hp1 HG01891.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.232+23631C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47881858 | ||||||
chr2:47881880
|
T | C | 6 | a0001c0001t0002g0281a0001c0001t0002g0285a0001c0001t0002g0286others(3): Show | 6 | HG00738.hp1 HG01109.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.232+23609A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47881880 | ||||||
chr2:47882130
|
C | T | 1 | a0001c0001t0001g0123 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.232+23359G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47882130 | ||||||
chr2:47882182
|
A | G | 3 | a0001c0001t0002g0143a0001c0001t0002g0144a0001c0001t0002g0145 | 3 | HG01346.hp2 HG01515.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.232+23307T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47882182 | ||||||
chr2:47882368
|
C | T | 1 | a0001c0001t0003g0293 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.232+23121G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47882368 | ||||||
chr2:47882383
|
G | C | 1 | a0001c0001t0001g0270 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.232+23106C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47882383 | ||||||
chr2:47882443
|
T | TC | 12 | a0001c0001t0001g0264a0001c0001t0001g0287a0001c0001t0001g0288others(9): Show | 12 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.232+23045dupG | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47882443 | ||||||
chr2:47882474
|
C | T | 24 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(21): Show | 24 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.232+23015G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47882474 | ||||||
chr2:47882491
|
T | C | 5 | a0001c0001t0003g0107a0001c0001t0003g0243a0001c0001t0003g0282others(2): Show | 5 | HG02145.hp1 HG02257.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.232+22998A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47882491 | ||||||
chr2:47882596
|
A | G | 1 | a0001c0001t0002g0185 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.232+22893T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47882596 | ||||||
chr2:47882712
|
G | A | 5 | a0001c0001t0003g0107a0001c0001t0003g0243a0001c0001t0003g0282others(2): Show | 5 | HG02145.hp1 HG02257.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.232+22777C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47882712 | ||||||
chr2:47882780
|
T | C | 8 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(5): Show | 8 | HG01346.hp1 HG02615.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.232+22709A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47882780 | ||||||
chr2:47882829
|
T | C | 2 | a0001c0001t0001g0074a0001c0001t0001g0084 | 2 | NA19011.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.232+22660A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47882829 | ||||||
chr2:47882886
|
C | T | 3 | a0001c0001t0003g0282a0001c0001t0003g0294a0001c0001t0003g0295 | 3 | HG02145.hp1 HG02717.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.232+22603G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47882886 | ||||||
chr2:47883192
|
T | C | 1 | a0001c0001t0001g0201 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.232+22297A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47883192 | ||||||
chr2:47883318
|
C | A | 1 | a0001c0001t0001g0091 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.232+22171G>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47883318 | ||||||
chr2:47883410
|
C | G | 4 | a0001c0001t0003g0243a0001c0001t0003g0293a0001c0001t0003g0294others(1): Show | 4 | HG02717.hp1 HG03130.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.232+22079G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47883410 | ||||||
chr2:47883425
|
A | C | 27 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(24): Show | 27 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(24): Show |
intron_variant | MODIFIER | c.232+22064T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47883425 | ||||||
chr2:47883450
|
C | A | 1 | a0001c0001t0001g0072 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.232+22039G>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47883450 | ||||||
chr2:47883467
|
G | C | 4 | a0001c0001t0002g0281a0001c0001t0002g0285a0001c0001t0002g0286others(1): Show | 4 | HG00738.hp1 HG02559.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.232+22022C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47883467 | ||||||
chr2:47883701
|
T | A | 9 | a0001c0002t0002g0030a0001c0002t0002g0031a0001c0002t0002g0032others(6): Show | 9 | HG01109.hp2 HG01884.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.232+21788A>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47883701 | ||||||
chr2:47883715
|
A | G | 1 | a0001c0001t0001g0270 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.232+21774T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47883715 | ||||||
chr2:47883752
|
C | T | 1 | a0001c0001t0010g0132 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.232+21737G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47883752 | ||||||
chr2:47883880
|
T | C | 5 | a0001c0001t0003g0243a0001c0001t0003g0282a0001c0001t0003g0293others(2): Show | 5 | HG02145.hp1 HG02717.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.232+21609A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47883880 | ||||||
chr2:47884057
|
T | C | 57 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0036others(54): Show | 59 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.232+21432A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47884057 | ||||||
chr2:47884281
|
C | T | 1 | a0001c0001t0001g0119 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.232+21208G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47884281 | ||||||
chr2:47884396
|
C | A | 1 | a0001c0001t0001g0053 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.232+21093G>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47884396 | ||||||
chr2:47884445
|
G | A | 2 | a0001c0001t0001g0053a0001c0001t0001g0081 | 2 | HG01993.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.232+21044C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47884445 | ||||||
chr2:47884453
|
T | C | 2 | a0001c0001t0001g0186a0001c0001t0002g0179 | 2 | HG02572.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.232+21036A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47884453 | ||||||
chr2:47884701
|
GGTATTTT others(4): Show |
G | 7 | a0001c0001t0001g0264a0001c0001t0001g0287a0001c0001t0001g0288others(4): Show | 7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.232+20777_232+2078 others(15): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47884701 | ||||||
chr2:47884824
|
T | G | 1 | a0001c0001t0001g0252 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.232+20665A>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47884824 | ||||||
chr2:47884828
|
CA | C | 7 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(4): Show | 7 | HG01346.hp1 HG02615.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.232+20660delT | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47884828 | ||||||
chr2:47884880
|
C | A | 7 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(4): Show | 7 | HG01346.hp1 HG02615.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.232+20609G>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47884880 | ||||||
chr2:47884892
|
A | G | 1 | a0001c0001t0001g0276 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.232+20597T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47884892 | ||||||
chr2:47884914
|
A | T | 10 | a0001c0001t0001g0167a0001c0001t0001g0188a0001c0001t0002g0162others(7): Show | 10 | HG00280.hp1 HG00738.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.232+20575T>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47884914 | ||||||
chr2:47885203
|
T | C | 1 | a0001c0001t0001g0020 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.232+20286A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47885203 | ||||||
chr2:47885332
|
G | A | 1 | a0001c0001t0001g0204 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.232+20157C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47885332 | ||||||
chr2:47885449
|
C | G | 35 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(32): Show | 35 | HG00438.hp1 HG00544.hp1 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.232+20040G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47885449 | ||||||
chr2:47885467
|
C | T | 1 | a0001c0001t0001g0279 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.232+20022G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47885467 | ||||||
chr2:47885515
|
C | G | 1 | a0001c0001t0001g0111 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.232+19974G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47885515 | ||||||
chr2:47885687
|
T | C | 1 | a0001c0001t0001g0048 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.232+19802A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47885687 | ||||||
chr2:47885716
|
T | C | 1 | a0001c0001t0003g0293 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.232+19773A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47885716 | ||||||
chr2:47885789
|
A | C | 1 | a0001c0001t0001g0097 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.232+19700T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47885789 | ||||||
chr2:47885974
|
C | G | 1 | a0001c0001t0001g0073 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.232+19515G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47885974 | ||||||
chr2:47886007
|
A | ATGCATTG others(23): Show |
7 | a0001c0001t0001g0264a0001c0001t0001g0287a0001c0001t0001g0288others(4): Show | 7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.232+19481_232+1948 others(34): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47886007 | ||||||
chr2:47886008
|
A | C | 7 | a0001c0001t0001g0264a0001c0001t0001g0287a0001c0001t0001g0288others(4): Show | 7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.232+19481T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47886008 | ||||||
chr2:47886010
|
C | G | 5 | a0001c0001t0002g0196a0001c0001t0002g0248a0001c0001t0002g0249others(2): Show | 5 | HG01261.hp2 HG02055.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.232+19479G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47886010 | ||||||
chr2:47886265
|
G | C | 4 | a0001c0001t0003g0107a0001c0001t0003g0282a0001c0001t0003g0294others(1): Show | 4 | HG02145.hp1 HG02257.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.232+19224C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47886265 | ||||||
chr2:47886320
|
C | T | 1 | a0001c0002t0002g0283 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.232+19169G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47886320 | ||||||
chr2:47886501
|
C | CA | 13 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(10): Show | 13 | HG01346.hp1 HG02615.hp2 HG02723.hp1 others(10): Show |
intron_variant | MODIFIER | c.232+18987dupT | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47886501 | ||||||
chr2:47886501
|
CA | C | 10 | a0001c0001t0001g0264a0001c0001t0001g0287a0001c0001t0001g0288others(7): Show | 10 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.232+18987delT | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47886501 | ||||||
chr2:47886559
|
A | G | 1 | a0001c0001t0001g0087 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.232+18930T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47886559 | ||||||
chr2:47886563
|
T | C | 1 | a0001c0001t0002g0109 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.232+18926A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47886563 | ||||||
chr2:47886693
|
A | G | 1 | a0001c0001t0001g0097 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.232+18796T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47886693 | ||||||
chr2:47886778
|
T | C | 1 | a0001c0001t0002g0303 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.232+18711A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47886778 | ||||||
chr2:47886863
|
T | A | 5 | a0001c0001t0001g0052a0001c0001t0002g0054a0001c0001t0004g0011others(2): Show | 5 | HG02135.hp2 HG02523.hp2 NA18982.hp2 others(2): Show |
intron_variant | MODIFIER | c.232+18626A>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47886863 | ||||||
chr2:47886864
|
G | T | 5 | a0001c0001t0001g0052a0001c0001t0002g0054a0001c0001t0004g0011others(2): Show | 5 | HG02135.hp2 HG02523.hp2 NA18982.hp2 others(2): Show |
intron_variant | MODIFIER | c.232+18625C>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47886864 | ||||||
chr2:47886916
|
G | C | 3 | a0001c0001t0001g0036a0001c0001t0001g0039a0001c0001t0001g0041 | 3 | HG02280.hp2 HG02300.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.232+18573C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47886916 | ||||||
chr2:47886955
|
C | G | 25 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(22): Show | 25 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.232+18534G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47886955 | ||||||
chr2:47886972
|
C | A | 1 | a0001c0001t0003g0282 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.232+18517G>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47886972 | ||||||
chr2:47887070
|
G | A | 48 | a0001c0001t0001g0151a0001c0001t0001g0156a0001c0001t0001g0167others(45): Show | 49 | HG00280.hp1 HG00735.hp1 HG00738.hp2 others(46): Show |
intron_variant | MODIFIER | c.232+18419C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47887070 | ||||||
chr2:47887195
|
T | G | 27 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(24): Show | 27 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(24): Show |
intron_variant | MODIFIER | c.232+18294A>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47887195 | ||||||
chr2:47887248
|
G | T | 4 | a0001c0001t0002g0139a0002c0004t0002g0262a0002c0004t0002g0263others(1): Show | 4 | HG01884.hp1 HG02896.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.232+18241C>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47887248 | ||||||
chr2:47887299
|
G | T | 1 | a0001c0001t0007g0008 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.232+18190C>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47887299 | ||||||
chr2:47887450
|
C | T | 3 | a0001c0001t0003g0282a0001c0001t0003g0294a0001c0001t0003g0295 | 3 | HG02145.hp1 HG02717.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.232+18039G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47887450 | ||||||
chr2:47887635
|
C | T | 7 | a0001c0001t0001g0051a0001c0001t0001g0059a0001c0001t0001g0079others(4): Show | 7 | HG01074.hp1 NA18966.hp2 NA18979.hp2 others(4): Show |
intron_variant | MODIFIER | c.232+17854G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47887635 | ||||||
chr2:47888003
|
T | A | 7 | a0001c0001t0001g0264a0001c0001t0001g0287a0001c0001t0001g0288others(4): Show | 7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.232+17486A>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47888003 | ||||||
chr2:47888027
|
T | G | 7 | a0001c0001t0001g0264a0001c0001t0001g0287a0001c0001t0001g0288others(4): Show | 7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.232+17462A>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47888027 | ||||||
chr2:47888124
|
C | G | 27 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(24): Show | 27 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(24): Show |
intron_variant | MODIFIER | c.232+17365G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47888124 | ||||||
chr2:47888125
|
G | A | 9 | a0001c0002t0002g0030a0001c0002t0002g0031a0001c0002t0002g0032others(6): Show | 9 | HG01109.hp2 HG01884.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.232+17364C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47888125 | ||||||
