geneid | 5899 |
---|---|
ensemblid | ENSG00000144118.14 |
hgncid | 9840 |
symbol | RALB |
name | RAS like proto-oncogene B |
refseq_nuc | NM_002881.3 |
refseq_prot | NP_002872.1 |
ensembl_nuc | ENST00000272519.10 |
ensembl_prot | ENSP00000272519.4 |
mane_status | MANE Select |
chr | chr2 |
start | 120252852 |
end | 120294710 |
strand | + |
ver | v1.2 |
region | chr2:120252852-120294710 |
region5000 | chr2:120247852-120299710 |
regionname0 | RALB_chr2_120252852_120294710 |
regionname5000 | RALB_chr2_120247852_120299710 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 206 | 358 | 86 | 66 | 148 | 16 | 40 | 118 | RALB_chr2_120247852_120299710 | RALB | copy fasta | chr2 | 120247852 | 120299710 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 621 | 342 | 86 | 60 | 147 | 11 | 36 | RALB_chr2_120247852_120299710 | RALB | copy fasta | chr2 | 120247852 | 120299710 |
c0002 | 0/0 | 621 | 15 | 0 | 6 | 0 | 5 | 4 | RALB_chr2_120247852_120299710 | RALB | copy fasta | chr2 | 120247852 | 120299710 |
c0003 | 0/0 | 621 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | copy fasta | chr2 | 120247852 | 120299710 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 1627 | 172 | 39 | 34 | 58 | 13 | 28 | RALB_chr2_120247852_120299710 | RALB | copy fasta | chr2 | 120247852 | 120299710 |
t0002 | 1/1 | 1627 | 131 | 20 | 27 | 71 | 2 | 9 | RALB_chr2_120247852_120299710 | RALB | copy fasta | chr2 | 120247852 | 120299710 |
t0003 | 0/0 | 1627 | 15 | 0 | 1 | 14 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | copy fasta | chr2 | 120247852 | 120299710 |
t0004 | 0/0 | 1627 | 11 | 10 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | copy fasta | chr2 | 120247852 | 120299710 |
t0005 | 0/0 | 1627 | 10 | 10 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | copy fasta | chr2 | 120247852 | 120299710 |
t0006 | 0/0 | 1627 | 6 | 4 | 2 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | copy fasta | chr2 | 120247852 | 120299710 |
t0007 | 0/0 | 1627 | 4 | 0 | 0 | 2 | 0 | 2 | RALB_chr2_120247852_120299710 | RALB | copy fasta | chr2 | 120247852 | 120299710 |
t0008 | 0/0 | 1627 | 2 | 1 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | copy fasta | chr2 | 120247852 | 120299710 |
t0009 | 0/0 | 1627 | 2 | 2 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | copy fasta | chr2 | 120247852 | 120299710 |
t0010 | 0/0 | 1627 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | copy fasta | chr2 | 120247852 | 120299710 |
t0011 | 0/0 | 1627 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | copy fasta | chr2 | 120247852 | 120299710 |
t0012 | 0/0 | 1627 | 1 | 0 | 0 | 0 | 0 | 1 | RALB_chr2_120247852_120299710 | RALB | copy fasta | chr2 | 120247852 | 120299710 |
t0013 | 0/0 | 1627 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | copy fasta | chr2 | 120247852 | 120299710 |
t0014 | 0/0 | 1627 | 1 | 0 | 0 | 0 | 1 | 0 | RALB_chr2_120247852_120299710 | RALB | copy fasta | chr2 | 120247852 | 120299710 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 1/0 | 27 | 6 | 10 | 8 | 0 | 2 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0002 | 0/0 | 11 | 0 | 1 | 10 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0003 | 0/0 | 11 | 0 | 0 | 11 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0004 | 0/0 | 8 | 3 | 1 | 4 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0005 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0006 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0007 | 0/0 | 5 | 0 | 3 | 0 | 0 | 2 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0008 | 0/0 | 5 | 0 | 2 | 0 | 0 | 3 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0009 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0010 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0012 | 0/0 | 4 | 0 | 0 | 0 | 4 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0013 | 0/0 | 4 | 3 | 0 | 0 | 1 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0015 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0016 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0018 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0019 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0021 | 0/0 | 3 | 2 | 0 | 0 | 0 | 1 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0026 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0027 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0029 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0036 | 0/1 | 2 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0040 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0043 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0044 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 621 | 342 | 86 | 60 | 147 | 11 | 36 | RALB_chr2_120247852_120299710 | RALB | copy fasta | chr2 | 120247852 | 120299710 |
a0001c0002 | 0/0 | 621 | 15 | 0 | 6 | 0 | 5 | 4 | RALB_chr2_120247852_120299710 | RALB | copy fasta | chr2 | 120247852 | 120299710 |
a0001c0003 | 0/0 | 621 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | copy fasta | chr2 | 120247852 | 120299710 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 2247 | 157 | 39 | 28 | 58 | 8 | 24 | RALB_chr2_120247852_120299710 | RALB | copy fasta | chr2 | 120247852 | 120299710 |
a0001c0001t0002 | 1/1 | 2247 | 131 | 20 | 27 | 71 | 2 | 9 | RALB_chr2_120247852_120299710 | RALB | copy fasta | chr2 | 120247852 | 120299710 |
a0001c0001t0003 | 0/0 | 2247 | 14 | 0 | 1 | 13 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | copy fasta | chr2 | 120247852 | 120299710 |
a0001c0001t0004 | 0/0 | 2247 | 11 | 10 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | copy fasta | chr2 | 120247852 | 120299710 |
a0001c0001t0005 | 0/0 | 2247 | 10 | 10 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | copy fasta | chr2 | 120247852 | 120299710 |
a0001c0001t0006 | 0/0 | 2247 | 6 | 4 | 2 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | copy fasta | chr2 | 120247852 | 120299710 |
a0001c0001t0007 | 0/0 | 2247 | 4 | 0 | 0 | 2 | 0 | 2 | RALB_chr2_120247852_120299710 | RALB | copy fasta | chr2 | 120247852 | 120299710 |
a0001c0001t0008 | 0/0 | 2247 | 2 | 1 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | copy fasta | chr2 | 120247852 | 120299710 |
a0001c0001t0009 | 0/0 | 2247 | 2 | 2 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | copy fasta | chr2 | 120247852 | 120299710 |
a0001c0001t0010 | 0/0 | 2247 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | copy fasta | chr2 | 120247852 | 120299710 |
a0001c0001t0011 | 0/0 | 2247 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | copy fasta | chr2 | 120247852 | 120299710 |
a0001c0001t0012 | 0/0 | 2247 | 1 | 0 | 0 | 0 | 0 | 1 | RALB_chr2_120247852_120299710 | RALB | copy fasta | chr2 | 120247852 | 120299710 |
a0001c0001t0013 | 0/0 | 2247 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | copy fasta | chr2 | 120247852 | 120299710 |
a0001c0001t0014 | 0/0 | 2247 | 1 | 0 | 0 | 0 | 1 | 0 | RALB_chr2_120247852_120299710 | RALB | copy fasta | chr2 | 120247852 | 120299710 |
a0001c0002t0001 | 0/0 | 2247 | 15 | 0 | 6 | 0 | 5 | 4 | RALB_chr2_120247852_120299710 | RALB | copy fasta | chr2 | 120247852 | 120299710 |
a0001c0003t0003 | 0/0 | 2247 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | copy fasta | chr2 | 120247852 | 120299710 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 11 | 0 | 1 | 10 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0001g0004 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0001g0006 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0001g0007 | 0/0 | 5 | 0 | 3 | 0 | 0 | 2 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0001g0008 | 0/0 | 4 | 0 | 2 | 0 | 0 | 2 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0001g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0001g0013 | 0/0 | 4 | 3 | 0 | 0 | 1 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0001g0018 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0001g0019 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0001g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0001g0021 | 0/0 | 3 | 2 | 0 | 0 | 0 | 1 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0001g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0001g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0002g0001 | 1/0 | 27 | 6 | 10 | 8 | 0 | 2 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0002g0003 | 0/0 | 11 | 0 | 0 | 11 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0002g0009 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0002g0010 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0002g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0002g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0002g0016 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0002g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0002g0036 | 0/1 | 2 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0002g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0002g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0002g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0002g0040 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0002g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0002g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0002g0043 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0002g0044 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0002g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0002g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0002g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0002g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0002g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0002g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0002g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0002g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0002g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0003g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0003g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0003g0026 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0004g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0004g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0004g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0004g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0004g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0004g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0004g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0004g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0004g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0004g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0005g0005 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0005g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0005g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0005g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0005g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0006g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0006g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0006g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0006g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0006g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0007g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0007g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0007g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0007g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0008g0029 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0009g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0010g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0011g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0012g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0013g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0001t0014g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0002t0001g0012 | 0/0 | 4 | 0 | 0 | 0 | 4 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0002t0001g0027 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0002t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0002t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0002t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0002t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0002t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
a0001c0003t0003g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0019 | EUR | GBR | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG00099 | hp2 | a0001 | c0002 | t0001 | g0012 | EUR | GBR | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG00280 | hp1 | a0001 | c0002 | t0001 | g0012 | EUR | FIN | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0018 | EUR | FIN | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0019 | EUR | FIN | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0108 | EUR | FIN | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | CHS | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG00609 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | CHS | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | CHS | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG00639 | hp2 | a0001 | c0001 | t0006 | g0052 | AMR | PUR | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0188 | AMR | PUR | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG00673 | hp1 | a0001 | c0001 | t0002 | g0200 | EAS | CHS | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG00673 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG00735 | hp1 | a0001 | c0001 | t0004 | g0094 | AMR | PUR | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG00735 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG00738 | hp1 | a0001 | c0002 | t0001 | g0027 | AMR | PUR | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG00738 | hp2 | a0001 | c0002 | t0001 | g0079 | AMR | PUR | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG00741 | hp2 | a0001 | c0002 | t0001 | g0080 | AMR | PUR | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG01069 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG01070 | hp1 | a0001 | c0002 | t0001 | g0077 | AMR | PUR | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG01071 | hp2 | a0001 | c0002 | t0001 | g0078 | AMR | PUR | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG01081 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG01109 | hp2 | a0001 | c0001 | t0002 | g0176 | AMR | PUR | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG01167 | hp2 | a0001 | c0001 | t0002 | g0224 | AMR | PUR | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG01168 | hp1 | a0001 | c0001 | t0002 | g0036 | AMR | PUR | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG01175 | hp1 | a0001 | c0001 | t0002 | g0223 | AMR | PUR | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0175 | AMR | PUR | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG01243 | hp1 | a0001 | c0001 | t0006 | g0054 | AMR | PUR | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG01243 | hp2 | a0001 | c0001 | t0008 | g0029 | AMR | PUR | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | CLM | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | CLM | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0044 | AMR | CLM | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0044 | AMR | CLM | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | CLM | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG01261 | hp1 | a0001 | c0001 | t0002 | g0178 | AMR | CLM | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0225 | AMR | CLM | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | CLM | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | CLM | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG01358 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | CLM | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | CLM | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0195 | AMR | CLM | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG01433 | hp2 | a0001 | c0001 | t0002 | g0213 | AMR | CLM | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | CLM | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG01515 | hp1 | a0001 | c0002 | t0001 | g0012 | EUR | IBS | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0169 | EUR | IBS | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG01516 | hp1 | a0001 | c0001 | t0002 | g0043 | EUR | IBS | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0128 | EUR | IBS | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG01517 | hp1 | a0001 | c0002 | t0001 | g0012 | EUR | IBS | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG01517 | hp2 | a0001 | c0001 | t0002 | g0043 | EUR | IBS | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG01884 | hp1 | a0001 | c0001 | t0002 | g0197 | AFR | ACB | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG01884 | hp2 | a0001 | c0001 | t0005 | g0005 | AFR | ACB | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG01891 | hp1 | a0001 | c0001 | t0002 | g0037 | AFR | ACB | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ACB | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0185 | AMR | PEL | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG01928 | hp2 | a0001 | c0001 | t0003 | g0026 | AMR | PEL | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG01943 | hp2 | a0001 | c0002 | t0001 | g0081 | AMR | PEL | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG01952 | hp1 | a0001 | c0001 | t0002 | g0186 | AMR | PEL | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG01952 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG01981 | hp1 | a0001 | c0001 | t0002 | g0192 | AMR | PEL | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0039 | AMR | PEL | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | PEL | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | KHV | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG02040 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | KHV | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | KHV | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | KHV | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | KHV | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | KHV | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | KHV | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | KHV | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | KHV | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0205 | EAS | KHV | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG02129 | hp2 | a0001 | c0001 | t0002 | g0203 | EAS | KHV | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG02135 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0219 | AMR | PEL | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PEL | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | CDX | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG02155 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | CDX | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | CDX | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG02165 | hp2 | a0001 | c0001 | t0003 | g0069 | EAS | CDX | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | ACB | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | ACB | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | ACB | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG02280 | hp2 | a0001 | c0001 | t0002 | g0190 | AFR | ACB | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PEL | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG02451 | hp1 | a0001 | c0001 | t0004 | g0028 | AFR | ACB | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | ACB | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | KHV | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG02523 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | KHV | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG02572 | hp1 | a0001 | c0001 | t0005 | g0005 | AFR | GWD | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | GWD | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0123 | SAS | PJL | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0151 | SAS | PJL | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG02615 | hp1 | a0001 | c0001 | t0004 | g0089 | AFR | GWD | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG02615 | hp2 | a0001 | c0001 | t0002 | g0206 | AFR | GWD | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | GWD | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG02622 | hp2 | a0001 | c0001 | t0002 | g0191 | AFR | GWD | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG02630 | hp2 | a0001 | c0001 | t0002 | g0189 | AFR | GWD | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | GWD | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG02683 | hp1 | a0001 | c0002 | t0001 | g0027 | SAS | PJL | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG02683 | hp2 | a0001 | c0001 | t0002 | g0222 | SAS | PJL | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG02717 | hp2 | a0001 | c0001 | t0002 | g0204 | AFR | GWD | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG02723 | hp1 | a0001 | c0001 | t0006 | g0025 | AFR | GWD | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG02723 | hp2 | a0001 | c0001 | t0004 | g0093 | AFR | GWD | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0124 | SAS | PJL | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG02809 | hp2 | a0001 | c0001 | t0005 | g0101 | AFR | GWD | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG02818 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | GWD | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG02818 | hp2 | a0001 | c0001 | t0008 | g0029 | AFR | GWD | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG02886 | hp1 | a0001 | c0001 | t0005 | g0005 | AFR | GWD | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | GWD | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG02895 | hp1 | a0001 | c0001 | t0005 | g0005 | AFR | GWD | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG02895 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | GWD | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG02897 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | GWD | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG02897 | hp2 | a0001 | c0001 | t0004 | g0092 | AFR | GWD | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG02922 | hp1 | a0001 | c0001 | t0002 | g0173 | AFR | ESN | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | ESN | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG02965 | hp1 | a0001 | c0001 | t0005 | g0102 | AFR | ESN | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG02970 | hp1 | a0001 | c0001 | t0004 | g0088 | AFR | ESN | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | ESN | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | PJL | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG03041 | hp1 | a0001 | c0001 | t0004 | g0087 | AFR | GWD | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | ESN | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG03130 | hp2 | a0001 | c0001 | t0006 | g0025 | AFR | ESN | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG03195 | hp1 | a0001 | c0001 | t0004 | g0090 | AFR | ESN | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG03195 | hp2 | a0001 | c0001 | t0002 | g0181 | AFR | ESN | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG03209 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | MSL | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG03209 | hp2 | a0001 | c0001 | t0009 | g0034 | AFR | MSL | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0161 | SAS | PJL | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG03453 | hp1 | a0001 | c0001 | t0002 | g0038 | AFR | MSL | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | MSL | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG03486 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | MSL | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | MSL | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG03490 | hp1 | a0001 | c0001 | t0007 | g0152 | SAS | PJL | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0160 | SAS | PJL | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0083 | SAS | PJL | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG03492 | hp1 | a0001 | c0001 | t0007 | g0150 | SAS | PJL | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG03516 | hp1 | a0001 | c0001 | t0002 | g0179 | AFR | ESN | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG03516 | hp2 | a0001 | c0001 | t0005 | g0005 | AFR | ESN | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG03540 | hp1 | a0001 | c0001 | t0009 | g0034 | AFR | GWD | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG03540 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | GWD | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG03579 | hp1 | a0001 | c0001 | t0002 | g0038 | AFR | MSL | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG03579 | hp2 | a0001 | c0001 | t0004 | g0048 | AFR | MSL | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0119 | SAS | PJL | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0208 | SAS | PJL | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0016 | SAS | STU | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0112 | SAS | STU | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG03834 | hp1 | a0001 | c0002 | t0001 | g0085 | SAS | BEB | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0071 | SAS | BEB | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0040 | SAS | BEB | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0018 | SAS | BEB | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0217 | SAS | BEB | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | BEB | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | STU | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0105 | SAS | STU | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0187 | SAS | BEB | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG04184 | hp2 | a0001 | c0002 | t0001 | g0146 | SAS | BEB | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0113 | SAS | STU | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0163 | SAS | STU | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG04228 | hp1 | a0001 | c0001 | t0012 | g0008 | SAS | STU | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG04228 | hp2 | a0001 | c0002 | t0001 | g0086 | SAS | STU | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | YRI | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA18522 | hp2 | a0001 | c0001 | t0002 | g0037 | AFR | YRI | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | CHB | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA18747 | hp2 | a0001 | c0001 | t0002 | g0184 | EAS | CHB | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA18906 | hp1 | a0001 | c0001 | t0006 | g0051 | AFR | YRI | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | YRI | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA18939 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA18939 | hp2 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA18940 | hp2 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA18942 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA18944 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA18945 | hp2 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA18946 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA18950 | hp2 | a0001 | c0001 | t0003 | g0065 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA18951 | hp1 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA18952 | hp2 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA18954 | hp1 | a0001 | c0001 | t0013 | g0035 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA18954 | hp2 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA18960 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA18961 | hp1 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA18964 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA18966 | hp1 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA18967 | hp1 | a0001 | c0001 | t0003 | g0049 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA18969 | hp1 | a0001 | c0001 | t0003 | g0063 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA18969 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA18970 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA18970 | hp2 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA18973 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA18974 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA18977 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA18977 | hp2 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA18978 | hp1 | a0001 | c0003 | t0003 | g0017 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA18978 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA18979 | hp2 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA18981 | hp1 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA18984 | hp2 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA18987 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA18990 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA18993 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA18993 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA18994 | hp1 | a0001 | c0001 | t0007 | g0015 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA18995 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA18997 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA18998 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA19000 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA19000 | hp2 | a0001 | c0001 | t0011 | g0135 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA19001 | hp1 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA19002 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA19004 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA19006 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA19009 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA19010 | hp1 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA19010 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA19011 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | LWK | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | LWK | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | LWK | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA19043 | hp2 | a0001 | c0001 | t0006 | g0053 | AFR | LWK | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA19054 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA19054 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA19055 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA19056 | hp1 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA19056 | hp2 | a0001 | c0001 | t0007 | g0129 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA19057 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA19058 | hp1 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA19058 | hp2 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA19060 | hp1 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA19062 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA19063 | hp1 | a0001 | c0001 | t0003 | g0026 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA19063 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA19064 | hp1 | a0001 | c0001 | t0003 | g0066 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA19064 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA19076 | hp1 | a0001 | c0001 | t0003 | g0072 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA19076 | hp2 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA19077 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA19079 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA19084 | hp2 | a0001 | c0001 | t0010 | g0198 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA19085 | hp1 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA19090 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA19091 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | YRI | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA19240 | hp2 | a0001 | c0001 | t0005 | g0005 | AFR | YRI | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ASW | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | ASW | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA20752 | hp1 | a0001 | c0001 | t0014 | g0154 | EUR | TSI | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0118 | EUR | TSI | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA20805 | hp1 | a0001 | c0002 | t0001 | g0084 | EUR | TSI | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0013 | EUR | TSI | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0116 | SAS | GIH | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0177 | SAS | GIH | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG01123 | hp2 | a0001 | c0001 | t0002 | g0039 | AMR | CLM | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG02109 | hp1 | a0001 | c0001 | t0005 | g0103 | AFR | ACB | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | ACB | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | ACB | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | ACB | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG02559 | hp1 | a0001 | c0001 | t0004 | g0091 | AFR | ACB | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | ACB | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | MSL | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG03471 | hp2 | a0001 | c0001 | t0005 | g0100 | AFR | MSL | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG06807 | hp1 | a0001 | c0001 | t0002 | g0040 | AFR | USA | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | USA | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA18955 | hp1 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA18955 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | USA | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | USA | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | LWK | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
NA21309 | hp2 | a0001 | c0001 | t0004 | g0028 | AFR | LWK | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0036 | REF | REF | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0001 | REF | REF | RALB_chr2_120247852_120299710 | RALB | chr2 | 120247852 | 120299710 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:120278757
|
G | A | 1 | a0001c0002 | 15 | HG00099.hp2 HG00280.hp1 HG00738.hp1 others(12): Show |
synonymous_variant | LOW | c.93G>A | p.Thr31Thr | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/5 | 269/2247 | 93/621 | 31/206 | chr2 | 120278757 | ||
chr2:120286029
|
T | A | 1 | a0001c0003 | 1 | NA18978.hp1 | synonymous_variant | LOW | c.270T>A | p.Leu90Leu | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 3/5 | 446/2247 | 270/621 | 90/206 | chr2 | 120286029 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:120252867
|
A | T | 13 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(10): Show | 224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-161A>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/5 | chr2 | 120252867 | ||||||
chr2:120252942
|
G | A | 1 | a0001c0001t0005 | 10 | HG01884.hp2 HG02109.hp1 HG02572.hp1 others(7): Show |
5_prime_UTR_variant | MODIFIER | c.-86G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/5 | 25723 | chr2 | 120252942 | |||||
chr2:120252943
|
C | A | 1 | a0001c0001t0011 | 1 | NA19000.hp2 | 5_prime_UTR_variant | MODIFIER | c.-85C>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/5 | 25722 | chr2 | 120252943 | |||||
chr2:120293413
|
T | A | 13 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(10): Show | 222 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(219): Show |
3_prime_UTR_variant | MODIFIER | c.*153T>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 5/5 | 153 | chr2 | 120293413 | |||||
chr2:120293564
|
A | G | 1 | a0001c0001t0006 | 6 | HG00639.hp2 HG01243.hp1 HG02723.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*304A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 5/5 | 304 | chr2 | 120293564 | |||||
chr2:120293605
|
C | T | 1 | a0001c0001t0014 | 1 | NA20752.hp1 | 3_prime_UTR_variant | MODIFIER | c.*345C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 5/5 | 345 | chr2 | 120293605 | |||||
chr2:120293619
|
G | A | 1 | a0001c0001t0009 | 2 | HG03209.hp2 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*359G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 5/5 | 359 | chr2 | 120293619 | |||||
chr2:120293818
|
G | A | 1 | a0001c0001t0004 | 11 | HG00735.hp1 HG02451.hp1 HG02559.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*558G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 5/5 | 558 | chr2 | 120293818 | |||||
chr2:120294196
|
C | T | 1 | a0001c0001t0013 | 1 | NA18954.hp1 | 3_prime_UTR_variant | MODIFIER | c.*936C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 5/5 | 936 | chr2 | 120294196 | |||||
chr2:120294224
|
T | A | 1 | a0001c0001t0012 | 1 | HG04228.hp1 | 3_prime_UTR_variant | MODIFIER | c.*964T>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 5/5 | 964 | chr2 | 120294224 | |||||
chr2:120294538
|
C | T | 1 | a0001c0001t0010 | 1 | NA19084.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1278C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 5/5 | 1278 | chr2 | 120294538 | |||||
chr2:120294558
|
C | A | 2 | a0001c0001t0003a0001c0003t0003 | 15 | HG00609.hp1 HG01928.hp2 HG02165.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1298C>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 5/5 | 1298 | chr2 | 120294558 | |||||
chr2:120294678
|
C | T | 1 | a0001c0001t0008 | 2 | HG01243.hp2 HG02818.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1418C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 5/5 | 1418 | chr2 | 120294678 | |||||
chr2:120294692
|
A | T | 13 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(10): Show | 222 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(219): Show |
3_prime_UTR_variant | MODIFIER | c.*1432A>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 5/5 | 1432 | chr2 | 120294692 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:120253200
|
CTGGGGCT others(3): Show |
C | 3 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0047 | 3 | HG02257.hp1 HG02486.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.-48+221_-48+230del others(10): Show |
RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120253200 | ||||||
chr2:120253333
|
C | A | 1 | a0001c0001t0004g0048 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-48+353C>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120253333 | ||||||
chr2:120253387
|
C | T | 1 | a0001c0001t0001g0225 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-48+407C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120253387 | ||||||
chr2:120253563
|
C | T | 1 | a0001c0001t0002g0044 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.-48+583C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120253563 | ||||||
chr2:120253586
|
T | C | 160 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(157): Show | 225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.-48+606T>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120253586 | ||||||
chr2:120253630
|
T | G | 1 | a0001c0001t0003g0049 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-48+650T>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120253630 | ||||||
chr2:120254084
|
C | G | 160 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(157): Show | 225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.-48+1104C>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120254084 | ||||||
chr2:120254194
|
A | G | 160 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(157): Show | 225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.-48+1214A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120254194 | ||||||
chr2:120254353
|
A | G | 1 | a0001c0001t0002g0224 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-48+1373A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120254353 | ||||||
chr2:120254404
|
A | C | 88 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(85): Show | 129 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.-48+1424A>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120254404 | ||||||
chr2:120254453
|
A | G | 160 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(157): Show | 225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.-48+1473A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120254453 | ||||||
chr2:120254457
|
A | G | 160 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(157): Show | 225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.-48+1477A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120254457 | ||||||
chr2:120254655
|
A | G | 5 | a0001c0001t0005g0005a0001c0001t0005g0100a0001c0001t0005g0101others(2): Show | 10 | HG01884.hp2 HG02109.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.-48+1675A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120254655 | ||||||
chr2:120254681
|
TTTTG | T | 159 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(156): Show | 224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.-48+1709_-48+1712d others(6): Show |
RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr2 | 120254681 | |||||
