geneid | 10447 |
---|---|
ensemblid | ENSG00000196937.11 |
hgncid | 18664 |
symbol | FAM3C |
name | FAM3 metabolism regulating signaling molecule C |
refseq_nuc | NM_014888.3 |
refseq_prot | NP_055703.1 |
ensembl_nuc | ENST00000359943.8 |
ensembl_prot | ENSP00000353025.3 |
mane_status | MANE Select |
chr | chr7 |
start | 121348878 |
end | 121396308 |
strand | - |
ver | v1.2 |
region | chr7:121348878-121396308 |
region5000 | chr7:121343878-121401308 |
regionname0 | FAM3C_chr7_121348878_121396308 |
regionname5000 | FAM3C_chr7_121343878_121401308 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 227 | 270 | 82 | 64 | 82 | 14 | 26 | 60 | FAM3C_chr7_121343878_121401308 | FAM3C | copy fasta | chr7 | 121343878 | 121401308 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 684 | 270 | 82 | 64 | 82 | 14 | 26 | FAM3C_chr7_121343878_121401308 | FAM3C | copy fasta | chr7 | 121343878 | 121401308 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 1772 | 186 | 39 | 45 | 73 | 10 | 18 | FAM3C_chr7_121343878_121401308 | FAM3C | copy fasta | chr7 | 121343878 | 121401308 |
t0002 | 0/0 | 1772 | 22 | 19 | 2 | 0 | 0 | 1 | FAM3C_chr7_121343878_121401308 | FAM3C | copy fasta | chr7 | 121343878 | 121401308 |
t0003 | 0/0 | 1772 | 20 | 12 | 0 | 4 | 0 | 4 | FAM3C_chr7_121343878_121401308 | FAM3C | copy fasta | chr7 | 121343878 | 121401308 |
t0004 | 0/0 | 1772 | 18 | 1 | 13 | 0 | 3 | 1 | FAM3C_chr7_121343878_121401308 | FAM3C | copy fasta | chr7 | 121343878 | 121401308 |
t0005 | 0/0 | 1772 | 7 | 7 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | copy fasta | chr7 | 121343878 | 121401308 |
t0006 | 0/0 | 1772 | 3 | 0 | 0 | 3 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | copy fasta | chr7 | 121343878 | 121401308 |
t0007 | 0/0 | 1772 | 2 | 0 | 2 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | copy fasta | chr7 | 121343878 | 121401308 |
t0008 | 0/0 | 1772 | 2 | 2 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | copy fasta | chr7 | 121343878 | 121401308 |
t0009 | 0/0 | 1772 | 1 | 0 | 0 | 0 | 1 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | copy fasta | chr7 | 121343878 | 121401308 |
t0010 | 0/0 | 1772 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | copy fasta | chr7 | 121343878 | 121401308 |
t0011 | 0/0 | 1772 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3C_chr7_121343878_121401308 | FAM3C | copy fasta | chr7 | 121343878 | 121401308 |
t0012 | 0/0 | 1772 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3C_chr7_121343878_121401308 | FAM3C | copy fasta | chr7 | 121343878 | 121401308 |
t0013 | 0/0 | 1772 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | copy fasta | chr7 | 121343878 | 121401308 |
t0014 | 0/0 | 1772 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | copy fasta | chr7 | 121343878 | 121401308 |
t0015 | 0/0 | 1772 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | copy fasta | chr7 | 121343878 | 121401308 |
t0016 | 0/0 | 1772 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | copy fasta | chr7 | 121343878 | 121401308 |
t0017 | 0/0 | 1772 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | copy fasta | chr7 | 121343878 | 121401308 |
t0018 | 1/0 | 1772 | 1 | 0 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | copy fasta | chr7 | 121343878 | 121401308 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 11 | 1 | 1 | 7 | 1 | 1 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0002 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0003 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0004 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0009 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0015 | 0/1 | 2 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0018 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0021 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0025 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0220 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 684 | 270 | 82 | 64 | 82 | 14 | 26 | FAM3C_chr7_121343878_121401308 | FAM3C | copy fasta | chr7 | 121343878 | 121401308 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 2455 | 186 | 39 | 45 | 73 | 10 | 18 | FAM3C_chr7_121343878_121401308 | FAM3C | copy fasta | chr7 | 121343878 | 121401308 |
a0001c0001t0002 | 0/0 | 2455 | 22 | 19 | 2 | 0 | 0 | 1 | FAM3C_chr7_121343878_121401308 | FAM3C | copy fasta | chr7 | 121343878 | 121401308 |
a0001c0001t0003 | 0/0 | 2455 | 20 | 12 | 0 | 4 | 0 | 4 | FAM3C_chr7_121343878_121401308 | FAM3C | copy fasta | chr7 | 121343878 | 121401308 |
a0001c0001t0004 | 0/0 | 2455 | 18 | 1 | 13 | 0 | 3 | 1 | FAM3C_chr7_121343878_121401308 | FAM3C | copy fasta | chr7 | 121343878 | 121401308 |
a0001c0001t0005 | 0/0 | 2455 | 7 | 7 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | copy fasta | chr7 | 121343878 | 121401308 |
a0001c0001t0006 | 0/0 | 2455 | 3 | 0 | 0 | 3 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | copy fasta | chr7 | 121343878 | 121401308 |
a0001c0001t0007 | 0/0 | 2455 | 2 | 0 | 2 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | copy fasta | chr7 | 121343878 | 121401308 |
a0001c0001t0008 | 0/0 | 2455 | 2 | 2 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | copy fasta | chr7 | 121343878 | 121401308 |
a0001c0001t0009 | 0/0 | 2455 | 1 | 0 | 0 | 0 | 1 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | copy fasta | chr7 | 121343878 | 121401308 |
a0001c0001t0010 | 0/0 | 2455 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | copy fasta | chr7 | 121343878 | 121401308 |
a0001c0001t0011 | 0/0 | 2455 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3C_chr7_121343878_121401308 | FAM3C | copy fasta | chr7 | 121343878 | 121401308 |
a0001c0001t0012 | 0/0 | 2455 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3C_chr7_121343878_121401308 | FAM3C | copy fasta | chr7 | 121343878 | 121401308 |
a0001c0001t0013 | 0/0 | 2455 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | copy fasta | chr7 | 121343878 | 121401308 |
a0001c0001t0014 | 0/0 | 2455 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | copy fasta | chr7 | 121343878 | 121401308 |
a0001c0001t0015 | 0/0 | 2455 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | copy fasta | chr7 | 121343878 | 121401308 |
a0001c0001t0016 | 0/0 | 2455 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | copy fasta | chr7 | 121343878 | 121401308 |
a0001c0001t0017 | 0/0 | 2455 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | copy fasta | chr7 | 121343878 | 121401308 |
a0001c0001t0018 | 1/0 | 2455 | 1 | 0 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | copy fasta | chr7 | 121343878 | 121401308 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 11 | 1 | 1 | 7 | 1 | 1 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0002 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0003 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0015 | 0/1 | 2 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0021 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0002g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0002g0018 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0002g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0003g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0003g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0003g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0003g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0003g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0003g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0003g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0003g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0003g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0003g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0003g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0003g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0003g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0003g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0004g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0004g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0004g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0004g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0004g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0004g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0004g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0004g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0004g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0004g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0004g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0004g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0004g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0004g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0004g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0004g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0005g0004 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0005g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0005g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0005g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0006g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0006g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0006g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0007g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0007g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0008g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0008g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0009g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0010g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0011g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0012g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0013g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0014g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0015g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0016g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0017g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
a0001c0001t0018g0220 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0004 | g0037 | EUR | GBR | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG00140 | hp2 | a0001 | c0001 | t0009 | g0089 | EUR | GBR | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0187 | EUR | FIN | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG00280 | hp2 | a0001 | c0001 | t0004 | g0197 | EUR | FIN | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0074 | EUR | FIN | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0196 | EUR | FIN | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | CHS | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG00438 | hp2 | a0001 | c0001 | t0003 | g0206 | EAS | CHS | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG00544 | hp2 | a0001 | c0001 | t0003 | g0199 | EAS | CHS | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG00558 | hp2 | a0001 | c0001 | t0013 | g0049 | EAS | CHS | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | CHS | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | CHS | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | CHS | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | CHS | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG00639 | hp2 | a0001 | c0001 | t0004 | g0031 | AMR | PUR | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | CHS | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG00673 | hp2 | a0001 | c0001 | t0006 | g0129 | EAS | CHS | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG00738 | hp1 | a0001 | c0001 | t0004 | g0033 | AMR | PUR | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG01074 | hp2 | a0001 | c0001 | t0002 | g0018 | AMR | PUR | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | PUR | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG01099 | hp1 | a0001 | c0001 | t0014 | g0100 | AMR | PUR | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG01106 | hp1 | a0001 | c0001 | t0004 | g0211 | AMR | PUR | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG01106 | hp2 | a0001 | c0001 | t0004 | g0032 | AMR | PUR | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0140 | AMR | PUR | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG01255 | hp1 | a0001 | c0001 | t0007 | g0216 | AMR | CLM | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | CLM | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG01258 | hp1 | a0001 | c0001 | t0004 | g0041 | AMR | CLM | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | CLM | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | CLM | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | CLM | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | CLM | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | CLM | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG01358 | hp2 | a0001 | c0001 | t0004 | g0039 | AMR | CLM | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG01361 | hp2 | a0001 | c0001 | t0004 | g0010 | AMR | CLM | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG01433 | hp1 | a0001 | c0001 | t0017 | g0058 | AMR | CLM | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | CLM | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0009 | EUR | IBS | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0021 | EUR | IBS | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0009 | EUR | IBS | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | ACB | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | ACB | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | ACB | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG01891 | hp2 | a0001 | c0001 | t0005 | g0217 | AFR | ACB | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | PEL | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG01928 | hp2 | a0001 | c0001 | t0007 | g0215 | AMR | PEL | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG01943 | hp1 | a0001 | c0001 | t0004 | g0010 | AMR | PEL | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | PEL | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PEL | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | PEL | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG01975 | hp1 | a0001 | c0001 | t0004 | g0011 | AMR | PEL | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PEL | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0214 | AMR | PEL | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG01978 | hp2 | a0001 | c0001 | t0004 | g0038 | AMR | PEL | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | ACB | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | KHV | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | KHV | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | KHV | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | KHV | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | KHV | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | ACB | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG02145 | hp2 | a0001 | c0001 | t0015 | g0116 | AFR | ACB | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PEL | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | CDX | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | ACB | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG02258 | hp1 | a0001 | c0001 | t0003 | g0146 | AFR | ACB | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PEL | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG02273 | hp2 | a0001 | c0001 | t0004 | g0011 | AMR | PEL | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG02280 | hp1 | a0001 | c0001 | t0002 | g0194 | AFR | ACB | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | ACB | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG02293 | hp1 | a0001 | c0001 | t0004 | g0040 | AMR | PEL | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG02300 | hp2 | a0001 | c0001 | t0004 | g0036 | AMR | PEL | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | ACB | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | ACB | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | KHV | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | KHV | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | PJL | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG02602 | hp2 | a0001 | c0001 | t0012 | g0203 | SAS | PJL | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG02615 | hp1 | a0001 | c0001 | t0005 | g0004 | AFR | GWD | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | GWD | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG02630 | hp1 | a0001 | c0001 | t0003 | g0144 | AFR | GWD | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | GWD | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0188 | SAS | PJL | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | GWD | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG02723 | hp1 | a0001 | c0001 | t0005 | g0004 | AFR | GWD | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG02723 | hp2 | a0001 | c0001 | t0016 | g0195 | AFR | GWD | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | GWD | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG02809 | hp2 | a0001 | c0001 | t0002 | g0055 | AFR | GWD | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | GWD | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | GWD | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG02886 | hp2 | a0001 | c0001 | t0005 | g0004 | AFR | GWD | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG02895 | hp1 | a0001 | c0001 | t0002 | g0017 | AFR | GWD | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG02895 | hp2 | a0001 | c0001 | t0008 | g0218 | AFR | GWD | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | GWD | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | GWD | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG02897 | hp2 | a0001 | c0001 | t0002 | g0017 | AFR | GWD | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG02922 | hp1 | a0001 | c0001 | t0002 | g0138 | AFR | ESN | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG02922 | hp2 | a0001 | c0001 | t0002 | g0044 | AFR | ESN | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG02965 | hp1 | a0001 | c0001 | t0003 | g0149 | AFR | ESN | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG02965 | hp2 | a0001 | c0001 | t0002 | g0192 | AFR | ESN | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG02970 | hp1 | a0001 | c0001 | t0003 | g0145 | AFR | ESN | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | ESN | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG02976 | hp1 | a0001 | c0001 | t0002 | g0071 | AFR | ESN | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG02976 | hp2 | a0001 | c0001 | t0003 | g0028 | AFR | ESN | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | GWD | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG03139 | hp1 | a0001 | c0001 | t0002 | g0139 | AFR | ESN | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG03139 | hp2 | a0001 | c0001 | t0005 | g0004 | AFR | ESN | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG03195 | hp1 | a0001 | c0001 | t0003 | g0028 | AFR | ESN | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG03195 | hp2 | a0001 | c0001 | t0002 | g0045 | AFR | ESN | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG03209 | hp2 | a0001 | c0001 | t0005 | g0222 | AFR | MSL | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | MSL | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG03225 | hp2 | a0001 | c0001 | t0003 | g0143 | AFR | MSL | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG03453 | hp1 | a0001 | c0001 | t0002 | g0141 | AFR | MSL | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG03453 | hp2 | a0001 | c0001 | t0002 | g0070 | AFR | MSL | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0213 | SAS | PJL | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0082 | SAS | PJL | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG03540 | hp1 | a0001 | c0001 | t0008 | g0219 | AFR | GWD | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | GWD | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG03579 | hp1 | a0001 | c0001 | t0003 | g0201 | AFR | MSL | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG03579 | hp2 | a0001 | c0001 | t0002 | g0191 | AFR | MSL | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG03669 | hp1 | a0001 | c0001 | t0003 | g0204 | SAS | PJL | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0168 | SAS | PJL | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | STU | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG03688 | hp2 | a0001 | c0001 | t0003 | g0207 | SAS | STU | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0160 | SAS | PJL | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0209 | SAS | PJL | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG03710 | hp2 | a0001 | c0001 | t0003 | g0200 | SAS | PJL | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG03834 | hp1 | a0001 | c0001 | t0011 | g0103 | SAS | BEB | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0150 | SAS | BEB | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0121 | SAS | BEB | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0127 | SAS | BEB | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0179 | SAS | BEB | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | BEB | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG04184 | hp2 | a0001 | c0001 | t0004 | g0035 | SAS | BEB | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0171 | SAS | STU | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0120 | SAS | STU | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0067 | SAS | STU | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG04228 | hp2 | a0001 | c0001 | t0003 | g0208 | SAS | STU | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
NA18522 | hp1 | a0001 | c0001 | t0002 | g0069 | AFR | YRI | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
NA18522 | hp2 | a0001 | c0001 | t0002 | g0054 | AFR | YRI | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
NA18906 | hp1 | a0001 | c0001 | t0003 | g0019 | AFR | YRI | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
NA18906 | hp2 | a0001 | c0001 | t0002 | g0137 | AFR | YRI | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
NA18954 | hp1 | a0001 | c0001 | t0003 | g0205 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
NA19030 | hp1 | a0001 | c0001 | t0002 | g0142 | AFR | LWK | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | LWK | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | LWK | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | LWK | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
NA19059 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
NA19059 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
NA19065 | hp1 | a0001 | c0001 | t0006 | g0064 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
NA19068 | hp2 | a0001 | c0001 | t0010 | g0092 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
NA19081 | hp1 | a0001 | c0001 | t0003 | g0202 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
NA19082 | hp1 | a0001 | c0001 | t0006 | g0115 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | YRI | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | YRI | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ASW | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
NA20129 | hp2 | a0001 | c0001 | t0003 | g0148 | AFR | ASW | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
NA20752 | hp1 | a0001 | c0001 | t0004 | g0034 | EUR | TSI | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0093 | EUR | TSI | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0097 | EUR | TSI | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0186 | EUR | TSI | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG02109 | hp1 | a0001 | c0001 | t0002 | g0131 | AFR | ACB | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG02109 | hp2 | a0001 | c0001 | t0002 | g0018 | AFR | ACB | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG02486 | hp1 | a0001 | c0001 | t0003 | g0147 | AFR | ACB | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | ACB | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG02559 | hp1 | a0001 | c0001 | t0004 | g0042 | AFR | ACB | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG02559 | hp2 | a0001 | c0001 | t0003 | g0019 | AFR | ACB | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG03471 | hp1 | a0001 | c0001 | t0005 | g0221 | AFR | MSL | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | MSL | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0015 | REF | REF | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0018 | g0220 | REF | REF | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
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 |
---|
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 |
---|
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:121349108
|
G | C | 4 | a0001c0001t0002a0001c0001t0005a0001c0001t0008others(1): Show | 32 | HG01074.hp2 HG01192.hp1 HG01433.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*1353C>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 10/10 | 1353 | chr7 | 121349108 | |||||
chr7:121349144
|
G | A | 2 | a0001c0001t0003a0001c0001t0012 | 21 | HG00438.hp2 HG00544.hp2 HG02258.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*1317C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 10/10 | 1317 | chr7 | 121349144 | |||||
chr7:121349384
|
T | C | 1 | a0001c0001t0011 | 1 | HG03834.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1077A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 10/10 | 1077 | chr7 | 121349384 | |||||
chr7:121349463
|
T | C | 2 | a0001c0001t0006a0001c0001t0010 | 4 | HG00673.hp2 NA19065.hp1 NA19068.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*998A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 10/10 | 998 | chr7 | 121349463 | |||||
chr7:121349477
|
A | G | 4 | a0001c0001t0002a0001c0001t0005a0001c0001t0008others(1): Show | 32 | HG01074.hp2 HG01192.hp1 HG01433.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*984T>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 10/10 | 984 | chr7 | 121349477 | |||||
chr7:121349484
|
T | C | 1 | a0001c0001t0012 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*977A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 10/10 | 977 | chr7 | 121349484 | |||||
chr7:121349625
|
A | T | 3 | a0001c0001t0004a0001c0001t0007a0001c0001t0016 | 21 | HG00140.hp1 HG00280.hp2 HG00639.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*836T>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 10/10 | 836 | chr7 | 121349625 | |||||
chr7:121349644
|
T | C | 1 | a0001c0001t0013 | 1 | HG00558.hp2 | 3_prime_UTR_variant | MODIFIER | c.*817A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 10/10 | 817 | chr7 | 121349644 | |||||
chr7:121349664
|
T | C | 1 | a0001c0001t0014 | 1 | HG01099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*797A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 10/10 | 797 | chr7 | 121349664 | |||||
chr7:121349694
|
T | A | 1 | a0001c0001t0015 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*767A>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 10/10 | 767 | chr7 | 121349694 | |||||
chr7:121349883
|
C | T | 3 | a0001c0001t0004a0001c0001t0007a0001c0001t0016 | 21 | HG00140.hp1 HG00280.hp2 HG00639.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*578G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 10/10 | 578 | chr7 | 121349883 | |||||
chr7:121349888
|
C | T | 3 | a0001c0001t0004a0001c0001t0007a0001c0001t0016 | 21 | HG00140.hp1 HG00280.hp2 HG00639.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*573G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 10/10 | 573 | chr7 | 121349888 | |||||
chr7:121349932
|
T | C | 1 | a0001c0001t0016 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*529A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 10/10 | 529 | chr7 | 121349932 | |||||
chr7:121349989
|
A | T | 1 | a0001c0001t0010 | 1 | NA19068.hp2 | 3_prime_UTR_variant | MODIFIER | c.*472T>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 10/10 | 472 | chr7 | 121349989 | |||||
chr7:121350066
|
C | T | 7 | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(4): Show | 53 | HG00140.hp1 HG00280.hp2 HG00639.hp2 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*395G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 10/10 | 395 | chr7 | 121350066 | |||||
chr7:121350122
|
T | C | 6 | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(3): Show | 51 | HG00140.hp1 HG00280.hp2 HG00639.hp2 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*339A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 10/10 | 339 | chr7 | 121350122 | |||||
chr7:121350172
|
C | T | 1 | a0001c0001t0009 | 1 | HG00140.hp2 | 3_prime_UTR_variant | MODIFIER | c.*289G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 10/10 | 289 | chr7 | 121350172 | |||||
chr7:121350279
|
T | C | 1 | a0001c0001t0017 | 1 | HG01433.hp1 | 3_prime_UTR_variant | MODIFIER | c.*182A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 10/10 | 182 | chr7 | 121350279 | |||||
chr7:121396185
|
C | A | 1 | a0001c0001t0007 | 2 | HG01255.hp1 HG01928.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-65G>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/10 | chr7 | 121396185 | ||||||
chr7:121396187
|
C | T | 15 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(12): Show | 260 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(257): Show |
5_prime_UTR_variant | MODIFIER | c.-67G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/10 | 13218 | chr7 | 121396187 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:121350673
|
C | A | 1 | a0001c0001t0001g0113 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.595-123G>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 9/9 | chr7 | 121350673 | ||||||
chr7:121350783
|
C | G | 111 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0020others(108): Show | 138 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.595-233G>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 9/9 | chr7 | 121350783 | ||||||
chr7:121350836
|
C | T | 1 | a0001c0001t0001g0053 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.595-286G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 9/9 | chr7 | 121350836 | ||||||
chr7:121350843
|
T | G | 1 | a0001c0001t0004g0041 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.595-293A>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 9/9 | chr7 | 121350843 | ||||||
chr7:121350901
|
T | C | 1 | a0001c0001t0002g0192 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.594+242A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 9/9 | chr7 | 121350901 | ||||||
chr7:121350931
|
T | C | 3 | a0001c0001t0002g0044a0001c0001t0002g0054a0001c0001t0002g0055 | 3 | HG02809.hp2 HG02922.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.594+212A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 9/9 | chr7 | 121350931 | ||||||
chr7:121351047
|
C | T | 1 | a0001c0001t0001g0050 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.594+96G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 9/9 | chr7 | 121351047 | ||||||
chr7:121351435
|
T | C | 38 | a0001c0001t0002g0209a0001c0001t0003g0019a0001c0001t0003g0028others(35): Show | 42 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(39): Show |
intron_variant | MODIFIER | c.468-166A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121351435 | ||||||
chr7:121351857
|
G | A | 1 | a0001c0001t0001g0193 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.468-588C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121351857 | ||||||
chr7:121352020
|
AAAG | A | 4 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0002g0191others(1): Show | 4 | HG02055.hp2 HG02965.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.468-754_468-752del others(3): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121352020 | ||||||
chr7:121352319
|
G | GT | 50 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0002g0017others(47): Show | 57 | HG00438.hp2 HG00544.hp2 HG01074.hp2 others(54): Show |
intron_variant | MODIFIER | c.468-1051dupA | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121352319 | ||||||
chr7:121352319
|
G | GTT | 17 | a0001c0001t0004g0010a0001c0001t0004g0011a0001c0001t0004g0031others(14): Show | 19 | HG00140.hp1 HG00280.hp2 HG00639.hp2 others(16): Show |
intron_variant | MODIFIER | c.468-1052_468-1051d others(4): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121352319 | ||||||
chr7:121352427
|
GC | G | 19 | a0001c0001t0003g0019a0001c0001t0003g0028a0001c0001t0003g0143others(16): Show | 21 | HG00438.hp2 HG00544.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.468-1159delG | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121352427 | ||||||
chr7:121352517
|
G | A | 1 | a0001c0001t0006g0129 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.468-1248C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121352517 | ||||||
chr7:121352654
|
C | T | 67 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0002g0017others(64): Show | 76 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.468-1385G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121352654 | ||||||
chr7:121352677
|
G | A | 67 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0002g0017others(64): Show | 76 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.468-1408C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121352677 | ||||||
chr7:121352724
|
T | C | 1 | a0001c0001t0001g0156 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.468-1455A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121352724 | ||||||
chr7:121352952
|
T | C | 39 | a0001c0001t0002g0209a0001c0001t0003g0019a0001c0001t0003g0028others(36): Show | 43 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.468-1683A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121352952 | ||||||
chr7:121353135
|
T | A | 1 | a0001c0001t0001g0102 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.468-1866A>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121353135 | ||||||
chr7:121353191
|
G | A | 2 | a0001c0001t0002g0191a0001c0001t0002g0192 | 2 | HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.468-1922C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121353191 | ||||||
chr7:121353272
|
C | T | 17 | a0001c0001t0001g0179a0001c0001t0002g0044a0001c0001t0002g0054others(14): Show | 20 | HG01891.hp2 HG02109.hp1 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.468-2003G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121353272 | ||||||