chr2:47888289
|
T | C | 1 | a0001c0001t0003g0293 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.232+17200A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47888289 | ||||||
chr2:47888577
|
C | A | 1 | a0001c0001t0001g0216 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.232+16912G>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47888577 | ||||||
chr2:47888608
|
T | C | 3 | a0002c0004t0002g0262a0002c0004t0002g0263a0002c0004t0002g0266 | 3 | HG01884.hp1 HG02896.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.232+16881A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47888608 | ||||||
chr2:47888748
|
G | A | 15 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(12): Show | 15 | HG01433.hp1 HG01891.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.232+16741C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47888748 | ||||||
chr2:47888803
|
T | C | 10 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(7): Show | 10 | HG01346.hp1 HG02615.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.232+16686A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47888803 | ||||||
chr2:47888813
|
T | C | 10 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(7): Show | 10 | HG01346.hp1 HG02615.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.232+16676A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47888813 | ||||||
chr2:47888929
|
T | C | 3 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0187 | 3 | HG01243.hp2 HG02886.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.232+16560A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47888929 | ||||||
chr2:47888987
|
G | A | 255 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(252): Show | 259 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(256): Show |
intron_variant | MODIFIER | c.232+16502C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47888987 | ||||||
chr2:47889044
|
TTCAC | T | 5 | a0001c0001t0001g0217a0001c0001t0001g0220a0001c0001t0001g0221others(2): Show | 5 | HG00099.hp2 HG00741.hp2 HG01070.hp2 others(2): Show |
intron_variant | MODIFIER | c.232+16441_232+1644 others(8): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47889044 | ||||||
chr2:47889093
|
T | C | 7 | a0001c0001t0001g0264a0001c0001t0001g0287a0001c0001t0001g0288others(4): Show | 7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.232+16396A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47889093 | ||||||
chr2:47889159
|
A | G | 6 | a0001c0001t0001g0078a0001c0001t0001g0093a0001c0001t0001g0094others(3): Show | 6 | HG00597.hp1 NA18946.hp1 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.232+16330T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47889159 | ||||||
chr2:47889177
|
C | T | 4 | a0001c0001t0001g0052a0001c0001t0004g0011a0001c0001t0004g0012others(1): Show | 4 | HG02135.hp2 HG02523.hp2 NA18982.hp2 others(1): Show |
intron_variant | MODIFIER | c.232+16312G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47889177 | ||||||
chr2:47889209
|
C | T | 1 | a0001c0001t0001g0038 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.232+16280G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47889209 | ||||||
chr2:47889432
|
C | A | 4 | a0001c0001t0003g0282a0001c0001t0003g0293a0001c0001t0003g0294others(1): Show | 4 | HG02145.hp1 HG02717.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.232+16057G>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47889432 | ||||||
chr2:47889496
|
T | A | 25 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(22): Show | 25 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.232+15993A>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47889496 | ||||||
chr2:47889627
|
G | A | 1 | a0004c0005t0002g0308 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.232+15862C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47889627 | ||||||
chr2:47889633
|
GT | G | 192 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(189): Show | 196 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.232+15855delA | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47889633 | ||||||
chr2:47889633
|
GTT | G | 12 | a0001c0001t0001g0264a0001c0001t0001g0287a0001c0001t0001g0288others(9): Show | 12 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.232+15854_232+1585 others(6): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47889633 | ||||||
chr2:47889736
|
G | C | 1 | a0001c0001t0001g0209 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.232+15753C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47889736 | ||||||
chr2:47889745
|
A | G | 1 | a0001c0001t0001g0275 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.232+15744T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47889745 | ||||||
chr2:47890020
|
C | A | 1 | a0001c0001t0003g0107 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.232+15469G>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47890020 | ||||||
chr2:47890123
|
A | ATTAT | 10 | a0001c0001t0001g0110a0001c0001t0001g0167a0001c0001t0001g0275others(7): Show | 10 | HG01261.hp2 HG01891.hp2 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.232+15362_232+1536 others(8): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47890123 | ||||||
chr2:47890222
|
C | G | 1 | a0001c0001t0001g0106 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.232+15267G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47890222 | ||||||
chr2:47890235
|
A | C | 10 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(7): Show | 10 | HG01346.hp1 HG02615.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.232+15254T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47890235 | ||||||
chr2:47890292
|
T | G | 1 | a0001c0001t0001g0072 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.232+15197A>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47890292 | ||||||
chr2:47890358
|
T | C | 3 | a0001c0001t0001g0274a0001c0001t0002g0272a0001c0001t0002g0273 | 3 | HG01074.hp2 NA20129.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.232+15131A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47890358 | ||||||
chr2:47890436
|
T | C | 1 | a0001c0001t0001g0278 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.232+15053A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47890436 | ||||||
chr2:47890517
|
A | G | 1 | a0001c0001t0001g0094 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.232+14972T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47890517 | ||||||
chr2:47890660
|
C | T | 2 | a0001c0001t0001g0066a0001c0001t0001g0067 | 2 | NA18999.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.232+14829G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47890660 | ||||||
chr2:47890736
|
A | T | 10 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(7): Show | 10 | HG01346.hp1 HG02615.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.232+14753T>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47890736 | ||||||
chr2:47890777
|
C | G | 7 | a0001c0001t0001g0264a0001c0001t0001g0287a0001c0001t0001g0288others(4): Show | 7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.232+14712G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47890777 | ||||||
chr2:47890787
|
G | C | 3 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027 | 3 | HG01433.hp1 HG03130.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.232+14702C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47890787 | ||||||
chr2:47890791
|
G | A | 1 | a0001c0001t0001g0209 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.232+14698C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47890791 | ||||||
chr2:47890811
|
GA | G | 28 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0029others(25): Show | 28 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(25): Show |
intron_variant | MODIFIER | c.232+14677delT | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47890811 | ||||||
chr2:47890821
|
A | T | 1 | a0001c0001t0002g0250 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.232+14668T>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47890821 | ||||||
chr2:47890826
|
T | G | 4 | a0001c0001t0003g0107a0001c0001t0003g0282a0001c0001t0003g0294others(1): Show | 4 | HG02145.hp1 HG02257.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.232+14663A>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47890826 | ||||||
chr2:47890855
|
T | C | 1 | a0001c0001t0002g0178 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.232+14634A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47890855 | ||||||
chr2:47890875
|
T | C | 1 | a0001c0001t0001g0297 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.232+14614A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47890875 | ||||||
chr2:47890901
|
T | G | 1 | a0001c0001t0001g0200 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.232+14588A>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47890901 | ||||||
chr2:47890994
|
T | A | 10 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(7): Show | 10 | HG01346.hp1 HG02615.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.232+14495A>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47890994 | ||||||
chr2:47890994
|
T | TTA | 7 | a0001c0001t0001g0264a0001c0001t0001g0287a0001c0001t0001g0288others(4): Show | 7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.232+14494_232+1449 others(6): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47890994 | ||||||
chr2:47890996
|
A | AT | 19 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(16): Show | 19 | HG00738.hp1 HG01346.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.232+14492dupA | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47890996 | ||||||
chr2:47890996
|
A | T | 7 | a0001c0001t0001g0264a0001c0001t0001g0287a0001c0001t0001g0288others(4): Show | 7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.232+14493T>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47890996 | ||||||
chr2:47891481
|
G | A | 2 | a0001c0001t0003g0294a0001c0001t0003g0295 | 2 | HG02717.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.232+14008C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47891481 | ||||||
chr2:47891499
|
T | C | 3 | a0001c0001t0001g0274a0001c0001t0002g0272a0001c0001t0002g0273 | 3 | HG01074.hp2 NA20129.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.232+13990A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47891499 | ||||||
chr2:47891590
|
T | C | 2 | a0001c0001t0001g0094a0001c0001t0001g0096 | 2 | NA18946.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.232+13899A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47891590 | ||||||
chr2:47891676
|
A | T | 1 | a0001c0001t0002g0181 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.232+13813T>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47891676 | ||||||
chr2:47891678
|
T | A | 1 | a0001c0001t0002g0181 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.232+13811A>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47891678 | ||||||
chr2:47891749
|
G | C | 2 | a0001c0001t0001g0192a0001c0001t0001g0242 | 2 | HG03492.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.232+13740C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47891749 | ||||||
chr2:47891757
|
T | C | 53 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0092others(50): Show | 55 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.232+13732A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47891757 | ||||||
chr2:47892096
|
T | C | 5 | a0001c0001t0002g0281a0001c0001t0002g0285a0001c0001t0002g0286others(2): Show | 5 | HG00738.hp1 HG01109.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.232+13393A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47892096 | ||||||
chr2:47892117
|
T | A | 1 | a0001c0001t0002g0225 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.232+13372A>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47892117 | ||||||
chr2:47892134
|
C | T | 51 | a0001c0001t0001g0151a0001c0001t0001g0156a0001c0001t0001g0167others(48): Show | 52 | HG00280.hp1 HG00735.hp1 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.232+13355G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47892134 | ||||||
chr2:47892278
|
T | A | 7 | a0001c0001t0001g0264a0001c0001t0001g0287a0001c0001t0001g0288others(4): Show | 7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.232+13211A>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47892278 | ||||||
chr2:47892307
|
A | C | 10 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(7): Show | 10 | HG01346.hp1 HG02615.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.232+13182T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47892307 | ||||||
chr2:47892363
|
T | C | 1 | a0001c0001t0002g0141 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.232+13126A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47892363 | ||||||
chr2:47892524
|
T | A | 3 | a0001c0001t0001g0274a0001c0001t0002g0272a0001c0001t0002g0273 | 3 | HG01074.hp2 NA20129.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.232+12965A>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47892524 | ||||||
chr2:47892531
|
G | T | 1 | a0001c0001t0001g0003 | 2 | HG02257.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.232+12958C>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47892531 | ||||||
chr2:47892641
|
A | T | 4 | a0001c0001t0003g0282a0001c0001t0003g0293a0001c0001t0003g0294others(1): Show | 4 | HG02145.hp1 HG02717.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.232+12848T>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47892641 | ||||||
chr2:47892698
|
A | G | 10 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(7): Show | 10 | HG01346.hp1 HG02615.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.232+12791T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47892698 | ||||||
chr2:47892763
|
G | C | 1 | a0001c0001t0007g0008 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.232+12726C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47892763 | ||||||
chr2:47892791
|
A | G | 1 | a0001c0001t0002g0185 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.232+12698T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47892791 | ||||||
chr2:47892821
|
T | C | 5 | a0001c0001t0003g0243a0001c0001t0003g0282a0001c0001t0003g0293others(2): Show | 5 | HG02145.hp1 HG02717.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.232+12668A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47892821 | ||||||
chr2:47892856
|
C | T | 1 | a0001c0001t0001g0212 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.232+12633G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47892856 | ||||||
chr2:47892949
|
T | C | 109 | a0001c0001t0001g0004a0001c0001t0001g0064a0001c0001t0001g0065others(106): Show | 110 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.232+12540A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47892949 | ||||||
chr2:47893019
|
G | T | 25 | a0001c0001t0001g0193a0001c0001t0001g0197a0001c0001t0001g0198others(22): Show | 25 | HG00438.hp1 HG00544.hp1 HG02155.hp2 others(22): Show |
intron_variant | MODIFIER | c.232+12470C>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47893019 | ||||||
chr2:47893042
|
C | G | 4 | a0001c0001t0002g0140a0001c0001t0002g0141a0001c0001t0002g0157others(1): Show | 4 | HG02027.hp1 HG02165.hp1 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.232+12447G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47893042 | ||||||
chr2:47893048
|
C | G | 3 | a0001c0001t0001g0274a0001c0001t0002g0272a0001c0001t0002g0273 | 3 | HG01074.hp2 NA20129.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.232+12441G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47893048 | ||||||
chr2:47893107
|
T | C | 1 | a0001c0001t0001g0264 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.232+12382A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47893107 | ||||||
