geneid | 131177 |
---|---|
ensemblid | ENSG00000198643.7 |
hgncid | 18665 |
symbol | FAM3D |
name | FAM3 metabolism regulating signaling molecule D |
refseq_nuc | NM_138805.3 |
refseq_prot | NP_620160.1 |
ensembl_nuc | ENST00000358781.7 |
ensembl_prot | ENSP00000351632.2 |
mane_status | MANE Select |
chr | chr3 |
start | 58633946 |
end | 58666774 |
strand | - |
ver | v1.2 |
region | chr3:58633946-58666774 |
region5000 | chr3:58628946-58671774 |
regionname0 | FAM3D_chr3_58633946_58666774 |
regionname5000 | FAM3D_chr3_58628946_58671774 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 224 | 364 | 84 | 62 | 161 | 9 | 46 | 125 | FAM3D_chr3_58628946_58671774 | FAM3D | copy fasta | chr3 | 58628946 | 58671774 |
a0002 | 0/0 | 224 | 28 | 8 | 11 | 1 | 4 | 4 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | copy fasta | chr3 | 58628946 | 58671774 |
a0003 | 0/0 | 224 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | FAM3D_chr3_58628946_58671774 | FAM3D | copy fasta | chr3 | 58628946 | 58671774 |
a0004 | 0/0 | 224 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | copy fasta | chr3 | 58628946 | 58671774 |
a0005 | 0/0 | 224 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | copy fasta | chr3 | 58628946 | 58671774 |
a0006 | 0/0 | 224 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | copy fasta | chr3 | 58628946 | 58671774 |
a0007 | 0/0 | 224 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | copy fasta | chr3 | 58628946 | 58671774 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 675 | 350 | 81 | 61 | 158 | 9 | 39 | FAM3D_chr3_58628946_58671774 | FAM3D | copy fasta | chr3 | 58628946 | 58671774 |
c0002 | 0/0 | 675 | 28 | 8 | 11 | 1 | 4 | 4 | FAM3D_chr3_58628946_58671774 | FAM3D | copy fasta | chr3 | 58628946 | 58671774 |
c0003 | 0/0 | 675 | 5 | 1 | 1 | 0 | 0 | 3 | FAM3D_chr3_58628946_58671774 | FAM3D | copy fasta | chr3 | 58628946 | 58671774 |
c0004 | 0/0 | 675 | 4 | 0 | 0 | 0 | 0 | 4 | FAM3D_chr3_58628946_58671774 | FAM3D | copy fasta | chr3 | 58628946 | 58671774 |
c0005 | 0/0 | 675 | 3 | 0 | 0 | 3 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | copy fasta | chr3 | 58628946 | 58671774 |
c0006 | 0/0 | 675 | 2 | 2 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | copy fasta | chr3 | 58628946 | 58671774 |
c0007 | 0/0 | 675 | 2 | 0 | 0 | 2 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | copy fasta | chr3 | 58628946 | 58671774 |
c0008 | 0/0 | 675 | 1 | 0 | 0 | 0 | 1 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | copy fasta | chr3 | 58628946 | 58671774 |
c0009 | 0/0 | 675 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | copy fasta | chr3 | 58628946 | 58671774 |
c0010 | 0/0 | 675 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | copy fasta | chr3 | 58628946 | 58671774 |
c0011 | 0/0 | 675 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | copy fasta | chr3 | 58628946 | 58671774 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 571 | 372 | 77 | 71 | 158 | 14 | 50 | FAM3D_chr3_58628946_58671774 | FAM3D | copy fasta | chr3 | 58628946 | 58671774 |
t0002 | 0/0 | 571 | 12 | 11 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | copy fasta | chr3 | 58628946 | 58671774 |
t0003 | 0/0 | 571 | 6 | 0 | 0 | 6 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | copy fasta | chr3 | 58628946 | 58671774 |
t0004 | 0/0 | 571 | 4 | 3 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | copy fasta | chr3 | 58628946 | 58671774 |
t0005 | 0/0 | 571 | 2 | 2 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | copy fasta | chr3 | 58628946 | 58671774 |
t0006 | 0/0 | 571 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | copy fasta | chr3 | 58628946 | 58671774 |
t0007 | 0/0 | 571 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | copy fasta | chr3 | 58628946 | 58671774 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/1 | 20 | 0 | 3 | 12 | 3 | 1 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0002 | 0/0 | 20 | 0 | 1 | 17 | 0 | 2 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0003 | 0/0 | 12 | 1 | 2 | 6 | 1 | 2 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0004 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0005 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0006 | 0/0 | 5 | 0 | 2 | 0 | 1 | 2 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0007 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0008 | 0/0 | 5 | 1 | 4 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0009 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0010 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0011 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0013 | 0/0 | 4 | 0 | 2 | 1 | 1 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0014 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0020 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0022 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0023 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0026 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0027 | 1/0 | 3 | 2 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0033 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0034 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0035 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0039 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0042 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0044 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0045 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0046 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0048 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0049 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0050 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0051 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0052 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0053 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0054 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0055 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0056 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0057 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0058 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 675 | 350 | 81 | 61 | 158 | 9 | 39 | FAM3D_chr3_58628946_58671774 | FAM3D | copy fasta | chr3 | 58628946 | 58671774 |
a0001c0003 | 0/0 | 675 | 5 | 1 | 1 | 0 | 0 | 3 | FAM3D_chr3_58628946_58671774 | FAM3D | copy fasta | chr3 | 58628946 | 58671774 |
a0001c0004 | 0/0 | 675 | 4 | 0 | 0 | 0 | 0 | 4 | FAM3D_chr3_58628946_58671774 | FAM3D | copy fasta | chr3 | 58628946 | 58671774 |
a0001c0005 | 0/0 | 675 | 3 | 0 | 0 | 3 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | copy fasta | chr3 | 58628946 | 58671774 |
a0001c0006 | 0/0 | 675 | 2 | 2 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | copy fasta | chr3 | 58628946 | 58671774 |
a0002c0002 | 0/0 | 675 | 28 | 8 | 11 | 1 | 4 | 4 | FAM3D_chr3_58628946_58671774 | FAM3D | copy fasta | chr3 | 58628946 | 58671774 |
a0003c0007 | 0/0 | 675 | 2 | 0 | 0 | 2 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | copy fasta | chr3 | 58628946 | 58671774 |
a0004c0008 | 0/0 | 675 | 1 | 0 | 0 | 0 | 1 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | copy fasta | chr3 | 58628946 | 58671774 |
a0005c0009 | 0/0 | 675 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | copy fasta | chr3 | 58628946 | 58671774 |
a0006c0010 | 0/0 | 675 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | copy fasta | chr3 | 58628946 | 58671774 |
a0007c0011 | 0/0 | 675 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | copy fasta | chr3 | 58628946 | 58671774 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 1245 | 326 | 66 | 58 | 152 | 9 | 39 | FAM3D_chr3_58628946_58671774 | FAM3D | copy fasta | chr3 | 58628946 | 58671774 |
a0001c0001t0002 | 0/0 | 1245 | 12 | 11 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | copy fasta | chr3 | 58628946 | 58671774 |
a0001c0001t0003 | 0/0 | 1245 | 6 | 0 | 0 | 6 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | copy fasta | chr3 | 58628946 | 58671774 |
a0001c0001t0004 | 0/0 | 1245 | 3 | 2 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | copy fasta | chr3 | 58628946 | 58671774 |
a0001c0001t0005 | 0/0 | 1245 | 2 | 2 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | copy fasta | chr3 | 58628946 | 58671774 |
a0001c0001t0007 | 0/0 | 1245 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | copy fasta | chr3 | 58628946 | 58671774 |
a0001c0003t0001 | 0/0 | 1245 | 5 | 1 | 1 | 0 | 0 | 3 | FAM3D_chr3_58628946_58671774 | FAM3D | copy fasta | chr3 | 58628946 | 58671774 |
a0001c0004t0001 | 0/0 | 1245 | 4 | 0 | 0 | 0 | 0 | 4 | FAM3D_chr3_58628946_58671774 | FAM3D | copy fasta | chr3 | 58628946 | 58671774 |
a0001c0005t0001 | 0/0 | 1245 | 3 | 0 | 0 | 3 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | copy fasta | chr3 | 58628946 | 58671774 |
a0001c0006t0001 | 0/0 | 1245 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | copy fasta | chr3 | 58628946 | 58671774 |
a0001c0006t0006 | 0/0 | 1245 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | copy fasta | chr3 | 58628946 | 58671774 |
a0002c0002t0001 | 0/0 | 1245 | 28 | 8 | 11 | 1 | 4 | 4 | FAM3D_chr3_58628946_58671774 | FAM3D | copy fasta | chr3 | 58628946 | 58671774 |
a0003c0007t0001 | 0/0 | 1245 | 2 | 0 | 0 | 2 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | copy fasta | chr3 | 58628946 | 58671774 |
a0004c0008t0001 | 0/0 | 1245 | 1 | 0 | 0 | 0 | 1 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | copy fasta | chr3 | 58628946 | 58671774 |
a0005c0009t0001 | 0/0 | 1245 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | copy fasta | chr3 | 58628946 | 58671774 |
a0006c0010t0004 | 0/0 | 1245 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | copy fasta | chr3 | 58628946 | 58671774 |
a0007c0011t0001 | 0/0 | 1245 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | copy fasta | chr3 | 58628946 | 58671774 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/1 | 20 | 0 | 3 | 12 | 3 | 1 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0002 | 0/0 | 20 | 0 | 1 | 17 | 0 | 2 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0003 | 0/0 | 12 | 1 | 2 | 6 | 1 | 2 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0004 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0005 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0007 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0008 | 0/0 | 5 | 1 | 4 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0009 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0013 | 0/0 | 4 | 0 | 2 | 1 | 1 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0014 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0020 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0023 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0026 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0027 | 1/0 | 3 | 2 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0033 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0034 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0045 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0051 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0052 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0053 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0054 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0055 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0056 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0057 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0058 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0002g0011 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0002g0046 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0003g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0003g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0004g0022 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0005g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0005g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0001t0007g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0003t0001g0048 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0003t0001g0049 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0003t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0004t0001g0039 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0004t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0004t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0005t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0005t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0005t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0006t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0001c0006t0006g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0002c0002t0001g0006 | 0/0 | 5 | 0 | 2 | 0 | 1 | 2 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0002c0002t0001g0010 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0002c0002t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0002c0002t0001g0042 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0002c0002t0001g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0002c0002t0001g0044 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0002c0002t0001g0050 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0002c0002t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0002c0002t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0002c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0002c0002t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0002c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0002c0002t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0002c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0002c0002t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0002c0002t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0003c0007t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0004c0008t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0005c0009t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0006c0010t0004g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
a0007c0011t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | GBR | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0023 | EUR | GBR | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0013 | EUR | FIN | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0095 | EUR | FIN | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | CHS | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | CHS | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | CHS | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | CHS | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | CHS | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | CHS | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | CHS | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | CHS | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | CHS | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | CHS | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG00639 | hp1 | a0002 | c0002 | t0001 | g0006 | AMR | PUR | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | CHS | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | CHS | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG00733 | hp2 | a0002 | c0002 | t0001 | g0214 | AMR | PUR | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | PUR | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0235 | AMR | PUR | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG01069 | hp2 | a0002 | c0002 | t0001 | g0043 | AMR | PUR | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG01070 | hp2 | a0002 | c0002 | t0001 | g0191 | AMR | PUR | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG01071 | hp1 | a0002 | c0002 | t0001 | g0043 | AMR | PUR | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG01081 | hp1 | a0001 | c0003 | t0001 | g0048 | AMR | PUR | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG01099 | hp1 | a0007 | c0011 | t0001 | g0239 | AMR | PUR | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0222 | AMR | PUR | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0247 | AMR | PUR | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG01109 | hp2 | a0001 | c0001 | t0002 | g0046 | AMR | PUR | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG01192 | hp2 | a0002 | c0002 | t0001 | g0006 | AMR | PUR | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG01255 | hp1 | a0002 | c0002 | t0001 | g0182 | AMR | CLM | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG01255 | hp2 | a0001 | c0001 | t0004 | g0022 | AMR | CLM | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG01258 | hp1 | a0002 | c0002 | t0001 | g0050 | AMR | CLM | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | CLM | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG01346 | hp2 | a0002 | c0002 | t0001 | g0184 | AMR | CLM | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | CLM | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | CLM | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | CLM | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG01496 | hp2 | a0002 | c0002 | t0001 | g0050 | AMR | CLM | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG01515 | hp1 | a0002 | c0002 | t0001 | g0042 | EUR | IBS | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0202 | EUR | IBS | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG01516 | hp2 | a0002 | c0002 | t0001 | g0006 | EUR | IBS | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG01517 | hp1 | a0002 | c0002 | t0001 | g0042 | EUR | IBS | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | ACB | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG01891 | hp2 | a0001 | c0001 | t0002 | g0110 | AFR | ACB | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PEL | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0207 | AMR | PEL | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PEL | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PEL | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG01981 | hp1 | a0001 | c0001 | t0007 | g0153 | AMR | PEL | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PEL | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG02027 | hp2 | a0003 | c0007 | t0001 | g0037 | EAS | KHV | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | KHV | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | KHV | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG02055 | hp1 | a0001 | c0001 | t0002 | g0046 | AFR | ACB | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | ACB | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | KHV | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | KHV | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG02074 | hp2 | a0002 | c0002 | t0001 | g0215 | EAS | KHV | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | KHV | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | KHV | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | KHV | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0249 | AFR | ACB | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | CDX | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | CDX | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | CDX | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | ACB | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | ACB | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0244 | AFR | ACB | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | ACB | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PEL | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | PEL | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG02280 | hp1 | a0001 | c0001 | t0002 | g0011 | AFR | ACB | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | ACB | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PEL | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG02300 | hp2 | a0002 | c0002 | t0001 | g0044 | AMR | PEL | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG02451 | hp1 | a0002 | c0002 | t0001 | g0010 | AFR | ACB | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | KHV | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | KHV | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG02572 | hp1 | a0001 | c0001 | t0004 | g0022 | AFR | GWD | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG02572 | hp2 | a0001 | c0001 | t0002 | g0105 | AFR | GWD | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0225 | SAS | PJL | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG02615 | hp1 | a0001 | c0001 | t0002 | g0193 | AFR | GWD | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | GWD | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | GWD | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | GWD | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | GWD | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | GWD | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | GWD | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | GWD | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG02683 | hp1 | a0001 | c0004 | t0001 | g0039 | SAS | PJL | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0169 | SAS | PJL | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG02698 | hp1 | a0002 | c0002 | t0001 | g0185 | SAS | PJL | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG02698 | hp2 | a0001 | c0004 | t0001 | g0039 | SAS | PJL | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG02717 | hp1 | a0001 | c0001 | t0002 | g0087 | AFR | GWD | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | GWD | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG02723 | hp1 | a0001 | c0001 | t0002 | g0172 | AFR | GWD | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | GWD | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0118 | SAS | PJL | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG02735 | hp2 | a0002 | c0002 | t0001 | g0206 | SAS | PJL | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0035 | SAS | PJL | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0123 | SAS | PJL | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG02818 | hp1 | a0001 | c0001 | t0002 | g0011 | AFR | GWD | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG02818 | hp2 | a0001 | c0001 | t0004 | g0022 | AFR | GWD | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0243 | AFR | GWD | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | GWD | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG02895 | hp1 | a0002 | c0002 | t0001 | g0030 | AFR | GWD | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG02897 | hp1 | a0002 | c0002 | t0001 | g0030 | AFR | GWD | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG02922 | hp1 | a0002 | c0002 | t0001 | g0010 | AFR | ESN | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | ESN | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | ESN | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | ESN | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | ESN | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | ESN | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | ESN | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0205 | SAS | PJL | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0226 | SAS | PJL | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | GWD | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | GWD | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG03098 | hp2 | a0001 | c0006 | t0001 | g0111 | AFR | MSL | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ESN | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | ESN | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | ESN | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG03139 | hp2 | a0006 | c0010 | t0004 | g0173 | AFR | ESN | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG03195 | hp1 | a0001 | c0001 | t0002 | g0192 | AFR | ESN | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG03195 | hp2 | a0002 | c0002 | t0001 | g0250 | AFR | ESN | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | MSL | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | MSL | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG03239 | hp2 | a0002 | c0002 | t0001 | g0006 | SAS | PJL | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0227 | AFR | MSL | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | MSL | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG03490 | hp1 | a0001 | c0003 | t0001 | g0049 | SAS | PJL | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0134 | SAS | PJL | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0052 | SAS | PJL | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG03492 | hp1 | a0001 | c0003 | t0001 | g0049 | SAS | PJL | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0052 | SAS | PJL | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | ESN | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG03516 | hp2 | a0002 | c0002 | t0001 | g0010 | AFR | ESN | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | GWD | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | GWD | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | MSL | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | MSL | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0072 | SAS | PJL | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0137 | SAS | PJL | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0200 | SAS | STU | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG03688 | hp2 | a0001 | c0003 | t0001 | g0048 | SAS | STU | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0220 | SAS | PJL | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0204 | SAS | PJL | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0133 | SAS | PJL | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG03831 | hp1 | a0002 | c0002 | t0001 | g0006 | SAS | BEB | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG03831 | hp2 | a0001 | c0004 | t0001 | g0113 | SAS | BEB | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0086 | SAS | BEB | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0149 | SAS | BEB | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0035 | SAS | BEB | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0233 | SAS | BEB | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0099 | SAS | BEB | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0167 | SAS | STU | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0165 | SAS | STU | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0231 | SAS | BEB | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0147 | SAS | BEB | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0094 | SAS | STU | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG04199 | hp2 | a0001 | c0004 | t0001 | g0083 | SAS | STU | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0136 | SAS | STU | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0208 | SAS | STU | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0168 | SAS | STU | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0230 | SAS | STU | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA18522 | hp1 | a0001 | c0003 | t0001 | g0176 | AFR | YRI | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | YRI | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA18612 | hp1 | a0001 | c0001 | t0003 | g0016 | EAS | CHB | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | CHB | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | YRI | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | YRI | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA18948 | hp1 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA18967 | hp1 | a0001 | c0005 | t0001 | g0135 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA18968 | hp2 | a0003 | c0007 | t0001 | g0037 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA18973 | hp2 | a0001 | c0001 | t0003 | g0081 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA19003 | hp1 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA19011 | hp1 | a0001 | c0001 | t0003 | g0073 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA19012 | hp1 | a0001 | c0005 | t0001 | g0143 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | LWK | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA19030 | hp2 | a0001 | c0006 | t0006 | g0179 | AFR | LWK | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA19043 | hp1 | a0001 | c0001 | t0002 | g0011 | AFR | LWK | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA19043 | hp2 | a0002 | c0002 | t0001 | g0010 | AFR | LWK | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA19056 | hp1 | a0001 | c0001 | t0003 | g0240 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA19066 | hp2 | a0001 | c0005 | t0001 | g0216 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA19240 | hp1 | a0001 | c0001 | t0005 | g0059 | AFR | YRI | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | YRI | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | ASW | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | ASW | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA20752 | hp1 | a0002 | c0002 | t0001 | g0044 | EUR | TSI | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0125 | EUR | TSI | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA20805 | hp2 | a0004 | c0008 | t0001 | g0183 | EUR | TSI | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | GIH | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0209 | SAS | GIH | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | CLM | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG02109 | hp1 | a0002 | c0002 | t0001 | g0251 | AFR | ACB | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG02109 | hp2 | a0001 | c0001 | t0002 | g0011 | AFR | ACB | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | ACB | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | ACB | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0241 | AFR | ACB | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG02559 | hp2 | a0001 | c0001 | t0005 | g0060 | AFR | ACB | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG03471 | hp2 | a0005 | c0009 | t0001 | g0242 | AFR | MSL | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | USA | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0248 | AFR | USA | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0246 | AFR | USA | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | USA | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | LWK | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | LWK | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0001 | REF | REF | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0027 | REF | REF | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:58637187
|
C | T | 1 | a0006 | 1 | HG03139.hp2 | missense_variant | MODERATE | c.412G>A | p.Gly138Arg | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 8/10 | 649/1245 | 412/675 | 138/224 | chr3 | 58637187 | ||
chr3:58637189
|
G | A | 1 | a0007 | 1 | HG01099.hp1 | missense_variant | MODERATE | c.410C>T | p.Pro137Leu | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 8/10 | 647/1245 | 410/675 | 137/224 | chr3 | 58637189 | ||
chr3:58640148
|
C | A | 3 | a0002a0004a0007 | 30 | HG00639.hp1 HG00733.hp2 HG01069.hp2 others(27): Show |
missense_variant | MODERATE | c.352G>T | p.Ala118Ser | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 7/10 | 589/1245 | 352/675 | 118/224 | chr3 | 58640148 | ||
chr3:58645512
|
C | T | 1 | a0005 | 1 | HG03471.hp2 | missense_variant | MODERATE | c.260G>A | p.Arg87His | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 5/10 | 497/1245 | 260/675 | 87/224 | chr3 | 58645512 | ||
chr3:58645594
|
G | A | 1 | a0003 | 2 | HG02027.hp2 NA18968.hp2 |
missense_variant | MODERATE | c.178C>T | p.Pro60Ser | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 5/10 | 415/1245 | 178/675 | 60/224 | chr3 | 58645594 | ||
chr3:58653691
|
C | T | 1 | a0004 | 1 | NA20805.hp2 | missense_variant | MODERATE | c.104G>A | p.Arg35His | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/10 | 341/1245 | 104/675 | 35/224 | chr3 | 58653691 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:58636303
|
G | A | 1 | a0001c0005 | 3 | NA18967.hp1 NA19012.hp1 NA19066.hp2 |
synonymous_variant | LOW | c.576C>T | p.Pro192Pro | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 9/10 | 813/1245 | 576/675 | 192/224 | chr3 | 58636303 | ||
chr3:58637155
|
G | A | 1 | a0001c0006 | 2 | HG03098.hp2 NA19030.hp2 |
synonymous_variant | LOW | c.444C>T | p.Asp148Asp | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 8/10 | 681/1245 | 444/675 | 148/224 | chr3 | 58637155 | ||
chr3:58645541
|
G | A | 1 | a0001c0004 | 4 | HG02683.hp1 HG02698.hp2 HG03831.hp2 others(1): Show |
synonymous_variant | LOW | c.231C>T | p.Val77Val | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 5/10 | 468/1245 | 231/675 | 77/224 | chr3 | 58645541 | ||
chr3:58653738
|
T | G | 1 | a0001c0003 | 5 | HG01081.hp1 HG03490.hp1 HG03492.hp1 others(2): Show |
synonymous_variant | LOW | c.57A>C | p.Thr19Thr | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/10 | 294/1245 | 57/675 | 19/224 | chr3 | 58653738 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:58634104
|
G | A | 1 | a0001c0001t0007 | 1 | HG01981.hp1 | 3_prime_UTR_variant | MODIFIER | c.*175C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 10/10 | 175 | chr3 | 58634104 | |||||
chr3:58634151
|
G | T | 2 | a0001c0001t0004a0006c0010t0004 | 4 | HG01255.hp2 HG02572.hp1 HG02818.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*128C>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 10/10 | 128 | chr3 | 58634151 | |||||
chr3:58634169
|
C | A | 1 | a0001c0001t0003 | 6 | NA18612.hp1 NA18948.hp1 NA18973.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*110G>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 10/10 | 110 | chr3 | 58634169 | |||||
chr3:58634183
|
C | G | 1 | a0001c0006t0006 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*96G>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 10/10 | 96 | chr3 | 58634183 | |||||
chr3:58634184
|
C | T | 1 | a0001c0006t0006 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*95G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 10/10 | 95 | chr3 | 58634184 | |||||
chr3:58634187
|
C | T | 1 | a0001c0006t0006 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*92G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 10/10 | 92 | chr3 | 58634187 | |||||
chr3:58634265
|
G | C | 1 | a0001c0001t0002 | 12 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*14C>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 10/10 | 14 | chr3 | 58634265 | |||||
chr3:58666728
|
C | T | 1 | a0001c0001t0005 | 2 | HG02559.hp2 NA19240.hp1 |
5_prime_UTR_variant | MODIFIER | c.-191G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/10 | 11165 | chr3 | 58666728 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:58634378
|
G | A | 2 | a0001c0001t0001g0021a0001c0001t0001g0199 | 4 | HG02257.hp1 HG02965.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.586-10C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 9/9 | chr3 | 58634378 | ||||||
chr3:58634378
|
G | C | 2 | a0001c0001t0001g0150a0003c0007t0001g0037 | 3 | HG02027.hp2 HG02135.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.586-10C>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 9/9 | chr3 | 58634378 | ||||||
chr3:58634624
|
T | C | 2 | a0001c0001t0001g0047a0001c0001t0001g0245 | 3 | HG02922.hp2 HG03516.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.586-256A>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 9/9 | chr3 | 58634624 | ||||||
chr3:58634661
|
T | A | 2 | a0001c0003t0001g0048a0001c0003t0001g0049 | 4 | HG01081.hp1 HG03490.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.586-293A>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 9/9 | chr3 | 58634661 | ||||||
chr3:58634940
|
