geneid | 10681 |
---|---|
ensemblid | ENSG00000069966.19 |
hgncid | 4401 |
symbol | GNB5 |
name | G protein subunit beta 5 |
refseq_nuc | NM_016194.4 |
refseq_prot | NP_057278.2 |
ensembl_nuc | ENST00000261837.12 |
ensembl_prot | ENSP00000261837.7 |
mane_status | MANE Select |
chr | chr15 |
start | 52115100 |
end | 52191392 |
strand | - |
ver | v1.2 |
region | chr15:52115100-52191392 |
region5000 | chr15:52110100-52196392 |
regionname0 | GNB5_chr15_52115100_52191392 |
regionname5000 | GNB5_chr15_52110100_52196392 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 395 | 362 | 86 | 74 | 154 | 10 | 36 | 112 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0002 | 0/0 | 395 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0003 | 0/0 | 395 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0004 | 0/0 | 265 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1188 | 296 | 47 | 60 | 144 | 10 | 33 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
c0002 | 0/0 | 1188 | 37 | 21 | 6 | 9 | 0 | 1 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
c0003 | 0/0 | 1188 | 14 | 14 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
c0004 | 0/0 | 1188 | 9 | 0 | 7 | 0 | 0 | 2 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
c0005 | 0/0 | 1188 | 3 | 2 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
c0006 | 0/0 | 1188 | 2 | 2 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
c0007 | 0/0 | 1188 | 2 | 2 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
c0008 | 0/0 | 1188 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
c0009 | 0/0 | 1188 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
c0010 | 0/0 | 1188 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 7753 | 41 | 1 | 6 | 32 | 0 | 2 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0002 | 0/1 | 7751 | 35 | 3 | 16 | 1 | 4 | 10 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0003 | 0/0 | 7753 | 11 | 0 | 0 | 11 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0004 | 0/0 | 7751 | 9 | 0 | 0 | 9 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0005 | 0/0 | 7753 | 9 | 0 | 2 | 4 | 0 | 3 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0006 | 0/0 | 7747 | 6 | 6 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0007 | 0/0 | 7823 | 5 | 0 | 0 | 3 | 0 | 2 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0008 | 0/0 | 7823 | 5 | 1 | 0 | 2 | 0 | 2 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0009 | 0/0 | 7747 | 5 | 0 | 0 | 5 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0010 | 0/0 | 7753 | 5 | 0 | 0 | 5 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0011 | 0/0 | 7780 | 5 | 5 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0012 | 0/0 | 7754 | 5 | 0 | 0 | 3 | 0 | 2 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0013 | 0/0 | 7751 | 4 | 0 | 3 | 0 | 1 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0014 | 0/0 | 7852 | 4 | 0 | 2 | 0 | 0 | 2 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0015 | 0/0 | 7823 | 3 | 0 | 0 | 3 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0016 | 0/0 | 7835 | 3 | 0 | 0 | 3 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0017 | 0/0 | 7851 | 3 | 0 | 3 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0018 | 0/0 | 7856 | 2 | 0 | 0 | 2 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0019 | 0/0 | 7851 | 2 | 2 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0020 | 0/0 | 7752 | 2 | 0 | 0 | 2 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0021 | 0/0 | 7786 | 2 | 2 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0022 | 0/0 | 7779 | 2 | 2 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0023 | 0/0 | 7779 | 2 | 2 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0024 | 0/0 | 7772 | 2 | 2 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0025 | 0/0 | 7772 | 2 | 2 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0026 | 0/0 | 7772 | 2 | 2 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0027 | 0/0 | 7780 | 2 | 2 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0028 | 0/0 | 7770 | 2 | 0 | 0 | 2 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0029 | 0/0 | 7752 | 2 | 0 | 0 | 2 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0030 | 0/0 | 7753 | 2 | 0 | 0 | 1 | 0 | 1 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0031 | 0/0 | 7836 | 2 | 0 | 0 | 1 | 0 | 1 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0032 | 0/0 | 7829 | 2 | 0 | 2 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0033 | 0/0 | 7825 | 2 | 0 | 2 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0034 | 0/0 | 7813 | 2 | 0 | 0 | 0 | 1 | 1 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0035 | 0/0 | 7747 | 2 | 1 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0036 | 0/0 | 7751 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0037 | 0/0 | 7865 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0038 | 0/0 | 7854 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0039 | 0/0 | 7825 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0040 | 0/0 | 7853 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0041 | 0/0 | 7858 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0042 | 0/0 | 7870 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0043 | 0/0 | 7871 | 1 | 0 | 0 | 0 | 0 | 1 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0044 | 0/0 | 7827 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0045 | 0/0 | 7826 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0046 | 0/0 | 7851 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0047 | 0/0 | 7866 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0048 | 0/0 | 7856 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0049 | 0/0 | 7834 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0050 | 0/0 | 7849 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0051 | 0/0 | 7854 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0052 | 0/0 | 7861 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0053 | 0/0 | 7859 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0054 | 0/0 | 7857 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0055 | 0/0 | 7862 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0056 | 0/0 | 7857 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0057 | 0/0 | 7853 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0058 | 0/0 | 7845 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0059 | 0/0 | 7833 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0060 | 0/0 | 7850 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0061 | 0/0 | 7840 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0062 | 0/0 | 7836 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0063 | 0/0 | 7847 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0064 | 0/0 | 7827 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0065 | 0/0 | 7888 | 1 | 0 | 0 | 0 | 1 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0066 | 0/0 | 7833 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0067 | 0/0 | 7865 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0068 | 0/0 | 7853 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0069 | 0/0 | 7856 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0070 | 0/0 | 7825 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0071 | 0/0 | 7861 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0072 | 0/0 | 7855 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0073 | 0/0 | 7840 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0074 | 0/0 | 7855 | 1 | 0 | 0 | 0 | 0 | 1 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0075 | 0/0 | 7839 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0076 | 0/0 | 7826 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0077 | 0/0 | 7825 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0078 | 0/0 | 7849 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0079 | 0/0 | 7831 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0080 | 0/0 | 7823 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0081 | 0/0 | 7824 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0082 | 