chr2:47893166
|
T | TTAAATAA others(5): Show |
6 | a0001c0001t0001g0289a0001c0001t0002g0281a0001c0001t0002g0285others(3): Show | 6 | HG00738.hp1 HG01257.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.232+12311_232+1232 others(16): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47893166 | ||||||
chr2:47893166
|
T | TTAAATAA others(9): Show |
4 | a0001c0001t0001g0288a0001c0001t0003g0293a0001c0001t0003g0294others(1): Show | 4 | HG01081.hp1 HG02717.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.232+12307_232+1232 others(20): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47893166 | ||||||
chr2:47893166
|
T | TTAAATAA others(13): Show |
5 | a0001c0001t0001g0264a0001c0001t0001g0287a0001c0001t0001g0290others(2): Show | 5 | HG00280.hp2 HG01070.hp1 HG01255.hp1 others(2): Show |
intron_variant | MODIFIER | c.232+12303_232+1232 others(24): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47893166 | ||||||
chr2:47893178
|
A | ATAAATAA others(5): Show |
9 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(6): Show | 9 | HG01346.hp1 HG02615.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.232+12310_232+1231 others(16): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47893178 | ||||||
chr2:47893178
|
A | C | 1 | a0001c0001t0001g0237 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.232+12311T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47893178 | ||||||
chr2:47893281
|
C | T | 6 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0002g0196others(3): Show | 6 | HG01261.hp2 HG01891.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.232+12208G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47893281 | ||||||
chr2:47893353
|
C | CAT | 4 | a0001c0001t0001g0106a0001c0001t0001g0274a0001c0001t0002g0272others(1): Show | 4 | HG01074.hp2 NA19005.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.232+12134_232+1213 others(6): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47893353 | ||||||
chr2:47893353
|
CAT | C | 20 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(17): Show | 20 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.232+12134_232+1213 others(6): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47893353 | ||||||
chr2:47893367
|
T | C | 8 | a0001c0001t0001g0264a0001c0001t0001g0287a0001c0001t0001g0288others(5): Show | 8 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.232+12122A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47893367 | ||||||
chr2:47893381
|
A | C | 1 | a0001c0001t0002g0181 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.232+12108T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47893381 | ||||||
chr2:47893559
|
G | C | 21 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(18): Show | 21 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(18): Show |
intron_variant | MODIFIER | c.232+11930C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47893559 | ||||||
chr2:47893678
|
G | A | 1 | a0001c0001t0001g0021 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.232+11811C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47893678 | ||||||
chr2:47893679
|
C | T | 1 | a0001c0001t0001g0021 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.232+11810G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47893679 | ||||||
chr2:47893727
|
G | A | 9 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(6): Show | 9 | HG01346.hp1 HG02615.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.232+11762C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47893727 | ||||||
chr2:47893992
|
G | C | 9 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(6): Show | 9 | HG01346.hp1 HG02615.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.232+11497C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47893992 | ||||||
chr2:47894049
|
T | C | 2 | a0001c0001t0002g0080a0001c0001t0002g0101 | 2 | HG01169.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.232+11440A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47894049 | ||||||
chr2:47894464
|
T | C | 7 | a0001c0001t0001g0264a0001c0001t0001g0287a0001c0001t0001g0288others(4): Show | 7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.232+11025A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47894464 | ||||||
chr2:47894571
|
A | G | 1 | a0001c0001t0001g0110 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.232+10918T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47894571 | ||||||
chr2:47894577
|
C | A | 1 | a0001c0001t0001g0097 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.232+10912G>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47894577 | ||||||
chr2:47894606
|
A | C | 4 | a0001c0001t0002g0140a0001c0001t0002g0141a0001c0001t0002g0157others(1): Show | 4 | HG02027.hp1 HG02165.hp1 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.232+10883T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47894606 | ||||||
chr2:47894855
|
T | C | 5 | a0001c0001t0001g0052a0001c0001t0002g0054a0001c0001t0004g0011others(2): Show | 5 | HG02135.hp2 HG02523.hp2 NA18982.hp2 others(2): Show |
intron_variant | MODIFIER | c.232+10634A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47894855 | ||||||
chr2:47894925
|
C | G | 1 | a0001c0001t0001g0304 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.232+10564G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47894925 | ||||||
chr2:47895107
|
A | G | 1 | a0001c0001t0002g0148 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.232+10382T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47895107 | ||||||
chr2:47895115
|
T | C | 1 | a0001c0001t0001g0237 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.232+10374A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47895115 | ||||||
chr2:47895122
|
G | C | 6 | a0001c0001t0003g0107a0001c0001t0003g0243a0001c0001t0003g0282others(3): Show | 6 | HG02145.hp1 HG02257.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.232+10367C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47895122 | ||||||
chr2:47895137
|
G | A | 1 | a0001c0001t0001g0226 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.232+10352C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47895137 | ||||||
chr2:47895238
|
C | G | 3 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0029 | 3 | HG01891.hp1 HG02559.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.232+10251G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47895238 | ||||||
chr2:47895418
|
G | T | 11 | a0001c0001t0001g0264a0001c0001t0001g0287a0001c0001t0001g0288others(8): Show | 11 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(8): Show |
intron_variant | MODIFIER | c.232+10071C>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47895418 | ||||||
chr2:47895540
|
T | C | 5 | a0001c0001t0002g0281a0001c0001t0002g0285a0001c0001t0002g0286others(2): Show | 5 | HG00738.hp1 HG01109.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.232+9949A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47895540 | ||||||
chr2:47895582
|
G | A | 9 | a0001c0002t0002g0030a0001c0002t0002g0031a0001c0002t0002g0032others(6): Show | 9 | HG01109.hp2 HG01884.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.232+9907C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47895582 | ||||||
chr2:47895654
|
G | A | 312 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(309): Show | 317 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(314): Show |
intron_variant | MODIFIER | c.232+9835C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47895654 | ||||||
chr2:47895684
|
A | G | 3 | a0001c0001t0001g0110a0001c0001t0001g0275a0001c0001t0001g0276 | 3 | HG01891.hp2 NA19043.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.232+9805T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47895684 | ||||||
chr2:47895703
|
T | G | 3 | a0001c0001t0001g0004a0001c0001t0001g0215a0001c0001t0001g0304 | 4 | HG02055.hp2 HG03209.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.232+9786A>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47895703 | ||||||
chr2:47895709
|
T | C | 5 | a0001c0001t0001g0121a0001c0001t0001g0124a0001c0001t0001g0125others(2): Show | 5 | HG02109.hp1 HG02280.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.232+9780A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47895709 | ||||||
chr2:47895752
|
G | T | 10 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(7): Show | 10 | HG01346.hp1 HG02615.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.232+9737C>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47895752 | ||||||
chr2:47895818
|
G | A | 3 | a0001c0001t0001g0274a0001c0001t0002g0272a0001c0001t0002g0273 | 3 | HG01074.hp2 NA20129.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.232+9671C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47895818 | ||||||
chr2:47895883
|
G | A | 4 | a0001c0001t0002g0281a0001c0001t0002g0285a0001c0001t0002g0286others(1): Show | 4 | HG00738.hp1 HG02559.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.232+9606C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47895883 | ||||||
chr2:47895903
|
G | C | 5 | a0001c0001t0001g0052a0001c0001t0002g0054a0001c0001t0004g0011others(2): Show | 5 | HG02135.hp2 HG02523.hp2 NA18982.hp2 others(2): Show |
intron_variant | MODIFIER | c.232+9586C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47895903 | ||||||
chr2:47895930
|
C | A | 1 | a0001c0001t0001g0209 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.232+9559G>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47895930 | ||||||
chr2:47895954
|
C | T | 1 | a0001c0001t0001g0226 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.232+9535G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47895954 | ||||||
chr2:47895990
|
C | T | 11 | a0001c0001t0001g0264a0001c0001t0001g0287a0001c0001t0001g0288others(8): Show | 11 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(8): Show |
intron_variant | MODIFIER | c.232+9499G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47895990 | ||||||
chr2:47896016
|
T | G | 1 | a0001c0001t0002g0141 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.232+9473A>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47896016 | ||||||
chr2:47896247
|
T | C | 22 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(19): Show | 22 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.232+9242A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47896247 | ||||||
chr2:47896321
|
G | GTTTCT | 19 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(16): Show | 19 | HG01346.hp1 HG02145.hp1 HG02615.hp2 others(16): Show |
intron_variant | MODIFIER | c.232+9163_232+9167d others(7): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47896321 | ||||||
chr2:47896330
|
C | CT | 18 | a0001c0001t0001g0038a0001c0001t0001g0122a0001c0001t0001g0127others(15): Show | 18 | HG00639.hp2 HG00642.hp1 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.232+9158dupA | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47896330 | ||||||
chr2:47896330
|
C | CTTTTCT | 11 | a0001c0001t0001g0264a0001c0001t0001g0287a0001c0001t0001g0288others(8): Show | 11 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(8): Show |
intron_variant | MODIFIER | c.232+9158_232+9159i others(8): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47896330 | ||||||
chr2:47896491
|
C | G | 2 | a0001c0001t0002g0285a0001c0002t0002g0283 | 2 | HG01109.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.232+8998G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47896491 | ||||||
chr2:47896540
|
G | C | 6 | a0001c0001t0002g0154a0001c0001t0002g0155a0001c0001t0002g0159others(3): Show | 6 | HG01884.hp1 HG01978.hp1 HG02273.hp2 others(3): Show |
intron_variant | MODIFIER | c.232+8949C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47896540 | ||||||
chr2:47896611
|
C | T | 3 | a0001c0001t0002g0142a0001c0001t0002g0160a0001c0001t0002g0301 | 3 | HG00735.hp1 HG01981.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.232+8878G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47896611 | ||||||
chr2:47896613
|
T | C | 1 | a0001c0001t0001g0199 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.232+8876A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47896613 | ||||||
chr2:47896720
|
T | C | 6 | a0001c0001t0002g0281a0001c0001t0002g0285a0001c0001t0002g0286others(3): Show | 6 | HG00738.hp1 HG01109.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.232+8769A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47896720 | ||||||
chr2:47896749
|
G | T | 1 | a0001c0001t0001g0071 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.232+8740C>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47896749 | ||||||
chr2:47896756
|
A | C | 10 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(7): Show | 10 | HG01346.hp1 HG02615.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.232+8733T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47896756 | ||||||
chr2:47896766
|
G | A | 1 | a0001c0001t0014g0284 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.232+8723C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47896766 | ||||||
chr2:47896776
|
A | T | 31 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(28): Show | 31 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(28): Show |
intron_variant | MODIFIER | c.232+8713T>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47896776 | ||||||
chr2:47896931
|
A | C | 28 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(25): Show | 28 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.232+8558T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47896931 | ||||||
chr2:47897039
|
G | C | 10 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(7): Show | 10 | HG01346.hp1 HG02615.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.232+8450C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47897039 | ||||||
chr2:47897088
|
A | C | 2 | a0001c0001t0001g0239a0003c0003t0001g0016 | 2 | HG02647.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.232+8401T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47897088 | ||||||
chr2:47897090
|
A | C | 28 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(25): Show | 28 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.232+8399T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47897090 | ||||||
chr2:47897365
|
G | C | 101 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0038others(98): Show | 102 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.232+8124C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47897365 | ||||||
chr2:47897525
|
C | T | 1 | a0001c0001t0002g0172 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.232+7964G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47897525 | ||||||
chr2:47897563
|
G | T | 1 | a0001c0001t0002g0249 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.232+7926C>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47897563 | ||||||
chr2:47897616
|
G | C | 1 | a0001c0001t0001g0271 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.232+7873C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47897616 | ||||||
chr2:47897701
|
C | CA | 75 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0092others(72): Show | 77 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(74): Show |
intron_variant | MODIFIER | c.232+7787dupT | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47897701 | ||||||
chr2:47897701
|
CA | C | 94 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0038others(91): Show | 95 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.232+7787delT | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47897701 | ||||||
chr2:47897930
|
A | C | 1 | a0002c0004t0002g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.232+7559T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47897930 | ||||||
