Item | Value |
---|---|
geneid | 167555 |
ensemblid | ENSG00000152380.10 |
hgncid | 33716 |
symbol | FAM151B |
name | family with sequence similarity 151 member B |
refseq_nuc | NM_205548.3 |
refseq_prot | NP_991111.2 |
ensembl_nuc | ENST00000282226.5 |
ensembl_prot | ENSP00000282226.4 |
mane_status | MANE Select |
chr | chr5 |
start | 80488100 |
end | 80542563 |
strand | + |
ver | v1.2 |
region | chr5:80488100-80542563 |
region5000 | chr5:80483100-80547563 |
regionname0 | FAM151B_chr5_80488100_80542563 |
regionname5000 | FAM151B_chr5_80483100_80547563 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 276 | 251 | 73 | 50 | 87 | 11 | 30 | 64 | FAM151B_chr5_80483100_80547563 | FAM151B | copy fasta | chr5 | 80483100 | 80547563 |
a0002 | 1/1 | 276 | 103 | 14 | 19 | 55 | 1 | 12 | 44 | FAM151B_chr5_80483100_80547563 | FAM151B | copy fasta | chr5 | 80483100 | 80547563 |
a0003 | 0/0 | 276 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | copy fasta | chr5 | 80483100 | 80547563 |
a0004 | 0/0 | 276 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | copy fasta | chr5 | 80483100 | 80547563 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 831 | 241 | 72 | 45 | 87 | 9 | 28 | FAM151B_chr5_80483100_80547563 | FAM151B | copy fasta | chr5 | 80483100 | 80547563 |
c0002 | 1/1 | 831 | 103 | 14 | 19 | 55 | 1 | 12 | FAM151B_chr5_80483100_80547563 | FAM151B | copy fasta | chr5 | 80483100 | 80547563 |
c0003 | 0/0 | 831 | 10 | 1 | 5 | 0 | 2 | 2 | FAM151B_chr5_80483100_80547563 | FAM151B | copy fasta | chr5 | 80483100 | 80547563 |
c0004 | 0/0 | 831 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | copy fasta | chr5 | 80483100 | 80547563 |
c0005 | 0/0 | 831 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | copy fasta | chr5 | 80483100 | 80547563 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 756 | 334 | 71 | 70 | 137 | 12 | 42 | FAM151B_chr5_80483100_80547563 | FAM151B | copy fasta | chr5 | 80483100 | 80547563 |
t0002 | 0/0 | 756 | 14 | 14 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | copy fasta | chr5 | 80483100 | 80547563 |
t0003 | 0/0 | 756 | 2 | 2 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | copy fasta | chr5 | 80483100 | 80547563 |
t0004 | 0/0 | 756 | 2 | 0 | 0 | 2 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | copy fasta | chr5 | 80483100 | 80547563 |
t0005 | 0/0 | 756 | 2 | 0 | 0 | 2 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | copy fasta | chr5 | 80483100 | 80547563 |
t0006 | 0/0 | 756 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | copy fasta | chr5 | 80483100 | 80547563 |
t0007 | 0/0 | 756 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | copy fasta | chr5 | 80483100 | 80547563 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0190 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0287 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0293 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0295 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0328 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0343 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0350 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0352 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 831 | 241 | 72 | 45 | 87 | 9 | 28 | FAM151B_chr5_80483100_80547563 | FAM151B | copy fasta | chr5 | 80483100 | 80547563 |
a0001c0003 | 0/0 | 831 | 10 | 1 | 5 | 0 | 2 | 2 | FAM151B_chr5_80483100_80547563 | FAM151B | copy fasta | chr5 | 80483100 | 80547563 |
a0002c0002 | 1/1 | 831 | 103 | 14 | 19 | 55 | 1 | 12 | FAM151B_chr5_80483100_80547563 | FAM151B | copy fasta | chr5 | 80483100 | 80547563 |
a0003c0005 | 0/0 | 831 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | copy fasta | chr5 | 80483100 | 80547563 |
a0004c0004 | 0/0 | 831 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | copy fasta | chr5 | 80483100 | 80547563 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 1586 | 222 | 55 | 45 | 85 | 9 | 28 | FAM151B_chr5_80483100_80547563 | FAM151B | copy fasta | chr5 | 80483100 | 80547563 |
a0001c0001t0002 | 0/0 | 1586 | 14 | 14 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | copy fasta | chr5 | 80483100 | 80547563 |
a0001c0001t0003 | 0/0 | 1586 | 2 | 2 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | copy fasta | chr5 | 80483100 | 80547563 |
a0001c0001t0004 | 0/0 | 1586 | 2 | 0 | 0 | 2 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | copy fasta | chr5 | 80483100 | 80547563 |
a0001c0001t0006 | 0/0 | 1586 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | copy fasta | chr5 | 80483100 | 80547563 |
a0001c0003t0001 | 0/0 | 1586 | 10 | 1 | 5 | 0 | 2 | 2 | FAM151B_chr5_80483100_80547563 | FAM151B | copy fasta | chr5 | 80483100 | 80547563 |
a0002c0002t0001 | 1/1 | 1586 | 100 | 14 | 19 | 52 | 1 | 12 | FAM151B_chr5_80483100_80547563 | FAM151B | copy fasta | chr5 | 80483100 | 80547563 |
a0002c0002t0005 | 0/0 | 1586 | 2 | 0 | 0 | 2 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | copy fasta | chr5 | 80483100 | 80547563 |
a0002c0002t0007 | 0/0 | 1586 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | copy fasta | chr5 | 80483100 | 80547563 |
a0003c0005t0001 | 0/0 | 1586 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | copy fasta | chr5 | 80483100 | 80547563 |
a0004c0004t0001 | 0/0 | 1586 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | copy fasta | chr5 | 80483100 | 80547563 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0352 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0001g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0002g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0002g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0002g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0002g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0002g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0002g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0002g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0002g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0002g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0003g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0003g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0004g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0004g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0001t0006g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0003t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0003t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0003t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0003t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0003t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0003t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0003t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0003t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0001c0003t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0002c0002t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0002c0002t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0002c0002t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0002c0002t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0002c0002t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0002c0002t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0002c0002t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0002c0002t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0002c0002t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0002c0002t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0002c0002t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0002c0002t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0002c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0002c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0002c0002t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0002c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0002c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0002c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0002c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0002c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0002c0002t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0002c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0002c0002t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0002c0002t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0002c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0002c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0002c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0002c0002t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0002c0002t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0002c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0002c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0002c0002t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0002c0002t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0002c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0002c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0002c0002t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0002c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0002c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0002c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0002c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0002c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0002c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0002c0002t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0002c0002t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0002c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0002c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0002c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0002c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0002c0002t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0002c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0002c0002t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0002c0002t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0002c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0002c0002t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0002c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0002c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0002c0002t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0002c0002t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0002c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0002c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0002c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0002c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0002c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0002c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0002c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0002c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0002c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0002c0002t0001g0190 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0002c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0002c0002t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0002c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0002c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0002c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0002c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0002c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0002c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0002c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0002c0002t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0002c0002t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0002c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0002c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0002c0002t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0002c0002t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0002c0002t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0002c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0002c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0002c0002t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0002c0002t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0002c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0002c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0002c0002t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0002c0002t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0002c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0002c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0002c0002t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0002c0002t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0002c0002t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0002c0002t0001g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0002c0002t0001g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0002c0002t0001g0350 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0002c0002t0005g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0002c0002t0005g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0002c0002t0007g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0003c0005t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
a0004c0004t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00280 | hp1 | a0001 | c0003 | t0001 | g0295 | EUR | FIN | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0153 | EUR | FIN | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0343 | EUR | FIN | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG00323 | hp2 | a0002 | c0002 | t0001 | g0115 | EUR | FIN | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG00408 | hp1 | a0002 | c0002 | t0001 | g0072 | EAS | CHS | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | CHS | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG00438 | hp1 | a0002 | c0002 | t0007 | g0101 | EAS | CHS | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG00438 | hp2 | a0001 | c0001 | t0004 | g0104 | EAS | CHS | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG00544 | hp1 | a0002 | c0002 | t0001 | g0136 | EAS | CHS | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | CHS | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | CHS | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG00558 | hp2 | a0002 | c0002 | t0001 | g0069 | EAS | CHS | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | CHS | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG00621 | hp2 | a0002 | c0002 | t0001 | g0210 | EAS | CHS | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0255 | AMR | PUR | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG00639 | hp2 | a0002 | c0002 | t0001 | g0110 | AMR | PUR | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG00642 | hp1 | a0002 | c0002 | t0001 | g0038 | AMR | PUR | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | CHS | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | CHS | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG00735 | hp1 | a0002 | c0002 | t0001 | g0259 | AMR | PUR | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG00738 | hp1 | a0001 | c0003 | t0001 | g0187 | AMR | PUR | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0355 | AMR | PUR | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG01069 | hp2 | a0002 | c0002 | t0001 | g0094 | AMR | PUR | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG01070 | hp1 | a0002 | c0002 | t0001 | g0301 | AMR | PUR | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG01099 | hp1 | a0002 | c0002 | t0001 | g0245 | AMR | PUR | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0266 | AMR | PUR | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0335 | AMR | PUR | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG01109 | hp2 | a0001 | c0003 | t0001 | g0294 | AMR | PUR | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0318 | AMR | PUR | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG01168 | hp1 | a0001 | c0003 | t0001 | g0001 | AMR | PUR | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG01168 | hp2 | a0002 | c0002 | t0001 | g0084 | AMR | PUR | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0239 | AMR | PUR | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG01169 | hp2 | a0001 | c0003 | t0001 | g0001 | AMR | PUR | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0299 | AMR | PUR | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG01243 | hp1 | a0002 | c0002 | t0001 | g0132 | AMR | PUR | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0326 | AMR | PUR | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0247 | AMR | CLM | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG01255 | hp2 | a0002 | c0002 | t0001 | g0053 | AMR | CLM | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG01257 | hp1 | a0002 | c0002 | t0001 | g0134 | AMR | CLM | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | CLM | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG01258 | hp1 | a0002 | c0002 | t0001 | g0111 | AMR | CLM | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | CLM | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG01261 | hp1 | a0001 | c0003 | t0001 | g0186 | AMR | CLM | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0271 | AMR | CLM | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0275 | AMR | CLM | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0260 | AMR | CLM | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | CLM | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0248 | AMR | CLM | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | CLM | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0257 | AMR | CLM | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG01433 | hp1 | a0002 | c0002 | t0001 | g0232 | AMR | CLM | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | CLM | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0306 | AMR | CLM | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | CLM | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG01515 | hp1 | a0001 | c0003 | t0001 | g0293 | EUR | IBS | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0075 | EUR | IBS | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0108 | EUR | IBS | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0121 | EUR | IBS | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG01884 | hp1 | a0001 | c0001 | t0002 | g0285 | AFR | ACB | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0279 | AFR | ACB | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG01928 | hp1 | a0002 | c0002 | t0001 | g0117 | AMR | PEL | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | PEL | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG01943 | hp1 | a0002 | c0002 | t0001 | g0227 | AMR | PEL | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG01943 | hp2 | a0002 | c0002 | t0001 | g0122 | AMR | PEL | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG01975 | hp1 | a0002 | c0002 | t0001 | g0138 | AMR | PEL | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0205 | AMR | PEL | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | PEL | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG01978 | hp2 | a0003 | c0005 | t0001 | g0254 | AMR | PEL | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | PEL | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0347 | AMR | PEL | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | PEL | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | PEL | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | KHV | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | KHV | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG02071 | hp1 | a0002 | c0002 | t0001 | g0026 | EAS | KHV | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG02071 | hp2 | a0002 | c0002 | t0001 | g0179 | EAS | KHV | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | KHV | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | KHV | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | KHV | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | KHV | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | KHV | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | KHV | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0349 | EAS | KHV | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG02132 | hp1 | a0002 | c0002 | t0001 | g0022 | EAS | KHV | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | KHV | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG02135 | hp1 | a0002 | c0002 | t0001 | g0176 | EAS | KHV | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG02135 | hp2 | a0002 | c0002 | t0001 | g0025 | EAS | KHV | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0302 | AFR | ACB | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0253 | AFR | ACB | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | CDX | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | CDX | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG02257 | hp1 | a0001 | c0001 | t0003 | g0296 | AFR | ACB | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | ACB | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG02258 | hp1 | a0002 | c0002 | t0001 | g0083 | AFR | ACB | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0334 | AFR | ACB | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PEL | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG02273 | hp2 | a0002 | c0002 | t0001 | g0236 | AMR | PEL | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG02280 | hp1 | a0002 | c0002 | t0001 | g0220 | AFR | ACB | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0265 | AFR | ACB | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | PEL | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | PEL | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | PEL | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG02300 | hp2 | a0002 | c0002 | t0001 | g0226 | AMR | PEL | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG02451 | hp1 | a0001 | c0001 | t0002 | g0298 | AFR | ACB | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG02451 | hp2 | a0001 | c0001 | t0006 | g0286 | AFR | ACB | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | KHV | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | KHV | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0289 | AFR | GWD | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0270 | AFR | GWD | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG02622 | hp1 | a0002 | c0002 | t0001 | g0154 | AFR | GWD | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG02622 | hp2 | a0001 | c0001 | t0002 | g0297 | AFR | GWD | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0327 | AFR | GWD | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0311 | AFR | GWD | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG02683 | hp1 | a0002 | c0002 | t0001 | g0041 | SAS | PJL | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0261 | SAS | PJL | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0346 | SAS | PJL | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0035 | SAS | PJL | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | GWD | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0316 | AFR | GWD | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG02723 | hp1 | a0004 | c0004 | t0001 | g0324 | AFR | GWD | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0258 | AFR | GWD | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0106 | SAS | PJL | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG02735 | hp2 | a0002 | c0002 | t0001 | g0241 | SAS | PJL | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0240 | SAS | PJL | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0123 | SAS | PJL | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG02809 | hp1 | a0001 | c0001 | t0002 | g0320 | AFR | GWD | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG02809 | hp2 | a0001 | c0001 | t0002 | g0118 | AFR | GWD | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0340 | AFR | GWD | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | GWD | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0231 | AFR | GWD | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0284 | AFR | GWD | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0234 | AFR | GWD | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG02896 | hp2 | a0001 | c0001 | t0002 | g0206 | AFR | GWD | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | GWD | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG02897 | hp2 | a0001 | c0001 | t0002 | g0204 | AFR | GWD | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | ESN | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0300 | AFR | ESN | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | ESN | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0222 | AFR | ESN | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG02970 | hp1 | a0001 | c0001 | t0003 | g0282 | AFR | ESN | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0338 | AFR | ESN | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0092 | SAS | PJL | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0268 | SAS | PJL | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG03041 | hp1 | a0001 | c0003 | t0001 | g0292 | AFR | GWD | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG03041 | hp2 | a0002 | c0002 | t0001 | g0274 | AFR | GWD | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG03098 | hp1 | a0001 | c0001 | t0002 | g0281 | AFR | MSL | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0332 | AFR | MSL | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | ESN | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG03130 | hp2 | a0002 | c0002 | t0001 | g0194 | AFR | ESN | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG03139 | hp1 | a0002 | c0002 | t0001 | g0052 | AFR | ESN | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | ESN | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG03195 | hp1 | a0002 | c0002 | t0001 | g0344 | AFR | ESN | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0310 | AFR | ESN | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0341 | AFR | MSL | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG03209 | hp2 | a0001 | c0001 | t0002 | g0113 | AFR | MSL | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0307 | AFR | MSL | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0304 | AFR | MSL | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG03239 | hp1 | a0002 | c0002 | t0001 | g0112 | SAS | PJL | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0319 | SAS | PJL | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0336 | AFR | MSL | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG03453 | hp2 | a0002 | c0002 | t0001 | g0283 | AFR | MSL | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG03486 | hp1 | a0001 | c0001 | t0002 | g0278 | AFR | MSL | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0315 | AFR | MSL | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0321 | SAS | PJL | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG03490 | hp2 | a0002 | c0002 | t0001 | g0088 | SAS | PJL | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0157 | SAS | PJL | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG03491 | hp2 | a0002 | c0002 | t0001 | g0061 | SAS | PJL | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0166 | SAS | PJL | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG03492 | hp2 | a0002 | c0002 | t0001 | g0086 | SAS | PJL | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0308 | AFR | ESN | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG03516 | hp2 | a0002 | c0002 | t0001 | g0345 | AFR | ESN | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0353 | AFR | GWD | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG03540 | hp2 | a0002 | c0002 | t0001 | g0221 | AFR | GWD | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0331 | AFR | MSL | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0313 | AFR | MSL | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0305 | SAS | PJL | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0211 | SAS | PJL | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0246 | SAS | PJL | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG03669 | hp2 | a0001 | c0003 | t0001 | g0290 | SAS | PJL | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0337 | SAS | STU | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0235 | SAS | STU | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0352 | SAS | PJL | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG03710 | hp1 | a0002 | c0002 | t0001 | g0193 | SAS | PJL | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0263 | SAS | PJL | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0124 | SAS | BEB | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG03831 | hp2 | a0002 | c0002 | t0001 | g0244 | SAS | BEB | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | BEB | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0264 | SAS | BEB | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG03942 | hp1 | a0002 | c0002 | t0001 | g0037 | SAS | BEB | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0256 | SAS | BEB | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0267 | SAS | STU | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG04115 | hp2 | a0002 | c0002 | t0001 | g0016 | SAS | STU | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0125 | SAS | BEB | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG04184 | hp2 | a0002 | c0002 | t0001 | g0096 | SAS | BEB | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0329 | SAS | STU | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0330 | SAS | STU | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA18522 | hp1 | a0001 | c0001 | t0002 | g0238 | AFR | YRI | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA18522 | hp2 | a0001 | c0001 | t0002 | g0303 | AFR | YRI | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | CHB | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA18612 | hp2 | a0002 | c0002 | t0001 | g0018 | EAS | CHB | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0342 | AFR | YRI | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0317 | AFR | YRI | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA18940 | hp1 | a0002 | c0002 | t0001 | g0171 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA18941 | hp1 | a0002 | c0002 | t0001 | g0198 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA18942 | hp1 | a0002 | c0002 | t0001 | g0170 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA18943 | hp1 | a0002 | c0002 | t0001 | g0079 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA18945 | hp2 | a0002 | c0002 | t0001 | g0230 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA18946 | hp1 | a0002 | c0002 | t0001 | g0044 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA18946 | hp2 | a0002 | c0002 | t0001 | g0024 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA18947 | hp1 | a0002 | c0002 | t0001 | g0169 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0351 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA18954 | hp1 | a0002 | c0002 | t0001 | g0023 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA18957 | hp2 | a0002 | c0002 | t0001 | g0116 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA18959 | hp2 | a0002 | c0002 | t0001 | g0105 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA18961 | hp1 | a0002 | c0002 | t0001 | g0133 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA18961 | hp2 | a0001 | c0001 | t0004 | g0103 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA18963 | hp1 | a0002 | c0002 | t0001 | g0050 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA18969 | hp2 | a0002 | c0002 | t0001 | g0028 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA18970 | hp1 | a0002 | c0002 | t0001 | g0223 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA18973 | hp1 | a0002 | c0002 | t0001 | g0273 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA18975 | hp1 | a0002 | c0002 | t0001 | g0224 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA18977 | hp1 | a0002 | c0002 | t0001 | g0097 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA18978 | hp2 | a0002 | c0002 | t0005 | g0087 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA18979 | hp2 | a0002 | c0002 | t0001 | g0209 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA18982 | hp1 | a0002 | c0002 | t0001 | g0212 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA18983 | hp2 | a0002 | c0002 | t0001 | g0119 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA18985 | hp1 | a0002 | c0002 | t0001 | g0217 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA18986 | hp2 | a0002 | c0002 | t0001 | g0272 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA18990 | hp1 | a0002 | c0002 | t0001 | g0027 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA18992 | hp2 | a0002 | c0002 | t0001 | g0043 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA19000 | hp2 | a0002 | c0002 | t0001 | g0107 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA19002 | hp2 | a0002 | c0002 | t0001 | g0184 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA19009 | hp2 | a0002 | c0002 | t0001 | g0099 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA19010 | hp1 | a0002 | c0002 | t0001 | g0156 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA19011 | hp1 | a0002 | c0002 | t0001 | g0178 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA19011 | hp2 | a0002 | c0002 | t0001 | g0042 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0309 | AFR | LWK | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA19030 | hp2 | a0002 | c0002 | t0001 | g0073 | AFR | LWK | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA19043 | hp1 | a0001 | c0001 | t0002 | g0288 | AFR | LWK | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0269 | AFR | LWK | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA19055 | hp2 | a0002 | c0002 | t0001 | g0135 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA19056 | hp2 | a0002 | c0002 | t0005 | g0081 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA19057 | hp2 | a0002 | c0002 | t0001 | g0032 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA19063 | hp2 | a0002 | c0002 | t0001 | g0098 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA19064 | hp1 | a0002 | c0002 | t0001 | g0029 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0348 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA19065 | hp2 | a0002 | c0002 | t0001 | g0229 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA19067 | hp1 | a0002 | c0002 | t0001 | g0034 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA19082 | hp1 | a0002 | c0002 | t0001 | g0213 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA19085 | hp2 | a0002 | c0002 | t0001 | g0155 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA19086 | hp1 | a0002 | c0002 | t0001 | g0040 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0354 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | YRI | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0339 | AFR | YRI | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | ASW | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0314 | AFR | ASW | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0328 | EUR | TSI | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0047 | EUR | TSI | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0068 | EUR | TSI | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0287 | EUR | TSI | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA20905 | hp1 | a0002 | c0002 | t0001 | g0114 | SAS | GIH | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA20905 | hp2 | a0001 | c0003 | t0001 | g0291 | SAS | GIH | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | CLM | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG01123 | hp2 | a0002 | c0002 | t0001 | g0076 | AMR | CLM | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0333 | AFR | ACB | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | ACB | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0312 | AFR | ACB | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0325 | AFR | ACB | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | ACB | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0322 | AFR | ACB | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG03471 | hp1 | a0002 | c0002 | t0001 | g0017 | AFR | MSL | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0280 | AFR | MSL | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | USA | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0262 | AFR | USA | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA18955 | hp1 | a0002 | c0002 | t0001 | g0216 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA18955 | hp2 | a0002 | c0002 | t0001 | g0080 | EAS | JPT | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0323 | AFR | USA | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA20300 | hp2 | a0002 | c0002 | t0001 | g0225 | AFR | USA | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA21309 | hp1 | a0002 | c0002 | t0001 | g0046 | AFR | LWK | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
NA21309 | hp2 | a0001 | c0001 | t0002 | g0237 | AFR | LWK | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
homoSapiens_chm13v2 | hp1 | a0002 | c0002 | t0001 | g0190 | REF | REF | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
homoSapiens_grch38 | hp1 | a0002 | c0002 | t0001 | g0350 | REF | REF | FAM151B_chr5_80483100_80547563 | FAM151B | chr5 | 80483100 | 80547563 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:80519781
|
C | A | 1 | a0004 | 1 | HG02723.hp1 | missense_variant | MODERATE | c.406C>A | p.Pro136Thr | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 4/6 | 430/1586 | 406/831 | 136/276 | chr5 | 80519781 | ||
chr5:80519839
|
T | C | 3 | a0001a0003a0004 | 253 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(250): Show |
missense_variant | MODERATE | c.464T>C | p.Ile155Thr | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 4/6 | 488/1586 | 464/831 | 155/276 | chr5 | 80519839 | ||
chr5:80522042
|
G | A | 1 | a0003 | 1 | HG01978.hp2 | missense_variant | MODERATE | c.575G>A | p.Cys192Tyr | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/6 | 599/1586 | 575/831 | 192/276 | chr5 | 80522042 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:80522079
|
A | G | 1 | a0001c0003 | 10 | HG00280.hp1 HG00738.hp1 HG01109.hp2 others(7): Show |
synonymous_variant | LOW | c.612A>G | p.Arg204Arg | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/6 | 636/1586 | 612/831 | 204/276 | chr5 | 80522079 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:80542255
|
G | A | 2 | a0001c0001t0003a0001c0001t0006 | 3 | HG02257.hp1 HG02451.hp2 HG02970.hp1 |
3_prime_UTR_variant | MODIFIER | c.*423G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 6/6 | 423 | chr5 | 80542255 | |||||
chr5:80542260
|
G | C | 1 | a0001c0001t0006 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*428G>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 6/6 | 428 | chr5 | 80542260 | |||||
chr5:80542310
|
T | C | 1 | a0002c0002t0007 | 1 | HG00438.hp1 | 3_prime_UTR_variant | MODIFIER | c.*478T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 6/6 | 478 | chr5 | 80542310 | |||||
chr5:80542340
|
G | A | 1 | a0001c0001t0004 | 2 | HG00438.hp2 NA18961.hp2 |
3_prime_UTR_variant | MODIFIER | c.*508G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 6/6 | 508 | chr5 | 80542340 | |||||
chr5:80542402
|
G | T | 1 | a0001c0001t0002 | 14 | HG01884.hp1 HG02451.hp1 HG02622.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*570G>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 6/6 | 570 | chr5 | 80542402 | |||||
chr5:80542503
|
G | A | 2 | a0001c0001t0003a0001c0001t0006 | 3 | HG02257.hp1 HG02451.hp2 HG02970.hp1 |
3_prime_UTR_variant | MODIFIER | c.*671G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 6/6 | 671 | chr5 | 80542503 | |||||
chr5:80542521
|
C | T | 1 | a0002c0002t0005 | 2 | NA18978.hp2 NA19056.hp2 |
3_prime_UTR_variant | MODIFIER | c.*689C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 6/6 | 689 | chr5 | 80542521 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:80488365
|
G | C | 277 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(274): Show | 278 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(275): Show |
intron_variant | MODIFIER | c.25+217G>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80488365 | ||||||
chr5:80488390
|
T | G | 1 | a0001c0001t0002g0278 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.25+242T>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80488390 | ||||||
chr5:80488543
|
G | T | 2 | a0001c0001t0001g0276a0001c0001t0001g0277 | 2 | HG00408.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.25+395G>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80488543 | ||||||
chr5:80488557
|
C | G | 1 | a0001c0001t0001g0275 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.25+409C>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80488557 | ||||||
chr5:80488573
|
G | T | 1 | a0002c0002t0001g0274 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.25+425G>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80488573 | ||||||
chr5:80488578
|
G | C | 2 | a0001c0001t0001g0002a0001c0001t0001g0003 | 2 | NA19062.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.25+430G>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80488578 | ||||||
chr5:80489033
|
G | A | 1 | a0001c0001t0001g0002 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.25+885G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80489033 | ||||||
chr5:80489130
|
A | G | 1 | a0002c0002t0001g0273 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.25+982A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80489130 | ||||||
chr5:80489241
|
G | T | 1 | a0002c0002t0001g0272 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.25+1093G>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80489241 | ||||||
chr5:80489349
|
T | C | 11 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(8): Show | 11 | NA18948.hp1 NA18950.hp1 NA18963.hp2 others(8): Show |
intron_variant | MODIFIER | c.25+1201T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80489349 | ||||||
chr5:80489411
|
C | T | 1 | a0001c0001t0001g0355 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.25+1263C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80489411 | ||||||
chr5:80489433
|
T | C | 1 | a0001c0001t0001g0015 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.25+1285T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80489433 | ||||||
chr5:80489710
|
G | A | 3 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0002g0281 | 3 | HG01884.hp2 HG03098.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.25+1562G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80489710 | ||||||
chr5:80489872
|
C | A | 278 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(275): Show | 279 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(276): Show |
intron_variant | MODIFIER | c.25+1724C>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80489872 | ||||||
chr5:80489903
|
A | G | 19 | a0001c0001t0001g0253a0001c0001t0001g0255a0001c0001t0001g0256others(16): Show | 19 | HG00639.hp1 HG00735.hp1 HG01099.hp2 others(16): Show |
intron_variant | MODIFIER | c.25+1755A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80489903 | ||||||
chr5:80489937
|
AC | A | 3 | a0001c0001t0001g0284a0001c0001t0003g0282a0002c0002t0001g0283 | 3 | HG02895.hp2 HG02970.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.25+1790delC | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80489937 | ||||||
chr5:80489938
|
C | CAAAAACA others(6): Show |
2 | a0001c0001t0002g0285a0001c0001t0006g0286 | 2 | HG01884.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.25+1795_25+1796ins others(13): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 80489938 | |||||
chr5:80490019
|
T | TAAACACA others(3): Show |
1 | a0001c0001t0002g0285 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.25+1872_25+1873ins others(10): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 80490019 | |||||
chr5:80490019
|
T | TAC | 24 | a0001c0001t0001g0235a0001c0001t0001g0255a0001c0001t0001g0256others(21): Show | 24 | HG00639.hp1 HG00735.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.25+1903_25+1904dup others(2): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 80490019 | |||||
chr5:80490019
|
T | TACAC | 16 | a0001c0001t0001g0222a0001c0001t0001g0228a0001c0001t0001g0231others(13): Show | 16 | HG01192.hp2 HG01433.hp1 HG01943.hp1 others(13): Show |
intron_variant | MODIFIER | c.25+1901_25+1904dup others(4): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 80490019 | |||||
chr5:80490019
|
T | TACACAC | 18 | a0001c0001t0001g0211a0001c0001t0001g0214a0001c0001t0001g0215others(15): Show | 18 | HG02257.hp1 HG02280.hp1 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.25+1899_25+1904dup others(6): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 80490019 | |||||
chr5:80490019
|
T | TACACACA others(1): Show |
40 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(37): Show | 41 | HG00280.hp1 HG00621.hp2 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.25+1897_25+1904dup others(8): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 80490019 | |||||
chr5:80490019
|
T | TACACACA others(3): Show |
123 | a0001c0001t0001g0004a0001c0001t0001g0070a0001c0001t0001g0071others(120): Show | 123 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.25+1895_25+1904dup others(10): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 80490019 | |||||
chr5:80490019
|
T | TACACACA others(5): Show |
39 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0036others(36): Show | 39 | HG00558.hp2 HG00621.hp1 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.25+1893_25+1904dup others(12): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 80490019 | |||||
chr5:80490019
|
T | TACACACA others(7): Show |
15 | a0001c0001t0001g0021a0001c0001t0001g0030a0001c0001t0001g0031others(12): Show | 15 | HG00741.hp2 HG02071.hp1 HG02083.hp2 others(12): Show |
intron_variant | MODIFIER | c.25+1891_25+1904dup others(14): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 80490019 | |||||
chr5:80490019
|
T | TACACACA others(9): Show |
4 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0020others(1): Show | 4 | HG02155.hp2 HG03704.hp1 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.25+1889_25+1904dup others(16): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 80490019 | |||||
chr5:80490019
|
T | TACACACA others(11): Show |
3 | a0002c0002t0001g0016a0002c0002t0001g0017a0002c0002t0001g0018 | 3 | HG03471.hp1 HG04115.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.25+1887_25+1904dup others(18): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 80490019 | |||||
chr5:80490019
|
TAC | T | 16 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0240others(13): Show | 16 | HG01099.hp1 HG01255.hp1 HG01358.hp2 others(13): Show |
intron_variant | MODIFIER | c.25+1903_25+1904del others(2): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 80490019 | |||||
chr5:80490019
|
TACACACA others(3): Show |
T | 1 | a0001c0001t0001g0354 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.25+1895_25+1904del others(10): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 80490019 | |||||
chr5:80490020
|
A | ACACACAC others(6): Show |
1 | a0001c0001t0001g0252 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.25+1873_25+1885dup others(13): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 80490020 | |||||
chr5:80490053
|
T | C | 3 | a0001c0003t0001g0001a0001c0003t0001g0186a0001c0003t0001g0187 | 4 | HG00738.hp1 HG01168.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.25+1905T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80490053 | ||||||
chr5:80490109
|
C | T | 2 | a0001c0001t0002g0285a0001c0001t0006g0286 | 2 | HG01884.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.25+1961C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80490109 | ||||||
chr5:80490413
|
T | C | 2 | a0001c0001t0002g0285a0001c0001t0006g0286 | 2 | HG01884.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.25+2265T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80490413 | ||||||
chr5:80490417
|
A | G | 1 | a0001c0001t0002g0278 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.25+2269A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80490417 | ||||||
chr5:80490586
|
T | C | 310 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(307): Show | 311 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(308): Show |
intron_variant | MODIFIER | c.25+2438T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80490586 | ||||||
chr5:80490618
|
T | C | 1 | a0001c0001t0001g0314 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.25+2470T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80490618 | ||||||
chr5:80490638
|
A | G | 3 | a0002c0002t0001g0018a0002c0002t0001g0032a0002c0002t0001g0069 | 3 | HG00558.hp2 NA18612.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.25+2490A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80490638 | ||||||
chr5:80490698
|
A | G | 1 | a0001c0001t0001g0355 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.25+2550A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80490698 | ||||||
chr5:80490849
|
A | G | 6 | a0001c0003t0001g0290a0001c0003t0001g0291a0001c0003t0001g0292others(3): Show | 6 | HG00280.hp1 HG01109.hp2 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.25+2701A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80490849 | ||||||
chr5:80490906
|
A | C | 1 | a0001c0001t0001g0251 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.25+2758A>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80490906 | ||||||
chr5:80491050
|
C | T | 1 | a0001c0001t0001g0300 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.25+2902C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80491050 | ||||||
chr5:80491102
|
C | G | 21 | a0001c0001t0001g0185a0001c0001t0001g0235a0001c0001t0001g0253others(18): Show | 21 | HG00639.hp1 HG00735.hp1 HG01099.hp2 others(18): Show |
intron_variant | MODIFIER | c.25+2954C>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80491102 | ||||||
chr5:80491153
|
G | A | 1 | a0001c0001t0001g0287 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.25+3005G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80491153 | ||||||
chr5:80491202
|
CTAT | C | 328 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(325): Show | 329 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(326): Show |
intron_variant | MODIFIER | c.25+3079_25+3081del others(3): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 80491202 | |||||
chr5:80491227
|
T | C | 2 | a0001c0001t0001g0211a0002c0002t0001g0301 | 2 | HG01070.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.25+3079T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80491227 | ||||||
chr5:80491294
|
C | T | 2 | a0001c0001t0001g0346a0001c0001t0001g0347 | 2 | HG01981.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.25+3146C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80491294 | ||||||
chr5:80491469
|
C | T | 1 | a0001c0001t0001g0250 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.25+3321C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80491469 | ||||||
chr5:80491774
|
G | A | 16 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0001g0284others(13): Show | 16 | HG00280.hp1 HG01109.hp2 HG01515.hp1 others(13): Show |
intron_variant | MODIFIER | c.25+3626G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80491774 | ||||||
chr5:80491782
|
G | A | 1 | a0001c0001t0001g0070 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.25+3634G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80491782 | ||||||
chr5:80491788
|
C | T | 2 | a0001c0001t0001g0183a0002c0002t0001g0184 | 2 | NA18943.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.25+3640C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80491788 | ||||||
chr5:80491821
|
A | G | 11 | a0001c0001t0001g0299a0001c0001t0001g0300a0001c0001t0001g0306others(8): Show | 11 | HG01192.hp2 HG01496.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.25+3673A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80491821 | ||||||
chr5:80492018
|
C | T | 2 | a0002c0002t0001g0344a0002c0002t0001g0345 | 2 | HG03195.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.25+3870C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80492018 | ||||||
chr5:80492297
|
A | G | 1 | a0001c0001t0001g0353 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.25+4149A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80492297 | ||||||
chr5:80492312
|
A | C | 1 | a0001c0001t0006g0286 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.25+4164A>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80492312 | ||||||
chr5:80492330
|
G | A | 1 | a0001c0001t0001g0299 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.25+4182G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80492330 | ||||||
chr5:80492349
|
C | A | 1 | a0001c0001t0002g0285 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.25+4201C>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80492349 | ||||||
chr5:80492465
|
T | C | 2 | a0002c0002t0001g0032a0002c0002t0001g0069 | 2 | HG00558.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.25+4317T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80492465 | ||||||
chr5:80492695
|
G | A | 2 | a0001c0001t0001g0222a0002c0002t0001g0274 | 2 | HG02965.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.25+4547G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80492695 | ||||||
chr5:80492742
|
C | T | 1 | a0001c0001t0006g0286 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.25+4594C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80492742 | ||||||
chr5:80492803
|
A | T | 3 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0067 | 3 | HG00738.hp2 HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.25+4655A>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80492803 | ||||||
chr5:80492826
|
C | T | 3 | a0001c0001t0001g0284a0001c0001t0003g0282a0002c0002t0001g0283 | 3 | HG02895.hp2 HG02970.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.25+4678C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80492826 | ||||||
chr5:80492963
|
A | G | 1 | a0001c0001t0001g0182 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.25+4815A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80492963 | ||||||
chr5:80493015
|
G | A | 3 | a0001c0001t0001g0284a0001c0001t0003g0282a0002c0002t0001g0283 | 3 | HG02895.hp2 HG02970.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.25+4867G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80493015 | ||||||
chr5:80493174
|
C | T | 2 | a0001c0001t0001g0180a0001c0001t0001g0181 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.25+5026C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80493174 | ||||||
chr5:80493202
|
C | A | 1 | a0001c0001t0001g0071 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.25+5054C>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80493202 | ||||||
chr5:80493368
|
CAT | C | 9 | a0001c0001t0001g0299a0001c0001t0001g0306a0001c0001t0001g0307others(6): Show | 9 | HG01192.hp2 HG01496.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.25+5221_25+5222del others(2): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80493368 | ||||||
chr5:80493423
|
G | A | 1 | a0001c0001t0001g0287 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.25+5275G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80493423 | ||||||
chr5:80493452
|
C | T | 1 | a0001c0001t0002g0298 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.25+5304C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80493452 | ||||||
chr5:80493454
|
T | C | 7 | a0001c0001t0001g0188a0001c0001t0001g0214a0001c0001t0001g0215others(4): Show | 7 | NA18955.hp1 NA18982.hp1 NA18985.hp1 others(4): Show |
intron_variant | MODIFIER | c.25+5306T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80493454 | ||||||
chr5:80493487
|
C | T | 1 | a0002c0002t0001g0179 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.25+5339C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80493487 | ||||||
chr5:80493552
|
A | G | 8 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(5): Show | 8 | HG01496.hp1 HG02486.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.25+5404A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80493552 | ||||||
chr5:80493726
|
A | G | 279 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(276): Show | 280 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(277): Show |
intron_variant | MODIFIER | c.25+5578A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80493726 | ||||||
chr5:80493770
|
T | G | 1 | a0001c0001t0001g0315 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.25+5622T>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80493770 | ||||||
chr5:80494085
|
G | A | 2 | a0002c0002t0001g0072a0002c0002t0001g0301 | 2 | HG00408.hp1 HG01070.hp1 |
intron_variant | MODIFIER | c.25+5937G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80494085 | ||||||
chr5:80494104
|
G | A | 1 | a0001c0001t0001g0189 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.25+5956G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80494104 | ||||||
chr5:80494105
|
T | G | 1 | a0001c0001t0001g0070 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.25+5957T>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80494105 | ||||||
chr5:80494127
|
T | C | 10 | a0001c0001t0001g0299a0001c0001t0001g0306a0001c0001t0001g0307others(7): Show | 10 | HG01192.hp2 HG01496.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.25+5979T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80494127 | ||||||