chr7:121353505
|
C | T | 2 | a0001c0001t0001g0022a0001c0001t0001g0170 | 3 | NA18955.hp1 NA18956.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.468-2236G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121353505 | ||||||
chr7:121353560
|
A | G | 3 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0072 | 3 | HG02055.hp2 HG02970.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.468-2291T>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121353560 | ||||||
chr7:121353681
|
C | A | 12 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0002g0017others(9): Show | 14 | HG01074.hp2 HG01192.hp1 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.468-2412G>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121353681 | ||||||
chr7:121353788
|
G | GT | 3 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0094 | 3 | NA18988.hp2 NA19065.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.468-2520dupA | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121353788 | ||||||
chr7:121353917
|
T | C | 1 | a0001c0001t0002g0131 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.468-2648A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121353917 | ||||||
chr7:121353968
|
A | C | 7 | a0001c0001t0003g0019a0001c0001t0003g0143a0001c0001t0003g0144others(4): Show | 8 | HG02486.hp1 HG02559.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.468-2699T>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121353968 | ||||||
chr7:121354046
|
T | G | 67 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0002g0017others(64): Show | 76 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.468-2777A>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121354046 | ||||||
chr7:121354115
|
G | T | 64 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0020others(61): Show | 84 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.468-2846C>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121354115 | ||||||
chr7:121354193
|
G | A | 1 | a0001c0001t0001g0097 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.468-2924C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121354193 | ||||||
chr7:121354557
|
A | G | 1 | a0001c0001t0001g0094 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.468-3288T>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121354557 | ||||||
chr7:121354619
|
T | C | 129 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0020others(126): Show | 158 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.468-3350A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121354619 | ||||||
chr7:121354697
|
C | T | 1 | a0001c0001t0001g0135 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.468-3428G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121354697 | ||||||
chr7:121354772
|
T | C | 67 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0002g0017others(64): Show | 76 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.468-3503A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121354772 | ||||||
chr7:121354781
|
C | T | 1 | a0001c0001t0001g0130 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.468-3512G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121354781 | ||||||
chr7:121354782
|
G | A | 67 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0002g0017others(64): Show | 76 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.468-3513C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121354782 | ||||||
chr7:121354818
|
C | A | 67 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0002g0017others(64): Show | 76 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.468-3549G>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121354818 | ||||||
chr7:121355280
|
T | C | 1 | a0001c0001t0001g0074 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.468-4011A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121355280 | ||||||
chr7:121355342
|
A | G | 2 | a0001c0001t0002g0191a0001c0001t0002g0192 | 2 | HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.468-4073T>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121355342 | ||||||
chr7:121355373
|
C | T | 6 | a0001c0001t0005g0004a0001c0001t0005g0217a0001c0001t0005g0221others(3): Show | 9 | HG01891.hp2 HG02615.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.468-4104G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121355373 | ||||||
chr7:121355392
|
C | G | 67 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0002g0017others(64): Show | 76 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.468-4123G>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121355392 | ||||||
chr7:121355409
|
T | C | 1 | a0001c0001t0002g0044 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.468-4140A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121355409 | ||||||
chr7:121355717
|
G | C | 1 | a0001c0001t0002g0131 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.467+4326C>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121355717 | ||||||
chr7:121355741
|
G | C | 1 | a0001c0001t0002g0209 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.467+4302C>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121355741 | ||||||
chr7:121355864
|
G | C | 67 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0002g0017others(64): Show | 76 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.467+4179C>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121355864 | ||||||
chr7:121356039
|
GA | G | 67 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0002g0017others(64): Show | 76 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.467+4003delT | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121356039 | ||||||
chr7:121356120
|
T | C | 67 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0002g0017others(64): Show | 76 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.467+3923A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121356120 | ||||||
chr7:121356186
|
G | A | 131 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0020others(128): Show | 160 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.467+3857C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121356186 | ||||||
chr7:121356196
|
A | AG | 67 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0002g0017others(64): Show | 76 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.467+3846dupC | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121356196 | ||||||
chr7:121356405
|
A | T | 1 | a0001c0001t0013g0049 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.467+3638T>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121356405 | ||||||
chr7:121356420
|
A | G | 3 | a0001c0001t0001g0007a0001c0001t0001g0029a0001c0001t0001g0210 | 6 | HG02055.hp1 HG02647.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.467+3623T>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121356420 | ||||||
chr7:121356453
|
C | A | 5 | a0001c0001t0001g0006a0001c0001t0001g0024a0001c0001t0001g0066others(2): Show | 8 | HG02083.hp2 NA18948.hp1 NA18980.hp1 others(5): Show |
intron_variant | MODIFIER | c.467+3590G>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121356453 | ||||||
chr7:121356483
|
A | T | 1 | a0001c0001t0002g0209 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.467+3560T>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121356483 | ||||||
chr7:121356489
|
A | G | 1 | a0001c0001t0001g0190 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.467+3554T>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121356489 | ||||||
chr7:121356541
|
C | T | 131 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0020others(128): Show | 160 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.467+3502G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121356541 | ||||||
chr7:121356873
|
A | G | 1 | a0001c0001t0001g0050 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.467+3170T>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121356873 | ||||||
chr7:121356910
|
G | C | 67 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0002g0017others(64): Show | 76 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.467+3133C>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121356910 | ||||||
chr7:121356985
|
T | C | 66 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0002g0017others(63): Show | 75 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.467+3058A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121356985 | ||||||
chr7:121357298
|
G | A | 1 | a0001c0001t0017g0058 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.467+2745C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121357298 | ||||||
chr7:121357315
|
G | T | 67 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0002g0017others(64): Show | 76 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.467+2728C>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121357315 | ||||||
chr7:121357464
|
C | T | 1 | a0001c0001t0002g0069 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.467+2579G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121357464 | ||||||
chr7:121357506
|
T | A | 136 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(133): Show | 168 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.467+2537A>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121357506 | ||||||
chr7:121357528
|
T | C | 1 | a0001c0001t0004g0211 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.467+2515A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121357528 | ||||||
chr7:121358031
|
G | GC | 67 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0002g0017others(64): Show | 76 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.467+2011dupG | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121358031 | ||||||
chr7:121358223
|
T | G | 64 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0020others(61): Show | 84 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.467+1820A>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121358223 | ||||||
chr7:121358582
|
TG | T | 17 | a0001c0001t0004g0010a0001c0001t0004g0011a0001c0001t0004g0031others(14): Show | 19 | HG00140.hp1 HG00280.hp2 HG00639.hp2 others(16): Show |
intron_variant | MODIFIER | c.467+1460delC | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121358582 | ||||||
chr7:121358730
|
C | T | 67 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0002g0017others(64): Show | 76 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.467+1313G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121358730 | ||||||
chr7:121358912
|
C | T | 28 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0002g0017others(25): Show | 33 | HG01074.hp2 HG01192.hp1 HG01433.hp1 others(30): Show |
intron_variant | MODIFIER | c.467+1131G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121358912 | ||||||
chr7:121359031
|
A | G | 7 | a0001c0001t0002g0131a0001c0001t0005g0004a0001c0001t0005g0217others(4): Show | 10 | HG01891.hp2 HG02109.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.467+1012T>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121359031 | ||||||
chr7:121359099
|
G | A | 1 | a0001c0001t0005g0221 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.467+944C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121359099 | ||||||
chr7:121359127
|
T | TA | 39 | a0001c0001t0002g0209a0001c0001t0003g0019a0001c0001t0003g0028others(36): Show | 43 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.467+915dupT | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121359127 | ||||||
chr7:121359283
|
T | C | 67 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0002g0017others(64): Show | 76 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.467+760A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121359283 | ||||||
chr7:121359407
|
CGTAAGTG others(5): Show |
C | 1 | a0001c0001t0002g0044 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.467+624_467+635del others(12): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121359407 | ||||||
chr7:121359546
|
T | C | 1 | a0001c0001t0002g0194 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.467+497A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121359546 | ||||||
chr7:121359967
|
A | AT | 129 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0020others(126): Show | 158 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.467+75dupA | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121359967 | ||||||
chr7:121360030
|
A | AAAGTTTT | 67 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0002g0017others(64): Show | 76 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.467+12_467+13insAA others(5): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121360030 | ||||||
chr7:121360585
|
C | A | 16 | a0001c0001t0002g0044a0001c0001t0002g0054a0001c0001t0002g0055others(13): Show | 19 | HG01891.hp2 HG02109.hp1 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.383-458G>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 7/9 | chr7 | 121360585 | ||||||
chr7:121360664
|
C | T | 64 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0020others(61): Show | 84 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.383-537G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 7/9 | chr7 | 121360664 | ||||||
chr7:121360690
|
C | T | 1 | a0001c0001t0001g0135 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.383-563G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 7/9 | chr7 | 121360690 | ||||||
chr7:121360708
|
C | T | 1 | a0001c0001t0001g0124 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.383-581G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 7/9 | chr7 | 121360708 | ||||||
chr7:121360729
|
G | A | 1 | a0001c0001t0014g0100 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.383-602C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 7/9 | chr7 | 121360729 | ||||||
chr7:121360733
|
T | C | 5 | a0001c0001t0001g0075a0001c0001t0001g0083a0001c0001t0001g0108others(2): Show | 5 | HG01261.hp1 HG01346.hp2 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.383-606A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 7/9 | chr7 | 121360733 | ||||||
chr7:121360877
|
A | G | 65 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0020others(62): Show | 85 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.383-750T>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 7/9 | chr7 | 121360877 | ||||||
chr7:121360914
|
A | G | 16 | a0001c0001t0002g0044a0001c0001t0002g0054a0001c0001t0002g0055others(13): Show | 19 | HG01891.hp2 HG02109.hp1 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.383-787T>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 7/9 | chr7 | 121360914 | ||||||
chr7:121361104
|
A | T | 16 | a0001c0001t0002g0044a0001c0001t0002g0054a0001c0001t0002g0055others(13): Show | 19 | HG01891.hp2 HG02109.hp1 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.383-977T>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 7/9 | chr7 | 121361104 | ||||||
chr7:121361132
|
A | C | 1 | a0001c0001t0002g0192 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.383-1005T>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 7/9 | chr7 | 121361132 | ||||||
chr7:121361186
|
A | C | 66 | a0001c0001t0001g0056a0001c0001t0002g0017a0001c0001t0002g0018others(63): Show | 75 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.383-1059T>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 7/9 | chr7 | 121361186 | ||||||
chr7:121361510
|
A | G | 1 | a0001c0001t0002g0131 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.383-1383T>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 7/9 | chr7 | 121361510 | ||||||
chr7:121361541
|
T | C | 1 | a0001c0001t0001g0185 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.382+1356A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 7/9 | chr7 | 121361541 | ||||||
chr7:121361676
|
G | A | 1 | a0001c0001t0002g0142 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.382+1221C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 7/9 | chr7 | 121361676 | ||||||
chr7:121361922
|
C | G | 1 | a0001c0001t0002g0044 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.382+975G>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 7/9 | chr7 | 121361922 | ||||||
chr7:121361929
|
G | A | 1 | a0001c0001t0002g0071 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.382+968C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 7/9 | chr7 | 121361929 | ||||||
chr7:121362134
|
C | T | 67 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0002g0017others(64): Show | 76 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.382+763G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 7/9 | chr7 | 121362134 | ||||||
chr7:121362212
|
C | T | 1 | a0001c0001t0001g0130 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.382+685G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 7/9 | chr7 | 121362212 | ||||||
chr7:121362247
|
G | A | 1 | a0001c0001t0016g0195 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.382+650C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 7/9 | chr7 | 121362247 | ||||||
chr7:121362274
|