chr2:120254695
|
G | T | 1 | a0001c0001t0001g0050 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.-48+1715G>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120254695 | ||||||
chr2:120254779
|
G | C | 1 | a0001c0001t0001g0050 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.-48+1799G>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120254779 | ||||||
chr2:120254783
|
G | T | 160 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(157): Show | 225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.-48+1803G>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120254783 | ||||||
chr2:120254852
|
T | A | 5 | a0001c0001t0006g0025a0001c0001t0006g0051a0001c0001t0006g0052others(2): Show | 6 | HG00639.hp2 HG01243.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.-48+1872T>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120254852 | ||||||
chr2:120254895
|
C | T | 3 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0047 | 3 | HG02257.hp1 HG02486.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.-48+1915C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120254895 | ||||||
chr2:120254948
|
A | G | 1 | a0001c0001t0002g0223 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-48+1968A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120254948 | ||||||
chr2:120254965
|
C | G | 4 | a0001c0001t0001g0030a0001c0001t0001g0097a0001c0001t0001g0098others(1): Show | 5 | HG02809.hp1 HG03041.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.-48+1985C>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120254965 | ||||||
chr2:120254966
|
C | G | 4 | a0001c0001t0001g0030a0001c0001t0001g0097a0001c0001t0001g0098others(1): Show | 5 | HG02809.hp1 HG03041.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.-48+1986C>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120254966 | ||||||
chr2:120254967
|
C | A | 4 | a0001c0001t0001g0030a0001c0001t0001g0097a0001c0001t0001g0098others(1): Show | 5 | HG02809.hp1 HG03041.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.-48+1987C>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120254967 | ||||||
chr2:120255082
|
TA | T | 5 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(2): Show | 5 | HG01192.hp2 HG01257.hp1 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.-48+2103delA | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120255082 | ||||||
chr2:120255090
|
T | A | 160 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(157): Show | 225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.-48+2110T>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120255090 | ||||||
chr2:120255255
|
G | A | 1 | a0001c0001t0002g0036 | 2 | HG01168.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-48+2275G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120255255 | ||||||
chr2:120255258
|
TG | T | 5 | a0001c0001t0005g0005a0001c0001t0005g0100a0001c0001t0005g0101others(2): Show | 10 | HG01884.hp2 HG02109.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.-48+2280delG | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr2 | 120255258 | |||||
chr2:120255259
|
G | GT | 9 | a0001c0001t0001g0096a0001c0001t0001g0167a0001c0001t0001g0168others(6): Show | 11 | HG00639.hp2 HG01243.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.-48+2279_-48+2280i others(3): Show |
RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120255259 | ||||||
chr2:120255260
|
G | T | 155 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(152): Show | 215 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.-48+2280G>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120255260 | ||||||
chr2:120255293
|
T | C | 160 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(157): Show | 225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.-48+2313T>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120255293 | ||||||
chr2:120255326
|
C | T | 160 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(157): Show | 225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.-48+2346C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120255326 | ||||||
chr2:120255335
|
A | G | 160 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(157): Show | 225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.-48+2355A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120255335 | ||||||
chr2:120255480
|
T | C | 160 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(157): Show | 225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.-48+2500T>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120255480 | ||||||
chr2:120255593
|
G | A | 162 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(159): Show | 227 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.-48+2613G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120255593 | ||||||
chr2:120255716
|
A | G | 1 | a0001c0001t0002g0222 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-48+2736A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120255716 | ||||||
chr2:120255765
|
C | T | 1 | a0001c0001t0001g0095 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-48+2785C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120255765 | ||||||
chr2:120255781
|
T | G | 1 | a0001c0001t0001g0104 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.-48+2801T>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120255781 | ||||||
chr2:120255930
|
C | CTATGTGA others(10): Show |
160 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(157): Show | 225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.-48+2953_-48+2954i others(19): Show |
RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr2 | 120255930 | |||||
chr2:120255936
|
G | A | 1 | a0001c0001t0001g0105 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-48+2956G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120255936 | ||||||
chr2:120256040
|
C | A | 1 | a0001c0001t0002g0174 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.-48+3060C>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120256040 | ||||||
chr2:120256096
|
T | TTC | 160 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(157): Show | 225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.-48+3117_-48+3118i others(4): Show |
RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr2 | 120256096 | |||||
chr2:120256099
|
A | G | 160 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(157): Show | 225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.-48+3119A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120256099 | ||||||
chr2:120256135
|
A | G | 1 | a0001c0001t0004g0094 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-48+3155A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120256135 | ||||||
chr2:120256205
|
G | A | 160 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(157): Show | 225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.-48+3225G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120256205 | ||||||
chr2:120256256
|
G | C | 160 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(157): Show | 225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.-48+3276G>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120256256 | ||||||
chr2:120256286
|
C | G | 10 | a0001c0001t0004g0028a0001c0001t0004g0048a0001c0001t0004g0087others(7): Show | 11 | HG00735.hp1 HG02451.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.-48+3306C>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120256286 | ||||||
chr2:120256306
|
C | T | 12 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0002t0001g0012others(9): Show | 16 | HG00099.hp2 HG00280.hp1 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.-48+3326C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120256306 | ||||||
chr2:120256338
|
GATA | G | 12 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0002t0001g0012others(9): Show | 16 | HG00099.hp2 HG00280.hp1 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.-48+3361_-48+3363d others(5): Show |
RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr2 | 120256338 | |||||
chr2:120256470
|
T | C | 1 | a0001c0001t0001g0097 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-48+3490T>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120256470 | ||||||
chr2:120256531
|
G | C | 25 | a0001c0001t0001g0007a0001c0001t0001g0018a0001c0001t0001g0031others(22): Show | 32 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(29): Show |
intron_variant | MODIFIER | c.-48+3551G>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120256531 | ||||||
chr2:120256546
|
G | A | 3 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0047 | 3 | HG02257.hp1 HG02486.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.-48+3566G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120256546 | ||||||
chr2:120256558
|
C | T | 1 | a0001c0001t0001g0166 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-48+3578C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120256558 | ||||||
chr2:120256568
|
A | G | 160 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(157): Show | 225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.-48+3588A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120256568 | ||||||
chr2:120256647
|
C | T | 4 | a0001c0002t0001g0012a0001c0002t0001g0084a0001c0002t0001g0085others(1): Show | 7 | HG00099.hp2 HG00280.hp1 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.-48+3667C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120256647 | ||||||
chr2:120256696
|
C | T | 3 | a0001c0001t0002g0024a0001c0001t0002g0220a0001c0001t0002g0221 | 5 | NA18939.hp1 NA18973.hp1 NA19002.hp1 others(2): Show |
intron_variant | MODIFIER | c.-48+3716C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120256696 | ||||||
chr2:120256734
|
C | A | 1 | a0001c0001t0002g0175 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-48+3754C>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120256734 | ||||||
chr2:120256794
|
C | T | 160 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(157): Show | 225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.-48+3814C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120256794 | ||||||
chr2:120257013
|
C | T | 159 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(156): Show | 224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.-48+4033C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120257013 | ||||||
chr2:120257014
|
G | T | 1 | a0001c0001t0001g0104 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.-48+4034G>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120257014 | ||||||
chr2:120257107
|
T | TG | 160 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(157): Show | 225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.-48+4128dupG | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr2 | 120257107 | |||||
chr2:120257115
|
T | G | 12 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0002t0001g0012others(9): Show | 16 | HG00099.hp2 HG00280.hp1 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.-48+4135T>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120257115 | ||||||
chr2:120257128
|
A | G | 1 | a0001c0001t0001g0121 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-48+4148A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120257128 | ||||||
chr2:120257225
|
C | T | 1 | a0001c0001t0002g0219 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-48+4245C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120257225 | ||||||
chr2:120257254
|
G | A | 12 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0002t0001g0012others(9): Show | 16 | HG00099.hp2 HG00280.hp1 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.-48+4274G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120257254 | ||||||
chr2:120257277
|
C | T | 2 | a0001c0001t0002g0173a0001c0001t0002g0223 | 2 | HG01175.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-48+4297C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120257277 | ||||||
chr2:120257319
|
G | A | 160 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(157): Show | 225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.-48+4339G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120257319 | ||||||
chr2:120257422
|
A | G | 1 | a0001c0001t0001g0076 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-48+4442A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120257422 | ||||||
chr2:120257511
|
AT | A | 159 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(156): Show | 224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.-48+4541delT | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr2 | 120257511 | |||||
chr2:120257526
|
C | T | 1 | a0001c0001t0002g0218 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-48+4546C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120257526 | ||||||
chr2:120257769
|
C | T | 12 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0002t0001g0012others(9): Show | 16 | HG00099.hp2 HG00280.hp1 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.-48+4789C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120257769 | ||||||
chr2:120257773
|
C | T | 5 | a0001c0001t0006g0025a0001c0001t0006g0051a0001c0001t0006g0052others(2): Show | 6 | HG00639.hp2 HG01243.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.-48+4793C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120257773 | ||||||
chr2:120257938
|
A | G | 1 | a0001c0001t0002g0217 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-48+4958A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120257938 | ||||||
chr2:120258071
|
G | T | 11 | a0001c0001t0001g0075a0001c0001t0004g0028a0001c0001t0004g0048others(8): Show | 12 | HG00735.hp1 HG02451.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.-48+5091G>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120258071 | ||||||
chr2:120258171
|
G | A | 30 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0047others(27): Show | 40 | HG00099.hp2 HG00280.hp1 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.-48+5191G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120258171 | ||||||
chr2:120258231
|
C | T | 3 | a0001c0001t0001g0023a0001c0001t0001g0164a0001c0001t0001g0165 | 5 | HG01891.hp2 HG02486.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.-48+5251C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120258231 | ||||||
chr2:120258254
|
T | A | 10 | a0001c0001t0004g0028a0001c0001t0004g0048a0001c0001t0004g0087others(7): Show | 11 | HG00735.hp1 HG02451.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.-48+5274T>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120258254 | ||||||
chr2:120258471
|
A | G | 1 | a0001c0001t0002g0217 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-48+5491A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120258471 | ||||||
chr2:120258488
|
G | A | 12 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0002t0001g0012others(9): Show | 16 | HG00099.hp2 HG00280.hp1 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.-48+5508G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120258488 | ||||||
chr2:120258613
|
G | C | 11 | a0001c0001t0001g0030a0001c0001t0001g0055a0001c0001t0001g0056others(8): Show | 12 | HG02109.hp2 HG02451.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.-48+5633G>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120258613 | ||||||
chr2:120258794
|
G | A | 1 | a0001c0001t0002g0176 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-48+5814G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120258794 | ||||||
chr2:120258834
|
G | T | 4 | a0001c0001t0001g0030a0001c0001t0001g0097a0001c0001t0001g0098others(1): Show | 5 | HG02809.hp1 HG03041.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.-48+5854G>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120258834 | ||||||
chr2:120258858
|
C | T | 2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | HG03017.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.-48+5878C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120258858 | ||||||
chr2:120258860
|
C | G | 1 | a0001c0001t0002g0218 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-48+5880C>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120258860 | ||||||
chr2:120258898
|
A | G | 160 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(157): Show | 225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.-48+5918A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120258898 | ||||||
chr2:120258931
|
G | A | 88 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(85): Show | 129 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.-48+5951G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120258931 | ||||||
chr2:120259002
|
G | C | 1 | a0001c0001t0001g0060 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-48+6022G>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120259002 | ||||||
chr2:120259155
|
G | T | 4 | a0001c0001t0002g0010a0001c0001t0002g0214a0001c0001t0002g0215others(1): Show | 8 | NA18944.hp1 NA18964.hp1 NA18977.hp2 others(5): Show |
intron_variant | MODIFIER | c.-48+6175G>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120259155 | ||||||
chr2:120259175
|
T | C | 160 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(157): Show | 225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.-48+6195T>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120259175 | ||||||
chr2:120259197
|
C | T | 1 | a0001c0001t0008g0029 | 2 | HG01243.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-48+6217C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120259197 | ||||||
chr2:120259198
|
G | A | 10 | a0001c0001t0004g0028a0001c0001t0004g0048a0001c0001t0004g0087others(7): Show | 11 | HG00735.hp1 HG02451.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.-48+6218G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120259198 | ||||||
chr2:120259294
|
C | T | 1 | a0001c0001t0001g0059 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-48+6314C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120259294 | ||||||
chr2:120259295
|
G | A | 2 | a0001c0001t0002g0177a0001c0001t0002g0222 | 2 | HG02683.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.-48+6315G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120259295 | ||||||
chr2:120259316
|
C | T | 1 | a0001c0001t0002g0213 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-48+6336C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120259316 | ||||||
chr2:120259443
|
G | A | 1 | a0001c0001t0002g0037 | 2 | HG01891.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-48+6463G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120259443 | ||||||
chr2:120259535
|
G | T | 1 | a0001c0001t0001g0163 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-48+6555G>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120259535 | ||||||
chr2:120259650
|
C | G | 1 | a0001c0001t0001g0162 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-48+6670C>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120259650 | ||||||
chr2:120259705
|
C | T | 1 | a0001c0001t0001g0161 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-48+6725C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120259705 | ||||||
chr2:120259712
|
G | A | 25 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0050others(22): Show | 36 | HG00609.hp1 HG01081.hp1 HG01928.hp2 others(33): Show |
intron_variant | MODIFIER | c.-48+6732G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120259712 | ||||||
chr2:120259742
|
A | G | 160 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(157): Show | 225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.-48+6762A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120259742 | ||||||
chr2:120259781
|
C | T | 6 | a0001c0001t0006g0025a0001c0001t0006g0051a0001c0001t0006g0052others(3): Show | 8 | HG00639.hp2 HG01243.hp1 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.-48+6801C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120259781 | ||||||
chr2:120259787
|
G | A | 5 | a0001c0001t0005g0005a0001c0001t0005g0100a0001c0001t0005g0101others(2): Show | 10 | HG01884.hp2 HG02109.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.-48+6807G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120259787 | ||||||
chr2:120259797
|
A | AG | 8 | a0001c0001t0001g0061a0001c0001t0001g0122a0001c0001t0001g0164others(5): Show | 8 | HG00735.hp1 HG01261.hp1 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.-48+6822dupG | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr2 | 120259797 | |||||
chr2:120259813
|
C | T | 3 | a0001c0001t0001g0023a0001c0001t0001g0164a0001c0001t0001g0165 | 5 | HG01891.hp2 HG02486.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.-48+6833C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120259813 | ||||||
