geneid | 54097 |
---|---|
ensemblid | ENSG00000183844.17 |
hgncid | 1253 |
symbol | FAM3B |
name | FAM3 metabolism regulating signaling molecule B |
refseq_nuc | NM_058186.4 |
refseq_prot | NP_478066.3 |
ensembl_nuc | ENST00000357985.7 |
ensembl_prot | ENSP00000350673.2 |
mane_status | MANE Select |
chr | chr21 |
start | 41316801 |
end | 41357727 |
strand | + |
ver | v1.2 |
region | chr21:41316801-41357727 |
region5000 | chr21:41311801-41362727 |
regionname0 | FAM3B_chr21_41316801_41357727 |
regionname5000 | FAM3B_chr21_41311801_41362727 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 235 | 266 | 64 | 60 | 92 | 13 | 35 | 64 | FAM3B_chr21_41311801_41362727 | FAM3B | copy fasta | chr21 | 41311801 | 41362727 |
a0002 | 0/0 | 235 | 27 | 21 | 4 | 1 | 0 | 1 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | copy fasta | chr21 | 41311801 | 41362727 |
a0003 | 0/0 | 235 | 18 | 5 | 1 | 11 | 1 | 0 | 8 | FAM3B_chr21_41311801_41362727 | FAM3B | copy fasta | chr21 | 41311801 | 41362727 |
a0004 | 0/0 | 235 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | FAM3B_chr21_41311801_41362727 | FAM3B | copy fasta | chr21 | 41311801 | 41362727 |
a0005 | 0/0 | 136 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | copy fasta | chr21 | 41311801 | 41362727 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 708 | 220 | 61 | 44 | 74 | 11 | 30 | FAM3B_chr21_41311801_41362727 | FAM3B | copy fasta | chr21 | 41311801 | 41362727 |
c0002 | 1/1 | 708 | 41 | 0 | 15 | 18 | 2 | 4 | FAM3B_chr21_41311801_41362727 | FAM3B | copy fasta | chr21 | 41311801 | 41362727 |
c0003 | 0/0 | 708 | 27 | 21 | 4 | 1 | 0 | 1 | FAM3B_chr21_41311801_41362727 | FAM3B | copy fasta | chr21 | 41311801 | 41362727 |
c0004 | 0/0 | 708 | 18 | 5 | 1 | 11 | 1 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | copy fasta | chr21 | 41311801 | 41362727 |
c0005 | 0/0 | 708 | 4 | 3 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | copy fasta | chr21 | 41311801 | 41362727 |
c0006 | 0/0 | 708 | 2 | 0 | 0 | 2 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | copy fasta | chr21 | 41311801 | 41362727 |
c0007 | 0/0 | 708 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3B_chr21_41311801_41362727 | FAM3B | copy fasta | chr21 | 41311801 | 41362727 |
c0008 | 0/0 | 487 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | copy fasta | chr21 | 41311801 | 41362727 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 610 | 241 | 39 | 58 | 100 | 11 | 31 | FAM3B_chr21_41311801_41362727 | FAM3B | copy fasta | chr21 | 41311801 | 41362727 |
t0002 | 0/0 | 610 | 65 | 44 | 8 | 5 | 3 | 5 | FAM3B_chr21_41311801_41362727 | FAM3B | copy fasta | chr21 | 41311801 | 41362727 |
t0003 | 0/0 | 610 | 3 | 3 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | copy fasta | chr21 | 41311801 | 41362727 |
t0004 | 0/0 | 610 | 2 | 2 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | copy fasta | chr21 | 41311801 | 41362727 |
t0005 | 0/0 | 610 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | copy fasta | chr21 | 41311801 | 41362727 |
t0006 | 0/0 | 610 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | copy fasta | chr21 | 41311801 | 41362727 |
t0007 | 0/0 | 610 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | copy fasta | chr21 | 41311801 | 41362727 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 8 | 0 | 2 | 4 | 1 | 1 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0002 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0003 | 0/0 | 4 | 1 | 2 | 0 | 1 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0006 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0009 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0010 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0013 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0017 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0018 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0021 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0022 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0024 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0025 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0030 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0180 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0262 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 708 | 220 | 61 | 44 | 74 | 11 | 30 | FAM3B_chr21_41311801_41362727 | FAM3B | copy fasta | chr21 | 41311801 | 41362727 |
a0001c0002 | 1/1 | 708 | 41 | 0 | 15 | 18 | 2 | 4 | FAM3B_chr21_41311801_41362727 | FAM3B | copy fasta | chr21 | 41311801 | 41362727 |
a0001c0005 | 0/0 | 708 | 4 | 3 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | copy fasta | chr21 | 41311801 | 41362727 |
a0001c0007 | 0/0 | 708 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3B_chr21_41311801_41362727 | FAM3B | copy fasta | chr21 | 41311801 | 41362727 |
a0002c0003 | 0/0 | 708 | 27 | 21 | 4 | 1 | 0 | 1 | FAM3B_chr21_41311801_41362727 | FAM3B | copy fasta | chr21 | 41311801 | 41362727 |
a0003c0004 | 0/0 | 708 | 18 | 5 | 1 | 11 | 1 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | copy fasta | chr21 | 41311801 | 41362727 |
a0004c0006 | 0/0 | 708 | 2 | 0 | 0 | 2 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | copy fasta | chr21 | 41311801 | 41362727 |
a0005c0008 | 0/0 | 487 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | copy fasta | chr21 | 41311801 | 41362727 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 1317 | 174 | 28 | 39 | 73 | 9 | 25 | FAM3B_chr21_41311801_41362727 | FAM3B | copy fasta | chr21 | 41311801 | 41362727 |
a0001c0001t0002 | 0/0 | 1317 | 41 | 28 | 5 | 1 | 2 | 5 | FAM3B_chr21_41311801_41362727 | FAM3B | copy fasta | chr21 | 41311801 | 41362727 |
a0001c0001t0003 | 0/0 | 1317 | 3 | 3 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | copy fasta | chr21 | 41311801 | 41362727 |
a0001c0001t0004 | 0/0 | 1317 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | copy fasta | chr21 | 41311801 | 41362727 |
a0001c0001t0005 | 0/0 | 1317 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | copy fasta | chr21 | 41311801 | 41362727 |
a0001c0002t0001 | 1/1 | 1317 | 41 | 0 | 15 | 18 | 2 | 4 | FAM3B_chr21_41311801_41362727 | FAM3B | copy fasta | chr21 | 41311801 | 41362727 |
a0001c0005t0001 | 0/0 | 1317 | 2 | 1 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | copy fasta | chr21 | 41311801 | 41362727 |
a0001c0005t0002 | 0/0 | 1317 | 2 | 2 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | copy fasta | chr21 | 41311801 | 41362727 |
a0001c0007t0001 | 0/0 | 1317 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3B_chr21_41311801_41362727 | FAM3B | copy fasta | chr21 | 41311801 | 41362727 |
a0002c0003t0001 | 0/0 | 1317 | 13 | 9 | 2 | 1 | 0 | 1 | FAM3B_chr21_41311801_41362727 | FAM3B | copy fasta | chr21 | 41311801 | 41362727 |
a0002c0003t0002 | 0/0 | 1317 | 12 | 10 | 2 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | copy fasta | chr21 | 41311801 | 41362727 |
a0002c0003t0004 | 0/0 | 1317 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | copy fasta | chr21 | 41311801 | 41362727 |
a0002c0003t0007 | 0/0 | 1317 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | copy fasta | chr21 | 41311801 | 41362727 |
a0003c0004t0001 | 0/0 | 1317 | 7 | 1 | 0 | 6 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | copy fasta | chr21 | 41311801 | 41362727 |
a0003c0004t0002 | 0/0 | 1317 | 10 | 4 | 1 | 4 | 1 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | copy fasta | chr21 | 41311801 | 41362727 |
a0003c0004t0006 | 0/0 | 1317 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | copy fasta | chr21 | 41311801 | 41362727 |
a0004c0006t0001 | 0/0 | 1317 | 2 | 0 | 0 | 2 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | copy fasta | chr21 | 41311801 | 41362727 |
a0005c0008t0001 | 0/0 | 1096 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | copy fasta | chr21 | 41311801 | 41362727 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 8 | 0 | 2 | 4 | 1 | 1 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0002 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0003 | 0/0 | 4 | 1 | 2 | 0 | 1 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0009 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0010 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0002g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0002g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0002g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0002g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0002g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0002g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0002g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0002g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0003g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0003g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0003g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0004g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0001t0005g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0002t0001g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0002t0001g0006 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0002t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0002t0001g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0002t0001g0030 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0002t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0002t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0002t0001g0180 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0002t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0002t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0002t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0002t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0002t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0002t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0002t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0002t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0002t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0002t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0002t0001g0262 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0005t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0005t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0005t0002g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0005t0002g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0001c0007t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0002c0003t0001g0013 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0002c0003t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0002c0003t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0002c0003t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0002c0003t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0002c0003t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0002c0003t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0002c0003t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0002c0003t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0002c0003t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0002c0003t0002g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0002c0003t0002g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0002c0003t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0002c0003t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0002c0003t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0002c0003t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0002c0003t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0002c0003t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0002c0003t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0002c0003t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0002c0003t0004g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0002c0003t0007g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0003c0004t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0003c0004t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0003c0004t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0003c0004t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0003c0004t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0003c0004t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0003c0004t0002g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0003c0004t0002g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0003c0004t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0003c0004t0002g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0003c0004t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0003c0004t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0003c0004t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0003c0004t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0003c0004t0006g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0004c0006t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0004c0006t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
a0005c0008t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0125 | EUR | GBR | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG00099 | hp2 | a0001 | c0002 | t0001 | g0237 | EUR | GBR | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | GBR | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG00140 | hp2 | a0003 | c0004 | t0002 | g0094 | EUR | GBR | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0057 | EUR | FIN | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0188 | EUR | FIN | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG00558 | hp1 | a0003 | c0004 | t0001 | g0113 | EAS | CHS | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | CHS | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | CHS | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | CHS | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | CHS | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG00673 | hp2 | a0001 | c0002 | t0001 | g0263 | EAS | CHS | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG00733 | hp1 | a0001 | c0002 | t0001 | g0029 | AMR | PUR | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG00735 | hp1 | a0001 | c0002 | t0001 | g0029 | AMR | PUR | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG00738 | hp2 | a0001 | c0002 | t0001 | g0255 | AMR | PUR | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG01070 | hp1 | a0003 | c0004 | t0002 | g0114 | AMR | PUR | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG01070 | hp2 | a0002 | c0003 | t0002 | g0012 | AMR | PUR | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG01071 | hp1 | a0002 | c0003 | t0002 | g0012 | AMR | PUR | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG01106 | hp1 | a0001 | c0005 | t0001 | g0228 | AMR | PUR | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG01106 | hp2 | a0001 | c0002 | t0001 | g0183 | AMR | PUR | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0106 | AMR | PUR | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG01109 | hp2 | a0002 | c0003 | t0001 | g0013 | AMR | PUR | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG01167 | hp1 | a0001 | c0002 | t0001 | g0240 | AMR | PUR | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG01175 | hp2 | a0001 | c0002 | t0001 | g0126 | AMR | PUR | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0190 | AMR | CLM | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | CLM | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG01256 | hp1 | a0001 | c0001 | t0002 | g0169 | AMR | CLM | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | CLM | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | CLM | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0165 | AMR | CLM | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | CLM | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG01346 | hp1 | a0001 | c0002 | t0001 | g0229 | AMR | CLM | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | CLM | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG01358 | hp1 | a0002 | c0003 | t0001 | g0045 | AMR | CLM | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | CLM | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | CLM | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG01433 | hp1 | a0001 | c0002 | t0001 | g0006 | AMR | CLM | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | CLM | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0176 | EUR | IBS | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0175 | EUR | IBS | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0186 | EUR | IBS | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG01884 | hp1 | a0001 | c0001 | t0002 | g0234 | AFR | ACB | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | ACB | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG01891 | hp2 | a0001 | c0001 | t0002 | g0220 | AFR | ACB | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | PEL | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PEL | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG01943 | hp2 | a0001 | c0002 | t0001 | g0227 | AMR | PEL | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | PEL | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | PEL | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG01978 | hp1 | a0001 | c0002 | t0001 | g0248 | AMR | PEL | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0250 | AMR | PEL | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG01981 | hp1 | a0001 | c0002 | t0001 | g0254 | AMR | PEL | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG01981 | hp2 | a0001 | c0001 | t0002 | g0155 | AMR | PEL | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG01993 | hp2 | a0001 | c0002 | t0001 | g0184 | AMR | PEL | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG02004 | hp1 | a0001 | c0002 | t0001 | g0147 | AMR | PEL | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | PEL | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | KHV | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG02027 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | KHV | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | KHV | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG02040 | hp2 | a0002 | c0003 | t0001 | g0051 | EAS | KHV | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | ACB | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG02055 | hp2 | a0001 | c0001 | t0002 | g0026 | AFR | ACB | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | KHV | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG02080 | hp2 | a0003 | c0004 | t0002 | g0070 | EAS | KHV | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | KHV | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG02083 | hp2 | a0003 | c0004 | t0001 | g0112 | EAS | KHV | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | KHV | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG02132 | hp2 | a0001 | c0002 | t0001 | g0087 | EAS | KHV | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG02135 | hp1 | a0001 | c0002 | t0001 | g0241 | EAS | KHV | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | KHV | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG02145 | hp1 | a0001 | c0001 | t0002 | g0261 | AFR | ACB | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | ACB | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG02148 | hp1 | a0001 | c0002 | t0001 | g0252 | AMR | PEL | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | CDX | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG02155 | hp2 | a0001 | c0002 | t0001 | g0264 | EAS | CDX | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | CDX | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | CDX | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0232 | AFR | ACB | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | ACB | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | ACB | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG02258 | hp2 | a0003 | c0004 | t0002 | g0206 | AFR | ACB | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0222 | AFR | ACB | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | ACB | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG02293 | hp2 | a0005 | c0008 | t0001 | g0251 | AMR | PEL | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | PEL | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG02300 | hp2 | a0001 | c0002 | t0001 | g0253 | AMR | PEL | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | ACB | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG02451 | hp2 | a0002 | c0003 | t0002 | g0049 | AFR | ACB | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | KHV | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | KHV | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG02572 | hp1 | a0001 | c0001 | t0002 | g0124 | AFR | GWD | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG02572 | hp2 | a0002 | c0003 | t0004 | g0038 | AFR | GWD | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0212 | SAS | PJL | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | GWD | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG02615 | hp2 | a0002 | c0003 | t0007 | g0102 | AFR | GWD | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG02622 | hp1 | a0001 | c0001 | t0002 | g0218 | AFR | GWD | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG02630 | hp1 | a0003 | c0004 | t0001 | g0133 | AFR | GWD | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | GWD | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG02683 | hp2 | a0001 | c0002 | t0001 | g0043 | SAS | PJL | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG02717 | hp1 | a0003 | c0004 | t0002 | g0019 | AFR | GWD | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG02717 | hp2 | a0001 | c0005 | t0002 | g0257 | AFR | GWD | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | GWD | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG02723 | hp2 | a0001 | c0001 | t0002 | g0225 | AFR | GWD | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG02735 | hp1 | a0002 | c0003 | t0001 | g0013 | SAS | PJL | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0159 | SAS | PJL | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG02809 | hp1 | a0003 | c0004 | t0002 | g0019 | AFR | GWD | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | GWD | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG02886 | hp1 | a0002 | c0003 | t0002 | g0041 | AFR | GWD | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG02886 | hp2 | a0001 | c0001 | t0002 | g0223 | AFR | GWD | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG02895 | hp1 | a0001 | c0001 | t0002 | g0195 | AFR | GWD | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG02895 | hp2 | a0002 | c0003 | t0001 | g0040 | AFR | GWD | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG02897 | hp1 | a0002 | c0003 | t0001 | g0039 | AFR | GWD | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG02897 | hp2 | a0002 | c0003 | t0002 | g0034 | AFR | GWD | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG02922 | hp1 | a0001 | c0001 | t0002 | g0150 | AFR | ESN | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG02922 | hp2 | a0001 | c0001 | t0002 | g0107 | AFR | ESN | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG02965 | hp1 | a0001 | c0001 | t0002 | g0209 | AFR | ESN | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG02965 | hp2 | a0001 | c0001 | t0002 | g0023 | AFR | ESN | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | ESN | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG02970 | hp2 | a0001 | c0001 | t0002 | g0215 | AFR | ESN | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG02976 | hp1 | a0001 | c0001 | t0003 | g0198 | AFR | ESN | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG02976 | hp2 | a0002 | c0003 | t0001 | g0050 | AFR | ESN | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0100 | SAS | PJL | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0158 | SAS | PJL | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG03041 | hp1 | a0002 | c0003 | t0002 | g0011 | AFR | GWD | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | GWD | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | MSL | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG03098 | hp2 | a0001 | c0001 | t0003 | g0217 | AFR | MSL | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | ESN | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG03130 | hp2 | a0001 | c0001 | t0002 | g0224 | AFR | ESN | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG03139 | hp1 | a0002 | c0003 | t0001 | g0042 | AFR | ESN | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG03139 | hp2 | a0001 | c0001 | t0002 | g0104 | AFR | ESN | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG03195 | hp1 | a0002 | c0003 | t0002 | g0036 | AFR | ESN | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG03195 | hp2 | a0001 | c0001 | t0002 | g0023 | AFR | ESN | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG03209 | hp1 | a0002 | c0003 | t0002 | g0047 | AFR | MSL | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG03209 | hp2 | a0001 | c0001 | t0004 | g0137 | AFR | MSL | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG03225 | hp1 | a0001 | c0001 | t0002 | g0109 | AFR | MSL | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG03225 | hp2 | a0002 | c0003 | t0001 | g0014 | AFR | MSL | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG03239 | hp1 | a0001 | c0002 | t0001 | g0071 | SAS | PJL | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0163 | SAS | PJL | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG03453 | hp1 | a0001 | c0001 | t0002 | g0131 | AFR | MSL | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG03453 | hp2 | a0001 | c0001 | t0002 | g0026 | AFR | MSL | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | MSL | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG03486 | hp2 | a0002 | c0003 | t0001 | g0015 | AFR | MSL | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG03490 | hp1 | a0001 | c0001 | t0002 | g0031 | SAS | PJL | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0196 | SAS | PJL | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG03516 | hp1 | a0001 | c0001 | t0003 | g0200 | AFR | ESN | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG03516 | hp2 | a0002 | c0003 | t0001 | g0015 | AFR | ESN | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG03540 | hp1 | a0001 | c0001 | t0002 | g0145 | AFR | GWD | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0221 | AFR | GWD | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0231 | AFR | MSL | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG03579 | hp2 | a0002 | c0003 | t0002 | g0035 | AFR | MSL | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0088 | SAS | PJL | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0135 | SAS | PJL | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | STU | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG03688 | hp2 | a0001 | c0001 | t0002 | g0141 | SAS | STU | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0089 | SAS | PJL | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0181 | SAS | PJL | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0214 | SAS | BEB | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0090 | SAS | BEB | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG03834 | hp1 | a0001 | c0002 | t0001 | g0030 | SAS | BEB | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0174 | SAS | BEB | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG03927 | hp1 | a0001 | c0007 | t0001 | g0033 | SAS | BEB | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | BEB | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG04204 | hp2 | a0001 | c0002 | t0001 | g0193 | SAS | STU | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0197 | SAS | STU | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0249 | SAS | STU | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | CHB | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHB | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
NA18906 | hp1 | a0002 | c0003 | t0002 | g0048 | AFR | YRI | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
NA18906 | hp2 | a0001 | c0001 | t0002 | g0105 | AFR | YRI | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
NA18940 | hp1 | a0001 | c0002 | t0001 | g0028 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
NA18940 | hp2 | a0003 | c0004 | t0001 | g0016 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
NA18943 | hp1 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
NA18944 | hp1 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
NA18957 | hp1 | a0001 | c0002 | t0001 | g0238 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
NA18963 | hp2 | a0001 | c0002 | t0001 | g0236 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
NA18965 | hp2 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
NA18967 | hp2 | a0003 | c0004 | t0002 | g0115 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
NA18984 | hp2 | a0001 | c0002 | t0001 | g0235 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
NA18985 | hp2 | a0001 | c0002 | t0001 | g0028 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
NA18994 | hp1 | a0001 | c0002 | t0001 | g0242 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
NA19011 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
NA19030 | hp1 | a0001 | c0001 | t0002 | g0130 | AFR | LWK | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
NA19030 | hp2 | a0001 | c0005 | t0002 | g0256 | AFR | LWK | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
NA19056 | hp1 | a0004 | c0006 | t0001 | g0230 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
NA19057 | hp2 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
NA19060 | hp2 | a0003 | c0004 | t0001 | g0053 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
NA19065 | hp2 | a0004 | c0006 | t0001 | g0247 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
NA19077 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
NA19077 | hp2 | a0003 | c0004 | t0001 | g0016 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
NA19079 | hp1 | a0001 | c0002 | t0001 | g0239 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
NA19079 | hp2 | a0003 | c0004 | t0002 | g0008 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
NA19083 | hp2 | a0003 | c0004 | t0006 | g0008 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
NA19084 | hp2 | a0003 | c0004 | t0002 | g0008 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
NA19090 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
NA19090 | hp2 | a0003 | c0004 | t0001 | g0111 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
NA19240 | hp1 | a0001 | c0001 | t0002 | g0151 | AFR | YRI | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0260 | AFR | YRI | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | ASW | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | ASW | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
NA20752 | hp1 | a0001 | c0002 | t0001 | g0030 | EUR | TSI | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0022 | EUR | TSI | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
NA20805 | hp1 | a0001 | c0001 | t0002 | g0146 | EUR | TSI | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0166 | EUR | TSI | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | GIH | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0194 | SAS | GIH | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG02109 | hp1 | a0002 | c0003 | t0002 | g0037 | AFR | ACB | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG02109 | hp2 | a0001 | c0001 | t0005 | g0123 | AFR | ACB | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | ACB | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG02486 | hp2 | a0002 | c0003 | t0001 | g0014 | AFR | ACB | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG02559 | hp1 | a0001 | c0001 | t0002 | g0108 | AFR | ACB | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG02559 | hp2 | a0001 | c0005 | t0001 | g0258 | AFR | ACB | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG03471 | hp1 | a0001 | c0001 | t0002 | g0208 | AFR | MSL | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG03471 | hp2 | a0001 | c0001 | t0002 | g0127 | AFR | MSL | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | USA | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
HG06807 | hp2 | a0003 | c0004 | t0002 | g0205 | AFR | USA | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
NA20300 | hp1 | a0002 | c0003 | t0002 | g0011 | AFR | USA | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | USA | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
NA21309 | hp1 | a0002 | c0003 | t0001 | g0046 | AFR | LWK | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
NA21309 | hp2 | a0001 | c0001 | t0002 | g0259 | AFR | LWK | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0001 | g0262 | REF | REF | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
homoSapiens_grch38 | hp1 | a0001 | c0002 | t0001 | g0180 | REF | REF | FAM3B_chr21_41311801_41362727 | FAM3B | chr21 | 41311801 | 41362727 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr21:41322943
|
G | A | 1 | a0002 | 27 | HG01070.hp2 HG01071.hp1 HG01109.hp2 others(24): Show |
missense_variant | MODERATE | c.40G>A | p.Val14Met | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/8 | 119/1317 | 40/708 | 14/235 | chr21 | 41322943 | ||
chr21:41346027
|
AAAAAAAA others(5917): Show |
A | 1 | a0005 | 1 | HG02293.hp2 | exon_loss_variant | HIGH | c.397+293_618+3228de others(1): Show |
FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr21 | 41346027 | |||||
chr21:41348652
|
G | A | 1 | a0003 | 18 | HG00140.hp2 HG00558.hp1 HG01070.hp1 others(15): Show |
missense_variant | MODERATE | c.546G>A | p.Met182Ile | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/8 | 625/1317 | 546/708 | 182/235 | chr21 | 41348652 | ||
chr21:41357190
|
G | A | 1 | a0004 | 2 | NA19056.hp1 NA19065.hp2 |
missense_variant | MODERATE | c.701G>A | p.Arg234Gln | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 8/8 | 780/1317 | 701/708 | 234/235 | chr21 | 41357190 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr21:41322951
|
C | T | 1 | a0001c0005 | 4 | HG01106.hp1 HG02559.hp2 HG02717.hp2 others(1): Show |
synonymous_variant | LOW | c.48C>T | p.Phe16Phe | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/8 | 127/1317 | 48/708 | 16/235 | chr21 | 41322951 | ||
chr21:41338403
|
T | C | 1 | a0001c0007 | 1 | HG03927.hp1 | synonymous_variant | LOW | c.189T>C | p.Cys63Cys | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/8 | 268/1317 | 189/708 | 63/235 | chr21 | 41338403 | ||
chr21:41345735
|
T | C | 7 | a0001c0001a0001c0005a0001c0007others(4): Show | 273 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(270): Show |
splice_region_variant&synonymous_variant | LOW | c.396T>C | p.Gly132Gly | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 5/8 | 475/1317 | 396/708 | 132/235 | chr21 | 41345735 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr21:41316825
|
G | T | 1 | a0002c0003t0007 | 1 | HG02615.hp2 | 5_prime_UTR_variant | MODIFIER | c.-55G>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/8 | 55 | chr21 | 41316825 | |||||
chr21:41357220
|
G | T | 1 | a0003c0004t0006 | 1 | NA19083.hp2 | 3_prime_UTR_variant | MODIFIER | c.*23G>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 8/8 | 23 | chr21 | 41357220 | |||||
chr21:41357550
|
A | G | 2 | a0001c0001t0003a0001c0001t0005 | 4 | HG02109.hp2 HG02976.hp1 HG03098.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*353A>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 8/8 | 353 | chr21 | 41357550 | |||||
chr21:41357664
|
C | G | 9 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(6): Show | 72 | HG00099.hp1 HG00140.hp2 HG01070.hp1 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*467C>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 8/8 | 467 | chr21 | 41357664 | |||||
chr21:41357686
|
G | A | 2 | a0001c0001t0004a0002c0003t0004 | 2 | HG02572.hp2 HG03209.hp2 |
3_prime_UTR_variant | MODIFIER | c.*489G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 8/8 | 489 | chr21 | 41357686 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr21:41317004
|
C | G | 57 | a0001c0001t0001g0004a0001c0001t0001g0027a0001c0001t0001g0216others(54): Show | 70 | HG00099.hp2 HG00621.hp2 HG00673.hp2 others(67): Show |
intron_variant | MODIFIER | c.19+106C>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | chr21 | 41317004 | ||||||
chr21:41317005
|
GGGAGGGC others(16): Show |
G | 1 | a0001c0001t0001g0214 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.19+110_19+132delAG others(21): Show |
FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr21 | 41317005 | |||||
chr21:41317032
|
T | G | 1 | a0001c0001t0001g0214 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.19+134T>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | chr21 | 41317032 | ||||||
chr21:41317130
|
C | G | 1 | a0001c0001t0001g0213 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.19+232C>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | chr21 | 41317130 | ||||||
chr21:41317169
|
G | C | 2 | a0001c0001t0001g0032a0001c0001t0002g0031 | 2 | HG02602.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.19+271G>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | chr21 | 41317169 | ||||||
chr21:41317258
|
C | T | 1 | a0001c0001t0002g0212 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.19+360C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | chr21 | 41317258 | ||||||