G | T | 4 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(1): Show | 4 | HG00280.hp2 HG00735.hp2 HG02040.hp2 others(1): Show |
intron_variant | MODIFIER | c.586-572C>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 9/9 | chr3 | 58634940 | ||||||
chr3:58634985
|
G | A | 1 | a0001c0001t0001g0244 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.586-617C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 9/9 | chr3 | 58634985 | ||||||
chr3:58635049
|
C | G | 2 | a0001c0003t0001g0048a0001c0003t0001g0049 | 4 | HG01081.hp1 HG03490.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.586-681G>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 9/9 | chr3 | 58635049 | ||||||
chr3:58635114
|
G | A | 1 | a0001c0001t0001g0119 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.586-746C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 9/9 | chr3 | 58635114 | ||||||
chr3:58635121
|
G | T | 1 | a0001c0001t0001g0147 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.586-753C>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 9/9 | chr3 | 58635121 | ||||||
chr3:58635162
|
G | A | 2 | a0001c0001t0001g0203a0005c0009t0001g0242 | 2 | HG02630.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.586-794C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 9/9 | chr3 | 58635162 | ||||||
chr3:58635175
|
T | A | 18 | a0001c0001t0001g0045a0001c0001t0001g0053a0001c0001t0001g0066others(15): Show | 20 | HG00642.hp2 HG01099.hp2 HG01175.hp2 others(17): Show |
intron_variant | MODIFIER | c.586-807A>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 9/9 | chr3 | 58635175 | ||||||
chr3:58635209
|
A | G | 3 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0090 | 3 | HG02622.hp2 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.586-841T>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 9/9 | chr3 | 58635209 | ||||||
chr3:58635251
|
T | C | 1 | a0001c0001t0001g0142 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.586-883A>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 9/9 | chr3 | 58635251 | ||||||
chr3:58635390
|
C | T | 1 | a0001c0001t0001g0229 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.585+904G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 9/9 | chr3 | 58635390 | ||||||
chr3:58635509
|
G | C | 1 | a0001c0001t0001g0181 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.585+785C>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 9/9 | chr3 | 58635509 | ||||||
chr3:58635521
|
C | T | 1 | a0001c0001t0001g0181 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.585+773G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 9/9 | chr3 | 58635521 | ||||||
chr3:58635532
|
G | A | 4 | a0001c0001t0002g0011a0001c0001t0002g0087a0001c0001t0002g0192others(1): Show | 7 | HG02109.hp2 HG02280.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.585+762C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 9/9 | chr3 | 58635532 | ||||||
chr3:58635628
|
C | T | 18 | a0001c0001t0001g0045a0001c0001t0001g0053a0001c0001t0001g0066others(15): Show | 20 | HG00642.hp2 HG01099.hp2 HG01175.hp2 others(17): Show |
intron_variant | MODIFIER | c.585+666G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 9/9 | chr3 | 58635628 | ||||||
chr3:58635633
|
C | T | 1 | a0001c0001t0001g0167 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.585+661G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 9/9 | chr3 | 58635633 | ||||||
chr3:58635806
|
C | T | 3 | a0001c0001t0001g0244a0001c0001t0004g0022a0006c0010t0004g0173 | 5 | HG01255.hp2 HG02258.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.585+488G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 9/9 | chr3 | 58635806 | ||||||
chr3:58635997
|
C | T | 8 | a0001c0001t0001g0024a0001c0001t0002g0046a0001c0001t0002g0105others(5): Show | 13 | HG01081.hp1 HG01109.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.585+297G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 9/9 | chr3 | 58635997 | ||||||
chr3:58636043
|
C | T | 1 | a0001c0001t0001g0244 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.585+251G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 9/9 | chr3 | 58636043 | ||||||
chr3:58636171
|
G | C | 1 | a0001c0001t0005g0059 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.585+123C>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 9/9 | chr3 | 58636171 | ||||||
chr3:58636208
|
C | T | 243 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(240): Show | 385 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(382): Show |
intron_variant | MODIFIER | c.585+86G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 9/9 | chr3 | 58636208 | ||||||
chr3:58636501
|
G | T | 1 | a0001c0001t0001g0121 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.459-81C>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 8/9 | chr3 | 58636501 | ||||||
chr3:58636758
|
T | C | 1 | a0001c0001t0001g0052 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.459-338A>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 8/9 | chr3 | 58636758 | ||||||
chr3:58636762
|
A | T | 103 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(100): Show | 158 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.459-342T>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 8/9 | chr3 | 58636762 | ||||||
chr3:58636769
|
GT | G | 239 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(236): Show | 379 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(376): Show |
intron_variant | MODIFIER | c.459-350delA | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 8/9 | chr3 | 58636769 | ||||||
chr3:58636778
|
T | C | 5 | a0001c0001t0001g0024a0001c0003t0001g0048a0001c0003t0001g0049others(2): Show | 9 | HG01081.hp1 HG02109.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.459-358A>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 8/9 | chr3 | 58636778 | ||||||
chr3:58636818
|
C | T | 2 | a0001c0001t0001g0109a0001c0003t0001g0176 | 2 | NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.458+323G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 8/9 | chr3 | 58636818 | ||||||
chr3:58636893
|
G | T | 85 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(82): Show | 145 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(142): Show |
intron_variant | MODIFIER | c.458+248C>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 8/9 | chr3 | 58636893 | ||||||
chr3:58637004
|
G | T | 1 | a0001c0001t0001g0221 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.458+137C>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 8/9 | chr3 | 58637004 | ||||||
chr3:58637058
|
A | G | 1 | a0001c0001t0001g0084 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.458+83T>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 8/9 | chr3 | 58637058 | ||||||
chr3:58637109
|
G | A | 1 | a0001c0001t0001g0158 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.458+32C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 8/9 | chr3 | 58637109 | ||||||
chr3:58637458
|
T | C | 122 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(119): Show | 192 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.374-233A>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 7/9 | chr3 | 58637458 | ||||||
chr3:58637513
|
C | G | 118 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(115): Show | 191 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(188): Show |
intron_variant | MODIFIER | c.374-288G>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 7/9 | chr3 | 58637513 | ||||||
chr3:58637531
|
C | T | 96 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(93): Show | 161 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.374-306G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 7/9 | chr3 | 58637531 | ||||||
chr3:58637616
|
C | T | 1 | a0001c0006t0001g0111 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.374-391G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 7/9 | chr3 | 58637616 | ||||||
chr3:58637617
|
G | A | 95 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(92): Show | 160 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(157): Show |
intron_variant | MODIFIER | c.374-392C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 7/9 | chr3 | 58637617 | ||||||
chr3:58637746
|
G | C | 3 | a0001c0001t0001g0036a0001c0001t0001g0148a0001c0001t0001g0202 | 4 | HG00639.hp2 HG00741.hp2 HG01123.hp2 others(1): Show |
intron_variant | MODIFIER | c.374-521C>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 7/9 | chr3 | 58637746 | ||||||
chr3:58637789
|
C | T | 1 | a0001c0001t0002g0087 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.374-564G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 7/9 | chr3 | 58637789 | ||||||
chr3:58637878
|
G | GATTATT | 6 | a0001c0001t0001g0045a0001c0001t0001g0180a0001c0001t0001g0190others(3): Show | 8 | HG01109.hp2 HG01243.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.374-659_374-654dup others(6): Show |
FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 7/9 | chr3 | 58637878 | ||||||
chr3:58637878
|
G | GATTATTA others(2): Show |
29 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0015others(26): Show | 47 | HG00609.hp1 HG00673.hp1 HG01074.hp2 others(44): Show |
intron_variant | MODIFIER | c.374-662_374-654dup others(9): Show |
FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 7/9 | chr3 | 58637878 | ||||||
chr3:58637878
|
G | GATTATTA others(5): Show |
182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(179): Show | 298 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.374-665_374-654dup others(12): Show |
FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 7/9 | chr3 | 58637878 | ||||||
chr3:58637878
|
G | GATTATTA others(8): Show |
22 | a0001c0001t0001g0026a0001c0001t0001g0035a0001c0001t0001g0054others(19): Show | 29 | HG00438.hp2 HG00621.hp2 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.374-668_374-654dup others(15): Show |
FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 7/9 | chr3 | 58637878 | ||||||
chr3:58637878
|
G | GATTATTA others(11): Show |
4 | a0001c0001t0001g0112a0001c0001t0001g0232a0001c0001t0001g0241others(1): Show | 4 | HG02486.hp1 HG02559.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.374-671_374-654dup others(18): Show |
FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 7/9 | chr3 | 58637878 | ||||||
chr3:58637878
|
G | GATTATTA others(14): Show |
5 | a0001c0001t0001g0171a0001c0001t0005g0059a0001c0004t0001g0039others(2): Show | 6 | HG02683.hp1 HG02698.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.374-674_374-654dup others(21): Show |
FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 7/9 | chr3 | 58637878 | ||||||
chr3:58637878
|
G | GATTATTA others(20): Show |
1 | a0006c0010t0004g0173 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.374-654_374-653ins others(27): Show |
FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 7/9 | chr3 | 58637878 | ||||||
chr3:58637909
|
A | G | 249 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(246): Show | 393 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(390): Show |
intron_variant | MODIFIER | c.374-684T>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 7/9 | chr3 | 58637909 | ||||||
chr3:58637915
|
T | G | 249 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(246): Show | 393 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(390): Show |
intron_variant | MODIFIER | c.374-690A>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 7/9 | chr3 | 58637915 | ||||||
chr3:58638076
|
G | A | 1 | a0001c0001t0001g0226 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.374-851C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 7/9 | chr3 | 58638076 | ||||||
chr3:58638176
|
C | G | 104 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(101): Show | 176 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(173): Show |
intron_variant | MODIFIER | c.374-951G>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 7/9 | chr3 | 58638176 | ||||||
chr3:58638213
|
T | C | 1 | a0001c0001t0001g0072 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.374-988A>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 7/9 | chr3 | 58638213 | ||||||
chr3:58638260
|
T | C | 3 | a0001c0001t0001g0177a0001c0001t0001g0199a0001c0001t0001g0243 | 3 | HG02257.hp1 HG02886.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.374-1035A>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 7/9 | chr3 | 58638260 | ||||||
chr3:58638484
|
G | A | 14 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0032others(11): Show | 22 | HG00609.hp1 HG00673.hp1 HG02129.hp2 others(19): Show |
intron_variant | MODIFIER | c.374-1259C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 7/9 | chr3 | 58638484 | ||||||
chr3:58638521
|
T | C | 1 | a0001c0001t0001g0128 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.374-1296A>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 7/9 | chr3 | 58638521 | ||||||
chr3:58638781
|
C | T | 2 | a0001c0004t0001g0039a0001c0004t0001g0113 | 3 | HG02683.hp1 HG02698.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.373+1346G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 7/9 | chr3 | 58638781 | ||||||
chr3:58638786
|
C | G | 1 | a0001c0001t0001g0194 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.373+1341G>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 7/9 | chr3 | 58638786 | ||||||
chr3:58638807
|
C | T | 2 | a0001c0004t0001g0039a0001c0004t0001g0113 | 3 | HG02683.hp1 HG02698.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.373+1320G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 7/9 | chr3 | 58638807 | ||||||
chr3:58638913
|
C | T | 250 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(247): Show | 394 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(391): Show |
intron_variant | MODIFIER | c.373+1214G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 7/9 | chr3 | 58638913 | ||||||
chr3:58638980
|
C | A | 1 | a0001c0001t0001g0056 | 2 | HG03225.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.373+1147G>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 7/9 | chr3 | 58638980 | ||||||
chr3:58639023
|
G | A | 1 | a0001c0001t0001g0008 | 5 | HG01256.hp1 HG01258.hp2 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.373+1104C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 7/9 | chr3 | 58639023 | ||||||
chr3:58639043
|
A | G | 112 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(109): Show | 165 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.373+1084T>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 7/9 | chr3 | 58639043 | ||||||
chr3:58639344
|
C | G | 1 | a0001c0001t0001g0220 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.373+783G>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 7/9 | chr3 | 58639344 | ||||||
chr3:58639347
|
T | C | 1 | a0001c0001t0001g0219 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.373+780A>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 7/9 | chr3 | 58639347 | ||||||
chr3:58639447
|
G | C | 7 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0084others(4): Show | 7 | HG00642.hp2 HG01099.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.373+680C>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 7/9 | chr3 | 58639447 | ||||||
chr3:58639479
|
C | A | 1 | a0001c0001t0001g0144 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.373+648G>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 7/9 | chr3 | 58639479 | ||||||
chr3:58639504
|
C | T | 21 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0032others(18): Show | 31 | HG00609.hp1 HG00673.hp1 HG01081.hp1 others(28): Show |
intron_variant | MODIFIER | c.373+623G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 7/9 | chr3 | 58639504 | ||||||
chr3:58639578
|
C | T | 1 | a0001c0001t0001g0210 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.373+549G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 7/9 | chr3 | 58639578 | ||||||
chr3:58639598
|
G | T | 19 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0032others(16): Show | 27 | HG00609.hp1 HG00673.hp1 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.373+529C>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 7/9 | chr3 | 58639598 | ||||||
chr3:58639607
|
A | G | 1 | a0005c0009t0001g0242 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.373+520T>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 7/9 | chr3 | 58639607 | ||||||
chr3:58639740
|
A | G | 1 | a0001c0006t0001g0111 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.373+387T>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 7/9 | chr3 | 58639740 | ||||||
chr3:58639832
|
T | C | 137 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(134): Show | 206 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.373+295A>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 7/9 | chr3 | 58639832 | ||||||
chr3:58639889
|
G | T | 1 | a0001c0001t0001g0208 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.373+238C>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 7/9 | chr3 | 58639889 | ||||||
chr3:58639904
|
C | T | 15 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0032others(12): Show | 23 | HG00609.hp1 HG00673.hp1 HG02129.hp2 others(20): Show |
intron_variant | MODIFIER | c.373+223G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 7/9 | chr3 | 58639904 | ||||||
chr3:58639973
|
A | G | 2 | a0001c0001t0001g0005a0001c0001t0001g0175 | 6 | NA18944.hp2 NA18962.hp1 NA18966.hp2 others(3): Show |
intron_variant | MODIFIER | c.373+154T>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 7/9 | chr3 | 58639973 | ||||||
chr3:58640086
|
G | A | 2 | a0001c0003t0001g0048a0001c0003t0001g0049 | 4 | HG01081.hp1 HG03490.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.373+41C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 7/9 | chr3 | 58640086 | ||||||
chr3:58640248
|
C | G | 113 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(110): Show | 169 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.323-71G>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 6/9 | chr3 | 58640248 | ||||||