chr2:47898009
|
T | C | 1 | a0001c0001t0001g0092 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.232+7480A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47898009 | ||||||
chr2:47898097
|
T | C | 1 | a0001c0001t0007g0008 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.232+7392A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47898097 | ||||||
chr2:47898154
|
A | G | 2 | a0001c0001t0002g0163a0001c0001t0002g0164 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.232+7335T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47898154 | ||||||
chr2:47898288
|
A | G | 1 | a0001c0001t0008g0009 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.232+7201T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47898288 | ||||||
chr2:47898361
|
T | C | 6 | a0001c0001t0002g0281a0001c0001t0002g0285a0001c0001t0002g0286others(3): Show | 6 | HG00738.hp1 HG01109.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.232+7128A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47898361 | ||||||
chr2:47898399
|
A | G | 1 | a0001c0001t0001g0041 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.232+7090T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47898399 | ||||||
chr2:47898569
|
C | T | 1 | a0001c0001t0001g0065 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.232+6920G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47898569 | ||||||
chr2:47898589
|
A | G | 1 | a0001c0001t0001g0060 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.232+6900T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47898589 | ||||||
chr2:47898692
|
A | G | 1 | a0001c0001t0001g0252 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.232+6797T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47898692 | ||||||
chr2:47898784
|
G | C | 5 | a0001c0001t0002g0281a0001c0001t0002g0285a0001c0001t0002g0286others(2): Show | 5 | HG00738.hp1 HG01109.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.232+6705C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47898784 | ||||||
chr2:47899002
|
C | T | 1 | a0001c0001t0001g0117 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.232+6487G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47899002 | ||||||
chr2:47899059
|
G | C | 3 | a0001c0001t0003g0282a0001c0001t0003g0294a0001c0001t0003g0295 | 3 | HG02145.hp1 HG02717.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.232+6430C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47899059 | ||||||
chr2:47899147
|
A | G | 1 | a0001c0001t0001g0039 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.232+6342T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47899147 | ||||||
chr2:47899223
|
G | C | 1 | a0001c0001t0001g0184 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.232+6266C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47899223 | ||||||
chr2:47899263
|
G | C | 1 | a0001c0001t0003g0293 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.232+6226C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47899263 | ||||||
chr2:47899273
|
C | CA | 33 | a0001c0001t0001g0051a0001c0001t0001g0065a0001c0001t0001g0066others(30): Show | 33 | HG00280.hp2 HG00597.hp1 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.232+6215dupT | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47899273 | ||||||
chr2:47899273
|
CA | C | 13 | a0001c0001t0001g0041a0001c0001t0001g0070a0001c0001t0001g0075others(10): Show | 13 | HG00280.hp1 HG00609.hp2 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.232+6215delT | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47899273 | ||||||
chr2:47899357
|
T | C | 2 | a0001c0001t0001g0053a0001c0001t0001g0081 | 2 | HG01993.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.232+6132A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47899357 | ||||||
chr2:47899397
|
C | G | 1 | a0001c0001t0002g0054 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.232+6092G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47899397 | ||||||
chr2:47899455
|
A | T | 309 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(306): Show | 314 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(311): Show |
intron_variant | MODIFIER | c.232+6034T>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47899455 | ||||||
chr2:47899600
|
T | G | 34 | a0001c0001t0001g0003a0001c0001t0001g0186a0001c0001t0001g0208others(31): Show | 35 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(32): Show |
intron_variant | MODIFIER | c.232+5889A>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47899600 | ||||||
chr2:47899619
|
C | T | 1 | a0001c0001t0008g0009 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.232+5870G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47899619 | ||||||
chr2:47899682
|
G | A | 1 | a0001c0001t0001g0156 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.232+5807C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47899682 | ||||||
chr2:47899682
|
G | C | 3 | a0001c0001t0001g0227a0001c0001t0001g0228a0001c0001t0002g0225 | 3 | NA18962.hp2 NA18991.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.232+5807C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47899682 | ||||||
chr2:47899811
|
C | A | 1 | a0001c0001t0002g0138 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.232+5678G>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47899811 | ||||||
chr2:47899837
|
C | A | 1 | a0001c0001t0002g0138 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.232+5652G>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47899837 | ||||||
chr2:47899926
|
T | C | 6 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(3): Show | 6 | HG00621.hp1 HG01993.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.232+5563A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47899926 | ||||||
chr2:47900116
|
C | A | 19 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(16): Show | 19 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(16): Show |
intron_variant | MODIFIER | c.232+5373G>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900116 | ||||||
chr2:47900121
|
T | C | 7 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(4): Show | 7 | HG01346.hp1 HG02615.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.232+5368A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900121 | ||||||
chr2:47900133
|
T | A | 5 | a0001c0001t0001g0274a0001c0001t0001g0275a0001c0001t0001g0276others(2): Show | 5 | HG01074.hp2 HG01891.hp2 NA19240.hp2 others(2): Show |
intron_variant | MODIFIER | c.232+5356A>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900133 | ||||||
chr2:47900173
|
T | C | 1 | a0001c0001t0002g0185 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.232+5316A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900173 | ||||||
chr2:47900182
|
T | C | 3 | a0001c0001t0001g0218a0001c0001t0001g0222a0001c0001t0001g0223 | 3 | HG00099.hp1 HG00741.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.232+5307A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900182 | ||||||
chr2:47900192
|
A | C | 1 | a0001c0001t0001g0226 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.232+5297T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900192 | ||||||
chr2:47900199
|
T | C | 1 | a0001c0001t0001g0085 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.232+5290A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900199 | ||||||
chr2:47900423
|
A | G | 1 | a0001c0001t0001g0055 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.232+5066T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900423 | ||||||
chr2:47900450
|
A | C | 1 | a0001c0001t0002g0134 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.232+5039T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900450 | ||||||
chr2:47900553
|
TACACGTA others(7): Show |
T | 5 | a0001c0001t0002g0281a0001c0001t0002g0285a0001c0001t0002g0286others(2): Show | 5 | HG00738.hp1 HG01109.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.232+4922_232+4935d others(16): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900553 | ||||||
chr2:47900557
|
C | CGTATATA others(19): Show |
7 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(4): Show | 7 | HG01346.hp1 HG02615.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.232+4931_232+4932i others(28): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900557 | ||||||
chr2:47900557
|
C | CGTATATA others(45): Show |
1 | a0001c0001t0003g0282 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.232+4931_232+4932i others(54): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900557 | ||||||
chr2:47900558
|
G | GTATATAT others(21): Show |
1 | a0001c0001t0001g0044 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.232+4903_232+4930d others(30): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900558 | ||||||
chr2:47900560
|
ATATATAC others(73): Show |
A | 2 | a0001c0001t0002g0272a0001c0001t0002g0273 | 2 | HG01074.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.232+4849_232+4928d others(82): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900560 | ||||||
chr2:47900565
|
T | C | 7 | a0001c0001t0001g0264a0001c0001t0001g0287a0001c0001t0001g0288others(4): Show | 7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.232+4924A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900565 | ||||||
chr2:47900575
|
T | TATACGTG others(21): Show |
1 | a0001c0001t0003g0293 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.232+4913_232+4914i others(30): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900575 | ||||||
chr2:47900577
|
C | CACGTGTG others(153): Show |
2 | a0001c0001t0001g0290a0001c0001t0001g0291 | 2 | HG01255.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.232+4911_232+4912i others(162): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900577 | ||||||
chr2:47900577
|
C | CACGTGTG others(181): Show |
1 | a0001c0001t0001g0288 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.232+4911_232+4912i others(190): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900577 | ||||||
chr2:47900577
|
C | CACGTGTG others(209): Show |
2 | a0001c0001t0001g0264a0001c0001t0001g0287 | 2 | HG00280.hp2 HG01070.hp1 |
intron_variant | MODIFIER | c.232+4911_232+4912i others(218): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900577 | ||||||
chr2:47900577
|
C | CACGTGTG others(237): Show |
1 | a0001c0001t0001g0292 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.232+4911_232+4912i others(246): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900577 | ||||||
chr2:47900577
|
C | CACGTGTG others(154): Show |
1 | a0001c0001t0001g0289 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.232+4911_232+4912i others(163): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900577 | ||||||
chr2:47900577
|
C | T | 3 | a0001c0001t0003g0107a0001c0001t0003g0294a0001c0001t0003g0295 | 3 | HG02257.hp2 HG02717.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.232+4912G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900577 | ||||||
chr2:47900580
|
A | G | 1 | a0001c0001t0003g0293 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.232+4909T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900580 | ||||||
chr2:47900581
|
C | T | 3 | a0001c0001t0003g0107a0001c0001t0003g0294a0001c0001t0003g0295 | 3 | HG02257.hp2 HG02717.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.232+4908G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900581 | ||||||
chr2:47900583
|
T | C | 7 | a0001c0001t0001g0264a0001c0001t0001g0287a0001c0001t0001g0288others(4): Show | 7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.232+4906A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900583 | ||||||
chr2:47900585
|
T | C | 9 | a0001c0001t0001g0264a0001c0001t0001g0287a0001c0001t0001g0288others(6): Show | 9 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.232+4904A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900585 | ||||||
chr2:47900586
|
A | G | 7 | a0001c0001t0001g0264a0001c0001t0001g0287a0001c0001t0001g0288others(4): Show | 7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.232+4903T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900586 | ||||||
chr2:47900586
|
ATACGTAT others(43): Show |
A | 2 | a0001c0001t0001g0005a0001c0001t0001g0191 | 3 | HG01243.hp1 HG02976.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.232+4853_232+4902d others(52): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900586 | ||||||
chr2:47900587
|
T | C | 4 | a0001c0001t0003g0107a0001c0001t0003g0293a0001c0001t0003g0294others(1): Show | 4 | HG02257.hp2 HG02717.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.232+4902A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900587 | ||||||
chr2:47900587
|
TACGTATA others(15): Show |
T | 3 | a0001c0001t0002g0134a0001c0001t0002g0157a0001c0001t0002g0158 | 3 | HG02080.hp1 NA18747.hp1 NA18953.hp1 |
intron_variant | MODIFIER | c.232+4880_232+4901d others(24): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900587 | ||||||
chr2:47900590
|
G | A | 2 | a0001c0001t0003g0294a0001c0001t0003g0295 | 2 | HG02717.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.232+4899C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900590 | ||||||
chr2:47900591
|
T | C | 2 | a0001c0001t0003g0294a0001c0001t0003g0295 | 2 | HG02717.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.232+4898A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900591 | ||||||
chr2:47900592
|
A | G | 2 | a0001c0001t0003g0294a0001c0001t0003g0295 | 2 | HG02717.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.232+4897T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900592 | ||||||
chr2:47900595
|
T | C | 23 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(20): Show | 23 | HG00738.hp1 HG01109.hp2 HG01256.hp2 others(20): Show |
intron_variant | MODIFIER | c.232+4894A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900595 | ||||||
chr2:47900602
|
GTATACAC others(5): Show |
G | 1 | a0001c0001t0001g0103 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.232+4875_232+4886d others(14): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900602 | ||||||
chr2:47900603
|
T | C | 3 | a0001c0001t0003g0293a0001c0001t0003g0294a0001c0001t0003g0295 | 3 | HG02717.hp1 HG03225.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.232+4886A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900603 | ||||||
chr2:47900607
|
C | T | 1 | a0001c0001t0003g0107 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.232+4882G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900607 | ||||||
chr2:47900609
|
C | CACACGT | 19 | a0001c0001t0001g0264a0001c0001t0001g0277a0001c0001t0001g0278others(16): Show | 19 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(16): Show |
intron_variant | MODIFIER | c.232+4879_232+4880i others(8): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900609 | ||||||
chr2:47900609
|
C | CACGTATA others(9): Show |
3 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0001g0211 | 3 | HG01346.hp1 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.232+4879_232+4880i others(18): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900609 | ||||||
chr2:47900609
|
CACGTATA others(21): Show |
C | 23 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0095others(20): Show | 23 | HG01069.hp2 HG01168.hp1 HG01261.hp1 others(20): Show |
intron_variant | MODIFIER | c.232+4852_232+4879d others(30): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900609 | ||||||
chr2:47900612
|
G | A | 1 | a0001c0001t0003g0107 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.232+4877C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900612 | ||||||
chr2:47900613
|
T | C | 1 | a0001c0001t0003g0107 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.232+4876A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900613 | ||||||
chr2:47900614
|