chr21:41317310
|
C | T | 2 | a0001c0002t0001g0263a0001c0002t0001g0264 | 2 | HG00673.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.19+412C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | chr21 | 41317310 | ||||||
chr21:41317356
|
T | C | 130 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(127): Show | 156 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.19+458T>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | chr21 | 41317356 | ||||||
chr21:41317477
|
G | A | 1 | a0001c0001t0002g0131 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.19+579G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | chr21 | 41317477 | ||||||
chr21:41317516
|
G | C | 86 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(83): Show | 106 | HG00140.hp2 HG00280.hp1 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.19+618G>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | chr21 | 41317516 | ||||||
chr21:41317710
|
G | T | 54 | a0001c0001t0001g0020a0001c0001t0001g0027a0001c0001t0001g0122others(51): Show | 65 | HG00099.hp1 HG00099.hp2 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.19+812G>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | chr21 | 41317710 | ||||||
chr21:41317727
|
C | T | 107 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(104): Show | 132 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(129): Show |
intron_variant | MODIFIER | c.19+829C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | chr21 | 41317727 | ||||||
chr21:41317773
|
A | G | 108 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(105): Show | 133 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(130): Show |
intron_variant | MODIFIER | c.19+875A>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | chr21 | 41317773 | ||||||
chr21:41317801
|
A | G | 2 | a0001c0001t0002g0223a0001c0001t0002g0224 | 2 | HG02886.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.19+903A>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | chr21 | 41317801 | ||||||
chr21:41317802
|
G | A | 1 | a0001c0002t0001g0227 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.19+904G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | chr21 | 41317802 | ||||||
chr21:41317874
|
G | A | 2 | a0002c0003t0002g0034a0002c0003t0002g0035 | 2 | HG02897.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.19+976G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | chr21 | 41317874 | ||||||
chr21:41318052
|
T | C | 11 | a0002c0003t0001g0039a0002c0003t0001g0040a0002c0003t0001g0042others(8): Show | 13 | HG01070.hp2 HG01071.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.19+1154T>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | chr21 | 41318052 | ||||||
chr21:41318169
|
C | T | 1 | a0001c0001t0002g0131 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.19+1271C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | chr21 | 41318169 | ||||||
chr21:41318218
|
G | C | 1 | a0001c0001t0001g0132 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.19+1320G>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | chr21 | 41318218 | ||||||
chr21:41318436
|
G | A | 66 | a0001c0001t0001g0004a0001c0001t0001g0027a0001c0001t0001g0110others(63): Show | 81 | HG00099.hp2 HG00558.hp1 HG00621.hp2 others(78): Show |
intron_variant | MODIFIER | c.19+1538G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | chr21 | 41318436 | ||||||
chr21:41318489
|
CAGAGTGG others(8): Show |
C | 1 | a0001c0001t0001g0103 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.19+1594_19+1608del others(15): Show |
FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr21 | 41318489 | |||||
chr21:41318497
|
C | T | 59 | a0001c0001t0001g0004a0001c0001t0001g0020a0001c0001t0001g0027others(56): Show | 73 | HG00099.hp1 HG00099.hp2 HG00621.hp2 others(70): Show |
intron_variant | MODIFIER | c.19+1599C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | chr21 | 41318497 | ||||||
chr21:41318506
|
G | A | 10 | a0001c0001t0001g0216a0001c0001t0001g0219a0001c0001t0001g0221others(7): Show | 10 | HG01891.hp2 HG02280.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.19+1608G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | chr21 | 41318506 | ||||||
chr21:41318529
|
T | G | 1 | a0001c0001t0001g0044 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.19+1631T>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | chr21 | 41318529 | ||||||
chr21:41318995
|
A | C | 24 | a0001c0001t0001g0020a0001c0001t0001g0122a0001c0001t0001g0128others(21): Show | 25 | HG00099.hp1 HG01074.hp1 HG01175.hp2 others(22): Show |
intron_variant | MODIFIER | c.19+2097A>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | chr21 | 41318995 | ||||||
chr21:41319040
|
A | G | 9 | a0001c0001t0001g0204a0001c0001t0001g0207a0001c0001t0001g0210others(6): Show | 10 | HG01243.hp2 HG02055.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.19+2142A>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | chr21 | 41319040 | ||||||
chr21:41319184
|
C | G | 10 | a0001c0001t0001g0216a0001c0001t0001g0219a0001c0001t0001g0221others(7): Show | 10 | HG01891.hp2 HG02280.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.19+2286C>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | chr21 | 41319184 | ||||||
chr21:41319189
|
C | T | 6 | a0001c0001t0001g0199a0001c0001t0001g0201a0001c0001t0001g0202others(3): Show | 6 | HG02055.hp1 HG02145.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.19+2291C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | chr21 | 41319189 | ||||||
chr21:41319311
|
G | A | 49 | a0001c0001t0001g0020a0001c0001t0001g0110a0001c0001t0001g0116others(46): Show | 52 | HG00099.hp1 HG00558.hp1 HG00642.hp2 others(49): Show |
intron_variant | MODIFIER | c.19+2413G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | chr21 | 41319311 | ||||||
chr21:41319471
|
C | T | 1 | a0001c0001t0001g0101 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.19+2573C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | chr21 | 41319471 | ||||||
chr21:41319520
|
C | G | 2 | a0001c0001t0001g0100a0001c0001t0001g0214 | 2 | HG03017.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.19+2622C>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | chr21 | 41319520 | ||||||
chr21:41319552
|
G | T | 9 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0196others(6): Show | 9 | HG01255.hp1 HG01952.hp2 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.19+2654G>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | chr21 | 41319552 | ||||||
chr21:41319574
|
C | T | 2 | a0001c0001t0001g0202a0001c0001t0001g0203 | 2 | HG02257.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.19+2676C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | chr21 | 41319574 | ||||||
chr21:41319695
|
G | A | 39 | a0001c0001t0001g0027a0001c0001t0001g0231a0001c0001t0001g0232others(36): Show | 49 | HG00099.hp2 HG00621.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.19+2797G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | chr21 | 41319695 | ||||||
chr21:41319718
|
T | C | 86 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(83): Show | 106 | HG00140.hp2 HG00280.hp1 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.19+2820T>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | chr21 | 41319718 | ||||||
chr21:41319993
|
C | A | 121 | a0001c0001t0001g0004a0001c0001t0001g0020a0001c0001t0001g0027others(118): Show | 143 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(140): Show |
intron_variant | MODIFIER | c.20-2930C>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | chr21 | 41319993 | ||||||
chr21:41319998
|
G | C | 15 | a0001c0001t0001g0110a0001c0001t0001g0132a0001c0001t0001g0199others(12): Show | 15 | HG01109.hp1 HG01884.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.20-2925G>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | chr21 | 41319998 | ||||||
chr21:41320143
|
C | T | 1 | a0001c0001t0001g0189 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.20-2780C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | chr21 | 41320143 | ||||||
chr21:41320173
|
A | G | 1 | a0001c0001t0002g0105 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.20-2750A>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | chr21 | 41320173 | ||||||
chr21:41320231
|
C | G | 4 | a0001c0001t0001g0025a0001c0001t0001g0186a0001c0001t0001g0187others(1): Show | 5 | HG00280.hp2 HG00738.hp1 HG01243.hp1 others(2): Show |
intron_variant | MODIFIER | c.20-2692C>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | chr21 | 41320231 | ||||||
chr21:41320241
|
T | G | 24 | a0001c0001t0001g0004a0001c0001t0002g0226a0002c0003t0001g0013others(21): Show | 32 | HG01070.hp2 HG01071.hp1 HG01109.hp2 others(29): Show |
intron_variant | MODIFIER | c.20-2682T>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | chr21 | 41320241 | ||||||
chr21:41320367
|
C | T | 5 | a0001c0001t0001g0110a0001c0001t0002g0106a0001c0001t0002g0107others(2): Show | 5 | HG01109.hp1 HG01884.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.20-2556C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | chr21 | 41320367 | ||||||
chr21:41320372
|
A | G | 2 | a0001c0005t0001g0258a0001c0005t0002g0257 | 2 | HG02559.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.20-2551A>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | chr21 | 41320372 | ||||||
chr21:41320392
|
G | T | 2 | a0001c0001t0001g0004a0001c0001t0002g0226 | 5 | NA18747.hp2 NA18952.hp2 NA18955.hp2 others(2): Show |
intron_variant | MODIFIER | c.20-2531G>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | chr21 | 41320392 | ||||||
chr21:41320536
|
G | A | 10 | a0001c0001t0001g0216a0001c0001t0001g0219a0001c0001t0001g0221others(7): Show | 10 | HG01891.hp2 HG02280.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.20-2387G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | chr21 | 41320536 | ||||||
chr21:41320738
|
T | G | 3 | a0001c0005t0001g0228a0001c0005t0001g0258a0001c0005t0002g0257 | 3 | HG01106.hp1 HG02559.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.20-2185T>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | chr21 | 41320738 | ||||||
chr21:41320934
|
C | T | 1 | a0001c0001t0001g0110 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.20-1989C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | chr21 | 41320934 | ||||||
chr21:41320935
|
C | A | 89 | a0001c0001t0001g0004a0001c0001t0001g0027a0001c0001t0001g0110others(86): Show | 107 | HG00099.hp2 HG00621.hp2 HG00673.hp2 others(104): Show |
intron_variant | MODIFIER | c.20-1988C>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | chr21 | 41320935 | ||||||
chr21:41321416
|
G | T | 1 | a0001c0001t0001g0098 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.20-1507G>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | chr21 | 41321416 | ||||||
chr21:41321438
|
G | A | 1 | a0001c0001t0001g0052 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.20-1485G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | chr21 | 41321438 | ||||||
chr21:41321603
|
C | A | 10 | a0001c0001t0001g0216a0001c0001t0001g0219a0001c0001t0001g0221others(7): Show | 10 | HG01891.hp2 HG02280.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.20-1320C>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | chr21 | 41321603 | ||||||
chr21:41321898
|
T | TCCTTTCC others(23): Show |
1 | a0001c0001t0001g0097 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.20-1020_20-991dupT others(29): Show |
FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr21 | 41321898 | |||||
chr21:41321906
|
T | C | 2 | a0001c0001t0001g0004a0001c0001t0002g0226 | 5 | NA18747.hp2 NA18952.hp2 NA18955.hp2 others(2): Show |
intron_variant | MODIFIER | c.20-1017T>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | chr21 | 41321906 | ||||||
chr21:41322008
|
A | T | 2 | a0001c0001t0001g0187a0001c0001t0001g0188 | 2 | HG00280.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.20-915A>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | chr21 | 41322008 | ||||||
chr21:41322190
|
AC | A | 18 | a0001c0001t0001g0020a0001c0001t0001g0116a0001c0001t0001g0117others(15): Show | 21 | HG00099.hp1 HG00558.hp1 HG01070.hp1 others(18): Show |
intron_variant | MODIFIER | c.20-727delC | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr21 | 41322190 | |||||
chr21:41322357
|
G | T | 122 | a0001c0001t0001g0004a0001c0001t0001g0020a0001c0001t0001g0027others(119): Show | 144 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(141): Show |
intron_variant | MODIFIER | c.20-566G>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | chr21 | 41322357 | ||||||
chr21:41322405
|
G | T | 9 | a0001c0001t0001g0204a0001c0001t0001g0207a0001c0001t0001g0210others(6): Show | 10 | HG01243.hp2 HG02055.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.20-518G>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | chr21 | 41322405 | ||||||
chr21:41322446
|
C | T | 22 | a0002c0003t0001g0013a0002c0003t0001g0014a0002c0003t0001g0015others(19): Show | 27 | HG01070.hp2 HG01071.hp1 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.20-477C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | chr21 | 41322446 | ||||||
chr21:41322706
|
A | T | 42 | a0001c0001t0001g0027a0001c0001t0001g0231a0001c0001t0001g0232others(39): Show | 52 | HG00099.hp2 HG00621.hp2 HG00673.hp2 others(49): Show |
intron_variant | MODIFIER | c.20-217A>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | chr21 | 41322706 | ||||||
chr21:41322740
|
T | C | 46 | a0001c0001t0001g0020a0001c0001t0001g0110a0001c0001t0001g0116others(43): Show | 50 | HG00099.hp1 HG00558.hp1 HG01070.hp1 others(47): Show |
intron_variant | MODIFIER | c.20-183T>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | chr21 | 41322740 | ||||||
chr21:41322758
|
T | C | 1 | a0003c0004t0001g0053 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.20-165T>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 1/7 | chr21 | 41322758 | ||||||
chr21:41323234
|
A | G | 17 | a0001c0001t0001g0020a0001c0001t0001g0116a0001c0001t0001g0117others(14): Show | 20 | HG00099.hp1 HG00558.hp1 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.163+168A>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41323234 | ||||||
chr21:41323518
|
G | C | 126 | a0001c0001t0001g0004a0001c0001t0001g0020a0001c0001t0001g0027others(123): Show | 148 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.163+452G>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41323518 | ||||||
chr21:41323774
|
G | A | 1 | a0001c0001t0001g0058 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.163+708G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41323774 | ||||||
chr21:41324214
|
A | G | 15 | a0001c0001t0001g0110a0001c0001t0001g0216a0001c0001t0001g0219others(12): Show | 15 | HG01109.hp1 HG01884.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.163+1148A>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41324214 | ||||||
chr21:41324495
|
A | T | 10 | a0001c0001t0001g0216a0001c0001t0001g0219a0001c0001t0001g0221others(7): Show | 10 | HG01891.hp2 HG02280.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.163+1429A>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41324495 | ||||||
chr21:41324872
|
C | T | 26 | a0001c0001t0001g0057a0001c0001t0001g0116a0001c0001t0001g0117others(23): Show | 31 | HG00280.hp1 HG01070.hp2 HG01071.hp1 others(28): Show |
intron_variant | MODIFIER | c.163+1806C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41324872 | ||||||
chr21:41324873
|
G | A | 1 | a0001c0001t0001g0135 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.163+1807G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41324873 | ||||||
chr21:41324881
|
C | A | 1 | a0001c0001t0002g0225 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.163+1815C>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41324881 | ||||||
chr21:41324960
|
G | C | 12 | a0002c0003t0001g0039a0002c0003t0001g0040a0002c0003t0001g0042others(9): Show | 14 | HG01070.hp2 HG01071.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.163+1894G>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41324960 | ||||||
chr21:41324963
|
A | G | 2 | a0001c0001t0001g0018a0001c0001t0001g0096 | 3 | HG02683.hp1 HG02738.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.163+1897A>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41324963 | ||||||
chr21:41324982
|
A | G | 1 | a0003c0004t0001g0133 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.163+1916A>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41324982 | ||||||
chr21:41324988
|
G | A | 2 | a0001c0001t0001g0128a0001c0001t0002g0127 | 2 | HG02258.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.163+1922G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41324988 | ||||||
chr21:41324994
|
C | T | 1 | a0001c0001t0001g0185 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.163+1928C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41324994 | ||||||
chr21:41325294
|
T | G | 36 | a0001c0001t0001g0057a0001c0001t0001g0116a0001c0001t0001g0117others(33): Show | 41 | HG00280.hp1 HG01070.hp2 HG01071.hp1 others(38): Show |
intron_variant | MODIFIER | c.163+2228T>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41325294 | ||||||
chr21:41325305
|
G | A | 5 | a0001c0001t0001g0110a0001c0001t0002g0106a0001c0001t0002g0107others(2): Show | 5 | HG01109.hp1 HG01884.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.163+2239G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41325305 | ||||||
chr21:41325480
|
T | C | 10 | a0001c0001t0001g0216a0001c0001t0001g0219a0001c0001t0001g0221others(7): Show | 10 | HG01891.hp2 HG02280.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.163+2414T>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41325480 | ||||||
chr21:41325525
|
T | G | 2 | a0001c0001t0001g0004a0001c0001t0002g0226 | 5 | NA18747.hp2 NA18952.hp2 NA18955.hp2 others(2): Show |
intron_variant | MODIFIER | c.163+2459T>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41325525 | ||||||
chr21:41325670
|
C | T | 2 | a0001c0001t0001g0095a0001c0001t0002g0197 | 2 | HG02165.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.163+2604C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41325670 | ||||||
chr21:41325787
|
C | G | 93 | a0001c0001t0001g0020a0001c0001t0001g0027a0001c0001t0001g0110others(90): Show | 107 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(104): Show |
intron_variant | MODIFIER | c.163+2721C>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41325787 | ||||||
chr21:41325791
|
G | A | 4 | a0001c0001t0001g0136a0001c0001t0001g0138a0001c0001t0001g0139others(1): Show | 4 | HG01167.hp2 HG02451.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.163+2725G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41325791 | ||||||
