geneid | 5911 |
---|---|
ensemblid | ENSG00000125249.7 |
hgncid | 9861 |
symbol | RAP2A |
name | RAP2A, member of RAS oncogene family |
refseq_nuc | NM_021033.7 |
refseq_prot | NP_066361.1 |
ensembl_nuc | ENST00000245304.5 |
ensembl_prot | ENSP00000245304.3 |
mane_status | MANE Select |
chr | chr13 |
start | 97434169 |
end | 97469128 |
strand | + |
ver | v1.2 |
region | chr13:97434169-97469128 |
region5000 | chr13:97429169-97474128 |
regionname0 | RAP2A_chr13_97434169_97469128 |
regionname5000 | RAP2A_chr13_97429169_97474128 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 183 | 344 | 84 | 60 | 152 | 10 | 36 | 108 | RAP2A_chr13_97429169_97474128 | RAP2A | copy fasta | chr13 | 97429169 | 97474128 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/0 | 4989 | 86 | 12 | 12 | 50 | 4 | 7 | RAP2A_chr13_97429169_97474128 | RAP2A | copy fasta | chr13 | 97429169 | 97474128 |
t0002 | 0/0 | 4990 | 79 | 10 | 14 | 39 | 3 | 13 | RAP2A_chr13_97429169_97474128 | RAP2A | copy fasta | chr13 | 97429169 | 97474128 |
t0003 | 0/1 | 4990 | 73 | 5 | 16 | 37 | 3 | 11 | RAP2A_chr13_97429169_97474128 | RAP2A | copy fasta | chr13 | 97429169 | 97474128 |
t0004 | 0/0 | 4990 | 53 | 30 | 3 | 16 | 0 | 4 | RAP2A_chr13_97429169_97474128 | RAP2A | copy fasta | chr13 | 97429169 | 97474128 |
t0005 | 0/0 | 4989 | 10 | 5 | 1 | 4 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | copy fasta | chr13 | 97429169 | 97474128 |
t0006 | 0/0 | 4988 | 5 | 1 | 3 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | copy fasta | chr13 | 97429169 | 97474128 |
t0007 | 0/0 | 4989 | 4 | 3 | 1 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | copy fasta | chr13 | 97429169 | 97474128 |
t0008 | 0/0 | 4990 | 4 | 3 | 1 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | copy fasta | chr13 | 97429169 | 97474128 |
t0009 | 0/0 | 4990 | 4 | 0 | 4 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | copy fasta | chr13 | 97429169 | 97474128 |
t0010 | 0/0 | 4990 | 3 | 3 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | copy fasta | chr13 | 97429169 | 97474128 |
t0011 | 0/0 | 4990 | 3 | 2 | 1 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | copy fasta | chr13 | 97429169 | 97474128 |
t0012 | 0/0 | 4990 | 3 | 3 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | copy fasta | chr13 | 97429169 | 97474128 |
t0013 | 0/0 | 4990 | 2 | 0 | 0 | 2 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | copy fasta | chr13 | 97429169 | 97474128 |
t0014 | 0/0 | 4990 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | copy fasta | chr13 | 97429169 | 97474128 |
t0015 | 0/0 | 4989 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | copy fasta | chr13 | 97429169 | 97474128 |
t0016 | 0/0 | 4990 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | copy fasta | chr13 | 97429169 | 97474128 |
t0017 | 0/0 | 4990 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | copy fasta | chr13 | 97429169 | 97474128 |
t0018 | 0/0 | 4990 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | copy fasta | chr13 | 97429169 | 97474128 |
t0019 | 0/0 | 4989 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | copy fasta | chr13 | 97429169 | 97474128 |
t0020 | 0/0 | 4989 | 1 | 0 | 1 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | copy fasta | chr13 | 97429169 | 97474128 |
t0021 | 0/0 | 4990 | 1 | 0 | 0 | 0 | 0 | 1 | RAP2A_chr13_97429169_97474128 | RAP2A | copy fasta | chr13 | 97429169 | 97474128 |
t0022 | 0/0 | 4990 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | copy fasta | chr13 | 97429169 | 97474128 |
t0023 | 0/0 | 4990 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | copy fasta | chr13 | 97429169 | 97474128 |
t0024 | 0/0 | 4990 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | copy fasta | chr13 | 97429169 | 97474128 |
t0025 | 0/0 | 4990 | 1 | 0 | 1 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | copy fasta | chr13 | 97429169 | 97474128 |
t0026 | 0/0 | 4989 | 1 | 0 | 1 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | copy fasta | chr13 | 97429169 | 97474128 |
t0027 | 0/0 | 4990 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | copy fasta | chr13 | 97429169 | 97474128 |
t0028 | 0/0 | 4989 | 1 | 0 | 1 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | copy fasta | chr13 | 97429169 | 97474128 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 29 | 1 | 7 | 19 | 0 | 2 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0002 | 0/0 | 15 | 1 | 5 | 6 | 2 | 1 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0003 | 0/0 | 13 | 1 | 5 | 4 | 2 | 1 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0004 | 0/0 | 12 | 3 | 2 | 6 | 1 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0005 | 1/0 | 12 | 0 | 0 | 10 | 0 | 1 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0006 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0007 | 0/0 | 6 | 0 | 0 | 5 | 0 | 1 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0008 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0011 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0013 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0014 | 0/0 | 4 | 1 | 1 | 2 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0015 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0016 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0017 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0018 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0019 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0021 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0022 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0023 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0025 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0028 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0032 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0033 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0034 | 0/1 | 2 | 0 | 0 | 0 | 0 | 1 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0035 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0039 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0041 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0045 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0046 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 552 | 342 | 84 | 60 | 150 | 10 | 36 | RAP2A_chr13_97429169_97474128 | RAP2A | copy fasta | chr13 | 97429169 | 97474128 |
a0001c0002 | 0/0 | 552 | 2 | 0 | 0 | 2 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | copy fasta | chr13 | 97429169 | 97474128 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 5540 | 86 | 12 | 12 | 50 | 4 | 7 | RAP2A_chr13_97429169_97474128 | RAP2A | copy fasta | chr13 | 97429169 | 97474128 |
a0001c0001t0002 | 0/0 | 5541 | 79 | 10 | 14 | 39 | 3 | 13 | RAP2A_chr13_97429169_97474128 | RAP2A | copy fasta | chr13 | 97429169 | 97474128 |
a0001c0001t0003 | 0/1 | 5541 | 71 | 5 | 16 | 35 | 3 | 11 | RAP2A_chr13_97429169_97474128 | RAP2A | copy fasta | chr13 | 97429169 | 97474128 |
a0001c0001t0004 | 0/0 | 5541 | 53 | 30 | 3 | 16 | 0 | 4 | RAP2A_chr13_97429169_97474128 | RAP2A | copy fasta | chr13 | 97429169 | 97474128 |
a0001c0001t0005 | 0/0 | 5540 | 10 | 5 | 1 | 4 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | copy fasta | chr13 | 97429169 | 97474128 |
a0001c0001t0006 | 0/0 | 5539 | 5 | 1 | 3 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | copy fasta | chr13 | 97429169 | 97474128 |
a0001c0001t0007 | 0/0 | 5540 | 4 | 3 | 1 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | copy fasta | chr13 | 97429169 | 97474128 |
a0001c0001t0008 | 0/0 | 5541 | 4 | 3 | 1 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | copy fasta | chr13 | 97429169 | 97474128 |
a0001c0001t0009 | 0/0 | 5541 | 4 | 0 | 4 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | copy fasta | chr13 | 97429169 | 97474128 |
a0001c0001t0010 | 0/0 | 5541 | 3 | 3 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | copy fasta | chr13 | 97429169 | 97474128 |
a0001c0001t0011 | 0/0 | 5541 | 3 | 2 | 1 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | copy fasta | chr13 | 97429169 | 97474128 |
a0001c0001t0012 | 0/0 | 5541 | 3 | 3 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | copy fasta | chr13 | 97429169 | 97474128 |
a0001c0001t0013 | 0/0 | 5541 | 2 | 0 | 0 | 2 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | copy fasta | chr13 | 97429169 | 97474128 |
a0001c0001t0014 | 0/0 | 5541 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | copy fasta | chr13 | 97429169 | 97474128 |
a0001c0001t0015 | 0/0 | 5540 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | copy fasta | chr13 | 97429169 | 97474128 |
a0001c0001t0016 | 0/0 | 5541 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | copy fasta | chr13 | 97429169 | 97474128 |
a0001c0001t0017 | 0/0 | 5541 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | copy fasta | chr13 | 97429169 | 97474128 |
a0001c0001t0018 | 0/0 | 5541 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | copy fasta | chr13 | 97429169 | 97474128 |
a0001c0001t0019 | 0/0 | 5540 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | copy fasta | chr13 | 97429169 | 97474128 |
a0001c0001t0020 | 0/0 | 5540 | 1 | 0 | 1 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | copy fasta | chr13 | 97429169 | 97474128 |
a0001c0001t0021 | 0/0 | 5541 | 1 | 0 | 0 | 0 | 0 | 1 | RAP2A_chr13_97429169_97474128 | RAP2A | copy fasta | chr13 | 97429169 | 97474128 |
a0001c0001t0022 | 0/0 | 5541 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | copy fasta | chr13 | 97429169 | 97474128 |
a0001c0001t0023 | 0/0 | 5541 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | copy fasta | chr13 | 97429169 | 97474128 |
a0001c0001t0024 | 0/0 | 5541 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | copy fasta | chr13 | 97429169 | 97474128 |
a0001c0001t0025 | 0/0 | 5541 | 1 | 0 | 1 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | copy fasta | chr13 | 97429169 | 97474128 |
a0001c0001t0026 | 0/0 | 5540 | 1 | 0 | 1 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | copy fasta | chr13 | 97429169 | 97474128 |
a0001c0001t0027 | 0/0 | 5541 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | copy fasta | chr13 | 97429169 | 97474128 |
a0001c0001t0028 | 0/0 | 5540 | 1 | 0 | 1 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | copy fasta | chr13 | 97429169 | 97474128 |
a0001c0002t0003 | 0/0 | 5541 | 2 | 0 | 0 | 2 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | copy fasta | chr13 | 97429169 | 97474128 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 14 | 1 | 5 | 5 | 2 | 1 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0001g0004 | 0/0 | 11 | 3 | 1 | 6 | 1 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0001g0005 | 1/0 | 11 | 0 | 0 | 9 | 0 | 1 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0001g0016 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0001g0023 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0001g0045 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0001g0046 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0001g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0001g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0002g0003 | 0/0 | 12 | 1 | 5 | 3 | 2 | 1 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0002g0006 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0002g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0002g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0002g0011 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0002g0018 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0002g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0002g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0002g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0002g0028 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0002g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0003g0001 | 0/0 | 26 | 1 | 7 | 16 | 0 | 2 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0003g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0003g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0003g0021 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0003g0025 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0003g0032 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0003g0033 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0003g0034 | 0/1 | 2 | 0 | 0 | 0 | 0 | 1 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0003g0035 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0003g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0003g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0003g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0003g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0003g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0003g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0003g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0003g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0003g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0003g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0003g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0003g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0003g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0003g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0003g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0004g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0004g0007 | 0/0 | 6 | 0 | 0 | 5 | 0 | 1 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0004g0008 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0004g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0004g0014 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0004g0015 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0004g0022 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0004g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0004g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0004g0039 