T | A | 67 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0002g0017others(64): Show | 76 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.382+623A>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 7/9 | chr7 | 121362274 | ||||||
chr7:121362403
|
A | G | 1 | a0001c0001t0001g0183 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.382+494T>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 7/9 | chr7 | 121362403 | ||||||
chr7:121362428
|
G | A | 2 | a0001c0001t0001g0086a0001c0001t0001g0088 | 2 | HG02074.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.382+469C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 7/9 | chr7 | 121362428 | ||||||
chr7:121362463
|
T | G | 1 | a0001c0001t0002g0209 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.382+434A>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 7/9 | chr7 | 121362463 | ||||||
chr7:121362539
|
T | C | 67 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0002g0017others(64): Show | 76 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.382+358A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 7/9 | chr7 | 121362539 | ||||||
chr7:121362648
|
T | A | 21 | a0001c0001t0001g0074a0001c0001t0002g0044a0001c0001t0003g0019others(18): Show | 23 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(20): Show |
intron_variant | MODIFIER | c.382+249A>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 7/9 | chr7 | 121362648 | ||||||
chr7:121362822
|
A | G | 67 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0002g0017others(64): Show | 76 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.382+75T>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 7/9 | chr7 | 121362822 | ||||||
chr7:121362856
|
C | T | 67 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0002g0017others(64): Show | 76 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.382+41G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 7/9 | chr7 | 121362856 | ||||||
chr7:121363001
|
G | A | 1 | a0001c0001t0001g0081 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.332-54C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 6/9 | chr7 | 121363001 | ||||||
chr7:121363239
|
C | T | 1 | a0001c0001t0001g0210 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.332-292G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 6/9 | chr7 | 121363239 | ||||||
chr7:121363258
|
G | C | 67 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0002g0017others(64): Show | 76 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.332-311C>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 6/9 | chr7 | 121363258 | ||||||
chr7:121363520
|
T | C | 1 | a0001c0001t0001g0133 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.332-573A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 6/9 | chr7 | 121363520 | ||||||
chr7:121363564
|
T | G | 19 | a0001c0001t0003g0019a0001c0001t0003g0028a0001c0001t0003g0143others(16): Show | 21 | HG00438.hp2 HG00544.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.331+566A>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 6/9 | chr7 | 121363564 | ||||||
chr7:121364036
|
G | A | 1 | a0001c0001t0001g0179 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.331+94C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 6/9 | chr7 | 121364036 | ||||||
chr7:121364270
|
G | T | 28 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0002g0017others(25): Show | 33 | HG01074.hp2 HG01192.hp1 HG01433.hp1 others(30): Show |
intron_variant | MODIFIER | c.273-82C>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121364270 | ||||||
chr7:121364380
|
C | T | 6 | a0001c0001t0005g0004a0001c0001t0005g0217a0001c0001t0005g0221others(3): Show | 9 | HG01891.hp2 HG02615.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.273-192G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121364380 | ||||||
chr7:121364503
|
G | A | 1 | a0001c0001t0001g0050 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.273-315C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121364503 | ||||||
chr7:121364530
|
G | C | 6 | a0001c0001t0005g0004a0001c0001t0005g0217a0001c0001t0005g0221others(3): Show | 9 | HG01891.hp2 HG02615.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.273-342C>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121364530 | ||||||
chr7:121364656
|
T | C | 1 | a0001c0001t0002g0044 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.273-468A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121364656 | ||||||
chr7:121364694
|
G | A | 1 | a0001c0001t0001g0127 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.273-506C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121364694 | ||||||
chr7:121364749
|
T | C | 39 | a0001c0001t0002g0209a0001c0001t0003g0019a0001c0001t0003g0028others(36): Show | 43 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.273-561A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121364749 | ||||||
chr7:121364876
|
T | C | 1 | a0001c0001t0001g0079 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.273-688A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121364876 | ||||||
chr7:121364935
|
G | A | 4 | a0001c0001t0001g0013a0001c0001t0001g0047a0001c0001t0001g0078others(1): Show | 5 | HG00741.hp2 HG01081.hp2 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.273-747C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121364935 | ||||||
chr7:121365102
|
G | T | 3 | a0001c0001t0001g0007a0001c0001t0001g0029a0001c0001t0001g0210 | 6 | HG02055.hp1 HG02647.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.273-914C>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121365102 | ||||||
chr7:121365357
|
A | C | 1 | a0001c0001t0002g0131 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.273-1169T>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121365357 | ||||||
chr7:121365368
|
T | C | 67 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0002g0017others(64): Show | 76 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.273-1180A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121365368 | ||||||
chr7:121365582
|
T | A | 64 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0020others(61): Show | 84 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.273-1394A>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121365582 | ||||||
chr7:121365672
|
T | C | 67 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0002g0017others(64): Show | 76 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.273-1484A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121365672 | ||||||
chr7:121365967
|
C | A | 1 | a0001c0001t0002g0131 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.273-1779G>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121365967 | ||||||
chr7:121366073
|
T | C | 2 | a0001c0001t0002g0142a0001c0001t0017g0058 | 2 | HG01433.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.273-1885A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121366073 | ||||||
chr7:121366302
|
TAATG | T | 2 | a0001c0001t0004g0211a0001c0001t0016g0195 | 2 | HG01106.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.273-2118_273-2115d others(6): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121366302 | ||||||
chr7:121366345
|
TATCGTTC others(45): Show |
T | 1 | a0001c0001t0001g0076 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.273-2209_273-2158d others(54): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121366345 | ||||||
chr7:121366687
|
A | G | 67 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0002g0017others(64): Show | 76 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.273-2499T>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121366687 | ||||||
chr7:121366749
|
C | A | 28 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0002g0017others(25): Show | 33 | HG01074.hp2 HG01192.hp1 HG01433.hp1 others(30): Show |
intron_variant | MODIFIER | c.273-2561G>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121366749 | ||||||
chr7:121367195
|
T | C | 131 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0020others(128): Show | 160 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.273-3007A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121367195 | ||||||
chr7:121367208
|
T | C | 1 | a0001c0001t0001g0198 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.273-3020A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121367208 | ||||||
chr7:121367289
|
C | T | 67 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0002g0017others(64): Show | 76 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.273-3101G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121367289 | ||||||
chr7:121367291
|
T | C | 1 | a0001c0001t0012g0203 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.273-3103A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121367291 | ||||||
chr7:121367509
|
T | C | 2 | a0001c0001t0002g0054a0001c0001t0002g0055 | 2 | HG02809.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.273-3321A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121367509 | ||||||
chr7:121367579
|
C | A | 1 | a0001c0001t0017g0058 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.273-3391G>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121367579 | ||||||
chr7:121367807
|
A | G | 1 | a0001c0001t0001g0109 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.272+3493T>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121367807 | ||||||
chr7:121367947
|
C | G | 67 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0002g0017others(64): Show | 76 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.272+3353G>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121367947 | ||||||
chr7:121368066
|
T | C | 1 | a0001c0001t0001g0061 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.272+3234A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121368066 | ||||||
chr7:121368149
|
T | C | 67 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0002g0017others(64): Show | 76 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.272+3151A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121368149 | ||||||
chr7:121368228
|
T | C | 67 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0002g0017others(64): Show | 76 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.272+3072A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121368228 | ||||||
chr7:121368264
|
A | G | 1 | a0001c0001t0001g0112 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.272+3036T>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121368264 | ||||||
chr7:121368486
|
C | T | 67 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0002g0017others(64): Show | 76 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.272+2814G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121368486 | ||||||
chr7:121368677
|
T | C | 1 | a0001c0001t0001g0053 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.272+2623A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121368677 | ||||||
chr7:121368755
|
C | T | 1 | a0001c0001t0001g0212 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.272+2545G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121368755 | ||||||
chr7:121368861
|
A | G | 1 | a0001c0001t0004g0211 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.272+2439T>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121368861 | ||||||
chr7:121368863
|
C | T | 1 | a0001c0001t0001g0169 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.272+2437G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121368863 | ||||||
chr7:121368871
|
T | C | 1 | a0001c0001t0001g0008 | 2 | HG01346.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.272+2429A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121368871 | ||||||
chr7:121368953
|
A | G | 67 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0002g0017others(64): Show | 76 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.272+2347T>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121368953 | ||||||
chr7:121368969
|
GTTGT | G | 12 | a0001c0001t0003g0028a0001c0001t0003g0146a0001c0001t0003g0199others(9): Show | 13 | HG00438.hp2 HG00544.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.272+2327_272+2330d others(6): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121368969 | ||||||
chr7:121368972
|
GT | G | 96 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(93): Show | 128 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.272+2327delA | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121368972 | ||||||
chr7:121368972
|
GTT | G | 6 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0135others(3): Show | 6 | HG00639.hp1 HG01243.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.272+2326_272+2327d others(4): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121368972 | ||||||
chr7:121368972
|
GTTT | G | 9 | a0001c0001t0002g0044a0001c0001t0004g0011a0001c0001t0004g0037others(6): Show | 10 | HG00140.hp1 HG01255.hp1 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.272+2325_272+2327d others(5): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121368972 | ||||||
chr7:121368972
|
GTTTT | G | 39 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0002g0017others(36): Show | 43 | HG00280.hp2 HG00639.hp2 HG00738.hp1 others(40): Show |
intron_variant | MODIFIER | c.272+2324_272+2327d others(6): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121368972 | ||||||
chr7:121368972
|
GTTTTT | G | 6 | a0001c0001t0005g0004a0001c0001t0005g0217a0001c0001t0005g0221others(3): Show | 9 | HG01891.hp2 HG02615.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.272+2323_272+2327d others(7): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121368972 | ||||||
chr7:121368974
|
T | G | 1 | a0001c0001t0001g0072 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.272+2326A>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121368974 | ||||||
chr7:121368975
|
T | G | 1 | a0001c0001t0001g0136 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.272+2325A>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121368975 | ||||||
chr7:121368976
|
T | G | 4 | a0001c0001t0001g0006a0001c0001t0001g0024a0001c0001t0001g0066others(1): Show | 7 | HG02083.hp2 NA18948.hp1 NA18980.hp1 others(4): Show |
intron_variant | MODIFIER | c.272+2324A>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121368976 | ||||||
chr7:121369033
|
G | A | 1 | a0001c0001t0002g0209 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.272+2267C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121369033 | ||||||
chr7:121369052
|
C | T | 67 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0002g0017others(64): Show | 76 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.272+2248G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121369052 | ||||||
chr7:121369234
|
A | G | 67 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0002g0017others(64): Show | 76 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.272+2066T>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121369234 | ||||||
chr7:121369271
|
A | G | 67 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0002g0017others(64): Show | 76 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.272+2029T>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121369271 | ||||||
chr7:121369316
|
G | A | 67 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0002g0017others(64): Show | 76 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.272+1984C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121369316 | ||||||
chr7:121369899
|
G | C | 67 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0002g0017others(64): Show | 76 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.272+1401C>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121369899 | ||||||
chr7:121369939
|
T | TAA | 67 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0002g0017others(64): Show | 76 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.272+1359_272+1360d others(4): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121369939 | ||||||
chr7:121369945
|
G | A | 6 | a0001c0001t0005g0004a0001c0001t0005g0217a0001c0001t0005g0221others(3): Show | 9 | HG01891.hp2 HG02615.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.272+1355C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121369945 | ||||||
chr7:121370112
|
T | C | 1 | a0001c0001t0010g0092 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.272+1188A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121370112 | ||||||
chr7:121370155
|
T | C | 67 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0002g0017others(64): Show | 76 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.272+1145A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121370155 | ||||||
chr7:121370358
|
G | C | 67 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0002g0017others(64): Show | 76 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.272+942C>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121370358 | ||||||
chr7:121370361
|
T | C | 39 | a0001c0001t0002g0209a0001c0001t0003g0019a0001c0001t0003g0028others(36): Show | 43 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.272+939A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121370361 | ||||||
chr7:121370462
|
T | C | 1 | a0001c0001t0001g0180 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.272+838A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121370462 | ||||||