chr3:58640348
|
G | T | 42 | a0001c0001t0001g0001a0001c0001t0001g0025a0001c0001t0001g0034others(39): Show | 66 | HG00408.hp2 HG00733.hp1 HG00735.hp1 others(63): Show |
intron_variant | MODIFIER | c.323-171C>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 6/9 | chr3 | 58640348 | ||||||
chr3:58640421
|
G | A | 1 | a0001c0001t0001g0139 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.323-244C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 6/9 | chr3 | 58640421 | ||||||
chr3:58640515
|
T | C | 104 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(101): Show | 157 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.323-338A>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 6/9 | chr3 | 58640515 | ||||||
chr3:58640615
|
C | T | 4 | a0001c0003t0001g0048a0001c0003t0001g0049a0001c0003t0001g0176others(1): Show | 6 | HG01081.hp1 HG03471.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.323-438G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 6/9 | chr3 | 58640615 | ||||||
chr3:58640896
|
G | T | 1 | a0001c0001t0001g0091 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.323-719C>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 6/9 | chr3 | 58640896 | ||||||
chr3:58640986
|
G | T | 1 | a0001c0001t0003g0073 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.323-809C>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 6/9 | chr3 | 58640986 | ||||||
chr3:58640992
|
C | G | 15 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0032others(12): Show | 23 | HG00609.hp1 HG00673.hp1 HG02129.hp2 others(20): Show |
intron_variant | MODIFIER | c.323-815G>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 6/9 | chr3 | 58640992 | ||||||
chr3:58640994
|
T | C | 1 | a0001c0001t0001g0249 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.323-817A>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 6/9 | chr3 | 58640994 | ||||||
chr3:58641055
|
C | T | 1 | a0001c0001t0001g0084 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.323-878G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 6/9 | chr3 | 58641055 | ||||||
chr3:58641091
|
C | T | 3 | a0001c0001t0001g0177a0001c0001t0001g0199a0001c0001t0001g0243 | 3 | HG02257.hp1 HG02886.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.323-914G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 6/9 | chr3 | 58641091 | ||||||
chr3:58641167
|
G | A | 218 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(215): Show | 345 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(342): Show |
intron_variant | MODIFIER | c.323-990C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 6/9 | chr3 | 58641167 | ||||||
chr3:58641321
|
C | T | 6 | a0001c0001t0001g0177a0001c0001t0001g0199a0001c0001t0001g0243others(3): Show | 7 | HG02257.hp1 HG02683.hp1 HG02698.hp2 others(4): Show |
intron_variant | MODIFIER | c.323-1144G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 6/9 | chr3 | 58641321 | ||||||
chr3:58641383
|
G | A | 1 | a0001c0001t0001g0222 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.323-1206C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 6/9 | chr3 | 58641383 | ||||||
chr3:58641536
|
G | T | 1 | a0001c0001t0001g0200 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.323-1359C>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 6/9 | chr3 | 58641536 | ||||||
chr3:58641544
|
G | A | 2 | a0001c0001t0001g0082a0001c0001t0001g0108 | 2 | HG01891.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.323-1367C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 6/9 | chr3 | 58641544 | ||||||
chr3:58641729
|
A | G | 3 | a0001c0004t0001g0039a0001c0004t0001g0083a0001c0004t0001g0113 | 4 | HG02683.hp1 HG02698.hp2 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.323-1552T>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 6/9 | chr3 | 58641729 | ||||||
chr3:58641753
|
A | C | 2 | a0001c0001t0001g0120a0001c0001t0001g0189 | 2 | HG01175.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.323-1576T>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 6/9 | chr3 | 58641753 | ||||||
chr3:58641879
|
T | G | 113 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(110): Show | 169 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.323-1702A>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 6/9 | chr3 | 58641879 | ||||||
chr3:58641880
|
T | G | 1 | a0001c0001t0005g0060 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.323-1703A>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 6/9 | chr3 | 58641880 | ||||||
chr3:58642185
|
A | T | 112 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(109): Show | 166 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.322+1477T>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 6/9 | chr3 | 58642185 | ||||||
chr3:58642210
|
C | A | 27 | a0001c0001t0001g0024a0001c0001t0001g0045a0001c0001t0001g0180others(24): Show | 44 | HG00639.hp1 HG00733.hp2 HG01069.hp2 others(41): Show |
intron_variant | MODIFIER | c.322+1452G>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 6/9 | chr3 | 58642210 | ||||||
chr3:58642276
|
C | T | 1 | a0001c0001t0001g0029 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.322+1386G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 6/9 | chr3 | 58642276 | ||||||
chr3:58642287
|
C | T | 1 | a0001c0001t0001g0229 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.322+1375G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 6/9 | chr3 | 58642287 | ||||||
chr3:58642310
|
T | C | 1 | a0001c0001t0001g0072 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.322+1352A>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 6/9 | chr3 | 58642310 | ||||||
chr3:58642339
|
T | C | 23 | a0001c0001t0001g0024a0001c0001t0001g0045a0001c0001t0001g0180others(20): Show | 38 | HG00639.hp1 HG00733.hp2 HG01069.hp2 others(35): Show |
intron_variant | MODIFIER | c.322+1323A>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 6/9 | chr3 | 58642339 | ||||||
chr3:58642375
|
G | A | 1 | a0001c0001t0001g0128 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.322+1287C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 6/9 | chr3 | 58642375 | ||||||
chr3:58642484
|
C | A | 6 | a0001c0001t0001g0177a0001c0001t0001g0199a0001c0001t0001g0243others(3): Show | 7 | HG02257.hp1 HG02683.hp1 HG02698.hp2 others(4): Show |
intron_variant | MODIFIER | c.322+1178G>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 6/9 | chr3 | 58642484 | ||||||
chr3:58642627
|
G | A | 114 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(111): Show | 168 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.322+1035C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 6/9 | chr3 | 58642627 | ||||||
chr3:58642642
|
G | A | 3 | a0001c0001t0001g0058a0001c0001t0001g0247a0001c0001t0001g0248 | 4 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(1): Show |
intron_variant | MODIFIER | c.322+1020C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 6/9 | chr3 | 58642642 | ||||||
chr3:58642648
|
C | T | 1 | a0001c0001t0001g0051 | 2 | NA18997.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.322+1014G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 6/9 | chr3 | 58642648 | ||||||
chr3:58642743
|
C | A | 1 | a0001c0001t0005g0060 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.322+919G>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 6/9 | chr3 | 58642743 | ||||||
chr3:58642743
|
C | G | 113 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(110): Show | 167 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.322+919G>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 6/9 | chr3 | 58642743 | ||||||
chr3:58642778
|
T | G | 114 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(111): Show | 168 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.322+884A>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 6/9 | chr3 | 58642778 | ||||||
chr3:58642812
|
C | T | 1 | a0001c0001t0005g0059 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.322+850G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 6/9 | chr3 | 58642812 | ||||||
chr3:58642927
|
C | T | 110 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(107): Show | 164 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.322+735G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 6/9 | chr3 | 58642927 | ||||||
chr3:58642952
|
T | C | 1 | a0001c0006t0001g0111 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.322+710A>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 6/9 | chr3 | 58642952 | ||||||
chr3:58642972
|
T | C | 111 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(108): Show | 165 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.322+690A>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 6/9 | chr3 | 58642972 | ||||||
chr3:58643012
|
C | T | 1 | a0001c0001t0001g0220 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.322+650G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 6/9 | chr3 | 58643012 | ||||||
chr3:58643017
|
A | T | 1 | a0001c0001t0001g0029 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.322+645T>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 6/9 | chr3 | 58643017 | ||||||
chr3:58643027
|
G | T | 109 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(106): Show | 162 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(159): Show |
intron_variant | MODIFIER | c.322+635C>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 6/9 | chr3 | 58643027 | ||||||
chr3:58643050
|
T | G | 160 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(157): Show | 239 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(236): Show |
intron_variant | MODIFIER | c.322+612A>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 6/9 | chr3 | 58643050 | ||||||
chr3:58643178
|
C | T | 5 | a0001c0001t0001g0177a0001c0001t0001g0199a0001c0001t0001g0243others(2): Show | 6 | HG02257.hp1 HG02683.hp1 HG02698.hp2 others(3): Show |
intron_variant | MODIFIER | c.322+484G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 6/9 | chr3 | 58643178 | ||||||
chr3:58643182
|
C | T | 1 | a0001c0001t0001g0166 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.322+480G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 6/9 | chr3 | 58643182 | ||||||
chr3:58643188
|
C | T | 2 | a0001c0001t0001g0171a0006c0010t0004g0173 | 2 | HG03139.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.322+474G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 6/9 | chr3 | 58643188 | ||||||
chr3:58643192
|
C | T | 19 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0032others(16): Show | 28 | HG00609.hp1 HG00673.hp1 HG02129.hp2 others(25): Show |
intron_variant | MODIFIER | c.322+470G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 6/9 | chr3 | 58643192 | ||||||
chr3:58643203
|
A | T | 1 | a0001c0003t0001g0176 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.322+459T>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 6/9 | chr3 | 58643203 | ||||||
chr3:58643212
|
C | T | 1 | a0001c0001t0001g0138 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.322+450G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 6/9 | chr3 | 58643212 | ||||||
chr3:58643244
|
T | C | 1 | a0001c0001t0001g0181 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.322+418A>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 6/9 | chr3 | 58643244 | ||||||
chr3:58643254
|
C | T | 2 | a0001c0001t0001g0137a0001c0001t0001g0149 | 2 | HG03669.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.322+408G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 6/9 | chr3 | 58643254 | ||||||
chr3:58643392
|
G | T | 2 | a0001c0001t0002g0110a0001c0006t0001g0111 | 2 | HG01891.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.322+270C>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 6/9 | chr3 | 58643392 | ||||||
chr3:58643531
|
C | T | 1 | a0001c0001t0001g0136 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.322+131G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 6/9 | chr3 | 58643531 | ||||||
chr3:58643608
|
C | T | 2 | a0001c0001t0001g0171a0006c0010t0004g0173 | 2 | HG03139.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.322+54G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 6/9 | chr3 | 58643608 | ||||||
chr3:58643960
|
G | C | 14 | a0002c0002t0001g0006a0002c0002t0001g0042a0002c0002t0001g0043others(11): Show | 22 | HG00639.hp1 HG00733.hp2 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.264-240C>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 5/9 | chr3 | 58643960 | ||||||
chr3:58644007
|
C | T | 1 | a0001c0001t0001g0018 | 3 | HG00423.hp1 HG00609.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.264-287G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 5/9 | chr3 | 58644007 | ||||||
chr3:58644113
|
A | T | 1 | a0001c0005t0001g0135 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.264-393T>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 5/9 | chr3 | 58644113 | ||||||
chr3:58644179
|
G | C | 2 | a0001c0001t0001g0020a0001c0001t0001g0130 | 4 | HG01074.hp2 HG01358.hp2 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.264-459C>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 5/9 | chr3 | 58644179 | ||||||
chr3:58644332
|
C | T | 86 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(83): Show | 138 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.264-612G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 5/9 | chr3 | 58644332 | ||||||
chr3:58644339
|
G | A | 1 | a0001c0003t0001g0176 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.264-619C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 5/9 | chr3 | 58644339 | ||||||
chr3:58644340
|
C | G | 1 | a0001c0003t0001g0176 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.264-620G>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 5/9 | chr3 | 58644340 | ||||||
chr3:58644498
|
T | C | 8 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0084others(5): Show | 8 | HG00642.hp2 HG01099.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.264-778A>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 5/9 | chr3 | 58644498 | ||||||
chr3:58644524
|
A | C | 1 | a0001c0001t0001g0082 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.264-804T>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 5/9 | chr3 | 58644524 | ||||||
chr3:58644576
|
C | A | 3 | a0001c0001t0001g0177a0001c0001t0001g0199a0001c0001t0001g0243 | 3 | HG02257.hp1 HG02886.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.264-856G>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 5/9 | chr3 | 58644576 | ||||||
chr3:58644594
|
C | T | 1 | a0001c0001t0001g0102 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.264-874G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 5/9 | chr3 | 58644594 | ||||||
chr3:58644632
|
A | G | 1 | a0001c0001t0001g0205 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.263+877T>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 5/9 | chr3 | 58644632 | ||||||
chr3:58644774
|
A | G | 111 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(108): Show | 166 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.263+735T>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 5/9 | chr3 | 58644774 | ||||||
chr3:58644924
|
C | T | 1 | a0001c0001t0001g0229 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.263+585G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 5/9 | chr3 | 58644924 | ||||||
chr3:58645264
|
A | G | 130 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(127): Show | 196 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(193): Show |
intron_variant | MODIFIER | c.263+245T>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 5/9 | chr3 | 58645264 | ||||||
chr3:58645278
|
T | G | 3 | a0001c0001t0001g0177a0001c0001t0001g0199a0001c0001t0001g0243 | 3 | HG02257.hp1 HG02886.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.263+231A>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 5/9 | chr3 | 58645278 | ||||||
chr3:58645283
|
G | A | 1 | a0001c0001t0001g0212 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.263+226C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 5/9 | chr3 | 58645283 | ||||||
chr3:58645289
|
C | T | 3 | a0001c0004t0001g0039a0001c0004t0001g0083a0001c0004t0001g0113 | 4 | HG02683.hp1 HG02698.hp2 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.263+220G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 5/9 | chr3 | 58645289 | ||||||
chr3:58645457
|
G | GAAATA | 117 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(114): Show | 176 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(173): Show |
intron_variant | MODIFIER | c.263+47_263+51dupTA others(3): Show |
FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 5/9 | chr3 | 58645457 | ||||||
chr3:58645457
|
G | GAAATAAA others(3): Show |
3 | a0001c0001t0001g0092a0001c0001t0001g0095a0001c0001t0001g0188 | 3 | HG00280.hp2 HG00735.hp2 HG02040.hp2 |
intron_variant | MODIFIER | c.263+42_263+51dupTA others(8): Show |
FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 5/9 | chr3 | 58645457 | ||||||
chr3:58645692
|
GAGGGCCA others(5): Show |
G | 2 | a0001c0003t0001g0048a0001c0003t0001g0049 | 4 | HG01081.hp1 HG03490.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.146-78_146-67delAG others(10): Show |
FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 4/9 | chr3 | 58645692 | ||||||
chr3:58645933
|
C | T | 2 | a0001c0001t0001g0181a0001c0006t0006g0179 | 2 | HG01243.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.146-307G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 4/9 | chr3 | 58645933 | ||||||
chr3:58646179
|
A | T | 105 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(102): Show | 156 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.146-553T>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 4/9 | chr3 | 58646179 | ||||||
chr3:58646414
|