chr5:80494442
|
TTTTTCTT others(6): Show |
T | 7 | a0001c0001t0001g0074a0001c0001t0001g0177a0001c0001t0002g0285others(4): Show | 7 | HG00621.hp2 HG01123.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.25+6311_25+6323del others(13): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 80494442 | |||||
chr5:80494443
|
T | TTTTCTTT others(1): Show |
25 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0015others(22): Show | 25 | HG00673.hp2 HG01168.hp2 HG02040.hp1 others(22): Show |
intron_variant | MODIFIER | c.25+6303_25+6310dup others(8): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 80494443 | |||||
chr5:80494443
|
TTTTCTTT others(22): Show |
T | 1 | a0003c0005t0001g0254 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.25+6311_25+6339del others(29): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 80494443 | |||||
chr5:80494447
|
CTTTCTTT others(2): Show |
C | 19 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0064others(16): Show | 19 | HG00738.hp2 HG01069.hp1 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.25+6311_25+6319del others(9): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 80494447 | |||||
chr5:80494451
|
CTTTCT | C | 45 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0031others(42): Show | 45 | HG00280.hp2 HG00408.hp2 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.25+6311_25+6315del others(5): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 80494451 | |||||
chr5:80494455
|
CT | C | 126 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0011others(123): Show | 127 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(124): Show |
intron_variant | MODIFIER | c.25+6311delT | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 80494455 | |||||
chr5:80494456
|
T | TTTC | 62 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(59): Show | 62 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.25+6310_25+6311ins others(3): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 80494456 | |||||
chr5:80494456
|
T | TTTCTTTC others(5): Show |
9 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0180others(6): Show | 9 | HG01070.hp2 HG01071.hp1 HG01496.hp2 others(6): Show |
intron_variant | MODIFIER | c.25+6310_25+6311ins others(12): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 80494456 | |||||
chr5:80494456
|
T | TTTCTTTC others(9): Show |
2 | a0001c0003t0001g0291a0002c0002t0001g0076 | 2 | HG01123.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.25+6310_25+6311ins others(16): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 80494456 | |||||
chr5:80494456
|
T | TTTCTTTC others(14): Show |
2 | a0001c0001t0001g0289a0001c0001t0002g0288 | 2 | HG02572.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.25+6310_25+6311ins others(21): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 80494456 | |||||
chr5:80494456
|
T | TTTCTTTC others(30): Show |
2 | a0001c0001t0001g0279a0001c0001t0001g0280 | 2 | HG01884.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.25+6310_25+6311ins others(37): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 80494456 | |||||
chr5:80494456
|
T | TTTTC | 4 | a0001c0001t0001g0302a0001c0001t0001g0314a0001c0001t0001g0316others(1): Show | 4 | HG02145.hp1 HG02717.hp2 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.25+6376_25+6379dup others(4): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 80494456 | |||||
chr5:80494456
|
TTTTC | T | 12 | a0001c0001t0001g0308a0001c0001t0001g0309a0001c0001t0001g0323others(9): Show | 12 | HG01243.hp2 HG01981.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.25+6376_25+6379del others(4): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 80494456 | |||||
chr5:80494456
|
TTTTCTTT others(1): Show |
T | 12 | a0001c0001t0001g0310a0001c0001t0001g0311a0001c0001t0001g0312others(9): Show | 12 | HG01109.hp1 HG02109.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.25+6372_25+6379del others(8): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 80494456 | |||||
chr5:80494456
|
TTTTCTTT others(5): Show |
T | 8 | a0001c0001t0001g0304a0001c0001t0001g0313a0001c0001t0001g0315others(5): Show | 8 | HG02886.hp1 HG02970.hp2 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.25+6368_25+6379del others(12): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 80494456 | |||||
chr5:80494456
|
TTTTCTTT others(9): Show |
T | 3 | a0001c0001t0001g0305a0001c0001t0001g0342a0001c0001t0001g0343 | 3 | HG00323.hp1 HG03654.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.25+6364_25+6379del others(16): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 80494456 | |||||
chr5:80494459
|
T | C | 1 | a0001c0003t0001g0295 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.25+6311T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80494459 | ||||||
chr5:80494460
|
C | CT | 59 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(56): Show | 59 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.25+6315dupT | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 80494460 | |||||
chr5:80494460
|
C | T | 1 | a0001c0003t0001g0295 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.25+6312C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80494460 | ||||||
chr5:80494463
|
T | TTC | 3 | a0001c0001t0001g0284a0001c0001t0003g0282a0002c0002t0001g0283 | 3 | HG02895.hp2 HG02970.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.25+6315_25+6316ins others(2): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80494463 | ||||||
chr5:80494464
|
C | A | 2 | a0001c0001t0001g0279a0001c0001t0001g0280 | 2 | HG01884.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.25+6316C>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80494464 | ||||||
chr5:80494464
|
C | CT | 61 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0011others(58): Show | 62 | HG00323.hp2 HG00639.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.25+6319dupT | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 80494464 | |||||
chr5:80494464
|
C | T | 3 | a0001c0001t0001g0284a0001c0001t0003g0282a0002c0002t0001g0283 | 3 | HG02895.hp2 HG02970.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.25+6316C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80494464 | ||||||
chr5:80494465
|
TTTC | T | 61 | a0001c0001t0001g0030a0001c0001t0001g0051a0001c0001t0001g0054others(58): Show | 61 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.25+6320_25+6322del others(3): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 80494465 | |||||
chr5:80494465
|
TTTCTTTC others(24): Show |
T | 2 | a0001c0001t0002g0297a0001c0001t0002g0298 | 2 | HG02451.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.25+6320_25+6350del others(31): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 80494465 | |||||
chr5:80494468
|
C | A | 1 | a0001c0001t0001g0279 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.25+6320C>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80494468 | ||||||
chr5:80494468
|
C | CT | 4 | a0001c0003t0001g0290a0001c0003t0001g0293a0001c0003t0001g0294others(1): Show | 4 | HG00280.hp1 HG01109.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.25+6323dupT | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 80494468 | |||||
chr5:80494469
|
TTTC | T | 44 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0031others(41): Show | 44 | HG00280.hp2 HG00408.hp2 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.25+6324_25+6326del others(3): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 80494469 | |||||
chr5:80494472
|
C | A | 1 | a0001c0001t0001g0279 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.25+6324C>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80494472 | ||||||
chr5:80494473
|
TTTC | T | 19 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0064others(16): Show | 19 | HG00738.hp2 HG01069.hp1 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.25+6328_25+6330del others(3): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 80494473 | |||||
chr5:80494477
|
TTTC | T | 6 | a0001c0001t0001g0177a0001c0001t0002g0285a0002c0002t0001g0176others(3): Show | 6 | HG00621.hp2 HG01884.hp1 HG02135.hp1 others(3): Show |
intron_variant | MODIFIER | c.25+6332_25+6334del others(3): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 80494477 | |||||
chr5:80494480
|
C | A | 2 | a0001c0001t0001g0289a0001c0001t0002g0288 | 2 | HG02572.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.25+6332C>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80494480 | ||||||
chr5:80494516
|
CTTTCTTT others(3): Show |
C | 1 | a0001c0001t0001g0328 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.25+6372_25+6381del others(10): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 80494516 | |||||
chr5:80494525
|
T | C | 1 | a0001c0001t0001g0075 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.25+6377T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80494525 | ||||||
chr5:80494572
|
G | A | 1 | a0002c0002t0001g0069 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.25+6424G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80494572 | ||||||
chr5:80494794
|
A | G | 1 | a0001c0001t0001g0106 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.25+6646A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80494794 | ||||||
chr5:80494850
|
AT | A | 6 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0001g0287others(3): Show | 6 | HG01884.hp2 HG02572.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.25+6704delT | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 80494850 | |||||
chr5:80495083
|
C | T | 3 | a0001c0001t0001g0203a0002c0002t0001g0046a0002c0002t0001g0073 | 3 | HG02559.hp1 NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.26-6709C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80495083 | ||||||
chr5:80495389
|
A | G | 1 | a0001c0001t0001g0322 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.26-6403A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80495389 | ||||||
chr5:80495528
|
G | A | 1 | a0001c0001t0001g0287 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.26-6264G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80495528 | ||||||
chr5:80495745
|
G | A | 3 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0260 | 3 | HG00639.hp1 HG01346.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.26-6047G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80495745 | ||||||
chr5:80495786
|
G | A | 279 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(276): Show | 280 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(277): Show |
intron_variant | MODIFIER | c.26-6006G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80495786 | ||||||
chr5:80495797
|
C | G | 1 | a0002c0002t0001g0272 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.26-5995C>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80495797 | ||||||
chr5:80495809
|
C | T | 2 | a0001c0001t0002g0285a0001c0001t0006g0286 | 2 | HG01884.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.26-5983C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80495809 | ||||||
chr5:80495830
|
CA | C | 27 | a0001c0001t0001g0304a0001c0001t0001g0314a0001c0001t0001g0315others(24): Show | 27 | HG00323.hp1 HG01070.hp1 HG01109.hp1 others(24): Show |
intron_variant | MODIFIER | c.26-5933delA | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 80495830 | |||||
chr5:80495830
|
CAAAA | C | 21 | a0001c0001t0001g0015a0001c0001t0001g0047a0001c0001t0001g0051others(18): Show | 21 | HG00280.hp2 HG01123.hp1 HG01361.hp1 others(18): Show |
intron_variant | MODIFIER | c.26-5936_26-5933del others(4): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 80495830 | |||||
chr5:80495830
|
CAAAAA | C | 244 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(241): Show | 245 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(242): Show |
intron_variant | MODIFIER | c.26-5937_26-5933del others(5): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 80495830 | |||||
chr5:80495830
|
CAAAAAA | C | 10 | a0001c0001t0001g0067a0001c0001t0001g0129a0001c0001t0001g0151others(7): Show | 10 | HG01069.hp1 HG02559.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.26-5938_26-5933del others(6): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 80495830 | |||||
chr5:80495830
|
CAAAAAAA | C | 30 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0001g0284others(27): Show | 30 | HG00280.hp1 HG00741.hp2 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.26-5939_26-5933del others(7): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 80495830 | |||||
chr5:80495830
|
CAAAAAAA others(5): Show |
C | 5 | a0001c0001t0001g0031a0001c0001t0001g0056a0001c0001t0001g0058others(2): Show | 5 | NA18973.hp2 NA18977.hp2 NA19000.hp1 others(2): Show |
intron_variant | MODIFIER | c.26-5944_26-5933del others(12): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 80495830 | |||||
chr5:80495830
|
CAAAAAAA others(8): Show |
C | 3 | a0001c0001t0001g0326a0001c0001t0001g0327a0001c0001t0001g0336 | 3 | HG01243.hp2 HG02630.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.26-5947_26-5933del others(15): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 80495830 | |||||
chr5:80495915
|
G | A | 7 | a0001c0001t0003g0296a0001c0003t0001g0290a0001c0003t0001g0291others(4): Show | 7 | HG00280.hp1 HG01109.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.26-5877G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80495915 | ||||||
chr5:80496184
|
A | C | 1 | a0001c0001t0001g0015 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.26-5608A>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80496184 | ||||||
chr5:80496430
|
A | C | 6 | a0001c0003t0001g0290a0001c0003t0001g0291a0001c0003t0001g0292others(3): Show | 6 | HG00280.hp1 HG01109.hp2 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.26-5362A>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80496430 | ||||||
chr5:80496456
|
A | G | 102 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0020others(99): Show | 102 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.26-5336A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80496456 | ||||||
chr5:80496511
|
A | G | 11 | a0001c0001t0001g0314a0001c0001t0001g0316a0001c0001t0001g0325others(8): Show | 11 | HG01109.hp1 HG02109.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.26-5281A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80496511 | ||||||
chr5:80496591
|
A | C | 1 | a0001c0001t0002g0278 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.26-5201A>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80496591 | ||||||
chr5:80496738
|
C | A | 354 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(351): Show | 355 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(352): Show |
intron_variant | MODIFIER | c.26-5054C>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80496738 | ||||||
chr5:80496771
|
G | T | 2 | a0001c0001t0002g0297a0001c0001t0002g0298 | 2 | HG02451.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.26-5021G>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80496771 | ||||||
chr5:80496783
|
T | A | 2 | a0001c0001t0001g0302a0001c0001t0001g0317 | 2 | HG02145.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.26-5009T>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80496783 | ||||||
chr5:80496799
|
A | AT | 10 | a0001c0001t0001g0323a0001c0001t0001g0327a0001c0001t0001g0333others(7): Show | 10 | HG01070.hp1 HG01109.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.26-4964dupT | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 80496799 | |||||
chr5:80496799
|
ATT | A | 33 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0070others(30): Show | 33 | HG00544.hp1 HG00673.hp2 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.26-4965_26-4964del others(2): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 80496799 | |||||
chr5:80496799
|
ATTT | A | 253 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(250): Show | 254 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(251): Show |
intron_variant | MODIFIER | c.26-4966_26-4964del others(3): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 80496799 | |||||
chr5:80496799
|
ATTTT | A | 17 | a0001c0001t0001g0011a0001c0001t0001g0108a0001c0001t0001g0121others(14): Show | 17 | HG00408.hp1 HG00408.hp2 HG00639.hp1 others(14): Show |
intron_variant | MODIFIER | c.26-4967_26-4964del others(4): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 80496799 | |||||
chr5:80496843
|
C | T | 1 | a0001c0001t0001g0130 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.26-4949C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80496843 | ||||||
chr5:80497018
|
C | A | 2 | a0002c0002t0001g0241a0002c0002t0001g0244 | 2 | HG02735.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.26-4774C>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80497018 | ||||||
chr5:80497154
|
G | A | 1 | a0002c0002t0001g0169 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.26-4638G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80497154 | ||||||
chr5:80497164
|
G | A | 6 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0001g0287others(3): Show | 6 | HG01884.hp2 HG02572.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.26-4628G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80497164 | ||||||
chr5:80497254
|
C | G | 1 | a0001c0001t0001g0207 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.26-4538C>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80497254 | ||||||
chr5:80497445
|
A | G | 3 | a0001c0001t0001g0321a0002c0002t0001g0344a0002c0002t0001g0345 | 3 | HG03195.hp1 HG03490.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.26-4347A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80497445 | ||||||
chr5:80497472
|
A | T | 1 | a0002c0002t0001g0273 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.26-4320A>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80497472 | ||||||
chr5:80497770
|
A | G | 279 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(276): Show | 280 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(277): Show |
intron_variant | MODIFIER | c.26-4022A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80497770 | ||||||
chr5:80497780
|
C | G | 2 | a0001c0001t0002g0285a0001c0001t0006g0286 | 2 | HG01884.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.26-4012C>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80497780 | ||||||
chr5:80497889
|
A | G | 1 | a0002c0002t0001g0176 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.26-3903A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80497889 | ||||||
chr5:80497931
|
T | G | 3 | a0001c0001t0001g0192a0001c0001t0001g0196a0001c0001t0001g0197 | 3 | HG02922.hp1 HG03139.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.26-3861T>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80497931 | ||||||
chr5:80497943
|
T | A | 1 | a0001c0001t0003g0296 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.26-3849T>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80497943 | ||||||
chr5:80497963
|
G | A | 1 | a0001c0001t0002g0285 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.26-3829G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80497963 | ||||||
chr5:80498017
|
T | C | 2 | a0001c0001t0002g0285a0001c0001t0006g0286 | 2 | HG01884.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.26-3775T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80498017 | ||||||
chr5:80498231
|
A | G | 4 | a0001c0001t0001g0074a0001c0001t0001g0126a0001c0001t0001g0127others(1): Show | 4 | HG01123.hp1 HG01433.hp2 HG01928.hp2 others(1): Show |
intron_variant | MODIFIER | c.26-3561A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80498231 | ||||||
chr5:80498283
|
A | G | 310 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(307): Show | 311 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(308): Show |
intron_variant | MODIFIER | c.26-3509A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80498283 | ||||||
chr5:80498302
|
G | A | 2 | a0002c0002t0001g0122a0002c0002t0001g0138 | 2 | HG01943.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.26-3490G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80498302 | ||||||
chr5:80498335
|
A | T | 2 | a0001c0001t0001g0265a0001c0001t0001g0266 | 2 | HG01099.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.26-3457A>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80498335 | ||||||
chr5:80498338
|
T | A | 277 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(274): Show | 278 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(275): Show |
intron_variant | MODIFIER | c.26-3454T>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80498338 | ||||||
chr5:80498351
|
C | A | 1 | a0001c0001t0003g0296 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.26-3441C>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80498351 | ||||||
chr5:80498351
|
C | T | 1 | a0001c0001t0001g0011 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.26-3441C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80498351 | ||||||
chr5:80498525
|
G | A | 10 | a0001c0001t0001g0299a0001c0001t0001g0306a0001c0001t0001g0307others(7): Show | 10 | HG01192.hp2 HG01496.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.26-3267G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80498525 | ||||||
chr5:80498638
|
T | A | 1 | a0001c0001t0002g0285 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.26-3154T>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80498638 | ||||||
chr5:80498904
|
T | C | 7 | a0001c0001t0003g0296a0001c0003t0001g0290a0001c0003t0001g0291others(4): Show | 7 | HG00280.hp1 HG01109.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.26-2888T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80498904 | ||||||
chr5:80498914
|
A | G | 1 | a0001c0001t0001g0347 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.26-2878A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80498914 | ||||||
chr5:80498985
|
G | T | 3 | a0001c0001t0001g0305a0001c0001t0001g0328a0001c0001t0001g0343 | 3 | HG00323.hp1 HG03654.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.26-2807G>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80498985 | ||||||
chr5:80499013
|
GA | G | 15 | a0001c0001t0001g0071a0001c0001t0001g0093a0001c0001t0001g0129others(12): Show | 15 | HG00741.hp1 HG01192.hp2 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.26-2765delA | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 80499013 | |||||
chr5:80499054
|
A | G | 1 | a0001c0001t0001g0347 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.26-2738A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80499054 | ||||||
chr5:80499061
|
G | A | 1 | a0002c0002t0001g0227 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.26-2731G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80499061 | ||||||
chr5:80499131
|
T | C | 1 | a0001c0001t0001g0328 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.26-2661T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80499131 | ||||||
chr5:80499365
|
G | A | 1 | a0001c0001t0001g0243 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.26-2427G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80499365 | ||||||
chr5:80499389
|
T | C | 9 | a0001c0001t0001g0299a0001c0001t0001g0306a0001c0001t0001g0307others(6): Show | 9 | HG01192.hp2 HG01496.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.26-2403T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80499389 | ||||||
chr5:80499588
|
G | C | 4 | a0001c0003t0001g0290a0001c0003t0001g0293a0001c0003t0001g0294others(1): Show | 4 | HG00280.hp1 HG01109.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.26-2204G>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80499588 | ||||||
chr5:80499594
|
G | A | 2 | a0001c0001t0002g0237a0001c0001t0002g0238 | 2 | NA18522.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.26-2198G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80499594 | ||||||
chr5:80499668
|
T | G | 2 | a0001c0001t0002g0297a0001c0001t0002g0298 | 2 | HG02451.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.26-2124T>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80499668 | ||||||
chr5:80499669
|
A | G | 18 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0001g0284others(15): Show | 18 | HG00280.hp1 HG01109.hp2 HG01515.hp1 others(15): Show |
intron_variant | MODIFIER | c.26-2123A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80499669 | ||||||
chr5:80499671
|
G | A | 1 | a0001c0001t0003g0296 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.26-2121G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80499671 | ||||||
chr5:80499778
|
G | A | 1 | a0001c0001t0001g0355 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.26-2014G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80499778 | ||||||
chr5:80499853
|
A | AT | 9 | a0001c0001t0001g0082a0001c0001t0001g0352a0001c0003t0001g0290others(6): Show | 9 | HG00280.hp1 HG01109.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.26-1922dupT | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 80499853 | |||||
chr5:80499950
|
C | G | 3 | a0002c0002t0001g0107a0002c0002t0001g0119a0002c0002t0001g0156 | 3 | NA18983.hp2 NA19000.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.26-1842C>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80499950 | ||||||
chr5:80499979
|
G | A | 2 | a0001c0001t0002g0285a0001c0001t0006g0286 | 2 | HG01884.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.26-1813G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80499979 | ||||||
chr5:80500060
|
A | G | 3 | a0001c0001t0001g0284a0001c0001t0003g0282a0002c0002t0001g0283 | 3 | HG02895.hp2 HG02970.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.26-1732A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80500060 | ||||||
chr5:80500215
|
T | C | 3 | a0002c0002t0001g0037a0002c0002t0001g0038a0002c0002t0001g0245 | 3 | HG00642.hp1 HG01099.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.26-1577T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80500215 | ||||||
chr5:80500242
|
G | A | 1 | a0001c0001t0001g0299 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.26-1550G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80500242 | ||||||
chr5:80500360
|
G | T | 1 | a0001c0001t0001g0304 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.26-1432G>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80500360 | ||||||
chr5:80500646
|
G | A | 2 | a0001c0001t0002g0297a0001c0001t0002g0298 | 2 | HG02451.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.26-1146G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80500646 | ||||||
chr5:80500713
|
T | C | 1 | a0002c0002t0001g0136 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.26-1079T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80500713 | ||||||
chr5:80500777
|
T | C | 9 | a0001c0001t0001g0299a0001c0001t0001g0306a0001c0001t0001g0307others(6): Show | 9 | HG01192.hp2 HG01496.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.26-1015T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80500777 | ||||||
chr5:80500797
|
C | T | 1 | a0001c0001t0006g0286 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.26-995C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80500797 | ||||||
chr5:80500807
|
G | A | 2 | a0001c0001t0002g0297a0001c0001t0002g0298 | 2 | HG02451.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.26-985G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80500807 | ||||||
chr5:80500937
|
A | C | 1 | a0002c0002t0001g0194 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.26-855A>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80500937 | ||||||
chr5:80501040
|
G | C | 1 | a0001c0001t0003g0296 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.26-752G>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80501040 | ||||||
chr5:80501180
|
A | AT | 8 | a0001c0001t0002g0278a0001c0003t0001g0290a0001c0003t0001g0291others(5): Show | 8 | HG00280.hp1 HG00408.hp1 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.26-599dupT | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 80501180 | |||||
chr5:80501193
|
T | A | 4 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0020others(1): Show | 4 | HG02071.hp1 HG02155.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.26-599T>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80501193 | ||||||
chr5:80501389
|
G | C | 1 | a0001c0001t0001g0172 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.26-403G>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80501389 | ||||||
chr5:80501414
|
T | G | 15 | a0001c0001t0001g0035a0001c0001t0001g0075a0001c0001t0001g0092others(12): Show | 16 | HG00738.hp1 HG00741.hp1 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.26-378T>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80501414 | ||||||
chr5:80501465
|
GA | G | 267 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(264): Show | 268 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(265): Show |