chr2:120259823
|
C | T | 1 | a0001c0001t0001g0160 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-48+6843C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120259823 | ||||||
chr2:120259829
|
G | A | 1 | a0001c0001t0001g0123 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-48+6849G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120259829 | ||||||
chr2:120259869
|
T | C | 1 | a0001c0002t0001g0084 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-48+6889T>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120259869 | ||||||
chr2:120259883
|
C | T | 1 | a0001c0002t0001g0084 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-48+6903C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120259883 | ||||||
chr2:120259884
|
A | G | 160 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(157): Show | 225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.-48+6904A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120259884 | ||||||
chr2:120259888
|
C | G | 3 | a0001c0001t0004g0028a0001c0001t0004g0092a0001c0001t0004g0093 | 4 | HG02451.hp1 HG02723.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-48+6908C>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120259888 | ||||||
chr2:120259936
|
T | C | 160 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(157): Show | 225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.-48+6956T>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120259936 | ||||||
chr2:120260006
|
T | C | 160 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(157): Show | 225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.-48+7026T>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120260006 | ||||||
chr2:120260014
|
C | T | 6 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0073others(3): Show | 6 | HG01943.hp2 HG02922.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.-48+7034C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120260014 | ||||||
chr2:120260041
|
C | T | 3 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0047 | 3 | HG02257.hp1 HG02486.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.-48+7061C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120260041 | ||||||
chr2:120260074
|
C | T | 5 | a0001c0001t0002g0173a0001c0001t0002g0223a0001c0001t0004g0028others(2): Show | 6 | HG01175.hp1 HG02451.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-48+7094C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120260074 | ||||||
chr2:120260112
|
C | T | 1 | a0001c0001t0002g0212 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.-48+7132C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120260112 | ||||||
chr2:120260198
|
C | T | 1 | a0001c0001t0001g0158 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.-48+7218C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120260198 | ||||||
chr2:120260278
|
C | T | 4 | a0001c0002t0001g0012a0001c0002t0001g0084a0001c0002t0001g0085others(1): Show | 7 | HG00099.hp2 HG00280.hp1 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.-48+7298C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120260278 | ||||||
chr2:120260279
|
G | A | 11 | a0001c0001t0001g0030a0001c0001t0001g0055a0001c0001t0001g0056others(8): Show | 12 | HG02109.hp2 HG02451.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.-48+7299G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120260279 | ||||||
chr2:120260437
|
G | A | 2 | a0001c0002t0001g0077a0001c0002t0001g0078 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.-48+7457G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120260437 | ||||||
chr2:120260577
|
C | A | 86 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(83): Show | 127 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.-48+7597C>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120260577 | ||||||
chr2:120260621
|
A | G | 11 | a0001c0001t0001g0030a0001c0001t0001g0055a0001c0001t0001g0056others(8): Show | 12 | HG02109.hp2 HG02451.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.-48+7641A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120260621 | ||||||
chr2:120260641
|
G | A | 1 | a0001c0001t0002g0181 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-48+7661G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120260641 | ||||||
chr2:120260893
|
A | G | 160 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(157): Show | 225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.-48+7913A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120260893 | ||||||
chr2:120260896
|
G | A | 12 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0002t0001g0012others(9): Show | 16 | HG00099.hp2 HG00280.hp1 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.-48+7916G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120260896 | ||||||
chr2:120260961
|
A | G | 154 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(151): Show | 217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.-48+7981A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120260961 | ||||||
chr2:120261032
|
C | T | 1 | a0001c0001t0001g0075 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-48+8052C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120261032 | ||||||
chr2:120261056
|
C | T | 1 | a0001c0001t0005g0103 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-48+8076C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120261056 | ||||||
chr2:120261063
|
A | C | 1 | a0001c0001t0002g0175 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-48+8083A>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120261063 | ||||||
chr2:120261070
|
T | G | 1 | a0001c0001t0001g0045 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-48+8090T>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120261070 | ||||||
chr2:120261111
|
C | T | 162 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(159): Show | 227 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.-48+8131C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120261111 | ||||||
chr2:120261171
|
A | G | 160 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(157): Show | 225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.-48+8191A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120261171 | ||||||
chr2:120261177
|
G | A | 1 | a0001c0001t0002g0182 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.-48+8197G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120261177 | ||||||
chr2:120261184
|
T | C | 162 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(159): Show | 227 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.-48+8204T>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120261184 | ||||||
chr2:120261185
|
G | A | 3 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0047 | 3 | HG02257.hp1 HG02486.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.-48+8205G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120261185 | ||||||
chr2:120261575
|
C | T | 3 | a0001c0001t0001g0030a0001c0001t0001g0097a0001c0001t0001g0099 | 4 | HG02809.hp1 HG03041.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-48+8595C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120261575 | ||||||
chr2:120261668
|
G | T | 160 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(157): Show | 225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.-48+8688G>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120261668 | ||||||
chr2:120261840
|
T | G | 1 | a0001c0001t0004g0087 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-48+8860T>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120261840 | ||||||
chr2:120261846
|
T | G | 5 | a0001c0001t0005g0005a0001c0001t0005g0100a0001c0001t0005g0101others(2): Show | 10 | HG01884.hp2 HG02109.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.-48+8866T>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120261846 | ||||||
chr2:120262023
|
G | A | 1 | a0001c0001t0004g0094 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-48+9043G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120262023 | ||||||
chr2:120262207
|
G | A | 5 | a0001c0001t0005g0005a0001c0001t0005g0100a0001c0001t0005g0101others(2): Show | 10 | HG01884.hp2 HG02109.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.-48+9227G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120262207 | ||||||
chr2:120262224
|
G | A | 124 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(121): Show | 177 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.-48+9244G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120262224 | ||||||
chr2:120262378
|
A | G | 6 | a0001c0001t0006g0025a0001c0001t0006g0051a0001c0001t0006g0052others(3): Show | 8 | HG00639.hp2 HG01243.hp1 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.-48+9398A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120262378 | ||||||
chr2:120262858
|
G | C | 1 | a0001c0001t0001g0097 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-48+9878G>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120262858 | ||||||
chr2:120262895
|
C | T | 1 | a0001c0001t0001g0120 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-48+9915C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120262895 | ||||||
chr2:120263065
|
A | C | 160 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(157): Show | 225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.-48+10085A>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120263065 | ||||||
chr2:120263207
|
C | T | 2 | a0001c0001t0002g0177a0001c0001t0002g0222 | 2 | HG02683.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.-48+10227C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120263207 | ||||||
chr2:120263226
|
C | T | 160 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(157): Show | 225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.-48+10246C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120263226 | ||||||
chr2:120263402
|
G | A | 1 | a0001c0001t0001g0062 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-48+10422G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120263402 | ||||||
chr2:120263579
|
A | T | 1 | a0001c0001t0001g0157 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-48+10599A>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120263579 | ||||||
chr2:120263772
|
C | T | 1 | a0001c0001t0001g0156 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-48+10792C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120263772 | ||||||
chr2:120263773
|
G | A | 1 | a0001c0001t0002g0222 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-48+10793G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120263773 | ||||||
chr2:120263827
|
G | T | 1 | a0001c0001t0001g0022 | 3 | HG02155.hp1 NA18951.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.-48+10847G>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120263827 | ||||||
chr2:120263886
|
C | T | 1 | a0001c0001t0004g0091 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-48+10906C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120263886 | ||||||
chr2:120263992
|
A | G | 160 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(157): Show | 225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.-48+11012A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120263992 | ||||||
chr2:120264049
|
A | G | 27 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0035others(24): Show | 38 | HG00609.hp1 HG01081.hp1 HG01928.hp2 others(35): Show |
intron_variant | MODIFIER | c.-48+11069A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120264049 | ||||||
chr2:120264205
|
T | C | 160 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(157): Show | 225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.-48+11225T>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120264205 | ||||||
chr2:120264219
|
C | T | 3 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0057 | 3 | HG02109.hp2 HG02622.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-48+11239C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120264219 | ||||||
chr2:120264260
|
C | T | 1 | a0001c0001t0002g0181 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-48+11280C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120264260 | ||||||
chr2:120264336
|
G | A | 3 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0096 | 3 | HG03453.hp2 HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-48+11356G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120264336 | ||||||
chr2:120264554
|
A | G | 1 | a0001c0001t0003g0072 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.-48+11574A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120264554 | ||||||
chr2:120264555
|
C | A | 1 | a0001c0001t0003g0072 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.-48+11575C>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120264555 | ||||||
chr2:120264555
|
CA | C | 159 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(156): Show | 224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.-48+11577delA | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr2 | 120264555 | |||||
chr2:120264556
|
A | C | 1 | a0001c0001t0003g0072 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.-48+11576A>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120264556 | ||||||
chr2:120264583
|
T | A | 1 | a0001c0001t0002g0183 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.-48+11603T>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120264583 | ||||||
chr2:120264610
|
A | G | 1 | a0001c0001t0004g0087 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-48+11630A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120264610 | ||||||
chr2:120264678
|
T | A | 1 | a0001c0001t0001g0157 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-48+11698T>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120264678 | ||||||
chr2:120264680
|
C | T | 27 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0035others(24): Show | 39 | HG00609.hp1 HG01081.hp1 HG01243.hp2 others(36): Show |
intron_variant | MODIFIER | c.-48+11700C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120264680 | ||||||
chr2:120264778
|
C | G | 74 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0030others(71): Show | 98 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(95): Show |
intron_variant | MODIFIER | c.-48+11798C>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120264778 | ||||||
chr2:120264786
|
C | A | 10 | a0001c0001t0004g0028a0001c0001t0004g0048a0001c0001t0004g0087others(7): Show | 11 | HG00735.hp1 HG02451.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.-48+11806C>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120264786 | ||||||
chr2:120264820
|
A | G | 2 | a0001c0001t0001g0073a0001c0001t0001g0074 | 2 | HG02922.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.-48+11840A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120264820 | ||||||
chr2:120264864
|
T | G | 1 | a0001c0001t0004g0087 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-48+11884T>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120264864 | ||||||
chr2:120264946
|
A | AATAC | 12 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0002t0001g0012others(9): Show | 16 | HG00099.hp2 HG00280.hp1 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.-48+11967_-48+1196 others(8): Show |
RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr2 | 120264946 | |||||
chr2:120265157
|
A | G | 1 | a0001c0001t0002g0211 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-48+12177A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120265157 | ||||||
chr2:120265164
|
G | T | 161 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(158): Show | 226 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.-48+12184G>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120265164 | ||||||
chr2:120265588
|
A | C | 1 | a0001c0001t0001g0161 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-48+12608A>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120265588 | ||||||
chr2:120265772
|
ATAGAAG | A | 159 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(156): Show | 224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.-48+12808_-48+1281 others(10): Show |
RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr2 | 120265772 | |||||
chr2:120265920
|
C | T | 85 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(82): Show | 126 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.-47-12698C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120265920 | ||||||
chr2:120266175
|
G | A | 74 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0030others(71): Show | 98 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(95): Show |
intron_variant | MODIFIER | c.-47-12443G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120266175 | ||||||
chr2:120266305
|
C | T | 1 | a0001c0001t0002g0221 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.-47-12313C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120266305 | ||||||
chr2:120266321
|
T | G | 3 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0057 | 3 | HG02109.hp2 HG02622.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-47-12297T>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120266321 | ||||||
chr2:120266352
|
A | C | 1 | a0001c0001t0001g0119 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-47-12266A>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120266352 | ||||||
chr2:120266384
|
A | G | 1 | a0001c0001t0001g0155 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-47-12234A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120266384 | ||||||
chr2:120266401
|
C | T | 60 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(57): Show | 94 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.-47-12217C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120266401 | ||||||
chr2:120266414
|
T | A | 1 | a0001c0001t0002g0184 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-47-12204T>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120266414 | ||||||
chr2:120266571
|
C | T | 1 | a0001c0001t0002g0210 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-47-12047C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120266571 | ||||||
chr2:120266685
|
T | A | 10 | a0001c0001t0004g0028a0001c0001t0004g0048a0001c0001t0004g0087others(7): Show | 11 | HG00735.hp1 HG02451.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.-47-11933T>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120266685 | ||||||
chr2:120266777
|
A | T | 3 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0047 | 3 | HG02257.hp1 HG02486.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.-47-11841A>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120266777 | ||||||
chr2:120266843
|
A | G | 159 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(156): Show | 224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.-47-11775A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120266843 | ||||||
chr2:120266856
|
A | G | 123 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(120): Show | 176 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.-47-11762A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120266856 | ||||||
chr2:120266868
|
T | A | 1 | a0001c0001t0001g0161 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-47-11750T>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120266868 | ||||||
chr2:120267138
|
G | A | 1 | a0001c0001t0002g0185 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-47-11480G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120267138 | ||||||
chr2:120267220
|
G | A | 1 | a0001c0001t0002g0186 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-47-11398G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120267220 | ||||||
chr2:120267222
|
G | A | 10 | a0001c0002t0001g0012a0001c0002t0001g0027a0001c0002t0001g0077others(7): Show | 14 | HG00099.hp2 HG00280.hp1 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.-47-11396G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120267222 | ||||||
chr2:120267396
|
A | G | 1 | a0001c0001t0001g0071 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-47-11222A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120267396 | ||||||
chr2:120267403
|
GT | G | 159 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(156): Show | 224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.-47-11213delT | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr2 | 120267403 | |||||
chr2:120267411
|
A | G | 123 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(120): Show | 176 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.-47-11207A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120267411 | ||||||