C | T | 1 | a0001c0001t0001g0035 | 2 | HG02738.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.146-788G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 4/9 | chr3 | 58646414 | ||||||
chr3:58646460
|
C | T | 1 | a0001c0001t0001g0134 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.146-834G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 4/9 | chr3 | 58646460 | ||||||
chr3:58646539
|
T | C | 1 | a0001c0001t0001g0244 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.146-913A>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 4/9 | chr3 | 58646539 | ||||||
chr3:58646557
|
C | T | 3 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0090 | 3 | HG02622.hp2 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.146-931G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 4/9 | chr3 | 58646557 | ||||||
chr3:58646635
|
C | T | 3 | a0001c0004t0001g0039a0001c0004t0001g0083a0001c0004t0001g0113 | 4 | HG02683.hp1 HG02698.hp2 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.146-1009G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 4/9 | chr3 | 58646635 | ||||||
chr3:58646740
|
G | C | 1 | a0003c0007t0001g0037 | 2 | HG02027.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.146-1114C>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 4/9 | chr3 | 58646740 | ||||||
chr3:58646748
|
C | G | 1 | a0001c0001t0001g0178 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.146-1122G>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 4/9 | chr3 | 58646748 | ||||||
chr3:58646772
|
C | T | 1 | a0001c0001t0005g0060 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.146-1146G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 4/9 | chr3 | 58646772 | ||||||
chr3:58646788
|
G | A | 6 | a0001c0001t0001g0177a0001c0001t0001g0199a0001c0001t0001g0243others(3): Show | 7 | HG02257.hp1 HG02683.hp1 HG02698.hp2 others(4): Show |
intron_variant | MODIFIER | c.146-1162C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 4/9 | chr3 | 58646788 | ||||||
chr3:58646828
|
T | C | 6 | a0001c0001t0001g0177a0001c0001t0001g0199a0001c0001t0001g0243others(3): Show | 7 | HG02257.hp1 HG02683.hp1 HG02698.hp2 others(4): Show |
intron_variant | MODIFIER | c.146-1202A>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 4/9 | chr3 | 58646828 | ||||||
chr3:58646846
|
G | C | 6 | a0001c0001t0001g0177a0001c0001t0001g0199a0001c0001t0001g0243others(3): Show | 7 | HG02257.hp1 HG02683.hp1 HG02698.hp2 others(4): Show |
intron_variant | MODIFIER | c.146-1220C>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 4/9 | chr3 | 58646846 | ||||||
chr3:58646924
|
C | T | 23 | a0001c0001t0001g0024a0001c0001t0001g0045a0001c0001t0001g0180others(20): Show | 38 | HG00639.hp1 HG00733.hp2 HG01069.hp2 others(35): Show |
intron_variant | MODIFIER | c.146-1298G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 4/9 | chr3 | 58646924 | ||||||
chr3:58646950
|
C | A | 1 | a0001c0001t0001g0064 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.146-1324G>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 4/9 | chr3 | 58646950 | ||||||
chr3:58647009
|
C | T | 1 | a0001c0001t0001g0114 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.146-1383G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 4/9 | chr3 | 58647009 | ||||||
chr3:58647014
|
T | C | 124 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(121): Show | 187 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.146-1388A>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 4/9 | chr3 | 58647014 | ||||||
chr3:58647152
|
C | G | 3 | a0001c0004t0001g0039a0001c0004t0001g0083a0001c0004t0001g0113 | 4 | HG02683.hp1 HG02698.hp2 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.146-1526G>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 4/9 | chr3 | 58647152 | ||||||
chr3:58647244
|
C | T | 6 | a0001c0001t0001g0177a0001c0001t0001g0199a0001c0001t0001g0243others(3): Show | 7 | HG02257.hp1 HG02683.hp1 HG02698.hp2 others(4): Show |
intron_variant | MODIFIER | c.146-1618G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 4/9 | chr3 | 58647244 | ||||||
chr3:58647534
|
T | A | 158 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(155): Show | 235 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(232): Show |
intron_variant | MODIFIER | c.145+1781A>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 4/9 | chr3 | 58647534 | ||||||
chr3:58647547
|
C | G | 6 | a0001c0001t0001g0109a0001c0001t0005g0059a0001c0003t0001g0048others(3): Show | 8 | HG01081.hp1 HG03471.hp2 HG03490.hp1 others(5): Show |
intron_variant | MODIFIER | c.145+1768G>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 4/9 | chr3 | 58647547 | ||||||
chr3:58647777
|
G | A | 1 | a0001c0001t0005g0059 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.145+1538C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 4/9 | chr3 | 58647777 | ||||||
chr3:58647820
|
A | G | 1 | a0001c0001t0001g0213 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.145+1495T>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 4/9 | chr3 | 58647820 | ||||||
chr3:58647850
|
G | C | 1 | a0002c0002t0001g0043 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.145+1465C>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 4/9 | chr3 | 58647850 | ||||||
chr3:58647949
|
G | A | 3 | a0001c0004t0001g0039a0001c0004t0001g0083a0001c0004t0001g0113 | 4 | HG02683.hp1 HG02698.hp2 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.145+1366C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 4/9 | chr3 | 58647949 | ||||||
chr3:58647965
|
T | G | 1 | a0001c0001t0001g0248 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.145+1350A>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 4/9 | chr3 | 58647965 | ||||||
chr3:58648222
|
G | A | 23 | a0001c0001t0001g0024a0001c0001t0001g0045a0001c0001t0001g0180others(20): Show | 38 | HG00639.hp1 HG00733.hp2 HG01069.hp2 others(35): Show |
intron_variant | MODIFIER | c.145+1093C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 4/9 | chr3 | 58648222 | ||||||
chr3:58648236
|
A | G | 155 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(152): Show | 229 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(226): Show |
intron_variant | MODIFIER | c.145+1079T>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 4/9 | chr3 | 58648236 | ||||||
chr3:58648516
|
C | T | 12 | a0001c0001t0001g0015a0001c0001t0001g0032a0001c0001t0001g0069others(9): Show | 17 | HG00438.hp1 HG00609.hp1 HG00673.hp1 others(14): Show |
intron_variant | MODIFIER | c.145+799G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 4/9 | chr3 | 58648516 | ||||||
chr3:58648745
|
G | A | 1 | a0001c0001t0001g0196 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.145+570C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 4/9 | chr3 | 58648745 | ||||||
chr3:58648777
|
G | T | 137 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(134): Show | 205 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.145+538C>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 4/9 | chr3 | 58648777 | ||||||
chr3:58648818
|
A | G | 1 | a0001c0001t0001g0181 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.145+497T>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 4/9 | chr3 | 58648818 | ||||||
chr3:58648824
|
G | T | 122 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(119): Show | 185 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.145+491C>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 4/9 | chr3 | 58648824 | ||||||
chr3:58648884
|
T | G | 1 | a0001c0001t0001g0149 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.145+431A>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 4/9 | chr3 | 58648884 | ||||||
chr3:58648923
|
A | G | 1 | a0001c0001t0001g0133 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.145+392T>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 4/9 | chr3 | 58648923 | ||||||
chr3:58649104
|
AG | A | 18 | a0001c0001t0001g0015a0001c0001t0001g0032a0001c0001t0001g0069others(15): Show | 24 | HG00438.hp1 HG00609.hp1 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.145+210delC | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 4/9 | chr3 | 58649104 | ||||||
chr3:58649228
|
G | A | 1 | a0001c0001t0001g0224 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.145+87C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 4/9 | chr3 | 58649228 | ||||||
chr3:58649258
|
G | C | 3 | a0001c0004t0001g0039a0001c0004t0001g0083a0001c0004t0001g0113 | 4 | HG02683.hp1 HG02698.hp2 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.145+57C>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 4/9 | chr3 | 58649258 | ||||||
chr3:58649284
|
G | A | 1 | a0001c0001t0001g0091 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.145+31C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 4/9 | chr3 | 58649284 | ||||||
chr3:58649350
|
A | G | 2 | a0001c0001t0001g0181a0001c0006t0006g0179 | 2 | HG01243.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.122-12T>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58649350 | ||||||
chr3:58649374
|
A | G | 1 | a0001c0001t0001g0089 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.122-36T>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58649374 | ||||||
chr3:58649470
|
G | A | 150 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(147): Show | 224 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(221): Show |
intron_variant | MODIFIER | c.122-132C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58649470 | ||||||
chr3:58649548
|
C | T | 1 | a0001c0001t0001g0194 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.122-210G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58649548 | ||||||
chr3:58649558
|
T | C | 1 | a0001c0001t0001g0225 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.122-220A>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58649558 | ||||||
chr3:58649560
|
T | C | 1 | a0001c0001t0001g0225 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.122-222A>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58649560 | ||||||
chr3:58649567
|
GCA | G | 6 | a0001c0001t0001g0034a0001c0001t0001g0076a0001c0001t0001g0119others(3): Show | 7 | HG00621.hp1 HG00733.hp1 HG00741.hp1 others(4): Show |
intron_variant | MODIFIER | c.122-231_122-230del others(2): Show |
FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58649567 | ||||||
chr3:58649605
|
T | C | 1 | a0001c0001t0001g0150 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.122-267A>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58649605 | ||||||
chr3:58649647
|
C | T | 1 | a0001c0001t0001g0152 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.122-309G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58649647 | ||||||
chr3:58649665
|
C | CAT | 3 | a0001c0004t0001g0039a0001c0004t0001g0083a0001c0004t0001g0113 | 4 | HG02683.hp1 HG02698.hp2 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.122-328_122-327ins others(2): Show |
FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58649665 | ||||||
chr3:58649666
|
G | A | 15 | a0001c0001t0001g0015a0001c0001t0001g0032a0001c0001t0001g0069others(12): Show | 20 | HG00438.hp1 HG00609.hp1 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.122-328C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58649666 | ||||||
chr3:58649670
|
A | G | 15 | a0001c0001t0001g0015a0001c0001t0001g0032a0001c0001t0001g0069others(12): Show | 20 | HG00438.hp1 HG00609.hp1 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.122-332T>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58649670 | ||||||
chr3:58649671
|
C | T | 15 | a0001c0001t0001g0015a0001c0001t0001g0032a0001c0001t0001g0069others(12): Show | 20 | HG00438.hp1 HG00609.hp1 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.122-333G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58649671 | ||||||
chr3:58649677
|
C | T | 3 | a0001c0001t0001g0021a0001c0001t0001g0196a0001c0001t0001g0198 | 5 | HG02615.hp2 HG02965.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.122-339G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58649677 | ||||||
chr3:58649773
|
A | AC | 137 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(134): Show | 205 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.122-436dupG | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58649773 | ||||||
chr3:58649867
|
C | T | 1 | a0001c0001t0001g0195 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.122-529G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58649867 | ||||||
chr3:58650082
|
T | G | 1 | a0001c0001t0001g0151 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.122-744A>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58650082 | ||||||
chr3:58650224
|
A | G | 3 | a0001c0004t0001g0039a0001c0004t0001g0083a0001c0004t0001g0113 | 4 | HG02683.hp1 HG02698.hp2 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.122-886T>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58650224 | ||||||
chr3:58650400
|
A | G | 1 | a0005c0009t0001g0242 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.122-1062T>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58650400 | ||||||
chr3:58650417
|
C | G | 17 | a0001c0001t0001g0015a0001c0001t0001g0032a0001c0001t0001g0069others(14): Show | 23 | HG00438.hp1 HG00609.hp1 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.122-1079G>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58650417 | ||||||
chr3:58650452
|
G | T | 17 | a0001c0001t0001g0015a0001c0001t0001g0032a0001c0001t0001g0069others(14): Show | 23 | HG00438.hp1 HG00609.hp1 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.122-1114C>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58650452 | ||||||
chr3:58650467
|
C | T | 2 | a0001c0001t0001g0199a0001c0001t0001g0243 | 2 | HG02257.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.122-1129G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58650467 | ||||||
chr3:58650473
|
A | T | 1 | a0001c0001t0001g0132 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.122-1135T>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58650473 | ||||||
chr3:58650474
|
G | T | 3 | a0001c0004t0001g0039a0001c0004t0001g0083a0001c0004t0001g0113 | 4 | HG02683.hp1 HG02698.hp2 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.122-1136C>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58650474 | ||||||
chr3:58650502
|
A | G | 1 | a0001c0001t0001g0218 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.122-1164T>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58650502 | ||||||
chr3:58650749
|
G | A | 1 | a0002c0002t0001g0043 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.122-1411C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58650749 | ||||||
chr3:58650836
|
A | G | 140 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(137): Show | 209 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.122-1498T>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58650836 | ||||||
chr3:58650843
|
A | G | 1 | a0001c0001t0001g0084 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.122-1505T>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58650843 | ||||||
chr3:58651039
|
T | G | 1 | a0001c0001t0001g0249 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.122-1701A>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58651039 | ||||||
chr3:58651051
|
T | G | 3 | a0001c0001t0001g0009a0001c0001t0001g0152a0001c0001t0007g0153 | 6 | HG01192.hp1 HG01928.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.122-1713A>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58651051 | ||||||
chr3:58651126
|
T | C | 151 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(148): Show | 226 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(223): Show |
intron_variant | MODIFIER | c.122-1788A>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58651126 | ||||||
chr3:58651174
|
T | C | 1 | a0002c0002t0001g0215 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.122-1836A>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58651174 | ||||||
chr3:58651177
|
T | G | 3 | a0002c0002t0001g0050a0002c0002t0001g0214a0002c0002t0001g0215 | 4 | HG00733.hp2 HG01258.hp1 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.122-1839A>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58651177 | ||||||
chr3:58651273
|
T | C | 2 | a0001c0001t0001g0180a0001c0001t0001g0190 | 2 | HG02647.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.122-1935A>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58651273 | ||||||
chr3:58651300
|
G | A | 3 | a0001c0001t0001g0007a0001c0001t0001g0201a0001c0001t0004g0022 | 9 | HG01255.hp2 HG01884.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.122-1962C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58651300 | ||||||
chr3:58651333
|
A | C | 1 | a0001c0001t0001g0131 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.122-1995T>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58651333 | ||||||
chr3:58651436
|
T | A | 1 | a0001c0001t0001g0154 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.122-2098A>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58651436 | ||||||
chr3:58651530
|
G | C | 3 | a0001c0004t0001g0039a0001c0004t0001g0083a0001c0004t0001g0113 | 4 | HG02683.hp1 HG02698.hp2 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.121+2144C>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58651530 | ||||||
chr3:58651633
|
C | G | 1 | a0001c0001t0001g0199 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.121+2041G>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58651633 | ||||||
chr3:58651641
|
A | G | 1 | a0001c0001t0001g0130 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.121+2033T>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58651641 | ||||||
chr3:58651704
|
C | T | 5 | a0001c0001t0001g0078a0001c0001t0001g0129a0001c0001t0001g0160others(2): Show | 5 | NA18961.hp2 NA18964.hp2 NA19010.hp2 others(2): Show |
intron_variant | MODIFIER | c.121+1970G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58651704 | ||||||
chr3:58651790
|