intron_variant | MODIFIER | c.26-306delA | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 80501465 | |||||
chr5:80501465
|
GAA | G | 10 | a0001c0001t0001g0006a0001c0001t0001g0055a0001c0001t0001g0215others(7): Show | 10 | HG02897.hp1 HG02965.hp1 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.26-307_26-306delAA | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 80501465 | |||||
chr5:80501600
|
A | G | 1 | a0001c0001t0001g0284 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.26-192A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80501600 | ||||||
chr5:80501676
|
A | C | 3 | a0001c0001t0001g0185a0001c0001t0001g0299a0002c0002t0001g0076 | 3 | HG01123.hp2 HG01175.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.26-116A>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | chr5 | 80501676 | ||||||
chr5:80501983
|
T | G | 1 | a0001c0001t0001g0299 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.151+66T>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80501983 | ||||||
chr5:80502173
|
C | T | 2 | a0001c0001t0002g0285a0001c0001t0006g0286 | 2 | HG01884.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.151+256C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80502173 | ||||||
chr5:80502182
|
T | C | 1 | a0001c0001t0001g0257 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.151+265T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80502182 | ||||||
chr5:80502226
|
C | G | 1 | a0001c0001t0006g0286 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.151+309C>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80502226 | ||||||
chr5:80502263
|
G | T | 1 | a0001c0001t0001g0222 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.151+346G>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80502263 | ||||||
chr5:80502279
|
T | C | 18 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0001g0284others(15): Show | 18 | HG00280.hp1 HG01109.hp2 HG01515.hp1 others(15): Show |
intron_variant | MODIFIER | c.151+362T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80502279 | ||||||
chr5:80502668
|
T | C | 310 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(307): Show | 311 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(308): Show |
intron_variant | MODIFIER | c.151+751T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80502668 | ||||||
chr5:80502860
|
A | C | 5 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0001g0287others(2): Show | 5 | HG01884.hp2 HG02572.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.151+943A>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80502860 | ||||||
chr5:80503087
|
A | G | 1 | a0001c0001t0001g0077 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.151+1170A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80503087 | ||||||
chr5:80503096
|
G | A | 3 | a0001c0001t0002g0237a0001c0001t0002g0238a0001c0001t0002g0281 | 3 | HG03098.hp1 NA18522.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.151+1179G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80503096 | ||||||
chr5:80503258
|
A | T | 10 | a0002c0002t0001g0135a0002c0002t0001g0223a0002c0002t0001g0224others(7): Show | 10 | HG01433.hp1 HG01943.hp1 HG02273.hp2 others(7): Show |
intron_variant | MODIFIER | c.151+1341A>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80503258 | ||||||
chr5:80504111
|
C | T | 2 | a0001c0001t0002g0297a0001c0001t0002g0298 | 2 | HG02451.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.151+2194C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80504111 | ||||||
chr5:80504119
|
G | A | 1 | a0003c0005t0001g0254 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.151+2202G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80504119 | ||||||
chr5:80504201
|
A | G | 3 | a0001c0001t0001g0321a0002c0002t0001g0344a0002c0002t0001g0345 | 3 | HG03195.hp1 HG03490.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.151+2284A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80504201 | ||||||
chr5:80504255
|
G | A | 1 | a0001c0001t0002g0281 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.151+2338G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80504255 | ||||||
chr5:80504292
|
T | C | 1 | a0001c0001t0001g0268 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.151+2375T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80504292 | ||||||
chr5:80504380
|
T | C | 2 | a0001c0001t0002g0297a0001c0001t0002g0298 | 2 | HG02451.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.151+2463T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80504380 | ||||||
chr5:80504503
|
C | T | 289 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(286): Show | 290 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(287): Show |
intron_variant | MODIFIER | c.151+2586C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80504503 | ||||||
chr5:80504514
|
CT | C | 14 | a0001c0001t0001g0033a0001c0001t0001g0036a0001c0001t0001g0284others(11): Show | 14 | HG00741.hp2 HG02451.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.151+2622delT | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 80504514 | |||||
chr5:80504514
|
CTT | C | 59 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0019others(56): Show | 59 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.151+2621_151+2622d others(4): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 80504514 | |||||
chr5:80504514
|
CTTT | C | 211 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(208): Show | 212 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(209): Show |
intron_variant | MODIFIER | c.151+2620_151+2622d others(5): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 80504514 | |||||
chr5:80504514
|
CTTTT | C | 17 | a0001c0001t0001g0228a0001c0001t0001g0253a0001c0001t0001g0255others(14): Show | 17 | HG00639.hp1 HG00735.hp1 HG01261.hp2 others(14): Show |
intron_variant | MODIFIER | c.151+2619_151+2622d others(6): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 80504514 | |||||
chr5:80504583
|
C | T | 1 | a0001c0001t0001g0258 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.151+2666C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80504583 | ||||||
chr5:80504614
|
G | A | 10 | a0001c0001t0001g0247a0001c0001t0001g0299a0001c0001t0001g0306others(7): Show | 10 | HG01192.hp2 HG01255.hp1 HG01496.hp1 others(7): Show |
intron_variant | MODIFIER | c.151+2697G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80504614 | ||||||
chr5:80504660
|
T | C | 208 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(205): Show | 208 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.151+2743T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80504660 | ||||||
chr5:80504668
|
T | C | 3 | a0001c0001t0001g0305a0001c0001t0001g0328a0001c0001t0001g0343 | 3 | HG00323.hp1 HG03654.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.151+2751T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80504668 | ||||||
chr5:80504676
|
T | C | 5 | a0001c0001t0003g0296a0002c0002t0001g0212a0002c0002t0001g0213others(2): Show | 5 | HG02257.hp1 NA18955.hp1 NA18982.hp1 others(2): Show |
intron_variant | MODIFIER | c.151+2759T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80504676 | ||||||
chr5:80504708
|
T | C | 1 | a0001c0001t0002g0298 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.151+2791T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80504708 | ||||||
chr5:80504728
|
T | C | 34 | a0001c0001t0001g0031a0001c0001t0001g0047a0001c0001t0001g0048others(31): Show | 34 | HG00621.hp1 HG00639.hp2 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.151+2811T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80504728 | ||||||
chr5:80504732
|
A | C | 1 | a0001c0001t0003g0296 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.151+2815A>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80504732 | ||||||
chr5:80504788
|
G | A | 2 | a0001c0001t0001g0346a0002c0002t0001g0016 | 2 | HG02698.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.151+2871G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80504788 | ||||||
chr5:80504915
|
C | G | 1 | a0001c0001t0001g0339 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.151+2998C>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80504915 | ||||||
chr5:80504996
|
C | T | 1 | a0001c0001t0001g0309 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.151+3079C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80504996 | ||||||
chr5:80505051
|
G | A | 5 | a0001c0001t0001g0030a0001c0001t0001g0162a0001c0001t0001g0174others(2): Show | 5 | HG00408.hp2 HG02129.hp1 NA18964.hp1 others(2): Show |
intron_variant | MODIFIER | c.151+3134G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80505051 | ||||||
chr5:80505391
|
G | A | 5 | a0002c0002t0001g0037a0002c0002t0001g0038a0002c0002t0001g0111others(2): Show | 5 | HG00642.hp1 HG01099.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.151+3474G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80505391 | ||||||
chr5:80505394
|
C | CT | 7 | a0001c0001t0002g0118a0001c0001t0002g0288a0001c0001t0003g0282others(4): Show | 7 | HG01099.hp1 HG02809.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.151+3488dupT | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 80505394 | |||||
chr5:80505405
|
TC | T | 41 | a0001c0001t0001g0302a0001c0001t0001g0304a0001c0001t0001g0305others(38): Show | 41 | HG00323.hp1 HG01109.hp1 HG01167.hp2 others(38): Show |
intron_variant | MODIFIER | c.151+3489delC | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80505405 | ||||||
chr5:80505406
|
C | T | 112 | a0001c0001t0001g0003a0001c0001t0001g0078a0001c0001t0001g0085others(109): Show | 112 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.151+3489C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80505406 | ||||||
chr5:80505457
|
C | T | 4 | a0001c0001t0002g0204a0001c0001t0002g0206a0001c0001t0002g0297others(1): Show | 4 | HG02451.hp1 HG02622.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.151+3540C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80505457 | ||||||
chr5:80505481
|
G | A | 4 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0001g0289others(1): Show | 4 | HG01884.hp2 HG02572.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.151+3564G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80505481 | ||||||
chr5:80505487
|
T | C | 2 | a0001c0001t0003g0282a0002c0002t0001g0283 | 2 | HG02970.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.151+3570T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80505487 | ||||||
chr5:80505491
|
T | C | 157 | a0001c0001t0001g0003a0001c0001t0001g0078a0001c0001t0001g0085others(154): Show | 157 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.151+3574T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80505491 | ||||||
chr5:80505548
|
T | C | 1 | a0002c0002t0001g0111 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.151+3631T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80505548 | ||||||
chr5:80505646
|
G | A | 4 | a0001c0001t0002g0204a0001c0001t0002g0206a0001c0001t0002g0297others(1): Show | 4 | HG02451.hp1 HG02622.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.151+3729G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80505646 | ||||||
chr5:80505701
|
T | C | 156 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0019others(153): Show | 156 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.151+3784T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80505701 | ||||||
chr5:80505749
|
A | AT | 28 | a0001c0001t0001g0077a0001c0001t0001g0100a0001c0001t0001g0124others(25): Show | 28 | HG00280.hp1 HG00558.hp1 HG00639.hp2 others(25): Show |
intron_variant | MODIFIER | c.151+3857dupT | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 80505749 | |||||
chr5:80505749
|
A | ATT | 122 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0019others(119): Show | 122 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.151+3856_151+3857d others(4): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 80505749 | |||||
chr5:80505749
|
A | ATTT | 21 | a0001c0001t0001g0222a0001c0001t0001g0252a0001c0001t0001g0302others(18): Show | 21 | HG01167.hp2 HG02083.hp1 HG02135.hp2 others(18): Show |
intron_variant | MODIFIER | c.151+3855_151+3857d others(5): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 80505749 | |||||
chr5:80505749
|
AT | A | 20 | a0001c0001t0001g0004a0001c0001t0001g0093a0001c0001t0001g0120others(17): Show | 20 | HG01496.hp1 HG01884.hp1 HG02293.hp1 others(17): Show |
intron_variant | MODIFIER | c.151+3857delT | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 80505749 | |||||
chr5:80505749
|
ATT | A | 50 | a0001c0001t0001g0021a0001c0001t0001g0030a0001c0001t0001g0033others(47): Show | 50 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.151+3856_151+3857d others(4): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 80505749 | |||||
chr5:80505821
|
A | G | 1 | a0001c0001t0001g0353 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.151+3904A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80505821 | ||||||
chr5:80505858
|
G | A | 10 | a0001c0001t0001g0258a0001c0001t0001g0261a0001c0001t0001g0262others(7): Show | 10 | HG00735.hp1 HG01261.hp2 HG01978.hp2 others(7): Show |
intron_variant | MODIFIER | c.151+3941G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80505858 | ||||||
chr5:80505891
|
G | C | 3 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0001g0289 | 3 | HG01884.hp2 HG02572.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.151+3974G>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80505891 | ||||||
chr5:80505908
|
C | T | 1 | a0002c0002t0001g0117 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.151+3991C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80505908 | ||||||
chr5:80506013
|
C | G | 4 | a0002c0002t0001g0024a0002c0002t0001g0025a0002c0002t0001g0029others(1): Show | 4 | HG02135.hp2 NA18946.hp2 NA19055.hp2 others(1): Show |
intron_variant | MODIFIER | c.151+4096C>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80506013 | ||||||
chr5:80506015
|
C | T | 1 | a0001c0001t0002g0320 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.151+4098C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80506015 | ||||||
chr5:80506016
|
G | A | 1 | a0001c0001t0001g0055 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.151+4099G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80506016 | ||||||
chr5:80506183
|
T | C | 6 | a0001c0001t0001g0355a0001c0001t0002g0204a0001c0001t0002g0206others(3): Show | 6 | HG00741.hp2 HG02451.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.151+4266T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80506183 | ||||||
chr5:80506318
|
G | A | 8 | a0001c0001t0001g0078a0001c0001t0001g0085a0001c0001t0001g0095others(5): Show | 8 | NA18950.hp2 NA18955.hp1 NA18959.hp2 others(5): Show |
intron_variant | MODIFIER | c.151+4401G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80506318 | ||||||
chr5:80506520
|
C | T | 2 | a0001c0001t0004g0103a0001c0001t0004g0104 | 2 | HG00438.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.151+4603C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80506520 | ||||||
chr5:80506521
|
G | A | 1 | a0001c0001t0006g0286 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.151+4604G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80506521 | ||||||
chr5:80506672
|
G | T | 1 | a0002c0002t0001g0117 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.151+4755G>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80506672 | ||||||
chr5:80506826
|
T | A | 2 | a0001c0001t0001g0355a0002c0002t0001g0073 | 2 | HG00741.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.151+4909T>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80506826 | ||||||
chr5:80506888
|
C | T | 1 | a0001c0001t0001g0137 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.151+4971C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80506888 | ||||||
chr5:80507051
|
A | C | 1 | a0001c0001t0006g0286 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.151+5134A>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80507051 | ||||||
chr5:80507052
|
G | A | 1 | a0001c0001t0001g0258 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.151+5135G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80507052 | ||||||
chr5:80507118
|
C | CA | 31 | a0001c0001t0001g0006a0001c0001t0001g0074a0001c0001t0001g0093others(28): Show | 31 | HG00544.hp2 HG00639.hp1 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.151+5220dupA | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 80507118 | |||||
chr5:80507118
|
CA | C | 115 | a0001c0001t0001g0011a0001c0001t0001g0055a0001c0001t0001g0078others(112): Show | 115 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.151+5220delA | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 80507118 | |||||
chr5:80507118
|
CAA | C | 39 | a0001c0001t0001g0302a0001c0001t0001g0304a0001c0001t0001g0305others(36): Show | 39 | HG00323.hp1 HG01109.hp1 HG01167.hp2 others(36): Show |
intron_variant | MODIFIER | c.151+5219_151+5220d others(4): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 80507118 | |||||
chr5:80507137
|
A | T | 4 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0001g0289others(1): Show | 4 | HG01884.hp2 HG02572.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.151+5220A>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80507137 | ||||||
chr5:80507359
|
T | C | 1 | a0002c0002t0001g0135 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.151+5442T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80507359 | ||||||
chr5:80507419
|
G | A | 4 | a0001c0001t0002g0204a0001c0001t0002g0206a0001c0001t0002g0297others(1): Show | 4 | HG02451.hp1 HG02622.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.151+5502G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80507419 | ||||||
chr5:80507580
|
C | T | 1 | a0001c0001t0002g0285 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.151+5663C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80507580 | ||||||
chr5:80507709
|
T | C | 2 | a0002c0002t0001g0086a0002c0002t0001g0088 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.151+5792T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80507709 | ||||||
chr5:80507865
|
C | T | 9 | a0001c0001t0001g0314a0001c0001t0001g0316a0001c0001t0001g0325others(6): Show | 9 | HG01109.hp1 HG02109.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.152-5739C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80507865 | ||||||
chr5:80507952
|
C | T | 2 | a0002c0002t0001g0086a0002c0002t0001g0088 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.152-5652C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80507952 | ||||||
chr5:80508169
|
T | C | 7 | a0001c0001t0003g0296a0001c0003t0001g0290a0001c0003t0001g0291others(4): Show | 7 | HG00280.hp1 HG01109.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.152-5435T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80508169 | ||||||
chr5:80508209
|
A | G | 1 | a0001c0001t0001g0168 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.152-5395A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80508209 | ||||||
chr5:80508221
|
G | A | 2 | a0001c0001t0001g0218a0001c0001t0001g0287 | 2 | HG02965.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.152-5383G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80508221 | ||||||
chr5:80508311
|
C | T | 160 | a0001c0001t0001g0078a0001c0001t0001g0085a0001c0001t0001g0095others(157): Show | 160 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(157): Show |
intron_variant | MODIFIER | c.152-5293C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80508311 | ||||||
chr5:80508350
|
A | G | 1 | a0001c0001t0001g0222 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.152-5254A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80508350 | ||||||
chr5:80508445
|
CT | C | 10 | a0001c0001t0001g0192a0001c0001t0001g0196a0001c0001t0001g0197others(7): Show | 10 | HG01070.hp1 HG02451.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.152-5148delT | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 80508445 | |||||
chr5:80508456
|
T | A | 1 | a0002c0002t0001g0083 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.152-5148T>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80508456 | ||||||
chr5:80508575
|
T | C | 1 | a0001c0001t0001g0192 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.152-5029T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80508575 | ||||||
chr5:80508698
|
A | C | 1 | a0001c0001t0001g0199 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.152-4906A>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80508698 | ||||||
chr5:80508920
|
G | A | 1 | a0001c0001t0003g0282 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.152-4684G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80508920 | ||||||
chr5:80509026
|
T | C | 1 | a0002c0002t0001g0107 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.152-4578T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80509026 | ||||||
chr5:80509034
|
C | T | 1 | a0001c0001t0004g0104 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.152-4570C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80509034 | ||||||
chr5:80509094
|
C | T | 6 | a0001c0003t0001g0290a0001c0003t0001g0291a0001c0003t0001g0292others(3): Show | 6 | HG00280.hp1 HG01109.hp2 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.152-4510C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80509094 | ||||||
chr5:80509399
|
G | A | 1 | a0001c0001t0001g0355 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.152-4205G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80509399 | ||||||
chr5:80509492
|
C | G | 4 | a0001c0001t0002g0204a0001c0001t0002g0206a0001c0001t0002g0297others(1): Show | 4 | HG02451.hp1 HG02622.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.152-4112C>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80509492 | ||||||
chr5:80509522
|
C | T | 1 | a0001c0001t0001g0276 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.152-4082C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80509522 | ||||||
chr5:80509946
|
G | A | 159 | a0001c0001t0001g0078a0001c0001t0001g0085a0001c0001t0001g0095others(156): Show | 159 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.152-3658G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80509946 | ||||||
chr5:80509961
|
C | T | 1 | a0001c0001t0001g0068 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.152-3643C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80509961 | ||||||
chr5:80510394
|
T | C | 1 | a0002c0002t0001g0117 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.152-3210T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80510394 | ||||||
chr5:80510912
|
C | T | 1 | a0002c0002t0001g0107 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.152-2692C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80510912 | ||||||
chr5:80511221
|
T | C | 2 | a0001c0001t0001g0355a0002c0002t0001g0073 | 2 | HG00741.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.152-2383T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80511221 | ||||||
chr5:80511353
|
A | T | 2 | a0001c0001t0001g0355a0002c0002t0001g0073 | 2 | HG00741.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.152-2251A>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80511353 | ||||||
chr5:80511399
|
A | G | 1 | a0001c0001t0001g0035 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.152-2205A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80511399 | ||||||
chr5:80511407
|
C | G | 229 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0020others(226): Show | 229 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(226): Show |
intron_variant | MODIFIER | c.152-2197C>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80511407 | ||||||
chr5:80511435
|
C | CA | 16 | a0001c0001t0001g0010a0001c0001t0001g0051a0001c0001t0001g0121others(13): Show | 16 | HG01109.hp2 HG01361.hp1 HG01516.hp2 others(13): Show |
intron_variant | MODIFIER | c.152-2144dupA | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 80511435 | |||||
chr5:80511435
|
CA | C | 137 | a0001c0001t0001g0020a0001c0001t0001g0030a0001c0001t0001g0090others(134): Show | 137 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.152-2144delA | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 80511435 | |||||
chr5:80511435
|
CAAAAAAA others(4): Show |
C | 1 | a0002c0002t0001g0212 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.152-2154_152-2144d others(13): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 80511435 | |||||
chr5:80511501
|
C | T | 10 | a0001c0001t0001g0284a0001c0001t0001g0306a0001c0001t0001g0307others(7): Show | 10 | HG01496.hp1 HG01884.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.152-2103C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80511501 | ||||||
chr5:80511525
|
C | T | 1 | a0002c0002t0001g0236 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.152-2079C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80511525 | ||||||
chr5:80511615
|
T | A | 46 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0020others(43): Show | 46 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(43): Show |
intron_variant | MODIFIER | c.152-1989T>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80511615 | ||||||
chr5:80511692
|
C | T | 2 | a0001c0001t0001g0247a0001c0001t0001g0248 | 2 | HG01255.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.152-1912C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80511692 | ||||||
chr5:80511693
|
G | A | 6 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0242others(3): Show | 6 | NA18954.hp2 NA18975.hp2 NA19001.hp1 others(3): Show |
intron_variant | MODIFIER | c.152-1911G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80511693 | ||||||
chr5:80511795
|
C | T | 2 | a0001c0001t0003g0282a0002c0002t0001g0283 | 2 | HG02970.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.152-1809C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80511795 | ||||||
chr5:80511941
|
T | A | 2 | a0001c0001t0001g0355a0002c0002t0001g0073 | 2 | HG00741.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.152-1663T>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80511941 | ||||||
chr5:80511979
|
T | C | 4 | a0001c0001t0002g0204a0001c0001t0002g0206a0001c0001t0002g0297others(1): Show | 4 | HG02451.hp1 HG02622.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.152-1625T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80511979 | ||||||
chr5:80512121
|
C | T | 1 | a0002c0002t0001g0301 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.152-1483C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80512121 | ||||||
chr5:80512273
|
T | C | 156 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0020others(153): Show | 156 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.152-1331T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80512273 | ||||||
chr5:80512577
|
C | G | 1 | a0001c0001t0001g0108 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.152-1027C>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80512577 | ||||||
chr5:80512625
|
TA | T | 352 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(349): Show | 353 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(350): Show |
intron_variant | MODIFIER | c.152-972delA | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 80512625 | |||||
chr5:80512771
|
C | T | 2 | a0001c0001t0001g0302a0001c0001t0001g0317 | 2 | HG02145.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.152-833C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80512771 | ||||||
chr5:80512780
|
T | TAA | 11 | a0001c0001t0003g0296a0001c0001t0006g0286a0001c0003t0001g0290others(8): Show | 11 | HG00280.hp1 HG00639.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.152-810_152-809dup others(2): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 80512780 | |||||
chr5:80512780
|
T | TAAA | 134 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0020others(131): Show | 134 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.152-811_152-809dup others(3): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 80512780 | |||||
chr5:80512780
|
T | TAAAA | 12 | a0001c0001t0001g0302a0001c0001t0001g0317a0001c0001t0001g0319others(9): Show | 12 | HG01168.hp2 HG01243.hp2 HG01981.hp2 others(9): Show |
intron_variant | MODIFIER | c.152-812_152-809dup others(4): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 80512780 | |||||
chr5:80512780
|
TA | T | 11 | a0001c0001t0001g0009a0001c0001t0001g0030a0001c0001t0001g0033others(8): Show | 11 | HG01070.hp1 HG01070.hp2 HG01167.hp1 others(8): Show |
intron_variant | MODIFIER | c.152-809delA | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 80512780 | |||||
chr5:80512809
|
A | G | 1 | a0002c0002t0001g0301 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.152-795A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80512809 | ||||||
chr5:80512817
|