0/0 | 7831 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0083 | 0/0 | 7827 | 1 | 0 | 0 | 0 | 0 | 1 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0084 | 0/0 | 7832 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0085 | 0/0 | 7826 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0086 | 0/0 | 7823 | 1 | 0 | 0 | 0 | 0 | 1 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0087 | 0/0 | 7794 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0088 | 0/0 | 7850 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0089 | 0/0 | 7841 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0090 | 0/0 | 7828 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0091 | 0/0 | 7828 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0092 | 0/0 | 7824 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0093 | 0/0 | 7820 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0094 | 0/0 | 7780 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0095 | 0/0 | 7752 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0096 | 0/0 | 7748 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0097 | 0/0 | 7821 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0098 | 0/0 | 7801 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0099 | 0/0 | 7819 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0100 | 0/0 | 7873 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0101 | 0/0 | 7800 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0102 | 0/0 | 7753 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0103 | 0/0 | 7754 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0104 | 0/0 | 7751 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0105 | 0/0 | 7751 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0106 | 0/0 | 7752 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0107 | 0/0 | 7751 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0108 | 0/0 | 7751 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0109 | 0/0 | 7752 | 1 | 0 | 0 | 0 | 1 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0110 | 0/0 | 7734 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0111 | 0/0 | 7730 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0112 | 0/0 | 7804 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0113 | 0/0 | 7843 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0114 | 0/0 | 7821 | 1 | 0 | 0 | 0 | 1 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0115 | 0/0 | 7807 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0116 | 0/0 | 7847 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0117 | 0/0 | 7833 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0118 | 0/0 | 7805 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0119 | 0/0 | 7888 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0120 | 0/0 | 7747 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0121 | 0/0 | 7753 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0122 | 0/0 | 7767 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0123 | 0/0 | 7770 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0124 | 0/0 | 7758 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0125 | 0/0 | 7754 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0126 | 0/0 | 7768 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0127 | 0/0 | 7773 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0128 | 0/0 | 7830 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0129 | 0/0 | 7832 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0130 | 0/0 | 7834 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0131 | 0/0 | 7852 | 1 | 0 | 0 | 0 | 0 | 1 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0132 | 0/0 | 7848 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0133 | 0/0 | 7850 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0134 | 0/0 | 7852 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0135 | 0/0 | 7844 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0136 | 0/0 | 7848 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0137 | 0/0 | 7842 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0138 | 0/0 | 7866 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0139 | 0/0 | 7838 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0140 | 0/0 | 7850 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0141 | 0/0 | 7781 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0142 | 0/0 | 7780 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0143 | 0/0 | 7781 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0144 | 0/0 | 7780 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0145 | 0/0 | 7781 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0146 | 0/0 | 7782 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0147 | 0/0 | 7773 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0148 | 0/0 | 7781 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0149 | 0/0 | 7780 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0150 | 0/0 | 7822 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0151 | 0/0 | 7825 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0152 | 0/0 | 7830 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0153 | 0/0 | 7823 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0154 | 0/0 | 7754 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0155 | 1/0 | 7747 | 1 | 0 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0156 | 0/0 | 7832 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0157 | 0/0 | 7829 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0158 | 0/0 | 7752 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0159 | 0/0 | 7753 | 1 | 0 | 0 | 0 | 0 | 1 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0160 | 0/0 | 7753 | 1 | 0 | 0 | 0 | 0 | 1 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0161 | 0/0 | 7754 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0162 | 0/0 | 7751 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0163 | 0/0 | 7772 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0164 | 0/0 | 7847 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0165 | 0/0 | 7838 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0166 | 0/0 | 7834 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0167 | 0/0 | 7736 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0168 | 0/0 | 7834 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0169 | 0/0 | 7831 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0170 | 0/0 | 7838 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0171 | 0/0 | 7837 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0172 | 0/0 | 7808 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0173 | 0/0 | 7833 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0174 | 0/0 | 7835 | 1 | 0 | 0 | 0 | 0 | 1 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0175 | 0/0 | 7840 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0176 | 0/0 | 7841 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0177 | 0/0 | 7838 | 1 | 0 | 0 | 0 | 0 | 1 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0178 | 0/0 | 7836 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0179 | 0/0 | 7841 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0180 | 0/0 | 7839 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0181 | 0/0 | 7835 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0182 | 0/0 | 7842 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0183 | 0/0 | 7840 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0184 | 0/0 | 7846 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0185 | 0/0 | 7836 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0186 | 0/0 | 7836 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0187 | 0/0 | 7843 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0188 | 0/0 | 7854 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0189 | 0/0 | 7823 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0190 | 0/0 | 7834 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0191 | 0/0 | 7822 | 1 | 0 | 0 | 0 | 0 | 1 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0192 | 0/0 | 7831 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0193 | 0/0 | 7827 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0194 | 0/0 | 7821 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0195 | 0/0 | 7802 | 1 | 0 | 0 | 0 | 1 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0196 | 0/0 | 7837 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0197 | 0/0 | 7841 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0198 | 0/0 | 7837 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0199 | 0/0 | 7828 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0200 | 0/0 | 7803 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0201 | 0/0 | 7745 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0202 | 0/0 | 7747 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0203 | 0/0 | 7745 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0204 | 0/0 | 7854 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0205 | 0/0 | 7852 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0206 | 0/0 | 7754 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