A | C | 35 | a0001c0001t0001g0015a0001c0001t0001g0032a0001c0001t0001g0069others(32): Show | 53 | HG00438.hp1 HG00609.hp1 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.121+1884T>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58651790 | ||||||
chr3:58651818
|
G | A | 1 | a0001c0001t0001g0155 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.121+1856C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58651818 | ||||||
chr3:58651842
|
C | T | 1 | a0001c0001t0005g0059 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.121+1832G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58651842 | ||||||
chr3:58651870
|
A | G | 1 | a0001c0001t0001g0199 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.121+1804T>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58651870 | ||||||
chr3:58651884
|
C | G | 1 | a0001c0001t0001g0056 | 2 | HG03225.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.121+1790G>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58651884 | ||||||
chr3:58652374
|
C | CCATT | 215 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(212): Show | 342 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(339): Show |
intron_variant | MODIFIER | c.121+1296_121+1299d others(6): Show |
FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58652374 | ||||||
chr3:58652374
|
C | CCATTCAT others(5): Show |
1 | a0006c0010t0004g0173 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.121+1288_121+1299d others(14): Show |
FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58652374 | ||||||
chr3:58652400
|
A | G | 1 | a0001c0001t0001g0101 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.121+1274T>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58652400 | ||||||
chr3:58652416
|
ACCATCTA others(72): Show |
A | 2 | a0001c0001t0001g0171a0006c0010t0004g0173 | 2 | HG03139.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.121+1179_121+1257d others(81): Show |
FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58652416 | ||||||
chr3:58652499
|
T | A | 2 | a0001c0001t0001g0171a0006c0010t0004g0173 | 2 | HG03139.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.121+1175A>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58652499 | ||||||
chr3:58652515
|
C | G | 4 | a0001c0001t0001g0171a0002c0002t0001g0250a0002c0002t0001g0251others(1): Show | 4 | HG02109.hp1 HG03139.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.121+1159G>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58652515 | ||||||
chr3:58652559
|
T | TCATCCAT others(346): Show |
1 | a0001c0003t0001g0176 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.121+1114_121+1115i others(355): Show |
FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58652559 | ||||||
chr3:58652730
|
C | T | 1 | a0001c0001t0001g0128 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.121+944G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58652730 | ||||||
chr3:58652731
|
G | A | 34 | a0001c0001t0001g0015a0001c0001t0001g0032a0001c0001t0001g0069others(31): Show | 52 | HG00438.hp1 HG00609.hp1 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.121+943C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58652731 | ||||||
chr3:58652801
|
T | G | 2 | a0001c0004t0001g0039a0001c0004t0001g0113 | 3 | HG02683.hp1 HG02698.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.121+873A>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58652801 | ||||||
chr3:58652825
|
C | G | 1 | a0001c0001t0001g0217 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.121+849G>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58652825 | ||||||
chr3:58652861
|
T | C | 2 | a0001c0004t0001g0039a0001c0004t0001g0113 | 3 | HG02683.hp1 HG02698.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.121+813A>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58652861 | ||||||
chr3:58652862
|
G | A | 2 | a0001c0004t0001g0039a0001c0004t0001g0113 | 3 | HG02683.hp1 HG02698.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.121+812C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58652862 | ||||||
chr3:58652862
|
G | GTCCA | 77 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(74): Show | 126 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(123): Show |
intron_variant | MODIFIER | c.121+808_121+811dup others(4): Show |
FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58652862 | ||||||
chr3:58652862
|
G | GTCCATCC others(1): Show |
46 | a0001c0001t0001g0031a0001c0001t0001g0038a0001c0001t0001g0066others(43): Show | 60 | HG00280.hp2 HG00408.hp2 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.121+804_121+811dup others(8): Show |
FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58652862 | ||||||
chr3:58652862
|
G | GTCCATCC others(5): Show |
4 | a0001c0001t0001g0096a0001c0001t0001g0097a0002c0002t0001g0044others(1): Show | 6 | HG01258.hp1 HG01496.hp2 HG02300.hp2 others(3): Show |
intron_variant | MODIFIER | c.121+800_121+811dup others(12): Show |
FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58652862 | ||||||
chr3:58652862
|
G | GTCCATCC others(9): Show |
1 | a0001c0001t0001g0098 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.121+796_121+811dup others(16): Show |
FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58652862 | ||||||
chr3:58652862
|
GTCCA | G | 22 | a0001c0001t0001g0015a0001c0001t0001g0024a0001c0001t0001g0032others(19): Show | 30 | HG00438.hp1 HG00609.hp1 HG00673.hp1 others(27): Show |
intron_variant | MODIFIER | c.121+808_121+811del others(4): Show |
FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58652862 | ||||||
chr3:58652866
|
A | G | 1 | a0001c0001t0001g0199 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.121+808T>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58652866 | ||||||
chr3:58652870
|
A | ATCCATCT others(5): Show |
1 | a0001c0001t0001g0199 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.121+803_121+804ins others(12): Show |
FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58652870 | ||||||
chr3:58652955
|
C | A | 1 | a0001c0001t0001g0159 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.121+719G>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58652955 | ||||||
chr3:58652967
|
T | A | 1 | a0001c0001t0001g0126 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.121+707A>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58652967 | ||||||
chr3:58652977
|
C | CATCT | 17 | a0001c0001t0001g0015a0001c0001t0001g0032a0001c0001t0001g0066others(14): Show | 22 | HG00438.hp1 HG00609.hp1 HG00642.hp2 others(19): Show |
intron_variant | MODIFIER | c.121+696_121+697ins others(4): Show |
FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58652977 | ||||||
chr3:58652977
|
C | CATCTG | 37 | a0001c0001t0001g0031a0001c0001t0001g0092a0001c0001t0001g0094others(34): Show | 50 | HG00280.hp2 HG00639.hp1 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.121+696_121+697ins others(5): Show |
FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58652977 | ||||||
chr3:58652977
|
C | CATCTGT | 80 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(77): Show | 130 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.121+696_121+697ins others(6): Show |
FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58652977 | ||||||
chr3:58652977
|
C | T | 1 | a0001c0001t0001g0163 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.121+697G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58652977 | ||||||
chr3:58652978
|
G | A | 3 | a0001c0003t0001g0048a0001c0003t0001g0049a0001c0003t0001g0176 | 5 | HG01081.hp1 HG03490.hp1 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.121+696C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58652978 | ||||||
chr3:58652978
|
G | T | 119 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(116): Show | 182 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(179): Show |
intron_variant | MODIFIER | c.121+696C>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58652978 | ||||||
chr3:58652978
|
GT | G | 6 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0064others(3): Show | 7 | HG01358.hp1 HG02273.hp2 HG02683.hp1 others(4): Show |
intron_variant | MODIFIER | c.121+695delA | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58652978 | ||||||
chr3:58652979
|
T | TCTG | 3 | a0001c0003t0001g0048a0001c0003t0001g0049a0001c0003t0001g0176 | 5 | HG01081.hp1 HG03490.hp1 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.121+694_121+695ins others(3): Show |
FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58652979 | ||||||
chr3:58653326
|
C | T | 14 | a0002c0002t0001g0006a0002c0002t0001g0042a0002c0002t0001g0043others(11): Show | 22 | HG00639.hp1 HG00733.hp2 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.121+348G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58653326 | ||||||
chr3:58653462
|
G | A | 3 | a0001c0001t0001g0171a0001c0001t0001g0244a0006c0010t0004g0173 | 3 | HG02258.hp1 HG03139.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.121+212C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58653462 | ||||||
chr3:58654135
|
T | A | 136 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(133): Show | 204 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(201): Show |
intron_variant | MODIFIER | c.14-354A>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 2/9 | chr3 | 58654135 | ||||||
chr3:58654201
|
G | A | 2 | a0001c0004t0001g0039a0001c0004t0001g0113 | 3 | HG02683.hp1 HG02698.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.14-420C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 2/9 | chr3 | 58654201 | ||||||
chr3:58654334
|
A | T | 123 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(120): Show | 186 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.14-553T>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 2/9 | chr3 | 58654334 | ||||||
chr3:58654378
|
C | G | 4 | a0001c0001t0001g0034a0001c0001t0001g0119a0001c0001t0001g0125others(1): Show | 5 | HG00733.hp1 HG00741.hp1 HG01167.hp1 others(2): Show |
intron_variant | MODIFIER | c.14-597G>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 2/9 | chr3 | 58654378 | ||||||
chr3:58654538
|
G | A | 4 | a0001c0001t0001g0053a0001c0001t0001g0207a0001c0001t0001g0227others(1): Show | 5 | HG01934.hp2 HG02630.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.14-757C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 2/9 | chr3 | 58654538 | ||||||
chr3:58654572
|
G | A | 1 | a0001c0001t0001g0164 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.14-791C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 2/9 | chr3 | 58654572 | ||||||
chr3:58654617
|
C | T | 60 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(57): Show | 112 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.14-836G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 2/9 | chr3 | 58654617 | ||||||
chr3:58654628
|
T | G | 1 | a0001c0001t0001g0201 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.14-847A>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 2/9 | chr3 | 58654628 | ||||||
chr3:58654767
|
C | T | 1 | a0001c0001t0005g0059 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.13+784G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 2/9 | chr3 | 58654767 | ||||||
chr3:58654770
|
G | A | 3 | a0001c0001t0001g0023a0001c0001t0001g0197a0001c0001t0001g0235 | 5 | HG00099.hp2 HG00738.hp1 HG01069.hp1 others(2): Show |
intron_variant | MODIFIER | c.13+781C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 2/9 | chr3 | 58654770 | ||||||
chr3:58654782
|
G | A | 1 | a0001c0001t0001g0065 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.13+769C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 2/9 | chr3 | 58654782 | ||||||
chr3:58654809
|
C | T | 1 | a0001c0001t0001g0123 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.13+742G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 2/9 | chr3 | 58654809 | ||||||
chr3:58654821
|
T | C | 139 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(136): Show | 208 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(205): Show |
intron_variant | MODIFIER | c.13+730A>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 2/9 | chr3 | 58654821 | ||||||
chr3:58654915
|
C | A | 2 | a0001c0001t0001g0171a0006c0010t0004g0173 | 2 | HG03139.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.13+636G>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 2/9 | chr3 | 58654915 | ||||||
chr3:58654916
|
T | C | 1 | a0001c0001t0001g0099 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.13+635A>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 2/9 | chr3 | 58654916 | ||||||
chr3:58655020
|
C | T | 14 | a0002c0002t0001g0006a0002c0002t0001g0042a0002c0002t0001g0043others(11): Show | 22 | HG00639.hp1 HG00733.hp2 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.13+531G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 2/9 | chr3 | 58655020 | ||||||
chr3:58655060
|
AC | A | 6 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0090others(3): Show | 7 | HG01109.hp2 HG02055.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.13+490delG | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 2/9 | chr3 | 58655060 | ||||||
chr3:58655109
|
A | G | 4 | a0001c0001t0001g0024a0001c0001t0001g0045a0001c0001t0001g0180others(1): Show | 7 | HG01243.hp1 HG02486.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.13+442T>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 2/9 | chr3 | 58655109 | ||||||
chr3:58655184
|
A | G | 241 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(238): Show | 383 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(380): Show |
intron_variant | MODIFIER | c.13+367T>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 2/9 | chr3 | 58655184 | ||||||
chr3:58655189
|
G | A | 3 | a0001c0001t0001g0171a0001c0001t0002g0011a0006c0010t0004g0173 | 6 | HG02109.hp2 HG02280.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.13+362C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 2/9 | chr3 | 58655189 | ||||||
chr3:58655220
|
T | A | 2 | a0001c0001t0001g0047a0001c0001t0001g0245 | 3 | HG02922.hp2 HG03516.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.13+331A>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 2/9 | chr3 | 58655220 | ||||||
chr3:58655397
|
C | T | 2 | a0001c0001t0001g0171a0001c0001t0002g0011 | 5 | HG02109.hp2 HG02280.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.13+154G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 2/9 | chr3 | 58655397 | ||||||
chr3:58655447
|
C | T | 1 | a0001c0001t0002g0110 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.13+104G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 2/9 | chr3 | 58655447 | ||||||
chr3:58655457
|
C | T | 5 | a0001c0001t0001g0024a0001c0001t0001g0045a0001c0001t0001g0180others(2): Show | 9 | HG01109.hp2 HG01243.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.13+94G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 2/9 | chr3 | 58655457 | ||||||
chr3:58655620
|
C | A | 1 | a0001c0001t0005g0059 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-38-19G>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58655620 | ||||||
chr3:58655625
|
C | T | 58 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0021others(55): Show | 86 | HG00099.hp2 HG00438.hp1 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.-38-24G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58655625 | ||||||
chr3:58655710
|
T | C | 1 | a0001c0001t0001g0233 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-38-109A>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58655710 | ||||||
chr3:58655786
|
C | T | 2 | a0001c0001t0001g0204a0001c0001t0001g0205 | 2 | HG03017.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.-38-185G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58655786 | ||||||
chr3:58656001
|
T | C | 242 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(239): Show | 383 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(380): Show |
intron_variant | MODIFIER | c.-38-400A>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58656001 | ||||||
chr3:58656002
|
G | A | 1 | a0001c0001t0001g0234 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-38-401C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58656002 | ||||||
chr3:58656039
|
C | T | 2 | a0002c0002t0001g0250a0002c0002t0001g0251 | 2 | HG02109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-38-438G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58656039 | ||||||
chr3:58656073
|
CT | C | 26 | a0001c0001t0001g0045a0001c0001t0001g0177a0001c0001t0001g0180others(23): Show | 35 | HG00639.hp1 HG01069.hp2 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.-38-473delA | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58656073 | ||||||
chr3:58656121
|
G | A | 10 | a0001c0001t0001g0007a0001c0001t0001g0023a0001c0001t0001g0197others(7): Show | 20 | HG00099.hp2 HG00738.hp1 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.-38-520C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58656121 | ||||||
chr3:58656165
|
G | A | 26 | a0001c0001t0001g0045a0001c0001t0001g0177a0001c0001t0001g0180others(23): Show | 35 | HG00639.hp1 HG01069.hp2 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.-38-564C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58656165 | ||||||
chr3:58656181
|
A | G | 26 | a0001c0001t0001g0045a0001c0001t0001g0177a0001c0001t0001g0180others(23): Show | 35 | HG00639.hp1 HG01069.hp2 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.-38-580T>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58656181 | ||||||
chr3:58656201
|
C | T | 1 | a0001c0001t0001g0194 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-38-600G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58656201 | ||||||
chr3:58656208
|
C | T | 58 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(55): Show | 114 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.-38-607G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58656208 | ||||||
chr3:58656454
|