A | G | 3 | a0001c0001t0002g0237a0001c0001t0002g0238a0001c0001t0002g0281 | 3 | HG03098.hp1 NA18522.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.152-787A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80512817 | ||||||
chr5:80512967
|
G | C | 1 | a0001c0001t0002g0288 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.152-637G>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80512967 | ||||||
chr5:80513050
|
G | A | 1 | a0001c0001t0006g0286 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.152-554G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80513050 | ||||||
chr5:80513394
|
A | G | 1 | a0001c0001t0003g0296 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.152-210A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80513394 | ||||||
chr5:80513448
|
G | C | 2 | a0001c0001t0001g0351a0001c0001t0001g0354 | 2 | NA18948.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.152-156G>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80513448 | ||||||
chr5:80513479
|
G | A | 4 | a0001c0001t0001g0228a0001c0001t0001g0231a0001c0001t0001g0233others(1): Show | 4 | HG02717.hp1 HG02895.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.152-125G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80513479 | ||||||
chr5:80513522
|
C | T | 10 | a0001c0001t0001g0284a0001c0001t0001g0306a0001c0001t0001g0307others(7): Show | 10 | HG01496.hp1 HG01884.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.152-82C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80513522 | ||||||
chr5:80513574
|
G | A | 1 | a0002c0002t0001g0274 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.152-30G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 2/5 | chr5 | 80513574 | ||||||
chr5:80513807
|
G | A | 3 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0001g0289 | 3 | HG01884.hp2 HG02572.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.317+38G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | chr5 | 80513807 | ||||||
chr5:80513839
|
A | T | 187 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0020others(184): Show | 187 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(184): Show |
intron_variant | MODIFIER | c.317+70A>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | chr5 | 80513839 | ||||||
chr5:80514097
|
G | A | 1 | a0001c0001t0001g0343 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.317+328G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | chr5 | 80514097 | ||||||
chr5:80514106
|
A | G | 157 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0020others(154): Show | 157 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.317+337A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | chr5 | 80514106 | ||||||
chr5:80514348
|
G | A | 3 | a0001c0001t0001g0261a0001c0001t0001g0265a0001c0001t0001g0266 | 3 | HG01099.hp2 HG02280.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.317+579G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | chr5 | 80514348 | ||||||
chr5:80514432
|
G | A | 1 | a0001c0001t0003g0296 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.317+663G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | chr5 | 80514432 | ||||||
chr5:80514476
|
A | AAAT | 51 | a0001c0001t0001g0047a0001c0001t0001g0065a0001c0001t0001g0066others(48): Show | 51 | HG00544.hp2 HG00738.hp2 HG01069.hp1 others(48): Show |
intron_variant | MODIFIER | c.317+751_317+753dup others(3): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr5 | 80514476 | |||||
chr5:80514476
|
A | AAATAAT | 10 | a0001c0001t0001g0275a0001c0001t0001g0280a0001c0001t0002g0297others(7): Show | 10 | HG00558.hp2 HG01070.hp1 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.317+748_317+753dup others(6): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr5 | 80514476 | |||||
chr5:80514476
|
AAAT | A | 108 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(105): Show | 109 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.317+751_317+753del others(3): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr5 | 80514476 | |||||
chr5:80514476
|
AAATAAT | A | 20 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0106others(17): Show | 20 | HG01496.hp1 HG01884.hp1 HG02486.hp1 others(17): Show |
intron_variant | MODIFIER | c.317+748_317+753del others(6): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr5 | 80514476 | |||||
chr5:80514476
|
AAATAATA others(2): Show |
A | 5 | a0001c0001t0001g0160a0001c0001t0001g0219a0001c0001t0001g0355others(2): Show | 5 | HG00741.hp2 HG01109.hp2 NA18941.hp2 others(2): Show |
intron_variant | MODIFIER | c.317+745_317+753del others(9): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr5 | 80514476 | |||||
chr5:80514476
|
AAATAATA others(5): Show |
A | 1 | a0002c0002t0001g0107 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.317+742_317+753del others(12): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr5 | 80514476 | |||||
chr5:80514611
|
A | G | 1 | a0001c0001t0006g0286 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.317+842A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | chr5 | 80514611 | ||||||
chr5:80514836
|
C | A | 1 | a0001c0001t0001g0106 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.317+1067C>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | chr5 | 80514836 | ||||||
chr5:80514900
|
T | C | 2 | a0002c0002t0001g0344a0002c0002t0001g0345 | 2 | HG03195.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.317+1131T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | chr5 | 80514900 | ||||||
chr5:80514957
|
C | T | 2 | a0002c0002t0001g0034a0002c0002t0001g0155 | 2 | NA19067.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.317+1188C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | chr5 | 80514957 | ||||||
chr5:80515010
|
C | T | 2 | a0001c0001t0001g0333a0001c0001t0006g0286 | 2 | HG02109.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.317+1241C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | chr5 | 80515010 | ||||||
chr5:80515194
|
T | C | 168 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0020others(165): Show | 169 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(166): Show |
intron_variant | MODIFIER | c.317+1425T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | chr5 | 80515194 | ||||||
chr5:80515216
|
G | A | 1 | a0001c0001t0001g0164 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.317+1447G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | chr5 | 80515216 | ||||||
chr5:80515267
|
T | TA | 166 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0020others(163): Show | 167 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.317+1504dupA | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr5 | 80515267 | |||||
chr5:80515276
|
A | G | 1 | a0001c0001t0001g0269 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.317+1507A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | chr5 | 80515276 | ||||||
chr5:80515296
|
A | G | 2 | a0001c0001t0001g0279a0001c0001t0001g0280 | 2 | HG01884.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.317+1527A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | chr5 | 80515296 | ||||||
chr5:80515501
|
C | T | 10 | a0001c0001t0001g0075a0001c0001t0001g0092a0001c0001t0001g0124others(7): Show | 10 | HG00741.hp2 HG01515.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.317+1732C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | chr5 | 80515501 | ||||||
chr5:80515810
|
T | C | 5 | a0001c0001t0002g0204a0001c0001t0002g0206a0001c0001t0002g0297others(2): Show | 5 | HG02451.hp1 HG02622.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.317+2041T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | chr5 | 80515810 | ||||||
chr5:80515843
|
G | A | 193 | a0001c0001t0001g0039a0001c0001t0001g0068a0001c0001t0001g0074others(190): Show | 194 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.317+2074G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | chr5 | 80515843 | ||||||
chr5:80515846
|
G | T | 4 | a0001c0001t0001g0228a0001c0001t0001g0231a0001c0001t0001g0233others(1): Show | 4 | HG02717.hp1 HG02895.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.317+2077G>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | chr5 | 80515846 | ||||||
chr5:80515958
|
T | C | 13 | a0001c0001t0001g0039a0001c0001t0001g0074a0001c0001t0001g0123others(10): Show | 13 | HG01123.hp1 HG01257.hp2 HG01258.hp2 others(10): Show |
intron_variant | MODIFIER | c.317+2189T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | chr5 | 80515958 | ||||||
chr5:80516106
|
C | T | 1 | a0001c0001t0001g0139 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.317+2337C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | chr5 | 80516106 | ||||||
chr5:80516139
|
A | G | 2 | a0001c0001t0003g0282a0001c0001t0006g0286 | 2 | HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.317+2370A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | chr5 | 80516139 | ||||||
chr5:80516448
|
G | A | 1 | a0001c0001t0001g0322 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.317+2679G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | chr5 | 80516448 | ||||||
chr5:80516524
|
A | G | 29 | a0001c0001t0001g0284a0001c0001t0001g0306a0001c0001t0001g0307others(26): Show | 30 | HG00280.hp1 HG00738.hp1 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.317+2755A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | chr5 | 80516524 | ||||||
chr5:80516657
|
A | G | 2 | a0002c0002t0001g0041a0002c0002t0001g0053 | 2 | HG01255.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.317+2888A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | chr5 | 80516657 | ||||||
chr5:80516847
|
A | G | 1 | a0001c0001t0001g0145 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.318-2846A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | chr5 | 80516847 | ||||||
chr5:80517181
|
A | G | 1 | a0001c0001t0001g0145 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.318-2512A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | chr5 | 80517181 | ||||||
chr5:80517190
|
T | C | 1 | a0001c0001t0002g0278 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.318-2503T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | chr5 | 80517190 | ||||||
chr5:80517197
|
A | C | 3 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0002g0281 | 3 | HG01884.hp2 HG03098.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.318-2496A>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | chr5 | 80517197 | ||||||
chr5:80517295
|
A | C | 1 | a0001c0001t0001g0240 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.318-2398A>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | chr5 | 80517295 | ||||||
chr5:80517393
|
AT | A | 4 | a0001c0001t0001g0289a0001c0001t0001g0326a0001c0001t0001g0327others(1): Show | 4 | HG01243.hp2 HG02572.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.318-2296delT | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr5 | 80517393 | |||||
chr5:80517484
|
TCAAGTTT others(11): Show |
T | 2 | a0001c0001t0001g0071a0001c0001t0001g0129 | 2 | NA19056.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.318-2208_318-2191d others(20): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | chr5 | 80517484 | ||||||
chr5:80517537
|
G | A | 19 | a0001c0001t0001g0235a0001c0001t0001g0253a0001c0001t0001g0255others(16): Show | 19 | HG00639.hp1 HG01099.hp2 HG01261.hp2 others(16): Show |
intron_variant | MODIFIER | c.318-2156G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | chr5 | 80517537 | ||||||
chr5:80517558
|
C | T | 53 | a0001c0001t0001g0031a0001c0001t0001g0047a0001c0001t0001g0048others(50): Show | 53 | HG00323.hp1 HG00621.hp1 HG00738.hp2 others(50): Show |
intron_variant | MODIFIER | c.318-2135C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | chr5 | 80517558 | ||||||
chr5:80517564
|
T | TTTTGTTT others(6): Show |
248 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(245): Show | 249 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(246): Show |
intron_variant | MODIFIER | c.318-2126_318-2125i others(15): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr5 | 80517564 | |||||
chr5:80517564
|
T | TTTTGTTT others(1766): Show |
1 | a0001c0001t0002g0118 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.318-2126_318-2125i others(1775): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr5 | 80517564 | |||||
chr5:80517639
|
A | G | 2 | a0002c0002t0001g0086a0002c0002t0001g0088 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.318-2054A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | chr5 | 80517639 | ||||||
chr5:80517653
|
C | T | 2 | a0001c0001t0003g0282a0001c0001t0006g0286 | 2 | HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.318-2040C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | chr5 | 80517653 | ||||||
chr5:80517711
|
C | T | 1 | a0001c0001t0001g0164 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.318-1982C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | chr5 | 80517711 | ||||||
chr5:80517946
|
C | T | 155 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(152): Show | 155 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(152): Show |
intron_variant | MODIFIER | c.318-1747C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | chr5 | 80517946 | ||||||
chr5:80518032
|
G | C | 30 | a0001c0001t0001g0284a0001c0001t0001g0306a0001c0001t0001g0307others(27): Show | 31 | HG00280.hp1 HG00738.hp1 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.318-1661G>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | chr5 | 80518032 | ||||||
chr5:80518059
|
G | A | 1 | a0002c0002t0001g0301 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.318-1634G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | chr5 | 80518059 | ||||||
chr5:80518075
|
G | A | 2 | a0001c0001t0001g0228a0001c0001t0001g0231 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.318-1618G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | chr5 | 80518075 | ||||||
chr5:80518075
|
G | GA | 6 | a0001c0001t0001g0185a0001c0001t0001g0262a0001c0001t0002g0113others(3): Show | 6 | HG00639.hp2 HG01175.hp1 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.318-1599dupA | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr5 | 80518075 | |||||
chr5:80518075
|
GA | G | 80 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(77): Show | 80 | HG00621.hp1 HG00673.hp1 HG00738.hp2 others(77): Show |
intron_variant | MODIFIER | c.318-1599delA | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr5 | 80518075 | |||||
chr5:80518138
|
A | T | 4 | a0001c0001t0001g0289a0001c0001t0001g0326a0001c0001t0001g0327others(1): Show | 4 | HG01243.hp2 HG02572.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.318-1555A>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | chr5 | 80518138 | ||||||
chr5:80518240
|
C | T | 1 | a0001c0001t0001g0004 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.318-1453C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | chr5 | 80518240 | ||||||
chr5:80518446
|
T | C | 253 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(250): Show | 254 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(251): Show |
intron_variant | MODIFIER | c.318-1247T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | chr5 | 80518446 | ||||||
chr5:80518603
|
G | A | 1 | a0001c0001t0001g0218 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.318-1090G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | chr5 | 80518603 | ||||||
chr5:80519027
|
G | T | 2 | a0002c0002t0001g0107a0002c0002t0007g0101 | 2 | HG00438.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.318-666G>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | chr5 | 80519027 | ||||||
chr5:80519154
|
A | C | 1 | a0002c0002t0001g0136 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.318-539A>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | chr5 | 80519154 | ||||||
chr5:80519264
|
A | G | 1 | a0001c0001t0001g0167 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.318-429A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | chr5 | 80519264 | ||||||
chr5:80519288
|
G | A | 2 | a0001c0001t0003g0282a0001c0001t0006g0286 | 2 | HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.318-405G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | chr5 | 80519288 | ||||||
chr5:80519353
|
G | C | 252 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(249): Show | 253 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(250): Show |
intron_variant | MODIFIER | c.318-340G>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | chr5 | 80519353 | ||||||
chr5:80520086
|
A | G | 1 | a0001c0001t0001g0305 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.535+176A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 4/5 | chr5 | 80520086 | ||||||
chr5:80520095
|
G | A | 32 | a0001c0001t0001g0289a0001c0001t0001g0304a0001c0001t0001g0305others(29): Show | 32 | HG00323.hp1 HG01109.hp1 HG01167.hp2 others(29): Show |
intron_variant | MODIFIER | c.535+185G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 4/5 | chr5 | 80520095 | ||||||
chr5:80520341
|
T | G | 1 | a0001c0001t0001g0348 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.535+431T>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 4/5 | chr5 | 80520341 | ||||||
chr5:80520367
|
G | T | 1 | a0001c0001t0001g0348 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.535+457G>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 4/5 | chr5 | 80520367 | ||||||
chr5:80520391
|
T | G | 5 | a0001c0001t0002g0204a0001c0001t0002g0206a0001c0001t0002g0297others(2): Show | 5 | HG02451.hp1 HG02622.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.535+481T>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 4/5 | chr5 | 80520391 | ||||||
chr5:80520491
|
A | G | 3 | a0002c0002t0001g0017a0002c0002t0001g0220a0002c0002t0001g0221 | 3 | HG02280.hp1 HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.535+581A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 4/5 | chr5 | 80520491 | ||||||
chr5:80520644
|
C | CA | 6 | a0001c0001t0001g0185a0001c0001t0001g0287a0001c0001t0001g0321others(3): Show | 6 | HG00438.hp1 HG01175.hp1 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.535+749dupA | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 80520644 | |||||
chr5:80520644
|
CA | C | 10 | a0001c0003t0001g0001a0001c0003t0001g0186a0001c0003t0001g0187others(7): Show | 11 | HG00280.hp1 HG00738.hp1 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.535+749delA | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 80520644 | |||||
chr5:80520650
|
A | C | 1 | a0001c0001t0001g0128 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.535+740A>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 4/5 | chr5 | 80520650 | ||||||
chr5:80520686
|
G | GTA | 12 | a0001c0001t0002g0113a0001c0001t0002g0118a0001c0001t0002g0204others(9): Show | 12 | HG01884.hp1 HG02451.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.535+790_535+791dup others(2): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 80520686 | |||||
chr5:80520698
|
ATATT | A | 32 | a0001c0001t0001g0289a0001c0001t0001g0304a0001c0001t0001g0305others(29): Show | 32 | HG00323.hp1 HG01109.hp1 HG01167.hp2 others(29): Show |
intron_variant | MODIFIER | c.535+797_535+800del others(4): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 80520698 | |||||
chr5:80520813
|
G | GT | 8 | a0001c0001t0001g0137a0001c0001t0001g0279a0001c0001t0001g0280others(5): Show | 8 | HG01884.hp2 HG02257.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.535+917dupT | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 80520813 | |||||
chr5:80520827
|
T | A | 1 | a0001c0001t0001g0139 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.535+917T>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 4/5 | chr5 | 80520827 | ||||||
chr5:80520861
|
T | G | 1 | a0001c0001t0001g0277 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.535+951T>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 4/5 | chr5 | 80520861 | ||||||
chr5:80520935
|
A | G | 251 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(248): Show | 252 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(249): Show |
intron_variant | MODIFIER | c.535+1025A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 4/5 | chr5 | 80520935 | ||||||
chr5:80520957
|
C | G | 1 | a0001c0001t0001g0151 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.536-1046C>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 4/5 | chr5 | 80520957 | ||||||
chr5:80520995
|
T | C | 2 | a0001c0001t0001g0128a0001c0001t0001g0143 | 2 | NA18978.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.536-1008T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 4/5 | chr5 | 80520995 | ||||||
chr5:80521116
|
C | CT | 45 | a0001c0001t0001g0033a0001c0001t0001g0036a0001c0001t0001g0058others(42): Show | 45 | HG00438.hp1 HG00621.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.536-862dupT | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 80521116 | |||||
chr5:80521116
|
C | CTT | 100 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(97): Show | 100 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.536-863_536-862dup others(2): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 80521116 | |||||
chr5:80521116
|
C | CTTT | 32 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(29): Show | 32 | HG00408.hp2 HG00544.hp2 HG00621.hp1 others(29): Show |
intron_variant | MODIFIER | c.536-864_536-862dup others(3): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 80521116 | |||||
chr5:80521116
|
CT | C | 28 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0001g0304others(25): Show | 28 | HG00323.hp1 HG00323.hp2 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.536-862delT | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 80521116 | |||||
chr5:80521116
|
CTTTTTTT others(9): Show |
C | 4 | a0001c0001t0001g0228a0001c0001t0001g0231a0001c0001t0001g0233others(1): Show | 4 | HG02717.hp1 HG02895.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.536-877_536-862del others(16): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 80521116 | |||||
chr5:80521144
|
A | G | 354 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(351): Show | 355 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(352): Show |
intron_variant | MODIFIER | c.536-859A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 4/5 | chr5 | 80521144 | ||||||
chr5:80521152
|
G | A | 1 | a0001c0001t0001g0002 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.536-851G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 4/5 | chr5 | 80521152 | ||||||
chr5:80521156
|
G | T | 1 | a0001c0001t0002g0281 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.536-847G>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 4/5 | chr5 | 80521156 | ||||||
chr5:80521256
|
C | T | 1 | a0001c0001t0001g0010 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.536-747C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 4/5 | chr5 | 80521256 | ||||||
chr5:80521474
|
A | G | 1 | a0002c0002t0001g0176 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.536-529A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 4/5 | chr5 | 80521474 | ||||||
chr5:80521552
|
G | C | 17 | a0001c0001t0001g0284a0001c0001t0001g0306a0001c0001t0001g0307others(14): Show | 18 | HG00280.hp1 HG00738.hp1 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.536-451G>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 4/5 | chr5 | 80521552 | ||||||
chr5:80521559
|
A | G | 5 | a0001c0001t0002g0204a0001c0001t0002g0206a0001c0001t0002g0297others(2): Show | 5 | HG02451.hp1 HG02622.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.536-444A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 4/5 | chr5 | 80521559 | ||||||
chr5:80521574
|
A | G | 1 | a0001c0001t0006g0286 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.536-429A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 4/5 | chr5 | 80521574 | ||||||
chr5:80521708
|
A | G | 31 | a0001c0001t0001g0284a0001c0001t0001g0306a0001c0001t0001g0307others(28): Show | 32 | HG00280.hp1 HG00738.hp1 HG01109.hp2 others(29): Show |
intron_variant | MODIFIER | c.536-295A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 4/5 | chr5 | 80521708 | ||||||
chr5:80521824
|
C | T | 1 | a0001c0001t0001g0260 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.536-179C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 4/5 | chr5 | 80521824 | ||||||
chr5:80522261
|
A | C | 1 | a0001c0001t0002g0278 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.671+123A>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80522261 | ||||||
chr5:80522326
|
T | A | 1 | a0001c0001t0001g0287 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.671+188T>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80522326 | ||||||
chr5:80522352
|
C | T | 1 | a0001c0001t0002g0278 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.671+214C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80522352 | ||||||
chr5:80522410
|
T | C | 30 | a0001c0001t0001g0284a0001c0001t0001g0306a0001c0001t0001g0307others(27): Show | 31 | HG00280.hp1 HG00738.hp1 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.671+272T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80522410 | ||||||
chr5:80522588
|
C | T | 1 | a0002c0002t0001g0038 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.671+450C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80522588 | ||||||
chr5:80522634
|
C | T | 31 | a0001c0001t0001g0289a0001c0001t0001g0304a0001c0001t0001g0305others(28): Show | 31 | HG00323.hp1 HG01109.hp1 HG01167.hp2 others(28): Show |
intron_variant | MODIFIER | c.671+496C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80522634 | ||||||
chr5:80522734
|
C | T | 3 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0002g0281 | 3 | HG01884.hp2 HG03098.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.671+596C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80522734 | ||||||
chr5:80522783
|
C | A | 4 | a0001c0001t0001g0228a0001c0001t0001g0231a0001c0001t0001g0233others(1): Show | 4 | HG02717.hp1 HG02895.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.671+645C>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80522783 | ||||||
chr5:80522838
|
A | G | 1 | a0001c0001t0006g0286 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.671+700A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80522838 | ||||||
chr5:80522884
|
AT | A | 30 | a0001c0001t0001g0284a0001c0001t0001g0306a0001c0001t0001g0307others(27): Show | 31 | HG00280.hp1 HG00738.hp1 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.671+755delT | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80522884 | |||||
chr5:80523134
|
G | A | 3 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0002g0281 | 3 | HG01884.hp2 HG03098.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.671+996G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80523134 | ||||||
chr5:80523600
|
T | C | 1 | a0001c0001t0001g0342 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.671+1462T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80523600 | ||||||
chr5:80523749
|
T | C | 1 | a0001c0001t0001g0100 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.671+1611T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80523749 | ||||||
chr5:80523757
|
A | T | 1 | a0001c0001t0001g0195 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.671+1619A>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80523757 | ||||||
chr5:80523899
|
C | G | 4 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0302others(1): Show | 4 | HG02145.hp1 HG02922.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.671+1761C>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80523899 | ||||||
chr5:80523981
|
C | T | 1 | a0001c0001t0002g0303 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.671+1843C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80523981 | ||||||
chr5:80524046
|
T | C | 32 | a0001c0001t0001g0289a0001c0001t0001g0304a0001c0001t0001g0305others(29): Show | 32 | HG00323.hp1 HG01109.hp1 HG01167.hp2 others(29): Show |
intron_variant | MODIFIER | c.671+1908T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80524046 | ||||||
chr5:80524099
|
G | A | 248 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(245): Show | 249 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(246): Show |
intron_variant | MODIFIER | c.671+1961G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80524099 | ||||||
chr5:80524196
|
T | G | 3 | a0001c0001t0003g0282a0001c0001t0003g0296a0001c0001t0006g0286 | 3 | HG02257.hp1 HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.671+2058T>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80524196 | ||||||
chr5:80524262
|
C | T | 3 | a0001c0001t0003g0282a0001c0001t0003g0296a0001c0001t0006g0286 | 3 | HG02257.hp1 HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.671+2124C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80524262 | ||||||
chr5:80524310
|
A | G | 1 | a0002c0002t0001g0301 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.671+2172A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80524310 | ||||||