t0207 | 0/0 | 7741 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0026 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0311 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0337 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0346 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0362 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1188 | 296 | 47 | 60 | 144 | 10 | 33 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0002 | 0/0 | 1188 | 37 | 21 | 6 | 9 | 0 | 1 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0003 | 0/0 | 1188 | 14 | 14 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0004 | 0/0 | 1188 | 9 | 0 | 7 | 0 | 0 | 2 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0005 | 0/0 | 1188 | 3 | 2 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0006 | 0/0 | 1188 | 2 | 2 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0010 | 0/0 | 1188 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0002c0007 | 0/0 | 1188 | 2 | 2 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0003c0009 | 0/0 | 1188 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0004c0008 | 0/0 | 1188 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 8940 | 41 | 1 | 6 | 32 | 0 | 2 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0002 | 0/1 | 8938 | 35 | 3 | 16 | 1 | 4 | 10 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0003 | 0/0 | 8940 | 11 | 0 | 0 | 11 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0004 | 0/0 | 8938 | 9 | 0 | 0 | 9 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0005 | 0/0 | 8940 | 8 | 0 | 2 | 3 | 0 | 3 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0007 | 0/0 | 9010 | 5 | 0 | 0 | 3 | 0 | 2 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0008 | 0/0 | 9010 | 5 | 1 | 0 | 2 | 0 | 2 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0009 | 0/0 | 8934 | 5 | 0 | 0 | 5 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0010 | 0/0 | 8940 | 5 | 0 | 0 | 5 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0011 | 0/0 | 8967 | 5 | 5 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0012 | 0/0 | 8941 | 5 | 0 | 0 | 3 | 0 | 2 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0013 | 0/0 | 8938 | 4 | 0 | 3 | 0 | 1 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0015 | 0/0 | 9010 | 3 | 0 | 0 | 3 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0016 | 0/0 | 9022 | 3 | 0 | 0 | 3 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0018 | 0/0 | 9043 | 2 | 0 | 0 | 2 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0020 | 0/0 | 8939 | 2 | 0 | 0 | 2 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0022 | 0/0 | 8966 | 2 | 2 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0023 | 0/0 | 8966 | 2 | 2 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0027 | 0/0 | 8967 | 2 | 2 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0028 | 0/0 | 8957 | 2 | 0 | 0 | 2 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0029 | 0/0 | 8939 | 2 | 0 | 0 | 2 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0030 | 0/0 | 8940 | 2 | 0 | 0 | 1 | 0 | 1 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0031 | 0/0 | 9023 | 2 | 0 | 0 | 1 | 0 | 1 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0032 | 0/0 | 9016 | 2 | 0 | 2 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0033 | 0/0 | 9012 | 2 | 0 | 2 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0034 | 0/0 | 9000 | 2 | 0 | 0 | 0 | 1 | 1 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0036 | 0/0 | 8938 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0037 | 0/0 | 9052 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0038 | 0/0 | 9041 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0040 | 0/0 | 9040 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0041 | 0/0 | 9045 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0042 | 0/0 | 9057 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0043 | 0/0 | 9058 | 1 | 0 | 0 | 0 | 0 | 1 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0044 | 0/0 | 9014 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0045 | 0/0 | 9013 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0046 | 0/0 | 9038 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0047 | 0/0 | 9053 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0048 | 0/0 | 9043 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0049 | 0/0 | 9021 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0050 | 0/0 | 9036 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0051 | 0/0 | 9041 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0052 | 0/0 | 9048 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0053 | 0/0 | 9046 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0054 | 0/0 | 9044 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0055 | 0/0 | 9049 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0056 | 0/0 | 9044 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0057 | 0/0 | 9040 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0058 | 0/0 | 9032 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0059 | 0/0 | 9020 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0060 | 0/0 | 9037 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0061 | 0/0 | 9027 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0062 | 0/0 | 9023 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0063 | 0/0 | 9034 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0064 | 0/0 | 9014 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0065 | 0/0 | 9075 | 1 | 0 | 0 | 0 | 1 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0066 | 0/0 | 9020 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0067 | 0/0 | 9052 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0068 | 0/0 | 9040 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0069 | 0/0 | 9043 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0070 | 0/0 | 9012 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0071 | 0/0 | 9048 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0072 | 0/0 | 9042 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0073 | 0/0 | 9027 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0074 | 0/0 | 9042 | 1 | 0 | 0 | 0 | 0 | 1 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0075 | 0/0 | 9026 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0076 | 0/0 | 9013 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0077 | 0/0 | 9012 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0078 | 0/0 | 9036 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0079 | 0/0 | 9018 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0080 | 0/0 | 9010 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0082 | 0/0 | 9018 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0083 | 0/0 | 9014 | 1 | 0 | 0 | 0 | 0 | 1 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0084 | 0/0 | 9019 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0085 | 0/0 | 9013 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0086 | 0/0 | 9010 | 1 | 0 | 0 | 0 | 0 | 1 