chr2:120267449
|
G | A | 1 | a0001c0001t0001g0106 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-47-11169G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120267449 | ||||||
chr2:120267503
|
G | A | 1 | a0001c0001t0002g0173 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-47-11115G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120267503 | ||||||
chr2:120267536
|
G | GCTCC | 2 | a0001c0001t0002g0014a0001c0001t0002g0187 | 5 | HG02040.hp1 HG02155.hp2 HG04184.hp1 others(2): Show |
intron_variant | MODIFIER | c.-47-11082_-47-1108 others(8): Show |
RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120267536 | ||||||
chr2:120267609
|
A | T | 1 | a0001c0001t0001g0070 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-47-11009A>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120267609 | ||||||
chr2:120267665
|
G | T | 12 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0002t0001g0012others(9): Show | 16 | HG00099.hp2 HG00280.hp1 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.-47-10953G>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120267665 | ||||||
chr2:120267672
|
C | T | 1 | a0001c0001t0001g0097 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-47-10946C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120267672 | ||||||
chr2:120267679
|
C | T | 25 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0050others(22): Show | 36 | HG00609.hp1 HG01081.hp1 HG01928.hp2 others(33): Show |
intron_variant | MODIFIER | c.-47-10939C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120267679 | ||||||
chr2:120267686
|
A | T | 3 | a0001c0001t0002g0009a0001c0001t0002g0180a0001c0001t0002g0209 | 7 | NA18952.hp2 NA18955.hp2 NA18970.hp1 others(4): Show |
intron_variant | MODIFIER | c.-47-10932A>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120267686 | ||||||
chr2:120267753
|
G | A | 1 | a0001c0001t0002g0218 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-47-10865G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120267753 | ||||||
chr2:120267801
|
A | T | 2 | a0001c0001t0001g0035a0001c0001t0013g0035 | 2 | NA18954.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.-47-10817A>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120267801 | ||||||
chr2:120268025
|
C | T | 159 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(156): Show | 224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.-47-10593C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120268025 | ||||||
chr2:120268110
|
C | T | 3 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0047 | 3 | HG02257.hp1 HG02486.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.-47-10508C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120268110 | ||||||
chr2:120268192
|
G | A | 1 | a0001c0001t0001g0031 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-47-10426G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120268192 | ||||||
chr2:120268269
|
T | A | 1 | a0001c0001t0002g0214 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-47-10349T>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120268269 | ||||||
chr2:120268319
|
C | CA | 123 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(120): Show | 176 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.-47-10298dupA | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr2 | 120268319 | |||||
chr2:120268443
|
T | C | 1 | a0001c0001t0001g0124 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-47-10175T>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120268443 | ||||||
chr2:120268566
|
C | T | 2 | a0001c0002t0001g0079a0001c0002t0001g0080 | 2 | HG00738.hp2 HG00741.hp2 |
intron_variant | MODIFIER | c.-47-10052C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120268566 | ||||||
chr2:120268578
|
T | G | 2 | a0001c0001t0001g0020a0001c0001t0001g0130 | 4 | NA18961.hp2 NA18997.hp2 NA19079.hp2 others(1): Show |
intron_variant | MODIFIER | c.-47-10040T>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120268578 | ||||||
chr2:120268579
|
G | C | 1 | a0001c0001t0001g0131 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-47-10039G>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120268579 | ||||||
chr2:120268669
|
A | G | 1 | a0001c0001t0008g0029 | 2 | HG01243.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-47-9949A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120268669 | ||||||
chr2:120268696
|
T | A | 25 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0050others(22): Show | 36 | HG00609.hp1 HG01081.hp1 HG01928.hp2 others(33): Show |
intron_variant | MODIFIER | c.-47-9922T>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120268696 | ||||||
chr2:120268750
|
A | G | 1 | a0001c0001t0014g0154 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-47-9868A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120268750 | ||||||
chr2:120268794
|
C | T | 1 | a0001c0001t0004g0093 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-47-9824C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120268794 | ||||||
chr2:120268937
|
A | AT | 159 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(156): Show | 224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.-47-9674dupT | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr2 | 120268937 | |||||
chr2:120269006
|
A | G | 123 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(120): Show | 176 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.-47-9612A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120269006 | ||||||
chr2:120269076
|
T | A | 159 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(156): Show | 224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.-47-9542T>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120269076 | ||||||
chr2:120269085
|
T | C | 1 | a0001c0001t0001g0132 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-47-9533T>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120269085 | ||||||
chr2:120269117
|
G | A | 2 | a0001c0001t0002g0173a0001c0001t0002g0223 | 2 | HG01175.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-47-9501G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120269117 | ||||||
chr2:120269195
|
T | C | 87 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(84): Show | 128 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.-47-9423T>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120269195 | ||||||
chr2:120269213
|
TGGAGTTT others(17): Show |
T | 1 | a0001c0001t0001g0153 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.-47-9392_-47-9369d others(26): Show |
RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr2 | 120269213 | |||||
chr2:120269302
|
G | A | 1 | a0001c0001t0001g0073 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-47-9316G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120269302 | ||||||
chr2:120269315
|
T | C | 159 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(156): Show | 224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.-47-9303T>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120269315 | ||||||
chr2:120269397
|
C | T | 72 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0030others(69): Show | 96 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.-47-9221C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120269397 | ||||||
chr2:120269398
|
G | A | 2 | a0001c0001t0002g0184a0001c0001t0002g0188 | 2 | HG00642.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.-47-9220G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120269398 | ||||||
chr2:120269417
|
G | A | 5 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(2): Show | 5 | HG01192.hp2 HG01257.hp1 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.-47-9201G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120269417 | ||||||
chr2:120269417
|
G | C | 2 | a0001c0001t0001g0058a0001c0001t0001g0096 | 2 | HG03453.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-47-9201G>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120269417 | ||||||
chr2:120269425
|
C | T | 1 | a0001c0001t0001g0057 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-47-9193C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120269425 | ||||||
chr2:120269475
|
T | C | 1 | a0001c0001t0002g0215 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-47-9143T>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120269475 | ||||||
chr2:120269498
|
AG | A | 72 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0030others(69): Show | 96 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.-47-9119delG | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120269498 | ||||||
chr2:120269508
|
T | C | 25 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0050others(22): Show | 36 | HG00609.hp1 HG01081.hp1 HG01928.hp2 others(33): Show |
intron_variant | MODIFIER | c.-47-9110T>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120269508 | ||||||
chr2:120269592
|
C | T | 6 | a0001c0001t0006g0025a0001c0001t0006g0051a0001c0001t0006g0052others(3): Show | 8 | HG00639.hp2 HG01243.hp1 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.-47-9026C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120269592 | ||||||
chr2:120269785
|
T | G | 159 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(156): Show | 224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.-47-8833T>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120269785 | ||||||
chr2:120269995
|
A | G | 5 | a0001c0001t0005g0005a0001c0001t0005g0100a0001c0001t0005g0101others(2): Show | 10 | HG01884.hp2 HG02109.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.-47-8623A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120269995 | ||||||
chr2:120270178
|
GTTC | G | 11 | a0001c0001t0001g0030a0001c0001t0001g0055a0001c0001t0001g0056others(8): Show | 12 | HG02109.hp2 HG02451.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.-47-8434_-47-8432d others(5): Show |
RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr2 | 120270178 | |||||
chr2:120270600
|
A | G | 1 | a0001c0001t0001g0050 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.-47-8018A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120270600 | ||||||
chr2:120270615
|
C | CG | 159 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(156): Show | 224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.-47-8001dupG | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr2 | 120270615 | |||||
chr2:120270761
|
T | A | 5 | a0001c0001t0006g0025a0001c0001t0006g0051a0001c0001t0006g0052others(2): Show | 6 | HG00639.hp2 HG01243.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.-47-7857T>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120270761 | ||||||
chr2:120270873
|
G | A | 1 | a0001c0001t0001g0133 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-47-7745G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120270873 | ||||||
chr2:120270884
|
ATAT | A | 36 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0030others(33): Show | 48 | HG00609.hp1 HG01081.hp1 HG01928.hp2 others(45): Show |
intron_variant | MODIFIER | c.-47-7730_-47-7728d others(5): Show |
RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr2 | 120270884 | |||||
chr2:120270933
|
G | A | 1 | a0001c0001t0001g0062 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-47-7685G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120270933 | ||||||
chr2:120270968
|
G | A | 12 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0002t0001g0012others(9): Show | 16 | HG00099.hp2 HG00280.hp1 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.-47-7650G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120270968 | ||||||
chr2:120270999
|
G | A | 5 | a0001c0001t0005g0005a0001c0001t0005g0100a0001c0001t0005g0101others(2): Show | 10 | HG01884.hp2 HG02109.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.-47-7619G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120270999 | ||||||
chr2:120271161
|
A | G | 1 | a0001c0001t0001g0155 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-47-7457A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120271161 | ||||||
chr2:120271191
|
C | T | 1 | a0001c0001t0002g0208 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-47-7427C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120271191 | ||||||
chr2:120271192
|
G | A | 5 | a0001c0001t0006g0025a0001c0001t0006g0051a0001c0001t0006g0052others(2): Show | 6 | HG00639.hp2 HG01243.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.-47-7426G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120271192 | ||||||
chr2:120271257
|
T | TA | 11 | a0001c0001t0001g0030a0001c0001t0001g0055a0001c0001t0001g0056others(8): Show | 12 | HG02109.hp2 HG02451.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.-47-7360dupA | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr2 | 120271257 | |||||
chr2:120271267
|
T | C | 5 | a0001c0001t0006g0025a0001c0001t0006g0051a0001c0001t0006g0052others(2): Show | 6 | HG00639.hp2 HG01243.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.-47-7351T>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120271267 | ||||||
chr2:120271276
|
G | A | 5 | a0001c0001t0006g0025a0001c0001t0006g0051a0001c0001t0006g0052others(2): Show | 6 | HG00639.hp2 HG01243.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.-47-7342G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120271276 | ||||||
chr2:120271357
|
G | A | 3 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0047 | 3 | HG02257.hp1 HG02486.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.-47-7261G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120271357 | ||||||
chr2:120271437
|
T | C | 1 | a0001c0001t0003g0063 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-47-7181T>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120271437 | ||||||
chr2:120271489
|
A | G | 1 | a0001c0001t0002g0014 | 4 | HG02040.hp1 HG02155.hp2 NA18987.hp1 others(1): Show |
intron_variant | MODIFIER | c.-47-7129A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120271489 | ||||||
chr2:120271782
|
C | G | 1 | a0001c0001t0002g0175 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-47-6836C>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120271782 | ||||||
chr2:120271941
|
C | G | 159 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(156): Show | 224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.-47-6677C>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120271941 | ||||||
chr2:120272010
|
G | A | 159 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(156): Show | 224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.-47-6608G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120272010 | ||||||
chr2:120272096
|
C | A | 2 | a0001c0001t0002g0173a0001c0001t0002g0223 | 2 | HG01175.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-47-6522C>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120272096 | ||||||
chr2:120272262
|
A | G | 10 | a0001c0001t0004g0028a0001c0001t0004g0048a0001c0001t0004g0087others(7): Show | 11 | HG00735.hp1 HG02451.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.-47-6356A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120272262 | ||||||
chr2:120272264
|
G | A | 1 | a0001c0001t0008g0029 | 2 | HG01243.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-47-6354G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120272264 | ||||||
chr2:120272367
|
G | C | 2 | a0001c0001t0001g0055a0001c0001t0001g0057 | 2 | HG02109.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.-47-6251G>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120272367 | ||||||
chr2:120272673
|
GCTTCCTA others(21): Show |
G | 1 | a0001c0001t0002g0207 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-47-5938_-47-5911d others(30): Show |
RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr2 | 120272673 | |||||
chr2:120272771
|
C | T | 3 | a0001c0001t0001g0151a0001c0001t0007g0150a0001c0001t0007g0152 | 3 | HG02602.hp2 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-47-5847C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120272771 | ||||||
chr2:120272783
|
C | A | 10 | a0001c0001t0004g0028a0001c0001t0004g0048a0001c0001t0004g0087others(7): Show | 11 | HG00735.hp1 HG02451.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.-47-5835C>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120272783 | ||||||
chr2:120272879
|
C | A | 1 | a0001c0001t0008g0029 | 2 | HG01243.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-47-5739C>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120272879 | ||||||
chr2:120273042
|
C | T | 1 | a0001c0001t0002g0206 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-47-5576C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120273042 | ||||||
chr2:120273172
|
C | T | 15 | a0001c0001t0004g0028a0001c0001t0004g0048a0001c0001t0004g0087others(12): Show | 17 | HG00639.hp2 HG00735.hp1 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.-47-5446C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120273172 | ||||||
chr2:120273173
|
T | TA | 157 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(154): Show | 222 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.-47-5442dupA | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr2 | 120273173 | |||||
chr2:120273182
|
A | G | 1 | a0001c0001t0001g0149 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.-47-5436A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120273182 | ||||||
chr2:120273356
|
G | A | 1 | a0001c0001t0001g0076 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-47-5262G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120273356 | ||||||
chr2:120273377
|
A | G | 1 | a0001c0001t0002g0205 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-47-5241A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120273377 | ||||||
chr2:120273438
|
C | T | 1 | a0001c0001t0008g0029 | 2 | HG01243.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-47-5180C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120273438 | ||||||
chr2:120273490
|
G | A | 1 | a0001c0001t0004g0087 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-47-5128G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120273490 | ||||||
chr2:120273613
|
A | G | 1 | a0001c0001t0002g0204 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-47-5005A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120273613 | ||||||
chr2:120273684
|
G | A | 12 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0002t0001g0012others(9): Show | 16 | HG00099.hp2 HG00280.hp1 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.-47-4934G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120273684 | ||||||
chr2:120273686
|
C | T | 1 | a0001c0002t0001g0086 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-47-4932C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120273686 | ||||||
chr2:120273743
|
G | A | 2 | a0001c0001t0001g0169a0001c0001t0001g0170 | 2 | HG01515.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.-47-4875G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120273743 | ||||||
chr2:120273830
|
A | G | 1 | a0001c0001t0001g0060 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-47-4788A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120273830 | ||||||
chr2:120273857
|
G | A | 3 | a0001c0001t0004g0088a0001c0001t0004g0089a0001c0001t0004g0091 | 3 | HG02559.hp1 HG02615.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.-47-4761G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120273857 | ||||||
chr2:120274050
|
G | C | 1 | a0001c0001t0006g0051 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-47-4568G>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120274050 | ||||||
chr2:120274119
|
G | A | 159 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(156): Show | 224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.-47-4499G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120274119 | ||||||
chr2:120274157
|
G | A | 3 | a0001c0001t0004g0088a0001c0001t0004g0089a0001c0001t0004g0091 | 3 | HG02559.hp1 HG02615.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.-47-4461G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120274157 | ||||||
chr2:120274232
|
C | G | 1 | a0001c0001t0002g0217 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-47-4386C>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120274232 | ||||||
chr2:120274247
|
C | G | 1 | a0001c0001t0008g0029 | 2 | HG01243.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-47-4371C>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120274247 | ||||||
chr2:120274283
|