A | G | 5 | a0001c0001t0001g0004a0001c0001t0001g0174a0001c0001t0001g0210others(2): Show | 11 | NA18946.hp2 NA18950.hp1 NA18952.hp1 others(8): Show |
intron_variant | MODIFIER | c.-38-853T>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58656454 | ||||||
chr3:58656521
|
AC | A | 61 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0028others(58): Show | 72 | HG00280.hp2 HG00438.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.-38-921delG | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58656521 | ||||||
chr3:58656648
|
C | T | 1 | a0002c0002t0001g0182 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-38-1047G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58656648 | ||||||
chr3:58656686
|
T | C | 1 | a0001c0003t0001g0049 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-38-1085A>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58656686 | ||||||
chr3:58656725
|
A | G | 61 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0028others(58): Show | 72 | HG00280.hp2 HG00438.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.-38-1124T>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58656725 | ||||||
chr3:58656931
|
G | A | 89 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(86): Show | 152 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(149): Show |
intron_variant | MODIFIER | c.-38-1330C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58656931 | ||||||
chr3:58656948
|
C | T | 1 | a0001c0001t0001g0197 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-38-1347G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58656948 | ||||||
chr3:58656999
|
T | C | 2 | a0002c0002t0001g0250a0002c0002t0001g0251 | 2 | HG02109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-38-1398A>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58656999 | ||||||
chr3:58657012
|
A | G | 241 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(238): Show | 382 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(379): Show |
intron_variant | MODIFIER | c.-38-1411T>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58657012 | ||||||
chr3:58657046
|
C | T | 2 | a0001c0001t0001g0181a0001c0006t0006g0179 | 2 | HG01243.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-38-1445G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58657046 | ||||||
chr3:58657094
|
C | T | 241 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(238): Show | 382 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(379): Show |
intron_variant | MODIFIER | c.-38-1493G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58657094 | ||||||
chr3:58657143
|
C | T | 1 | a0001c0001t0001g0118 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-38-1542G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58657143 | ||||||
chr3:58657148
|
T | C | 1 | a0001c0001t0001g0165 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-38-1547A>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58657148 | ||||||
chr3:58657193
|
C | T | 241 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(238): Show | 382 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(379): Show |
intron_variant | MODIFIER | c.-38-1592G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58657193 | ||||||
chr3:58657228
|
G | A | 1 | a0001c0004t0001g0113 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-38-1627C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58657228 | ||||||
chr3:58657276
|
T | A | 2 | a0001c0001t0001g0177a0001c0003t0001g0176 | 2 | NA18522.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-38-1675A>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58657276 | ||||||
chr3:58657383
|
A | AAG | 54 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0028others(51): Show | 65 | HG00280.hp2 HG00438.hp1 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.-38-1784_-38-1783d others(4): Show |
FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58657383 | ||||||
chr3:58657383
|
A | AAGAG | 8 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0092others(5): Show | 8 | HG00735.hp2 HG01358.hp1 HG02273.hp2 others(5): Show |
intron_variant | MODIFIER | c.-38-1786_-38-1783d others(6): Show |
FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58657383 | ||||||
chr3:58657443
|
G | A | 62 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0028others(59): Show | 73 | HG00280.hp2 HG00438.hp1 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.-38-1842C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58657443 | ||||||
chr3:58657457
|
A | G | 149 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(146): Show | 269 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.-38-1856T>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58657457 | ||||||
chr3:58657468
|
C | G | 2 | a0001c0001t0005g0059a0001c0001t0005g0060 | 2 | HG02559.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-38-1867G>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58657468 | ||||||
chr3:58657638
|
G | A | 1 | a0001c0001t0001g0112 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-38-2037C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58657638 | ||||||
chr3:58657726
|
C | G | 87 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(84): Show | 149 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(146): Show |
intron_variant | MODIFIER | c.-38-2125G>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58657726 | ||||||
chr3:58657850
|
A | C | 150 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(147): Show | 270 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.-38-2249T>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58657850 | ||||||
chr3:58657915
|
C | T | 1 | a0001c0001t0001g0069 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-38-2314G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58657915 | ||||||
chr3:58657917
|
C | T | 1 | a0001c0001t0001g0196 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-38-2316G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58657917 | ||||||
chr3:58657947
|
G | T | 1 | a0001c0001t0001g0068 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-38-2346C>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58657947 | ||||||
chr3:58658002
|
T | G | 1 | a0001c0001t0001g0041 | 2 | NA18940.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.-38-2401A>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58658002 | ||||||
chr3:58658307
|
A | G | 2 | a0002c0002t0001g0250a0002c0002t0001g0251 | 2 | HG02109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-38-2706T>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58658307 | ||||||
chr3:58658368
|
G | A | 1 | a0001c0001t0001g0237 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-38-2767C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58658368 | ||||||
chr3:58658394
|
A | G | 1 | a0001c0001t0001g0028 | 2 | NA18939.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.-38-2793T>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58658394 | ||||||
chr3:58658475
|
G | A | 241 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(238): Show | 382 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(379): Show |
intron_variant | MODIFIER | c.-38-2874C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58658475 | ||||||
chr3:58658486
|
C | G | 89 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(86): Show | 152 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(149): Show |
intron_variant | MODIFIER | c.-38-2885G>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58658486 | ||||||
chr3:58658491
|
G | A | 1 | a0001c0001t0001g0238 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-38-2890C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58658491 | ||||||
chr3:58658497
|
C | A | 10 | a0001c0001t0001g0031a0001c0001t0001g0092a0001c0001t0001g0093others(7): Show | 11 | HG00280.hp2 HG00735.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.-38-2896G>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58658497 | ||||||
chr3:58658559
|
A | G | 1 | a0001c0001t0001g0194 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-38-2958T>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58658559 | ||||||
chr3:58658635
|
C | G | 61 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0028others(58): Show | 72 | HG00280.hp2 HG00438.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.-38-3034G>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58658635 | ||||||
chr3:58658638
|
G | A | 1 | a0001c0001t0001g0067 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-38-3037C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58658638 | ||||||
chr3:58658799
|
G | A | 1 | a0001c0001t0001g0244 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-38-3198C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58658799 | ||||||
chr3:58658810
|
C | T | 1 | a0001c0001t0001g0209 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-38-3209G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58658810 | ||||||
chr3:58658896
|
C | T | 22 | a0001c0001t0001g0045a0001c0001t0001g0180a0001c0001t0001g0181others(19): Show | 31 | HG00639.hp1 HG01069.hp2 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.-38-3295G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58658896 | ||||||
chr3:58658999
|
G | A | 92 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0028others(89): Show | 113 | HG00280.hp2 HG00438.hp1 HG00609.hp1 others(110): Show |
intron_variant | MODIFIER | c.-38-3398C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58658999 | ||||||
chr3:58659063
|
G | A | 1 | a0001c0001t0001g0203 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-38-3462C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58659063 | ||||||
chr3:58659181
|
C | T | 1 | a0001c0001t0001g0117 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-38-3580G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58659181 | ||||||
chr3:58659229
|
G | C | 29 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0177others(26): Show | 39 | HG00639.hp1 HG01069.hp2 HG01070.hp2 others(36): Show |
intron_variant | MODIFIER | c.-38-3628C>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58659229 | ||||||
chr3:58659654
|
G | A | 243 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(240): Show | 384 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(381): Show |
intron_variant | MODIFIER | c.-38-4053C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58659654 | ||||||
chr3:58659868
|
A | G | 91 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(88): Show | 154 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(151): Show |
intron_variant | MODIFIER | c.-38-4267T>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58659868 | ||||||
chr3:58659990
|
C | T | 237 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(234): Show | 377 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(374): Show |
intron_variant | MODIFIER | c.-38-4389G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58659990 | ||||||
chr3:58660076
|
A | G | 1 | a0001c0004t0001g0113 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-38-4475T>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58660076 | ||||||
chr3:58660262
|
C | G | 1 | a0001c0001t0001g0207 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-38-4661G>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58660262 | ||||||
chr3:58660482
|
G | A | 217 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(214): Show | 349 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(346): Show |
intron_variant | MODIFIER | c.-38-4881C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58660482 | ||||||
chr3:58660493
|
C | G | 70 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(67): Show | 128 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.-38-4892G>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58660493 | ||||||
chr3:58660493
|
C | T | 28 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0028others(25): Show | 37 | HG00438.hp1 HG00609.hp1 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.-38-4892G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58660493 | ||||||
chr3:58660638
|
T | G | 1 | a0001c0001t0001g0100 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-38-5037A>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58660638 | ||||||
chr3:58660721
|
G | A | 7 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0103others(4): Show | 7 | HG01496.hp1 HG02572.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-38-5120C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58660721 | ||||||
chr3:58660757
|
A | G | 243 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(240): Show | 384 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(381): Show |
intron_variant | MODIFIER | c.-38-5156T>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58660757 | ||||||
chr3:58660825
|
T | A | 1 | a0001c0001t0001g0194 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-38-5224A>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58660825 | ||||||
chr3:58660825
|
T | C | 237 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(234): Show | 378 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(375): Show |
intron_variant | MODIFIER | c.-38-5224A>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58660825 | ||||||
chr3:58660975
|
G | C | 1 | a0001c0001t0001g0194 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-38-5374C>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58660975 | ||||||
chr3:58661154
|
C | A | 4 | a0001c0001t0001g0045a0001c0001t0001g0180a0001c0001t0001g0190others(1): Show | 6 | HG01109.hp2 HG01243.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.-39+5422G>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58661154 | ||||||
chr3:58661170
|
C | T | 1 | a0001c0001t0001g0180 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-39+5406G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58661170 | ||||||
chr3:58661191
|
G | C | 179 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(176): Show | 309 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.-39+5385C>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58661191 | ||||||
chr3:58661209
|
C | A | 1 | a0007c0011t0001g0239 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-39+5367G>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58661209 | ||||||
chr3:58661235
|
T | C | 1 | a0001c0004t0001g0113 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-39+5341A>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58661235 | ||||||
chr3:58661237
|
G | A | 177 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(174): Show | 307 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.-39+5339C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58661237 | ||||||
chr3:58661308
|
C | T | 1 | a0001c0004t0001g0113 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-39+5268G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58661308 | ||||||
chr3:58661310
|
T | C | 1 | a0001c0001t0001g0252 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-39+5266A>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58661310 | ||||||
chr3:58661431
|
T | C | 177 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(174): Show | 307 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.-39+5145A>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58661431 | ||||||
chr3:58661442
|
G | C | 2 | a0001c0001t0001g0055a0001c0001t0003g0240 | 3 | HG02040.hp1 NA19004.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.-39+5134C>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58661442 | ||||||
chr3:58661464
|
C | T | 1 | a0001c0001t0001g0056 | 2 | HG03225.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-39+5112G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58661464 | ||||||
chr3:58661584
|
G | A | 176 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(173): Show | 306 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.-39+4992C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58661584 | ||||||
chr3:58661654
|
C | A | 1 | a0001c0004t0001g0113 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-39+4922G>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58661654 | ||||||
chr3:58661658
|
T | C | 1 | a0001c0001t0001g0106 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-39+4918A>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58661658 | ||||||
chr3:58661669
|
T | C | 2 | a0001c0001t0002g0110a0001c0006t0001g0111 | 2 | HG01891.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-39+4907A>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58661669 | ||||||
chr3:58661716
|
C | T | 1 | a0001c0006t0006g0179 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-39+4860G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58661716 | ||||||
chr3:58661725
|
A | G | 1 | a0001c0001t0001g0056 | 2 | HG03225.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-39+4851T>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58661725 | ||||||
chr3:58661809
|
C | G | 1 | a0001c0001t0001g0115 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-39+4767G>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58661809 | ||||||
chr3:58661848
|
C | T | 2 | a0001c0001t0001g0066a0001c0001t0001g0067 | 2 | HG01099.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.-39+4728G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58661848 | ||||||
chr3:58661985
|
C | T | 1 | a0001c0004t0001g0113 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-39+4591G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58661985 | ||||||
chr3:58662147
|
G | C | 179 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(176): Show | 309 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.-39+4429C>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58662147 | ||||||
chr3:58662148
|
G | C | 2 | a0002c0002t0001g0250a0002c0002t0001g0251 | 2 | HG02109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-39+4428C>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58662148 | ||||||