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0087 | 0/0 | 8981 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0088 | 0/0 | 9037 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0089 | 0/0 | 9028 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0090 | 0/0 | 9015 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0091 | 0/0 | 9015 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0092 | 0/0 | 9011 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0093 | 0/0 | 9007 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0094 | 0/0 | 8967 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0095 | 0/0 | 8939 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0096 | 0/0 | 8935 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0102 | 0/0 | 8940 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0103 | 0/0 | 8941 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0104 | 0/0 | 8938 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0105 | 0/0 | 8938 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0106 | 0/0 | 8939 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0107 | 0/0 | 8938 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0108 | 0/0 | 8938 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0109 | 0/0 | 8939 | 1 | 0 | 0 | 0 | 1 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0110 | 0/0 | 8921 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0111 | 0/0 | 8917 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0113 | 0/0 | 9030 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0114 | 0/0 | 9008 | 1 | 0 | 0 | 0 | 1 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0115 | 0/0 | 8994 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0116 | 0/0 | 9034 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0117 | 0/0 | 9020 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0118 | 0/0 | 8992 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0121 | 0/0 | 8940 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0141 | 0/0 | 8968 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0144 | 0/0 | 8967 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0145 | 0/0 | 8968 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0146 | 0/0 | 8969 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0148 | 0/0 | 8968 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0149 | 0/0 | 8967 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0151 | 0/0 | 9012 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0152 | 0/0 | 9017 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0153 | 0/0 | 9010 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0154 | 0/0 | 8941 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0155 | 1/0 | 8934 | 1 | 0 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0158 | 0/0 | 8939 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0159 | 0/0 | 8940 | 1 | 0 | 0 | 0 | 0 | 1 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0160 | 0/0 | 8940 | 1 | 0 | 0 | 0 | 0 | 1 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0161 | 0/0 | 8941 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0162 | 0/0 | 8938 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0163 | 0/0 | 8959 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0164 | 0/0 | 9034 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0165 | 0/0 | 9025 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0166 | 0/0 | 9021 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0167 | 0/0 | 8923 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0168 | 0/0 | 9021 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0169 | 0/0 | 9018 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0170 | 0/0 | 9025 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0171 | 0/0 | 9024 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0173 | 0/0 | 9020 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0174 | 0/0 | 9022 | 1 | 0 | 0 | 0 | 0 | 1 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0175 | 0/0 | 9027 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0176 | 0/0 | 9028 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0177 | 0/0 | 9025 | 1 | 0 | 0 | 0 | 0 | 1 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0178 | 0/0 | 9023 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0179 | 0/0 | 9028 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0180 | 0/0 | 9026 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0181 | 0/0 | 9022 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0182 | 0/0 | 9029 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0183 | 0/0 | 9027 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0184 | 0/0 | 9033 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0185 | 0/0 | 9023 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0186 | 0/0 | 9023 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0187 | 0/0 | 9030 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0188 | 0/0 | 9041 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0190 | 0/0 | 9021 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0191 | 0/0 | 9009 | 1 | 0 | 0 | 0 | 0 | 1 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0192 | 0/0 | 9018 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0193 | 0/0 | 9014 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0194 | 0/0 | 9008 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0195 | 0/0 | 8989 | 1 | 0 | 0 | 0 | 1 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0196 | 0/0 | 9024 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0197 | 0/0 | 9028 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0198 | 0/0 | 9024 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0199 | 0/0 | 9015 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0001t0200 | 0/0 | 8990 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0002t0006 | 0/0 | 8934 | 6 | 6 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0002t0019 | 0/0 | 9038 | 2 | 2 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0002t0024 | 0/0 | 8959 | 2 | 2 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0002t0025 | 0/0 | 8959 | 2 | 2 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0002t0026 | 0/0 | 8959 | 2 | 2 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0002t0035 | 0/0 | 8934 | 2 | 1 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0002t0120 | 0/0 | 8934 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0002t0128 | 0/0 | 9017 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0002t0129 | 0/0 | 9019 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0002t0130 | 0/0 | 9021 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0002t0131 | 0/0 | 9039 | 1 | 0 | 0 | 0 | 0 | 1 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0002t0132 | 0/0 | 9035 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0002t0133 | 0/0 | 9037 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0002t0134 | 0/0 | 9039 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0002t0135 | 0/0 | 9031 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0002t0136 | 0/0 | 9035 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0002t0137 | 0/0 | 9029 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0002t0138 | 0/0 | 9053 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0002t0139 | 0/0 | 9025 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0002t0140 | 0/0 | 9037 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0002t0147 | 0/0 | 8960 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0002t0150 | 0/0 | 9009 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0002t0201 | 0/0 | 8932 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0002t0202 | 0/0 | 8934 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0002t0203 | 0/0 | 8932 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0002t0206 | 0/0 | 8941 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0002t0207 | 0/0 | 8928 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0003t0021 | 0/0 | 8973 | 2 | 2 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0003t0097 | 