T | C | 6 | a0001c0001t0002g0038a0001c0001t0002g0175a0001c0001t0002g0189others(3): Show | 7 | HG01192.hp1 HG02280.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.-47-4335T>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120274283 | ||||||
chr2:120274342
|
T | A | 5 | a0001c0001t0005g0005a0001c0001t0005g0100a0001c0001t0005g0101others(2): Show | 10 | HG01884.hp2 HG02109.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.-47-4276T>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120274342 | ||||||
chr2:120274386
|
C | T | 1 | a0001c0001t0004g0091 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-47-4232C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120274386 | ||||||
chr2:120274414
|
A | G | 12 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0002t0001g0012others(9): Show | 16 | HG00099.hp2 HG00280.hp1 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.-47-4204A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120274414 | ||||||
chr2:120274467
|
A | T | 159 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(156): Show | 224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.-47-4151A>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120274467 | ||||||
chr2:120274507
|
T | C | 1 | a0001c0001t0001g0098 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-47-4111T>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120274507 | ||||||
chr2:120275156
|
G | A | 159 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(156): Show | 224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.-47-3462G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120275156 | ||||||
chr2:120275164
|
G | A | 1 | a0001c0001t0004g0087 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-47-3454G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120275164 | ||||||
chr2:120275283
|
C | T | 5 | a0001c0001t0001g0030a0001c0001t0001g0097a0001c0001t0001g0098others(2): Show | 6 | HG02809.hp1 HG03041.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.-47-3335C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120275283 | ||||||
chr2:120275373
|
C | G | 1 | a0001c0001t0009g0034 | 2 | HG03209.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-47-3245C>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120275373 | ||||||
chr2:120275495
|
C | T | 1 | a0001c0001t0002g0219 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-47-3123C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120275495 | ||||||
chr2:120275690
|
C | T | 1 | a0001c0001t0001g0118 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-47-2928C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120275690 | ||||||
chr2:120275842
|
C | T | 159 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(156): Show | 224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.-47-2776C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120275842 | ||||||
chr2:120275914
|
T | A | 159 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(156): Show | 224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.-47-2704T>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120275914 | ||||||
chr2:120275935
|
T | G | 12 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0002t0001g0012others(9): Show | 16 | HG00099.hp2 HG00280.hp1 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.-47-2683T>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120275935 | ||||||
chr2:120276049
|
C | T | 1 | a0001c0001t0001g0117 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-47-2569C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120276049 | ||||||
chr2:120276131
|
TG | T | 12 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0002t0001g0012others(9): Show | 16 | HG00099.hp2 HG00280.hp1 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.-47-2482delG | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr2 | 120276131 | |||||
chr2:120276195
|
C | T | 4 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116others(1): Show | 4 | HG01175.hp2 HG02293.hp1 NA20752.hp2 others(1): Show |
intron_variant | MODIFIER | c.-47-2423C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120276195 | ||||||
chr2:120276419
|
A | G | 5 | a0001c0001t0005g0005a0001c0001t0005g0100a0001c0001t0005g0101others(2): Show | 10 | HG01884.hp2 HG02109.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.-47-2199A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120276419 | ||||||
chr2:120276557
|
C | T | 27 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0035others(24): Show | 38 | HG00609.hp1 HG01081.hp1 HG01928.hp2 others(35): Show |
intron_variant | MODIFIER | c.-47-2061C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120276557 | ||||||
chr2:120276722
|
A | T | 1 | a0001c0001t0002g0043 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.-47-1896A>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120276722 | ||||||
chr2:120276954
|
A | G | 159 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(156): Show | 224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.-47-1664A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120276954 | ||||||
chr2:120277075
|
G | A | 3 | a0001c0001t0001g0023a0001c0001t0001g0164a0001c0001t0001g0165 | 5 | HG01891.hp2 HG02486.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.-47-1543G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120277075 | ||||||
chr2:120277243
|
G | A | 14 | a0001c0001t0001g0007a0001c0001t0001g0018a0001c0001t0001g0031others(11): Show | 21 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.-47-1375G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120277243 | ||||||
chr2:120277290
|
C | A | 3 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0047 | 3 | HG02257.hp1 HG02486.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.-47-1328C>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120277290 | ||||||
chr2:120277290
|
C | T | 2 | a0001c0001t0005g0102a0001c0001t0005g0103 | 2 | HG02109.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.-47-1328C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120277290 | ||||||
chr2:120277293
|
G | A | 1 | a0001c0001t0003g0049 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-47-1325G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120277293 | ||||||
chr2:120277326
|
TTG | T | 12 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0002t0001g0012others(9): Show | 16 | HG00099.hp2 HG00280.hp1 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.-47-1285_-47-1284d others(4): Show |
RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr2 | 120277326 | |||||
chr2:120277330
|
G | C | 12 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0002t0001g0012others(9): Show | 16 | HG00099.hp2 HG00280.hp1 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.-47-1288G>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120277330 | ||||||
chr2:120277350
|
C | CATGT | 37 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0047others(34): Show | 49 | HG00099.hp2 HG00280.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.-47-1267_-47-1264d others(6): Show |
RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr2 | 120277350 | |||||
chr2:120277353
|
G | GTA | 122 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(119): Show | 175 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.-47-1264_-47-1263i others(4): Show |
RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr2 | 120277353 | |||||
chr2:120277360
|
A | T | 122 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(119): Show | 175 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.-47-1258A>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120277360 | ||||||
chr2:120277365
|
ATG | A | 159 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(156): Show | 224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.-47-1246_-47-1245d others(4): Show |
RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr2 | 120277365 | |||||
chr2:120277411
|
G | A | 1 | a0001c0001t0001g0105 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-47-1207G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120277411 | ||||||
chr2:120277418
|
CAT | C | 5 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0047others(2): Show | 6 | HG01243.hp2 HG02257.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.-47-1199_-47-1198d others(4): Show |
RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120277418 | ||||||
chr2:120277429
|
C | A | 64 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0035others(61): Show | 87 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(84): Show |
intron_variant | MODIFIER | c.-47-1189C>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120277429 | ||||||
chr2:120277431
|
C | G | 159 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(156): Show | 224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.-47-1187C>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120277431 | ||||||
chr2:120277458
|
G | A | 1 | a0001c0001t0001g0149 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.-47-1160G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120277458 | ||||||
chr2:120277463
|
T | TGTGA | 148 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(145): Show | 212 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.-47-1153_-47-1152i others(6): Show |
RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr2 | 120277463 | |||||
chr2:120277511
|
C | CAT | 159 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(156): Show | 224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.-47-1107_-47-1106i others(4): Show |
RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120277511 | ||||||
chr2:120277519
|
CGTAT | C | 5 | a0001c0001t0005g0005a0001c0001t0005g0100a0001c0001t0005g0101others(2): Show | 10 | HG01884.hp2 HG02109.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.-47-1096_-47-1093d others(6): Show |
RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr2 | 120277519 | |||||
chr2:120277520
|
G | A | 1 | a0001c0001t0004g0088 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-47-1098G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120277520 | ||||||
chr2:120277523
|
TGTGA | T | 5 | a0001c0001t0006g0025a0001c0001t0006g0051a0001c0001t0006g0052others(2): Show | 6 | HG00639.hp2 HG01243.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.-47-1091_-47-1088d others(6): Show |
RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr2 | 120277523 | |||||
chr2:120277536
|
T | TTG | 10 | a0001c0001t0004g0028a0001c0001t0004g0048a0001c0001t0004g0087others(7): Show | 11 | HG00735.hp1 HG02451.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.-47-1069_-47-1068d others(4): Show |
RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr2 | 120277536 | |||||
chr2:120277537
|
TGTG | T | 15 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0131others(12): Show | 19 | HG00099.hp2 HG00280.hp1 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.-47-1080_-47-1078d others(5): Show |
RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120277537 | ||||||
chr2:120277594
|
A | G | 1 | a0001c0001t0001g0060 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-47-1024A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120277594 | ||||||
chr2:120277641
|
C | G | 1 | a0001c0001t0002g0203 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-47-977C>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120277641 | ||||||
chr2:120277654
|
GTGT | G | 67 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0011others(64): Show | 88 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(85): Show |
intron_variant | MODIFIER | c.-47-960_-47-958del others(3): Show |
RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr2 | 120277654 | |||||
chr2:120277681
|
ATGAG | A | 86 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(83): Show | 127 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.-47-933_-47-930del others(4): Show |
RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr2 | 120277681 | |||||
chr2:120277684
|
AGT | A | 73 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0030others(70): Show | 97 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(94): Show |
intron_variant | MODIFIER | c.-47-932_-47-931del others(2): Show |
RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr2 | 120277684 | |||||
chr2:120277687
|
G | A | 73 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0030others(70): Show | 97 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(94): Show |
intron_variant | MODIFIER | c.-47-931G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120277687 | ||||||
chr2:120277689
|
A | G | 73 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0030others(70): Show | 97 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(94): Show |
intron_variant | MODIFIER | c.-47-929A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120277689 | ||||||
chr2:120277690
|
A | T | 73 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0030others(70): Show | 97 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(94): Show |
intron_variant | MODIFIER | c.-47-928A>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120277690 | ||||||
chr2:120277697
|
A | G | 1 | a0001c0001t0001g0098 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-47-921A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120277697 | ||||||
chr2:120277699
|
G | A | 1 | a0001c0001t0001g0098 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-47-919G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120277699 | ||||||
chr2:120277702
|
G | T | 1 | a0001c0001t0001g0098 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-47-916G>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120277702 | ||||||
chr2:120277704
|
T | G | 1 | a0001c0001t0001g0098 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-47-914T>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120277704 | ||||||
chr2:120277759
|
GTA | G | 1 | a0001c0001t0001g0022 | 3 | HG02155.hp1 NA18951.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.-47-857_-47-856del others(2): Show |
RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr2 | 120277759 | |||||
chr2:120277768
|
CGT | C | 3 | a0001c0001t0002g0189a0001c0001t0002g0190a0001c0001t0002g0206 | 3 | HG02280.hp2 HG02615.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.-47-846_-47-845del others(2): Show |
RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr2 | 120277768 | |||||
chr2:120277781
|
G | A | 5 | a0001c0001t0006g0025a0001c0001t0006g0051a0001c0001t0006g0052others(2): Show | 6 | HG00639.hp2 HG01243.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.-47-837G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120277781 | ||||||
chr2:120277828
|
AAT | A | 15 | a0001c0001t0004g0028a0001c0001t0004g0048a0001c0001t0004g0087others(12): Show | 17 | HG00639.hp2 HG00735.hp1 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.-47-787_-47-786del others(2): Show |
RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr2 | 120277828 | |||||
chr2:120277831
|
ATG | A | 84 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(81): Show | 125 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.-47-781_-47-780del others(2): Show |
RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr2 | 120277831 | |||||
chr2:120277843
|
A | T | 1 | a0001c0001t0001g0119 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-47-775A>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120277843 | ||||||
chr2:120277867
|
ATG | A | 12 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0002t0001g0012others(9): Show | 16 | HG00099.hp2 HG00280.hp1 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.-47-748_-47-747del others(2): Show |
RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr2 | 120277867 | |||||
chr2:120277877
|
A | ATG | 158 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(155): Show | 223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.-47-740_-47-739dup others(2): Show |
RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr2 | 120277877 | |||||
chr2:120277877
|
A | G | 1 | a0001c0001t0001g0059 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-47-741A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120277877 | ||||||
chr2:120277900
|
CGT | C | 3 | a0001c0001t0002g0015a0001c0001t0002g0193a0001c0001t0007g0015 | 5 | NA18990.hp1 NA18994.hp1 NA19001.hp1 others(2): Show |
intron_variant | MODIFIER | c.-47-710_-47-709del others(2): Show |
RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr2 | 120277900 | |||||
chr2:120277920
|
A | G | 1 | a0001c0001t0001g0148 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-47-698A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120277920 | ||||||
chr2:120277928
|
C | A | 1 | a0001c0001t0001g0071 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-47-690C>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120277928 | ||||||
chr2:120277947
|
A | ATG | 158 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(155): Show | 223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.-47-666_-47-665dup others(2): Show |
RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr2 | 120277947 | |||||
chr2:120277976
|
T | G | 85 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(82): Show | 126 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.-47-642T>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120277976 | ||||||
chr2:120277984
|
T | C | 1 | a0001c0001t0001g0059 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-47-634T>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120277984 | ||||||
chr2:120278000
|
C | T | 1 | a0001c0001t0002g0192 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-47-618C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120278000 | ||||||
chr2:120278036
|
C | CGT | 153 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(150): Show | 213 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.-47-580_-47-579dup others(2): Show |
RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr2 | 120278036 | |||||
chr2:120278038
|
TGA | T | 6 | a0001c0001t0001g0138a0001c0001t0005g0005a0001c0001t0005g0100others(3): Show | 11 | HG01884.hp2 HG02109.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.-47-578_-47-577del others(2): Show |
RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr2 | 120278038 | |||||
chr2:120278347
|
AC | A | 3 | a0001c0001t0001g0033a0001c0001t0001g0133a0001c0001t0001g0134 | 4 | HG02071.hp2 HG02074.hp1 HG02165.hp1 others(1): Show |
intron_variant | MODIFIER | c.-47-270delC | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120278347 | ||||||
chr2:120278348
|
CT | C | 156 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(153): Show | 220 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.-47-269delT | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120278348 | ||||||
chr2:120278449
|
G | C | 12 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0002t0001g0012others(9): Show | 16 | HG00099.hp2 HG00280.hp1 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.-47-169G>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120278449 | ||||||
chr2:120278476
|
A | G | 1 | a0001c0001t0002g0210 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-47-142A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120278476 | ||||||
chr2:120278482
|
G | A | 1 | a0001c0001t0003g0049 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-47-136G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120278482 | ||||||
chr2:120278483
|
C | T | 1 | a0001c0001t0002g0042 | 2 | NA18946.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.-47-135C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120278483 | ||||||
chr2:120278587
|
G | A | 1 | a0001c0001t0002g0038 | 2 | HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-47-31G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120278587 | ||||||
chr2:120278591
|
C | G | 1 | a0001c0001t0001g0225 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-47-27C>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 1/4 | chr2 | 120278591 | ||||||
chr2:120278800
|
C | T | 1 | a0001c0001t0002g0202 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.114+22C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120278800 | ||||||
chr2:120278809
|
T | G | 159 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(156): Show | 224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.114+31T>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120278809 | ||||||
chr2:120278810
|
T | A | 159 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(156): Show | 224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.114+32T>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120278810 | ||||||
chr2:120278983
|