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0004g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0004g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0004g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0004g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0004g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0004g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0004g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0004g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0004g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0004g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0004g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0004g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0004g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0004g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0004g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0004g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0004g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0004g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0004g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0004g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0004g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0004g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0004g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0004g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0004g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0005g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0005g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0005g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0005g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0005g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0005g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0005g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0006g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0006g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0006g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0006g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0006g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0007g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0007g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0007g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0008g0041 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0008g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0009g0019 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0009g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0010g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0010g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0010g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0011g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0011g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0011g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0012g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0012g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0012g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0013g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0013g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0014g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0015g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0016g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0017g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0018g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0019g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0020g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0021g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0022g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0023g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0024g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0025g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0026g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0027g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0001t0028g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
a0001c0002t0003g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0002 | g0094 | EUR | GBR | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | FIN | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG00280 | hp2 | a0001 | c0001 | t0002 | g0003 | EUR | FIN | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG00408 | hp1 | a0001 | c0001 | t0003 | g0107 | EAS | CHS | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG00408 | hp2 | a0001 | c0001 | t0003 | g0126 | EAS | CHS | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG00423 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | CHS | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG00423 | hp2 | a0001 | c0001 | t0003 | g0119 | EAS | CHS | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0073 | EAS | CHS | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG00438 | hp2 | a0001 | c0001 | t0013 | g0001 | EAS | CHS | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG00544 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | CHS | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG00544 | hp2 | a0001 | c0001 | t0005 | g0013 | EAS | CHS | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG00558 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | CHS | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG00558 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | CHS | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG00609 | hp2 | a0001 | c0001 | t0004 | g0132 | EAS | CHS | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0050 | EAS | CHS | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG00639 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG00639 | hp2 | a0001 | c0001 | t0026 | g0108 | AMR | PUR | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG00642 | hp1 | a0001 | c0001 | t0006 | g0014 | AMR | PUR | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0011 | AMR | PUR | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | CHS | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG00673 | hp2 | a0001 | c0001 | t0003 | g0049 | EAS | CHS | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG00735 | hp2 | a0001 | c0001 | t0006 | g0142 | AMR | PUR | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG00741 | hp1 | a0001 | c0001 | t0003 | g0021 | AMR | PUR | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG00741 | hp2 | a0001 | c0001 | t0006 | g0123 | AMR | PUR | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG01069 | hp1 | a0001 | c0001 | t0003 | g0067 | AMR | PUR | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG01069 | hp2 | a0001 | c0001 | t0002 | g0027 | AMR | PUR | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG01070 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | PUR | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG01070 | hp2 | a0001 | c0001 | t0003 | g0021 | AMR | PUR | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0027 | AMR | PUR | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG01071 | hp2 | a0001 | c0001 | t0003 | g0021 | AMR | PUR | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG01081 | hp2 | a0001 | c0001 | t0002 | g0028 | AMR | PUR | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG01106 | hp1 | a0001 | c0001 | t0003 | g0139 | AMR | PUR | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG01106 | hp2 | a0001 | c0001 | t0025 | g0117 | AMR | PUR | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG01109 | hp1 | a0001 | c0001 | t0004 | g0039 | AMR | PUR | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG01109 | hp2 | a0001 | c0001 | t0004 | g0022 | AMR | PUR | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG01167 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG01175 | hp1 | a0001 | c0001 | t0002 | g0069 | AMR | PUR | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG01175 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG01192 | hp1 | a0001 | c0001 | t0007 | g0157 | AMR | PUR | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG01192 | hp2 | a0001 | c0001 | t0008 | g0041 | AMR | PUR | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG01243 | hp1 | a0001 | c0001 | t0005 | g0098 | AMR | PUR | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG01243 | hp2 | a0001 | c0001 | t0011 | g0147 | AMR | PUR | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG01261 | hp1 | a0001 | c0001 | t0002 | g0076 | AMR | CLM | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | CLM | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG01346 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG01346 | hp2 | a0001 | c0001 | t0003 | g0032 | AMR | CLM | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG01358 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | CLM | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG01358 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | CLM | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG01361 | hp1 | a0001 | c0001 | t0003 | g0109 | AMR | CLM | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG01361 | hp2 | a0001 | c0001 | t0020 | g0004 | AMR | CLM | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG01496 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | CLM | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0045 | EUR | IBS | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG01516 | hp2 | a0001 | c0001 | t0003 | g0033 | EUR | IBS | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG01884 | hp1 | a0001 | c0001 | t0006 | g0138 | AFR | ACB | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG01884 | hp2 | a0001 | c0001 | t0027 | g0140 | AFR | ACB | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG01891 | hp1 | a0001 | c0001 | t0004 | g0039 | AFR | ACB | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG01891 | hp2 | a0001 | c0001 | t0010 | g0163 | AFR | ACB | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG01928 | hp1 | a0001 | c0001 | t0009 | g0019 | AMR | PEL | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG01934 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | PEL | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG01943 | hp1 | a0001 | c0001 | t0009 | g0120 | AMR | PEL | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG01952 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | PEL | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG01975 | hp2 | a0001 | c0001 | t0028 | g0017 | AMR | PEL | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG01978 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG01981 | hp1 | a0001 | c0001 | t0004 | g0090 | AMR | PEL | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | PEL | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG02015 | hp1 | a0001 | c0001 | t0003 | g0127 | EAS | KHV | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | KHV | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG02027 | hp1 | a0001 | c0001 | t0014 | g0003 | EAS | KHV | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG02027 | hp2 | a0001 | c0001 | t0023 | g0137 | EAS | KHV | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG02040 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG02040 | hp2 | a0001 | c0001 | t0004 | g0007 | EAS | KHV | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG02055 | hp1 | a0001 | c0001 | t0005 | g0031 | AFR | ACB | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG02055 | hp2 | a0001 | c0001 | t0003 | g0088 | AFR | ACB | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG02056 | hp1 | a0001 | c0001 | t0004 | g0007 | EAS | KHV | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG02071 | hp1 | a0001 | c0001 | t0002 | g0075 | EAS | KHV | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | KHV | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG02074 | hp1 | a0001 | c0001 | t0004 | g0037 | EAS | KHV | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG02074 | hp2 | a0001 | c0001 | t0004 | g0135 | EAS | KHV | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG02080 | hp1 | a0001 | c0001 | t0003 | g0068 | EAS | KHV | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | KHV | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG02083 | hp1 | a0001 | c0001 | t0024 | g0112 | EAS | KHV | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | KHV | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG02132 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | KHV | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG02135 | hp2 | a0001 | c0001 | t0003 | g0114 | EAS | KHV | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG02148 | hp1 | a0001 | c0001 | t0003 | g0113 | AMR | PEL | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | CDX | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | CDX | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG02257 | hp1 | a0001 | c0001 | t0011 | g0057 | AFR | ACB | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG02257 | hp2 | a0001 | c0001 | t0004 | g0058 | AFR | ACB | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG02258 | hp1 | a0001 | c0001 | t0003 | g0001 | AFR | ACB | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | ACB | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG02273 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG02273 | hp2 | a0001 | c0001 | t0009 | g0019 | AMR | PEL | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG02280 | hp1 | a0001 | c0001 | t0011 | g0144 | AFR | ACB | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG02280 | hp2 | a0001 | c0001 | t0004 | g0141 | AFR | ACB | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG02293 | hp1 | a0001 | c0001 | t0003 | g0025 | AMR | PEL | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG02293 | hp2 | a0001 | c0001 | t0009 | g0019 | AMR | PEL | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | ACB | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | ACB | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | KHV | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG02602 | hp1 | a0001 | c0001 | t0003 | g0001 | SAS | PJL | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0018 | SAS | PJL | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | GWD | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG02615 | hp2 | a0001 | c0001 | t0004 | g0014 | AFR | GWD | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG02622 | hp1 | a0001 | c0001 | t0010 | g0102 | AFR | GWD | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG02622 | hp2 | a0001 | c0001 | t0002 | g0093 | AFR | GWD | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG02630 | hp1 | a0001 | c0001 | t0012 | g0166 | AFR | GWD | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG02630 | hp2 | a0001 | c0001 | t0004 | g0150 | AFR | GWD | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG02647 | hp1 | a0001 | c0001 | t0004 | g0042 | AFR | GWD | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG02647 | hp2 | a0001 | c0001 | t0005 | g0101 | AFR | GWD | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG02723 | hp1 | a0001 | c0001 | t0012 | g0165 | AFR | GWD | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG02723 | hp2 | a0001 | c0001 | t0004 | g0042 | AFR | GWD | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG02735 | hp1 | a0001 | c0001 | t0004 | g0133 | SAS | PJL | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG02735 | hp2 | a0001 | c0001 | t0003 | g0034 | SAS | PJL | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG02738 | hp1 | a0001 | c0001 | t0003 | g0115 | SAS | PJL | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG02809 | hp1 | a0001 | c0001 | t0004 | g0091 | AFR | GWD | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG02809 | hp2 | a0001 | c0001 | t0004 | g0089 | AFR | GWD | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG02886 | hp1 | a0001 | c0001 | t0004 | g0022 | AFR | GWD | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG02886 | hp2 | a0001 | c0001 | t0004 | g0008 | AFR | GWD | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG02895 | hp1 | a0001 | c0001 | t0002 | g0029 | AFR | GWD | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG02895 | hp2 | a0001 | c0001 | t0004 | g0153 | AFR | GWD | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG02896 | hp1 | a0001 | c0001 | t0004 | g0162 | AFR | GWD | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG02896 | hp2 | a0001 | c0001 | t0004 | g0038 | AFR | GWD | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG02897 | hp1 | a0001 | c0001 | t0004 | g0038 | AFR | GWD | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG02897 | hp2 | a0001 | c0001 | t0002 | g0029 | AFR | GWD | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG02922 | hp1 | a0001 | c0001 | t0003 | g0036 | AFR | ESN | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG02922 | hp2 | a0001 | c0001 | t0004 | g0156 | AFR | ESN | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG02965 | hp1 | a0001 | c0001 | t0004 | g0143 | AFR | ESN | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG02965 | hp2 | a0001 | c0001 | t0004 | g0015 | AFR | ESN | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG02976 | hp1 | a0001 | c0001 | t0022 | g0152 | AFR | ESN | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG02976 | hp2 | a0001 | c0001 | t0008 | g0043 | AFR | ESN | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG03017 | hp1 | a0001 | c0001 | t0003 | g0032 | SAS | PJL | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG03017 | hp2 | a0001 | c0001 | t0002 | g0018 | SAS | PJL | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG03041 | hp1 | a0001 | c0001 | t0004 | g0015 | AFR | GWD | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG03041 | hp2 | a0001 | c0001 | t0004 | g0008 | AFR | GWD | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG03098 | hp1 | a0001 | c0001 | t0004 | g0008 | AFR | MSL | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG03098 | hp2 | a0001 | c0001 | t0018 | g0164 | AFR | MSL | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG03130 | hp1 | a0001 | c0001 | t0004 | g0161 | AFR | ESN | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG03130 | hp2 | a0001 | c0001 | t0010 | g0103 | AFR | ESN | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG03139 | hp1 | a0001 | c0001 | t0004 | g0015 | AFR | ESN | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG03139 | hp2 | a0001 | c0001 | t0017 | g0151 | AFR | ESN | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG03195 | hp1 | a0001 | c0001 | t0019 | g0168 | AFR | ESN | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG03195 | hp2 | a0001 | c0001 | t0015 | g0100 | AFR | ESN | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG03209 | hp1 | a0001 | c0001 | t0004 | g0055 | AFR | MSL | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG03209 | hp2 | a0001 | c0001 | t0004 | g0096 | AFR | MSL | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG03239 | hp1 | a0001 | c0001 | t0003 | g0104 | SAS | PJL | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG03453 | hp1 | a0001 | c0001 | t0004 | g0008 | AFR | MSL | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG03453 | hp2 | a0001 | c0001 | t0004 | g0015 | AFR | MSL | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG03486 | hp2 | a0001 | c0001 | t0007 | g0158 | AFR | MSL | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG03490 | hp1 | a0001 | c0001 | t0002 | g0077 | SAS | PJL | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG03490 | hp2 | a0001 | c0001 | t0003 | g0035 | SAS | PJL | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0177 | SAS | PJL | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG03492 | hp2 | a0001 | c0001 | t0003 | g0035 | SAS | PJL | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG03516 | hp2 | a0001 | c0001 | t0004 | g0022 | AFR | ESN | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG03540 | hp1 | a0001 | c0001 | t0002 | g0092 | AFR | GWD | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG03579 | hp1 | a0001 | c0001 | t0004 | g0155 | AFR | MSL | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG03579 | hp2 | a0001 | c0001 | t0002 | g0080 | AFR | MSL | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0028 | SAS | PJL | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0175 | SAS | PJL | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG03669 | hp1 | a0001 | c0001 | t0003 | g0001 | SAS | PJL | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG03669 | hp2 | a0001 | c0001 | t0002 | g0084 | SAS | PJL | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0184 | SAS | STU | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG03688 | hp2 | a0001 | c0001 | t0003 | g0095 | SAS | STU | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0178 | SAS | PJL | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG03831 | hp1 | a0001 | c0001 | t0004 | g0013 | SAS | BEB | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0065 | SAS | BEB | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG03927 | hp1 | a0001 | c0001 | t0003 | g0106 | SAS | BEB | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG03927 | hp2 | a0001 | c0001 | t0004 | g0007 | SAS | BEB | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0018 | SAS | BEB | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG03942 | hp2 | a0001 | c0001 | t0004 | g0136 | SAS | BEB | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0051 | SAS | STU | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG04115 | hp2 | a0001 | c0001 | t0021 | g0086 | SAS | STU | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0187 | SAS | BEB | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0052 | SAS | BEB | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG04204 | hp1 | a0001 | c0001 | t0003 | g0033 | SAS | STU | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0079 | SAS | STU | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA18522 | hp1 | a0001 | c0001 | t0005 | g0030 | AFR | YRI | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | YRI | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0060 | EAS | CHB | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA18612 | hp2 | a0001 | c0001 | t0004 | g0007 | EAS | CHB | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA18747 | hp1 | a0001 | c0001 | t0004 | g0130 | EAS | CHB | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA18747 | hp2 | a0001 | c0001 | t0002 | g0062 | EAS | CHB | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA18906 | hp1 | a0001 | c0001 | t0008 | g0043 | AFR | YRI | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA18906 | hp2 | a0001 | c0001 | t0007 | g0017 | AFR | YRI | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA18939 | hp2 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA18941 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA18941 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA18942 | hp2 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA18944 | hp2 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA18945 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA18946 | hp2 | a0001 | c0001 | t0003 | g0160 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA18947 | hp1 | a0001 | c0001 | t0004 | g0044 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA18947 | hp2 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA18949 | hp1 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA18949 | hp2 | a0001 | c0001 | t0003 | g0025 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA18954 | hp1 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA18956 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA18956 | hp2 | a0001 | c0001 | t0003 | g0064 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA18959 | hp1 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA18959 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA18960 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA18960 | hp2 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA18963 | hp1 | a0001 | c0001 | t0004 | g0124 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA18965 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA18968 | hp2 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA18969 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA18973 | hp1 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA18975 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA18975 | hp2 | a0001 | c0001 | t0003 | g0125 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA18977 | hp1 | a0001 | c0001 | t0013 | g0110 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA18983 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA18985 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA18990 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA18993 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA18994 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA18998 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA18998 | hp2 | a0001 | c0001 | t0005 | g0013 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA18999 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA19000 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA19003 | hp1 | a0001 | c0001 | t0005 | g0128 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA19005 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA19010 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA19012 | hp1 | a0001 | c0001 | t0003 | g0116 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA19043 | hp1 | a0001 | c0001 | t0002 | g0070 | AFR | LWK | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA19043 | hp2 | a0001 | c0001 | t0016 | g0008 | AFR | LWK | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA19056 | hp1 | a0001 | c0001 | t0004 | g0014 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA19056 | hp2 | a0001 | c0001 | t0004 | g0131 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA19058 | hp1 | a0001 | c0001 | t0005 | g0044 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA19058 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA19060 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA19060 | hp2 | a0001 | c0001 | t0004 | g0129 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA19062 | hp1 | a0001 | c0001 | t0004 | g0037 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA19062 | hp2 | a0001 | c0001 | t0003 | g0066 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA19063 | hp1 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA19065 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA19067 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA19072 | hp2 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA19074 | hp1 | a0001 | c0001 | t0006 | g0024 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA19074 | hp2 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA19075 | hp1 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA19076 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA19076 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA19077 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA19077 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA19084 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA19084 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA19085 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA19086 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA19086 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA19088 | hp1 | a0001 | c0001 | t0003 | g0063 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA19088 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ASW | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA20129 | hp2 | a0001 | c0001 | t0012 | g0167 | AFR | ASW | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA20752 | hp1 | a0001 | c0001 | t0003 | g0118 | EUR | TSI | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA20805 | hp1 | a0001 | c0001 | t0003 | g0105 | EUR | TSI | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA20805 | hp2 | a0001 | c0001 | t0002 | g0003 | EUR | TSI | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0072 | SAS | GIH | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0122 | SAS | GIH | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | ACB | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG02109 | hp2 | a0001 | c0001 | t0007 | g0017 | AFR | ACB | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG02486 | hp1 | a0001 | c0001 | t0002 | g0078 | AFR | ACB | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG02486 | hp2 | a0001 | c0001 | t0004 | g0099 | AFR | ACB | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG02559 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | ACB | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG02559 | hp2 | a0001 | c0001 | t0002 | g0061 | AFR | ACB | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | MSL | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG03471 | hp2 | a0001 | c0001 | t0005 | g0031 | AFR | MSL | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG06807 | hp1 | a0001 | c0001 | t0002 | g0121 | AFR | USA | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