0/0 | 9008 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0003t0098 | 0/0 | 8988 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0003t0099 | 0/0 | 9006 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0003t0101 | 0/0 | 8987 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0003t0112 | 0/0 | 8991 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0003t0119 | 0/0 | 9075 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0003t0122 | 0/0 | 8954 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0003t0123 | 0/0 | 8957 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0003t0124 | 0/0 | 8945 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0003t0125 | 0/0 | 8941 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0003t0126 | 0/0 | 8955 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0003t0127 | 0/0 | 8960 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0004t0014 | 0/0 | 9039 | 4 | 0 | 2 | 0 | 0 | 2 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0004t0017 | 0/0 | 9038 | 3 | 0 | 3 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0004t0204 | 0/0 | 9041 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0004t0205 | 0/0 | 9039 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0005t0100 | 0/0 | 9060 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0005t0156 | 0/0 | 9019 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0005t0157 | 0/0 | 9016 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0006t0142 | 0/0 | 8967 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0006t0143 | 0/0 | 8968 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0001c0010t0189 | 0/0 | 9010 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0002c0007t0039 | 0/0 | 9012 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0002c0007t0081 | 0/0 | 9011 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0003c0009t0172 | 0/0 | 8995 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
a0004c0008t0005 | 0/0 | 8940 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | copy fasta | chr15 | 52110100 | 52196392 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0002g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0002g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0002g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0002g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0002g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0002g0026 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0002g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0002g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0003g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0003g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0003g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0003g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0003g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0003g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0003g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0003g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0003g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0003g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0004g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0004g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0004g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0004g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0004g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0004g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0004g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0004g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0004g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0005g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0005g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0005g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0005g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0005g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0005g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0005g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0005g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0007g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0007g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0007g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0007g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0007g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0008g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0008g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0008g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0008g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0008g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0009g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0009g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0009g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0009g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0009g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0010g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0010g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0010g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0010g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0010g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0011g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0011g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0011g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0011g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0011g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0012g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0012g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0012g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0012g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0012g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0013g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0013g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0013g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0013g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0015g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0015g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0015g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0016g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0016g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0016g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0018g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0018g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0020g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0020g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0022g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0022g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0023g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0023g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0027g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0027g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0028g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0028g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0029g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0029g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0030g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0030g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0031g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0031g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0032g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0032g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0033g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0033g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0034g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0034g0346 