chr5:80524361
|
A | C | 252 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(249): Show | 253 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(250): Show |
intron_variant | MODIFIER | c.671+2223A>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80524361 | ||||||
chr5:80524611
|
G | A | 1 | a0001c0001t0003g0282 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.671+2473G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80524611 | ||||||
chr5:80524706
|
A | G | 30 | a0001c0001t0001g0284a0001c0001t0001g0306a0001c0001t0001g0307others(27): Show | 31 | HG00280.hp1 HG00738.hp1 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.671+2568A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80524706 | ||||||
chr5:80524905
|
T | C | 253 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(250): Show | 254 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(251): Show |
intron_variant | MODIFIER | c.671+2767T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80524905 | ||||||
chr5:80525038
|
G | GGTGTTTA others(14): Show |
1 | a0002c0002t0001g0135 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.671+2901_671+2921d others(23): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80525038 | |||||
chr5:80525086
|
C | A | 1 | a0002c0002t0001g0016 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.671+2948C>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80525086 | ||||||
chr5:80525224
|
C | T | 1 | a0002c0002t0001g0193 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.671+3086C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80525224 | ||||||
chr5:80525242
|
C | T | 1 | a0001c0001t0006g0286 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.671+3104C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80525242 | ||||||
chr5:80525291
|
T | C | 4 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0139others(1): Show | 4 | HG02074.hp1 NA18954.hp2 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.671+3153T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80525291 | ||||||
chr5:80525370
|
C | G | 3 | a0001c0001t0003g0282a0001c0001t0003g0296a0001c0001t0006g0286 | 3 | HG02257.hp1 HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.671+3232C>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80525370 | ||||||
chr5:80525413
|
A | G | 253 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(250): Show | 254 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(251): Show |
intron_variant | MODIFIER | c.671+3275A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80525413 | ||||||
chr5:80525534
|
G | A | 251 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(248): Show | 252 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(249): Show |
intron_variant | MODIFIER | c.671+3396G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80525534 | ||||||
chr5:80525663
|
A | G | 1 | a0001c0001t0002g0278 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.671+3525A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80525663 | ||||||
chr5:80525875
|
CAT | C | 241 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(238): Show | 242 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(239): Show |
intron_variant | MODIFIER | c.671+3756_671+3757d others(4): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80525875 | |||||
chr5:80525977
|
T | A | 1 | a0001c0001t0001g0182 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.671+3839T>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80525977 | ||||||
chr5:80526058
|
G | A | 7 | a0001c0001t0001g0035a0001c0001t0001g0075a0001c0001t0001g0092others(4): Show | 7 | HG01515.hp2 HG01516.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.671+3920G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80526058 | ||||||
chr5:80526133
|
G | C | 4 | a0001c0001t0001g0192a0001c0001t0001g0300a0001c0001t0001g0308others(1): Show | 4 | HG00741.hp2 HG02922.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.671+3995G>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80526133 | ||||||
chr5:80526214
|
A | C | 1 | a0001c0001t0002g0278 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.671+4076A>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80526214 | ||||||
chr5:80526268
|
G | A | 4 | a0001c0001t0001g0192a0001c0001t0001g0300a0001c0001t0001g0308others(1): Show | 4 | HG00741.hp2 HG02922.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.671+4130G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80526268 | ||||||
chr5:80526453
|
C | CA | 158 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(155): Show | 159 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(156): Show |
intron_variant | MODIFIER | c.671+4332dupA | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80526453 | |||||
chr5:80526516
|
A | G | 1 | a0002c0002t0001g0179 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.671+4378A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80526516 | ||||||
chr5:80526648
|
T | A | 4 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0302others(1): Show | 4 | HG02145.hp1 HG02922.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.671+4510T>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80526648 | ||||||
chr5:80527016
|
G | A | 3 | a0001c0001t0001g0021a0001c0001t0004g0103a0001c0001t0004g0104 | 3 | HG00438.hp2 HG02083.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.671+4878G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80527016 | ||||||
chr5:80527097
|
C | T | 32 | a0001c0001t0001g0289a0001c0001t0001g0304a0001c0001t0001g0305others(29): Show | 32 | HG00323.hp1 HG01109.hp1 HG01167.hp2 others(29): Show |
intron_variant | MODIFIER | c.671+4959C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80527097 | ||||||
chr5:80527307
|
C | G | 1 | a0001c0001t0001g0310 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.671+5169C>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80527307 | ||||||
chr5:80527426
|
TA | T | 199 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(196): Show | 199 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(196): Show |
intron_variant | MODIFIER | c.671+5303delA | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80527426 | |||||
chr5:80527710
|
G | A | 1 | a0001c0001t0001g0355 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.671+5572G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80527710 | ||||||
chr5:80527807
|
A | C | 1 | a0001c0001t0001g0203 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.671+5669A>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80527807 | ||||||
chr5:80527909
|
T | A | 1 | a0001c0001t0002g0278 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.671+5771T>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80527909 | ||||||
chr5:80527996
|
A | G | 1 | a0001c0003t0001g0292 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.671+5858A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80527996 | ||||||
chr5:80528118
|
G | A | 2 | a0001c0001t0001g0033a0001c0001t0001g0036 | 2 | HG03130.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.671+5980G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80528118 | ||||||
chr5:80528150
|
A | G | 5 | a0001c0001t0001g0090a0002c0002t0001g0212a0002c0002t0001g0213others(2): Show | 5 | HG02040.hp1 NA18955.hp1 NA18982.hp1 others(2): Show |
intron_variant | MODIFIER | c.671+6012A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80528150 | ||||||
chr5:80528252
|
C | G | 1 | a0001c0001t0002g0113 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.671+6114C>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80528252 | ||||||
chr5:80528346
|
A | C | 20 | a0001c0001t0001g0185a0001c0001t0001g0235a0001c0001t0001g0253others(17): Show | 20 | HG00639.hp1 HG01099.hp2 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.671+6208A>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80528346 | ||||||
chr5:80528373
|
A | G | 4 | a0001c0001t0001g0192a0001c0001t0001g0300a0001c0001t0001g0308others(1): Show | 4 | HG00741.hp2 HG02922.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.671+6235A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80528373 | ||||||
chr5:80528438
|
A | G | 133 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(130): Show | 133 | HG00323.hp1 HG00621.hp1 HG00673.hp1 others(130): Show |
intron_variant | MODIFIER | c.671+6300A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80528438 | ||||||
chr5:80528601
|
A | C | 4 | a0001c0001t0001g0192a0001c0001t0001g0300a0001c0001t0001g0308others(1): Show | 4 | HG00741.hp2 HG02922.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.671+6463A>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80528601 | ||||||
chr5:80528655
|
G | A | 1 | a0001c0001t0002g0278 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.671+6517G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80528655 | ||||||
chr5:80528687
|
C | T | 1 | a0002c0002t0001g0073 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.671+6549C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80528687 | ||||||
chr5:80528803
|
C | T | 1 | a0001c0001t0001g0338 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.671+6665C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80528803 | ||||||
chr5:80528919
|
A | G | 1 | a0001c0001t0001g0102 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.671+6781A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80528919 | ||||||
chr5:80528978
|
T | C | 1 | a0001c0001t0001g0208 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.671+6840T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80528978 | ||||||
chr5:80529095
|
G | A | 57 | a0001c0001t0001g0021a0001c0001t0001g0030a0001c0001t0001g0033others(54): Show | 57 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(54): Show |
intron_variant | MODIFIER | c.671+6957G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80529095 | ||||||
chr5:80529141
|
G | A | 2 | a0001c0001t0001g0192a0001c0001t0001g0355 | 2 | HG00741.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.671+7003G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80529141 | ||||||
chr5:80529217
|
C | T | 2 | a0002c0002t0001g0037a0002c0002t0001g0038 | 2 | HG00642.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.671+7079C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80529217 | ||||||
chr5:80529241
|
T | G | 2 | a0001c0001t0001g0250a0001c0001t0001g0251 | 2 | NA18975.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.671+7103T>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80529241 | ||||||
chr5:80529329
|
T | G | 4 | a0001c0001t0001g0078a0001c0001t0001g0085a0001c0001t0001g0095others(1): Show | 4 | HG02074.hp1 NA18950.hp2 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.671+7191T>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80529329 | ||||||
chr5:80529434
|
G | T | 17 | a0001c0001t0001g0284a0001c0001t0001g0306a0001c0001t0001g0307others(14): Show | 18 | HG00280.hp1 HG00738.hp1 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.671+7296G>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80529434 | ||||||
chr5:80529485
|
C | T | 2 | a0001c0001t0001g0192a0001c0001t0001g0355 | 2 | HG00741.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.671+7347C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80529485 | ||||||
chr5:80529508
|
A | G | 30 | a0001c0001t0001g0284a0001c0001t0001g0306a0001c0001t0001g0307others(27): Show | 31 | HG00280.hp1 HG00738.hp1 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.671+7370A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80529508 | ||||||
chr5:80529531
|
C | T | 1 | a0002c0002t0001g0032 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.671+7393C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80529531 | ||||||
chr5:80529551
|
C | G | 12 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(9): Show | 12 | HG03491.hp2 NA18948.hp1 NA18950.hp1 others(9): Show |
intron_variant | MODIFIER | c.671+7413C>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80529551 | ||||||
chr5:80529551
|
C | T | 2 | a0001c0001t0001g0279a0001c0001t0001g0280 | 2 | HG01884.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.671+7413C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80529551 | ||||||
chr5:80529626
|
G | T | 2 | a0001c0001t0001g0279a0001c0001t0003g0282 | 2 | HG01884.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.671+7488G>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80529626 | ||||||
chr5:80529716
|
T | C | 32 | a0001c0001t0001g0289a0001c0001t0001g0304a0001c0001t0001g0305others(29): Show | 32 | HG00323.hp1 HG01109.hp1 HG01167.hp2 others(29): Show |
intron_variant | MODIFIER | c.671+7578T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80529716 | ||||||
chr5:80529790
|
G | C | 1 | a0001c0001t0001g0256 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.671+7652G>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80529790 | ||||||
chr5:80529894
|
G | A | 1 | a0002c0002t0001g0179 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.671+7756G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80529894 | ||||||
chr5:80529907
|
T | TACCAAAG others(53): Show |
29 | a0001c0001t0001g0284a0001c0001t0001g0306a0001c0001t0001g0307others(26): Show | 30 | HG00280.hp1 HG00738.hp1 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.671+7770_671+7829d others(62): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80529907 | |||||
chr5:80529958
|
G | GTGATGAA others(53): Show |
1 | a0001c0001t0002g0298 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.671+7829_671+7830i others(62): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80529958 | |||||
chr5:80529970
|
G | A | 3 | a0001c0001t0003g0282a0001c0001t0003g0296a0001c0001t0006g0286 | 3 | HG02257.hp1 HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.671+7832G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80529970 | ||||||
chr5:80530151
|
T | C | 4 | a0001c0001t0001g0192a0001c0001t0001g0300a0001c0001t0001g0308others(1): Show | 4 | HG00741.hp2 HG02922.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.671+8013T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80530151 | ||||||
chr5:80530176
|
A | C | 1 | a0001c0001t0001g0137 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.671+8038A>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80530176 | ||||||
chr5:80530368
|
G | A | 58 | a0001c0001t0001g0021a0001c0001t0001g0030a0001c0001t0001g0033others(55): Show | 58 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(55): Show |
intron_variant | MODIFIER | c.671+8230G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80530368 | ||||||
chr5:80530462
|
G | T | 2 | a0002c0002t0001g0034a0002c0002t0001g0155 | 2 | NA19067.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.671+8324G>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80530462 | ||||||
chr5:80530472
|
T | A | 34 | a0001c0001t0001g0289a0001c0001t0001g0304a0001c0001t0001g0305others(31): Show | 34 | HG00323.hp1 HG01109.hp1 HG01167.hp2 others(31): Show |
intron_variant | MODIFIER | c.671+8334T>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80530472 | ||||||
chr5:80530501
|
C | T | 30 | a0001c0001t0001g0284a0001c0001t0001g0306a0001c0001t0001g0307others(27): Show | 31 | HG00280.hp1 HG00738.hp1 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.671+8363C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80530501 | ||||||
chr5:80530520
|
T | A | 1 | a0001c0001t0002g0278 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.671+8382T>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80530520 | ||||||
chr5:80530826
|
T | G | 30 | a0001c0001t0001g0284a0001c0001t0001g0306a0001c0001t0001g0307others(27): Show | 31 | HG00280.hp1 HG00738.hp1 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.671+8688T>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80530826 | ||||||
chr5:80530827
|
G | A | 30 | a0001c0001t0001g0284a0001c0001t0001g0306a0001c0001t0001g0307others(27): Show | 31 | HG00280.hp1 HG00738.hp1 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.671+8689G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80530827 | ||||||
chr5:80530840
|
A | C | 20 | a0001c0001t0001g0185a0001c0001t0001g0235a0001c0001t0001g0253others(17): Show | 20 | HG00639.hp1 HG01099.hp2 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.671+8702A>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80530840 | ||||||
chr5:80530882
|
A | C | 1 | a0001c0001t0001g0047 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.671+8744A>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80530882 | ||||||
chr5:80531267
|
C | T | 5 | a0001c0001t0002g0204a0001c0001t0002g0206a0001c0001t0002g0297others(2): Show | 5 | HG02451.hp1 HG02622.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.671+9129C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80531267 | ||||||
chr5:80531273
|
C | T | 1 | a0001c0001t0002g0278 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.671+9135C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80531273 | ||||||
chr5:80531359
|
T | C | 30 | a0001c0001t0001g0284a0001c0001t0001g0306a0001c0001t0001g0307others(27): Show | 31 | HG00280.hp1 HG00738.hp1 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.671+9221T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80531359 | ||||||
chr5:80531427
|
A | G | 1 | a0001c0001t0001g0068 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.671+9289A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80531427 | ||||||
chr5:80531558
|
C | G | 19 | a0001c0001t0001g0235a0001c0001t0001g0253a0001c0001t0001g0255others(16): Show | 19 | HG00639.hp1 HG01099.hp2 HG01261.hp2 others(16): Show |
intron_variant | MODIFIER | c.671+9420C>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80531558 | ||||||
chr5:80531565
|
A | G | 1 | a0001c0001t0002g0118 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.671+9427A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80531565 | ||||||
chr5:80531569
|
T | C | 1 | a0002c0002t0001g0301 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.671+9431T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80531569 | ||||||
chr5:80531577
|
G | A | 1 | a0001c0001t0001g0021 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.671+9439G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80531577 | ||||||
chr5:80531895
|
C | T | 2 | a0001c0001t0001g0192a0001c0001t0001g0355 | 2 | HG00741.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.671+9757C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80531895 | ||||||
chr5:80532017
|
GA | G | 32 | a0001c0001t0001g0289a0001c0001t0001g0304a0001c0001t0001g0305others(29): Show | 32 | HG00323.hp1 HG01109.hp1 HG01167.hp2 others(29): Show |
intron_variant | MODIFIER | c.672-9652delA | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80532017 | |||||
chr5:80532035
|
C | T | 1 | a0001c0001t0001g0269 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.672-9638C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80532035 | ||||||
chr5:80532127
|
C | A | 20 | a0001c0001t0001g0185a0001c0001t0001g0235a0001c0001t0001g0253others(17): Show | 20 | HG00639.hp1 HG01099.hp2 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.672-9546C>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80532127 | ||||||
chr5:80532137
|
T | C | 30 | a0001c0001t0001g0284a0001c0001t0001g0306a0001c0001t0001g0307others(27): Show | 31 | HG00280.hp1 HG00738.hp1 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.672-9536T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80532137 | ||||||
chr5:80532217
|
T | A | 4 | a0001c0001t0001g0192a0001c0001t0001g0300a0001c0001t0001g0308others(1): Show | 4 | HG00741.hp2 HG02922.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.672-9456T>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80532217 | ||||||
chr5:80532230
|
G | T | 1 | a0001c0001t0001g0258 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.672-9443G>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80532230 | ||||||
chr5:80532370
|
A | T | 1 | a0001c0001t0006g0286 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.672-9303A>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80532370 | ||||||
chr5:80532464
|
A | G | 1 | a0002c0002t0001g0034 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.672-9209A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80532464 | ||||||
chr5:80532539
|
A | G | 1 | a0001c0001t0001g0312 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.672-9134A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80532539 | ||||||
chr5:80532759
|
A | G | 162 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(159): Show | 162 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(159): Show |
intron_variant | MODIFIER | c.672-8914A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80532759 | ||||||
chr5:80532889
|
C | T | 1 | a0001c0001t0001g0075 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.672-8784C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80532889 | ||||||
chr5:80533038
|
C | T | 51 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0020others(48): Show | 51 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(48): Show |
intron_variant | MODIFIER | c.672-8635C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80533038 | ||||||
chr5:80533192
|
A | G | 2 | a0002c0002t0001g0086a0002c0002t0001g0088 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.672-8481A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80533192 | ||||||
chr5:80533309
|
G | A | 19 | a0001c0001t0001g0235a0001c0001t0001g0253a0001c0001t0001g0255others(16): Show | 19 | HG00639.hp1 HG01099.hp2 HG01261.hp2 others(16): Show |
intron_variant | MODIFIER | c.672-8364G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80533309 | ||||||
chr5:80533325
|
C | T | 3 | a0002c0002t0001g0017a0002c0002t0001g0220a0002c0002t0001g0221 | 3 | HG02280.hp1 HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.672-8348C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80533325 | ||||||
chr5:80533371
|
C | T | 1 | a0001c0001t0002g0278 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.672-8302C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80533371 | ||||||
chr5:80533427
|
A | AAACCCAA others(4): Show |
1 | a0001c0001t0001g0211 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.672-8244_672-8234d others(13): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80533427 | |||||
chr5:80533471
|
G | A | 1 | a0001c0001t0001g0200 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.672-8202G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80533471 | ||||||
chr5:80533609
|
G | A | 2 | a0001c0001t0001g0033a0001c0001t0001g0036 | 2 | HG03130.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.672-8064G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80533609 | ||||||
chr5:80533621
|
G | A | 32 | a0001c0001t0001g0289a0001c0001t0001g0304a0001c0001t0001g0305others(29): Show | 32 | HG00323.hp1 HG01109.hp1 HG01167.hp2 others(29): Show |
intron_variant | MODIFIER | c.672-8052G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80533621 | ||||||
chr5:80533660
|
G | T | 9 | a0001c0003t0001g0001a0001c0003t0001g0186a0001c0003t0001g0187others(6): Show | 10 | HG00280.hp1 HG00738.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.672-8013G>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80533660 | ||||||
chr5:80533698
|
C | T | 1 | a0001c0001t0003g0282 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.672-7975C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80533698 | ||||||
chr5:80533702
|
A | T | 1 | a0001c0001t0006g0286 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.672-7971A>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80533702 | ||||||
chr5:80533736
|
C | T | 2 | a0001c0001t0001g0128a0001c0001t0001g0143 | 2 | NA18978.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.672-7937C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80533736 | ||||||
chr5:80533749
|
C | CA | 36 | a0001c0001t0001g0054a0001c0001t0001g0257a0001c0001t0001g0279others(33): Show | 36 | HG00323.hp1 HG01109.hp1 HG01167.hp2 others(33): Show |
intron_variant | MODIFIER | c.672-7905dupA | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80533749 | |||||
chr5:80533749
|
C | CAA | 24 | a0001c0001t0001g0177a0001c0001t0001g0196a0001c0001t0001g0235others(21): Show | 24 | HG00639.hp1 HG01099.hp2 HG01261.hp2 others(21): Show |
intron_variant | MODIFIER | c.672-7906_672-7905d others(4): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80533749 | |||||
chr5:80533749
|
C | CAAA | 59 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0020others(56): Show | 59 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.672-7907_672-7905d others(5): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80533749 | |||||
chr5:80533749
|
C | CAAAA | 93 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(90): Show | 93 | HG00621.hp1 HG00673.hp1 HG00738.hp2 others(90): Show |
intron_variant | MODIFIER | c.672-7908_672-7905d others(6): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80533749 | |||||
chr5:80533749
|
CA | C | 24 | a0001c0001t0001g0284a0001c0001t0001g0306a0001c0001t0001g0307others(21): Show | 25 | HG00280.hp1 HG00738.hp1 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.672-7905delA | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80533749 | |||||
chr5:80533769
|
G | A | 1 | a0001c0001t0001g0054 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.672-7904G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80533769 | ||||||
chr5:80533934
|
T | A | 1 | a0001c0001t0002g0320 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.672-7739T>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80533934 | ||||||
chr5:80533952
|
G | C | 30 | a0001c0001t0001g0284a0001c0001t0001g0306a0001c0001t0001g0307others(27): Show | 31 | HG00280.hp1 HG00738.hp1 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.672-7721G>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80533952 | ||||||
chr5:80534036
|
C | A | 1 | a0001c0001t0001g0085 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.672-7637C>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80534036 | ||||||
chr5:80534148
|
G | T | 5 | a0001c0001t0002g0204a0001c0001t0002g0206a0001c0001t0002g0297others(2): Show | 5 | HG02451.hp1 HG02622.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.672-7525G>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80534148 | ||||||
chr5:80534296
|
C | G | 5 | a0002c0002t0001g0037a0002c0002t0001g0038a0002c0002t0001g0111others(2): Show | 5 | HG00642.hp1 HG01099.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.672-7377C>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80534296 | ||||||
chr5:80534352
|
C | T | 190 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(187): Show | 190 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.672-7321C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80534352 | ||||||
chr5:80534490
|
C | T | 1 | a0001c0001t0002g0278 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.672-7183C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80534490 | ||||||
chr5:80534723
|
C | G | 1 | a0001c0001t0001g0092 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.672-6950C>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80534723 | ||||||
chr5:80534806
|
A | G | 1 | a0002c0002t0001g0073 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.672-6867A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80534806 | ||||||
chr5:80534858
|
C | T | 1 | a0001c0001t0001g0354 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.672-6815C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80534858 | ||||||
chr5:80534939
|
G | A | 247 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(244): Show | 248 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(245): Show |
intron_variant | MODIFIER | c.672-6734G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80534939 | ||||||
chr5:80535137
|
G | A | 1 | a0001c0001t0002g0278 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.672-6536G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80535137 | ||||||
chr5:80535175
|
C | T | 1 | a0001c0001t0001g0143 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.672-6498C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80535175 | ||||||
chr5:80535280
|
A | C | 2 | a0001c0001t0002g0118a0001c0001t0002g0288 | 2 | HG02809.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.672-6393A>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80535280 | ||||||
chr5:80535443
|
G | A | 34 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0001g0289others(31): Show | 34 | HG00323.hp1 HG01109.hp1 HG01167.hp2 others(31): Show |
intron_variant | MODIFIER | c.672-6230G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80535443 | ||||||
chr5:80535480
|