C | T | 18 | a0001c0001t0002g0003a0001c0001t0002g0024a0001c0001t0002g0041others(15): Show | 32 | HG00673.hp1 HG00673.hp2 HG01433.hp2 others(29): Show |
intron_variant | MODIFIER | c.114+205C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120278983 | ||||||
chr2:120278996
|
G | A | 1 | a0001c0001t0001g0125 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.114+218G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120278996 | ||||||
chr2:120279001
|
C | T | 25 | a0001c0001t0001g0007a0001c0001t0001g0018a0001c0001t0001g0031others(22): Show | 32 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(29): Show |
intron_variant | MODIFIER | c.114+223C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120279001 | ||||||
chr2:120279022
|
T | C | 1 | a0001c0001t0002g0043 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.114+244T>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120279022 | ||||||
chr2:120279085
|
T | G | 5 | a0001c0001t0006g0025a0001c0001t0006g0051a0001c0001t0006g0052others(2): Show | 6 | HG00639.hp2 HG01243.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.114+307T>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120279085 | ||||||
chr2:120279325
|
C | T | 3 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0057 | 3 | HG02109.hp2 HG02622.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.114+547C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120279325 | ||||||
chr2:120279353
|
G | C | 1 | a0001c0001t0002g0036 | 2 | HG01168.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.114+575G>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120279353 | ||||||
chr2:120279353
|
G | T | 2 | a0001c0001t0003g0069a0001c0001t0003g0072 | 2 | HG02165.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.114+575G>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120279353 | ||||||
chr2:120279442
|
A | G | 85 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(82): Show | 126 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.114+664A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120279442 | ||||||
chr2:120279486
|
C | G | 1 | a0001c0001t0002g0201 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.114+708C>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120279486 | ||||||
chr2:120279622
|
T | C | 74 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0030others(71): Show | 98 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(95): Show |
intron_variant | MODIFIER | c.114+844T>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120279622 | ||||||
chr2:120279657
|
A | C | 159 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(156): Show | 224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.114+879A>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120279657 | ||||||
chr2:120279703
|
CA | C | 74 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0030others(71): Show | 98 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(95): Show |
intron_variant | MODIFIER | c.114+926delA | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120279703 | ||||||
chr2:120279707
|
G | A | 1 | a0001c0001t0001g0155 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.114+929G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120279707 | ||||||
chr2:120279799
|
A | G | 1 | a0001c0001t0001g0060 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.114+1021A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120279799 | ||||||
chr2:120279954
|
T | G | 74 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0030others(71): Show | 98 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(95): Show |
intron_variant | MODIFIER | c.114+1176T>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120279954 | ||||||
chr2:120280075
|
T | C | 74 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0030others(71): Show | 98 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(95): Show |
intron_variant | MODIFIER | c.114+1297T>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120280075 | ||||||
chr2:120280080
|
C | T | 74 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0030others(71): Show | 98 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(95): Show |
intron_variant | MODIFIER | c.114+1302C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120280080 | ||||||
chr2:120280221
|
C | A | 10 | a0001c0001t0001g0030a0001c0001t0001g0055a0001c0001t0001g0056others(7): Show | 11 | HG02109.hp2 HG02451.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.114+1443C>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120280221 | ||||||
chr2:120280506
|
C | T | 1 | a0001c0001t0001g0147 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.114+1728C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120280506 | ||||||
chr2:120280508
|
C | T | 4 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0047others(1): Show | 4 | HG02257.hp1 HG02486.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.114+1730C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120280508 | ||||||
chr2:120280543
|
C | A | 1 | a0001c0001t0001g0082 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.114+1765C>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120280543 | ||||||
chr2:120280668
|
A | G | 1 | a0001c0001t0001g0170 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.114+1890A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120280668 | ||||||
chr2:120280714
|
GA | G | 158 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(155): Show | 223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.114+1949delA | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr2 | 120280714 | |||||
chr2:120280774
|
C | G | 1 | a0001c0001t0002g0197 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.114+1996C>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120280774 | ||||||
chr2:120280774
|
CAA | C | 27 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0035others(24): Show | 38 | HG00609.hp1 HG01081.hp1 HG01928.hp2 others(35): Show |
intron_variant | MODIFIER | c.114+1999_114+2000d others(4): Show |
RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr2 | 120280774 | |||||
chr2:120280982
|
G | GT | 74 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0030others(71): Show | 98 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(95): Show |
intron_variant | MODIFIER | c.114+2212dupT | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr2 | 120280982 | |||||
chr2:120281035
|
C | T | 85 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(82): Show | 126 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.114+2257C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120281035 | ||||||
chr2:120281093
|
C | T | 1 | a0001c0001t0002g0200 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.114+2315C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120281093 | ||||||
chr2:120281198
|
T | C | 4 | a0001c0001t0002g0010a0001c0001t0002g0194a0001c0001t0002g0214others(1): Show | 8 | NA18944.hp1 NA18955.hp1 NA18964.hp1 others(5): Show |
intron_variant | MODIFIER | c.114+2420T>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120281198 | ||||||
chr2:120281241
|
C | T | 1 | a0001c0001t0002g0181 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.114+2463C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120281241 | ||||||
chr2:120281261
|
G | C | 5 | a0001c0001t0006g0025a0001c0001t0006g0051a0001c0001t0006g0052others(2): Show | 6 | HG00639.hp2 HG01243.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.114+2483G>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120281261 | ||||||
chr2:120281302
|
C | T | 1 | a0001c0002t0001g0085 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.114+2524C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120281302 | ||||||
chr2:120281324
|
C | T | 1 | a0001c0001t0001g0137 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.114+2546C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120281324 | ||||||
chr2:120281687
|
G | A | 159 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(156): Show | 224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.114+2909G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120281687 | ||||||
chr2:120281732
|
T | G | 159 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(156): Show | 224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.114+2954T>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120281732 | ||||||
chr2:120281816
|
G | C | 158 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(155): Show | 223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.114+3038G>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120281816 | ||||||
chr2:120281818
|
G | C | 1 | a0001c0001t0001g0105 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.114+3040G>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120281818 | ||||||
chr2:120281890
|
G | C | 12 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0002t0001g0012others(9): Show | 16 | HG00099.hp2 HG00280.hp1 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.114+3112G>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120281890 | ||||||
chr2:120281997
|
C | T | 4 | a0001c0001t0001g0011a0001c0001t0001g0050a0001c0001t0001g0067others(1): Show | 7 | NA18948.hp1 NA18982.hp1 NA18995.hp2 others(4): Show |
intron_variant | MODIFIER | c.114+3219C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120281997 | ||||||
chr2:120282137
|
G | A | 10 | a0001c0001t0001g0030a0001c0001t0001g0055a0001c0001t0001g0056others(7): Show | 11 | HG02109.hp2 HG02451.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.114+3359G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120282137 | ||||||
chr2:120282176
|
C | T | 1 | a0001c0001t0001g0160 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.114+3398C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120282176 | ||||||
chr2:120282342
|
G | A | 5 | a0001c0001t0005g0005a0001c0001t0005g0100a0001c0001t0005g0101others(2): Show | 10 | HG01884.hp2 HG02109.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.115-3532G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120282342 | ||||||
chr2:120282392
|
C | T | 5 | a0001c0001t0006g0025a0001c0001t0006g0051a0001c0001t0006g0052others(2): Show | 6 | HG00639.hp2 HG01243.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.115-3482C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120282392 | ||||||
chr2:120282432
|
C | T | 1 | a0001c0001t0002g0184 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.115-3442C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120282432 | ||||||
chr2:120282478
|
CA | C | 73 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0030others(70): Show | 97 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(94): Show |
intron_variant | MODIFIER | c.115-3385delA | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr2 | 120282478 | |||||
chr2:120282518
|
C | T | 1 | a0001c0001t0001g0122 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.115-3356C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120282518 | ||||||
chr2:120282564
|
A | AG | 9 | a0001c0001t0001g0133a0001c0001t0001g0145a0001c0001t0002g0040others(6): Show | 10 | HG01261.hp1 HG02074.hp1 HG02080.hp1 others(7): Show |
intron_variant | MODIFIER | c.115-3304dupG | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr2 | 120282564 | |||||
chr2:120282609
|
G | T | 1 | a0001c0001t0002g0207 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.115-3265G>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120282609 | ||||||
chr2:120282816
|
A | C | 17 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0005g0005others(14): Show | 26 | HG00099.hp2 HG00280.hp1 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.115-3058A>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120282816 | ||||||
chr2:120282822
|
G | T | 1 | a0001c0001t0001g0121 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.115-3052G>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120282822 | ||||||
chr2:120283104
|
G | A | 1 | a0001c0001t0002g0208 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.115-2770G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120283104 | ||||||
chr2:120283142
|
C | T | 1 | a0001c0001t0001g0136 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.115-2732C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120283142 | ||||||
chr2:120283143
|
T | G | 12 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0002t0001g0012others(9): Show | 16 | HG00099.hp2 HG00280.hp1 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.115-2731T>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120283143 | ||||||
chr2:120283427
|
C | G | 1 | a0001c0001t0001g0057 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.115-2447C>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120283427 | ||||||
chr2:120283458
|
G | T | 74 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0030others(71): Show | 98 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(95): Show |
intron_variant | MODIFIER | c.115-2416G>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120283458 | ||||||
chr2:120283575
|
G | A | 1 | a0001c0001t0001g0074 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.115-2299G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120283575 | ||||||
chr2:120283586
|
C | A | 21 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0047others(18): Show | 30 | HG00099.hp2 HG00280.hp1 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.115-2288C>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120283586 | ||||||
chr2:120283738
|
A | G | 154 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(151): Show | 214 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.115-2136A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120283738 | ||||||
chr2:120283771
|
A | C | 159 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(156): Show | 224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.115-2103A>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120283771 | ||||||
chr2:120283898
|
A | T | 1 | a0001c0002t0001g0146 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.115-1976A>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120283898 | ||||||
chr2:120284220
|
T | C | 5 | a0001c0001t0005g0005a0001c0001t0005g0100a0001c0001t0005g0101others(2): Show | 10 | HG01884.hp2 HG02109.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.115-1654T>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120284220 | ||||||
chr2:120284274
|
C | T | 1 | a0001c0001t0001g0151 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.115-1600C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120284274 | ||||||
chr2:120284403
|
AT | A | 154 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(151): Show | 218 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.115-1459delT | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr2 | 120284403 | |||||
chr2:120284416
|
G | A | 1 | a0001c0001t0001g0166 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.115-1458G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120284416 | ||||||
chr2:120284578
|
T | G | 2 | a0001c0001t0001g0019a0001c0001t0001g0126 | 4 | HG00099.hp1 HG00323.hp1 HG01074.hp2 others(1): Show |
intron_variant | MODIFIER | c.115-1296T>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120284578 | ||||||
chr2:120284634
|
A | T | 10 | a0001c0001t0004g0028a0001c0001t0004g0048a0001c0001t0004g0087others(7): Show | 11 | HG00735.hp1 HG02451.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.115-1240A>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120284634 | ||||||
chr2:120284684
|
T | G | 5 | a0001c0001t0006g0025a0001c0001t0006g0051a0001c0001t0006g0052others(2): Show | 6 | HG00639.hp2 HG01243.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.115-1190T>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120284684 | ||||||
chr2:120284755
|
C | A | 1 | a0001c0001t0001g0032 | 2 | HG02630.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.115-1119C>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120284755 | ||||||
chr2:120284757
|
A | C | 1 | a0001c0001t0001g0032 | 2 | HG02630.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.115-1117A>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120284757 | ||||||
chr2:120284758
|
AC | A | 191 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(188): Show | 281 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(278): Show |
intron_variant | MODIFIER | c.115-1114delC | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr2 | 120284758 | |||||
chr2:120284759
|
C | A | 1 | a0001c0001t0001g0032 | 2 | HG02630.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.115-1115C>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120284759 | ||||||
chr2:120284782
|
C | T | 3 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0047 | 3 | HG02257.hp1 HG02486.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.115-1092C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120284782 | ||||||
chr2:120284965
|
C | T | 1 | a0001c0001t0002g0196 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.115-909C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120284965 | ||||||
chr2:120284969
|
C | T | 4 | a0001c0002t0001g0027a0001c0002t0001g0077a0001c0002t0001g0078others(1): Show | 5 | HG00738.hp1 HG01070.hp1 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.115-905C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120284969 | ||||||
chr2:120285270
|
G | A | 11 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0002t0001g0012others(8): Show | 15 | HG00099.hp2 HG00280.hp1 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.115-604G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120285270 | ||||||
chr2:120285270
|
G | GC | 5 | a0001c0001t0005g0005a0001c0001t0005g0100a0001c0001t0005g0101others(2): Show | 10 | HG01884.hp2 HG02109.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.115-599dupC | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr2 | 120285270 | |||||
chr2:120285359
|
G | A | 2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | HG03017.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.115-515G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120285359 | ||||||
chr2:120285570
|
T | TAAAA | 141 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(138): Show | 197 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.115-301_115-298dup others(4): Show |
RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr2 | 120285570 | |||||
chr2:120285570
|
T | TAAAAA | 16 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0005g0005others(13): Show | 25 | HG00099.hp2 HG00280.hp1 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.115-302_115-298dup others(5): Show |
RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr2 | 120285570 | |||||
chr2:120285614
|
A | T | 157 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(154): Show | 222 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.115-260A>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120285614 | ||||||
chr2:120285827
|
G | A | 157 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(154): Show | 222 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.115-47G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120285827 | ||||||
chr2:120285853
|
C | T | 28 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0032others(25): Show | 40 | HG00609.hp1 HG01081.hp1 HG01928.hp2 others(37): Show |
intron_variant | MODIFIER | c.115-21C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 2/4 | chr2 | 120285853 | ||||||
chr2:120286138
|
A | G | 2 | a0001c0001t0001g0106a0001c0001t0001g0108 | 2 | HG00323.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.323+56A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 3/4 | chr2 | 120286138 | ||||||
chr2:120286337
|
G | A | 1 | a0001c0001t0001g0124 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.323+255G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 3/4 | chr2 | 120286337 | ||||||
chr2:120286570
|
C | T | 5 | a0001c0001t0006g0025a0001c0001t0006g0051a0001c0001t0006g0052others(2): Show | 6 | HG00639.hp2 HG01243.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.323+488C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 3/4 | chr2 | 120286570 | ||||||
chr2:120286573
|
G | C | 28 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0032others(25): Show | 40 | HG00609.hp1 HG01081.hp1 HG01928.hp2 others(37): Show |
intron_variant | MODIFIER | c.323+491G>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 3/4 | chr2 | 120286573 | ||||||
chr2:120286719
|