HG06807 | hp2 | a0001 | c0001 | t0005 | g0030 | AFR | USA | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA18955 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA18955 | hp2 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA20300 | hp1 | a0001 | c0001 | t0008 | g0041 | AFR | USA | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA20300 | hp2 | a0001 | c0001 | t0003 | g0036 | AFR | USA | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA21309 | hp1 | a0001 | c0001 | t0003 | g0111 | AFR | LWK | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | LWK | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0003 | g0034 | REF | REF | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0005 | REF | REF | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:97434740
|
C | T | 1 | a0001c0002 | 2 | NA18944.hp2 NA19072.hp2 |
synonymous_variant | LOW | c.270C>T | p.Phe90Phe | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/2 | 572/5540 | 270/552 | 90/183 | chr13 | 97434740 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:97434249
|
G | A | 1 | a0001c0001t0014 | 1 | HG02027.hp1 | 5_prime_UTR_variant | MODIFIER | c.-222G>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/2 | 222 | chr13 | 97434249 | |||||
chr13:97464501
|
C | T | 1 | a0001c0001t0012 | 3 | HG02630.hp1 HG02723.hp1 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*59C>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 2/2 | 59 | chr13 | 97464501 | |||||
chr13:97464506
|
A | C | 1 | a0001c0001t0028 | 1 | HG01975.hp2 | 3_prime_UTR_variant | MODIFIER | c.*64A>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 2/2 | 64 | chr13 | 97464506 | |||||
chr13:97464683
|
C | G | 1 | a0001c0001t0027 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*241C>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 2/2 | 241 | chr13 | 97464683 | |||||
chr13:97464910
|
A | G | 9 | a0001c0001t0002a0001c0001t0003a0001c0001t0009others(6): Show | 162 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(159): Show |
3_prime_UTR_variant | MODIFIER | c.*468A>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 2/2 | 468 | chr13 | 97464910 | |||||
chr13:97465535
|
G | A | 1 | a0001c0001t0010 | 3 | HG01891.hp2 HG02622.hp1 HG03130.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1093G>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 2/2 | 1093 | chr13 | 97465535 | |||||
chr13:97465680
|
C | G | 1 | a0001c0001t0023 | 1 | HG02027.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1238C>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 2/2 | 1238 | chr13 | 97465680 | |||||
chr13:97465698
|
T | C | 1 | a0001c0001t0023 | 1 | HG02027.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1256T>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 2/2 | 1256 | chr13 | 97465698 | |||||
chr13:97465704
|
A | G | 1 | a0001c0001t0023 | 1 | HG02027.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1262A>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 2/2 | 1262 | chr13 | 97465704 | |||||
chr13:97465709
|
G | A | 1 | a0001c0001t0023 | 1 | HG02027.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1267G>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 2/2 | 1267 | chr13 | 97465709 | |||||
chr13:97465710
|
C | G | 1 | a0001c0001t0023 | 1 | HG02027.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1268C>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 2/2 | 1268 | chr13 | 97465710 | |||||
chr13:97465712
|
C | G | 1 | a0001c0001t0023 | 1 | HG02027.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1270C>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 2/2 | 1270 | chr13 | 97465712 | |||||
chr13:97465716
|
C | G | 1 | a0001c0001t0023 | 1 | HG02027.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1274C>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 2/2 | 1274 | chr13 | 97465716 | |||||
chr13:97465718
|
C | T | 1 | a0001c0001t0023 | 1 | HG02027.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1276C>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 2/2 | 1276 | chr13 | 97465718 | |||||
chr13:97465726
|
T | A | 1 | a0001c0001t0023 | 1 | HG02027.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1284T>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 2/2 | 1284 | chr13 | 97465726 | |||||
chr13:97465727
|
T | G | 1 | a0001c0001t0023 | 1 | HG02027.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1285T>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 2/2 | 1285 | chr13 | 97465727 | |||||
chr13:97465732
|
T | A | 1 | a0001c0001t0023 | 1 | HG02027.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1290T>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 2/2 | 1290 | chr13 | 97465732 | |||||
chr13:97465733
|
T | G | 1 | a0001c0001t0023 | 1 | HG02027.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1291T>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 2/2 | 1291 | chr13 | 97465733 | |||||
chr13:97465734
|
T | G | 1 | a0001c0001t0023 | 1 | HG02027.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1292T>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 2/2 | 1292 | chr13 | 97465734 | |||||
chr13:97465735
|
C | T | 1 | a0001c0001t0023 | 1 | HG02027.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1293C>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 2/2 | 1293 | chr13 | 97465735 | |||||
chr13:97465736
|
A | C | 1 | a0001c0001t0023 | 1 | HG02027.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1294A>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 2/2 | 1294 | chr13 | 97465736 | |||||
chr13:97465745
|
A | C | 1 | a0001c0001t0023 | 1 | HG02027.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1303A>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 2/2 | 1303 | chr13 | 97465745 | |||||
chr13:97465752
|
T | C | 1 | a0001c0001t0023 | 1 | HG02027.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1310T>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 2/2 | 1310 | chr13 | 97465752 | |||||
chr13:97465753
|
A | C | 1 | a0001c0001t0023 | 1 | HG02027.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1311A>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 2/2 | 1311 | chr13 | 97465753 | |||||
chr13:97465756
|
A | T | 1 | a0001c0001t0023 | 1 | HG02027.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1314A>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 2/2 | 1314 | chr13 | 97465756 | |||||
chr13:97465757
|
T | A | 1 | a0001c0001t0023 | 1 | HG02027.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1315T>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 2/2 | 1315 | chr13 | 97465757 | |||||
chr13:97465780
|
A | C | 1 | a0001c0001t0023 | 1 | HG02027.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1338A>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 2/2 | 1338 | chr13 | 97465780 | |||||
chr13:97465784
|
C | T | 1 | a0001c0001t0023 | 1 | HG02027.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1342C>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 2/2 | 1342 | chr13 | 97465784 | |||||
chr13:97465791
|
A | T | 1 | a0001c0001t0023 | 1 | HG02027.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1349A>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 2/2 | 1349 | chr13 | 97465791 | |||||
chr13:97465798
|
T | G | 1 | a0001c0001t0023 | 1 | HG02027.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1356T>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 2/2 | 1356 | chr13 | 97465798 | |||||
chr13:97465822
|
T | A | 1 | a0001c0001t0023 | 1 | HG02027.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1380T>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 2/2 | 1380 | chr13 | 97465822 | |||||
chr13:97465830
|
C | A | 1 | a0001c0001t0023 | 1 | HG02027.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1388C>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 2/2 | 1388 | chr13 | 97465830 | |||||
chr13:97465836
|
T | C | 1 | a0001c0001t0023 | 1 | HG02027.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1394T>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 2/2 | 1394 | chr13 | 97465836 | |||||
chr13:97465853
|
A | G | 1 | a0001c0001t0013 | 2 | HG00438.hp2 NA18977.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1411A>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 2/2 | 1411 | chr13 | 97465853 | |||||
chr13:97465900
|
C | A | 1 | a0001c0001t0015 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1458C>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 2/2 | 1458 | chr13 | 97465900 | |||||
chr13:97466086
|
A | G | 1 | a0001c0001t0022 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1644A>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 2/2 | 1644 | chr13 | 97466086 | |||||
chr13:97466209
|
GA | G | 4 | a0001c0001t0005a0001c0001t0006a0001c0001t0015others(1): Show | 17 | HG00544.hp2 HG00639.hp2 HG00642.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*1781delA | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 2/2 | 1781 | INFO_REALIGN_3_PRIME | chr13 | 97466209 | ||||
chr13:97466290
|
C | T | 1 | a0001c0001t0027 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1848C>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 2/2 | 1848 | chr13 | 97466290 | |||||
chr13:97466451
|
T | C | 1 | a0001c0001t0016 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2009T>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 2/2 | 2009 | chr13 | 97466451 | |||||
chr13:97466675
|
T | C | 2 | a0001c0001t0017a0001c0001t0022 | 2 | HG02976.hp1 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2233T>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 2/2 | 2233 | chr13 | 97466675 | |||||
chr13:97466974
|
G | A | 1 | a0001c0001t0018 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2532G>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 2/2 | 2532 | chr13 | 97466974 | |||||
chr13:97467270
|
T | C | 3 | a0001c0001t0002a0001c0001t0009a0001c0001t0014 | 84 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(81): Show |
3_prime_UTR_variant | MODIFIER | c.*2828T>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 2/2 | 2828 | chr13 | 97467270 | |||||
chr13:97467588
|
AT | A | 3 | a0001c0001t0007a0001c0001t0019a0001c0001t0028 | 6 | HG01192.hp1 HG01975.hp2 HG02109.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3153delT | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 2/2 | 3153 | INFO_REALIGN_3_PRIME | chr13 | 97467588 | ||||
chr13:97467677
|
C | CT | 26 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(23): Show | 252 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(249): Show |
3_prime_UTR_variant | MODIFIER | c.*3246dupT | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 2/2 | 3247 | INFO_REALIGN_3_PRIME | chr13 | 97467677 | ||||
chr13:97467678
|
T | C | 1 | a0001c0001t0020 | 1 | HG01361.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3236T>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 2/2 | 3236 | chr13 | 97467678 | |||||
chr13:97467767
|
T | C | 1 | a0001c0001t0024 | 1 | HG02083.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3325T>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 2/2 | 3325 | chr13 | 97467767 | |||||
chr13:97467986
|
A | C | 1 | a0001c0001t0009 | 4 | HG01928.hp1 HG01943.hp1 HG02273.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3544A>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 2/2 | 3544 | chr13 | 97467986 | |||||
chr13:97468059
|
T | C | 1 | a0001c0001t0021 | 1 | HG04115.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3617T>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 2/2 | 3617 | chr13 | 97468059 | |||||
chr13:97468391
|
C | T | 2 | a0001c0001t0011a0001c0001t0027 | 4 | HG01243.hp2 HG01884.hp2 HG02257.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3949C>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 2/2 | 3949 | chr13 | 97468391 | |||||
chr13:97468394
|
A | T | 1 | a0001c0001t0008 | 4 | HG01192.hp2 HG02976.hp2 NA18906.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3952A>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 2/2 | 3952 | chr13 | 97468394 | |||||
chr13:97468461
|
A | T | 3 | a0001c0001t0007a0001c0001t0019a0001c0001t0028 | 6 | HG01192.hp1 HG01975.hp2 HG02109.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4019A>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 2/2 | 4019 | chr13 | 97468461 | |||||
chr13:97468551
|
G | A | 1 | a0001c0001t0025 | 1 | HG01106.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4109G>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 2/2 | 4109 | chr13 | 97468551 | |||||
chr13:97468962
|
C | T | 1 | a0001c0001t0019 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4520C>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 2/2 | 4520 | chr13 | 97468962 | |||||
chr13:97468993
|
G | A | 1 | a0001c0001t0019 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4551G>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 2/2 | 4551 | chr13 | 97468993 | |||||
chr13:97469117
|
T | G | 1 | a0001c0001t0018 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4675T>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 2/2 | 4675 | chr13 | 97469117 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:97434801
|
G | A | 1 | a0001c0001t0003g0049 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.314+17G>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97434801 | ||||||
chr13:97434842
|
T | C | 170 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0014others(167): Show | 280 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(277): Show |
intron_variant | MODIFIER | c.314+58T>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97434842 | ||||||
chr13:97434844
|
G | T | 1 | a0001c0001t0019g0168 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.314+60G>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97434844 | ||||||
chr13:97434911
|
A | G | 3 | a0001c0001t0012g0165a0001c0001t0012g0166a0001c0001t0012g0167 | 3 | HG02630.hp1 HG02723.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.314+127A>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97434911 | ||||||
chr13:97435183
|
A | C | 1 | a0001c0001t0018g0164 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.314+399A>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97435183 | ||||||