C | T | 2 | a0002c0002t0001g0111a0002c0002t0001g0193 | 2 | HG01258.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.672-6193C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80535480 | ||||||
chr5:80535562
|
G | A | 1 | a0002c0002t0001g0171 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.672-6111G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80535562 | ||||||
chr5:80535658
|
C | T | 1 | a0001c0001t0006g0286 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.672-6015C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80535658 | ||||||
chr5:80535663
|
G | C | 251 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(248): Show | 252 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(249): Show |
intron_variant | MODIFIER | c.672-6010G>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80535663 | ||||||
chr5:80535768
|
C | T | 1 | a0002c0002t0001g0179 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.672-5905C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80535768 | ||||||
chr5:80536074
|
A | C | 1 | a0001c0001t0002g0297 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.672-5599A>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80536074 | ||||||
chr5:80536141
|
T | TTTTAG | 5 | a0001c0001t0002g0118a0001c0001t0002g0288a0001c0001t0002g0303others(2): Show | 5 | HG02451.hp2 HG02809.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.672-5513_672-5509d others(7): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80536141 | |||||
chr5:80536141
|
TTTTAG | T | 9 | a0001c0003t0001g0001a0001c0003t0001g0186a0001c0003t0001g0187others(6): Show | 10 | HG00280.hp1 HG00738.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.672-5513_672-5509d others(7): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80536141 | |||||
chr5:80536160
|
A | T | 3 | a0001c0001t0001g0033a0001c0001t0001g0036a0002c0002t0001g0154 | 3 | HG02622.hp1 HG03130.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.672-5513A>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80536160 | ||||||
chr5:80536160
|
AGTTTTGT others(3): Show |
A | 1 | a0002c0002t0001g0122 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.672-5497_672-5488d others(12): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80536160 | |||||
chr5:80536165
|
T | A | 3 | a0002c0002t0001g0274a0002c0002t0001g0344a0002c0002t0001g0345 | 3 | HG03041.hp2 HG03195.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.672-5508T>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80536165 | ||||||
chr5:80536216
|
G | A | 32 | a0001c0001t0001g0289a0001c0001t0001g0304a0001c0001t0001g0305others(29): Show | 32 | HG00323.hp1 HG01109.hp1 HG01167.hp2 others(29): Show |
intron_variant | MODIFIER | c.672-5457G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80536216 | ||||||
chr5:80536219
|
G | A | 55 | a0001c0001t0001g0021a0001c0001t0001g0030a0001c0001t0001g0033others(52): Show | 55 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(52): Show |
intron_variant | MODIFIER | c.672-5454G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80536219 | ||||||
chr5:80536231
|
C | T | 1 | a0001c0001t0002g0278 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.672-5442C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80536231 | ||||||
chr5:80536273
|
C | T | 2 | a0001c0001t0001g0279a0001c0001t0001g0280 | 2 | HG01884.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.672-5400C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80536273 | ||||||
chr5:80536316
|
G | A | 3 | a0001c0001t0003g0282a0001c0001t0003g0296a0001c0001t0006g0286 | 3 | HG02257.hp1 HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.672-5357G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80536316 | ||||||
chr5:80536337
|
A | AT | 31 | a0001c0001t0001g0284a0001c0001t0001g0306a0001c0001t0001g0307others(28): Show | 32 | HG00280.hp1 HG00738.hp1 HG01109.hp2 others(29): Show |
intron_variant | MODIFIER | c.672-5326dupT | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80536337 | |||||
chr5:80536398
|
A | C | 30 | a0001c0001t0001g0284a0001c0001t0001g0306a0001c0001t0001g0307others(27): Show | 31 | HG00280.hp1 HG00738.hp1 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.672-5275A>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80536398 | ||||||
chr5:80536418
|
T | C | 33 | a0001c0001t0001g0284a0001c0001t0001g0306a0001c0001t0001g0307others(30): Show | 34 | HG00280.hp1 HG00738.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.672-5255T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80536418 | ||||||
chr5:80536474
|
A | T | 1 | a0002c0002t0001g0042 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.672-5199A>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80536474 | ||||||
chr5:80536489
|
TTGAGGAA others(14): Show |
T | 1 | a0001c0001t0001g0228 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.672-5183_672-5163d others(23): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80536489 | ||||||
chr5:80536542
|
C | T | 1 | a0001c0001t0001g0300 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.672-5131C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80536542 | ||||||
chr5:80536699
|
A | G | 1 | a0002c0002t0001g0132 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.672-4974A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80536699 | ||||||
chr5:80536942
|
A | G | 1 | a0002c0002t0001g0244 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.672-4731A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80536942 | ||||||
chr5:80537230
|
A | C | 1 | a0002c0002t0001g0194 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.672-4443A>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80537230 | ||||||
chr5:80537467
|
G | C | 1 | a0002c0002t0001g0210 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.672-4206G>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80537467 | ||||||
chr5:80537482
|
G | A | 59 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0020others(56): Show | 59 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.672-4191G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80537482 | ||||||
chr5:80537794
|
C | T | 1 | a0001c0001t0001g0143 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.672-3879C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80537794 | ||||||
chr5:80537910
|
TAATAG | T | 60 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0020others(57): Show | 60 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(57): Show |
intron_variant | MODIFIER | c.672-3758_672-3754d others(7): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80537910 | |||||
chr5:80537954
|
A | C | 1 | a0001c0003t0001g0290 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.672-3719A>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80537954 | ||||||
chr5:80538002
|
A | G | 30 | a0001c0001t0001g0284a0001c0001t0001g0306a0001c0001t0001g0307others(27): Show | 31 | HG00280.hp1 HG00738.hp1 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.672-3671A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538002 | ||||||
chr5:80538006
|
A | G | 1 | a0001c0001t0002g0113 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.672-3667A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538006 | ||||||
chr5:80538014
|
G | A | 1 | a0002c0002t0001g0229 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.672-3659G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538014 | ||||||
chr5:80538073
|
A | AT | 6 | a0001c0001t0001g0185a0001c0001t0001g0253a0001c0001t0001g0264others(3): Show | 6 | HG01070.hp1 HG01175.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.672-3587dupT | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538073 | |||||
chr5:80538073
|
AT | A | 229 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(226): Show | 230 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(227): Show |
intron_variant | MODIFIER | c.672-3587delT | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538073 | |||||
chr5:80538103
|
C | T | 2 | a0002c0002t0001g0086a0002c0002t0001g0088 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.672-3570C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538103 | ||||||
chr5:80538136
|
C | T | 3 | a0002c0002t0001g0016a0002c0002t0001g0096a0002c0002t0001g0114 | 3 | HG04115.hp2 HG04184.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.672-3537C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538136 | ||||||
chr5:80538146
|
C | T | 1 | a0001c0001t0001g0057 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.672-3527C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538146 | ||||||
chr5:80538153
|
C | T | 3 | a0002c0002t0001g0122a0002c0002t0001g0138a0002c0002t0001g0198 | 3 | HG01943.hp2 HG01975.hp1 NA18941.hp1 |
intron_variant | MODIFIER | c.672-3520C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538153 | ||||||
chr5:80538245
|
T | C | 3 | a0002c0002t0001g0122a0002c0002t0001g0138a0002c0002t0001g0198 | 3 | HG01943.hp2 HG01975.hp1 NA18941.hp1 |
intron_variant | MODIFIER | c.672-3428T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538245 | ||||||
chr5:80538284
|
A | G | 30 | a0001c0001t0001g0284a0001c0001t0001g0306a0001c0001t0001g0307others(27): Show | 31 | HG00280.hp1 HG00738.hp1 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.672-3389A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538284 | ||||||
chr5:80538319
|
G | A | 60 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0020others(57): Show | 60 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(57): Show |
intron_variant | MODIFIER | c.672-3354G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538319 | ||||||
chr5:80538372
|
T | TTTTC | 12 | a0001c0001t0001g0185a0001c0001t0001g0235a0001c0001t0002g0113others(9): Show | 12 | HG01069.hp2 HG01175.hp1 HG01943.hp2 others(9): Show |
intron_variant | MODIFIER | c.672-3227_672-3224d others(6): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538372 | |||||
chr5:80538372
|
T | TTTTCTTT others(1): Show |
5 | a0002c0002t0001g0037a0002c0002t0001g0038a0002c0002t0001g0052others(2): Show | 5 | HG00642.hp1 HG01258.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.672-3231_672-3224d others(10): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538372 | |||||
chr5:80538372
|
T | TTTTCTTT others(5): Show |
3 | a0001c0001t0001g0258a0002c0002t0001g0028a0002c0002t0001g0209 | 3 | HG02723.hp2 NA18969.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.672-3235_672-3224d others(14): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538372 | |||||
chr5:80538372
|
T | TTTTCTTT others(9): Show |
2 | a0002c0002t0001g0080a0002c0002t0001g0135 | 2 | NA18955.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.672-3239_672-3224d others(18): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538372 | |||||
chr5:80538372
|
TTTTC | T | 9 | a0001c0001t0001g0055a0001c0001t0001g0205a0002c0002t0001g0017others(6): Show | 9 | HG01975.hp2 HG02622.hp1 HG03239.hp1 others(6): Show |
intron_variant | MODIFIER | c.672-3227_672-3224d others(6): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538372 | |||||
chr5:80538372
|
TTTTCTTT others(1): Show |
T | 6 | a0001c0001t0001g0144a0001c0001t0001g0180a0001c0001t0001g0181others(3): Show | 6 | HG01070.hp2 HG01071.hp1 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.672-3231_672-3224d others(10): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538372 | |||||
chr5:80538372
|
TTTTCTTT others(5): Show |
T | 1 | a0002c0002t0001g0053 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.672-3235_672-3224d others(14): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538372 | |||||
chr5:80538372
|
TTTTCTTT others(9): Show |
T | 1 | a0002c0002t0001g0114 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.672-3239_672-3224d others(18): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538372 | |||||
chr5:80538402
|
T | G | 1 | a0001c0001t0001g0188 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.672-3271T>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538402 | ||||||
chr5:80538418
|
TTCTTTCT others(23): Show |
T | 1 | a0001c0001t0001g0300 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.672-3223_672-3194d others(32): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538418 | |||||
chr5:80538424
|
CTTTCTTT others(21): Show |
C | 1 | a0002c0002t0001g0096 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.672-3247_672-3220d others(30): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538424 | |||||
chr5:80538426
|
T | TTCTTTCT others(3): Show |
2 | a0001c0001t0002g0237a0001c0003t0001g0290 | 2 | HG03669.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.672-3245_672-3236d others(12): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538426 | |||||
chr5:80538426
|
T | TTCTTTCT others(7): Show |
2 | a0001c0001t0001g0284a0001c0001t0001g0306 | 2 | HG01496.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.672-3245_672-3232d others(16): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538426 | |||||
chr5:80538426
|
T | TTCTTTCT others(11): Show |
1 | a0001c0003t0001g0291 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.672-3245_672-3228d others(20): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538426 | |||||
chr5:80538428
|
CTTTCTTT others(17): Show |
C | 1 | a0001c0001t0001g0128 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.672-3243_672-3220d others(26): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538428 | |||||
chr5:80538431
|
T | C | 1 | a0001c0001t0001g0308 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.672-3242T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538431 | ||||||
chr5:80538432
|
CTTTCTT | C | 3 | a0002c0002t0001g0105a0002c0002t0001g0344a0002c0002t0001g0345 | 3 | HG03195.hp1 HG03516.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.672-3239_672-3234d others(8): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538432 | |||||
chr5:80538432
|
CTTTCTTT others(13): Show |
C | 2 | a0001c0001t0001g0143a0001c0001t0001g0214 | 2 | NA18989.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.672-3239_672-3220d others(22): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538432 | |||||
chr5:80538435
|
T | C | 1 | a0001c0001t0001g0308 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.672-3238T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538435 | ||||||
chr5:80538436
|
CTT | C | 3 | a0001c0001t0001g0271a0001c0001t0001g0280a0002c0002t0001g0274 | 3 | HG01261.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.672-3235_672-3234d others(4): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538436 | |||||
chr5:80538436
|
CTTTCTTT others(9): Show |
C | 8 | a0001c0001t0001g0062a0001c0001t0001g0064a0001c0001t0001g0065others(5): Show | 8 | HG00738.hp2 HG01069.hp1 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.672-3235_672-3220d others(18): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538436 | |||||
chr5:80538436
|
CTTTCTTT others(13): Show |
C | 1 | a0002c0002t0001g0084 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.672-3235_672-3216d others(22): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538436 | |||||
chr5:80538436
|
CTTTCTTT others(17): Show |
C | 1 | a0001c0001t0001g0233 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.672-3235_672-3212d others(26): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538436 | |||||
chr5:80538438
|
TTCTTTCT others(3): Show |
T | 3 | a0001c0001t0001g0163a0001c0001t0001g0196a0001c0001t0001g0197 | 3 | HG02074.hp2 HG02922.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.672-3223_672-3214d others(12): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538438 | |||||
chr5:80538440
|
CTTTCTTT others(5): Show |
C | 11 | a0001c0001t0001g0048a0001c0001t0001g0057a0001c0001t0001g0077others(8): Show | 11 | HG00621.hp1 HG00741.hp1 HG01496.hp2 others(8): Show |
intron_variant | MODIFIER | c.672-3231_672-3220d others(14): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538440 | |||||
chr5:80538440
|
CTTTCTTT others(9): Show |
C | 1 | a0001c0001t0001g0328 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.672-3231_672-3216d others(18): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538440 | |||||
chr5:80538440
|
CTTTCTTT others(13): Show |
C | 2 | a0001c0001t0001g0078a0001c0001t0001g0161 | 2 | HG00558.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.672-3231_672-3212d others(22): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538440 | |||||
chr5:80538441
|
TTTCTTTC others(39): Show |
T | 1 | a0001c0001t0001g0192 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.672-3228_672-3183d others(48): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538441 | |||||
chr5:80538442
|
T | C | 8 | a0001c0001t0001g0049a0001c0001t0001g0095a0001c0001t0001g0203others(5): Show | 8 | HG00323.hp1 HG00738.hp1 HG02080.hp2 others(5): Show |
intron_variant | MODIFIER | c.672-3231T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538442 | ||||||
chr5:80538442
|
TTCTTTC | T | 9 | a0001c0001t0001g0015a0001c0001t0001g0139a0001c0001t0001g0145others(6): Show | 9 | HG00323.hp2 HG00438.hp2 HG00642.hp2 others(6): Show |
intron_variant | MODIFIER | c.672-3223_672-3218d others(8): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538442 | |||||
chr5:80538444
|
C | CTCTTTCT others(25): Show |
2 | a0001c0001t0001g0312a0001c0001t0001g0313 | 2 | HG02486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.672-3228_672-3227i others(34): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538444 | |||||
chr5:80538444
|
C | T | 3 | a0001c0001t0001g0095a0001c0001t0002g0288a0001c0003t0001g0187 | 3 | HG00738.hp1 NA19043.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.672-3229C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538444 | ||||||
chr5:80538444
|
CTTTCTCT others(1): Show |
C | 10 | a0001c0001t0001g0014a0001c0001t0001g0054a0001c0001t0001g0063others(7): Show | 10 | HG02293.hp1 HG02300.hp1 HG03669.hp1 others(7): Show |
intron_variant | MODIFIER | c.672-3227_672-3220d others(10): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538444 | |||||
chr5:80538444
|
CTTTCTCT others(5): Show |
C | 2 | a0001c0001t0001g0325a0001c0001t0001g0334 | 2 | HG02258.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.672-3227_672-3216d others(14): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538444 | |||||
chr5:80538444
|
CTTTCTCT others(9): Show |
C | 4 | a0001c0001t0001g0019a0001c0001t0001g0106a0001c0001t0001g0164others(1): Show | 4 | HG02109.hp2 HG02735.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.672-3227_672-3212d others(18): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538444 | |||||
chr5:80538445
|
TTTCTCTT others(35): Show |
T | 1 | a0001c0001t0001g0355 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.672-3224_672-3183d others(44): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538445 | |||||
chr5:80538446
|
T | C | 39 | a0001c0001t0001g0002a0001c0001t0001g0047a0001c0001t0001g0049others(36): Show | 39 | HG00323.hp1 HG00738.hp1 HG01099.hp1 others(36): Show |
intron_variant | MODIFIER | c.672-3227T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538446 | ||||||
chr5:80538446
|
TTC | T | 25 | a0001c0001t0001g0030a0001c0001t0001g0051a0001c0001t0001g0056others(22): Show | 25 | HG00408.hp2 HG01070.hp1 HG01261.hp2 others(22): Show |
intron_variant | MODIFIER | c.672-3223_672-3222d others(4): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538446 | |||||
chr5:80538447
|
T | C | 1 | a0001c0001t0001g0211 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.672-3226T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538447 | ||||||
chr5:80538448
|
C | CTCTT | 7 | a0002c0002t0001g0116a0002c0002t0001g0178a0002c0002t0001g0210others(4): Show | 7 | HG00621.hp2 HG00735.hp1 HG02300.hp2 others(4): Show |
intron_variant | MODIFIER | c.672-3190_672-3187d others(6): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538448 | |||||
chr5:80538448
|
C | CTCTTCTT others(4): Show |
1 | a0002c0002t0001g0069 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.672-3221_672-3220i others(13): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538448 | |||||
chr5:80538448
|
C | CTT | 43 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(40): Show | 43 | HG00438.hp1 HG01109.hp1 HG01358.hp1 others(40): Show |
intron_variant | MODIFIER | c.672-3224_672-3223i others(4): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538448 | |||||
chr5:80538448
|
C | CTTTCTCT others(1): Show |
5 | a0001c0001t0001g0255a0002c0002t0001g0061a0002c0002t0001g0184others(2): Show | 5 | HG00639.hp1 HG03491.hp2 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.672-3224_672-3223i others(10): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538448 | |||||
chr5:80538448
|
C | CTTTCTCT others(5): Show |
2 | a0002c0002t0001g0170a0002c0002t0001g0272 | 2 | NA18942.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.672-3224_672-3223i others(14): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538448 | |||||
chr5:80538448
|
C | CTTTCTCT others(9): Show |
1 | a0002c0002t0001g0022 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.672-3224_672-3223i others(18): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538448 | |||||
chr5:80538448
|
C | CTTTCTCT others(23): Show |
1 | a0001c0003t0001g0001 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.672-3224_672-3223i others(32): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538448 | |||||
chr5:80538448
|
C | CTTTCTCT others(27): Show |
1 | a0001c0003t0001g0295 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.672-3224_672-3223i others(36): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538448 | |||||
chr5:80538448
|
C | CTTTCTTT others(5): Show |
3 | a0001c0001t0001g0252a0002c0002t0001g0136a0002c0002t0001g0224 | 3 | HG00544.hp1 HG02083.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.672-3224_672-3223i others(14): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538448 | |||||
chr5:80538448
|
C | CTTTCTTT others(9): Show |
1 | a0002c0002t0001g0076 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.672-3224_672-3223i others(18): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538448 | |||||
chr5:80538448
|
C | CTTTCTTT others(25): Show |
1 | a0002c0002t0001g0032 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.672-3224_672-3223i others(34): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538448 | |||||
chr5:80538448
|
C | CTTTCTTT others(9): Show |
2 | a0001c0001t0001g0260a0002c0002t0001g0133 | 2 | HG01346.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.672-3224_672-3223i others(18): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538448 | |||||
chr5:80538448
|
C | CTTTCTTT others(13): Show |
2 | a0002c0002t0001g0169a0002c0002t0001g0179 | 2 | HG02071.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.672-3224_672-3223i others(22): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538448 | |||||
chr5:80538448
|
C | CTTTCTTT others(13): Show |
1 | a0002c0002t0001g0046 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.672-3224_672-3223i others(22): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538448 | |||||
chr5:80538448
|
C | CTTTCTTT others(21): Show |
1 | a0002c0002t0001g0023 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.672-3224_672-3223i others(30): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538448 | |||||
chr5:80538448
|
C | CTTTCTTT others(15): Show |
1 | a0002c0002t0001g0171 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.672-3224_672-3223i others(24): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538448 | |||||
chr5:80538448
|
C | T | 20 | a0001c0001t0001g0095a0001c0001t0001g0262a0001c0001t0001g0310others(17): Show | 20 | HG00738.hp1 HG01099.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.672-3225C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538448 | ||||||
chr5:80538448
|
CTCTT | C | 12 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(9): Show | 12 | HG01257.hp2 HG01258.hp2 HG01515.hp2 others(9): Show |
intron_variant | MODIFIER | c.672-3190_672-3187d others(6): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538448 | |||||
chr5:80538448
|
CTCTTTCT others(1): Show |
C | 6 | a0001c0001t0001g0060a0001c0001t0001g0182a0001c0001t0001g0316others(3): Show | 6 | HG02004.hp2 HG02717.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.672-3194_672-3187d others(10): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538448 | |||||
chr5:80538448
|
CTCTTTCT others(5): Show |
C | 15 | a0001c0001t0001g0036a0001c0001t0001g0070a0001c0001t0001g0071others(12): Show | 15 | HG00544.hp2 HG00673.hp2 HG00735.hp2 others(12): Show |
intron_variant | MODIFIER | c.672-3198_672-3187d others(14): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538448 | |||||
chr5:80538449
|
TCTTTCTT others(31): Show |
T | 1 | a0001c0001t0001g0308 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.672-3223_672-3186d others(40): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538449 | ||||||
chr5:80538450
|
C | CTTTCTTT others(19): Show |
1 | a0001c0003t0001g0293 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.672-3206_672-3205i others(28): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538450 | |||||
chr5:80538450
|
C | CTTTCTTT others(23): Show |
3 | a0001c0001t0002g0285a0001c0003t0001g0292a0001c0003t0001g0294 | 3 | HG01109.hp2 HG01884.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.672-3202_672-3201i others(32): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538450 | |||||
chr5:80538450
|
C | G | 1 | a0001c0003t0001g0295 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.672-3223C>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538450 | ||||||
chr5:80538450
|
C | T | 23 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0020others(20): Show | 23 | HG00408.hp1 HG00639.hp2 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.672-3223C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538450 | ||||||
chr5:80538450
|
CTTTCTT | C | 9 | a0001c0001t0001g0137a0001c0001t0001g0142a0001c0001t0001g0207others(6): Show | 9 | HG01243.hp2 HG01978.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.672-3221_672-3216d others(8): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538450 | |||||
chr5:80538450
|
CTTTCTTT others(3): Show |
C | 8 | a0001c0001t0001g0002a0001c0001t0001g0130a0001c0001t0001g0318others(5): Show | 8 | HG01167.hp2 HG02523.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.672-3221_672-3212d others(12): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538450 | |||||
chr5:80538450
|
CTTTCTTT others(7): Show |
C | 4 | a0001c0001t0001g0049a0001c0001t0001g0208a0001c0001t0001g0305others(1): Show | 4 | HG00323.hp1 HG02080.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.672-3221_672-3208d others(16): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538450 | |||||
chr5:80538451
|
T | A | 1 | a0001c0001t0001g0211 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.672-3222T>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538451 | ||||||
chr5:80538451
|
T | C | 2 | a0001c0001t0001g0020a0002c0002t0001g0110 | 2 | HG00639.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.672-3222T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538451 | ||||||
chr5:80538452
|
T | C | 47 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0031others(44): Show | 47 | HG00408.hp1 HG00673.hp1 HG01070.hp2 others(44): Show |
intron_variant | MODIFIER | c.672-3221T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538452 | ||||||
chr5:80538452
|
T | TTC | 9 | a0001c0001t0001g0012a0001c0001t0001g0189a0001c0001t0001g0240others(6): Show | 9 | HG00438.hp1 HG01358.hp1 HG02129.hp2 others(6): Show |
intron_variant | MODIFIER | c.672-3219_672-3218d others(4): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538452 | |||||
chr5:80538454
|
C | CTTTCTTT others(19): Show |
1 | a0001c0003t0001g0186 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.672-3202_672-3201i others(28): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538454 | |||||
chr5:80538454
|
C | G | 2 | a0001c0001t0001g0310a0001c0003t0001g0001 | 3 | HG01168.hp1 HG01169.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.672-3219C>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538454 | ||||||
chr5:80538454
|
C | T | 6 | a0001c0001t0001g0045a0001c0001t0001g0191a0001c0001t0001g0247others(3): Show | 6 | HG00673.hp1 HG01255.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.672-3219C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538454 | ||||||
chr5:80538454
|
CTT | C | 5 | a0001c0001t0001g0056a0001c0001t0001g0058a0001c0001t0001g0059others(2): Show | 5 | HG00408.hp2 HG03490.hp1 NA18973.hp2 others(2): Show |
intron_variant | MODIFIER | c.672-3217_672-3216d others(4): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538454 | |||||
chr5:80538456
|
T | C | 86 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(83): Show | 86 | HG00621.hp1 HG00673.hp1 HG00738.hp2 others(83): Show |