A | G | 1 | a0001c0001t0003g0107 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.232+4875T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900614 | ||||||
chr2:47900617
|
T | C | 11 | a0001c0001t0001g0038a0001c0001t0001g0064a0001c0001t0001g0070others(8): Show | 11 | HG00609.hp2 HG00639.hp2 HG00738.hp1 others(8): Show |
intron_variant | MODIFIER | c.232+4872A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900617 | ||||||
chr2:47900617
|
T | TACACACG others(9): Show |
1 | a0001c0001t0001g0092 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.232+4871_232+4872i others(18): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900617 | ||||||
chr2:47900617
|
TACACACG others(5): Show |
T | 3 | a0001c0001t0001g0097a0001c0001t0001g0189a0001c0001t0007g0008 | 3 | HG03669.hp1 HG04204.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.232+4860_232+4871d others(14): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900617 | ||||||
chr2:47900621
|
C | CACGT | 29 | a0001c0001t0001g0051a0001c0001t0001g0055a0001c0001t0001g0056others(26): Show | 29 | HG00597.hp1 HG00609.hp2 HG00621.hp2 others(26): Show |
intron_variant | MODIFIER | c.232+4864_232+4867d others(6): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900621 | ||||||
chr2:47900625
|
T | C | 1 | a0001c0001t0003g0294 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.232+4864A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900625 | ||||||
chr2:47900625
|
TATACACA others(17): Show |
T | 3 | a0001c0001t0001g0098a0001c0001t0001g0190a0001c0001t0001g0232 | 3 | HG00639.hp2 NA18991.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.232+4840_232+4863d others(26): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900625 | ||||||
chr2:47900626
|
A | ACG | 44 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0039others(41): Show | 45 | HG00323.hp2 HG00438.hp2 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.232+4862_232+4863i others(4): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900626 | ||||||
chr2:47900627
|
TACACACA others(33): Show |
T | 2 | a0001c0001t0001g0265a0001c0001t0001g0268 | 2 | HG02717.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.232+4822_232+4861d others(42): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900627 | ||||||
chr2:47900629
|
C | T | 63 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0039others(60): Show | 64 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.232+4860G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900629 | ||||||
chr2:47900631
|
C | CGTACGTA others(61): Show |
1 | a0001c0001t0003g0294 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.232+4857_232+4858i others(70): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900631 | ||||||
chr2:47900631
|
C | T | 4 | a0001c0001t0001g0052a0001c0001t0001g0100a0001c0001t0003g0293others(1): Show | 4 | HG02027.hp2 HG03225.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.232+4858G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900631 | ||||||
chr2:47900635
|
CGT | C | 45 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0039others(42): Show | 46 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(43): Show |
intron_variant | MODIFIER | c.232+4852_232+4853d others(4): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900635 | ||||||
chr2:47900637
|
T | TATACACA others(1): Show |
28 | a0001c0001t0001g0038a0001c0001t0001g0051a0001c0001t0001g0055others(25): Show | 28 | HG00597.hp1 HG00609.hp2 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.232+4851_232+4852i others(10): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900637 | ||||||
chr2:47900639
|
C | T | 1 | a0001c0001t0001g0212 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.232+4850G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900639 | ||||||
chr2:47900640
|
G | A | 2 | a0001c0001t0001g0212a0001c0001t0002g0299 | 2 | HG03927.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.232+4849C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900640 | ||||||
chr2:47900641
|
T | C | 1 | a0001c0001t0002g0299 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.232+4848A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900641 | ||||||
chr2:47900642
|
A | G | 1 | a0001c0001t0002g0299 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.232+4847T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900642 | ||||||
chr2:47900645
|
T | C | 82 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0036others(79): Show | 83 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.232+4844A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900645 | ||||||
chr2:47900645
|
TACACACG others(33): Show |
T | 7 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0220others(4): Show | 7 | HG00741.hp1 HG00741.hp2 HG01070.hp2 others(4): Show |
intron_variant | MODIFIER | c.232+4804_232+4843d others(42): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900645 | ||||||
chr2:47900647
|
C | T | 1 | a0001c0001t0001g0038 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.232+4842G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900647 | ||||||
chr2:47900647
|
CACACGTA others(61): Show |
C | 1 | a0001c0001t0001g0226 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.232+4774_232+4841d others(70): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900647 | ||||||
chr2:47900649
|
C | CGT | 9 | a0001c0001t0001g0001a0001c0001t0001g0074a0001c0001t0001g0082others(6): Show | 10 | HG00544.hp2 HG00597.hp2 NA18942.hp2 others(7): Show |
intron_variant | MODIFIER | c.232+4839_232+4840i others(4): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900649 | ||||||
chr2:47900652
|
GTATA | G | 5 | a0001c0001t0003g0107a0001c0001t0003g0282a0001c0001t0003g0293others(2): Show | 5 | HG02145.hp1 HG02257.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.232+4833_232+4836d others(6): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900652 | ||||||
chr2:47900654
|
A | G | 3 | a0001c0001t0001g0069a0001c0001t0001g0277a0001c0001t0001g0278 | 3 | HG03831.hp1 NA18977.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.232+4835T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900654 | ||||||
chr2:47900655
|
T | C | 1 | a0001c0001t0002g0250 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.232+4834A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900655 | ||||||
chr2:47900657
|
C | T | 4 | a0001c0001t0001g0069a0001c0001t0001g0232a0001c0001t0001g0277others(1): Show | 4 | HG00639.hp2 HG03831.hp1 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.232+4832G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900657 | ||||||
chr2:47900657
|
CACACACG others(9): Show |
C | 1 | a0001c0001t0001g0097 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.232+4816_232+4831d others(18): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900657 | ||||||
chr2:47900659
|
C | T | 8 | a0001c0001t0001g0069a0001c0001t0001g0277a0001c0001t0001g0278others(5): Show | 8 | HG02145.hp1 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.232+4830G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900659 | ||||||
chr2:47900659
|
CACACGTA others(49): Show |
C | 9 | a0001c0001t0001g0004a0001c0001t0001g0195a0001c0001t0001g0215others(6): Show | 10 | HG02055.hp2 HG03130.hp1 NA18522.hp1 others(7): Show |
intron_variant | MODIFIER | c.232+4774_232+4829d others(58): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900659 | ||||||
chr2:47900659
|
CACACGTA others(77): Show |
C | 1 | a0001c0001t0001g0129 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.232+4746_232+4829d others(86): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900659 | ||||||
chr2:47900661
|
C | G | 1 | a0001c0001t0001g0069 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.232+4828G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900661 | ||||||
chr2:47900661
|
C | T | 2 | a0001c0001t0001g0277a0001c0001t0001g0278 | 2 | NA18977.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.232+4828G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900661 | ||||||
chr2:47900661
|
CACGT | C | 112 | a0001c0001t0001g0001a0001c0001t0001g0042a0001c0001t0001g0043others(109): Show | 113 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.232+4824_232+4827d others(6): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900661 | ||||||
chr2:47900663
|
C | T | 3 | a0001c0001t0001g0069a0001c0001t0001g0277a0001c0001t0001g0278 | 3 | HG03831.hp1 NA18977.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.232+4826G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900663 | ||||||
chr2:47900664
|
G | A | 3 | a0001c0001t0001g0069a0001c0001t0001g0277a0001c0001t0001g0278 | 3 | HG03831.hp1 NA18977.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.232+4825C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900664 | ||||||
chr2:47900665
|
T | C | 3 | a0001c0001t0001g0069a0001c0001t0001g0277a0001c0001t0001g0278 | 3 | HG03831.hp1 NA18977.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.232+4824A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900665 | ||||||
chr2:47900665
|
T | TATACACA others(57): Show |
1 | a0001c0001t0001g0110 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.232+4823_232+4824i others(66): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900665 | ||||||
chr2:47900665
|
T | TATACACA others(17): Show |
6 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0047others(3): Show | 6 | HG00639.hp1 HG01109.hp1 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.232+4823_232+4824i others(26): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900665 | ||||||
chr2:47900665
|
T | TATACACA others(45): Show |
2 | a0001c0002t0002g0031a0001c0002t0002g0032 | 2 | HG02895.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.232+4823_232+4824i others(54): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900665 | ||||||
chr2:47900665
|
T | TGTATATA others(7): Show |
1 | a0001c0001t0001g0212 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.232+4823_232+4824i others(16): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900665 | ||||||
chr2:47900665
|
TAC | T | 8 | a0001c0001t0001g0086a0001c0001t0001g0103a0001c0001t0001g0216others(5): Show | 8 | HG00099.hp1 HG00099.hp2 HG01516.hp1 others(5): Show |
intron_variant | MODIFIER | c.232+4822_232+4823d others(4): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900665 | ||||||
chr2:47900665
|
TACGTATA others(5): Show |
T | 4 | a0001c0001t0002g0281a0001c0001t0002g0285a0001c0001t0002g0286others(1): Show | 4 | HG00738.hp1 HG01109.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.232+4812_232+4823d others(14): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900665 | ||||||
chr2:47900666
|
A | G | 34 | a0001c0001t0001g0036a0001c0001t0001g0038a0001c0001t0001g0039others(31): Show | 34 | HG00323.hp1 HG00597.hp1 HG00609.hp2 others(31): Show |
intron_variant | MODIFIER | c.232+4823T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900666 | ||||||
chr2:47900667
|
C | T | 36 | a0001c0001t0001g0036a0001c0001t0001g0038a0001c0001t0001g0039others(33): Show | 36 | HG00323.hp1 HG00597.hp1 HG00609.hp2 others(33): Show |
intron_variant | MODIFIER | c.232+4822G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900667 | ||||||
chr2:47900668
|
G | A | 36 | a0001c0001t0001g0036a0001c0001t0001g0038a0001c0001t0001g0039others(33): Show | 36 | HG00323.hp1 HG00597.hp1 HG00609.hp2 others(33): Show |
intron_variant | MODIFIER | c.232+4821C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900668 | ||||||
chr2:47900668
|
G | GTA | 5 | a0001c0001t0002g0196a0001c0001t0002g0248a0001c0001t0002g0249others(2): Show | 5 | HG01261.hp2 HG02055.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.232+4819_232+4820d others(4): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900668 | ||||||
chr2:47900668
|
G | GTATATAC others(93): Show |
1 | a0001c0001t0003g0293 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.232+4820_232+4821i others(102): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900668 | ||||||
chr2:47900673
|
T | C | 142 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0018others(139): Show | 143 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(140): Show |
intron_variant | MODIFIER | c.232+4816A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900673 | ||||||
chr2:47900674
|
ACACACG | A | 8 | a0001c0001t0001g0086a0001c0001t0001g0103a0001c0001t0001g0216others(5): Show | 8 | HG00099.hp1 HG00099.hp2 HG01516.hp1 others(5): Show |
intron_variant | MODIFIER | c.232+4809_232+4814d others(8): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900674 | ||||||
chr2:47900675
|
C | T | 39 | a0001c0001t0001g0036a0001c0001t0001g0038a0001c0001t0001g0039others(36): Show | 39 | HG00323.hp1 HG00597.hp1 HG00609.hp2 others(36): Show |
intron_variant | MODIFIER | c.232+4814G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900675 | ||||||
chr2:47900678
|
A | ACGTATAC others(9): Show |
1 | a0001c0001t0014g0284 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.232+4810_232+4811i others(18): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900678 | ||||||
chr2:47900678
|
A | G | 2 | a0001c0001t0002g0281a0001c0001t0002g0286 | 2 | HG00738.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.232+4811T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900678 | ||||||
chr2:47900680
|
G | GTATATAT others(53): Show |
12 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0020others(9): Show | 12 | HG01433.hp1 HG01891.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.232+4808_232+4809i others(62): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900680 | ||||||
chr2:47900680
|
G | GTATATAT others(81): Show |
1 | a0001c0001t0001g0028 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.232+4808_232+4809i others(90): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900680 | ||||||
chr2:47900680
|
G | GTGTA | 122 | a0001c0001t0001g0001a0001c0001t0001g0042a0001c0001t0001g0043others(119): Show | 123 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(120): Show |
intron_variant | MODIFIER | c.232+4808_232+4809i others(6): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900680 | ||||||
chr2:47900680
|
G | GTGTATAT others(53): Show |
1 | a0001c0001t0001g0018 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.232+4808_232+4809i others(62): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900680 | ||||||
chr2:47900681
|
T | C | 4 | a0001c0001t0003g0107a0001c0001t0003g0282a0001c0001t0003g0294others(1): Show | 4 | HG02145.hp1 HG02257.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.232+4808A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900681 | ||||||
chr2:47900683
|
TACAC | T | 8 | a0001c0001t0001g0086a0001c0001t0001g0103a0001c0001t0001g0216others(5): Show | 8 | HG00099.hp1 HG00099.hp2 HG01516.hp1 others(5): Show |
intron_variant | MODIFIER | c.232+4802_232+4805d others(6): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900683 | ||||||
chr2:47900685
|
C | CACACACG others(9): Show |
7 | a0001c0001t0001g0264a0001c0001t0001g0287a0001c0001t0001g0288others(4): Show | 7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.232+4803_232+4804i others(18): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900685 | ||||||
chr2:47900685
|
C | CACACACG others(39): Show |
1 | a0001c0001t0001g0208 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.232+4803_232+4804i others(48): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900685 | ||||||
chr2:47900685
|
C | CACACACG others(67): Show |
3 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0001g0211 | 3 | HG01346.hp1 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.232+4803_232+4804i others(76): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900685 | ||||||
chr2:47900685
|
C | CACACACG others(95): Show |
1 | a0001c0001t0001g0213 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.232+4803_232+4804i others(104): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900685 | ||||||