chr13:97435465
|
C | CA | 59 | a0001c0001t0001g0023a0001c0001t0001g0045a0001c0001t0001g0046others(56): Show | 107 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.314+703dupA | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 97435465 | |||||
chr13:97435465
|
C | CAA | 9 | a0001c0001t0002g0050a0001c0001t0002g0051a0001c0001t0002g0052others(6): Show | 10 | HG00558.hp1 HG00621.hp2 HG01975.hp2 others(7): Show |
intron_variant | MODIFIER | c.314+702_314+703dup others(2): Show |
RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 97435465 | |||||
chr13:97435465
|
CA | C | 9 | a0001c0001t0001g0016a0001c0001t0001g0185a0001c0001t0001g0186others(6): Show | 12 | HG01943.hp2 HG02148.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.314+703delA | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 97435465 | |||||
chr13:97435465
|
CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0010g0163 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.314+692_314+703del others(12): Show |
RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 97435465 | |||||
chr13:97435540
|
A | G | 1 | a0001c0001t0001g0159 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.314+756A>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97435540 | ||||||
chr13:97435641
|
G | A | 1 | a0001c0001t0003g0095 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.314+857G>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97435641 | ||||||
chr13:97435724
|
A | G | 1 | a0001c0001t0001g0184 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.314+940A>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97435724 | ||||||
chr13:97436268
|
T | TA | 6 | a0001c0001t0001g0097a0001c0001t0004g0008a0001c0001t0004g0058others(3): Show | 9 | HG02257.hp1 HG02257.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.314+1487dupA | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 97436268 | |||||
chr13:97436454
|
A | G | 1 | a0001c0001t0002g0056 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.314+1670A>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97436454 | ||||||
chr13:97436507
|
C | G | 6 | a0001c0001t0007g0017a0001c0001t0007g0157a0001c0001t0007g0158others(3): Show | 7 | HG01192.hp1 HG01975.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.314+1723C>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97436507 | ||||||
chr13:97436517
|
G | T | 1 | a0001c0001t0019g0168 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.314+1733G>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97436517 | ||||||
chr13:97436790
|
C | T | 1 | a0001c0001t0004g0156 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.314+2006C>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97436790 | ||||||
chr13:97436881
|
C | T | 1 | a0001c0001t0002g0094 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.314+2097C>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97436881 | ||||||
chr13:97436962
|
A | G | 6 | a0001c0001t0007g0017a0001c0001t0007g0157a0001c0001t0007g0158others(3): Show | 7 | HG01192.hp1 HG01975.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.314+2178A>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97436962 | ||||||
chr13:97436990
|
C | T | 4 | a0001c0001t0002g0092a0001c0001t0002g0093a0001c0001t0004g0091others(1): Show | 4 | HG02622.hp2 HG02809.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.314+2206C>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97436990 | ||||||
chr13:97436994
|
C | G | 1 | a0001c0001t0007g0158 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.314+2210C>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97436994 | ||||||
chr13:97437155
|
T | C | 1 | a0001c0001t0004g0096 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.314+2371T>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97437155 | ||||||
chr13:97437171
|
A | G | 2 | a0001c0001t0001g0048a0001c0001t0001g0183 | 3 | HG02132.hp1 NA18993.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.314+2387A>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97437171 | ||||||
chr13:97437383
|
ATGCT | A | 6 | a0001c0001t0004g0099a0001c0001t0005g0030a0001c0001t0005g0031others(3): Show | 8 | HG01243.hp1 HG02055.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.314+2605_314+2608d others(6): Show |
RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 97437383 | |||||
chr13:97437561
|
GT | G | 3 | a0001c0001t0010g0102a0001c0001t0010g0103a0001c0001t0010g0163 | 3 | HG01891.hp2 HG02622.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.314+2778delT | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97437561 | ||||||
chr13:97438510
|
AGACCTTA others(5): Show |
A | 2 | a0001c0001t0004g0044a0001c0001t0005g0044 | 2 | NA18947.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.314+3733_314+3744d others(14): Show |
RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 97438510 | |||||
chr13:97438695
|
C | T | 1 | a0001c0001t0001g0154 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.314+3911C>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97438695 | ||||||
chr13:97438754
|
T | C | 83 | a0001c0001t0001g0085a0001c0001t0002g0003a0001c0001t0002g0006others(80): Show | 156 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.314+3970T>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97438754 | ||||||
chr13:97438858
|
A | T | 1 | a0001c0001t0008g0043 | 2 | HG02976.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.314+4074A>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97438858 | ||||||
chr13:97439074
|
A | C | 1 | a0001c0001t0002g0094 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.314+4290A>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97439074 | ||||||
chr13:97439214
|
T | G | 1 | a0001c0001t0001g0183 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.314+4430T>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97439214 | ||||||
chr13:97439224
|
T | A | 3 | a0001c0001t0001g0169a0001c0001t0001g0172a0001c0001t0001g0173 | 3 | HG00673.hp1 NA18969.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.314+4440T>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97439224 | ||||||
chr13:97439364
|
G | A | 1 | a0001c0001t0002g0059 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.314+4580G>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97439364 | ||||||
chr13:97439425
|
G | GGAATGTT others(5): Show |
6 | a0001c0001t0007g0017a0001c0001t0007g0157a0001c0001t0007g0158others(3): Show | 7 | HG01192.hp1 HG01975.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.314+4647_314+4658d others(14): Show |
RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 97439425 | |||||
chr13:97439531
|
A | T | 1 | a0001c0001t0004g0042 | 2 | HG02647.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.314+4747A>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97439531 | ||||||
chr13:97439671
|
G | C | 1 | a0001c0001t0002g0060 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.314+4887G>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97439671 | ||||||
chr13:97439780
|
G | T | 3 | a0001c0001t0001g0047a0001c0001t0001g0181a0001c0001t0001g0182 | 4 | HG02258.hp2 HG02615.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.314+4996G>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97439780 | ||||||
chr13:97440129
|
CT | C | 17 | a0001c0001t0001g0013a0001c0001t0001g0134a0001c0001t0004g0007others(14): Show | 23 | HG00544.hp2 HG00609.hp2 HG02027.hp2 others(20): Show |
intron_variant | MODIFIER | c.314+5346delT | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97440129 | ||||||
chr13:97440209
|
G | A | 2 | a0001c0001t0003g0032a0001c0001t0003g0104 | 3 | HG01346.hp2 HG03017.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.314+5425G>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97440209 | ||||||
chr13:97440408
|
C | G | 1 | a0001c0001t0005g0101 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.314+5624C>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97440408 | ||||||
chr13:97440499
|
T | G | 4 | a0001c0001t0007g0017a0001c0001t0007g0157a0001c0001t0007g0158others(1): Show | 5 | HG01192.hp1 HG01975.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.314+5715T>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97440499 | ||||||
chr13:97440502
|
T | C | 1 | a0001c0001t0001g0087 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.314+5718T>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97440502 | ||||||
chr13:97440615
|
G | A | 6 | a0001c0001t0007g0017a0001c0001t0007g0157a0001c0001t0007g0158others(3): Show | 7 | HG01192.hp1 HG01975.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.314+5831G>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97440615 | ||||||
chr13:97440629
|
CT | C | 4 | a0001c0001t0007g0017a0001c0001t0007g0157a0001c0001t0007g0158others(1): Show | 5 | HG01192.hp1 HG01975.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.314+5852delT | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 97440629 | |||||
chr13:97440696
|
T | C | 1 | a0001c0001t0004g0161 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.314+5912T>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97440696 | ||||||
chr13:97440778
|
A | G | 1 | a0001c0001t0001g0085 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.314+5994A>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97440778 | ||||||
chr13:97440806
|
CCATT | C | 2 | a0001c0001t0008g0041a0001c0001t0008g0043 | 4 | HG01192.hp2 HG02976.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.314+6043_314+6046d others(6): Show |
RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 97440806 | |||||
chr13:97441172
|
G | A | 1 | a0001c0001t0019g0168 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.314+6388G>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97441172 | ||||||
chr13:97441172
|
G | C | 1 | a0001c0001t0002g0050 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.314+6388G>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97441172 | ||||||
chr13:97441618
|
T | G | 1 | a0001c0001t0001g0172 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.314+6834T>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97441618 | ||||||
chr13:97441752
|
C | T | 1 | a0001c0001t0019g0168 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.314+6968C>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97441752 | ||||||
chr13:97441767
|
G | A | 1 | a0001c0001t0005g0128 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.314+6983G>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97441767 | ||||||
chr13:97441832
|
G | A | 1 | a0001c0001t0003g0105 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.314+7048G>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97441832 | ||||||
chr13:97442314
|
T | C | 1 | a0001c0001t0004g0161 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.314+7530T>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97442314 | ||||||
chr13:97442348
|
C | A | 1 | a0001c0001t0006g0138 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.314+7564C>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97442348 | ||||||
chr13:97442392
|
A | G | 1 | a0001c0001t0003g0127 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.314+7608A>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97442392 | ||||||
chr13:97442414
|
A | G | 1 | a0001c0001t0012g0167 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.314+7630A>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97442414 | ||||||
chr13:97442669
|
C | G | 1 | a0001c0001t0003g0035 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.314+7885C>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97442669 | ||||||
chr13:97442675
|
A | G | 1 | a0001c0001t0004g0161 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.314+7891A>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97442675 | ||||||
chr13:97442710
|
A | G | 2 | a0001c0001t0002g0011a0001c0001t0002g0084 | 5 | HG00642.hp2 HG01070.hp1 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.314+7926A>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97442710 | ||||||
chr13:97443439
|
G | A | 17 | a0001c0001t0001g0013a0001c0001t0001g0134a0001c0001t0004g0007others(14): Show | 23 | HG00544.hp2 HG00609.hp2 HG02027.hp2 others(20): Show |
intron_variant | MODIFIER | c.314+8655G>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97443439 | ||||||
chr13:97443445
|
C | T | 2 | a0001c0001t0001g0179a0001c0001t0001g0180 | 2 | NA18985.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.314+8661C>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97443445 | ||||||
chr13:97443448
|
C | T | 3 | a0001c0001t0004g0015a0001c0001t0004g0153a0001c0001t0004g0156 | 6 | HG02895.hp2 HG02922.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.314+8664C>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97443448 | ||||||
chr13:97443511
|
C | G | 1 | a0001c0001t0023g0137 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.314+8727C>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97443511 | ||||||
chr13:97443575
|
A | G | 1 | a0001c0001t0003g0126 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.314+8791A>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97443575 | ||||||
chr13:97443727
|
T | C | 1 | a0001c0001t0002g0009 | 4 | NA18964.hp2 NA18965.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.314+8943T>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97443727 | ||||||
chr13:97443872
|
T | G | 1 | a0001c0001t0002g0061 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.314+9088T>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97443872 | ||||||
chr13:97443937
|
G | A | 1 | a0001c0001t0018g0164 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.314+9153G>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97443937 | ||||||
chr13:97444014
|
A | T | 1 | a0001c0001t0022g0152 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.314+9230A>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97444014 | ||||||
chr13:97444166
|
C | T | 1 | a0001c0001t0001g0182 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.314+9382C>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97444166 | ||||||
chr13:97444167
|
G | A | 3 | a0001c0001t0003g0036a0001c0001t0003g0088a0001c0001t0003g0139 | 4 | HG01106.hp1 HG02055.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.314+9383G>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97444167 | ||||||