intron_variant | MODIFIER | c.672-3217T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538456 | ||||||
chr5:80538456
|
T | TTC | 4 | a0001c0001t0001g0248a0001c0001t0001g0332a0001c0001t0001g0335others(1): Show | 4 | HG01109.hp1 HG01358.hp2 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.672-3215_672-3214d others(4): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538456 | |||||
chr5:80538458
|
C | G | 8 | a0001c0001t0001g0284a0001c0001t0001g0306a0001c0001t0001g0307others(5): Show | 8 | HG01496.hp1 HG02630.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.672-3215C>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538458 | ||||||
chr5:80538458
|
CTT | C | 20 | a0001c0001t0001g0015a0001c0001t0001g0030a0001c0001t0001g0033others(17): Show | 20 | HG00323.hp2 HG00438.hp2 HG00642.hp2 others(17): Show |
intron_variant | MODIFIER | c.672-3213_672-3212d others(4): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538458 | |||||
chr5:80538460
|
T | C | 115 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(112): Show | 115 | HG00621.hp1 HG00673.hp1 HG00738.hp2 others(112): Show |
intron_variant | MODIFIER | c.672-3213T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538460 | ||||||
chr5:80538460
|
T | TTC | 7 | a0001c0001t0001g0021a0001c0001t0001g0093a0001c0001t0001g0121others(4): Show | 7 | HG00738.hp1 HG01516.hp2 HG02083.hp2 others(4): Show |
intron_variant | MODIFIER | c.672-3211_672-3210d others(4): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538460 | |||||
chr5:80538462
|
CTT | C | 6 | a0001c0001t0001g0163a0001c0001t0001g0196a0001c0001t0001g0197others(3): Show | 6 | HG02074.hp2 HG02145.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.672-3209_672-3208d others(4): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538462 | |||||
chr5:80538463
|
T | C | 1 | a0001c0001t0001g0153 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.672-3210T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538463 | ||||||
chr5:80538464
|
T | C | 121 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(118): Show | 121 | HG00621.hp1 HG00673.hp1 HG00738.hp2 others(118): Show |
intron_variant | MODIFIER | c.672-3209T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538464 | ||||||
chr5:80538464
|
T | TTC | 4 | a0001c0001t0002g0118a0001c0001t0002g0204a0001c0001t0002g0206others(1): Show | 4 | HG02451.hp1 HG02809.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.672-3207_672-3206d others(4): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538464 | |||||
chr5:80538465
|
T | C | 1 | a0001c0001t0001g0160 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.672-3208T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538465 | ||||||
chr5:80538466
|
C | T | 1 | a0001c0001t0001g0160 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.672-3207C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538466 | ||||||
chr5:80538467
|
T | C | 1 | a0001c0001t0001g0160 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.672-3206T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538467 | ||||||
chr5:80538468
|
T | C | 111 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(108): Show | 111 | HG00323.hp1 HG00621.hp1 HG00673.hp1 others(108): Show |
intron_variant | MODIFIER | c.672-3205T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538468 | ||||||
chr5:80538468
|
T | TTC | 3 | a0001c0001t0002g0113a0001c0001t0002g0238a0001c0001t0002g0297 | 3 | HG02622.hp2 HG03209.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.672-3203_672-3202d others(4): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538468 | |||||
chr5:80538469
|
T | C | 2 | a0001c0001t0001g0095a0001c0001t0001g0211 | 2 | HG03654.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.672-3204T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538469 | ||||||
chr5:80538470
|
C | G | 2 | a0001c0001t0002g0288a0001c0003t0001g0187 | 2 | HG00738.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.672-3203C>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538470 | ||||||
chr5:80538471
|
T | C | 3 | a0001c0001t0001g0031a0001c0001t0001g0183a0001c0001t0001g0203 | 3 | HG02559.hp1 NA18943.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.672-3202T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538471 | ||||||
chr5:80538472
|
T | C | 21 | a0001c0001t0001g0003a0001c0001t0001g0091a0001c0001t0001g0130others(18): Show | 21 | HG01255.hp1 HG01358.hp2 HG01981.hp2 others(18): Show |
intron_variant | MODIFIER | c.672-3201T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538472 | ||||||
chr5:80538473
|
T | C | 2 | a0001c0001t0001g0095a0001c0001t0001g0211 | 2 | HG03654.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.672-3200T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538473 | ||||||
chr5:80538474
|
C | G | 5 | a0001c0001t0002g0118a0001c0001t0002g0204a0001c0001t0002g0206others(2): Show | 5 | HG02451.hp1 HG02809.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.672-3199C>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538474 | ||||||
chr5:80538475
|
T | C | 5 | a0001c0001t0001g0047a0001c0001t0001g0126a0001c0001t0001g0203others(2): Show | 5 | HG01261.hp2 HG01433.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.672-3198T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538475 | ||||||
chr5:80538476
|
T | C | 1 | a0001c0001t0001g0331 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.672-3197T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538476 | ||||||
chr5:80538477
|
T | C | 1 | a0001c0001t0001g0095 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.672-3196T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538477 | ||||||
chr5:80538478
|
C | G | 3 | a0001c0001t0002g0113a0001c0001t0002g0238a0001c0001t0002g0297 | 3 | HG02622.hp2 HG03209.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.672-3195C>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538478 | ||||||
chr5:80538479
|
T | C | 24 | a0001c0001t0001g0035a0001c0001t0001g0039a0001c0001t0001g0047others(21): Show | 24 | HG01123.hp1 HG01167.hp1 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.672-3194T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538479 | ||||||
chr5:80538479
|
T | TTTCCTTC others(1): Show |
5 | a0001c0001t0001g0258a0001c0001t0001g0261a0001c0001t0001g0265others(2): Show | 5 | HG02280.hp2 HG02683.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.672-3191_672-3190i others(10): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538479 | |||||
chr5:80538480
|
T | C | 1 | a0001c0001t0001g0331 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.672-3193T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538480 | ||||||
chr5:80538480
|
TTCTTTCC others(37): Show |
T | 1 | a0001c0001t0001g0211 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.672-3192_672-3149d others(46): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538480 | ||||||
chr5:80538482
|
C | G | 1 | a0001c0001t0002g0303 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.672-3191C>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538482 | ||||||
chr5:80538483
|
T | C | 144 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(141): Show | 144 | HG00323.hp1 HG00408.hp2 HG00621.hp1 others(141): Show |
intron_variant | MODIFIER | c.672-3190T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538483 | ||||||
chr5:80538483
|
T | TTTCCTTC others(5): Show |
2 | a0001c0001t0001g0266a0001c0001t0001g0270 | 2 | HG01099.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.672-3183_672-3172d others(14): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538483 | |||||
chr5:80538484
|
T | C | 1 | a0001c0001t0001g0331 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.672-3189T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538484 | ||||||
chr5:80538485
|
TC | T | 13 | a0001c0001t0001g0310a0001c0001t0001g0311a0001c0001t0002g0118others(10): Show | 13 | HG00738.hp1 HG02257.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.672-3186delC | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538485 | |||||
chr5:80538486
|
C | CTTT | 8 | a0001c0001t0001g0284a0001c0001t0001g0306a0001c0001t0001g0307others(5): Show | 8 | HG01496.hp1 HG02622.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.672-3187_672-3186i others(5): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538486 | ||||||
chr5:80538487
|
C | T | 16 | a0001c0001t0001g0121a0001c0001t0001g0257a0001c0001t0001g0300others(13): Show | 17 | HG00280.hp1 HG01109.hp2 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.672-3186C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538487 | ||||||
chr5:80538490
|
C | T | 22 | a0001c0001t0001g0228a0001c0001t0001g0284a0001c0001t0001g0306others(19): Show | 22 | HG00738.hp1 HG01496.hp1 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.672-3183C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538490 | ||||||
chr5:80538491
|
C | T | 5 | a0001c0001t0001g0095a0001c0001t0001g0203a0001c0001t0001g0257others(2): Show | 5 | HG01361.hp2 HG02559.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.672-3182C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538491 | ||||||
chr5:80538494
|
C | T | 23 | a0001c0001t0001g0203a0001c0001t0001g0228a0001c0001t0001g0284others(20): Show | 23 | HG00738.hp1 HG01496.hp1 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.672-3179C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538494 | ||||||
chr5:80538494
|
CCTTCCTT others(3): Show |
C | 1 | a0001c0001t0002g0278 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.672-3178_672-3169d others(12): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538494 | ||||||
chr5:80538495
|
C | T | 5 | a0001c0001t0001g0047a0001c0001t0001g0095a0001c0001t0001g0126others(2): Show | 5 | HG01433.hp2 HG02896.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.672-3178C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538495 | ||||||
chr5:80538498
|
C | T | 51 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0039others(48): Show | 51 | HG00408.hp2 HG00738.hp1 HG01123.hp1 others(48): Show |
intron_variant | MODIFIER | c.672-3175C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538498 | ||||||
chr5:80538500
|
T | C | 1 | a0001c0003t0001g0290 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.672-3173T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538500 | ||||||
chr5:80538500
|
T | TTCC | 7 | a0001c0001t0001g0185a0001c0001t0001g0235a0001c0001t0001g0255others(4): Show | 7 | HG00639.hp1 HG01175.hp1 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.672-3172_672-3171i others(5): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538500 | |||||
chr5:80538502
|
T | C | 12 | a0001c0001t0001g0095a0001c0001t0001g0121a0001c0001t0001g0201others(9): Show | 12 | HG01255.hp1 HG01358.hp2 HG01361.hp2 others(9): Show |
intron_variant | MODIFIER | c.672-3171T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538502 | ||||||
chr5:80538503
|
C | T | 25 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0039others(22): Show | 25 | HG00408.hp2 HG01123.hp1 HG01167.hp1 others(22): Show |
intron_variant | MODIFIER | c.672-3170C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538503 | ||||||
chr5:80538503
|
CT | C | 18 | a0001c0001t0001g0126a0001c0001t0001g0203a0001c0001t0001g0234others(15): Show | 18 | HG00738.hp1 HG01433.hp2 HG01496.hp1 others(15): Show |
intron_variant | MODIFIER | c.672-3166delT | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538503 | |||||
chr5:80538504
|
T | C | 36 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0039others(33): Show | 36 | HG00408.hp2 HG00639.hp1 HG01123.hp1 others(33): Show |
intron_variant | MODIFIER | c.672-3169T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538504 | ||||||
chr5:80538504
|
T | TTTC | 4 | a0001c0001t0001g0307a0001c0001t0001g0309a0001c0001t0002g0113others(1): Show | 4 | HG00639.hp2 HG03209.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.672-3167_672-3166i others(5): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538504 | |||||
chr5:80538505
|
T | C | 1 | a0001c0001t0001g0203 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.672-3168T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538505 | ||||||
chr5:80538505
|
T | TTCC | 3 | a0001c0001t0001g0047a0001c0001t0001g0228a0001c0001t0003g0282 | 3 | HG02897.hp1 HG02970.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.672-3167_672-3166i others(5): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538505 | |||||
chr5:80538507
|
T | C | 12 | a0001c0001t0001g0121a0001c0001t0001g0201a0001c0001t0001g0243others(9): Show | 12 | HG01255.hp1 HG01358.hp2 HG01516.hp2 others(9): Show |
intron_variant | MODIFIER | c.672-3166T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538507 | ||||||
chr5:80538508
|
C | CT | 8 | a0001c0001t0001g0185a0001c0001t0001g0235a0001c0001t0001g0255others(5): Show | 8 | HG00639.hp1 HG01175.hp1 HG01346.hp2 others(5): Show |
intron_variant | MODIFIER | c.672-3162dupT | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538508 | |||||
chr5:80538508
|
C | T | 9 | a0001c0001t0001g0121a0001c0001t0001g0201a0001c0001t0001g0243others(6): Show | 9 | HG01255.hp1 HG01358.hp2 HG01516.hp2 others(6): Show |
intron_variant | MODIFIER | c.672-3165C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538508 | ||||||
chr5:80538509
|
T | C | 10 | a0001c0001t0001g0047a0001c0001t0001g0095a0001c0001t0001g0126others(7): Show | 10 | HG00639.hp2 HG01361.hp2 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.672-3164T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538509 | ||||||
chr5:80538509
|
T | TTTCC | 3 | a0001c0001t0001g0035a0001c0001t0001g0108a0002c0002t0001g0083 | 3 | HG01516.hp1 HG02258.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.672-3161_672-3160i others(6): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538509 | |||||
chr5:80538509
|
TTTCTTTC others(9): Show |
T | 2 | a0001c0001t0001g0300a0001c0001t0001g0308 | 2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.672-3160_672-3145d others(18): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538509 | |||||
chr5:80538511
|
T | C | 1 | a0001c0001t0002g0281 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.672-3162T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538511 | ||||||
chr5:80538513
|
T | C | 42 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0039others(39): Show | 42 | HG00408.hp2 HG00639.hp2 HG00738.hp1 others(39): Show |
intron_variant | MODIFIER | c.672-3160T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538513 | ||||||
chr5:80538513
|
T | TTTCC | 38 | a0001c0001t0001g0004a0001c0001t0001g0033a0001c0001t0001g0068others(35): Show | 38 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(35): Show |
intron_variant | MODIFIER | c.672-3103_672-3100d others(6): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538513 | |||||
chr5:80538513
|
T | TTTCCTTC others(1): Show |
29 | a0001c0001t0001g0091a0001c0001t0001g0252a0001c0001t0001g0262others(26): Show | 29 | HG00621.hp2 HG01069.hp2 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.672-3107_672-3100d others(10): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538513 | |||||
chr5:80538513
|
T | TTTCCTTC others(5): Show |
5 | a0002c0002t0001g0028a0002c0002t0001g0073a0002c0002t0001g0229others(2): Show | 5 | HG02735.hp2 NA18969.hp2 NA18973.hp1 others(2): Show |
intron_variant | MODIFIER | c.672-3111_672-3100d others(14): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538513 | |||||
chr5:80538513
|
T | TTTCCTTC others(9): Show |
5 | a0001c0001t0001g0137a0002c0002t0001g0025a0002c0002t0001g0061others(2): Show | 5 | HG02135.hp1 HG02135.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.672-3115_672-3100d others(18): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538513 | |||||
chr5:80538513
|
TTTCC | T | 43 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0015others(40): Show | 43 | HG00558.hp1 HG00642.hp2 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.672-3103_672-3100d others(6): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538513 | |||||
chr5:80538513
|
TTTCCTTC others(1): Show |
T | 31 | a0001c0001t0001g0021a0001c0001t0001g0045a0001c0001t0001g0065others(28): Show | 32 | HG00280.hp1 HG00544.hp2 HG00673.hp1 others(29): Show |
intron_variant | MODIFIER | c.672-3107_672-3100d others(10): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538513 | |||||
chr5:80538513
|
TTTCCTTC others(5): Show |
T | 10 | a0001c0001t0001g0070a0001c0001t0001g0082a0001c0001t0001g0100others(7): Show | 10 | HG00673.hp2 HG01167.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.672-3111_672-3100d others(14): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538513 | |||||
chr5:80538513
|
TTTCCTTC others(9): Show |
T | 11 | a0001c0001t0001g0077a0001c0001t0001g0302a0001c0001t0001g0305others(8): Show | 11 | HG00323.hp1 HG00438.hp2 HG01496.hp2 others(8): Show |
intron_variant | MODIFIER | c.672-3115_672-3100d others(18): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538513 | |||||
chr5:80538513
|
TTTCCTTC others(13): Show |
T | 20 | a0001c0001t0001g0289a0001c0001t0001g0304a0001c0001t0001g0314others(17): Show | 20 | HG01109.hp1 HG01243.hp2 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.672-3119_672-3100d others(22): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538513 | |||||
chr5:80538513
|
TTTCCTTC others(17): Show |
T | 1 | a0001c0001t0001g0340 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.672-3123_672-3100d others(26): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538513 | |||||
chr5:80538516
|
C | T | 1 | a0001c0001t0001g0257 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.672-3157C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538516 | ||||||
chr5:80538517
|
C | T | 18 | a0001c0001t0001g0121a0001c0001t0001g0185a0001c0001t0001g0201others(15): Show | 18 | HG00639.hp1 HG01175.hp1 HG01255.hp1 others(15): Show |
intron_variant | MODIFIER | c.672-3156C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538517 | ||||||
chr5:80538520
|
C | T | 1 | a0001c0001t0001g0331 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.672-3153C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538520 | ||||||
chr5:80538521
|
C | CTTTCTTT others(7): Show |
1 | a0001c0001t0001g0307 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.672-3150_672-3149i others(16): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538521 | |||||
chr5:80538521
|
C | T | 3 | a0001c0001t0001g0263a0001c0001t0002g0281a0001c0003t0001g0290 | 3 | HG03098.hp1 HG03669.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.672-3152C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538521 | ||||||
chr5:80538524
|
C | T | 3 | a0001c0001t0002g0118a0001c0001t0002g0288a0001c0003t0001g0187 | 3 | HG00738.hp1 HG02809.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.672-3149C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538524 | ||||||
chr5:80538525
|
C | CTT | 3 | a0001c0001t0002g0118a0001c0001t0002g0288a0001c0003t0001g0187 | 3 | HG00738.hp1 HG02809.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.672-3147_672-3146d others(4): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538525 | |||||
chr5:80538525
|
C | CTTTCTT | 6 | a0001c0001t0002g0204a0001c0001t0002g0206a0001c0001t0002g0297others(3): Show | 6 | HG02451.hp1 HG02622.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.672-3146_672-3145i others(8): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538525 | |||||
chr5:80538525
|
C | CTTTCTTT others(3): Show |
2 | a0001c0001t0002g0113a0001c0001t0003g0282 | 2 | HG02970.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.672-3146_672-3145i others(12): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538525 | |||||
chr5:80538525
|
C | CTTTCTTT others(7): Show |
5 | a0001c0001t0001g0284a0001c0001t0001g0306a0001c0001t0001g0309others(2): Show | 5 | HG01496.hp1 HG02630.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.672-3146_672-3145i others(16): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538525 | |||||
chr5:80538525
|
C | T | 4 | a0001c0001t0001g0257a0001c0001t0001g0263a0001c0001t0002g0238others(1): Show | 4 | HG01361.hp2 HG03098.hp1 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.672-3148C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538525 | ||||||
chr5:80538529
|
C | CTTTCTTT others(7): Show |
1 | a0001c0001t0003g0296 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.672-3142_672-3141i others(16): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538529 | |||||
chr5:80538529
|
C | T | 15 | a0001c0001t0001g0257a0001c0001t0001g0331a0001c0001t0001g0347others(12): Show | 15 | HG00738.hp1 HG01361.hp2 HG01981.hp2 others(12): Show |
intron_variant | MODIFIER | c.672-3144C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538529 | ||||||
chr5:80538532
|
C | T | 2 | a0001c0001t0001g0211a0001c0001t0002g0278 | 2 | HG03486.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.672-3141C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538532 | ||||||
chr5:80538533
|
C | T | 11 | a0001c0001t0001g0327a0001c0001t0001g0331a0001c0001t0002g0118others(8): Show | 11 | HG00738.hp1 HG02451.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.672-3140C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538533 | ||||||
chr5:80538541
|
C | T | 1 | a0001c0001t0002g0278 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.672-3132C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538541 | ||||||
chr5:80538545
|
C | T | 1 | a0001c0001t0002g0278 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.672-3128C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538545 | ||||||
chr5:80538570
|
T | C | 2 | a0001c0001t0001g0305a0001c0001t0001g0343 | 2 | HG00323.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.672-3103T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538570 | ||||||
chr5:80538653
|
G | A | 2 | a0001c0001t0001g0302a0001c0001t0001g0317 | 2 | HG02145.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.672-3020G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538653 | ||||||
chr5:80538745
|
C | A | 99 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(96): Show | 99 | HG00621.hp1 HG00673.hp1 HG00738.hp2 others(96): Show |
intron_variant | MODIFIER | c.672-2928C>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538745 | ||||||
chr5:80538745
|
C | T | 1 | a0001c0001t0002g0278 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.672-2928C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538745 | ||||||
chr5:80538801
|
A | G | 1 | a0001c0001t0002g0278 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.672-2872A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538801 | ||||||
chr5:80538808
|
A | G | 4 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0302others(1): Show | 4 | HG02145.hp1 HG02922.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.672-2865A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538808 | ||||||
chr5:80538941
|
C | T | 19 | a0001c0001t0001g0235a0001c0001t0001g0253a0001c0001t0001g0255others(16): Show | 19 | HG00639.hp1 HG01099.hp2 HG01261.hp2 others(16): Show |
intron_variant | MODIFIER | c.672-2732C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80538941 | ||||||
chr5:80538992
|
CT | C | 108 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0015others(105): Show | 109 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.672-2664delT | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538992 | |||||
chr5:80538992
|
CTT | C | 128 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(125): Show | 128 | HG00323.hp1 HG00639.hp1 HG00673.hp1 others(125): Show |
intron_variant | MODIFIER | c.672-2665_672-2664d others(4): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80538992 | |||||
chr5:80539226
|
A | G | 17 | a0001c0001t0001g0284a0001c0001t0001g0306a0001c0001t0001g0307others(14): Show | 18 | HG00280.hp1 HG00738.hp1 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.672-2447A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80539226 | ||||||
chr5:80539370
|
A | AT | 189 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(186): Show | 190 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(187): Show |
intron_variant | MODIFIER | c.672-2295dupT | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80539370 | |||||
chr5:80539407
|
G | A | 1 | a0001c0001t0002g0278 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.672-2266G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80539407 | ||||||
chr5:80539636
|
C | T | 57 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0035others(54): Show | 57 | HG00323.hp1 HG00741.hp1 HG01070.hp2 others(54): Show |
intron_variant | MODIFIER | c.672-2037C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80539636 | ||||||
chr5:80539637
|
G | A | 4 | a0001c0001t0001g0192a0001c0001t0001g0300a0001c0001t0001g0308others(1): Show | 4 | HG00741.hp2 HG02922.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.672-2036G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80539637 | ||||||
chr5:80539640
|
C | T | 2 | a0001c0001t0003g0282a0001c0001t0003g0296 | 2 | HG02257.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.672-2033C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80539640 | ||||||
chr5:80539791
|
C | CT | 7 | a0001c0001t0001g0054a0001c0001t0001g0125a0001c0001t0001g0353others(4): Show | 7 | HG02257.hp1 HG02451.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.672-1868dupT | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80539791 | |||||
chr5:80539844
|
A | G | 3 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0067 | 3 | HG00738.hp2 HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.672-1829A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80539844 | ||||||
chr5:80540051
|
C | T | 13 | a0001c0001t0002g0113a0001c0001t0002g0118a0001c0001t0002g0204others(10): Show | 13 | HG01884.hp1 HG02451.hp1 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.672-1622C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80540051 | ||||||
chr5:80540373
|
G | A | 250 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(247): Show | 251 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(248): Show |
intron_variant | MODIFIER | c.672-1300G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80540373 | ||||||
chr5:80540530
|
G | A | 9 | a0001c0003t0001g0001a0001c0003t0001g0186a0001c0003t0001g0187others(6): Show | 10 | HG00280.hp1 HG00738.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.672-1143G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80540530 | ||||||
chr5:80540835
|
G | T | 1 | a0001c0001t0002g0278 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.672-838G>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80540835 | ||||||
chr5:80540939
|
GGATTCT | G | 13 | a0001c0001t0001g0252a0002c0002t0001g0105a0002c0002t0001g0119others(10): Show | 13 | HG00621.hp2 HG02083.hp1 HG02135.hp1 others(10): Show |
intron_variant | MODIFIER | c.672-731_672-726del others(6): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 80540939 | |||||
chr5:80541057
|
G | A | 6 | a0002c0002t0001g0046a0002c0002t0001g0052a0002c0002t0001g0083others(3): Show | 6 | HG02258.hp1 HG02622.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.672-616G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80541057 | ||||||
chr5:80541062
|
A | G | 135 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(132): Show | 135 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.672-611A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80541062 | ||||||
chr5:80541187
|
G | A | 2 | a0001c0001t0001g0300a0001c0001t0001g0308 | 2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.672-486G>A | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80541187 | ||||||
chr5:80541225
|
C | G | 1 | a0001c0001t0001g0265 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.672-448C>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80541225 | ||||||
chr5:80541307
|
G | C | 1 | a0001c0001t0006g0286 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.672-366G>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80541307 | ||||||
chr5:80541352
|
A | G | 1 | a0001c0001t0001g0182 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.672-321A>G | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80541352 | ||||||
chr5:80541430
|
C | T | 30 | a0001c0001t0001g0284a0001c0001t0001g0306a0001c0001t0001g0307others(27): Show | 31 | HG00280.hp1 HG00738.hp1 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.672-243C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80541430 | ||||||
chr5:80541608
|
T | C | 1 | a0001c0001t0002g0288 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.672-65T>C | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80541608 | ||||||
chr5:80541635
|
C | T | 1 | a0001c0001t0003g0282 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.672-38C>T | FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | chr5 | 80541635 |