chr2:47900685
|
C | CACACACG others(99): Show |
1 | a0001c0001t0001g0214 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.232+4803_232+4804i others(108): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900685 | ||||||
chr2:47900685
|
C | G | 1 | a0001c0001t0001g0069 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.232+4804G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900685 | ||||||
chr2:47900685
|
C | T | 136 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0018others(133): Show | 137 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(134): Show |
intron_variant | MODIFIER | c.232+4804G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900685 | ||||||
chr2:47900687
|
C | CACACGTA others(119): Show |
1 | a0001c0001t0001g0123 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.232+4801_232+4802i others(128): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900687 | ||||||
chr2:47900687
|
C | CACACGTG others(9): Show |
22 | a0001c0001t0001g0041a0001c0001t0001g0051a0001c0001t0001g0058others(19): Show | 22 | HG00323.hp1 HG00597.hp1 HG01169.hp1 others(19): Show |
intron_variant | MODIFIER | c.232+4801_232+4802i others(18): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900687 | ||||||
chr2:47900687
|
C | CACACGTG others(37): Show |
14 | a0001c0001t0001g0036a0001c0001t0001g0039a0001c0001t0001g0055others(11): Show | 14 | HG00609.hp2 HG00621.hp2 HG01358.hp2 others(11): Show |
intron_variant | MODIFIER | c.232+4801_232+4802i others(46): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900687 | ||||||
chr2:47900687
|
C | CACACGTG others(65): Show |
1 | a0001c0001t0001g0038 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.232+4801_232+4802i others(74): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900687 | ||||||
chr2:47900687
|
C | CACACGTG others(93): Show |
2 | a0001c0001t0001g0297a0001c0001t0002g0248 | 2 | HG02055.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.232+4801_232+4802i others(102): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900687 | ||||||
chr2:47900687
|
C | CGTACGTA others(21): Show |
1 | a0004c0005t0002g0308 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.232+4801_232+4802i others(30): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900687 | ||||||
chr2:47900687
|
C | CGTACGTA others(225): Show |
1 | a0001c0001t0003g0282 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.232+4801_232+4802i others(234): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900687 | ||||||
chr2:47900687
|
C | T | 136 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0018others(133): Show | 137 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(134): Show |
intron_variant | MODIFIER | c.232+4802G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900687 | ||||||
chr2:47900688
|
A | G | 2 | a0001c0001t0003g0294a0001c0001t0003g0295 | 2 | HG02717.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.232+4801T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900688 | ||||||
chr2:47900689
|
C | T | 2 | a0001c0001t0003g0294a0001c0001t0003g0295 | 2 | HG02717.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.232+4800G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900689 | ||||||
chr2:47900693
|
T | TGTATATA others(205): Show |
1 | a0001c0001t0003g0107 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.232+4795_232+4796i others(214): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900693 | ||||||
chr2:47900697
|
C | T | 3 | a0001c0001t0003g0293a0001c0001t0003g0294a0001c0001t0003g0295 | 3 | HG02717.hp1 HG03225.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.232+4792G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900697 | ||||||
chr2:47900705
|
T | C | 3 | a0001c0001t0001g0100a0001c0001t0003g0294a0001c0001t0003g0295 | 3 | HG02027.hp2 HG02717.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.232+4784A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900705 | ||||||
chr2:47900706
|
G | A | 2 | a0001c0001t0003g0294a0001c0001t0003g0295 | 2 | HG02717.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.232+4783C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900706 | ||||||
chr2:47900706
|
G | GTA | 4 | a0001c0001t0002g0099a0001c0001t0004g0011a0001c0001t0004g0012others(1): Show | 4 | HG02135.hp2 HG02523.hp2 NA18982.hp2 others(1): Show |
intron_variant | MODIFIER | c.232+4781_232+4782d others(4): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900706 | ||||||
chr2:47900707
|
T | C | 4 | a0001c0001t0002g0285a0001c0001t0002g0286a0001c0001t0014g0284others(1): Show | 4 | HG00738.hp1 HG01109.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.232+4782A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900707 | ||||||
chr2:47900708
|
A | ACACGTAC others(97): Show |
1 | a0001c0001t0003g0295 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.232+4780_232+4781i others(106): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900708 | ||||||
chr2:47900708
|
A | ATACACAC others(47): Show |
1 | a0001c0001t0002g0281 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.232+4780_232+4781i others(56): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900708 | ||||||
chr2:47900708
|
A | G | 4 | a0001c0001t0002g0285a0001c0001t0002g0286a0001c0001t0014g0284others(1): Show | 4 | HG00738.hp1 HG01109.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.232+4781T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900708 | ||||||
chr2:47900713
|
T | C | 5 | a0001c0001t0002g0281a0001c0001t0002g0285a0001c0001t0002g0286others(2): Show | 5 | HG00738.hp1 HG01109.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.232+4776A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900713 | ||||||
chr2:47900715
|
T | C | 21 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(18): Show | 21 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(18): Show |
intron_variant | MODIFIER | c.232+4774A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900715 | ||||||
chr2:47900721
|
T | C | 1 | a0001c0001t0003g0295 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.232+4768A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900721 | ||||||
chr2:47900728
|
A | G | 1 | a0001c0001t0003g0294 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.232+4761T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900728 | ||||||
chr2:47900729
|
C | T | 1 | a0001c0001t0003g0294 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.232+4760G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900729 | ||||||
chr2:47900733
|
T | C | 1 | a0001c0001t0001g0100 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.232+4756A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900733 | ||||||
chr2:47900735
|
T | C | 5 | a0001c0001t0002g0281a0001c0001t0002g0285a0001c0001t0002g0286others(2): Show | 5 | HG00738.hp1 HG01109.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.232+4754A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900735 | ||||||
chr2:47900736
|
A | G | 5 | a0001c0001t0002g0281a0001c0001t0002g0285a0001c0001t0002g0286others(2): Show | 5 | HG00738.hp1 HG01109.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.232+4753T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900736 | ||||||
chr2:47900740
|
A | C | 4 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0047others(1): Show | 4 | HG00639.hp1 HG01109.hp1 HG01123.hp2 others(1): Show |
intron_variant | MODIFIER | c.232+4749T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900740 | ||||||
chr2:47900741
|
T | C | 5 | a0001c0001t0002g0281a0001c0001t0002g0285a0001c0001t0002g0286others(2): Show | 5 | HG00738.hp1 HG01109.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.232+4748A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900741 | ||||||
chr2:47900743
|
T | C | 22 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(19): Show | 22 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.232+4746A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900743 | ||||||
chr2:47900761
|
T | C | 1 | a0001c0001t0001g0100 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.232+4728A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900761 | ||||||
chr2:47900763
|
T | C | 4 | a0001c0001t0002g0281a0001c0001t0002g0285a0001c0001t0014g0284others(1): Show | 4 | HG01109.hp2 HG02559.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.232+4726A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900763 | ||||||
chr2:47900764
|
A | G | 5 | a0001c0001t0002g0281a0001c0001t0002g0285a0001c0001t0002g0286others(2): Show | 5 | HG00738.hp1 HG01109.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.232+4725T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900764 | ||||||
chr2:47900769
|
T | C | 5 | a0001c0001t0002g0281a0001c0001t0002g0285a0001c0001t0002g0286others(2): Show | 5 | HG00738.hp1 HG01109.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.232+4720A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900769 | ||||||
chr2:47900771
|
T | C | 22 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(19): Show | 22 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.232+4718A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900771 | ||||||
chr2:47900789
|
T | C | 1 | a0001c0001t0001g0100 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.232+4700A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900789 | ||||||
chr2:47900791
|
T | C | 3 | a0001c0001t0002g0285a0001c0001t0014g0284a0001c0002t0002g0283 | 3 | HG01109.hp2 HG02559.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.232+4698A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900791 | ||||||
chr2:47900792
|
A | G | 5 | a0001c0001t0002g0281a0001c0001t0002g0285a0001c0001t0002g0286others(2): Show | 5 | HG00738.hp1 HG01109.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.232+4697T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900792 | ||||||
chr2:47900797
|
T | C | 5 | a0001c0001t0002g0281a0001c0001t0002g0285a0001c0001t0002g0286others(2): Show | 5 | HG00738.hp1 HG01109.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.232+4692A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900797 | ||||||
chr2:47900799
|
T | C | 21 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(18): Show | 21 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(18): Show |
intron_variant | MODIFIER | c.232+4690A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900799 | ||||||
chr2:47900809
|
CACACACG others(19): Show |
C | 6 | a0001c0001t0001g0174a0001c0001t0002g0134a0001c0001t0002g0157others(3): Show | 6 | HG02080.hp1 HG04228.hp1 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.232+4654_232+4679d others(28): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900809 | ||||||
chr2:47900818
|
GTA | G | 5 | a0001c0001t0001g0213a0001c0001t0001g0287a0001c0001t0001g0288others(2): Show | 5 | HG00280.hp2 HG01081.hp1 HG01255.hp1 others(2): Show |
intron_variant | MODIFIER | c.232+4669_232+4670d others(4): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900818 | ||||||
chr2:47900820
|
A | ATATACAC others(71): Show |
1 | a0001c0001t0001g0212 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.232+4668_232+4669i others(80): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900820 | ||||||
chr2:47900820
|
A | G | 5 | a0001c0001t0002g0281a0001c0001t0002g0285a0001c0001t0002g0286others(2): Show | 5 | HG00738.hp1 HG01109.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.232+4669T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900820 | ||||||
chr2:47900825
|
T | C | 5 | a0001c0001t0002g0281a0001c0001t0002g0285a0001c0001t0002g0286others(2): Show | 5 | HG00738.hp1 HG01109.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.232+4664A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900825 | ||||||
chr2:47900827
|
T | C | 16 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(13): Show | 16 | HG00738.hp1 HG01070.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.232+4662A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900827 | ||||||
chr2:47900832
|
G | GTA | 6 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0047others(3): Show | 6 | HG00639.hp1 HG01109.hp1 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.232+4655_232+4656d others(4): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900832 | ||||||
chr2:47900832
|
G | GTATACAC others(21): Show |
1 | a0001c0001t0001g0287 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.232+4656_232+4657i others(30): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900832 | ||||||
chr2:47900832
|
G | GTATACAC others(23): Show |
1 | a0001c0001t0001g0069 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.232+4627_232+4656d others(32): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900832 | ||||||
chr2:47900835
|
T | TAC | 120 | a0001c0001t0001g0038a0001c0001t0001g0051a0001c0001t0001g0052others(117): Show | 120 | HG00323.hp2 HG00438.hp2 HG00544.hp2 others(117): Show |
intron_variant | MODIFIER | c.232+4652_232+4653d others(4): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900835 | ||||||
chr2:47900835
|
T | TACACACA others(25): Show |
1 | a0001c0001t0001g0041 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.232+4653_232+4654i others(34): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900835 | ||||||
chr2:47900835
|
T | TACACACA others(23): Show |
7 | a0001c0001t0002g0172a0001c0001t0002g0173a0001c0002t0002g0033others(4): Show | 7 | HG01099.hp1 HG01175.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.232+4624_232+4653d others(32): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900835 | ||||||
chr2:47900835
|
T | TACACACA others(53): Show |
2 | a0001c0001t0002g0163a0001c0001t0002g0164 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.232+4653_232+4654i others(62): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900835 | ||||||
chr2:47900835
|
T | TACACACA others(51): Show |
1 | a0001c0002t0002g0030 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.232+4653_232+4654i others(60): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900835 | ||||||
chr2:47900844
|
G | GTGTATAT others(79): Show |
3 | a0001c0001t0001g0264a0001c0001t0001g0291a0001c0001t0001g0292 | 3 | HG01070.hp1 HG01516.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.232+4644_232+4645i others(88): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900844 | ||||||
chr2:47900844
|
G | GTGTATAT others(53): Show |
3 | a0001c0001t0001g0288a0001c0001t0001g0289a0001c0001t0001g0290 | 3 | HG01081.hp1 HG01255.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.232+4644_232+4645i others(62): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900844 | ||||||
chr2:47900846
|
GTA | G | 3 | a0001c0001t0001g0208a0001c0001t0001g0210a0001c0001t0001g0211 | 3 | HG02723.hp1 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.232+4641_232+4642d others(4): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900846 | ||||||
chr2:47900848
|
A | G | 5 | a0001c0001t0002g0281a0001c0001t0002g0285a0001c0001t0002g0286others(2): Show | 5 | HG00738.hp1 HG01109.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.232+4641T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900848 | ||||||
chr2:47900853
|
T | C | 5 | a0001c0001t0002g0281a0001c0001t0002g0285a0001c0001t0002g0286others(2): Show | 5 | HG00738.hp1 HG01109.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.232+4636A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900853 | ||||||
chr2:47900855
|
T | C | 6 | a0001c0001t0001g0209a0001c0001t0002g0281a0001c0001t0002g0285others(3): Show | 6 | HG00738.hp1 HG01109.hp2 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.232+4634A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900855 | ||||||
chr2:47900860
|