chr21:41325822
|
C | T | 5 | a0001c0001t0001g0110a0001c0001t0002g0106a0001c0001t0002g0107others(2): Show | 5 | HG01109.hp1 HG01884.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.163+2756C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41325822 | ||||||
chr21:41326055
|
G | T | 1 | a0001c0001t0001g0222 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.163+2989G>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41326055 | ||||||
chr21:41326161
|
G | A | 1 | a0003c0004t0001g0133 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.163+3095G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41326161 | ||||||
chr21:41326211
|
T | G | 1 | a0001c0001t0001g0059 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.163+3145T>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41326211 | ||||||
chr21:41326276
|
T | C | 2 | a0001c0001t0001g0018a0001c0001t0001g0096 | 3 | HG02683.hp1 HG02738.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.163+3210T>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41326276 | ||||||
chr21:41326277
|
G | A | 12 | a0001c0001t0001g0110a0001c0001t0001g0132a0001c0001t0001g0199others(9): Show | 12 | HG01109.hp1 HG01884.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.163+3211G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41326277 | ||||||
chr21:41326351
|
C | G | 2 | a0001c0005t0001g0228a0003c0004t0001g0133 | 2 | HG01106.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.163+3285C>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41326351 | ||||||
chr21:41326463
|
G | T | 6 | a0001c0001t0001g0207a0001c0001t0001g0210a0001c0001t0001g0211others(3): Show | 7 | HG01243.hp2 HG02055.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.163+3397G>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41326463 | ||||||
chr21:41326586
|
C | T | 2 | a0001c0002t0001g0183a0001c0002t0001g0184 | 2 | HG01106.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.163+3520C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41326586 | ||||||
chr21:41326733
|
G | A | 2 | a0001c0001t0001g0004a0001c0001t0002g0226 | 5 | NA18747.hp2 NA18952.hp2 NA18955.hp2 others(2): Show |
intron_variant | MODIFIER | c.163+3667G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41326733 | ||||||
chr21:41326785
|
T | C | 4 | a0001c0001t0001g0004a0001c0001t0002g0226a0001c0005t0001g0228others(1): Show | 7 | HG01106.hp1 HG02630.hp1 NA18747.hp2 others(4): Show |
intron_variant | MODIFIER | c.163+3719T>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41326785 | ||||||
chr21:41326854
|
T | G | 27 | a0001c0001t0001g0057a0001c0001t0001g0116a0001c0001t0001g0117others(24): Show | 32 | HG00280.hp1 HG01070.hp2 HG01071.hp1 others(29): Show |
intron_variant | MODIFIER | c.163+3788T>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41326854 | ||||||
chr21:41326942
|
T | C | 13 | a0001c0001t0001g0129a0001c0001t0001g0204a0001c0001t0001g0207others(10): Show | 14 | HG01243.hp2 HG02055.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.163+3876T>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41326942 | ||||||
chr21:41326980
|
A | G | 127 | a0001c0001t0001g0004a0001c0001t0001g0020a0001c0001t0001g0027others(124): Show | 149 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.163+3914A>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41326980 | ||||||
chr21:41327198
|
C | T | 1 | a0001c0005t0001g0228 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.163+4132C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41327198 | ||||||
chr21:41327468
|
T | C | 2 | a0001c0001t0001g0100a0001c0001t0001g0214 | 2 | HG03017.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.163+4402T>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41327468 | ||||||
chr21:41327725
|
G | C | 2 | a0001c0001t0001g0021a0001c0001t0001g0140 | 3 | HG01192.hp1 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.163+4659G>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41327725 | ||||||
chr21:41327834
|
G | A | 2 | a0001c0001t0001g0191a0001c0001t0002g0190 | 2 | HG01255.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.163+4768G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41327834 | ||||||
chr21:41328086
|
G | A | 2 | a0001c0005t0001g0258a0001c0005t0002g0257 | 2 | HG02559.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.163+5020G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41328086 | ||||||
chr21:41328169
|
G | A | 1 | a0001c0001t0002g0215 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.163+5103G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41328169 | ||||||
chr21:41328219
|
T | C | 110 | a0001c0001t0001g0004a0001c0001t0001g0020a0001c0001t0001g0027others(107): Show | 130 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.163+5153T>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41328219 | ||||||
chr21:41328351
|
A | G | 1 | a0001c0001t0002g0225 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.163+5285A>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41328351 | ||||||
chr21:41328468
|
G | T | 1 | a0001c0002t0001g0255 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.163+5402G>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41328468 | ||||||
chr21:41328483
|
A | G | 113 | a0001c0001t0001g0004a0001c0001t0001g0020a0001c0001t0001g0027others(110): Show | 133 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.163+5417A>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41328483 | ||||||
chr21:41328553
|
G | T | 9 | a0001c0001t0001g0120a0003c0004t0001g0111a0003c0004t0001g0112others(6): Show | 11 | HG00558.hp1 HG01070.hp1 HG02083.hp2 others(8): Show |
intron_variant | MODIFIER | c.163+5487G>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41328553 | ||||||
chr21:41328608
|
G | C | 1 | a0001c0001t0001g0122 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.163+5542G>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41328608 | ||||||
chr21:41328785
|
G | A | 1 | a0001c0001t0002g0225 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.163+5719G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41328785 | ||||||
chr21:41328797
|
G | A | 1 | a0001c0001t0001g0207 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.163+5731G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41328797 | ||||||
chr21:41328822
|
A | C | 1 | a0002c0003t0001g0042 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.163+5756A>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41328822 | ||||||
chr21:41328860
|
G | T | 10 | a0001c0001t0001g0216a0001c0001t0001g0219a0001c0001t0001g0221others(7): Show | 10 | HG01891.hp2 HG02280.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.163+5794G>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41328860 | ||||||
chr21:41329139
|
C | T | 1 | a0001c0001t0001g0182 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.163+6073C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41329139 | ||||||
chr21:41329153
|
T | C | 1 | a0001c0001t0001g0027 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.163+6087T>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41329153 | ||||||
chr21:41329168
|
C | T | 2 | a0001c0001t0001g0100a0001c0001t0001g0214 | 2 | HG03017.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.163+6102C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41329168 | ||||||
chr21:41329347
|
A | T | 1 | a0001c0001t0002g0225 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.163+6281A>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41329347 | ||||||
chr21:41329382
|
C | T | 22 | a0001c0001t0001g0110a0001c0001t0001g0120a0001c0001t0001g0132others(19): Show | 24 | HG00558.hp1 HG01070.hp1 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.163+6316C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41329382 | ||||||
chr21:41329397
|
C | T | 1 | a0001c0001t0002g0225 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.163+6331C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41329397 | ||||||
chr21:41329398
|
G | A | 41 | a0001c0001t0001g0027a0001c0001t0001g0122a0001c0001t0001g0128others(38): Show | 51 | HG00099.hp2 HG00621.hp2 HG00673.hp2 others(48): Show |
intron_variant | MODIFIER | c.163+6332G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41329398 | ||||||
chr21:41329573
|
C | CT | 13 | a0001c0001t0001g0181a0001c0001t0001g0196a0001c0001t0001g0250others(10): Show | 15 | HG00140.hp2 HG00733.hp1 HG00735.hp1 others(12): Show |
intron_variant | MODIFIER | c.163+6521dupT | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr21 | 41329573 | |||||
chr21:41329673
|
G | A | 14 | a0001c0001t0001g0057a0001c0001t0001g0116a0001c0001t0001g0117others(11): Show | 17 | HG00280.hp1 HG01109.hp2 HG01256.hp2 others(14): Show |
intron_variant | MODIFIER | c.163+6607G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41329673 | ||||||
chr21:41329725
|
T | A | 59 | a0001c0001t0001g0004a0001c0001t0001g0020a0001c0001t0001g0057others(56): Show | 69 | HG00099.hp1 HG00280.hp1 HG01070.hp2 others(66): Show |
intron_variant | MODIFIER | c.163+6659T>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41329725 | ||||||
chr21:41329797
|
T | G | 1 | a0001c0001t0001g0204 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.163+6731T>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41329797 | ||||||
chr21:41329887
|
A | G | 1 | a0001c0001t0001g0058 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.163+6821A>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41329887 | ||||||
chr21:41330134
|
G | GA | 173 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(170): Show | 209 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(206): Show |
intron_variant | MODIFIER | c.163+7085dupA | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr21 | 41330134 | |||||
chr21:41330134
|
G | GAA | 41 | a0001c0001t0001g0054a0001c0001t0001g0060a0001c0001t0001g0061others(38): Show | 44 | HG00558.hp1 HG00673.hp2 HG00733.hp1 others(41): Show |
intron_variant | MODIFIER | c.163+7084_163+7085d others(4): Show |
FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr21 | 41330134 | |||||
chr21:41330134
|
GA | G | 25 | a0001c0001t0001g0004a0001c0001t0001g0020a0001c0001t0001g0129others(22): Show | 30 | HG00099.hp1 HG01074.hp1 HG01175.hp2 others(27): Show |
intron_variant | MODIFIER | c.163+7085delA | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr21 | 41330134 | |||||
chr21:41330151
|
A | T | 2 | a0001c0001t0001g0004a0001c0001t0002g0226 | 5 | NA18747.hp2 NA18952.hp2 NA18955.hp2 others(2): Show |
intron_variant | MODIFIER | c.163+7085A>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41330151 | ||||||
chr21:41330188
|
A | G | 22 | a0001c0001t0001g0110a0001c0001t0001g0120a0001c0001t0001g0132others(19): Show | 24 | HG00558.hp1 HG01070.hp1 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.163+7122A>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41330188 | ||||||
chr21:41330334
|
C | T | 2 | a0001c0001t0002g0104a0001c0001t0002g0105 | 2 | HG03139.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.163+7268C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41330334 | ||||||
chr21:41330443
|
G | C | 4 | a0001c0001t0001g0057a0002c0003t0001g0013a0002c0003t0001g0045others(1): Show | 5 | HG00280.hp1 HG01109.hp2 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.163+7377G>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41330443 | ||||||
chr21:41330493
|
T | G | 1 | a0001c0001t0001g0143 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.163+7427T>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41330493 | ||||||
chr21:41330582
|
C | T | 10 | a0001c0001t0001g0216a0001c0001t0001g0219a0001c0001t0001g0221others(7): Show | 10 | HG01891.hp2 HG02280.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.163+7516C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41330582 | ||||||
chr21:41330603
|
G | A | 2 | a0001c0001t0001g0022a0001c0001t0001g0144 | 3 | HG00733.hp2 HG01192.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.163+7537G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41330603 | ||||||
chr21:41330739
|
T | G | 58 | a0001c0001t0001g0004a0001c0001t0001g0020a0001c0001t0001g0057others(55): Show | 68 | HG00099.hp1 HG00280.hp1 HG01070.hp2 others(65): Show |
intron_variant | MODIFIER | c.164-7639T>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41330739 | ||||||
chr21:41330750
|
G | A | 41 | a0001c0001t0001g0027a0001c0001t0001g0122a0001c0001t0001g0128others(38): Show | 51 | HG00099.hp2 HG00621.hp2 HG00673.hp2 others(48): Show |
intron_variant | MODIFIER | c.164-7628G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41330750 | ||||||
chr21:41330846
|
G | A | 2 | a0001c0005t0001g0258a0001c0005t0002g0257 | 2 | HG02559.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.164-7532G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41330846 | ||||||
chr21:41330979
|
A | T | 1 | a0001c0001t0001g0179 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.164-7399A>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41330979 | ||||||
chr21:41331459
|
G | A | 60 | a0001c0001t0001g0004a0001c0001t0001g0057a0001c0001t0001g0110others(57): Show | 70 | HG00280.hp1 HG00558.hp1 HG01070.hp1 others(67): Show |
intron_variant | MODIFIER | c.164-6919G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41331459 | ||||||
chr21:41331550
|
A | G | 10 | a0001c0001t0001g0216a0001c0001t0001g0219a0001c0001t0001g0221others(7): Show | 10 | HG01891.hp2 HG02280.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.164-6828A>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41331550 | ||||||
chr21:41331575
|
T | C | 1 | a0001c0001t0002g0026 | 2 | HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.164-6803T>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41331575 | ||||||
chr21:41331680
|
A | G | 5 | a0001c0001t0001g0110a0001c0001t0002g0106a0001c0001t0002g0107others(2): Show | 5 | HG01109.hp1 HG01884.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.164-6698A>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41331680 | ||||||
chr21:41331843
|
A | G | 2 | a0001c0001t0002g0104a0001c0001t0002g0105 | 2 | HG03139.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.164-6535A>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41331843 | ||||||
chr21:41331892
|
A | G | 1 | a0001c0002t0001g0248 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.164-6486A>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41331892 | ||||||
chr21:41331894
|
A | C | 1 | a0001c0001t0002g0225 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.164-6484A>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41331894 | ||||||
chr21:41332016
|
C | T | 3 | a0002c0003t0002g0011a0002c0003t0002g0012a0002c0003t0002g0037 | 5 | HG01070.hp2 HG01071.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.164-6362C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41332016 | ||||||
chr21:41332136
|
G | A | 7 | a0001c0001t0001g0132a0001c0001t0001g0199a0001c0001t0001g0201others(4): Show | 7 | HG02055.hp1 HG02145.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.164-6242G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41332136 | ||||||
chr21:41332159
|
C | G | 21 | a0001c0001t0001g0110a0001c0001t0001g0132a0001c0001t0001g0199others(18): Show | 23 | HG00558.hp1 HG01070.hp1 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.164-6219C>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41332159 | ||||||
chr21:41332325
|
T | C | 1 | a0002c0003t0007g0102 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.164-6053T>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41332325 | ||||||
chr21:41332563
|
T | A | 13 | a0001c0001t0001g0121a0001c0001t0001g0191a0001c0001t0001g0192others(10): Show | 13 | HG00140.hp2 HG00642.hp2 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.164-5815T>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41332563 | ||||||
chr21:41332781
|
G | A | 1 | a0001c0002t0001g0147 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.164-5597G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41332781 | ||||||
chr21:41332874
|
C | CA | 74 | a0001c0001t0001g0004a0001c0001t0001g0027a0001c0001t0001g0054others(71): Show | 92 | HG00099.hp2 HG00280.hp1 HG00621.hp2 others(89): Show |
intron_variant | MODIFIER | c.164-5498dupA | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr21 | 41332874 | |||||
chr21:41333020
|
T | C | 124 | a0001c0001t0001g0004a0001c0001t0001g0020a0001c0001t0001g0027others(121): Show | 146 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.164-5358T>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41333020 | ||||||
chr21:41333024
|
A | C | 1 | a0001c0001t0001g0188 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.164-5354A>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41333024 | ||||||
chr21:41333056
|
C | T | 18 | a0001c0001t0001g0020a0001c0001t0001g0129a0001c0001t0001g0204others(15): Show | 20 | HG00099.hp1 HG01074.hp1 HG01175.hp2 others(17): Show |
intron_variant | MODIFIER | c.164-5322C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41333056 | ||||||
chr21:41333078
|
T | C | 1 | a0001c0001t0002g0225 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.164-5300T>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41333078 | ||||||
chr21:41333131
|
G | GT | 74 | a0001c0001t0001g0004a0001c0001t0001g0027a0001c0001t0001g0054others(71): Show | 92 | HG00099.hp2 HG00280.hp1 HG00621.hp2 others(89): Show |
intron_variant | MODIFIER | c.164-5234dupT | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr21 | 41333131 | |||||
chr21:41333131
|
G | GTT | 13 | a0001c0001t0001g0128a0001c0001t0001g0216a0001c0001t0001g0219others(10): Show | 13 | HG01891.hp2 HG02258.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.164-5235_164-5234d others(4): Show |
FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr21 | 41333131 | |||||
chr21:41333151
|
A | T | 1 | a0001c0005t0001g0228 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.164-5227A>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41333151 | ||||||
chr21:41333194
|
A | G | 124 | a0001c0001t0001g0004a0001c0001t0001g0020a0001c0001t0001g0027others(121): Show | 146 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.164-5184A>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41333194 | ||||||
chr21:41333397
|
T | G | 125 | a0001c0001t0001g0004a0001c0001t0001g0020a0001c0001t0001g0027others(122): Show | 147 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.164-4981T>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41333397 | ||||||
chr21:41333478
|
T | C | 35 | a0001c0001t0001g0057a0001c0001t0001g0116a0001c0001t0001g0117others(32): Show | 39 | HG00280.hp1 HG01109.hp2 HG01256.hp2 others(36): Show |