chr13:97444197
|
G | A | 1 | a0001c0001t0002g0062 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.314+9413G>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97444197 | ||||||
chr13:97444234
|
A | G | 1 | a0001c0001t0019g0168 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.314+9450A>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97444234 | ||||||
chr13:97444348
|
TTTG | T | 38 | a0001c0001t0002g0026a0001c0001t0002g0065a0001c0001t0003g0001others(35): Show | 75 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.314+9567_314+9569d others(5): Show |
RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 97444348 | |||||
chr13:97444628
|
G | A | 41 | a0001c0001t0001g0085a0001c0001t0002g0003a0001c0001t0002g0006others(38): Show | 77 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.314+9844G>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97444628 | ||||||
chr13:97444633
|
A | C | 7 | a0001c0001t0002g0006a0001c0001t0002g0020a0001c0001t0002g0050others(4): Show | 17 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(14): Show |
intron_variant | MODIFIER | c.314+9849A>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97444633 | ||||||
chr13:97444770
|
G | T | 104 | a0001c0001t0001g0085a0001c0001t0002g0003a0001c0001t0002g0006others(101): Show | 184 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(181): Show |
intron_variant | MODIFIER | c.314+9986G>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97444770 | ||||||
chr13:97444830
|
A | G | 1 | a0001c0001t0001g0178 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.314+10046A>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97444830 | ||||||
chr13:97444874
|
A | C | 8 | a0001c0001t0001g0149a0001c0001t0004g0099a0001c0001t0004g0161others(5): Show | 10 | HG01243.hp1 HG02055.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.314+10090A>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97444874 | ||||||
chr13:97445026
|
A | G | 6 | a0001c0001t0007g0017a0001c0001t0007g0157a0001c0001t0007g0158others(3): Show | 7 | HG01192.hp1 HG01975.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.314+10242A>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97445026 | ||||||
chr13:97445134
|
A | G | 1 | a0001c0001t0001g0148 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.314+10350A>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97445134 | ||||||
chr13:97445138
|
C | A | 1 | a0001c0001t0003g0106 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.314+10354C>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97445138 | ||||||
chr13:97445142
|
G | A | 3 | a0001c0001t0003g0012a0001c0001t0003g0063a0001c0001t0003g0160 | 6 | NA18946.hp2 NA18960.hp2 NA18968.hp2 others(3): Show |
intron_variant | MODIFIER | c.314+10358G>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97445142 | ||||||
chr13:97445464
|
T | C | 1 | a0001c0001t0004g0037 | 2 | HG02074.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.314+10680T>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97445464 | ||||||
chr13:97445724
|
C | T | 1 | a0001c0001t0018g0164 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.314+10940C>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97445724 | ||||||
chr13:97445898
|
C | T | 2 | a0001c0001t0002g0053a0001c0001t0002g0081 | 2 | NA18947.hp2 NA18949.hp1 |
intron_variant | MODIFIER | c.314+11114C>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97445898 | ||||||
chr13:97445930
|
A | C | 1 | a0001c0001t0011g0147 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.314+11146A>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97445930 | ||||||
chr13:97446114
|
C | G | 1 | a0001c0001t0008g0043 | 2 | HG02976.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.314+11330C>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97446114 | ||||||
chr13:97446270
|
T | C | 23 | a0001c0001t0001g0013a0001c0001t0001g0134a0001c0001t0004g0007others(20): Show | 29 | HG00544.hp2 HG00609.hp2 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.314+11486T>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97446270 | ||||||
chr13:97446684
|
T | C | 1 | a0001c0001t0004g0089 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.314+11900T>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97446684 | ||||||
chr13:97446703
|
G | A | 2 | a0001c0001t0001g0179a0001c0001t0001g0180 | 2 | NA18985.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.314+11919G>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97446703 | ||||||
chr13:97446728
|
G | A | 19 | a0001c0001t0001g0013a0001c0001t0001g0134a0001c0001t0004g0007others(16): Show | 25 | HG00544.hp2 HG00609.hp2 HG02027.hp2 others(22): Show |
intron_variant | MODIFIER | c.314+11944G>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97446728 | ||||||
chr13:97446992
|
C | T | 1 | a0001c0001t0008g0041 | 2 | HG01192.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.314+12208C>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97446992 | ||||||
chr13:97447044
|
T | C | 1 | a0001c0001t0002g0069 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.314+12260T>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97447044 | ||||||
chr13:97447249
|
A | G | 1 | a0001c0001t0002g0084 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.314+12465A>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97447249 | ||||||
chr13:97447510
|
A | G | 1 | a0001c0001t0002g0122 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.314+12726A>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97447510 | ||||||
chr13:97447585
|
C | T | 2 | a0001c0001t0001g0177a0001c0001t0001g0187 | 2 | HG03492.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.314+12801C>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97447585 | ||||||
chr13:97447667
|
C | T | 1 | a0001c0001t0003g0119 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.314+12883C>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97447667 | ||||||
chr13:97447668
|
G | A | 1 | a0001c0001t0004g0129 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.314+12884G>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97447668 | ||||||
chr13:97447845
|
G | T | 1 | a0001c0001t0002g0061 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.314+13061G>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97447845 | ||||||
chr13:97447846
|
C | T | 1 | a0001c0001t0002g0061 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.314+13062C>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97447846 | ||||||
chr13:97447971
|
GT | G | 5 | a0001c0001t0001g0045a0001c0001t0007g0017a0001c0001t0007g0157others(2): Show | 7 | HG01192.hp1 HG01516.hp1 HG01934.hp2 others(4): Show |
intron_variant | MODIFIER | c.314+13201delT | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 97447971 | |||||
chr13:97448019
|
A | G | 2 | a0001c0001t0002g0080a0001c0001t0002g0121 | 2 | HG03579.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.314+13235A>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97448019 | ||||||
chr13:97448529
|
A | G | 1 | a0001c0001t0006g0138 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.314+13745A>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97448529 | ||||||
chr13:97448798
|
A | C | 3 | a0001c0001t0010g0102a0001c0001t0010g0103a0001c0001t0010g0163 | 3 | HG01891.hp2 HG02622.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.314+14014A>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97448798 | ||||||
chr13:97449017
|
A | G | 1 | a0001c0001t0019g0168 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.314+14233A>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97449017 | ||||||
chr13:97449103
|
G | C | 2 | a0001c0001t0002g0080a0001c0001t0002g0121 | 2 | HG03579.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.314+14319G>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97449103 | ||||||
chr13:97449168
|
T | A | 8 | a0001c0001t0001g0149a0001c0001t0004g0099a0001c0001t0004g0161others(5): Show | 10 | HG01243.hp1 HG02055.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.314+14384T>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97449168 | ||||||
chr13:97449375
|
G | A | 2 | a0001c0001t0004g0055a0001c0001t0004g0089 | 2 | HG02809.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.314+14591G>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97449375 | ||||||
chr13:97449489
|
G | A | 1 | a0001c0001t0001g0170 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.314+14705G>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97449489 | ||||||
chr13:97449636
|
C | T | 4 | a0001c0001t0007g0017a0001c0001t0007g0157a0001c0001t0007g0158others(1): Show | 5 | HG01192.hp1 HG01975.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.315-14569C>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97449636 | ||||||
chr13:97449726
|
A | AT | 54 | a0001c0001t0001g0149a0001c0001t0001g0180a0001c0001t0002g0020others(51): Show | 98 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.315-14469dupT | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 97449726 | |||||
chr13:97449792
|
C | T | 1 | a0001c0001t0002g0078 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.315-14413C>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97449792 | ||||||
chr13:97449964
|
G | A | 3 | a0001c0001t0001g0169a0001c0001t0001g0172a0001c0001t0001g0173 | 3 | HG00673.hp1 NA18969.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.315-14241G>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97449964 | ||||||
chr13:97449965
|
G | GT | 8 | a0001c0001t0001g0149a0001c0001t0004g0099a0001c0001t0005g0030others(5): Show | 10 | HG01243.hp1 HG02055.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.315-14228dupT | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 97449965 | |||||
chr13:97449965
|
GT | G | 5 | a0001c0001t0004g0022a0001c0001t0004g0055a0001c0001t0004g0089others(2): Show | 7 | HG01109.hp2 HG01981.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.315-14228delT | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 97449965 | |||||
chr13:97450163
|
G | A | 1 | a0001c0001t0004g0130 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.315-14042G>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97450163 | ||||||
chr13:97450259
|
T | G | 1 | a0001c0001t0003g0107 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.315-13946T>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97450259 | ||||||
chr13:97450474
|
T | C | 4 | a0001c0001t0007g0017a0001c0001t0007g0157a0001c0001t0007g0158others(1): Show | 5 | HG01192.hp1 HG01975.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.315-13731T>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97450474 | ||||||
chr13:97450551
|
G | A | 1 | a0001c0001t0026g0108 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.315-13654G>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97450551 | ||||||
chr13:97450658
|
T | TA | 5 | a0001c0001t0002g0070a0001c0001t0004g0008a0001c0001t0004g0058others(2): Show | 8 | HG02257.hp2 HG02886.hp2 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.315-13535dupA | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 97450658 | |||||
chr13:97450695
|
G | GT | 6 | a0001c0001t0001g0149a0001c0001t0005g0030a0001c0001t0005g0031others(3): Show | 8 | HG01243.hp1 HG02055.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.315-13504dupT | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 97450695 | |||||
chr13:97450809
|
A | C | 1 | a0001c0001t0002g0029 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.315-13396A>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97450809 | ||||||
chr13:97450944
|
G | A | 1 | a0001c0001t0008g0043 | 2 | HG02976.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.315-13261G>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97450944 | ||||||
chr13:97451001
|
T | G | 1 | a0001c0001t0002g0060 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.315-13204T>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97451001 | ||||||
chr13:97451256
|
G | A | 1 | a0001c0001t0003g0109 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.315-12949G>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97451256 | ||||||
chr13:97451663
|
T | C | 1 | a0001c0001t0004g0131 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.315-12542T>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97451663 | ||||||
chr13:97451664
|
GTATACTT | G | 35 | a0001c0001t0001g0085a0001c0001t0001g0087a0001c0001t0002g0003others(32): Show | 67 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(64): Show |
intron_variant | MODIFIER | c.315-12539_315-1253 others(11): Show |
RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 97451664 | |||||
chr13:97451672
|
T | C | 1 | a0001c0001t0004g0124 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.315-12533T>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97451672 | ||||||
chr13:97451687
|
T | C | 6 | a0001c0001t0002g0029a0001c0001t0004g0022a0001c0001t0004g0055others(3): Show | 9 | HG01109.hp2 HG01981.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.315-12518T>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97451687 | ||||||
chr13:97451816
|
A | C | 6 | a0001c0001t0002g0029a0001c0001t0004g0022a0001c0001t0004g0055others(3): Show | 9 | HG01109.hp2 HG01981.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.315-12389A>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97451816 | ||||||
chr13:97451881
|
T | C | 1 | a0001c0001t0004g0038 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.315-12324T>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97451881 | ||||||
chr13:97452058
|
T | C | 2 | a0001c0001t0002g0080a0001c0001t0002g0121 | 2 | HG03579.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.315-12147T>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97452058 | ||||||
chr13:97452517
|
C | T | 1 | a0001c0001t0003g0068 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.315-11688C>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97452517 | ||||||
chr13:97452616
|
T | C | 1 | a0001c0001t0019g0168 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.315-11589T>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97452616 | ||||||
chr13:97452648
|
A | G | 1 | a0001c0001t0008g0041 | 2 | HG01192.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.315-11557A>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97452648 | ||||||