G | GTA | 10 | a0001c0001t0001g0212a0001c0001t0001g0213a0001c0001t0001g0214others(7): Show | 10 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.232+4627_232+4628d others(4): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900860 | ||||||
chr2:47900860
|
G | GTATACAC others(57): Show |
1 | a0001c0001t0002g0251 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.232+4628_232+4629i others(66): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900860 | ||||||
chr2:47900860
|
G | GTATACAC others(23): Show |
3 | a0001c0001t0001g0208a0001c0001t0001g0210a0001c0001t0001g0211 | 3 | HG02723.hp1 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.232+4628_232+4629i others(32): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900860 | ||||||
chr2:47900863
|
TAC | T | 3 | a0001c0001t0001g0209a0001c0001t0003g0107a0001c0001t0003g0293 | 3 | HG01346.hp1 HG02257.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.232+4624_232+4625d others(4): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900863 | ||||||
chr2:47900865
|
C | CACACACA others(23): Show |
34 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0036others(31): Show | 36 | HG00280.hp1 HG00323.hp1 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.232+4594_232+4623d others(32): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900865 | ||||||
chr2:47900865
|
C | CACACACG others(51): Show |
7 | a0001c0001t0001g0186a0001c0001t0002g0002a0001c0001t0002g0133others(4): Show | 8 | HG01257.hp1 HG01258.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.232+4623_232+4624i others(60): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900865 | ||||||
chr2:47900865
|
C | CACACACG others(101): Show |
1 | a0001c0001t0001g0267 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.232+4623_232+4624i others(110): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900865 | ||||||
chr2:47900865
|
C | CACACACG others(79): Show |
2 | a0001c0001t0001g0200a0001c0001t0015g0130 | 2 | NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.232+4623_232+4624i others(88): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900865 | ||||||
chr2:47900865
|
C | CACACACG others(77): Show |
1 | a0001c0001t0001g0247 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.232+4623_232+4624i others(86): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900865 | ||||||
chr2:47900865
|
C | CACACACG others(77): Show |
1 | a0001c0001t0001g0193 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.232+4623_232+4624i others(86): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900865 | ||||||
chr2:47900865
|
C | CACACACG others(49): Show |
3 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0187 | 3 | HG01243.hp2 HG02886.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.232+4623_232+4624i others(58): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900865 | ||||||
chr2:47900865
|
C | CACACACG others(21): Show |
12 | a0001c0001t0001g0042a0001c0001t0001g0064a0001c0001t0001g0203others(9): Show | 12 | HG00438.hp1 HG00544.hp1 HG01993.hp2 others(9): Show |
intron_variant | MODIFIER | c.232+4623_232+4624i others(30): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900865 | ||||||
chr2:47900865
|
C | CACACACG others(51): Show |
1 | a0001c0001t0001g0049 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.232+4623_232+4624i others(60): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900865 | ||||||
chr2:47900865
|
C | CACACACG others(49): Show |
1 | a0001c0001t0001g0238 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.232+4623_232+4624i others(58): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900865 | ||||||
chr2:47900865
|
C | T | 193 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0017others(190): Show | 195 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(192): Show |
intron_variant | MODIFIER | c.232+4624G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900865 | ||||||
chr2:47900867
|
C | A | 1 | a0001c0001t0001g0060 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.232+4622G>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900867 | ||||||
chr2:47900872
|
A | G | 3 | a0001c0001t0003g0282a0001c0001t0003g0294a0001c0001t0003g0295 | 3 | HG02145.hp1 HG02717.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.232+4617T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900872 | ||||||
chr2:47900873
|
C | CGT | 5 | a0001c0001t0002g0281a0001c0001t0002g0285a0001c0001t0002g0286others(2): Show | 5 | HG00738.hp1 HG01109.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.232+4614_232+4615d others(4): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900873 | ||||||
chr2:47900873
|
C | T | 16 | a0001c0001t0001g0208a0001c0001t0001g0210a0001c0001t0001g0211others(13): Show | 16 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.232+4616G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900873 | ||||||
chr2:47900874
|
G | A | 13 | a0001c0001t0001g0208a0001c0001t0001g0210a0001c0001t0001g0211others(10): Show | 13 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.232+4615C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900874 | ||||||
chr2:47900874
|
G | GTGTATAT others(51): Show |
1 | a0001c0001t0001g0209 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.232+4614_232+4615i others(60): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900874 | ||||||
chr2:47900876
|
G | A | 3 | a0001c0001t0003g0282a0001c0001t0003g0294a0001c0001t0003g0295 | 3 | HG02145.hp1 HG02717.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.232+4613C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900876 | ||||||
chr2:47900880
|
A | ATATATAC others(3): Show |
1 | a0001c0001t0003g0282 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.232+4599_232+4608d others(12): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900880 | ||||||
chr2:47900880
|
A | ATATATAT others(3): Show |
1 | a0001c0001t0003g0293 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.232+4608_232+4609i others(12): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900880 | ||||||
chr2:47900883
|
T | C | 6 | a0001c0001t0001g0215a0001c0001t0002g0281a0001c0001t0002g0285others(3): Show | 6 | HG00738.hp1 HG01109.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.232+4606A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900883 | ||||||
chr2:47900885
|
T | TACACGTA others(3): Show |
1 | a0001c0001t0003g0107 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.232+4603_232+4604i others(12): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900885 | ||||||
chr2:47900892
|
A | G | 1 | a0001c0001t0001g0274 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.232+4597T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900892 | ||||||
chr2:47900897
|
T | C | 14 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0044others(11): Show | 14 | HG00639.hp1 HG00735.hp2 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.232+4592A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900897 | ||||||
chr2:47900903
|
CAT | C | 5 | a0001c0001t0002g0281a0001c0001t0002g0285a0001c0001t0002g0286others(2): Show | 5 | HG00738.hp1 HG01109.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.232+4584_232+4585d others(4): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900903 | ||||||
chr2:47900912
|
G | GTATA | 4 | a0001c0001t0003g0282a0001c0001t0003g0293a0001c0001t0003g0294others(1): Show | 4 | HG02145.hp1 HG02717.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.232+4573_232+4576d others(6): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900912 | ||||||
chr2:47900951
|
A | T | 1 | a0001c0001t0002g0138 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.232+4538T>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900951 | ||||||
chr2:47900998
|
G | A | 1 | a0001c0001t0013g0165 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.232+4491C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900998 | ||||||
chr2:47901014
|
T | C | 6 | a0001c0001t0001g0215a0001c0001t0002g0281a0001c0001t0002g0285others(3): Show | 6 | HG00738.hp1 HG01109.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.232+4475A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47901014 | ||||||
chr2:47901018
|
TATGTATA others(103): Show |
T | 35 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(32): Show | 35 | HG00438.hp1 HG00544.hp1 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.232+4361_232+4470d others(2): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47901018 | ||||||
chr2:47901037
|
G | A | 2 | a0001c0001t0001g0005a0001c0001t0001g0191 | 3 | HG01243.hp1 HG02976.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.232+4452C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47901037 | ||||||
chr2:47901052
|
C | T | 24 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(21): Show | 24 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.232+4437G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47901052 | ||||||
chr2:47901058
|
T | C | 107 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0038others(104): Show | 108 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.232+4431A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47901058 | ||||||
chr2:47901065
|
A | G | 1 | a0001c0001t0001g0003 | 2 | HG02257.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.232+4424T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47901065 | ||||||
chr2:47901071
|
A | G | 1 | a0001c0001t0001g0215 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.232+4418T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47901071 | ||||||
chr2:47901072
|
T | TAC | 9 | a0001c0001t0001g0229a0001c0001t0001g0230a0001c0001t0001g0231others(6): Show | 9 | HG00639.hp2 HG00642.hp1 HG01069.hp2 others(6): Show |
intron_variant | MODIFIER | c.232+4415_232+4416d others(4): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47901072 | ||||||
chr2:47901086
|
C | T | 2 | a0001c0001t0001g0201a0001c0001t0001g0238 | 2 | HG02615.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.232+4403G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47901086 | ||||||
chr2:47901094
|
T | C | 14 | a0001c0001t0001g0201a0001c0001t0001g0238a0001c0001t0001g0264others(11): Show | 14 | HG00280.hp2 HG01070.hp1 HG01074.hp2 others(11): Show |
intron_variant | MODIFIER | c.232+4395A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47901094 | ||||||
chr2:47901095
|
A | G | 6 | a0001c0001t0001g0215a0001c0001t0002g0281a0001c0001t0002g0285others(3): Show | 6 | HG00738.hp1 HG01109.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.232+4394T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47901095 | ||||||
chr2:47901096
|
C | T | 15 | a0001c0001t0001g0201a0001c0001t0001g0215a0001c0001t0001g0238others(12): Show | 15 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.232+4393G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47901096 | ||||||
chr2:47901096
|
CAT | C | 4 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(1): Show | 4 | HG01346.hp1 HG02723.hp1 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.232+4391_232+4392d others(4): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47901096 | ||||||
chr2:47901100
|
TATATGTA others(21): Show |
T | 3 | a0001c0001t0001g0212a0001c0001t0001g0213a0001c0001t0001g0214 | 3 | HG02615.hp2 HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.232+4361_232+4388d others(30): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47901100 | ||||||
chr2:47901103
|
A | ATG | 35 | a0001c0001t0001g0005a0001c0001t0001g0122a0001c0001t0001g0127others(32): Show | 36 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.232+4384_232+4385d others(4): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47901103 | ||||||
chr2:47901103
|
A | G | 7 | a0001c0001t0001g0264a0001c0001t0001g0287a0001c0001t0001g0288others(4): Show | 7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.232+4386T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47901103 | ||||||
chr2:47901105
|
G | A | 13 | a0001c0001t0001g0215a0001c0001t0001g0264a0001c0001t0001g0287others(10): Show | 13 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.232+4384C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47901105 | ||||||
chr2:47901108
|
T | C | 6 | a0001c0001t0001g0215a0001c0001t0002g0281a0001c0001t0002g0285others(3): Show | 6 | HG00738.hp1 HG01109.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.232+4381A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47901108 | ||||||
chr2:47901109
|
A | ACACG | 6 | a0001c0001t0001g0215a0001c0001t0002g0281a0001c0001t0002g0285others(3): Show | 6 | HG00738.hp1 HG01109.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.232+4379_232+4380i others(6): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47901109 | ||||||
chr2:47901111
|
A | G | 6 | a0001c0001t0001g0215a0001c0001t0002g0281a0001c0001t0002g0285others(3): Show | 6 | HG00738.hp1 HG01109.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.232+4378T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47901111 | ||||||
chr2:47901113
|
G | A | 11 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(8): Show | 11 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.232+4376C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47901113 | ||||||
chr2:47901118
|
C | T | 6 | a0001c0001t0001g0215a0001c0001t0002g0281a0001c0001t0002g0285others(3): Show | 6 | HG00738.hp1 HG01109.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.232+4371G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47901118 | ||||||
chr2:47901120
|
C | T | 6 | a0001c0001t0001g0215a0001c0001t0002g0281a0001c0001t0002g0285others(3): Show | 6 | HG00738.hp1 HG01109.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.232+4369G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47901120 | ||||||
chr2:47901121
|
G | A | 6 | a0001c0001t0001g0215a0001c0001t0002g0281a0001c0001t0002g0285others(3): Show | 6 | HG00738.hp1 HG01109.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.232+4368C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47901121 | ||||||
chr2:47901122
|
T | TAC | 6 | a0001c0001t0001g0215a0001c0001t0002g0281a0001c0001t0002g0285others(3): Show | 6 | HG00738.hp1 HG01109.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.232+4366_232+4367i others(4): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47901122 | ||||||
chr2:47901123
|
G | A | 6 | a0001c0001t0001g0215a0001c0001t0002g0281a0001c0001t0002g0285others(3): Show | 6 | HG00738.hp1 HG01109.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.232+4366C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47901123 | ||||||
chr2:47901125
|
G | A | 6 | a0001c0001t0001g0215a0001c0001t0002g0281a0001c0001t0002g0285others(3): Show | 6 | HG00738.hp1 HG01109.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.232+4364C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47901125 | ||||||
chr2:47901128
|
C | CATATATA others(7): Show |
7 | a0001c0001t0001g0264a0001c0001t0001g0287a0001c0001t0001g0288others(4): Show | 7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.232+4360_232+4361i others(16): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47901128 | ||||||
chr2:47901128
|
C | CATATATA others(155): Show |
1 | a0001c0001t0001g0208 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.232+4360_232+4361i others(164): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47901128 | ||||||
chr2:47901128
|
C | CATATATA others(157): Show |
2 | a0001c0001t0001g0210a0001c0001t0001g0211 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.232+4360_232+4361i others(166): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47901128 | ||||||
chr2:47901128
|
C | CATATATA others(155): Show |
1 | a0001c0001t0001g0209 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.232+4360_232+4361i others(164): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47901128 | ||||||
chr2:47901128
|