intron_variant | MODIFIER | c.164-4900T>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41333478 | ||||||
chr21:41333523
|
T | C | 2 | a0001c0001t0001g0136a0001c0001t0004g0137 | 2 | HG01167.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.164-4855T>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41333523 | ||||||
chr21:41333762
|
A | G | 1 | a0001c0001t0002g0104 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.164-4616A>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41333762 | ||||||
chr21:41334013
|
A | T | 21 | a0001c0001t0001g0110a0001c0001t0001g0132a0001c0001t0001g0199others(18): Show | 23 | HG00558.hp1 HG01070.hp1 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.164-4365A>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41334013 | ||||||
chr21:41334035
|
G | T | 1 | a0001c0001t0001g0177 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.164-4343G>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41334035 | ||||||
chr21:41334047
|
T | G | 2 | a0001c0001t0001g0128a0001c0001t0002g0127 | 2 | HG02258.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.164-4331T>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41334047 | ||||||
chr21:41334303
|
T | G | 28 | a0001c0001t0001g0004a0001c0001t0001g0057a0001c0001t0001g0116others(25): Show | 36 | HG00280.hp1 HG01070.hp2 HG01071.hp1 others(33): Show |
intron_variant | MODIFIER | c.164-4075T>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41334303 | ||||||
chr21:41334362
|
G | C | 58 | a0001c0001t0001g0004a0001c0001t0001g0020a0001c0001t0001g0057others(55): Show | 68 | HG00099.hp1 HG00280.hp1 HG01070.hp2 others(65): Show |
intron_variant | MODIFIER | c.164-4016G>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41334362 | ||||||
chr21:41334376
|
A | G | 1 | a0001c0001t0001g0091 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.164-4002A>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41334376 | ||||||
chr21:41334384
|
A | G | 26 | a0001c0001t0001g0057a0001c0001t0001g0116a0001c0001t0001g0117others(23): Show | 31 | HG00280.hp1 HG01070.hp2 HG01071.hp1 others(28): Show |
intron_variant | MODIFIER | c.164-3994A>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41334384 | ||||||
chr21:41334573
|
G | T | 1 | a0001c0001t0001g0007 | 3 | HG00609.hp1 HG00621.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.164-3805G>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41334573 | ||||||
chr21:41334682
|
G | C | 21 | a0001c0001t0001g0110a0001c0001t0001g0132a0001c0001t0001g0199others(18): Show | 23 | HG00558.hp1 HG01070.hp1 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.164-3696G>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41334682 | ||||||
chr21:41334737
|
G | T | 2 | a0001c0001t0001g0175a0001c0001t0001g0176 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.164-3641G>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41334737 | ||||||
chr21:41334794
|
C | T | 2 | a0001c0001t0001g0004a0001c0001t0002g0226 | 5 | NA18747.hp2 NA18952.hp2 NA18955.hp2 others(2): Show |
intron_variant | MODIFIER | c.164-3584C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41334794 | ||||||
chr21:41334844
|
G | T | 1 | a0001c0001t0001g0132 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.164-3534G>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41334844 | ||||||
chr21:41334846
|
A | G | 132 | a0001c0001t0001g0004a0001c0001t0001g0020a0001c0001t0001g0027others(129): Show | 154 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.164-3532A>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41334846 | ||||||
chr21:41335146
|
G | A | 1 | a0001c0001t0001g0064 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.164-3232G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41335146 | ||||||
chr21:41335239
|
A | G | 91 | a0001c0001t0001g0004a0001c0001t0001g0020a0001c0001t0001g0027others(88): Show | 111 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.164-3139A>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41335239 | ||||||
chr21:41335399
|
G | A | 2 | a0001c0001t0001g0004a0001c0001t0002g0226 | 5 | NA18747.hp2 NA18952.hp2 NA18955.hp2 others(2): Show |
intron_variant | MODIFIER | c.164-2979G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41335399 | ||||||
chr21:41335679
|
G | T | 1 | a0001c0001t0002g0131 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.164-2699G>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41335679 | ||||||
chr21:41335705
|
G | T | 1 | a0001c0001t0002g0225 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.164-2673G>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41335705 | ||||||
chr21:41335802
|
T | G | 1 | a0001c0001t0002g0106 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.164-2576T>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41335802 | ||||||
chr21:41335989
|
T | G | 1 | a0003c0004t0001g0133 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.164-2389T>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41335989 | ||||||
chr21:41336064
|
TC | T | 3 | a0001c0001t0001g0196a0001c0001t0002g0195a0003c0004t0002g0094 | 3 | HG00140.hp2 HG02895.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.164-2313delC | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41336064 | ||||||
chr21:41336073
|
G | C | 22 | a0001c0001t0001g0110a0001c0001t0001g0120a0001c0001t0001g0132others(19): Show | 24 | HG00558.hp1 HG01070.hp1 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.164-2305G>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41336073 | ||||||
chr21:41336086
|
G | A | 16 | a0001c0001t0001g0002a0001c0001t0001g0065a0001c0001t0001g0066others(13): Show | 19 | HG01255.hp2 HG01257.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.164-2292G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41336086 | ||||||
chr21:41336207
|
T | G | 1 | a0001c0001t0002g0225 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.164-2171T>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41336207 | ||||||
chr21:41336233
|
A | T | 4 | a0001c0001t0001g0129a0001c0001t0002g0104a0001c0001t0002g0105others(1): Show | 4 | HG02723.hp1 HG03139.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.164-2145A>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41336233 | ||||||
chr21:41336558
|
A | G | 6 | a0001c0001t0001g0199a0001c0001t0001g0201a0001c0001t0001g0202others(3): Show | 6 | HG02055.hp1 HG02145.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.164-1820A>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41336558 | ||||||
chr21:41336658
|
A | G | 1 | a0001c0005t0001g0228 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.164-1720A>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41336658 | ||||||
chr21:41336829
|
C | T | 1 | a0002c0003t0002g0011 | 2 | HG03041.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.164-1549C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41336829 | ||||||
chr21:41336859
|
G | A | 2 | a0001c0001t0001g0004a0001c0001t0002g0226 | 5 | NA18747.hp2 NA18952.hp2 NA18955.hp2 others(2): Show |
intron_variant | MODIFIER | c.164-1519G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41336859 | ||||||
chr21:41336913
|
A | G | 1 | a0001c0001t0002g0130 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.164-1465A>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41336913 | ||||||
chr21:41336926
|
G | A | 2 | a0001c0001t0001g0004a0001c0001t0002g0226 | 5 | NA18747.hp2 NA18952.hp2 NA18955.hp2 others(2): Show |
intron_variant | MODIFIER | c.164-1452G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41336926 | ||||||
chr21:41336958
|
A | G | 1 | a0001c0001t0001g0132 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.164-1420A>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41336958 | ||||||
chr21:41336969
|
C | G | 1 | a0001c0001t0001g0174 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.164-1409C>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41336969 | ||||||
chr21:41337058
|
T | A | 8 | a0001c0001t0001g0204a0001c0001t0001g0207a0001c0001t0001g0210others(5): Show | 9 | HG01243.hp2 HG02055.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.164-1320T>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41337058 | ||||||
chr21:41337077
|
G | C | 1 | a0001c0001t0001g0148 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.164-1301G>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41337077 | ||||||
chr21:41337201
|
C | A | 2 | a0001c0001t0001g0004a0001c0001t0002g0226 | 5 | NA18747.hp2 NA18952.hp2 NA18955.hp2 others(2): Show |
intron_variant | MODIFIER | c.164-1177C>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41337201 | ||||||
chr21:41337331
|
C | T | 12 | a0001c0001t0001g0211a0001c0001t0002g0145a0002c0003t0001g0039others(9): Show | 14 | HG01070.hp2 HG01071.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.164-1047C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41337331 | ||||||
chr21:41337669
|
G | T | 54 | a0001c0001t0001g0020a0001c0001t0001g0110a0001c0001t0001g0129others(51): Show | 58 | HG00099.hp1 HG00558.hp1 HG01070.hp1 others(55): Show |
intron_variant | MODIFIER | c.164-709G>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41337669 | ||||||
chr21:41337682
|
C | G | 1 | a0001c0007t0001g0033 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.164-696C>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41337682 | ||||||
chr21:41337720
|
T | C | 15 | a0001c0001t0001g0027a0001c0001t0001g0216a0001c0001t0001g0219others(12): Show | 16 | HG01257.hp2 HG01258.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.164-658T>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41337720 | ||||||
chr21:41337729
|
T | C | 8 | a0001c0001t0001g0204a0001c0001t0001g0207a0001c0001t0001g0210others(5): Show | 9 | HG01243.hp2 HG02055.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.164-649T>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41337729 | ||||||
chr21:41337731
|
C | T | 5 | a0001c0001t0001g0004a0001c0001t0001g0088a0001c0001t0001g0089others(2): Show | 8 | HG03669.hp1 HG03710.hp1 HG03831.hp2 others(5): Show |
intron_variant | MODIFIER | c.164-647C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41337731 | ||||||
chr21:41337810
|
G | C | 56 | a0001c0001t0001g0004a0001c0001t0001g0020a0001c0001t0001g0021others(53): Show | 71 | HG00099.hp1 HG00099.hp2 HG00673.hp2 others(68): Show |
intron_variant | MODIFIER | c.164-568G>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41337810 | ||||||
chr21:41337837
|
G | A | 2 | a0001c0002t0001g0030a0001c0002t0001g0262 | 3 | HG03834.hp1 NA20752.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.164-541G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41337837 | ||||||
chr21:41337883
|
G | A | 2 | a0001c0001t0001g0004a0001c0001t0002g0226 | 5 | NA18747.hp2 NA18952.hp2 NA18955.hp2 others(2): Show |
intron_variant | MODIFIER | c.164-495G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41337883 | ||||||
chr21:41338027
|
C | G | 1 | a0002c0003t0001g0046 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.164-351C>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41338027 | ||||||
chr21:41338138
|
C | T | 11 | a0001c0001t0001g0057a0001c0001t0001g0116a0001c0001t0001g0117others(8): Show | 14 | HG00280.hp1 HG01109.hp2 HG01256.hp2 others(11): Show |
intron_variant | MODIFIER | c.164-240C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41338138 | ||||||
chr21:41338248
|
T | C | 109 | a0001c0001t0001g0004a0001c0001t0001g0020a0001c0001t0001g0027others(106): Show | 126 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(123): Show |
intron_variant | MODIFIER | c.164-130T>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41338248 | ||||||
chr21:41338308
|
G | A | 2 | a0001c0001t0002g0105a0001c0001t0002g0107 | 2 | HG02922.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.164-70G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 2/7 | chr21 | 41338308 | ||||||
chr21:41338533
|
C | T | 1 | a0001c0001t0001g0173 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.287+32C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41338533 | ||||||
chr21:41338595
|
A | C | 2 | a0001c0001t0001g0068a0001c0001t0001g0069 | 2 | NA18964.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.287+94A>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41338595 | ||||||
chr21:41338609
|
T | C | 1 | a0001c0001t0001g0097 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.287+108T>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41338609 | ||||||
chr21:41338639
|
A | G | 36 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0056others(33): Show | 45 | HG00099.hp2 HG00673.hp2 HG00733.hp1 others(42): Show |
intron_variant | MODIFIER | c.287+138A>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41338639 | ||||||
chr21:41338692
|
C | G | 1 | a0001c0002t0001g0262 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.287+191C>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41338692 | ||||||
chr21:41338709
|
CT | C | 15 | a0001c0001t0001g0136a0001c0001t0001g0204a0001c0001t0001g0207others(12): Show | 15 | HG01167.hp2 HG01243.hp2 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.287+210delT | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr21 | 41338709 | |||||
chr21:41338745
|
A | C | 6 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0085others(3): Show | 6 | HG02027.hp1 HG02132.hp2 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.287+244A>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41338745 | ||||||
chr21:41338795
|
C | T | 2 | a0001c0001t0002g0105a0001c0001t0002g0107 | 2 | HG02922.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.287+294C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41338795 | ||||||
chr21:41339012
|
G | A | 13 | a0001c0001t0001g0057a0001c0001t0001g0116a0001c0001t0001g0117others(10): Show | 16 | HG00280.hp1 HG01109.hp2 HG01256.hp2 others(13): Show |
intron_variant | MODIFIER | c.287+511G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41339012 | ||||||
chr21:41339063
|
G | T | 1 | a0001c0002t0001g0248 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.287+562G>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41339063 | ||||||
chr21:41339280
|
C | A | 1 | a0001c0001t0001g0065 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.287+779C>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41339280 | ||||||
chr21:41339352
|
C | T | 85 | a0001c0001t0001g0027a0001c0001t0001g0057a0001c0001t0001g0110others(82): Show | 91 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.287+851C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41339352 | ||||||
chr21:41339529
|
G | A | 104 | a0001c0001t0001g0020a0001c0001t0001g0027a0001c0001t0001g0110others(101): Show | 118 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(115): Show |
intron_variant | MODIFIER | c.287+1028G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41339529 | ||||||
chr21:41339592
|
A | T | 31 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0028others(28): Show | 40 | HG00099.hp2 HG00673.hp2 HG00733.hp1 others(37): Show |
intron_variant | MODIFIER | c.287+1091A>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41339592 | ||||||
chr21:41339751
|
T | G | 189 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(186): Show | 228 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.287+1250T>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41339751 | ||||||
chr21:41339758
|
G | A | 1 | a0001c0005t0001g0228 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.287+1257G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41339758 | ||||||
chr21:41339786
|
C | T | 40 | a0001c0001t0001g0027a0001c0001t0001g0110a0001c0001t0001g0121others(37): Show | 41 | HG00140.hp2 HG00642.hp2 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.287+1285C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41339786 | ||||||
chr21:41339862
|
G | A | 7 | a0001c0001t0001g0132a0001c0001t0001g0199a0001c0001t0001g0201others(4): Show | 8 | HG02055.hp1 HG02055.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.287+1361G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41339862 | ||||||
chr21:41339885
|
A | G | 1 | a0001c0005t0001g0258 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.287+1384A>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41339885 | ||||||
chr21:41339966
|
G | C | 4 | a0001c0001t0002g0208a0001c0001t0002g0209a0001c0005t0002g0257others(1): Show | 4 | HG02717.hp2 HG02965.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.287+1465G>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41339966 | ||||||
chr21:41340009
|
T | C | 160 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(157): Show | 195 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(192): Show |
intron_variant | MODIFIER | c.287+1508T>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41340009 | ||||||
chr21:41340054
|
G | A | 22 | a0001c0001t0001g0121a0001c0001t0001g0128a0001c0001t0001g0129others(19): Show | 22 | HG00140.hp2 HG00642.hp2 HG01255.hp1 others(19): Show |
intron_variant | MODIFIER | c.287+1553G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41340054 | ||||||
chr21:41340074
|
T | A | 1 | a0001c0001t0001g0060 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.287+1573T>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41340074 | ||||||
chr21:41340099
|
G | A | 1 | a0001c0001t0001g0149 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.287+1598G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41340099 | ||||||
chr21:41340152
|
C | CT | 13 | a0001c0001t0001g0069a0001c0001t0001g0090a0001c0001t0001g0128others(10): Show | 13 | HG02258.hp1 HG02300.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.287+1671dupT | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr21 | 41340152 | |||||
chr21:41340152
|
CTT | C | 14 | a0001c0002t0001g0235a0003c0004t0001g0053a0003c0004t0001g0111others(11): Show | 16 | HG00558.hp1 HG01070.hp1 HG02080.hp2 others(13): Show |
intron_variant | MODIFIER | c.287+1670_287+1671d others(4): Show |
FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr21 | 41340152 | |||||
chr21:41340215
|
G | A | 1 | a0001c0001t0001g0136 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.287+1714G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41340215 | ||||||
chr21:41340223
|
G | A | 1 | a0001c0005t0001g0228 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.287+1722G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41340223 | ||||||
chr21:41340388
|
A | G | 14 | a0001c0001t0001g0020a0001c0001t0001g0132a0001c0001t0001g0199others(11): Show | 16 | HG00099.hp1 HG01074.hp1 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.287+1887A>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41340388 | ||||||