G | A | 2 | a0001c0001t0006g0052a0001c0001t0006g0053 | 2 | HG00639.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.323+637G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 3/4 | chr2 | 120286719 | ||||||
chr2:120286818
|
A | G | 1 | a0001c0001t0005g0101 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.323+736A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 3/4 | chr2 | 120286818 | ||||||
chr2:120286831
|
G | A | 5 | a0001c0001t0006g0025a0001c0001t0006g0051a0001c0001t0006g0052others(2): Show | 6 | HG00639.hp2 HG01243.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.323+749G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 3/4 | chr2 | 120286831 | ||||||
chr2:120286878
|
T | C | 157 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(154): Show | 222 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.323+796T>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 3/4 | chr2 | 120286878 | ||||||
chr2:120286917
|
A | C | 11 | a0001c0001t0004g0028a0001c0001t0004g0048a0001c0001t0004g0087others(8): Show | 13 | HG00735.hp1 HG01243.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.323+835A>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 3/4 | chr2 | 120286917 | ||||||
chr2:120286917
|
A | T | 1 | a0001c0001t0001g0059 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.323+835A>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 3/4 | chr2 | 120286917 | ||||||
chr2:120286945
|
T | G | 1 | a0001c0001t0001g0127 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.323+863T>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 3/4 | chr2 | 120286945 | ||||||
chr2:120286980
|
C | CA | 157 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(154): Show | 222 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.323+898_323+899ins others(1): Show |
RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 3/4 | chr2 | 120286980 | ||||||
chr2:120287008
|
A | C | 22 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0022others(19): Show | 32 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(29): Show |
intron_variant | MODIFIER | c.323+926A>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 3/4 | chr2 | 120287008 | ||||||
chr2:120287228
|
C | T | 1 | a0001c0001t0004g0087 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.323+1146C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 3/4 | chr2 | 120287228 | ||||||
chr2:120287230
|
C | T | 1 | a0001c0001t0001g0116 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.323+1148C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 3/4 | chr2 | 120287230 | ||||||
chr2:120287257
|
C | A | 1 | a0001c0001t0004g0089 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.323+1175C>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 3/4 | chr2 | 120287257 | ||||||
chr2:120287271
|
T | C | 11 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0002t0001g0012others(8): Show | 15 | HG00099.hp2 HG00280.hp1 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.323+1189T>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 3/4 | chr2 | 120287271 | ||||||
chr2:120287346
|
G | A | 11 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0002t0001g0012others(8): Show | 15 | HG00099.hp2 HG00280.hp1 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.323+1264G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 3/4 | chr2 | 120287346 | ||||||
chr2:120287397
|
T | C | 1 | a0001c0001t0002g0195 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.323+1315T>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 3/4 | chr2 | 120287397 | ||||||
chr2:120287478
|
G | A | 1 | a0001c0002t0001g0146 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.323+1396G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 3/4 | chr2 | 120287478 | ||||||
chr2:120287537
|
C | T | 11 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0002t0001g0012others(8): Show | 15 | HG00099.hp2 HG00280.hp1 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.323+1455C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 3/4 | chr2 | 120287537 | ||||||
chr2:120287553
|
C | T | 2 | a0001c0001t0002g0179a0001c0001t0002g0181 | 2 | HG03195.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.323+1471C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 3/4 | chr2 | 120287553 | ||||||
chr2:120287599
|
G | A | 1 | a0001c0001t0008g0029 | 2 | HG01243.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.323+1517G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 3/4 | chr2 | 120287599 | ||||||
chr2:120288083
|
C | G | 1 | a0001c0001t0001g0131 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.324-1497C>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 3/4 | chr2 | 120288083 | ||||||
chr2:120288197
|
C | T | 3 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0047 | 3 | HG02257.hp1 HG02486.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.324-1383C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 3/4 | chr2 | 120288197 | ||||||
chr2:120288308
|
G | A | 157 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(154): Show | 222 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.324-1272G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 3/4 | chr2 | 120288308 | ||||||
chr2:120288342
|
G | GTT | 27 | a0001c0001t0001g0030a0001c0001t0001g0055a0001c0001t0001g0057others(24): Show | 39 | HG00099.hp2 HG00280.hp1 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.324-1228_324-1227d others(4): Show |
RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr2 | 120288342 | |||||
chr2:120288342
|
G | GTTT | 41 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0032others(38): Show | 53 | HG00609.hp1 HG00741.hp2 HG01081.hp1 others(50): Show |
intron_variant | MODIFIER | c.324-1229_324-1227d others(5): Show |
RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr2 | 120288342 | |||||
chr2:120288342
|
G | GTTTT | 60 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(57): Show | 97 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.324-1230_324-1227d others(6): Show |
RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr2 | 120288342 | |||||
chr2:120288342
|
G | GTTTTT | 26 | a0001c0001t0001g0018a0001c0001t0001g0021a0001c0001t0001g0104others(23): Show | 30 | HG00280.hp2 HG00323.hp2 HG00609.hp2 others(27): Show |
intron_variant | MODIFIER | c.324-1231_324-1227d others(7): Show |
RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr2 | 120288342 | |||||
chr2:120288354
|
G | T | 159 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(156): Show | 225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.324-1226G>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 3/4 | chr2 | 120288354 | ||||||
chr2:120288431
|
C | T | 28 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0032others(25): Show | 40 | HG00609.hp1 HG01081.hp1 HG01928.hp2 others(37): Show |
intron_variant | MODIFIER | c.324-1149C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 3/4 | chr2 | 120288431 | ||||||
chr2:120288477
|
G | A | 1 | a0001c0001t0001g0076 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.324-1103G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 3/4 | chr2 | 120288477 | ||||||
chr2:120288540
|
C | G | 157 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(154): Show | 222 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.324-1040C>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 3/4 | chr2 | 120288540 | ||||||
chr2:120288701
|
C | T | 7 | a0001c0001t0004g0028a0001c0001t0004g0088a0001c0001t0004g0089others(4): Show | 8 | HG00735.hp1 HG02451.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.324-879C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 3/4 | chr2 | 120288701 | ||||||
chr2:120288857
|
C | T | 1 | a0001c0001t0002g0194 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-723C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 3/4 | chr2 | 120288857 | ||||||
chr2:120288977
|
C | T | 1 | a0001c0001t0002g0211 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.324-603C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 3/4 | chr2 | 120288977 | ||||||
chr2:120288997
|
T | C | 157 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(154): Show | 222 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.324-583T>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 3/4 | chr2 | 120288997 | ||||||
chr2:120289048
|
G | C | 3 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0010g0198 | 3 | NA18994.hp2 NA19077.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.324-532G>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 3/4 | chr2 | 120289048 | ||||||
chr2:120289109
|
A | G | 3 | a0001c0001t0004g0088a0001c0001t0004g0089a0001c0001t0004g0091 | 3 | HG02559.hp1 HG02615.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.324-471A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 3/4 | chr2 | 120289109 | ||||||
chr2:120289238
|
C | CT | 5 | a0001c0001t0001g0047a0001c0001t0001g0050a0001c0001t0001g0059others(2): Show | 5 | HG02486.hp1 HG03486.hp2 NA18948.hp1 others(2): Show |
intron_variant | MODIFIER | c.324-337dupT | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr2 | 120289238 | |||||
chr2:120289238
|
C | CTT | 5 | a0001c0001t0005g0005a0001c0001t0005g0100a0001c0001t0005g0101others(2): Show | 10 | HG01884.hp2 HG02109.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.324-338_324-337dup others(2): Show |
RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr2 | 120289238 | |||||
chr2:120289243
|
TG | T | 18 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0004g0028others(15): Show | 24 | HG00099.hp2 HG00280.hp1 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.324-336delG | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 3/4 | chr2 | 120289243 | ||||||
chr2:120289244
|
G | T | 52 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0030others(49): Show | 71 | HG00609.hp1 HG00639.hp2 HG01081.hp1 others(68): Show |
intron_variant | MODIFIER | c.324-336G>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 3/4 | chr2 | 120289244 | ||||||
chr2:120289244
|
GT | G | 83 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(80): Show | 123 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.324-325delT | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr2 | 120289244 | |||||
chr2:120289254
|
T | G | 12 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0004g0087others(9): Show | 16 | HG00099.hp2 HG00280.hp1 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.324-326T>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 3/4 | chr2 | 120289254 | ||||||
chr2:120289313
|
C | CACTT | 157 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(154): Show | 222 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.324-266_324-263dup others(4): Show |
RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr2 | 120289313 | |||||
chr2:120289534
|
G | A | 1 | a0001c0001t0008g0029 | 2 | HG01243.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.324-46G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 3/4 | chr2 | 120289534 | ||||||
chr2:120289941
|
C | T | 3 | a0001c0001t0004g0028a0001c0001t0004g0092a0001c0001t0004g0093 | 4 | HG02451.hp1 HG02723.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.501+184C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 4/4 | chr2 | 120289941 | ||||||
chr2:120289999
|
TG | T | 18 | a0001c0001t0001g0059a0001c0001t0001g0082a0001c0001t0001g0083others(15): Show | 28 | HG00099.hp2 HG00280.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.501+243delG | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 4/4 | chr2 | 120289999 | ||||||
chr2:120290099
|
A | G | 124 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(121): Show | 177 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.501+342A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 4/4 | chr2 | 120290099 | ||||||
chr2:120290163
|
G | A | 1 | a0001c0001t0002g0196 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.501+406G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 4/4 | chr2 | 120290163 | ||||||
chr2:120290273
|
G | A | 1 | a0001c0002t0001g0084 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.501+516G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 4/4 | chr2 | 120290273 | ||||||
chr2:120290287
|
C | T | 13 | a0001c0001t0001g0030a0001c0001t0001g0045a0001c0001t0001g0046others(10): Show | 14 | HG02109.hp2 HG02257.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.501+530C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 4/4 | chr2 | 120290287 | ||||||
chr2:120290353
|
G | C | 1 | a0001c0001t0001g0156 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.501+596G>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 4/4 | chr2 | 120290353 | ||||||
chr2:120290433
|
G | C | 1 | a0001c0001t0002g0183 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.501+676G>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 4/4 | chr2 | 120290433 | ||||||
chr2:120290434
|
C | G | 1 | a0001c0001t0002g0183 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.501+677C>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 4/4 | chr2 | 120290434 | ||||||
chr2:120290435
|
G | A | 5 | a0001c0001t0005g0005a0001c0001t0005g0100a0001c0001t0005g0101others(2): Show | 10 | HG01884.hp2 HG02109.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.501+678G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 4/4 | chr2 | 120290435 | ||||||
chr2:120290626
|
G | T | 3 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0047 | 3 | HG02257.hp1 HG02486.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.501+869G>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 4/4 | chr2 | 120290626 | ||||||
chr2:120290632
|
C | CT | 7 | a0001c0001t0001g0120a0001c0001t0001g0142a0001c0001t0002g0193others(4): Show | 8 | HG00639.hp2 HG01074.hp1 HG01928.hp2 others(5): Show |
intron_variant | MODIFIER | c.501+887dupT | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 120290632 | |||||
chr2:120290632
|
C | CTT | 128 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(125): Show | 186 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.501+886_501+887dup others(2): Show |
RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 120290632 | |||||
chr2:120290632
|
C | CTTT | 12 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0099others(9): Show | 16 | HG00099.hp2 HG00280.hp1 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.501+885_501+887dup others(3): Show |
RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 120290632 | |||||
chr2:120290632
|
C | CTTTT | 11 | a0001c0001t0004g0028a0001c0001t0004g0048a0001c0001t0004g0087others(8): Show | 13 | HG00735.hp1 HG01243.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.501+884_501+887dup others(4): Show |
RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 120290632 | |||||
chr2:120290830
|
G | T | 1 | a0001c0001t0003g0065 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.501+1073G>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 4/4 | chr2 | 120290830 | ||||||
chr2:120291136
|
T | C | 157 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(154): Show | 222 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.501+1379T>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 4/4 | chr2 | 120291136 | ||||||
chr2:120291276
|
A | T | 3 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0057 | 3 | HG02109.hp2 HG02622.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.501+1519A>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 4/4 | chr2 | 120291276 | ||||||
chr2:120291302
|
C | T | 74 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0030others(71): Show | 99 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(96): Show |
intron_variant | MODIFIER | c.501+1545C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 4/4 | chr2 | 120291302 | ||||||
chr2:120291500
|
G | A | 1 | a0001c0001t0001g0112 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.502-1641G>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 4/4 | chr2 | 120291500 | ||||||
chr2:120291502
|
G | T | 3 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0057 | 3 | HG02109.hp2 HG02622.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.502-1639G>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 4/4 | chr2 | 120291502 | ||||||
chr2:120291590
|
G | T | 157 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(154): Show | 222 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.502-1551G>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 4/4 | chr2 | 120291590 | ||||||
chr2:120291635
|
G | T | 1 | a0001c0001t0002g0199 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.502-1506G>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 4/4 | chr2 | 120291635 | ||||||
chr2:120291878
|
C | T | 1 | a0001c0001t0006g0051 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.502-1263C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 4/4 | chr2 | 120291878 | ||||||
chr2:120292029
|
C | G | 1 | a0001c0001t0001g0064 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.502-1112C>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 4/4 | chr2 | 120292029 | ||||||
chr2:120292037
|
G | T | 33 | a0001c0001t0001g0059a0001c0001t0001g0082a0001c0001t0001g0083others(30): Show | 45 | HG00099.hp2 HG00280.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.502-1104G>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 4/4 | chr2 | 120292037 | ||||||
chr2:120292515
|
C | T | 1 | a0001c0002t0001g0086 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.502-626C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 4/4 | chr2 | 120292515 | ||||||
chr2:120292560
|
T | C | 1 | a0001c0001t0001g0064 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.502-581T>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 4/4 | chr2 | 120292560 | ||||||
chr2:120292598
|
C | T | 1 | a0001c0001t0002g0215 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.502-543C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 4/4 | chr2 | 120292598 | ||||||
chr2:120292790
|
T | A | 28 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0020others(25): Show | 43 | HG00609.hp2 HG01123.hp1 HG01255.hp2 others(40): Show |
intron_variant | MODIFIER | c.502-351T>A | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 4/4 | chr2 | 120292790 | ||||||
chr2:120292803
|
A | G | 1 | a0001c0001t0001g0151 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.502-338A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 4/4 | chr2 | 120292803 | ||||||
chr2:120292830
|
C | T | 2 | a0001c0001t0001g0035a0001c0001t0013g0035 | 2 | NA18954.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.502-311C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 4/4 | chr2 | 120292830 | ||||||
chr2:120292839
|
T | C | 5 | a0001c0001t0005g0005a0001c0001t0005g0100a0001c0001t0005g0101others(2): Show | 10 | HG01884.hp2 HG02109.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.502-302T>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 4/4 | chr2 | 120292839 | ||||||
chr2:120292848
|
C | T | 3 | a0001c0001t0001g0033a0001c0001t0001g0133a0001c0001t0001g0134 | 4 | HG02071.hp2 HG02074.hp1 HG02165.hp1 others(1): Show |
intron_variant | MODIFIER | c.502-293C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 4/4 | chr2 | 120292848 | ||||||
chr2:120292851
|
G | C | 4 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0167others(1): Show | 4 | HG00609.hp2 HG02040.hp2 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.502-290G>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 4/4 | chr2 | 120292851 | ||||||
chr2:120292861
|
G | T | 1 | a0001c0001t0002g0209 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.502-280G>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 4/4 | chr2 | 120292861 | ||||||
chr2:120292888
|
T | G | 1 | a0001c0001t0004g0048 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.502-253T>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 4/4 | chr2 | 120292888 | ||||||
chr2:120292984
|
A | G | 157 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(154): Show | 222 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.502-157A>G | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 4/4 | chr2 | 120292984 | ||||||
chr2:120293013
|
C | T | 2 | a0001c0001t0001g0138a0001c0001t0001g0155 | 2 | HG01496.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.502-128C>T | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 4/4 | chr2 | 120293013 | ||||||
chr2:120293022
|
T | C | 1 | a0001c0001t0001g0075 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.502-119T>C | RALB | ENSG00000144118.14 | transcript | ENST00000272519.10 | protein_coding | 4/4 | chr2 | 120293022 |