chr7:121370469
|
C | T | 1 | a0001c0001t0001g0093 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.272+831G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121370469 | ||||||
chr7:121370844
|
C | T | 67 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0002g0017others(64): Show | 76 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.272+456G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121370844 | ||||||
chr7:121371157
|
G | GA | 6 | a0001c0001t0005g0004a0001c0001t0005g0217a0001c0001t0005g0221others(3): Show | 9 | HG01891.hp2 HG02615.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.272+142dupT | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121371157 | ||||||
chr7:121371561
|
G | T | 67 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0002g0017others(64): Show | 76 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.149-138C>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 4/9 | chr7 | 121371561 | ||||||
chr7:121371593
|
A | T | 1 | a0001c0001t0002g0131 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.149-170T>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 4/9 | chr7 | 121371593 | ||||||
chr7:121371600
|
T | A | 1 | a0001c0001t0017g0058 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.149-177A>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 4/9 | chr7 | 121371600 | ||||||
chr7:121371614
|
A | C | 1 | a0001c0001t0001g0128 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.149-191T>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 4/9 | chr7 | 121371614 | ||||||
chr7:121371789
|
T | C | 1 | a0001c0001t0001g0021 | 2 | HG01517.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.148+321A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 4/9 | chr7 | 121371789 | ||||||
chr7:121372010
|
C | T | 1 | a0001c0001t0001g0157 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.148+100G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 4/9 | chr7 | 121372010 | ||||||
chr7:121372022
|
A | T | 1 | a0001c0001t0001g0135 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.148+88T>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 4/9 | chr7 | 121372022 | ||||||
chr7:121372142
|
GA | G | 13 | a0001c0001t0002g0017a0001c0001t0002g0018a0001c0001t0002g0045others(10): Show | 18 | HG01074.hp2 HG01192.hp1 HG01891.hp2 others(15): Show |
splice_region_variant&intron_variant | LOW | c.119-4delT | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 3/9 | chr7 | 121372142 | ||||||
chr7:121372181
|
T | C | 1 | a0001c0001t0002g0209 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.119-42A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 3/9 | chr7 | 121372181 | ||||||
chr7:121372215
|
C | T | 1 | a0001c0001t0015g0116 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.119-76G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 3/9 | chr7 | 121372215 | ||||||
chr7:121372241
|
A | G | 1 | a0001c0001t0001g0091 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.119-102T>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 3/9 | chr7 | 121372241 | ||||||
chr7:121372337
|
G | A | 1 | a0001c0001t0001g0052 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.119-198C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 3/9 | chr7 | 121372337 | ||||||
chr7:121372527
|
C | T | 2 | a0001c0001t0002g0054a0001c0001t0002g0055 | 2 | HG02809.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.119-388G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 3/9 | chr7 | 121372527 | ||||||
chr7:121372639
|
A | T | 2 | a0001c0001t0001g0099a0001c0001t0001g0125 | 2 | HG02523.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.119-500T>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 3/9 | chr7 | 121372639 | ||||||
chr7:121372718
|
T | G | 67 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0002g0017others(64): Show | 76 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.119-579A>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 3/9 | chr7 | 121372718 | ||||||
chr7:121372821
|
T | C | 19 | a0001c0001t0003g0019a0001c0001t0003g0028a0001c0001t0003g0143others(16): Show | 21 | HG00438.hp2 HG00544.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.119-682A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 3/9 | chr7 | 121372821 | ||||||
chr7:121372861
|
A | G | 1 | a0001c0001t0002g0191 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.119-722T>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 3/9 | chr7 | 121372861 | ||||||
chr7:121373176
|
G | GTCAGGAT others(15): Show |
6 | a0001c0001t0001g0020a0001c0001t0001g0052a0001c0001t0001g0159others(3): Show | 7 | HG01891.hp1 HG02258.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.119-1059_119-1038d others(24): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 3/9 | chr7 | 121373176 | ||||||
chr7:121373176
|
GTCAGGAT others(15): Show |
G | 67 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0002g0017others(64): Show | 76 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.119-1059_119-1038d others(24): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 3/9 | chr7 | 121373176 | ||||||
chr7:121373353
|
T | G | 1 | a0001c0001t0001g0187 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.119-1214A>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 3/9 | chr7 | 121373353 | ||||||
chr7:121373747
|
G | A | 1 | a0001c0001t0001g0160 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.119-1608C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 3/9 | chr7 | 121373747 | ||||||
chr7:121373818
|
C | T | 1 | a0001c0001t0002g0044 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.119-1679G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 3/9 | chr7 | 121373818 | ||||||
chr7:121373831
|
G | C | 4 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(1): Show | 4 | NA18969.hp2 NA18994.hp2 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.119-1692C>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 3/9 | chr7 | 121373831 | ||||||
chr7:121373866
|
C | CA | 12 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0002g0017others(9): Show | 14 | HG01074.hp2 HG01192.hp1 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.119-1728dupT | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 3/9 | chr7 | 121373866 | ||||||
chr7:121373888
|
C | T | 1 | a0001c0001t0003g0148 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.119-1749G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 3/9 | chr7 | 121373888 | ||||||
chr7:121373922
|
C | G | 67 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0002g0017others(64): Show | 76 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.119-1783G>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 3/9 | chr7 | 121373922 | ||||||
chr7:121373995
|
CA | C | 67 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0002g0017others(64): Show | 76 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.119-1857delT | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 3/9 | chr7 | 121373995 | ||||||
chr7:121374121
|
C | T | 1 | a0001c0001t0002g0209 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.119-1982G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 3/9 | chr7 | 121374121 | ||||||
chr7:121374144
|
G | A | 1 | a0001c0001t0001g0030 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.119-2005C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 3/9 | chr7 | 121374144 | ||||||
chr7:121374338
|
G | A | 1 | a0001c0001t0001g0193 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.119-2199C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 3/9 | chr7 | 121374338 | ||||||
chr7:121374351
|
C | G | 1 | a0001c0001t0001g0176 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.119-2212G>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 3/9 | chr7 | 121374351 | ||||||
chr7:121374498
|
A | G | 1 | a0001c0001t0017g0058 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.119-2359T>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 3/9 | chr7 | 121374498 | ||||||
chr7:121374572
|
A | G | 1 | a0001c0001t0003g0200 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.119-2433T>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 3/9 | chr7 | 121374572 | ||||||
chr7:121374661
|
C | T | 1 | a0001c0001t0001g0122 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.119-2522G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 3/9 | chr7 | 121374661 | ||||||
chr7:121374759
|
G | A | 67 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0002g0017others(64): Show | 76 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.119-2620C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 3/9 | chr7 | 121374759 | ||||||
chr7:121374906
|
A | C | 1 | a0001c0001t0016g0195 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.119-2767T>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 3/9 | chr7 | 121374906 | ||||||
chr7:121374960
|
C | T | 6 | a0001c0001t0005g0004a0001c0001t0005g0217a0001c0001t0005g0221others(3): Show | 9 | HG01891.hp2 HG02615.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.119-2821G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 3/9 | chr7 | 121374960 | ||||||
chr7:121375013
|
G | C | 1 | a0001c0001t0001g0009 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.119-2874C>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 3/9 | chr7 | 121375013 | ||||||
chr7:121375193
|
G | A | 1 | a0001c0001t0001g0076 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.119-3054C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 3/9 | chr7 | 121375193 | ||||||
chr7:121375274
|
G | C | 6 | a0001c0001t0002g0017a0001c0001t0002g0018a0001c0001t0002g0045others(3): Show | 8 | HG01074.hp2 HG01192.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.119-3135C>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 3/9 | chr7 | 121375274 | ||||||
chr7:121375404
|
C | A | 67 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0002g0017others(64): Show | 76 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.119-3265G>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 3/9 | chr7 | 121375404 | ||||||
chr7:121375474
|
T | A | 1 | a0001c0001t0001g0163 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.119-3335A>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 3/9 | chr7 | 121375474 | ||||||
chr7:121375554
|
A | C | 1 | a0001c0001t0012g0203 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.118+3356T>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 3/9 | chr7 | 121375554 | ||||||
chr7:121375833
|
T | G | 2 | a0001c0001t0003g0028a0001c0001t0003g0146 | 3 | HG02258.hp1 HG02976.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.118+3077A>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 3/9 | chr7 | 121375833 | ||||||
chr7:121376049
|
T | A | 1 | a0001c0001t0001g0168 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.118+2861A>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 3/9 | chr7 | 121376049 | ||||||
chr7:121376157
|
T | C | 1 | a0001c0001t0007g0215 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.118+2753A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 3/9 | chr7 | 121376157 | ||||||
chr7:121376342
|
G | C | 1 | a0001c0001t0001g0098 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.118+2568C>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 3/9 | chr7 | 121376342 | ||||||
chr7:121376368
|
A | T | 6 | a0001c0001t0005g0004a0001c0001t0005g0217a0001c0001t0005g0221others(3): Show | 9 | HG01891.hp2 HG02615.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.118+2542T>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 3/9 | chr7 | 121376368 | ||||||
chr7:121376750
|
T | C | 1 | a0001c0001t0001g0084 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.118+2160A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 3/9 | chr7 | 121376750 | ||||||
chr7:121376830
|
A | G | 2 | a0001c0001t0003g0147a0001c0001t0003g0149 | 2 | HG02486.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.118+2080T>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 3/9 | chr7 | 121376830 | ||||||
chr7:121377077
|
A | T | 1 | a0001c0001t0001g0124 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.118+1833T>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 3/9 | chr7 | 121377077 | ||||||
chr7:121377089
|
G | A | 1 | a0001c0001t0001g0082 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.118+1821C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 3/9 | chr7 | 121377089 | ||||||
chr7:121377106
|
G | A | 5 | a0001c0001t0001g0007a0001c0001t0001g0029a0001c0001t0001g0061others(2): Show | 8 | HG02055.hp1 HG02647.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.118+1804C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 3/9 | chr7 | 121377106 | ||||||
chr7:121377407
|
C | T | 1 | a0001c0001t0001g0061 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.118+1503G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 3/9 | chr7 | 121377407 | ||||||
chr7:121377420
|
C | A | 69 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(66): Show | 92 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.118+1490G>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 3/9 | chr7 | 121377420 | ||||||
chr7:121377758
|
T | C | 202 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(199): Show | 248 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.118+1152A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 3/9 | chr7 | 121377758 | ||||||
chr7:121378525
|
C | T | 71 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(68): Show | 94 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(91): Show |
intron_variant | MODIFIER | c.118+385G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 3/9 | chr7 | 121378525 | ||||||
chr7:121378605
|
T | G | 19 | a0001c0001t0003g0019a0001c0001t0003g0028a0001c0001t0003g0143others(16): Show | 21 | HG00438.hp2 HG00544.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.118+305A>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 3/9 | chr7 | 121378605 | ||||||
chr7:121378713
|
T | TAGAA | 110 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(107): Show | 137 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.118+193_118+196dup others(4): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 3/9 | chr7 | 121378713 | ||||||
chr7:121378786
|
A | G | 3 | a0001c0001t0001g0043a0001c0001t0001g0176a0001c0001t0001g0177 | 3 | HG01099.hp2 HG01261.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.118+124T>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 3/9 | chr7 | 121378786 | ||||||
chr7:121378803
|
A | T | 69 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(66): Show | 92 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.118+107T>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 3/9 | chr7 | 121378803 | ||||||
chr7:121378810
|
C | T | 1 | a0001c0001t0001g0080 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.118+100G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 3/9 | chr7 | 121378810 | ||||||
chr7:121379065
|
A | G | 2 | a0001c0001t0001g0056a0001c0001t0001g0057 | 2 | HG02055.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.14-51T>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 2/9 | chr7 | 121379065 | ||||||
chr7:121379199
|
T | C | 5 | a0001c0001t0001g0007a0001c0001t0001g0029a0001c0001t0001g0061others(2): Show | 8 | HG02055.hp1 HG02647.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.14-185A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 2/9 | chr7 | 121379199 | ||||||
chr7:121379408
|
G | A | 5 | a0001c0001t0001g0007a0001c0001t0001g0029a0001c0001t0001g0061others(2): Show | 8 | HG02055.hp1 HG02647.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.14-394C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 2/9 | chr7 | 121379408 | ||||||
chr7:121379425
|
T | C | 1 | a0001c0001t0008g0219 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.14-411A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 2/9 | chr7 | 121379425 | ||||||
chr7:121379466
|
A | G | 3 | a0001c0001t0001g0043a0001c0001t0001g0176a0001c0001t0001g0177 | 3 | HG01099.hp2 HG01261.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.14-452T>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 2/9 | chr7 | 121379466 | ||||||
chr7:121379517
|
A | G | 1 | a0001c0001t0003g0148 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.14-503T>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 2/9 | chr7 | 121379517 | ||||||
chr7:121379550
|
T | C | 1 | a0001c0001t0001g0085 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.14-536A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 2/9 | chr7 | 121379550 | ||||||
chr7:121379751
|
G | A | 1 | a0001c0001t0002g0194 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.14-737C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 2/9 | chr7 | 121379751 | ||||||
chr7:121379908
|
T | C | 6 | a0001c0001t0002g0017a0001c0001t0002g0018a0001c0001t0002g0045others(3): Show | 8 | HG01074.hp2 HG01192.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.14-894A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 2/9 | chr7 | 121379908 | ||||||
chr7:121380596
|