chr21:41340590
|
A | G | 15 | a0001c0001t0001g0020a0001c0001t0001g0132a0001c0001t0001g0199others(12): Show | 17 | HG00099.hp1 HG01074.hp1 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.287+2089A>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41340590 | ||||||
chr21:41340592
|
C | A | 15 | a0001c0001t0001g0020a0001c0001t0001g0132a0001c0001t0001g0199others(12): Show | 17 | HG00099.hp1 HG01074.hp1 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.287+2091C>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41340592 | ||||||
chr21:41340696
|
G | T | 1 | a0001c0001t0001g0032 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.287+2195G>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41340696 | ||||||
chr21:41341003
|
T | C | 1 | a0001c0001t0001g0243 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.287+2502T>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41341003 | ||||||
chr21:41341069
|
A | G | 15 | a0001c0001t0001g0020a0001c0001t0001g0132a0001c0001t0001g0199others(12): Show | 17 | HG00099.hp1 HG01074.hp1 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.287+2568A>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41341069 | ||||||
chr21:41341142
|
G | GTTAATAG others(27): Show |
1 | a0001c0001t0001g0072 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.287+2644_287+2677d others(36): Show |
FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr21 | 41341142 | |||||
chr21:41341163
|
T | C | 1 | a0001c0001t0001g0174 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.287+2662T>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41341163 | ||||||
chr21:41341237
|
T | G | 1 | a0001c0001t0002g0023 | 2 | HG02965.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.287+2736T>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41341237 | ||||||
chr21:41341444
|
C | T | 31 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0028others(28): Show | 40 | HG00099.hp2 HG00673.hp2 HG00733.hp1 others(37): Show |
intron_variant | MODIFIER | c.287+2943C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41341444 | ||||||
chr21:41341595
|
A | G | 1 | a0001c0001t0001g0084 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.288-2881A>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41341595 | ||||||
chr21:41341936
|
G | A | 6 | a0001c0001t0001g0020a0001c0001t0002g0124a0001c0001t0002g0125others(3): Show | 7 | HG00099.hp1 HG01074.hp1 HG01934.hp2 others(4): Show |
intron_variant | MODIFIER | c.288-2540G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41341936 | ||||||
chr21:41341985
|
G | A | 2 | a0001c0001t0002g0105a0001c0001t0002g0107 | 2 | HG02922.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.288-2491G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41341985 | ||||||
chr21:41342021
|
A | G | 1 | a0001c0001t0001g0054 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.288-2455A>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41342021 | ||||||
chr21:41342161
|
T | C | 21 | a0001c0001t0001g0121a0001c0001t0001g0128a0001c0001t0001g0129others(18): Show | 21 | HG00140.hp2 HG00642.hp2 HG01255.hp1 others(18): Show |
intron_variant | MODIFIER | c.288-2315T>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41342161 | ||||||
chr21:41342181
|
G | T | 15 | a0001c0001t0001g0020a0001c0001t0001g0199a0001c0001t0001g0201others(12): Show | 17 | HG00099.hp1 HG01074.hp1 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.288-2295G>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41342181 | ||||||
chr21:41342210
|
C | T | 1 | a0001c0001t0001g0072 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.288-2266C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41342210 | ||||||
chr21:41342226
|
C | T | 1 | a0001c0001t0002g0026 | 2 | HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.288-2250C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41342226 | ||||||
chr21:41342361
|
T | A | 142 | a0001c0001t0001g0020a0001c0001t0001g0027a0001c0001t0001g0057others(139): Show | 161 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.288-2115T>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41342361 | ||||||
chr21:41342544
|
A | C | 1 | a0003c0004t0002g0114 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.288-1932A>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41342544 | ||||||
chr21:41342547
|
A | G | 48 | a0001c0001t0001g0020a0001c0001t0001g0054a0001c0001t0001g0055others(45): Show | 59 | HG00099.hp1 HG00099.hp2 HG00673.hp2 others(56): Show |
intron_variant | MODIFIER | c.288-1929A>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41342547 | ||||||
chr21:41342556
|
G | A | 1 | a0001c0001t0001g0092 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.288-1920G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41342556 | ||||||
chr21:41342605
|
C | T | 4 | a0001c0001t0004g0137a0002c0003t0001g0039a0002c0003t0001g0040others(1): Show | 4 | HG02572.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.288-1871C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41342605 | ||||||
chr21:41342640
|
A | G | 50 | a0001c0001t0001g0020a0001c0001t0001g0054a0001c0001t0001g0055others(47): Show | 61 | HG00099.hp1 HG00099.hp2 HG00673.hp2 others(58): Show |
intron_variant | MODIFIER | c.288-1836A>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41342640 | ||||||
chr21:41342709
|
A | G | 1 | a0001c0001t0002g0026 | 2 | HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.288-1767A>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41342709 | ||||||
chr21:41342764
|
T | C | 13 | a0003c0004t0001g0053a0003c0004t0001g0111a0003c0004t0001g0112others(10): Show | 15 | HG00558.hp1 HG01070.hp1 HG02080.hp2 others(12): Show |
intron_variant | MODIFIER | c.288-1712T>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41342764 | ||||||
chr21:41342781
|
T | C | 14 | a0001c0001t0001g0057a0001c0001t0001g0116a0001c0001t0001g0117others(11): Show | 17 | HG00280.hp1 HG01109.hp2 HG01256.hp2 others(14): Show |
intron_variant | MODIFIER | c.288-1695T>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41342781 | ||||||
chr21:41342858
|
G | A | 1 | a0001c0001t0001g0060 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.288-1618G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41342858 | ||||||
chr21:41342872
|
G | A | 27 | a0001c0001t0001g0057a0001c0001t0001g0116a0001c0001t0001g0117others(24): Show | 30 | HG00280.hp1 HG01109.hp2 HG01167.hp2 others(27): Show |
intron_variant | MODIFIER | c.288-1604G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41342872 | ||||||
chr21:41342910
|
A | G | 7 | a0001c0001t0001g0110a0001c0001t0001g0132a0001c0001t0001g0139others(4): Show | 7 | HG01109.hp1 HG01884.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.288-1566A>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41342910 | ||||||
chr21:41342992
|
A | G | 34 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0056others(31): Show | 43 | HG00099.hp2 HG00673.hp2 HG00733.hp1 others(40): Show |
intron_variant | MODIFIER | c.288-1484A>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41342992 | ||||||
chr21:41343351
|
T | C | 2 | a0001c0001t0001g0152a0001c0001t0001g0153 | 2 | HG02040.hp1 NA18942.hp2 |
intron_variant | MODIFIER | c.288-1125T>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41343351 | ||||||
chr21:41343355
|
G | A | 1 | a0001c0001t0001g0260 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.288-1121G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41343355 | ||||||
chr21:41343367
|
ATCTTTAA others(7): Show |
A | 1 | a0001c0002t0001g0235 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.288-1108_288-1095d others(16): Show |
FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41343367 | ||||||
chr21:41343389
|
A | C | 15 | a0001c0001t0001g0057a0001c0001t0001g0116a0001c0001t0001g0117others(12): Show | 18 | HG00280.hp1 HG01109.hp2 HG01256.hp2 others(15): Show |
intron_variant | MODIFIER | c.288-1087A>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41343389 | ||||||
chr21:41343422
|
A | G | 4 | a0001c0001t0004g0137a0002c0003t0001g0039a0002c0003t0001g0040others(1): Show | 4 | HG02572.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.288-1054A>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41343422 | ||||||
chr21:41343480
|
A | C | 1 | a0001c0001t0001g0135 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.288-996A>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41343480 | ||||||
chr21:41343548
|
A | C | 13 | a0003c0004t0001g0053a0003c0004t0001g0111a0003c0004t0001g0112others(10): Show | 15 | HG00558.hp1 HG01070.hp1 HG02080.hp2 others(12): Show |
intron_variant | MODIFIER | c.288-928A>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41343548 | ||||||
chr21:41343763
|
G | A | 14 | a0001c0001t0001g0057a0001c0001t0001g0116a0001c0001t0001g0117others(11): Show | 17 | HG00280.hp1 HG01109.hp2 HG01256.hp2 others(14): Show |
intron_variant | MODIFIER | c.288-713G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41343763 | ||||||
chr21:41343770
|
G | A | 1 | a0001c0002t0001g0236 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.288-706G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41343770 | ||||||
chr21:41343771
|
G | A | 1 | a0001c0001t0001g0192 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.288-705G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41343771 | ||||||
chr21:41343947
|
G | A | 1 | a0001c0001t0001g0073 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.288-529G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41343947 | ||||||
chr21:41343961
|
A | T | 1 | a0001c0001t0001g0189 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.288-515A>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41343961 | ||||||
chr21:41343962
|
T | A | 1 | a0001c0001t0001g0084 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.288-514T>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41343962 | ||||||
chr21:41343963
|
T | G | 1 | a0001c0001t0001g0129 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.288-513T>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41343963 | ||||||
chr21:41344059
|
G | T | 30 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0028others(27): Show | 39 | HG00099.hp2 HG00673.hp2 HG00733.hp1 others(36): Show |
intron_variant | MODIFIER | c.288-417G>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41344059 | ||||||
chr21:41344064
|
G | A | 1 | a0003c0004t0001g0016 | 2 | NA18940.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.288-412G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41344064 | ||||||
chr21:41344267
|
G | A | 1 | a0001c0001t0002g0131 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.288-209G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41344267 | ||||||
chr21:41344324
|
C | T | 1 | a0001c0005t0001g0228 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.288-152C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41344324 | ||||||
chr21:41344330
|
C | T | 2 | a0001c0001t0002g0105a0001c0001t0002g0107 | 2 | HG02922.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.288-146C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41344330 | ||||||
chr21:41344348
|
G | A | 44 | a0001c0001t0001g0027a0001c0001t0001g0110a0001c0001t0001g0121others(41): Show | 45 | HG00140.hp2 HG00642.hp2 HG01109.hp1 others(42): Show |
intron_variant | MODIFIER | c.288-128G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41344348 | ||||||
chr21:41344360
|
T | C | 1 | a0001c0001t0001g0182 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.288-116T>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41344360 | ||||||
chr21:41344379
|
C | T | 15 | a0001c0001t0002g0105a0001c0001t0002g0107a0003c0004t0001g0053others(12): Show | 17 | HG00558.hp1 HG01070.hp1 HG02080.hp2 others(14): Show |
intron_variant | MODIFIER | c.288-97C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41344379 | ||||||
chr21:41344434
|
G | A | 11 | a0001c0001t0002g0145a0001c0001t0002g0150a0001c0001t0002g0151others(8): Show | 13 | HG01070.hp2 HG01071.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.288-42G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41344434 | ||||||
chr21:41344468
|
C | T | 1 | a0001c0001t0001g0083 | 1 | NA19010.hp2 | splice_region_variant&intron_variant | LOW | c.288-8C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 3/7 | chr21 | 41344468 | ||||||
chr21:41344621
|
G | A | 44 | a0001c0001t0001g0027a0001c0001t0001g0110a0001c0001t0001g0121others(41): Show | 45 | HG00140.hp2 HG00642.hp2 HG01109.hp1 others(42): Show |
intron_variant | MODIFIER | c.346+87G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 4/7 | chr21 | 41344621 | ||||||
chr21:41344765
|
G | C | 13 | a0001c0001t0001g0057a0001c0001t0001g0116a0001c0001t0001g0117others(10): Show | 16 | HG00280.hp1 HG01109.hp2 HG01256.hp2 others(13): Show |
intron_variant | MODIFIER | c.346+231G>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 4/7 | chr21 | 41344765 | ||||||
chr21:41344780
|
A | T | 1 | a0001c0001t0001g0024 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.346+246A>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 4/7 | chr21 | 41344780 | ||||||
chr21:41344804
|
C | T | 2 | a0001c0001t0001g0121a0001c0001t0001g0192 | 2 | HG00642.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.346+270C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 4/7 | chr21 | 41344804 | ||||||
chr21:41344820
|
G | C | 2 | a0001c0001t0001g0074a0001c0001t0001g0083 | 2 | NA18979.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.346+286G>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 4/7 | chr21 | 41344820 | ||||||
chr21:41344933
|
G | A | 1 | a0001c0005t0001g0228 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.346+399G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 4/7 | chr21 | 41344933 | ||||||
chr21:41345040
|
G | A | 40 | a0001c0001t0001g0027a0001c0001t0001g0110a0001c0001t0001g0121others(37): Show | 41 | HG00140.hp2 HG00642.hp2 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.346+506G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 4/7 | chr21 | 41345040 | ||||||
chr21:41345070
|
C | T | 1 | a0003c0004t0002g0094 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.346+536C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 4/7 | chr21 | 41345070 | ||||||
chr21:41345136
|
A | G | 1 | a0001c0001t0001g0095 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.347-550A>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 4/7 | chr21 | 41345136 | ||||||
chr21:41345152
|
A | AGGCTGAG others(85): Show |
2 | a0001c0002t0001g0237a0001c0002t0001g0255 | 2 | HG00099.hp2 HG00738.hp2 |
intron_variant | MODIFIER | c.347-457_347-366dup others(92): Show |
FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr21 | 41345152 | |||||
chr21:41345183
|
TGAGGCGG others(39): Show |
T | 2 | a0001c0001t0002g0105a0001c0001t0002g0107 | 2 | HG02922.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.347-457_347-412del others(46): Show |
FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr21 | 41345183 | |||||
chr21:41345229
|
A | AGAGGCGG others(39): Show |
2 | a0001c0001t0002g0151a0001c0001t0002g0261 | 2 | HG02145.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.347-348_347-303dup others(46): Show |
FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr21 | 41345229 | |||||
chr21:41345229
|
AGAGGCGG others(39): Show |
A | 1 | a0001c0005t0001g0228 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.347-348_347-303del others(46): Show |
FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr21 | 41345229 | |||||
chr21:41345234
|
C | T | 44 | a0001c0001t0001g0027a0001c0001t0001g0110a0001c0001t0001g0121others(41): Show | 45 | HG00140.hp2 HG00642.hp2 HG01109.hp1 others(42): Show |
intron_variant | MODIFIER | c.347-452C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 4/7 | chr21 | 41345234 | ||||||
chr21:41345280
|
C | T | 1 | a0001c0005t0001g0228 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.347-406C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 4/7 | chr21 | 41345280 | ||||||
chr21:41345338
|
G | A | 1 | a0001c0001t0001g0088 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.347-348G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 4/7 | chr21 | 41345338 | ||||||
chr21:41345339
|
C | G | 1 | a0001c0001t0001g0088 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.347-347C>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 4/7 | chr21 | 41345339 | ||||||
chr21:41345372
|
C | T | 3 | a0001c0001t0001g0010a0001c0001t0001g0171a0001c0001t0001g0179 | 5 | HG01358.hp2 HG01943.hp1 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.347-314C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 4/7 | chr21 | 41345372 | ||||||
chr21:41345539
|
C | T | 1 | a0001c0001t0004g0137 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.347-147C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 4/7 | chr21 | 41345539 | ||||||
chr21:41345631
|
A | G | 11 | a0001c0001t0001g0027a0001c0001t0001g0122a0001c0001t0001g0219others(8): Show | 12 | HG01257.hp2 HG01258.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.347-55A>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 4/7 | chr21 | 41345631 | ||||||
chr21:41345649
|
G | A | 2 | a0003c0004t0002g0205a0003c0004t0002g0206 | 2 | HG02258.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.347-37G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 4/7 | chr21 | 41345649 | ||||||
chr21:41345683
|
C | T | 2 | a0002c0003t0001g0039a0002c0003t0001g0040 | 2 | HG02895.hp2 HG02897.hp1 |
splice_region_variant&intron_variant | LOW | c.347-3C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 4/7 | chr21 | 41345683 | ||||||
chr21:41345753
|
T | A | 6 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0118others(3): Show | 7 | HG01256.hp2 HG01361.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.397+17T>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 5/7 | chr21 | 41345753 | ||||||
chr21:41345866
|
T | C | 1 | a0001c0007t0001g0033 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.397+130T>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 5/7 | chr21 | 41345866 | ||||||
chr21:41345992
|
TATA | T | 18 | a0001c0001t0001g0027a0001c0001t0001g0110a0001c0001t0001g0122others(15): Show | 19 | HG01109.hp1 HG01257.hp2 HG01258.hp2 others(16): Show |
intron_variant | MODIFIER | c.397+261_397+263del others(3): Show |
FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr21 | 41345992 | |||||
chr21:41346014
|
C | CT | 33 | a0001c0001t0002g0105a0001c0001t0002g0107a0001c0001t0002g0130others(30): Show | 42 | HG00099.hp2 HG00673.hp2 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.397+286dupT | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr21 | 41346014 | |||||