chr13:97452650
|
G | GCA | 56 | a0001c0001t0001g0085a0001c0001t0001g0087a0001c0001t0001g0097others(53): Show | 96 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.315-11536_315-1153 others(6): Show |
RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 97452650 | |||||
chr13:97452650
|
G | GCACA | 32 | a0001c0001t0002g0020a0001c0001t0002g0026a0001c0001t0002g0065others(29): Show | 68 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(65): Show |
intron_variant | MODIFIER | c.315-11538_315-1153 others(8): Show |
RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 97452650 | |||||
chr13:97452650
|
G | GCACACAC others(1): Show |
5 | a0001c0001t0003g0033a0001c0001t0003g0034a0001c0001t0003g0067others(2): Show | 7 | HG01069.hp1 HG01106.hp2 HG01516.hp2 others(4): Show |
intron_variant | MODIFIER | c.315-11542_315-1153 others(12): Show |
RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 97452650 | |||||
chr13:97452650
|
GCA | G | 8 | a0001c0001t0004g0129a0001c0001t0004g0161a0001c0001t0005g0030others(5): Show | 10 | HG01243.hp1 HG02055.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.315-11536_315-1153 others(6): Show |
RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 97452650 | |||||
chr13:97452750
|
A | G | 1 | a0001c0001t0003g0066 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.315-11455A>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97452750 | ||||||
chr13:97452764
|
A | G | 1 | a0001c0001t0001g0184 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.315-11441A>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97452764 | ||||||
chr13:97453091
|
A | G | 6 | a0001c0001t0004g0099a0001c0001t0005g0030a0001c0001t0005g0031others(3): Show | 8 | HG01243.hp1 HG02055.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.315-11114A>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97453091 | ||||||
chr13:97453238
|
T | C | 1 | a0001c0001t0003g0068 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.315-10967T>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97453238 | ||||||
chr13:97453402
|
C | G | 1 | a0001c0001t0005g0101 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.315-10803C>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97453402 | ||||||
chr13:97453578
|
G | A | 39 | a0001c0001t0002g0065a0001c0001t0003g0001a0001c0001t0003g0012others(36): Show | 76 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.315-10627G>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97453578 | ||||||
chr13:97453745
|
G | C | 1 | a0001c0001t0002g0072 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.315-10460G>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97453745 | ||||||
chr13:97453842
|
C | T | 1 | a0001c0001t0004g0099 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.315-10363C>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97453842 | ||||||
chr13:97453989
|
G | T | 4 | a0001c0001t0007g0017a0001c0001t0007g0157a0001c0001t0007g0158others(1): Show | 5 | HG01192.hp1 HG01975.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.315-10216G>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97453989 | ||||||
chr13:97454030
|
A | G | 2 | a0001c0001t0001g0040a0001c0001t0001g0154 | 3 | HG02015.hp2 NA18950.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.315-10175A>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97454030 | ||||||
chr13:97454057
|
C | T | 1 | a0001c0001t0004g0136 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.315-10148C>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97454057 | ||||||
chr13:97454166
|
T | C | 2 | a0001c0001t0017g0151a0001c0001t0022g0152 | 2 | HG02976.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.315-10039T>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97454166 | ||||||
chr13:97454240
|
T | C | 1 | a0001c0001t0018g0164 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.315-9965T>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97454240 | ||||||
chr13:97454268
|
G | A | 1 | a0001c0001t0005g0101 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.315-9937G>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97454268 | ||||||
chr13:97454429
|
A | G | 4 | a0001c0001t0007g0017a0001c0001t0007g0157a0001c0001t0007g0158others(1): Show | 5 | HG01192.hp1 HG01975.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.315-9776A>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97454429 | ||||||
chr13:97454794
|
C | T | 6 | a0001c0001t0007g0017a0001c0001t0007g0157a0001c0001t0007g0158others(3): Show | 7 | HG01192.hp1 HG01975.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.315-9411C>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97454794 | ||||||
chr13:97454800
|
A | G | 1 | a0001c0001t0019g0168 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.315-9405A>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97454800 | ||||||
chr13:97454997
|
T | TCTC | 6 | a0001c0001t0007g0017a0001c0001t0007g0157a0001c0001t0007g0158others(3): Show | 7 | HG01192.hp1 HG01975.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.315-9206_315-9205i others(5): Show |
RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 97454997 | |||||
chr13:97455052
|
T | C | 1 | a0001c0001t0022g0152 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.315-9153T>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97455052 | ||||||
chr13:97455304
|
T | C | 1 | a0001c0001t0019g0168 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.315-8901T>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97455304 | ||||||
chr13:97455434
|
T | G | 1 | a0001c0001t0006g0142 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.315-8771T>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97455434 | ||||||
chr13:97455592
|
G | A | 1 | a0001c0001t0004g0131 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.315-8613G>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97455592 | ||||||
chr13:97455680
|
T | C | 2 | a0001c0001t0002g0061a0001c0001t0002g0078 | 2 | HG02486.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.315-8525T>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97455680 | ||||||
chr13:97455911
|
A | G | 1 | a0001c0001t0019g0168 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.315-8294A>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97455911 | ||||||
chr13:97455949
|
G | C | 3 | a0001c0001t0012g0165a0001c0001t0012g0166a0001c0001t0012g0167 | 3 | HG02630.hp1 HG02723.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.315-8256G>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97455949 | ||||||
chr13:97455967
|
G | A | 2 | a0001c0001t0004g0143a0001c0001t0022g0152 | 2 | HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.315-8238G>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97455967 | ||||||
chr13:97455992
|
T | C | 6 | a0001c0001t0007g0017a0001c0001t0007g0157a0001c0001t0007g0158others(3): Show | 7 | HG01192.hp1 HG01975.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.315-8213T>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97455992 | ||||||
chr13:97456397
|
T | G | 1 | a0001c0001t0024g0112 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.315-7808T>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97456397 | ||||||
chr13:97456438
|
T | C | 1 | a0001c0001t0004g0132 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.315-7767T>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97456438 | ||||||
chr13:97456513
|
A | G | 3 | a0001c0001t0001g0169a0001c0001t0001g0172a0001c0001t0001g0173 | 3 | HG00673.hp1 NA18969.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.315-7692A>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97456513 | ||||||
chr13:97456781
|
C | T | 6 | a0001c0001t0002g0029a0001c0001t0004g0022a0001c0001t0004g0055others(3): Show | 9 | HG01109.hp2 HG01981.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.315-7424C>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97456781 | ||||||
chr13:97456953
|
T | C | 1 | a0001c0001t0018g0164 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.315-7252T>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97456953 | ||||||
chr13:97456977
|
G | A | 1 | a0001c0001t0003g0104 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.315-7228G>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97456977 | ||||||
chr13:97456999
|
T | C | 1 | a0001c0001t0004g0132 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.315-7206T>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97456999 | ||||||
chr13:97457141
|
C | T | 5 | a0001c0001t0007g0017a0001c0001t0007g0157a0001c0001t0007g0158others(2): Show | 6 | HG01192.hp1 HG01975.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.315-7064C>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97457141 | ||||||
chr13:97457182
|
A | T | 5 | a0001c0001t0007g0017a0001c0001t0007g0157a0001c0001t0007g0158others(2): Show | 6 | HG01192.hp1 HG01975.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.315-7023A>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97457182 | ||||||
chr13:97457240
|
C | T | 5 | a0001c0001t0005g0030a0001c0001t0005g0031a0001c0001t0005g0098others(2): Show | 7 | HG01243.hp1 HG02055.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.315-6965C>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97457240 | ||||||
chr13:97457249
|
T | G | 5 | a0001c0001t0001g0097a0001c0001t0004g0008a0001c0001t0004g0058others(2): Show | 8 | HG02257.hp2 HG02451.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.315-6956T>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97457249 | ||||||
chr13:97457449
|
C | T | 1 | a0001c0001t0019g0168 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.315-6756C>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97457449 | ||||||
chr13:97457455
|
A | G | 1 | a0001c0001t0002g0072 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.315-6750A>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97457455 | ||||||
chr13:97457529
|
G | A | 1 | a0001c0001t0018g0164 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.315-6676G>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97457529 | ||||||
chr13:97457614
|
T | C | 4 | a0001c0001t0004g0162a0001c0001t0012g0165a0001c0001t0012g0166others(1): Show | 4 | HG02630.hp1 HG02723.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.315-6591T>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97457614 | ||||||
chr13:97457827
|
T | C | 2 | a0001c0001t0002g0018a0001c0001t0002g0079 | 4 | HG02602.hp2 HG03017.hp2 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.315-6378T>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97457827 | ||||||
chr13:97457889
|
A | AT | 6 | a0001c0001t0007g0017a0001c0001t0007g0157a0001c0001t0007g0158others(3): Show | 7 | HG01192.hp1 HG01975.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.315-6315dupT | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 97457889 | |||||
chr13:97458005
|
G | C | 6 | a0001c0001t0007g0017a0001c0001t0007g0157a0001c0001t0007g0158others(3): Show | 7 | HG01192.hp1 HG01975.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.315-6200G>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97458005 | ||||||
chr13:97458091
|
C | G | 1 | a0001c0001t0019g0168 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.315-6114C>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97458091 | ||||||
chr13:97458131
|
A | G | 7 | a0001c0001t0004g0099a0001c0001t0004g0161a0001c0001t0005g0030others(4): Show | 9 | HG01243.hp1 HG02055.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.315-6074A>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97458131 | ||||||
chr13:97458193
|
A | C | 1 | a0001c0001t0003g0116 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.315-6012A>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97458193 | ||||||
chr13:97458346
|
G | A | 2 | a0001c0001t0010g0102a0001c0001t0010g0103 | 2 | HG02622.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.315-5859G>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97458346 | ||||||
chr13:97458439
|
T | G | 1 | a0001c0001t0018g0164 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.315-5766T>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97458439 | ||||||
chr13:97458456
|
G | A | 1 | a0001c0001t0025g0117 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.315-5749G>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97458456 | ||||||
chr13:97458579
|
C | T | 1 | a0001c0001t0003g0126 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.315-5626C>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97458579 | ||||||
chr13:97458720
|
A | G | 5 | a0001c0001t0007g0017a0001c0001t0007g0157a0001c0001t0007g0158others(2): Show | 6 | HG01192.hp1 HG01975.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.315-5485A>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97458720 | ||||||
chr13:97458736
|
G | A | 1 | a0001c0001t0002g0073 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.315-5469G>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97458736 | ||||||
chr13:97458827
|
A | G | 2 | a0001c0001t0005g0031a0001c0001t0005g0098 | 3 | HG01243.hp1 HG02055.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.315-5378A>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97458827 | ||||||
chr13:97458860
|
T | G | 3 | a0001c0001t0012g0165a0001c0001t0012g0166a0001c0001t0012g0167 | 3 | HG02630.hp1 HG02723.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.315-5345T>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97458860 | ||||||
chr13:97458914
|
G | A | 1 | a0001c0001t0004g0161 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.315-5291G>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97458914 | ||||||
chr13:97459187
|
G | A | 5 | a0001c0001t0001g0097a0001c0001t0004g0008a0001c0001t0004g0058others(2): Show | 8 | HG02257.hp2 HG02451.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.315-5018G>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97459187 | ||||||
chr13:97459245
|
CAAATGAT others(18): Show |
C | 1 | a0001c0001t0002g0074 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.315-4942_315-4918d others(27): Show |
RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 97459245 | |||||
chr13:97459269
|
AGAAATGA others(10): Show |