G | T | 1 | a0001c0001t0004g0211 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.14-1582C>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 2/9 | chr7 | 121380596 | ||||||
chr7:121380604
|
C | T | 1 | a0001c0001t0001g0132 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.14-1590G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 2/9 | chr7 | 121380604 | ||||||
chr7:121380733
|
T | TTA | 14 | a0001c0001t0001g0013a0001c0001t0001g0023a0001c0001t0001g0047others(11): Show | 16 | HG00642.hp1 HG00741.hp2 HG01069.hp1 others(13): Show |
intron_variant | MODIFIER | c.14-1721_14-1720dup others(2): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 2/9 | chr7 | 121380733 | ||||||
chr7:121380733
|
T | TTATA | 4 | a0001c0001t0001g0061a0001c0001t0001g0080a0001c0001t0001g0198others(1): Show | 4 | HG01884.hp2 NA19030.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.14-1723_14-1720dup others(4): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 2/9 | chr7 | 121380733 | ||||||
chr7:121380733
|
T | TTATATA | 10 | a0001c0001t0001g0007a0001c0001t0001g0029a0001c0001t0001g0210others(7): Show | 14 | HG02055.hp1 HG02486.hp1 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.14-1725_14-1720dup others(6): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 2/9 | chr7 | 121380733 | ||||||
chr7:121380733
|
T | TTATATAT others(1): Show |
4 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0003g0144others(1): Show | 4 | HG02055.hp2 HG02630.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.14-1727_14-1720dup others(8): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 2/9 | chr7 | 121380733 | ||||||
chr7:121380733
|
T | TTATATAT others(3): Show |
11 | a0001c0001t0002g0017a0001c0001t0002g0018a0001c0001t0002g0139others(8): Show | 13 | HG00544.hp2 HG01074.hp2 HG01192.hp1 others(10): Show |
intron_variant | MODIFIER | c.14-1729_14-1720dup others(10): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 2/9 | chr7 | 121380733 | ||||||
chr7:121380733
|
T | TTATATAT others(5): Show |
7 | a0001c0001t0002g0045a0001c0001t0002g0141a0001c0001t0002g0194others(4): Show | 8 | HG00438.hp2 HG02258.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.14-1731_14-1720dup others(12): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 2/9 | chr7 | 121380733 | ||||||
chr7:121380733
|
T | TTATATAT others(7): Show |
4 | a0001c0001t0002g0191a0001c0001t0003g0208a0001c0001t0004g0032others(1): Show | 4 | HG00738.hp1 HG01106.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.14-1733_14-1720dup others(14): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 2/9 | chr7 | 121380733 | ||||||
chr7:121380733
|
T | TTATATAT others(9): Show |
1 | a0001c0001t0004g0036 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.14-1735_14-1720dup others(16): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 2/9 | chr7 | 121380733 | ||||||
chr7:121380733
|
T | TTATATAT others(13): Show |
5 | a0001c0001t0002g0055a0001c0001t0004g0010a0001c0001t0004g0037others(2): Show | 6 | HG00140.hp1 HG01106.hp1 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.14-1739_14-1720dup others(20): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 2/9 | chr7 | 121380733 | ||||||
chr7:121380733
|
T | TTATATAT others(15): Show |
4 | a0001c0001t0004g0035a0001c0001t0004g0038a0001c0001t0004g0197others(1): Show | 4 | HG00280.hp2 HG01978.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.14-1741_14-1720dup others(22): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 2/9 | chr7 | 121380733 | ||||||
chr7:121380733
|
T | TTATATAT others(17): Show |
6 | a0001c0001t0002g0054a0001c0001t0004g0034a0001c0001t0004g0039others(3): Show | 6 | HG01255.hp1 HG01358.hp2 HG02293.hp1 others(3): Show |
intron_variant | MODIFIER | c.14-1720_14-1719ins others(24): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 2/9 | chr7 | 121380733 | ||||||
chr7:121380733
|
T | TTATATAT others(19): Show |
3 | a0001c0001t0002g0044a0001c0001t0004g0011a0001c0001t0004g0031 | 4 | HG00639.hp2 HG01975.hp1 HG02273.hp2 others(1): Show |
intron_variant | MODIFIER | c.14-1720_14-1719ins others(26): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 2/9 | chr7 | 121380733 | ||||||
chr7:121380733
|
T | TTATATAT others(21): Show |
1 | a0001c0001t0004g0041 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.14-1720_14-1719ins others(28): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 2/9 | chr7 | 121380733 | ||||||
chr7:121380757
|
G | A | 2 | a0001c0001t0002g0137a0001c0001t0002g0138 | 2 | HG02922.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.14-1743C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 2/9 | chr7 | 121380757 | ||||||
chr7:121380758
|
A | T | 2 | a0001c0001t0002g0137a0001c0001t0002g0138 | 2 | HG02922.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.14-1744T>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 2/9 | chr7 | 121380758 | ||||||
chr7:121380759
|
C | A | 2 | a0001c0001t0002g0137a0001c0001t0002g0138 | 2 | HG02922.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.14-1745G>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 2/9 | chr7 | 121380759 | ||||||
chr7:121380760
|
A | T | 2 | a0001c0001t0002g0137a0001c0001t0002g0138 | 2 | HG02922.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.14-1746T>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 2/9 | chr7 | 121380760 | ||||||
chr7:121380761
|
C | A | 2 | a0001c0001t0002g0137a0001c0001t0002g0138 | 2 | HG02922.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.14-1747G>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 2/9 | chr7 | 121380761 | ||||||
chr7:121380762
|
T | TATATATA others(9): Show |
1 | a0001c0001t0002g0138 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.14-1749_14-1748ins others(16): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 2/9 | chr7 | 121380762 | ||||||
chr7:121380762
|
T | TATATATA others(5): Show |
1 | a0001c0001t0002g0137 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.14-1749_14-1748ins others(12): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 2/9 | chr7 | 121380762 | ||||||
chr7:121380995
|
C | G | 1 | a0001c0001t0002g0137 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.13+1962G>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 2/9 | chr7 | 121380995 | ||||||
chr7:121381316
|
T | A | 1 | a0001c0001t0001g0087 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.13+1641A>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 2/9 | chr7 | 121381316 | ||||||
chr7:121381360
|
T | C | 2 | a0001c0001t0007g0215a0001c0001t0007g0216 | 2 | HG01255.hp1 HG01928.hp2 |
intron_variant | MODIFIER | c.13+1597A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 2/9 | chr7 | 121381360 | ||||||
chr7:121381425
|
AAACACAA others(3): Show |
A | 1 | a0001c0001t0001g0119 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.13+1522_13+1531del others(10): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 2/9 | chr7 | 121381425 | ||||||
chr7:121381556
|
CTTACT | C | 2 | a0001c0001t0002g0191a0001c0001t0002g0192 | 2 | HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.13+1396_13+1400del others(5): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 2/9 | chr7 | 121381556 | ||||||
chr7:121381656
|
C | CCA | 21 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0026others(18): Show | 25 | HG00609.hp2 HG00621.hp1 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.13+1299_13+1300dup others(2): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 2/9 | chr7 | 121381656 | ||||||
chr7:121381656
|
C | CCACACAC others(1): Show |
15 | a0001c0001t0002g0209a0001c0001t0003g0019a0001c0001t0003g0143others(12): Show | 16 | HG00438.hp2 HG00544.hp2 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.13+1293_13+1300dup others(8): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 2/9 | chr7 | 121381656 | ||||||
chr7:121381656
|
C | CCACACAC others(3): Show |
18 | a0001c0001t0003g0201a0001c0001t0003g0205a0001c0001t0004g0010others(15): Show | 20 | HG00140.hp1 HG00280.hp2 HG00639.hp2 others(17): Show |
intron_variant | MODIFIER | c.13+1291_13+1300dup others(10): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 2/9 | chr7 | 121381656 | ||||||
chr7:121381656
|
C | CCACACAC others(5): Show |
2 | a0001c0001t0004g0042a0001c0001t0016g0195 | 2 | HG02559.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.13+1289_13+1300dup others(12): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 2/9 | chr7 | 121381656 | ||||||
chr7:121381656
|
CCA | C | 12 | a0001c0001t0001g0048a0001c0001t0001g0090a0001c0001t0001g0118others(9): Show | 12 | HG00558.hp2 HG01069.hp2 HG02922.hp1 others(9): Show |
intron_variant | MODIFIER | c.13+1299_13+1300del others(2): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 2/9 | chr7 | 121381656 | ||||||
chr7:121381656
|
CCACACAC others(3): Show |
C | 2 | a0001c0001t0003g0028a0001c0001t0003g0146 | 3 | HG02258.hp1 HG02976.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.13+1291_13+1300del others(10): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 2/9 | chr7 | 121381656 | ||||||
chr7:121381656
|
CCACACAC others(11): Show |
C | 2 | a0001c0001t0002g0054a0001c0001t0002g0055 | 2 | HG02809.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.13+1283_13+1300del others(18): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 2/9 | chr7 | 121381656 | ||||||
chr7:121381742
|
GTTC | G | 19 | a0001c0001t0003g0019a0001c0001t0003g0028a0001c0001t0003g0143others(16): Show | 21 | HG00438.hp2 HG00544.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.13+1212_13+1214del others(3): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 2/9 | chr7 | 121381742 | ||||||
chr7:121382133
|
G | A | 2 | a0001c0001t0002g0054a0001c0001t0002g0055 | 2 | HG02809.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.13+824C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 2/9 | chr7 | 121382133 | ||||||
chr7:121382214
|
C | T | 1 | a0001c0001t0001g0132 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.13+743G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 2/9 | chr7 | 121382214 | ||||||
chr7:121382301
|
T | C | 1 | a0001c0001t0002g0192 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.13+656A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 2/9 | chr7 | 121382301 | ||||||
chr7:121382350
|
T | G | 4 | a0001c0001t0002g0044a0001c0001t0002g0137a0001c0001t0002g0138others(1): Show | 4 | HG02280.hp1 HG02922.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.13+607A>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 2/9 | chr7 | 121382350 | ||||||
chr7:121382365
|
C | G | 11 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0135others(8): Show | 13 | HG01243.hp2 HG01496.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.13+592G>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 2/9 | chr7 | 121382365 | ||||||
chr7:121382418
|
C | T | 5 | a0001c0001t0001g0007a0001c0001t0001g0029a0001c0001t0001g0061others(2): Show | 8 | HG02055.hp1 HG02647.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.13+539G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 2/9 | chr7 | 121382418 | ||||||
chr7:121382549
|
G | GT | 7 | a0001c0001t0001g0009a0001c0001t0001g0073a0001c0001t0001g0074others(4): Show | 8 | HG00323.hp1 HG01169.hp2 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.13+407dupA | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 2/9 | chr7 | 121382549 | ||||||
chr7:121382549
|
GT | G | 70 | a0001c0001t0001g0007a0001c0001t0001g0029a0001c0001t0001g0051others(67): Show | 82 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.13+407delA | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 2/9 | chr7 | 121382549 | ||||||
chr7:121382549
|
GTT | G | 62 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0020others(59): Show | 82 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.13+406_13+407delAA | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 2/9 | chr7 | 121382549 | ||||||
chr7:121382567
|
T | C | 1 | a0001c0001t0001g0173 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.13+390A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 2/9 | chr7 | 121382567 | ||||||
chr7:121382767
|
A | C | 1 | a0001c0001t0003g0200 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.13+190T>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 2/9 | chr7 | 121382767 | ||||||
chr7:121382889
|
T | C | 3 | a0001c0001t0001g0043a0001c0001t0001g0176a0001c0001t0001g0177 | 3 | HG01099.hp2 HG01261.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.13+68A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 2/9 | chr7 | 121382889 | ||||||
chr7:121383142
|
TA | T | 47 | a0001c0001t0001g0135a0001c0001t0001g0163a0001c0001t0002g0209others(44): Show | 54 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.-41-133delT | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121383142 | ||||||
chr7:121383415
|
C | T | 39 | a0001c0001t0002g0209a0001c0001t0003g0019a0001c0001t0003g0028others(36): Show | 43 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.-41-405G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121383415 | ||||||
chr7:121383507
|
A | G | 39 | a0001c0001t0002g0209a0001c0001t0003g0019a0001c0001t0003g0028others(36): Show | 43 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.-41-497T>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121383507 | ||||||
chr7:121383520
|
G | A | 2 | a0001c0001t0001g0016a0001c0001t0001g0105 | 3 | HG01358.hp1 HG02148.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.-41-510C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121383520 | ||||||
chr7:121383530
|
C | T | 1 | a0001c0001t0001g0085 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-41-520G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121383530 | ||||||
chr7:121383577
|
T | C | 1 | a0001c0001t0001g0059 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-41-567A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121383577 | ||||||
chr7:121383724
|
T | C | 17 | a0001c0001t0004g0010a0001c0001t0004g0011a0001c0001t0004g0031others(14): Show | 19 | HG00140.hp1 HG00280.hp2 HG00639.hp2 others(16): Show |
intron_variant | MODIFIER | c.-41-714A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121383724 | ||||||
chr7:121383904
|
G | C | 1 | a0001c0001t0001g0094 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.-41-894C>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121383904 | ||||||
chr7:121384166
|
A | G | 1 | a0001c0001t0001g0185 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-41-1156T>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121384166 | ||||||
chr7:121384257
|
G | A | 1 | a0001c0001t0001g0097 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-41-1247C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121384257 | ||||||
chr7:121384473
|
T | A | 41 | a0001c0001t0002g0054a0001c0001t0002g0055a0001c0001t0002g0209others(38): Show | 45 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(42): Show |
intron_variant | MODIFIER | c.-41-1463A>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121384473 | ||||||
chr7:121384573
|
T | C | 5 | a0001c0001t0001g0007a0001c0001t0001g0029a0001c0001t0001g0061others(2): Show | 8 | HG02055.hp1 HG02647.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.-41-1563A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121384573 | ||||||
chr7:121384654
|
G | A | 39 | a0001c0001t0002g0209a0001c0001t0003g0019a0001c0001t0003g0028others(36): Show | 43 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.-41-1644C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121384654 | ||||||
chr7:121384808
|
A | T | 1 | a0001c0001t0001g0119 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-41-1798T>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121384808 | ||||||
chr7:121384817
|
C | G | 1 | a0001c0001t0001g0119 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-41-1807G>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121384817 | ||||||
chr7:121384818
|
C | A | 1 | a0001c0001t0001g0119 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-41-1808G>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121384818 | ||||||
chr7:121384826
|
G | T | 1 | a0001c0001t0001g0119 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-41-1816C>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121384826 | ||||||
chr7:121384827
|
C | T | 1 | a0001c0001t0001g0119 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-41-1817G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121384827 | ||||||
chr7:121384829
|
A | C | 1 | a0001c0001t0001g0119 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-41-1819T>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121384829 | ||||||
chr7:121384835
|
T | G | 1 | a0001c0001t0001g0119 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-41-1825A>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121384835 | ||||||
chr7:121384840
|
C | G | 1 | a0001c0001t0001g0119 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-41-1830G>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121384840 | ||||||
chr7:121384845
|
A | T | 1 | a0001c0001t0001g0119 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-41-1835T>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121384845 | ||||||
chr7:121384846
|