chr21:41346021
|
T | A | 1 | a0001c0005t0001g0228 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.397+285T>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 5/7 | chr21 | 41346021 | ||||||
chr21:41346022
|
T | A | 4 | a0001c0001t0001g0024a0001c0001t0001g0182a0001c0001t0002g0234others(1): Show | 5 | HG01106.hp1 HG01346.hp2 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.397+286T>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 5/7 | chr21 | 41346022 | ||||||
chr21:41346022
|
T | TA | 49 | a0001c0001t0001g0027a0001c0001t0001g0110a0001c0001t0001g0121others(46): Show | 51 | HG00140.hp2 HG00642.hp2 HG01070.hp1 others(48): Show |
intron_variant | MODIFIER | c.397+300dupA | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr21 | 41346022 | |||||
chr21:41346022
|
T | TAA | 12 | a0003c0004t0001g0016a0003c0004t0001g0053a0003c0004t0001g0111others(9): Show | 15 | HG00558.hp1 HG02080.hp2 HG02083.hp2 others(12): Show |
intron_variant | MODIFIER | c.397+299_397+300dup others(2): Show |
FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr21 | 41346022 | |||||
chr21:41346022
|
TA | T | 9 | a0001c0001t0001g0060a0001c0001t0001g0082a0001c0001t0001g0153others(6): Show | 10 | HG01069.hp1 HG01070.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.397+300delA | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr21 | 41346022 | |||||
chr21:41346023
|
A | T | 8 | a0001c0001t0001g0118a0001c0001t0001g0136a0001c0001t0001g0174others(5): Show | 8 | HG00673.hp2 HG01167.hp2 HG01256.hp2 others(5): Show |
intron_variant | MODIFIER | c.397+287A>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 5/7 | chr21 | 41346023 | ||||||
chr21:41346035
|
A | G | 5 | a0001c0001t0002g0124a0001c0001t0002g0125a0001c0001t0002g0212others(2): Show | 5 | HG00099.hp1 HG02109.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.397+299A>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 5/7 | chr21 | 41346035 | ||||||
chr21:41346149
|
G | A | 1 | a0001c0001t0002g0127 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.397+413G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 5/7 | chr21 | 41346149 | ||||||
chr21:41346193
|
G | C | 1 | a0001c0001t0001g0092 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.397+457G>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 5/7 | chr21 | 41346193 | ||||||
chr21:41346235
|
G | A | 1 | a0001c0001t0001g0154 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.397+499G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 5/7 | chr21 | 41346235 | ||||||
chr21:41346335
|
C | T | 40 | a0001c0001t0001g0027a0001c0001t0001g0110a0001c0001t0001g0121others(37): Show | 41 | HG00140.hp2 HG00642.hp2 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.397+599C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 5/7 | chr21 | 41346335 | ||||||
chr21:41346402
|
G | A | 1 | a0002c0003t0001g0042 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.398-611G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 5/7 | chr21 | 41346402 | ||||||
chr21:41346559
|
C | A | 2 | a0001c0001t0002g0141a0001c0001t0002g0146 | 2 | HG03688.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.398-454C>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 5/7 | chr21 | 41346559 | ||||||
chr21:41346588
|
C | T | 35 | a0001c0001t0001g0199a0001c0001t0001g0201a0001c0001t0001g0202others(32): Show | 44 | HG00099.hp2 HG00673.hp2 HG00733.hp1 others(41): Show |
intron_variant | MODIFIER | c.398-425C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 5/7 | chr21 | 41346588 | ||||||
chr21:41346640
|
C | G | 35 | a0001c0001t0001g0199a0001c0001t0001g0201a0001c0001t0001g0202others(32): Show | 44 | HG00099.hp2 HG00673.hp2 HG00733.hp1 others(41): Show |
intron_variant | MODIFIER | c.398-373C>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 5/7 | chr21 | 41346640 | ||||||
chr21:41346782
|
G | C | 1 | a0002c0003t0001g0050 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.398-231G>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 5/7 | chr21 | 41346782 | ||||||
chr21:41346786
|
C | A | 1 | a0001c0002t0001g0193 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.398-227C>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 5/7 | chr21 | 41346786 | ||||||
chr21:41346827
|
A | G | 4 | a0001c0001t0002g0208a0001c0001t0002g0209a0001c0005t0002g0257others(1): Show | 4 | HG02717.hp2 HG02965.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.398-186A>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 5/7 | chr21 | 41346827 | ||||||
chr21:41346912
|
C | A | 3 | a0001c0002t0001g0126a0001c0002t0001g0183a0001c0002t0001g0184 | 3 | HG01106.hp2 HG01175.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.398-101C>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 5/7 | chr21 | 41346912 | ||||||
chr21:41347140
|
A | C | 1 | a0001c0001t0001g0128 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.485+40A>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 6/7 | chr21 | 41347140 | ||||||
chr21:41347210
|
C | A | 35 | a0001c0001t0001g0199a0001c0001t0001g0201a0001c0001t0001g0202others(32): Show | 44 | HG00099.hp2 HG00673.hp2 HG00733.hp1 others(41): Show |
intron_variant | MODIFIER | c.485+110C>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 6/7 | chr21 | 41347210 | ||||||
chr21:41347522
|
A | C | 1 | a0001c0001t0002g0234 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.485+422A>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 6/7 | chr21 | 41347522 | ||||||
chr21:41347580
|
T | G | 1 | a0001c0001t0002g0234 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.485+480T>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 6/7 | chr21 | 41347580 | ||||||
chr21:41347723
|
A | G | 1 | a0001c0001t0001g0168 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.485+623A>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 6/7 | chr21 | 41347723 | ||||||
chr21:41347737
|
G | C | 1 | a0001c0001t0002g0155 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.485+637G>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 6/7 | chr21 | 41347737 | ||||||
chr21:41347749
|
C | CA | 6 | a0001c0001t0001g0017a0001c0001t0001g0075a0001c0001t0001g0085others(3): Show | 7 | HG00673.hp1 HG02027.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.485+669dupA | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr21 | 41347749 | |||||
chr21:41347749
|
C | CAA | 15 | a0001c0002t0001g0235a0003c0004t0001g0016a0003c0004t0001g0053others(12): Show | 18 | HG00558.hp1 HG01070.hp1 HG02080.hp2 others(15): Show |
intron_variant | MODIFIER | c.485+668_485+669dup others(2): Show |
FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr21 | 41347749 | |||||
chr21:41347749
|
C | CAAA | 31 | a0001c0001t0002g0234a0001c0002t0001g0005a0001c0002t0001g0006others(28): Show | 39 | HG00099.hp2 HG00140.hp2 HG00673.hp2 others(36): Show |
intron_variant | MODIFIER | c.485+667_485+669dup others(3): Show |
FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr21 | 41347749 | |||||
chr21:41347749
|
CA | C | 12 | a0001c0001t0001g0057a0001c0001t0001g0098a0001c0001t0001g0118others(9): Show | 13 | HG00280.hp1 HG01069.hp2 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.485+669delA | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr21 | 41347749 | |||||
chr21:41347749
|
CAAAAAAA others(4): Show |
C | 41 | a0001c0001t0001g0027a0001c0001t0001g0110a0001c0001t0001g0121others(38): Show | 42 | HG00642.hp2 HG01109.hp1 HG01255.hp1 others(39): Show |
intron_variant | MODIFIER | c.485+659_485+669del others(11): Show |
FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr21 | 41347749 | |||||
chr21:41347795
|
C | T | 15 | a0001c0001t0001g0003a0001c0001t0001g0135a0001c0001t0001g0154others(12): Show | 19 | HG00140.hp1 HG00735.hp2 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.485+695C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 6/7 | chr21 | 41347795 | ||||||
chr21:41347797
|
TAC | T | 41 | a0001c0001t0001g0027a0001c0001t0001g0110a0001c0001t0001g0121others(38): Show | 42 | HG00642.hp2 HG01109.hp1 HG01255.hp1 others(39): Show |
intron_variant | MODIFIER | c.485+701_485+702del others(2): Show |
FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr21 | 41347797 | |||||
chr21:41348274
|
C | T | 2 | a0001c0001t0002g0151a0001c0001t0002g0261 | 2 | HG02145.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.486-318C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 6/7 | chr21 | 41348274 | ||||||
chr21:41348284
|
A | G | 97 | a0001c0001t0001g0027a0001c0001t0001g0110a0001c0001t0001g0121others(94): Show | 110 | HG00099.hp2 HG00140.hp2 HG00558.hp1 others(107): Show |
intron_variant | MODIFIER | c.486-308A>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 6/7 | chr21 | 41348284 | ||||||
chr21:41348290
|
TGA | T | 15 | a0003c0004t0001g0016a0003c0004t0001g0053a0003c0004t0001g0111others(12): Show | 18 | HG00140.hp2 HG00558.hp1 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.486-300_486-299del others(2): Show |
FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr21 | 41348290 | |||||
chr21:41348493
|
C | T | 7 | a0001c0001t0001g0110a0001c0001t0001g0132a0001c0001t0001g0139others(4): Show | 7 | HG01109.hp1 HG01884.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.486-99C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 6/7 | chr21 | 41348493 | ||||||
chr21:41348764
|
T | C | 1 | a0001c0001t0001g0068 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.618+40T>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41348764 | ||||||
chr21:41349098
|
C | A | 1 | a0001c0001t0001g0093 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.618+374C>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41349098 | ||||||
chr21:41349180
|
A | C | 44 | a0001c0001t0001g0027a0001c0001t0001g0110a0001c0001t0001g0121others(41): Show | 45 | HG00642.hp2 HG01109.hp1 HG01255.hp1 others(42): Show |
intron_variant | MODIFIER | c.618+456A>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41349180 | ||||||
chr21:41349378
|
ATGCTGCA others(8): Show |
A | 1 | a0001c0001t0001g0075 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.618+673_618+687del others(15): Show |
FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr21 | 41349378 | |||||
chr21:41349406
|
C | T | 1 | a0001c0001t0001g0090 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.618+682C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41349406 | ||||||
chr21:41349462
|
A | G | 1 | a0001c0001t0001g0191 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.618+738A>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41349462 | ||||||
chr21:41349609
|
C | T | 1 | a0001c0001t0001g0144 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.618+885C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41349609 | ||||||
chr21:41349646
|
G | A | 3 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0002g0026 | 4 | HG02055.hp2 HG02257.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.618+922G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41349646 | ||||||
chr21:41349694
|
G | A | 17 | a0001c0001t0001g0121a0001c0001t0001g0129a0001c0001t0001g0191others(14): Show | 17 | HG00642.hp2 HG01255.hp1 HG01952.hp2 others(14): Show |
intron_variant | MODIFIER | c.618+970G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41349694 | ||||||
chr21:41349704
|
C | T | 1 | a0001c0002t0001g0087 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.618+980C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41349704 | ||||||
chr21:41349793
|
C | T | 1 | a0001c0001t0002g0259 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.618+1069C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41349793 | ||||||
chr21:41349857
|
C | T | 32 | a0001c0001t0001g0166a0001c0001t0001g0202a0001c0001t0001g0203others(29): Show | 41 | HG00099.hp2 HG00673.hp2 HG00733.hp1 others(38): Show |
intron_variant | MODIFIER | c.618+1133C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41349857 | ||||||
chr21:41349912
|
T | G | 2 | a0001c0001t0001g0100a0001c0001t0001g0214 | 2 | HG03017.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.618+1188T>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41349912 | ||||||
chr21:41349915
|
C | T | 1 | a0001c0001t0001g0173 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.618+1191C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41349915 | ||||||
chr21:41349919
|
G | A | 3 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0002g0026 | 4 | HG02055.hp2 HG02257.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.618+1195G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41349919 | ||||||
chr21:41349942
|
C | T | 44 | a0001c0001t0001g0027a0001c0001t0001g0110a0001c0001t0001g0121others(41): Show | 45 | HG00642.hp2 HG01109.hp1 HG01255.hp1 others(42): Show |
intron_variant | MODIFIER | c.618+1218C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41349942 | ||||||
chr21:41349949
|
C | T | 132 | a0001c0001t0001g0027a0001c0001t0001g0057a0001c0001t0001g0110others(129): Show | 148 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(145): Show |
intron_variant | MODIFIER | c.618+1225C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41349949 | ||||||
chr21:41349983
|
C | T | 8 | a0001c0001t0001g0060a0001c0001t0001g0149a0001c0001t0001g0152others(5): Show | 8 | HG02040.hp1 HG02523.hp2 NA18942.hp2 others(5): Show |
intron_variant | MODIFIER | c.618+1259C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41349983 | ||||||
chr21:41350043
|
C | T | 1 | a0001c0001t0002g0104 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.618+1319C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41350043 | ||||||
chr21:41350103
|
G | A | 1 | a0001c0001t0001g0140 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.618+1379G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41350103 | ||||||
chr21:41350141
|
C | T | 31 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0002g0026others(28): Show | 40 | HG00099.hp2 HG00673.hp2 HG00733.hp1 others(37): Show |
intron_variant | MODIFIER | c.618+1417C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41350141 | ||||||
chr21:41350240
|
G | A | 4 | a0001c0001t0001g0207a0001c0001t0001g0210a0001c0001t0001g0211others(1): Show | 4 | HG01243.hp2 HG02615.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.618+1516G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41350240 | ||||||
chr21:41350250
|
C | G | 1 | a0001c0002t0001g0184 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.618+1526C>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41350250 | ||||||
chr21:41350463
|
G | A | 1 | a0001c0001t0001g0073 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.618+1739G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41350463 | ||||||
chr21:41350523
|
G | A | 1 | a0001c0001t0002g0109 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.618+1799G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41350523 | ||||||
chr21:41350633
|
G | A | 5 | a0001c0001t0002g0105a0001c0001t0002g0107a0001c0001t0002g0234others(2): Show | 5 | HG01884.hp1 HG02717.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.618+1909G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41350633 | ||||||
chr21:41350699
|
C | T | 4 | a0001c0001t0002g0105a0001c0001t0002g0107a0001c0005t0002g0257others(1): Show | 4 | HG02717.hp2 HG02922.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.618+1975C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41350699 | ||||||
chr21:41350737
|
A | G | 1 | a0001c0001t0002g0234 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.618+2013A>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41350737 | ||||||
chr21:41350912
|
G | A | 15 | a0003c0004t0001g0016a0003c0004t0001g0053a0003c0004t0001g0111others(12): Show | 18 | HG00140.hp2 HG00558.hp1 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.618+2188G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41350912 | ||||||
chr21:41350962
|
G | C | 1 | a0001c0001t0001g0135 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.618+2238G>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41350962 | ||||||
chr21:41350996
|
C | G | 7 | a0003c0004t0001g0016a0003c0004t0001g0112a0003c0004t0001g0113others(4): Show | 9 | HG00558.hp1 HG02080.hp2 HG02083.hp2 others(6): Show |
intron_variant | MODIFIER | c.618+2272C>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41350996 | ||||||
chr21:41351025
|
TG | T | 31 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0002g0026others(28): Show | 40 | HG00099.hp2 HG00673.hp2 HG00733.hp1 others(37): Show |
intron_variant | MODIFIER | c.618+2303delG | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr21 | 41351025 | |||||
chr21:41351028
|
T | C | 31 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0002g0026others(28): Show | 40 | HG00099.hp2 HG00673.hp2 HG00733.hp1 others(37): Show |
intron_variant | MODIFIER | c.618+2304T>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41351028 | ||||||
chr21:41351045
|
T | A | 3 | a0001c0001t0001g0057a0002c0003t0001g0013a0002c0003t0001g0046 | 4 | HG00280.hp1 HG01109.hp2 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.618+2321T>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41351045 | ||||||
chr21:41351133
|
G | A | 1 | a0002c0003t0002g0035 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.618+2409G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41351133 | ||||||
chr21:41351133
|
G | T | 1 | a0001c0001t0001g0162 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.618+2409G>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41351133 | ||||||
chr21:41351164
|
A | C | 11 | a0001c0001t0001g0027a0001c0001t0001g0122a0001c0001t0001g0138others(8): Show | 12 | HG01257.hp2 HG01258.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.618+2440A>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41351164 | ||||||
chr21:41351397
|
A | G | 1 | a0001c0005t0001g0228 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.618+2673A>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41351397 | ||||||
chr21:41351572
|
G | C | 34 | a0001c0001t0001g0057a0001c0001t0001g0136a0001c0001t0001g0204others(31): Show | 37 | HG00280.hp1 HG01070.hp2 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.618+2848G>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41351572 | ||||||
chr21:41351644
|
A | C | 17 | a0001c0001t0001g0121a0001c0001t0001g0191a0001c0001t0001g0192others(14): Show | 17 | HG00642.hp2 HG01255.hp1 HG01952.hp2 others(14): Show |
intron_variant | MODIFIER | c.618+2920A>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41351644 | ||||||
chr21:41351666
|
G | A | 2 | a0001c0001t0001g0018a0001c0001t0001g0096 | 3 | HG02683.hp1 HG02738.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.618+2942G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41351666 | ||||||