C | T | 6 | a0001c0001t0001g0215a0001c0001t0002g0281a0001c0001t0002g0285others(3): Show | 6 | HG00738.hp1 HG01109.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.232+4361G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47901128 | ||||||
chr2:47901131
|
G | GTA | 14 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(11): Show | 14 | HG01433.hp1 HG01891.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.232+4356_232+4357d others(4): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47901131 | ||||||
chr2:47901147
|
G | A | 1 | a0001c0001t0002g0196 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.232+4342C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47901147 | ||||||
chr2:47901162
|
C | CACACGTG others(33): Show |
1 | a0001c0001t0001g0264 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.232+4326_232+4327i others(42): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47901162 | ||||||
chr2:47901162
|
C | CACACGTG others(13): Show |
6 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0001g0289others(3): Show | 6 | HG00280.hp2 HG01081.hp1 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.232+4326_232+4327i others(22): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47901162 | ||||||
chr2:47901164
|
T | C | 7 | a0001c0001t0001g0264a0001c0001t0001g0287a0001c0001t0001g0288others(4): Show | 7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.232+4325A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47901164 | ||||||
chr2:47901270
|
C | T | 7 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(4): Show | 7 | HG01346.hp1 HG02615.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.232+4219G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47901270 | ||||||
chr2:47901316
|
T | C | 1 | a0001c0001t0001g0123 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.232+4173A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47901316 | ||||||
chr2:47901534
|
T | C | 4 | a0001c0001t0001g0269a0001c0001t0001g0270a0001c0001t0001g0271others(1): Show | 4 | HG02922.hp2 HG03225.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.232+3955A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47901534 | ||||||
chr2:47901667
|
CTCAGT | C | 7 | a0001c0001t0001g0264a0001c0001t0001g0287a0001c0001t0001g0288others(4): Show | 7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.232+3817_232+3821d others(7): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47901667 | ||||||
chr2:47901720
|
A | T | 1 | a0001c0001t0002g0054 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.232+3769T>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47901720 | ||||||
chr2:47902252
|
T | C | 1 | a0001c0001t0001g0104 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.232+3237A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47902252 | ||||||
chr2:47902273
|
C | T | 9 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045others(6): Show | 9 | HG00639.hp1 HG00735.hp2 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.232+3216G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47902273 | ||||||
chr2:47902333
|
G | T | 2 | a0001c0001t0001g0265a0001c0001t0001g0268 | 2 | HG02717.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.232+3156C>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47902333 | ||||||
chr2:47902403
|
G | T | 1 | a0001c0001t0001g0063 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.232+3086C>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47902403 | ||||||
chr2:47902529
|
T | C | 1 | a0001c0001t0001g0110 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.232+2960A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47902529 | ||||||
chr2:47902725
|
T | C | 1 | a0001c0001t0002g0185 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.232+2764A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47902725 | ||||||
chr2:47902896
|
T | C | 1 | a0001c0001t0001g0105 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.232+2593A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47902896 | ||||||
chr2:47902919
|
TA | T | 6 | a0001c0001t0002g0137a0001c0001t0002g0196a0001c0001t0002g0248others(3): Show | 6 | HG01261.hp2 HG02055.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.232+2569delT | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47902919 | ||||||
chr2:47903075
|
G | A | 5 | a0001c0001t0003g0107a0001c0001t0003g0282a0001c0001t0003g0293others(2): Show | 5 | HG02145.hp1 HG02257.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.232+2414C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47903075 | ||||||
chr2:47903193
|
T | G | 7 | a0001c0001t0001g0121a0001c0001t0001g0124a0001c0001t0001g0125others(4): Show | 7 | HG02109.hp1 HG02280.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.232+2296A>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47903193 | ||||||
chr2:47903416
|
G | A | 4 | a0001c0001t0003g0282a0001c0001t0003g0293a0001c0001t0003g0294others(1): Show | 4 | HG02145.hp1 HG02717.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.232+2073C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47903416 | ||||||
chr2:47903453
|
T | C | 2 | a0001c0001t0001g0186a0001c0001t0002g0179 | 2 | HG02572.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.232+2036A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47903453 | ||||||
chr2:47903567
|
T | C | 1 | a0001c0001t0003g0107 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.232+1922A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47903567 | ||||||
chr2:47903703
|
T | C | 1 | a0001c0001t0001g0268 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.232+1786A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47903703 | ||||||
chr2:47903778
|
A | C | 4 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0298others(1): Show | 4 | HG01358.hp2 HG03017.hp1 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.232+1711T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47903778 | ||||||
chr2:47903782
|
A | G | 1 | a0001c0001t0002g0133 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.232+1707T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47903782 | ||||||
chr2:47903800
|
G | A | 22 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(19): Show | 22 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.232+1689C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47903800 | ||||||
chr2:47903810
|
G | C | 23 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(20): Show | 23 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.232+1679C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47903810 | ||||||
chr2:47903825
|
G | A | 1 | a0006c0008t0001g0305 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.232+1664C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47903825 | ||||||
chr2:47904150
|
A | C | 3 | a0001c0001t0001g0061a0001c0001t0001g0190a0001c0001t0002g0062 | 3 | HG02071.hp1 NA18967.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.232+1339T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47904150 | ||||||
chr2:47904176
|
T | C | 1 | a0006c0008t0001g0305 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.232+1313A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47904176 | ||||||
chr2:47904184
|
C | G | 46 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0122others(43): Show | 48 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.232+1305G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47904184 | ||||||
chr2:47904247
|
A | C | 6 | a0001c0001t0001g0215a0001c0001t0002g0281a0001c0001t0002g0285others(3): Show | 6 | HG00738.hp1 HG01109.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.232+1242T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47904247 | ||||||
chr2:47904284
|
A | G | 1 | a0001c0001t0001g0296 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.232+1205T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47904284 | ||||||
chr2:47904581
|
A | C | 1 | a0001c0001t0001g0036 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.232+908T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47904581 | ||||||
chr2:47904581
|
AAC | A | 20 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045others(17): Show | 21 | HG00639.hp1 HG00735.hp2 HG01074.hp2 others(18): Show |
intron_variant | MODIFIER | c.232+906_232+907del others(2): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47904581 | ||||||
chr2:47904581
|
AACAC | A | 44 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0057others(41): Show | 44 | HG00735.hp1 HG01069.hp1 HG01071.hp1 others(41): Show |
intron_variant | MODIFIER | c.232+904_232+907del others(4): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47904581 | ||||||
chr2:47904581
|
AACACAC | A | 89 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0063others(86): Show | 90 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.232+902_232+907del others(6): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47904581 | ||||||
chr2:47904581
|
AACACACA others(1): Show |
A | 33 | a0001c0001t0001g0106a0001c0001t0001g0122a0001c0001t0001g0123others(30): Show | 33 | HG00323.hp2 HG00438.hp1 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.232+900_232+907del others(8): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47904581 | ||||||
chr2:47904581
|
AACACACA others(3): Show |
A | 72 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(69): Show | 75 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.232+898_232+907del others(10): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47904581 | ||||||
chr2:47904581
|
AACACACA others(5): Show |
A | 23 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(20): Show | 23 | HG00738.hp1 HG01109.hp2 HG01433.hp1 others(20): Show |
intron_variant | MODIFIER | c.232+896_232+907del others(12): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47904581 | ||||||
chr2:47904581
|
AACACACA others(7): Show |
A | 5 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0269others(2): Show | 5 | HG02451.hp2 HG02559.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.232+894_232+907del others(14): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47904581 | ||||||
chr2:47904581
|
AACACACA others(9): Show |
A | 13 | a0001c0001t0001g0111a0001c0001t0001g0113a0001c0001t0001g0114others(10): Show | 13 | HG00280.hp2 HG01081.hp1 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.232+892_232+907del others(16): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47904581 | ||||||
chr2:47904581
|
AACACACA others(11): Show |
A | 2 | a0001c0001t0001g0118a0001c0001t0001g0292 | 2 | HG01516.hp2 NA18946.hp2 |
intron_variant | MODIFIER | c.232+890_232+907del others(18): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47904581 | ||||||
chr2:47904581
|
AACACACA others(13): Show |
A | 1 | a0001c0001t0001g0119 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.232+888_232+907del others(20): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47904581 | ||||||
chr2:47904584
|
A | G | 1 | a0001c0001t0002g0180 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.232+905T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47904584 | ||||||
chr2:47904587
|
C | A | 1 | a0001c0001t0002g0180 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.232+902G>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47904587 | ||||||
chr2:47904621
|
C | A | 2 | a0001c0001t0001g0005a0001c0001t0001g0191 | 3 | HG01243.hp1 HG02976.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.232+868G>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47904621 | ||||||
chr2:47904709
|
C | A | 210 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(207): Show | 214 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.232+780G>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47904709 | ||||||
chr2:47904797
|
T | C | 67 | a0001c0001t0001g0003a0001c0001t0001g0151a0001c0001t0001g0156others(64): Show | 69 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(66): Show |
intron_variant | MODIFIER | c.232+692A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47904797 | ||||||
chr2:47904885
|
T | A | 1 | a0001c0001t0001g0187 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.232+604A>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47904885 | ||||||
chr2:47905020
|
A | G | 1 | a0001c0001t0001g0191 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.232+469T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47905020 | ||||||
chr2:47905157
|
T | C | 2 | a0001c0001t0001g0277a0001c0001t0001g0278 | 2 | NA18977.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.232+332A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47905157 | ||||||
chr2:47905185
|
G | C | 1 | a0001c0001t0001g0188 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.232+304C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47905185 | ||||||
chr2:47905204
|
A | T | 1 | a0001c0001t0002g0035 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.232+285T>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47905204 | ||||||
chr2:47905224
|
G | C | 1 | a0001c0001t0001g0189 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.232+265C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47905224 | ||||||
chr2:47905235
|
T | A | 1 | a0001c0002t0002g0302 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.232+254A>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47905235 | ||||||
chr2:47905295
|
G | A | 1 | a0001c0001t0001g0190 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.232+194C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47905295 | ||||||
chr2:47905349
|
G | A | 3 | a0001c0001t0003g0293a0001c0001t0003g0294a0001c0001t0003g0295 | 3 | HG02717.hp1 HG03225.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.232+140C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47905349 | ||||||
chr2:47905355
|
C | T | 1 | a0004c0005t0002g0307 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.232+134G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47905355 | ||||||
chr2:47905400
|
GCCCCCGC others(9): Show |
G | 14 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(11): Show | 14 | HG01433.hp1 HG01891.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.232+73_232+88delGG others(14): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47905400 | ||||||
chr2:47905402
|
C | CCCCG | 5 | a0001c0002t0002g0030a0001c0002t0002g0031a0001c0002t0002g0032others(2): Show | 5 | HG01884.hp2 HG02109.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.232+83_232+86dupCG others(2): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47905402 | ||||||
chr2:47905402
|
CCCCG | C | 97 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0191others(94): Show | 99 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.232+83_232+86delCG others(2): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47905402 | ||||||
chr2:47905402
|
CCCCGCCC others(1): Show |
C | 17 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0001g0287others(14): Show | 17 | HG00280.hp2 HG00738.hp1 HG01081.hp1 others(14): Show |
intron_variant | MODIFIER | c.232+79_232+86delCG others(6): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47905402 | ||||||
chr2:47905402
|
CCCCGCCC others(5): Show |
C | 7 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0298others(4): Show | 7 | HG01358.hp2 HG01981.hp1 HG03017.hp1 others(4): Show |
intron_variant | MODIFIER | c.232+75_232+86delCG others(10): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47905402 | ||||||
chr2:47905402
|
CCCCGCCC others(9): Show |
C | 2 | a0001c0001t0001g0304a0001c0001t0002g0303 | 2 | HG02155.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.232+71_232+86delCG others(14): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47905402 | ||||||
chr2:47905467
|
T | C | 1 | a0001c0001t0001g0304 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.232+22A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47905467 |