T | G | 2 | a0001c0001t0002g0054a0001c0001t0002g0055 | 2 | HG02809.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-41-1836A>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121384846 | ||||||
chr7:121384847
|
C | G | 1 | a0001c0001t0001g0119 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-41-1837G>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121384847 | ||||||
chr7:121384849
|
A | G | 1 | a0001c0001t0001g0119 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-41-1839T>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121384849 | ||||||
chr7:121384850
|
C | A | 1 | a0001c0001t0001g0119 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-41-1840G>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121384850 | ||||||
chr7:121384853
|
C | A | 1 | a0001c0001t0001g0119 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-41-1843G>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121384853 | ||||||
chr7:121384854
|
A | T | 1 | a0001c0001t0001g0119 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-41-1844T>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121384854 | ||||||
chr7:121384855
|
G | T | 1 | a0001c0001t0001g0119 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-41-1845C>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121384855 | ||||||
chr7:121384856
|
G | T | 1 | a0001c0001t0001g0119 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-41-1846C>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121384856 | ||||||
chr7:121384857
|
A | T | 1 | a0001c0001t0001g0119 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-41-1847T>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121384857 | ||||||
chr7:121384859
|
A | G | 1 | a0001c0001t0001g0119 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-41-1849T>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121384859 | ||||||
chr7:121384860
|
G | A | 1 | a0001c0001t0001g0119 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-41-1850C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121384860 | ||||||
chr7:121384865
|
A | T | 1 | a0001c0001t0001g0119 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-41-1855T>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121384865 | ||||||
chr7:121384866
|
T | A | 1 | a0001c0001t0001g0119 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-41-1856A>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121384866 | ||||||
chr7:121384872
|
A | C | 1 | a0001c0001t0001g0119 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-41-1862T>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121384872 | ||||||
chr7:121384884
|
A | T | 1 | a0001c0001t0001g0119 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-41-1874T>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121384884 | ||||||
chr7:121384888
|
C | T | 1 | a0001c0001t0001g0119 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-41-1878G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121384888 | ||||||
chr7:121384891
|
G | A | 1 | a0001c0001t0001g0119 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-41-1881C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121384891 | ||||||
chr7:121384894
|
G | T | 1 | a0001c0001t0001g0119 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-41-1884C>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121384894 | ||||||
chr7:121384895
|
C | A | 1 | a0001c0001t0001g0119 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-41-1885G>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121384895 | ||||||
chr7:121384896
|
A | T | 1 | a0001c0001t0001g0119 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-41-1886T>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121384896 | ||||||
chr7:121384966
|
G | A | 1 | a0001c0001t0001g0088 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-41-1956C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121384966 | ||||||
chr7:121385032
|
C | T | 1 | a0001c0001t0001g0212 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-41-2022G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121385032 | ||||||
chr7:121385093
|
T | C | 1 | a0001c0001t0001g0174 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-41-2083A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121385093 | ||||||
chr7:121385162
|
C | T | 1 | a0001c0001t0001g0081 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-41-2152G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121385162 | ||||||
chr7:121385241
|
A | G | 39 | a0001c0001t0002g0209a0001c0001t0003g0019a0001c0001t0003g0028others(36): Show | 43 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.-41-2231T>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121385241 | ||||||
chr7:121385304
|
C | T | 2 | a0001c0001t0002g0137a0001c0001t0002g0138 | 2 | HG02922.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-41-2294G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121385304 | ||||||
chr7:121385330
|
T | C | 1 | a0001c0001t0001g0190 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-41-2320A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121385330 | ||||||
chr7:121385448
|
T | C | 64 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0020others(61): Show | 84 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.-41-2438A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121385448 | ||||||
chr7:121385523
|
A | C | 42 | a0001c0001t0001g0118a0001c0001t0002g0054a0001c0001t0002g0055others(39): Show | 46 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(43): Show |
intron_variant | MODIFIER | c.-41-2513T>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121385523 | ||||||
chr7:121385825
|
G | A | 5 | a0001c0001t0001g0007a0001c0001t0001g0029a0001c0001t0001g0061others(2): Show | 8 | HG02055.hp1 HG02647.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.-41-2815C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121385825 | ||||||
chr7:121385962
|
G | A | 3 | a0001c0001t0002g0069a0001c0001t0002g0070a0001c0001t0002g0071 | 3 | HG02976.hp1 HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-41-2952C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121385962 | ||||||
chr7:121386023
|
G | A | 1 | a0001c0001t0008g0218 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-41-3013C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121386023 | ||||||
chr7:121386043
|
T | C | 6 | a0001c0001t0005g0004a0001c0001t0005g0217a0001c0001t0005g0221others(3): Show | 9 | HG01891.hp2 HG02615.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.-41-3033A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121386043 | ||||||
chr7:121386067
|
A | G | 1 | a0001c0001t0001g0050 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-41-3057T>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121386067 | ||||||
chr7:121386435
|
T | C | 2 | a0001c0001t0002g0054a0001c0001t0002g0055 | 2 | HG02809.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-41-3425A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121386435 | ||||||
chr7:121386469
|
T | C | 1 | a0001c0001t0001g0185 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-41-3459A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121386469 | ||||||
chr7:121386569
|
C | A | 2 | a0001c0001t0001g0056a0001c0001t0001g0057 | 2 | HG02055.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.-41-3559G>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121386569 | ||||||
chr7:121386579
|
C | T | 2 | a0001c0001t0002g0054a0001c0001t0002g0055 | 2 | HG02809.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-41-3569G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121386579 | ||||||
chr7:121386664
|
T | C | 1 | a0001c0001t0009g0089 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-41-3654A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121386664 | ||||||
chr7:121386687
|
G | A | 1 | a0001c0001t0001g0187 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-41-3677C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121386687 | ||||||
chr7:121386687
|
G | GCA | 3 | a0001c0001t0002g0069a0001c0001t0002g0070a0001c0001t0002g0071 | 3 | HG02976.hp1 HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-41-3679_-41-3678d others(4): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121386687 | ||||||
chr7:121386689
|
A | G | 1 | a0001c0001t0001g0187 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-41-3679T>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121386689 | ||||||
chr7:121386692
|
C | CAT | 5 | a0001c0001t0001g0072a0001c0001t0001g0097a0001c0001t0002g0194others(2): Show | 5 | HG02280.hp1 HG03579.hp1 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.-41-3684_-41-3683d others(4): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121386692 | ||||||
chr7:121386692
|
CAT | C | 76 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0020others(73): Show | 98 | HG00323.hp2 HG00438.hp2 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.-41-3684_-41-3683d others(4): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121386692 | ||||||
chr7:121386694
|
T | C | 2 | a0001c0001t0001g0029a0001c0001t0001g0187 | 3 | HG00280.hp1 HG02647.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.-41-3684A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121386694 | ||||||
chr7:121386696
|
T | C | 1 | a0001c0001t0001g0175 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-41-3686A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121386696 | ||||||
chr7:121386920
|
T | A | 1 | a0001c0001t0002g0194 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-41-3910A>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121386920 | ||||||
chr7:121387026
|
C | T | 1 | a0001c0001t0001g0015 | 2 | HG01433.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-41-4016G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121387026 | ||||||
chr7:121387107
|
G | A | 2 | a0001c0001t0002g0054a0001c0001t0002g0055 | 2 | HG02809.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-41-4097C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121387107 | ||||||
chr7:121387380
|
C | T | 48 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0020others(45): Show | 65 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.-41-4370G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121387380 | ||||||
chr7:121387388
|
A | T | 2 | a0001c0001t0002g0054a0001c0001t0002g0055 | 2 | HG02809.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-41-4378T>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121387388 | ||||||
chr7:121387442
|
G | A | 1 | a0001c0001t0001g0163 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-41-4432C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121387442 | ||||||
chr7:121387836
|
G | A | 19 | a0001c0001t0003g0019a0001c0001t0003g0028a0001c0001t0003g0143others(16): Show | 21 | HG00438.hp2 HG00544.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.-41-4826C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121387836 | ||||||
chr7:121388235
|
A | AAC | 90 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(87): Show | 107 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.-41-5227_-41-5226d others(4): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121388235 | ||||||
chr7:121388235
|
A | AACAC | 9 | a0001c0001t0001g0063a0001c0001t0001g0096a0001c0001t0001g0117others(6): Show | 9 | HG00438.hp1 HG01496.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.-41-5229_-41-5226d others(6): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121388235 | ||||||
chr7:121388235
|
A | AACACAC | 61 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0020others(58): Show | 81 | HG00323.hp2 HG00558.hp1 HG00621.hp2 others(78): Show |
intron_variant | MODIFIER | c.-41-5231_-41-5226d others(8): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121388235 | ||||||
chr7:121388235
|
A | AACACACA others(1): Show |
22 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0001g0166others(19): Show | 25 | HG00140.hp1 HG00280.hp2 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.-41-5233_-41-5226d others(10): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121388235 | ||||||
chr7:121388235
|
A | AACACACA others(3): Show |
8 | a0001c0001t0001g0061a0001c0001t0004g0031a0001c0001t0004g0032others(5): Show | 11 | HG00639.hp2 HG00738.hp1 HG01106.hp2 others(8): Show |
intron_variant | MODIFIER | c.-41-5235_-41-5226d others(12): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121388235 | ||||||
chr7:121388235
|
A | AACACACA others(5): Show |
7 | a0001c0001t0001g0007a0001c0001t0001g0029a0001c0001t0001g0210others(4): Show | 10 | HG01891.hp2 HG02055.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.-41-5237_-41-5226d others(14): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121388235 | ||||||
chr7:121388235
|
AAC | A | 2 | a0001c0001t0001g0059a0001c0001t0001g0108 | 2 | NA18969.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.-41-5227_-41-5226d others(4): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121388235 | ||||||
chr7:121388286
|
C | T | 122 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(119): Show | 151 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.-41-5276G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121388286 | ||||||
chr7:121388398
|
G | A | 19 | a0001c0001t0004g0010a0001c0001t0004g0011a0001c0001t0004g0031others(16): Show | 21 | HG00140.hp1 HG00280.hp2 HG00639.hp2 others(18): Show |
intron_variant | MODIFIER | c.-41-5388C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121388398 | ||||||
chr7:121388434
|
G | A | 1 | a0001c0001t0001g0130 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.-41-5424C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121388434 | ||||||
chr7:121388623
|
T | C | 2 | a0001c0001t0002g0131a0001c0001t0002g0209 | 2 | HG02109.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.-41-5613A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121388623 | ||||||
chr7:121388934
|
T | C | 2 | a0001c0001t0002g0054a0001c0001t0002g0055 | 2 | HG02809.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-41-5924A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121388934 | ||||||
chr7:121389017
|
T | C | 2 | a0001c0001t0004g0032a0001c0001t0004g0033 | 2 | HG00738.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.-41-6007A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121389017 | ||||||
chr7:121389157
|
A | G | 1 | a0001c0001t0001g0165 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-41-6147T>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121389157 | ||||||
chr7:121389504
|
C | T | 1 | a0001c0001t0003g0205 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-41-6494G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121389504 | ||||||
chr7:121389751
|
C | G | 1 | a0001c0001t0004g0197 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-42+6411G>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121389751 | ||||||
chr7:121389762
|
C | CA | 14 | a0001c0001t0001g0067a0001c0001t0001g0132a0001c0001t0003g0028others(11): Show | 15 | HG00438.hp2 HG00544.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.-42+6399dupT | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121389762 | ||||||
chr7:121390063
|
T | C | 2 | a0001c0001t0002g0054a0001c0001t0002g0055 | 2 | HG02809.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-42+6099A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121390063 | ||||||
chr7:121390209
|
T | C | 2 | a0001c0001t0002g0137a0001c0001t0002g0138 | 2 | HG02922.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-42+5953A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121390209 | ||||||
chr7:121390260
|
C | A | 3 | a0001c0001t0002g0069a0001c0001t0002g0070a0001c0001t0002g0071 | 3 | HG02976.hp1 HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-42+5902G>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121390260 | ||||||
chr7:121390513
|
C | A | 4 | a0001c0001t0001g0046a0001c0001t0001g0095a0001c0001t0001g0109others(1): Show | 4 | HG00673.hp1 NA18968.hp1 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.-42+5649G>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121390513 | ||||||
chr7:121390692
|
C | T | 1 | a0001c0001t0015g0116 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-42+5470G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121390692 | ||||||
chr7:121390784
|
C | T | 1 | a0001c0001t0003g0205 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-42+5378G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121390784 | ||||||
chr7:121390813
|
C | T | 1 | a0001c0001t0001g0210 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-42+5349G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121390813 | ||||||
chr7:121390848
|
T | G | 1 | a0001c0001t0001g0184 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.-42+5314A>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121390848 | ||||||
chr7:121390850
|
G | GGGT | 2 | a0001c0001t0001g0027a0001c0001t0001g0188 | 3 | HG02647.hp1 HG02698.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-42+5311_-42+5312i others(5): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121390850 | ||||||
chr7:121390851
|
G | GGT | 6 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0185others(3): Show | 8 | HG00280.hp1 HG00323.hp2 HG01256.hp2 others(5): Show |