A | 1 | a0001c0001t0022g0152 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.315-4914_315-4898d others(19): Show |
RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 97459269 | |||||
chr13:97459283
|
G | T | 1 | a0001c0001t0001g0181 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.315-4922G>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97459283 | ||||||
chr13:97459303
|
G | T | 1 | a0001c0001t0004g0150 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.315-4902G>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97459303 | ||||||
chr13:97459345
|
C | T | 4 | a0001c0001t0007g0017a0001c0001t0007g0157a0001c0001t0007g0158others(1): Show | 5 | HG01192.hp1 HG01975.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.315-4860C>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97459345 | ||||||
chr13:97459352
|
GTAAC | G | 2 | a0001c0001t0001g0024a0001c0001t0006g0024 | 3 | NA18950.hp1 NA19010.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.315-4851_315-4848d others(6): Show |
RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 97459352 | |||||
chr13:97459398
|
CAG | C | 5 | a0001c0001t0002g0027a0001c0001t0002g0028a0001c0001t0002g0052others(2): Show | 7 | HG01069.hp2 HG01071.hp1 HG01081.hp2 others(4): Show |
intron_variant | MODIFIER | c.315-4804_315-4803d others(4): Show |
RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 97459398 | |||||
chr13:97459467
|
G | A | 1 | a0001c0001t0019g0168 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.315-4738G>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97459467 | ||||||
chr13:97459577
|
G | A | 1 | a0001c0001t0002g0084 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.315-4628G>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97459577 | ||||||
chr13:97459982
|
T | C | 4 | a0001c0001t0004g0162a0001c0001t0012g0165a0001c0001t0012g0166others(1): Show | 4 | HG02630.hp1 HG02723.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.315-4223T>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97459982 | ||||||
chr13:97460131
|
A | G | 1 | a0001c0001t0002g0078 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.315-4074A>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97460131 | ||||||
chr13:97460382
|
A | G | 6 | a0001c0001t0004g0099a0001c0001t0005g0030a0001c0001t0005g0031others(3): Show | 8 | HG01243.hp1 HG02055.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.315-3823A>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97460382 | ||||||
chr13:97460520
|
T | C | 1 | a0001c0001t0004g0153 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.315-3685T>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97460520 | ||||||
chr13:97460754
|
C | T | 1 | a0001c0001t0004g0135 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.315-3451C>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97460754 | ||||||
chr13:97460847
|
G | T | 1 | a0001c0001t0019g0168 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.315-3358G>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97460847 | ||||||
chr13:97460956
|
T | C | 1 | a0001c0001t0003g0021 | 3 | HG00741.hp1 HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.315-3249T>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97460956 | ||||||
chr13:97461114
|
G | A | 1 | a0001c0001t0004g0135 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.315-3091G>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97461114 | ||||||
chr13:97461256
|
A | T | 1 | a0001c0001t0018g0164 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.315-2949A>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97461256 | ||||||
chr13:97461269
|
A | G | 1 | a0001c0001t0001g0145 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.315-2936A>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97461269 | ||||||
chr13:97461398
|
C | CAATT | 15 | a0001c0001t0001g0149a0001c0001t0003g0115a0001c0001t0004g0099others(12): Show | 18 | HG01192.hp1 HG01243.hp1 HG01975.hp2 others(15): Show |
intron_variant | MODIFIER | c.315-2805_315-2804i others(6): Show |
RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 97461398 | |||||
chr13:97461451
|
C | T | 1 | a0001c0001t0015g0100 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.315-2754C>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97461451 | ||||||
chr13:97461680
|
C | T | 7 | a0001c0001t0003g0115a0001c0001t0007g0017a0001c0001t0007g0157others(4): Show | 8 | HG01192.hp1 HG01975.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.315-2525C>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97461680 | ||||||
chr13:97461715
|
G | A | 3 | a0001c0001t0003g0021a0001c0001t0003g0111a0001c0001t0003g0113 | 5 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.315-2490G>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97461715 | ||||||
chr13:97461778
|
A | G | 3 | a0001c0001t0007g0017a0001c0001t0007g0157a0001c0001t0028g0017 | 4 | HG01192.hp1 HG01975.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.315-2427A>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97461778 | ||||||
chr13:97461941
|
A | C | 7 | a0001c0001t0003g0115a0001c0001t0007g0017a0001c0001t0007g0157others(4): Show | 8 | HG01192.hp1 HG01975.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.315-2264A>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97461941 | ||||||
chr13:97461962
|
CA | C | 5 | a0001c0001t0001g0176a0001c0001t0007g0017a0001c0001t0007g0157others(2): Show | 6 | HG01192.hp1 HG01975.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.315-2233delA | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 97461962 | |||||
chr13:97461969
|
A | AAT | 15 | a0001c0001t0001g0013a0001c0001t0003g0125a0001c0001t0004g0007others(12): Show | 22 | HG00544.hp2 HG00609.hp2 HG02040.hp2 others(19): Show |
intron_variant | MODIFIER | c.315-2235_315-2234i others(4): Show |
RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 97461969 | |||||
chr13:97461969
|
A | T | 3 | a0001c0001t0001g0134a0001c0001t0003g0115a0001c0001t0004g0136 | 3 | HG02738.hp1 HG03942.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.315-2236A>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97461969 | ||||||
chr13:97461971
|
A | AAAATATA others(15): Show |
1 | a0001c0001t0019g0168 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.315-2233_315-2232i others(24): Show |
RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 97461971 | |||||
chr13:97461971
|
A | AAT | 16 | a0001c0001t0001g0097a0001c0001t0002g0070a0001c0001t0004g0008others(13): Show | 19 | HG01243.hp2 HG01884.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.315-2217_315-2216d others(4): Show |
RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 97461971 | |||||
chr13:97461971
|
A | T | 27 | a0001c0001t0001g0013a0001c0001t0001g0134a0001c0001t0002g0028others(24): Show | 37 | HG00544.hp2 HG00609.hp2 HG01081.hp2 others(34): Show |
intron_variant | MODIFIER | c.315-2234A>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97461971 | ||||||
chr13:97461973
|
T | A | 42 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(39): Show | 79 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(76): Show |
intron_variant | MODIFIER | c.315-2232T>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97461973 | ||||||
chr13:97461975
|
T | A | 1 | a0001c0001t0001g0171 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.315-2230T>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97461975 | ||||||
chr13:97461980
|
A | ATATATAT others(45): Show |
1 | a0001c0001t0001g0175 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.315-2207_315-2156d others(54): Show |
RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 97461980 | |||||
chr13:97461990
|
T | A | 1 | a0001c0001t0019g0168 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.315-2215T>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97461990 | ||||||
chr13:97462004
|
T | A | 1 | a0001c0001t0019g0168 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.315-2201T>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97462004 | ||||||
chr13:97462005
|
T | G | 1 | a0001c0001t0019g0168 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.315-2200T>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97462005 | ||||||
chr13:97462024
|
TTATATAT others(3): Show |
T | 3 | a0001c0001t0010g0102a0001c0001t0010g0103a0001c0001t0010g0163 | 3 | HG01891.hp2 HG02622.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.315-2163_315-2154d others(12): Show |
RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 97462024 | |||||
chr13:97462032
|
T | TTATATAT others(5): Show |
1 | a0001c0001t0004g0162 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.315-2143_315-2132d others(14): Show |
RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 97462032 | |||||
chr13:97462032
|
TTATATAT others(5): Show |
T | 6 | a0001c0001t0001g0174a0001c0001t0002g0062a0001c0001t0003g0115others(3): Show | 6 | HG00423.hp2 HG02071.hp2 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.315-2143_315-2132d others(14): Show |
RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 97462032 | |||||
chr13:97462033
|
T | G | 1 | a0001c0001t0002g0082 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.315-2172T>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97462033 | ||||||
chr13:97462056
|
A | T | 2 | a0001c0001t0004g0091a0001c0001t0004g0155 | 2 | HG02809.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.315-2149A>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97462056 | ||||||
chr13:97462061
|
T | G | 1 | a0001c0001t0018g0164 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.315-2144T>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97462061 | ||||||
chr13:97462065
|
T | G | 4 | a0001c0001t0007g0017a0001c0001t0007g0157a0001c0001t0007g0158others(1): Show | 5 | HG01192.hp1 HG01975.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.315-2140T>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97462065 | ||||||
chr13:97462074
|
T | C | 1 | a0001c0001t0026g0108 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.315-2131T>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97462074 | ||||||
chr13:97462155
|
A | T | 5 | a0001c0001t0004g0022a0001c0001t0004g0055a0001c0001t0004g0089others(2): Show | 7 | HG01109.hp2 HG01981.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.315-2050A>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97462155 | ||||||
chr13:97462160
|
TAGAC | T | 2 | a0001c0001t0008g0041a0001c0001t0008g0043 | 4 | HG01192.hp2 HG02976.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.315-2040_315-2037d others(6): Show |
RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 97462160 | |||||
chr13:97462244
|
A | G | 12 | a0001c0001t0001g0004a0001c0001t0001g0040a0001c0001t0001g0085others(9): Show | 24 | HG00140.hp1 HG00280.hp1 HG00609.hp1 others(21): Show |
intron_variant | MODIFIER | c.315-1961A>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97462244 | ||||||
chr13:97462299
|
T | C | 1 | a0001c0001t0010g0102 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.315-1906T>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97462299 | ||||||
chr13:97462395
|
A | G | 1 | a0001c0001t0004g0055 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.315-1810A>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97462395 | ||||||
chr13:97462429
|
TG | T | 2 | a0001c0001t0008g0041a0001c0001t0008g0043 | 4 | HG01192.hp2 HG02976.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.315-1774delG | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 97462429 | |||||
chr13:97462633
|
T | G | 1 | a0001c0001t0004g0161 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.315-1572T>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97462633 | ||||||
chr13:97462738
|
A | T | 3 | a0001c0001t0010g0102a0001c0001t0010g0103a0001c0001t0010g0163 | 3 | HG01891.hp2 HG02622.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.315-1467A>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97462738 | ||||||
chr13:97462911
|
G | A | 6 | a0001c0001t0004g0099a0001c0001t0005g0030a0001c0001t0005g0031others(3): Show | 8 | HG01243.hp1 HG02055.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.315-1294G>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97462911 | ||||||
chr13:97462938
|
G | C | 81 | a0001c0001t0002g0003a0001c0001t0002g0006a0001c0001t0002g0009others(78): Show | 154 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(151): Show |
intron_variant | MODIFIER | c.315-1267G>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97462938 | ||||||
chr13:97463014
|
AT | A | 104 | a0001c0001t0002g0003a0001c0001t0002g0006a0001c0001t0002g0009others(101): Show | 184 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(181): Show |
intron_variant | MODIFIER | c.315-1188delT | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 97463014 | |||||
chr13:97463119
|
AAC | A | 35 | a0001c0001t0002g0003a0001c0001t0002g0006a0001c0001t0002g0009others(32): Show | 67 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(64): Show |
intron_variant | MODIFIER | c.315-1072_315-1071d others(4): Show |
RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 97463119 | |||||
chr13:97463258
|
C | G | 1 | a0001c0001t0005g0101 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.315-947C>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97463258 | ||||||
chr13:97463663
|
C | T | 79 | a0001c0001t0002g0003a0001c0001t0002g0006a0001c0001t0002g0009others(76): Show | 152 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(149): Show |
intron_variant | MODIFIER | c.315-542C>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97463663 | ||||||
chr13:97463680
|
C | T | 4 | a0001c0001t0007g0017a0001c0001t0007g0157a0001c0001t0007g0158others(1): Show | 5 | HG01192.hp1 HG01975.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.315-525C>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97463680 | ||||||
chr13:97463790
|
A | G | 3 | a0001c0001t0002g0011a0001c0001t0002g0084a0001c0001t0002g0122 | 6 | HG00642.hp2 HG01070.hp1 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.315-415A>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97463790 | ||||||
chr13:97463815
|
A | G | 5 | a0001c0001t0004g0162a0001c0001t0012g0165a0001c0001t0012g0166others(2): Show | 5 | HG01106.hp2 HG02630.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.315-390A>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97463815 |