chr21:41351923
|
C | T | 4 | a0001c0001t0002g0105a0001c0001t0002g0107a0001c0005t0002g0257others(1): Show | 4 | HG02717.hp2 HG02922.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.618+3199C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41351923 | ||||||
chr21:41351953
|
T | G | 1 | a0005c0008t0001g0251 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.618+3229T>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41351953 | ||||||
chr21:41352013
|
G | A | 1 | a0001c0005t0001g0228 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.618+3289G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41352013 | ||||||
chr21:41352030
|
T | C | 49 | a0001c0001t0002g0105a0001c0001t0002g0107a0001c0001t0002g0195others(46): Show | 60 | HG00099.hp2 HG00140.hp2 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.618+3306T>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41352030 | ||||||
chr21:41352121
|
A | G | 1 | a0001c0001t0002g0130 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.618+3397A>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41352121 | ||||||
chr21:41352141
|
A | G | 1 | a0001c0001t0001g0139 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.618+3417A>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41352141 | ||||||
chr21:41352238
|
C | T | 2 | a0001c0001t0001g0128a0001c0001t0002g0104 | 2 | HG02258.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.618+3514C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41352238 | ||||||
chr21:41352263
|
T | C | 2 | a0001c0001t0002g0208a0001c0001t0002g0209 | 2 | HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.618+3539T>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41352263 | ||||||
chr21:41352771
|
G | A | 1 | a0001c0001t0001g0177 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.618+4047G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41352771 | ||||||
chr21:41352820
|
T | C | 1 | a0001c0001t0001g0249 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.618+4096T>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41352820 | ||||||
chr21:41352820
|
T | TAAATAAA others(1): Show |
124 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(121): Show | 155 | HG00140.hp1 HG00558.hp2 HG00597.hp1 others(152): Show |
intron_variant | MODIFIER | c.618+4103_618+4104i others(10): Show |
FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr21 | 41352820 | |||||
chr21:41352820
|
T | TAAATAAA others(5): Show |
32 | a0001c0001t0001g0057a0001c0001t0001g0136a0001c0001t0001g0204others(29): Show | 36 | HG00280.hp1 HG01070.hp2 HG01071.hp1 others(33): Show |
intron_variant | MODIFIER | c.618+4103_618+4104i others(14): Show |
FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr21 | 41352820 | |||||
chr21:41352820
|
T | TAAATAAA others(5): Show |
45 | a0001c0001t0001g0022a0001c0001t0001g0025a0001c0001t0001g0054others(42): Show | 49 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(46): Show |
intron_variant | MODIFIER | c.618+4103_618+4104i others(14): Show |
FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr21 | 41352820 | |||||
chr21:41352820
|
T | TAAATAAA others(9): Show |
5 | a0001c0001t0001g0199a0001c0001t0001g0201a0001c0001t0001g0202others(2): Show | 5 | HG02055.hp1 HG02145.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.618+4103_618+4104i others(18): Show |
FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr21 | 41352820 | |||||
chr21:41352820
|
T | TAAATAAA others(9): Show |
20 | a0001c0001t0001g0027a0001c0001t0001g0122a0001c0001t0001g0128others(17): Show | 22 | HG00558.hp1 HG01109.hp1 HG01257.hp2 others(19): Show |
intron_variant | MODIFIER | c.618+4103_618+4104i others(18): Show |
FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr21 | 41352820 | |||||
chr21:41352820
|
T | TAAATAAA others(13): Show |
2 | a0001c0001t0002g0208a0001c0001t0002g0209 | 2 | HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.618+4103_618+4104i others(22): Show |
FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr21 | 41352820 | |||||
chr21:41352820
|
T | TAAATAAA others(17): Show |
1 | a0001c0005t0001g0228 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.618+4103_618+4104i others(26): Show |
FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr21 | 41352820 | |||||
chr21:41352820
|
T | TAAATAAA others(13): Show |
5 | a0001c0001t0001g0110a0001c0001t0001g0132a0001c0001t0002g0104others(2): Show | 5 | HG01884.hp1 HG01884.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.618+4103_618+4104i others(22): Show |
FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr21 | 41352820 | |||||
chr21:41352857
|
G | A | 235 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(232): Show | 276 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(273): Show |
intron_variant | MODIFIER | c.618+4133G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41352857 | ||||||
chr21:41352964
|
C | T | 4 | a0001c0001t0002g0105a0001c0001t0002g0107a0001c0005t0002g0257others(1): Show | 4 | HG02717.hp2 HG02922.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.619-4144C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41352964 | ||||||
chr21:41352965
|
G | A | 6 | a0001c0001t0001g0199a0001c0001t0001g0201a0001c0001t0001g0202others(3): Show | 7 | HG02055.hp1 HG02055.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.619-4143G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41352965 | ||||||
chr21:41353028
|
C | T | 1 | a0001c0001t0001g0243 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.619-4080C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41353028 | ||||||
chr21:41353099
|
A | G | 1 | a0001c0002t0001g0241 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.619-4009A>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41353099 | ||||||
chr21:41353225
|
A | T | 1 | a0001c0001t0001g0158 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.619-3883A>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41353225 | ||||||
chr21:41353282
|
A | G | 1 | a0001c0001t0001g0158 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.619-3826A>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41353282 | ||||||
chr21:41353453
|
G | A | 132 | a0001c0001t0001g0027a0001c0001t0001g0057a0001c0001t0001g0110others(129): Show | 148 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(145): Show |
intron_variant | MODIFIER | c.619-3655G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41353453 | ||||||
chr21:41353541
|
C | T | 6 | a0001c0001t0001g0110a0001c0001t0001g0132a0001c0001t0001g0139others(3): Show | 6 | HG01884.hp2 HG02451.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.619-3567C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41353541 | ||||||
chr21:41353676
|
G | A | 1 | a0001c0001t0001g0069 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.619-3432G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41353676 | ||||||
chr21:41353722
|
G | T | 2 | a0001c0001t0002g0141a0001c0001t0002g0146 | 2 | HG03688.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.619-3386G>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41353722 | ||||||
chr21:41354182
|
G | A | 2 | a0001c0005t0002g0257a0002c0003t0001g0042 | 2 | HG02717.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.619-2926G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41354182 | ||||||
chr21:41354189
|
G | A | 1 | a0001c0002t0001g0239 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.619-2919G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41354189 | ||||||
chr21:41354192
|
G | A | 1 | a0001c0001t0001g0219 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.619-2916G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41354192 | ||||||
chr21:41354221
|
CAT | C | 40 | a0001c0001t0001g0024a0001c0001t0001g0027a0001c0001t0001g0110others(37): Show | 42 | HG00642.hp2 HG01109.hp1 HG01255.hp1 others(39): Show |
intron_variant | MODIFIER | c.619-2886_619-2885d others(4): Show |
FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41354221 | ||||||
chr21:41354310
|
T | C | 2 | a0001c0001t0001g0231a0001c0001t0001g0232 | 2 | HG02257.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.619-2798T>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41354310 | ||||||
chr21:41354832
|
C | CT | 134 | a0001c0001t0001g0027a0001c0001t0001g0057a0001c0001t0001g0110others(131): Show | 150 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.619-2276_619-2275i others(3): Show |
FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41354832 | ||||||
chr21:41355013
|
G | C | 134 | a0001c0001t0001g0027a0001c0001t0001g0057a0001c0001t0001g0110others(131): Show | 150 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.619-2095G>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41355013 | ||||||
chr21:41355370
|
C | A | 6 | a0001c0001t0001g0057a0002c0003t0001g0013a0002c0003t0001g0046others(3): Show | 7 | HG00280.hp1 HG01109.hp2 HG02040.hp2 others(4): Show |
intron_variant | MODIFIER | c.619-1738C>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41355370 | ||||||
chr21:41355375
|
G | A | 29 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0028others(26): Show | 37 | HG00099.hp2 HG00673.hp2 HG00733.hp1 others(34): Show |
intron_variant | MODIFIER | c.619-1733G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41355375 | ||||||
chr21:41355398
|
T | C | 2 | a0002c0003t0002g0047a0002c0003t0002g0048 | 2 | HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.619-1710T>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41355398 | ||||||
chr21:41355488
|
C | A | 1 | a0001c0001t0001g0207 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.619-1620C>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41355488 | ||||||
chr21:41355494
|
C | T | 1 | a0001c0001t0002g0259 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.619-1614C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41355494 | ||||||
chr21:41355556
|
G | GAAAC | 136 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(133): Show | 169 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.619-1530_619-1527d others(6): Show |
FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr21 | 41355556 | |||||
chr21:41355568
|
C | G | 1 | a0001c0001t0002g0026 | 2 | HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.619-1540C>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41355568 | ||||||
chr21:41355781
|
A | C | 79 | a0001c0001t0001g0027a0001c0001t0001g0110a0001c0001t0001g0121others(76): Show | 88 | HG00099.hp2 HG00642.hp2 HG00673.hp2 others(85): Show |
intron_variant | MODIFIER | c.619-1327A>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41355781 | ||||||
chr21:41355848
|
A | G | 18 | a0001c0001t0001g0027a0001c0001t0001g0110a0001c0001t0001g0122others(15): Show | 19 | HG01109.hp1 HG01257.hp2 HG01258.hp2 others(16): Show |
intron_variant | MODIFIER | c.619-1260A>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41355848 | ||||||
chr21:41355891
|
A | G | 1 | a0001c0001t0002g0026 | 2 | HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.619-1217A>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41355891 | ||||||
chr21:41356034
|
A | AATAC | 8 | a0001c0001t0001g0207a0001c0001t0001g0210a0001c0001t0001g0211others(5): Show | 8 | HG01243.hp2 HG02572.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.619-1068_619-1065d others(6): Show |
FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr21 | 41356034 | |||||
chr21:41356036
|
TACATACA others(3): Show |
T | 4 | a0001c0001t0001g0027a0001c0001t0001g0122a0001c0001t0001g0231others(1): Show | 5 | HG01257.hp2 HG01258.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.619-1068_619-1059d others(12): Show |
FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr21 | 41356036 | |||||
chr21:41356036
|
TACATACA others(7): Show |
T | 1 | a0001c0001t0001g0232 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.619-1068_619-1055d others(16): Show |
FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr21 | 41356036 | |||||
chr21:41356040
|
T | TAC | 39 | a0001c0001t0001g0021a0001c0001t0001g0024a0001c0001t0001g0025others(36): Show | 43 | HG00280.hp1 HG00673.hp2 HG00738.hp1 others(40): Show |
intron_variant | MODIFIER | c.619-1024_619-1023d others(4): Show |
FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr21 | 41356040 | |||||
chr21:41356040
|
T | TACAC | 8 | a0001c0001t0001g0007a0001c0001t0001g0066a0001c0001t0001g0091others(5): Show | 10 | HG00597.hp2 HG00609.hp1 HG00621.hp1 others(7): Show |
intron_variant | MODIFIER | c.619-1026_619-1023d others(6): Show |
FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr21 | 41356040 | |||||
chr21:41356040
|
T | TACACAC | 6 | a0001c0001t0001g0002a0001c0001t0001g0076a0001c0001t0001g0156others(3): Show | 9 | HG00642.hp1 HG01257.hp1 HG01975.hp2 others(6): Show |
intron_variant | MODIFIER | c.619-1028_619-1023d others(8): Show |
FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr21 | 41356040 | |||||
chr21:41356040
|
T | TACACACA others(5): Show |
1 | a0001c0001t0001g0250 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.619-1034_619-1023d others(14): Show |
FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr21 | 41356040 | |||||
chr21:41356040
|
TAC | T | 23 | a0001c0001t0001g0078a0001c0001t0001g0121a0001c0001t0001g0129others(20): Show | 25 | HG00558.hp2 HG00642.hp2 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.619-1024_619-1023d others(4): Show |
FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr21 | 41356040 | |||||
chr21:41356040
|
TACAC | T | 5 | a0001c0001t0001g0079a0001c0001t0001g0119a0001c0001t0001g0136others(2): Show | 6 | HG01167.hp2 HG01361.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.619-1026_619-1023d others(6): Show |
FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr21 | 41356040 | |||||
chr21:41356040
|
TACACAC | T | 12 | a0001c0001t0001g0128a0001c0001t0001g0199a0001c0001t0001g0201others(9): Show | 12 | HG01109.hp1 HG01167.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.619-1028_619-1023d others(8): Show |
FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr21 | 41356040 | |||||
chr21:41356040
|
TACACACA others(1): Show |
T | 28 | a0001c0001t0001g0110a0001c0001t0001g0132a0001c0001t0002g0108others(25): Show | 35 | HG00099.hp2 HG00733.hp1 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.619-1030_619-1023d others(10): Show |
FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr21 | 41356040 | |||||
chr21:41356044
|
C | T | 13 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0002g0026others(10): Show | 16 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.619-1064C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41356044 | ||||||
chr21:41356048
|
C | T | 3 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0002g0026 | 4 | HG02055.hp2 HG02257.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.619-1060C>T | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41356048 | ||||||
chr21:41356074
|
CACACACA others(5): Show |
C | 1 | a0001c0005t0001g0228 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.619-1032_619-1021d others(14): Show |
FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr21 | 41356074 | |||||
chr21:41356076
|
CACACACA others(3): Show |
C | 3 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0002g0026 | 4 | HG02055.hp2 HG02257.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.619-1030_619-1021d others(12): Show |
FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr21 | 41356076 | |||||
chr21:41356082
|
CACAT | C | 6 | a0001c0001t0002g0145a0001c0001t0002g0150a0002c0003t0002g0011others(3): Show | 8 | HG01070.hp2 HG01071.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.619-1024_619-1021d others(6): Show |
FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr21 | 41356082 | |||||
chr21:41356084
|
CAT | C | 10 | a0001c0001t0001g0189a0001c0001t0002g0125a0001c0001t0002g0151others(7): Show | 11 | HG00099.hp1 HG00140.hp2 HG01070.hp1 others(8): Show |
intron_variant | MODIFIER | c.619-1022_619-1021d others(4): Show |
FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr21 | 41356084 | |||||
chr21:41356086
|
T | C | 24 | a0001c0001t0001g0057a0001c0001t0001g0159a0001c0001t0001g0204others(21): Show | 25 | HG00280.hp1 HG01109.hp2 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.619-1022T>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41356086 | ||||||
chr21:41356506
|
T | C | 46 | a0001c0001t0001g0018a0001c0001t0001g0057a0001c0001t0001g0116others(43): Show | 50 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(47): Show |
intron_variant | MODIFIER | c.619-602T>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41356506 | ||||||
chr21:41356534
|
T | C | 92 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0060others(89): Show | 97 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.619-574T>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41356534 | ||||||
chr21:41356589
|
C | A | 11 | a0001c0001t0002g0108a0001c0001t0002g0226a0001c0002t0001g0087others(8): Show | 12 | HG02080.hp2 HG02132.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.619-519C>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41356589 | ||||||
chr21:41356620
|
G | A | 1 | a0001c0005t0002g0256 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.619-488G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41356620 | ||||||
chr21:41356639
|
C | A | 10 | a0001c0001t0001g0002a0001c0001t0001g0065a0001c0001t0001g0066others(7): Show | 13 | HG01255.hp2 HG01257.hp1 HG01975.hp2 others(10): Show |
intron_variant | MODIFIER | c.619-469C>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41356639 | ||||||
chr21:41356645
|
T | C | 1 | a0001c0001t0001g0204 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.619-463T>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41356645 | ||||||
chr21:41356675
|
C | G | 3 | a0001c0001t0002g0208a0001c0001t0002g0209a0001c0001t0002g0225 | 3 | HG02723.hp2 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.619-433C>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41356675 | ||||||
chr21:41356922
|
A | G | 2 | a0001c0001t0002g0105a0001c0001t0002g0107 | 2 | HG02922.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.619-186A>G | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41356922 | ||||||
chr21:41356974
|
G | A | 1 | a0001c0001t0002g0104 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.619-134G>A | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41356974 | ||||||
chr21:41357039
|
A | C | 1 | a0001c0001t0002g0124 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.619-69A>C | FAM3B | ENSG00000183844.17 | transcript | ENST00000357985.7 | protein_coding | 7/7 | chr21 | 41357039 |