intron_variant | MODIFIER | c.-42+5310_-42+5311i others(4): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121390851 | ||||||
chr7:121390852
|
G | GT | 10 | a0001c0001t0001g0043a0001c0001t0001g0066a0001c0001t0001g0178others(7): Show | 10 | HG00735.hp1 HG01099.hp2 HG01978.hp1 others(7): Show |
intron_variant | MODIFIER | c.-42+5309_-42+5310i others(3): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121390852 | ||||||
chr7:121390852
|
G | T | 1 | a0001c0001t0001g0184 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.-42+5310C>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121390852 | ||||||
chr7:121390852
|
GC | G | 11 | a0001c0001t0001g0020a0001c0001t0001g0150a0001c0001t0001g0156others(8): Show | 12 | HG00738.hp2 HG01069.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.-42+5309delG | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121390852 | ||||||
chr7:121390853
|
C | CGG | 19 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0060others(16): Show | 22 | HG00438.hp2 HG00544.hp2 HG00621.hp1 others(19): Show |
intron_variant | MODIFIER | c.-42+5307_-42+5308d others(4): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121390853 | ||||||
chr7:121390853
|
C | CGGG | 22 | a0001c0001t0001g0009a0001c0001t0001g0063a0001c0001t0001g0096others(19): Show | 24 | HG00558.hp2 HG00738.hp1 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.-42+5306_-42+5308d others(5): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121390853 | ||||||
chr7:121390853
|
C | CGGGG | 25 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0030others(22): Show | 30 | HG00140.hp2 HG00544.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.-42+5305_-42+5308d others(6): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121390853 | ||||||
chr7:121390853
|
C | CGGGGG | 18 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0059others(15): Show | 21 | HG00323.hp1 HG00642.hp1 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.-42+5304_-42+5308d others(7): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121390853 | ||||||
chr7:121390853
|
C | CGGGGGGG others(3): Show |
2 | a0001c0001t0001g0067a0001c0001t0003g0200 | 2 | HG03710.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.-42+5299_-42+5308d others(12): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121390853 | ||||||
chr7:121390853
|
C | CGGGGGGG others(4): Show |
1 | a0001c0001t0002g0142 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-42+5298_-42+5308d others(13): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121390853 | ||||||
chr7:121390853
|
C | CGGGGGGG others(5): Show |
1 | a0001c0001t0002g0191 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-42+5297_-42+5308d others(14): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121390853 | ||||||
chr7:121390853
|
C | CGGGGGGG others(9): Show |
1 | a0001c0001t0001g0065 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.-42+5293_-42+5308d others(18): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121390853 | ||||||
chr7:121390853
|
C | G | 21 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(18): Show | 24 | HG00280.hp1 HG00323.hp2 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.-42+5309G>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121390853 | ||||||
chr7:121390853
|
C | T | 25 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0021others(22): Show | 41 | HG00558.hp1 HG00621.hp2 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.-42+5309G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121390853 | ||||||
chr7:121390854
|
G | T | 11 | a0001c0001t0001g0020a0001c0001t0001g0150a0001c0001t0001g0156others(8): Show | 12 | HG00738.hp2 HG01069.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.-42+5308C>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121390854 | ||||||
chr7:121390855
|
G | T | 6 | a0001c0001t0001g0135a0001c0001t0001g0151a0001c0001t0001g0152others(3): Show | 6 | HG02135.hp2 HG03225.hp1 NA18988.hp1 others(3): Show |
intron_variant | MODIFIER | c.-42+5307C>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121390855 | ||||||
chr7:121390860
|
G | C | 3 | a0001c0001t0001g0007a0001c0001t0001g0029a0001c0001t0001g0210 | 6 | HG02055.hp1 HG02647.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.-42+5302C>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121390860 | ||||||
chr7:121390864
|
G | A | 1 | a0001c0001t0001g0198 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-42+5298C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121390864 | ||||||
chr7:121390865
|
G | T | 14 | a0001c0001t0001g0061a0001c0001t0002g0044a0001c0001t0002g0069others(11): Show | 17 | HG01891.hp2 HG02280.hp1 HG02615.hp1 others(14): Show |
intron_variant | MODIFIER | c.-42+5297C>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121390865 | ||||||
chr7:121390866
|
G | GAGC | 3 | a0001c0001t0001g0007a0001c0001t0001g0029a0001c0001t0001g0210 | 6 | HG02055.hp1 HG02647.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.-42+5295_-42+5296i others(5): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121390866 | ||||||
chr7:121390880
|
G | A | 1 | a0001c0001t0001g0061 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-42+5282C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121390880 | ||||||
chr7:121391571
|
G | A | 3 | a0001c0001t0001g0053a0001c0001t0002g0054a0001c0001t0002g0055 | 3 | HG02486.hp2 HG02809.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-42+4591C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121391571 | ||||||
chr7:121391825
|
C | T | 125 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(122): Show | 154 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.-42+4337G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121391825 | ||||||
chr7:121391895
|
A | T | 3 | a0001c0001t0001g0053a0001c0001t0002g0054a0001c0001t0002g0055 | 3 | HG02486.hp2 HG02809.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-42+4267T>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121391895 | ||||||
chr7:121391950
|
T | C | 3 | a0001c0001t0001g0053a0001c0001t0002g0054a0001c0001t0002g0055 | 3 | HG02486.hp2 HG02809.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-42+4212A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121391950 | ||||||
chr7:121391958
|
A | G | 2 | a0001c0001t0001g0067a0001c0001t0001g0068 | 2 | HG00639.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.-42+4204T>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121391958 | ||||||
chr7:121392218
|
C | T | 1 | a0001c0001t0001g0059 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-42+3944G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121392218 | ||||||
chr7:121392566
|
G | GT | 6 | a0001c0001t0002g0017a0001c0001t0002g0018a0001c0001t0002g0045others(3): Show | 8 | HG01074.hp2 HG01192.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.-42+3595dupA | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121392566 | ||||||
chr7:121392799
|
C | T | 4 | a0001c0001t0001g0053a0001c0001t0001g0150a0001c0001t0002g0054others(1): Show | 4 | HG02486.hp2 HG02809.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.-42+3363G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121392799 | ||||||
chr7:121393008
|
G | T | 1 | a0001c0001t0001g0065 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.-42+3154C>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121393008 | ||||||
chr7:121393009
|
G | C | 1 | a0001c0001t0002g0194 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-42+3153C>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121393009 | ||||||
chr7:121393067
|
T | C | 64 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0020others(61): Show | 84 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.-42+3095A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121393067 | ||||||
chr7:121393137
|
A | G | 121 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(118): Show | 150 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.-42+3025T>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121393137 | ||||||
chr7:121393147
|
T | C | 4 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0002g0191others(1): Show | 4 | HG02055.hp2 HG02965.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-42+3015A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121393147 | ||||||
chr7:121393362
|
G | T | 1 | a0001c0001t0003g0199 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-42+2800C>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121393362 | ||||||
chr7:121393542
|
C | T | 3 | a0001c0001t0001g0053a0001c0001t0002g0054a0001c0001t0002g0055 | 3 | HG02486.hp2 HG02809.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-42+2620G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121393542 | ||||||
chr7:121393614
|
A | T | 1 | a0001c0001t0001g0065 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.-42+2548T>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121393614 | ||||||
chr7:121393626
|
A | G | 1 | a0001c0001t0001g0053 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-42+2536T>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121393626 | ||||||
chr7:121393709
|
C | T | 2 | a0001c0001t0002g0137a0001c0001t0002g0138 | 2 | HG02922.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-42+2453G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121393709 | ||||||
chr7:121393795
|
T | G | 1 | a0001c0001t0001g0193 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-42+2367A>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121393795 | ||||||
chr7:121393854
|
T | C | 1 | a0001c0001t0002g0194 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-42+2308A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121393854 | ||||||
chr7:121394114
|
G | C | 1 | a0001c0001t0016g0195 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-42+2048C>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121394114 | ||||||
chr7:121394198
|
T | C | 3 | a0001c0001t0001g0053a0001c0001t0002g0054a0001c0001t0002g0055 | 3 | HG02486.hp2 HG02809.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-42+1964A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121394198 | ||||||
chr7:121394204
|
C | T | 4 | a0001c0001t0001g0007a0001c0001t0001g0029a0001c0001t0001g0198others(1): Show | 7 | HG02055.hp1 HG02647.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.-42+1958G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121394204 | ||||||
chr7:121394213
|
T | C | 1 | a0001c0001t0001g0133 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-42+1949A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121394213 | ||||||
chr7:121394537
|
T | C | 1 | a0001c0001t0005g0221 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-42+1625A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121394537 | ||||||
chr7:121394629
|
G | A | 3 | a0001c0001t0001g0053a0001c0001t0002g0054a0001c0001t0002g0055 | 3 | HG02486.hp2 HG02809.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-42+1533C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121394629 | ||||||
chr7:121394740
|
C | T | 3 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0006g0064 | 3 | NA18988.hp2 NA19065.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.-42+1422G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121394740 | ||||||
chr7:121394975
|
G | A | 2 | a0001c0001t0002g0054a0001c0001t0002g0055 | 2 | HG02809.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-42+1187C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121394975 | ||||||
chr7:121394987
|
G | A | 2 | a0001c0001t0001g0196a0001c0001t0004g0197 | 2 | HG00280.hp2 HG00323.hp2 |
intron_variant | MODIFIER | c.-42+1175C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121394987 | ||||||
chr7:121395029
|
T | A | 3 | a0001c0001t0001g0053a0001c0001t0002g0054a0001c0001t0002g0055 | 3 | HG02486.hp2 HG02809.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-42+1133A>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121395029 | ||||||
chr7:121395195
|
A | G | 1 | a0001c0001t0001g0136 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-42+967T>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121395195 | ||||||
chr7:121395204
|
T | G | 3 | a0001c0001t0001g0053a0001c0001t0002g0054a0001c0001t0002g0055 | 3 | HG02486.hp2 HG02809.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-42+958A>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121395204 | ||||||
chr7:121395210
|
CGGATACA others(33): Show |
C | 1 | a0001c0001t0001g0134 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-42+912_-42+951del others(40): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121395210 | ||||||
chr7:121395225
|
A | C | 1 | a0001c0001t0001g0135 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-42+937T>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121395225 | ||||||
chr7:121395234
|
C | CATACATA others(29): Show |
3 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061 | 3 | NA18948.hp2 NA19002.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-42+892_-42+927dup others(36): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121395234 | ||||||
chr7:121395234
|
CATACATA others(11): Show |
C | 113 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0020others(110): Show | 139 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.-42+910_-42+927del others(18): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121395234 | ||||||
chr7:121395234
|
CATACATA others(29): Show |
C | 7 | a0001c0001t0001g0007a0001c0001t0001g0029a0001c0001t0001g0053others(4): Show | 10 | HG02055.hp1 HG02486.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.-42+892_-42+927del others(36): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121395234 | ||||||
chr7:121395296
|
C | CATATATA others(73): Show |
1 | a0001c0001t0017g0058 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-42+865_-42+866ins others(80): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121395296 | ||||||
chr7:121395300
|
T | C | 2 | a0001c0001t0001g0056a0001c0001t0001g0057 | 2 | HG02055.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.-42+862A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121395300 | ||||||
chr7:121395302
|
TATGGATA others(9): Show |
T | 2 | a0001c0001t0001g0056a0001c0001t0001g0057 | 2 | HG02055.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.-42+844_-42+859del others(16): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121395302 | ||||||
chr7:121395464
|
T | TA | 11 | a0001c0001t0003g0028a0001c0001t0003g0199a0001c0001t0003g0200others(8): Show | 12 | HG00438.hp2 HG00544.hp2 HG02602.hp2 others(9): Show |
intron_variant | MODIFIER | c.-42+697dupT | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121395464 | ||||||
chr7:121395464
|
TA | T | 9 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0050others(6): Show | 9 | HG00558.hp2 HG01943.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.-42+697delT | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121395464 | ||||||
chr7:121395660
|
C | T | 1 | a0001c0001t0001g0046 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-42+502G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121395660 | ||||||
chr7:121395671
|
G | A | 1 | a0001c0001t0002g0209 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-42+491C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121395671 | ||||||
chr7:121395717
|
C | G | 1 | a0001c0001t0002g0045 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-42+445G>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121395717 | ||||||
chr7:121395753
|
G | A | 3 | a0001c0001t0001g0007a0001c0001t0001g0029a0001c0001t0001g0210 | 6 | HG02055.hp1 HG02647.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.-42+409C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121395753 | ||||||
chr7:121395821
|
C | G | 1 | a0001c0001t0002g0044 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-42+341G>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121395821 | ||||||
chr7:121395881
|
C | A | 1 | a0001c0001t0005g0222 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-42+281G>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121395881 | ||||||
chr7:121395925
|
C | T | 1 | a0001c0001t0001g0043 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-42+237G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121395925 | ||||||
chr7:121396050
|
G | T | 16 | a0001c0001t0004g0010a0001c0001t0004g0011a0001c0001t0004g0031others(13): Show | 18 | HG00140.hp1 HG00639.hp2 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.-42+112C>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121396050 | ||||||
chr7:121396063
|
G | T | 3 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0030 | 5 | HG00735.hp2 HG01346.hp1 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.-42+99C>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121396063 | ||||||
chr7:121396082
|
G | A | 1 | a0001c0001t0004g0211 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-42+80C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121396082 | ||||||
chr7:121396112
|
T | A | 3 | a0001c0001t0001g0212a0001c0001t0001g0213a0001c0001t0001g0214 | 3 | HG01884.hp1 HG01978.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.-42+50A>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121396112 |