chr3:58662149
|
T | C | 149 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(146): Show | 269 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.-39+4427A>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58662149 | ||||||
chr3:58662153
|
G | A | 61 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0028others(58): Show | 72 | HG00280.hp2 HG00438.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.-39+4423C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58662153 | ||||||
chr3:58662154
|
TA | T | 88 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(85): Show | 151 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(148): Show |
intron_variant | MODIFIER | c.-39+4421delT | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58662154 | ||||||
chr3:58662161
|
G | C | 2 | a0001c0001t0001g0195a0002c0002t0001g0010 | 5 | HG02280.hp2 HG02451.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.-39+4415C>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58662161 | ||||||
chr3:58662165
|
A | T | 1 | a0001c0001t0001g0115 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-39+4411T>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58662165 | ||||||
chr3:58662278
|
C | T | 1 | a0001c0001t0001g0194 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-39+4298G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58662278 | ||||||
chr3:58662304
|
T | C | 179 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(176): Show | 309 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.-39+4272A>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58662304 | ||||||
chr3:58662318
|
G | C | 179 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(176): Show | 309 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.-39+4258C>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58662318 | ||||||
chr3:58662362
|
A | G | 179 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(176): Show | 309 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.-39+4214T>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58662362 | ||||||
chr3:58662433
|
T | C | 1 | a0002c0002t0001g0191 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.-39+4143A>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58662433 | ||||||
chr3:58662452
|
A | T | 36 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0028others(33): Show | 46 | HG00438.hp1 HG00609.hp1 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.-39+4124T>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58662452 | ||||||
chr3:58662453
|
G | T | 36 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0028others(33): Show | 46 | HG00438.hp1 HG00609.hp1 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.-39+4123C>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58662453 | ||||||
chr3:58662797
|
C | A | 1 | a0001c0001t0001g0107 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-39+3779G>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58662797 | ||||||
chr3:58662828
|
C | A | 59 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(56): Show | 116 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.-39+3748G>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58662828 | ||||||
chr3:58662849
|
G | A | 3 | a0001c0001t0001g0047a0001c0001t0002g0192a0001c0001t0002g0193 | 4 | HG02615.hp1 HG02922.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-39+3727C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58662849 | ||||||
chr3:58662991
|
C | T | 176 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(173): Show | 305 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(302): Show |
intron_variant | MODIFIER | c.-39+3585G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58662991 | ||||||
chr3:58663001
|
C | T | 4 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0064others(1): Show | 4 | HG01358.hp1 HG02273.hp2 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.-39+3575G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58663001 | ||||||
chr3:58663019
|
C | G | 2 | a0001c0001t0005g0059a0001c0001t0005g0060 | 2 | HG02559.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-39+3557G>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58663019 | ||||||
chr3:58663048
|
G | A | 179 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(176): Show | 309 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.-39+3528C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58663048 | ||||||
chr3:58663233
|
G | A | 179 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(176): Show | 309 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.-39+3343C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58663233 | ||||||
chr3:58663310
|
C | T | 61 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0028others(58): Show | 72 | HG00280.hp2 HG00438.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.-39+3266G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58663310 | ||||||
chr3:58663316
|
C | T | 1 | a0001c0004t0001g0113 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-39+3260G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58663316 | ||||||
chr3:58663369
|
A | C | 2 | a0001c0001t0005g0059a0001c0001t0005g0060 | 2 | HG02559.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-39+3207T>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58663369 | ||||||
chr3:58663378
|
C | T | 180 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(177): Show | 310 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(307): Show |
intron_variant | MODIFIER | c.-39+3198G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58663378 | ||||||
chr3:58663390
|
G | T | 179 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(176): Show | 309 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.-39+3186C>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58663390 | ||||||
chr3:58663441
|
T | C | 2 | a0001c0001t0001g0177a0001c0003t0001g0176 | 2 | NA18522.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-39+3135A>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58663441 | ||||||
chr3:58663485
|
G | C | 179 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(176): Show | 309 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.-39+3091C>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58663485 | ||||||
chr3:58663552
|
C | T | 1 | a0001c0001t0001g0114 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-39+3024G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58663552 | ||||||
chr3:58663582
|
C | G | 179 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(176): Show | 309 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.-39+2994G>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58663582 | ||||||
chr3:58663608
|
G | C | 59 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0028others(56): Show | 70 | HG00280.hp2 HG00438.hp1 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.-39+2968C>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58663608 | ||||||
chr3:58663623
|
C | T | 1 | a0001c0001t0001g0243 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-39+2953G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58663623 | ||||||
chr3:58663630
|
C | T | 2 | a0001c0001t0005g0059a0001c0001t0005g0060 | 2 | HG02559.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-39+2946G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58663630 | ||||||
chr3:58663648
|
G | A | 241 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(238): Show | 382 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(379): Show |
intron_variant | MODIFIER | c.-39+2928C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58663648 | ||||||
chr3:58663784
|
G | A | 1 | a0001c0004t0001g0113 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-39+2792C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58663784 | ||||||
chr3:58663787
|
C | T | 2 | a0001c0001t0001g0204a0001c0001t0001g0205 | 2 | HG03017.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.-39+2789G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58663787 | ||||||
chr3:58663837
|
G | A | 87 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(84): Show | 150 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.-39+2739C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58663837 | ||||||
chr3:58663847
|
A | T | 152 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(149): Show | 272 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.-39+2729T>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58663847 | ||||||
chr3:58664002
|
T | G | 60 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(57): Show | 117 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.-39+2574A>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58664002 | ||||||
chr3:58664023
|
G | A | 1 | a0001c0001t0001g0108 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-39+2553C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58664023 | ||||||
chr3:58664076
|
G | A | 177 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(174): Show | 307 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.-39+2500C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58664076 | ||||||
chr3:58664087
|
T | C | 177 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(174): Show | 307 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.-39+2489A>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58664087 | ||||||
chr3:58664089
|
C | A | 177 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(174): Show | 307 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.-39+2487G>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58664089 | ||||||
chr3:58664091
|
C | CAGATAAA others(1): Show |
177 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(174): Show | 307 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.-39+2484_-39+2485i others(10): Show |
FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58664091 | ||||||
chr3:58664092
|
T | C | 177 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(174): Show | 307 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.-39+2484A>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58664092 | ||||||
chr3:58664106
|
C | A | 1 | a0001c0001t0001g0109 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-39+2470G>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58664106 | ||||||
chr3:58664195
|
T | C | 178 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(175): Show | 308 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.-39+2381A>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58664195 | ||||||
chr3:58664229
|
T | C | 177 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(174): Show | 307 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.-39+2347A>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58664229 | ||||||
chr3:58664230
|
G | A | 24 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0180others(21): Show | 34 | HG00639.hp1 HG01069.hp2 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.-39+2346C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58664230 | ||||||
chr3:58664251
|
T | G | 177 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(174): Show | 307 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.-39+2325A>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58664251 | ||||||
chr3:58664255
|
C | T | 2 | a0001c0001t0001g0195a0002c0002t0001g0010 | 5 | HG02280.hp2 HG02451.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.-39+2321G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58664255 | ||||||
chr3:58664267
|
G | A | 148 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(145): Show | 268 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.-39+2309C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58664267 | ||||||
chr3:58664368
|
G | A | 1 | a0001c0001t0001g0032 | 2 | NA18969.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.-39+2208C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58664368 | ||||||
chr3:58664383
|
G | A | 1 | a0001c0001t0001g0194 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-39+2193C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58664383 | ||||||
chr3:58664411
|
T | A | 1 | a0001c0001t0001g0194 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-39+2165A>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58664411 | ||||||
chr3:58664423
|
T | TA | 150 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(147): Show | 270 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.-39+2152_-39+2153i others(3): Show |
FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58664423 | ||||||
chr3:58664482
|
G | T | 1 | a0001c0001t0001g0178 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-39+2094C>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58664482 | ||||||
chr3:58664509
|
C | T | 59 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0028others(56): Show | 70 | HG00280.hp2 HG00438.hp1 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.-39+2067G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58664509 | ||||||
chr3:58664522
|
A | G | 1 | a0001c0001t0001g0056 | 2 | HG03225.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-39+2054T>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58664522 | ||||||
chr3:58664658
|
C | T | 2 | a0001c0001t0001g0177a0001c0003t0001g0176 | 2 | NA18522.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-39+1918G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58664658 | ||||||
chr3:58665012
|
G | C | 239 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(236): Show | 380 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(377): Show |
intron_variant | MODIFIER | c.-39+1564C>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58665012 | ||||||
chr3:58665036
|
T | G | 1 | a0001c0001t0001g0112 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-39+1540A>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58665036 | ||||||
chr3:58665310
|
T | G | 1 | a0001c0004t0001g0113 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-39+1266A>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58665310 | ||||||
chr3:58665351
|
A | T | 2 | a0001c0001t0001g0005a0001c0001t0001g0175 | 6 | NA18944.hp2 NA18962.hp1 NA18966.hp2 others(3): Show |
intron_variant | MODIFIER | c.-39+1225T>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58665351 | ||||||
chr3:58665372
|
T | C | 1 | a0001c0001t0001g0168 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-39+1204A>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58665372 | ||||||
chr3:58665373
|
C | G | 1 | a0001c0001t0001g0252 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-39+1203G>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58665373 | ||||||
chr3:58665431
|
C | T | 1 | a0001c0001t0001g0174 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-39+1145G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58665431 | ||||||
chr3:58665437
|
C | T | 1 | a0001c0001t0001g0061 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-39+1139G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58665437 | ||||||
chr3:58665459
|
T | C | 176 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(173): Show | 306 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.-39+1117A>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58665459 | ||||||
chr3:58665554
|
T | G | 239 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(236): Show | 380 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(377): Show |
intron_variant | MODIFIER | c.-39+1022A>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58665554 | ||||||
chr3:58665655
|
T | C | 1 | a0001c0004t0001g0113 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-39+921A>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58665655 | ||||||
chr3:58665747
|
C | G | 3 | a0001c0001t0001g0171a0001c0001t0002g0172a0006c0010t0004g0173 | 3 | HG02723.hp1 HG03139.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-39+829G>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58665747 | ||||||
chr3:58665748
|
G | A | 2 | a0001c0001t0005g0059a0001c0001t0005g0060 | 2 | HG02559.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-39+828C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58665748 | ||||||
chr3:58665878
|
T | C | 1 | a0001c0004t0001g0113 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-39+698A>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58665878 | ||||||
chr3:58666121
|
G | T | 1 | a0001c0004t0001g0113 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-39+455C>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58666121 | ||||||
chr3:58666126
|
C | T | 176 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(173): Show | 306 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.-39+450G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58666126 | ||||||
chr3:58666304
|
T | C | 1 | a0001c0001t0001g0170 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.-39+272A>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58666304 | ||||||
chr3:58666489
|
A | G | 72 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(69): Show | 120 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.-39+87T>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58666489 | ||||||
chr3:58666531
|
T | A | 1 | a0001c0001t0001g0252 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-39+45A>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58666531 | ||||||
chr3:58666534
|
G | T | 1 | a0001c0004t0001g0113 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-39+42C>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58666534 | ||||||
chr3:58666565
|
G | T | 60 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0028others(57): Show | 71 | HG00280.hp2 HG00438.hp1 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.-39+11C>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58666565 |