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0036g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0037g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0038g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0040g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0041g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0042g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0043g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0044g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0045g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0046g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0047g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0048g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0049g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0050g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0051g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0052g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0053g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0054g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0055g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0056g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0057g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0058g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0059g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0060g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0061g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0062g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0063g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0064g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0065g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0066g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0067g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0068g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0069g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0070g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0071g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0072g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0073g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0074g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0075g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0076g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0077g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0078g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0079g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0080g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0082g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0083g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0084g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0085g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0086g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0087g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0088g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0089g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0090g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0091g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0092g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0093g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0094g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0095g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0096g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0102g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0103g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0104g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0105g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0106g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0107g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0108g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0109g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0110g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0111g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0113g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0114g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0115g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0116g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0117g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0118g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0121g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0141g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0144g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0145g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0146g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0148g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0149g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0151g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0152g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0153g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0154g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0155g0311 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0158g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0159g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0160g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0161g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0162g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0163g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0164g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0165g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0166g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0167g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0168g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0169g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0170g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0171g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0173g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0174g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0175g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0176g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0177g0362 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0178g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0179g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0180g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0181g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0182g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0183g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0184g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0185g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0186g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0187g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0188g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0190g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0191g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0192g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0193g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0194g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0195g0337 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0196g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0197g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0198g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0199g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0001t0200g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0002t0006g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0002t0006g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0002t0006g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0002t0006g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0002t0006g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0002t0006g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0002t0019g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0002t0019g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0002t0024g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0002t0024g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0002t0025g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0002t0025g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0002t0026g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0002t0026g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0002t0035g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0002t0035g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0002t0120g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0002t0128g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0002t0129g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0002t0130g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0002t0131g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0002t0132g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0002t0133g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0002t0134g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0002t0135g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0002t0136g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0002t0137g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0002t0138g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0002t0139g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0002t0140g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0002t0147g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0002t0150g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0002t0201g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0002t0202g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0002t0203g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0002t0206g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0002t0207g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0003t0021g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0003t0021g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0003t0097g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0003t0098g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0003t0099g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0003t0101g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0003t0112g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0003t0119g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0003t0122g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0003t0123g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0003t0124g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0003t0125g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0003t0126g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0003t0127g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0004t0014g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0004t0014g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0004t0014g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0004t0017g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0004t0017g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0004t0204g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0004t0205g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0005t0100g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0005t0156g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0005t0157g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0006t0142g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0006t0143g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0001c0010t0189g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0002c0007t0039g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0002c0007t0081g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0003c0009t0172g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
a0004c0008t0005g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0043 | EUR | GBR | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG00099 | hp2 | a0001 | c0001 | t0034 | g0346 | EUR | GBR | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0051 | EUR | FIN | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG00323 | hp2 | a0001 | c0001 | t0065 | g0079 | EUR | FIN | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG00408 | hp1 | a0001 | c0001 | t0003 | g0014 | EAS | CHS | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG00408 | hp2 | a0001 | c0001 | t0016 | g0343 | EAS | CHS | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG00438 | hp1 | a0001 | c0001 | t0198 | g0351 | EAS | CHS | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | CHS | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG00544 | hp1 | a0001 | c0001 | t0005 | g0233 | EAS | CHS | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG00544 | hp2 | a0001 | c0001 | t0052 | g0121 | EAS | CHS | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG00558 | hp1 | a0001 | c0001 | t0113 | g0021 | EAS | CHS | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG00558 | hp2 | a0001 | c0001 | t0005 | g0207 | EAS | CHS | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG00597 | hp1 | a0001 | c0001 | t0053 | g0171 | EAS | CHS | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | CHS | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG00609 | hp1 | a0001 | c0001 | t0079 | g0138 | EAS | CHS | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG00609 | hp2 | a0001 | c0001 | t0173 | g0183 | EAS | CHS | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | CHS | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | CHS | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0239 | AMR | PUR | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0011 | AMR | PUR | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG00673 | hp1 | a0001 | c0001 | t0012 | g0257 | EAS | CHS | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG00673 | hp2 | a0001 | c0001 | t0063 | g0132 | EAS | CHS | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG00733 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0240 | AMR | PUR | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG00735 | hp1 | a0001 | c0001 | t0110 | g0009 | AMR | PUR | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG00735 | hp2 | a0001 | c0001 | t0170 | g0338 | AMR | PUR | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG00738 | hp1 | a0001 | c0001 | t0013 | g0035 | AMR | PUR | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG00738 | hp2 | a0001 | c0004 | t0017 | g0001 | AMR | PUR | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG00741 | hp1 | a0001 | c0004 | t0205 | g0289 | AMR | PUR | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG00741 | hp2 | a0001 | c0001 | t0186 | g0349 | AMR | PUR | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG01069 | hp1 | a0001 | c0004 | t0017 | g0293 | AMR | PUR | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0251 | AMR | PUR | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG01071 | hp1 | a0001 | c0004 | t0017 | g0001 | AMR | PUR | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0045 | AMR | PUR | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG01081 | hp1 | a0001 | c0001 | t0013 | g0067 | AMR | PUR | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG01081 | hp2 | a0001 | c0001 | t0002 | g0055 | AMR | PUR | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG01099 | hp1 | a0001 | c0001 | t0118 | g0032 | AMR | PUR | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG01099 | hp2 | a0001 | c0001 | t0185 | g0228 | AMR | PUR | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG01106 | hp1 | a0001 | c0001 | t0002 | g0046 | AMR | PUR | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG01106 | hp2 | a0001 | c0001 | t0062 | g0118 | AMR | PUR | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG01109 | hp1 | a0001 | c0005 | t0157 | g0278 | AMR | PUR | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG01109 | hp2 | a0001 | c0001 | t0013 | g0049 | AMR | PUR | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG01168 | hp1 | a0001 | c0004 | t0014 | g0280 | AMR | PUR | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG01168 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG01169 | hp1 | a0001 | c0004 | t0014 | g0290 | AMR | PUR | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0034 | AMR | PUR | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG01175 | hp1 | a0001 | c0001 | t0002 | g0053 | AMR | PUR | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG01175 | hp2 | a0001 | c0001 | t0200 | g0360 | AMR | PUR | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG01192 | hp1 | a0001 | c0001 | t0066 | g0164 | AMR | PUR | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG01192 | hp2 | a0001 | c0001 | t0117 | g0006 | AMR | PUR | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG01243 | hp1 | a0001 | c0002 | t0035 | g0322 | AMR | PUR | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG01243 | hp2 | a0001 | c0001 | t0196 | g0335 | AMR | PUR | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0081 | AMR | CLM | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG01255 | hp2 | a0001 | c0001 | t0162 | g0361 | AMR | CLM | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG01256 | hp1 | a0001 | c0001 | t0002 | g0054 | AMR | CLM | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG01256 | hp2 | a0001 | c0001 | t0046 | g0110 | AMR | CLM | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG01257 | hp1 | a0001 | c0001 | t0032 | g0350 | AMR | CLM | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0068 | AMR | CLM | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG01258 | hp1 | a0001 | c0001 | t0068 | g0111 | AMR | CLM | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0070 | AMR | CLM | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG01261 | hp1 | a0001 | c0001 | t0154 | g0255 | AMR | CLM | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG01261 | hp2 | a0001 | c0004 | t0204 | g0288 | AMR | CLM | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0249 | AMR | CLM | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG01358 | hp2 | a0001 | c0001 | t0002 | g0085 | AMR | CLM | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG01496 | hp1 | a0001 | c0002 | t0207 | g0177 | AMR | CLM | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG01496 | hp2 | a0001 | c0001 | t0163 | g0222 | AMR | CLM | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG01515 | hp1 | a0001 | c0001 | t0002 | g0039 | EUR | IBS | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG01515 | hp2 | a0001 | c0001 | t0013 | g0050 | EUR | IBS | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG01884 | hp1 | a0001 | c0003 | t0101 | g0089 | AFR | ACB | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG01884 | hp2 | a0001 | c0001 | t0002 | g0044 | AFR | ACB | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG01891 | hp1 | a0001 | c0001 | t0145 | g0279 | AFR | ACB | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG01891 | hp2 | a0001 | c0003 | t0021 | g0355 | AFR | ACB | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG01928 | hp1 | a0001 | c0001 | t0089 | g0097 | AMR | PEL | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0256 | AMR | PEL | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG01934 | hp1 | a0001 | c0001 | t0005 | g0232 | AMR | PEL | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG01934 | hp2 | a0001 | c0002 | t0133 | g0271 | AMR | PEL | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG01943 | hp1 | a0001 | c0001 | t0061 | g0096 | AMR | PEL | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG01943 | hp2 | a0001 | c0001 | t0192 | g0267 | AMR | PEL | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG01952 | hp1 | a0001 | c0002 | t0132 | g0276 | AMR | PEL | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG01952 | hp2 | a0001 | c0001 | t0033 | g0348 | AMR | PEL | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG01975 | hp1 | a0001 | c0001 | t0005 | g0231 | AMR | PEL | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG01975 | hp2 | a0001 | c0001 | t0032 | g0333 | AMR | PEL | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG01978 | hp1 | a0001 | c0001 | t0115 | g0024 | AMR | PEL | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG01978 | hp2 | a0001 | c0001 | t0050 | g0124 | AMR | PEL | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG01981 | hp1 | a0001 | c0001 | t0193 | g0329 | AMR | PEL | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG01981 | hp2 | a0001 | c0001 | t0002 | g0040 | AMR | PEL | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG01993 | hp1 | a0001 | c0001 | t0158 | g0247 | AMR | PEL | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG01993 | hp2 | a0001 | c0001 | t0194 | g0336 | AMR | PEL | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG02004 | hp1 | a0001 | c0002 | t0139 | g0269 | AMR | PEL | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0263 | AMR | PEL | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG02015 | hp1 | a0001 | c0001 | t0183 | g0359 | EAS | KHV | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG02015 | hp2 | a0001 | c0001 | t0018 | g0133 | EAS | KHV | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG02027 | hp1 | a0001 | c0001 | t0161 | g0214 | EAS | KHV | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG02027 | hp2 | a0001 | c0001 | t0082 | g0154 | EAS | KHV | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG02055 | hp1 | a0001 | c0003 | t0126 | g0313 | AFR | ACB | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG02055 | hp2 | a0001 | c0002 | t0201 | g0315 | AFR | ACB | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | KHV | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG02056 | hp2 | a0001 | c0001 | t0057 | g0129 | EAS | KHV | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG02074 | hp1 | a0001 | c0001 | t0004 | g0072 | EAS | KHV | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG02074 | hp2 | a0001 | c0001 | t0178 | g0226 | EAS | KHV | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG02080 | hp1 | a0001 | c0001 | t0048 | g0123 | EAS | KHV | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | KHV | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | KHV | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG02083 | hp2 | a0001 | c0001 | t0190 | g0358 | EAS | KHV | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG02129 | hp1 | a0001 | c0001 | t0179 | g0198 | EAS | KHV | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG02129 | hp2 | a0001 | c0001 | t0028 | g0184 | EAS | KHV | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | KHV | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG02132 | hp2 | a0001 | c0002 | t0134 | g0277 | EAS | KHV | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG02135 | hp1 | a0001 | c0001 | t0088 | g0114 | EAS | KHV | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG02135 | hp2 | a0001 | c0001 | t0010 | g0112 | EAS | KHV | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG02148 | hp1 | a0001 | c0001 | t0058 | g0098 | AMR | PEL | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG02148 | hp2 | a0001 | c0002 | t0140 | g0265 | AMR | PEL | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG02155 | hp1 | a0001 | c0001 | t0056 | g0130 | EAS | CDX | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG02155 | hp2 | a0001 | c0001 | t0030 | g0206 | EAS | CDX | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG02257 | hp1 | a0001 | c0002 | t0024 | g0281 | AFR | ACB | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG02257 | hp2 | a0001 | c0001 | t0108 | g0083 | AFR | ACB | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG02258 | hp1 | a0001 | c0001 | t0149 | g0300 | AFR | ACB | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG02258 | hp2 | a0001 | c0001 | t0069 | g0105 | AFR | ACB | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG02273 | hp1 | a0001 | c0001 | t0033 | g0328 | AMR | PEL | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG02273 | hp2 | a0001 | c0001 | t0167 | g0259 | AMR | PEL | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG02293 | hp1 | a0001 | c0001 | t0199 | g0327 | AMR | PEL | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG02293 | hp2 | a0001 | c0001 | t0002 | g0073 | AMR | PEL | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0084 | AMR | PEL | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG02300 | hp2 | a0001 | c0001 | t0180 | g0341 | AMR | PEL | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG02451 | hp1 | a0001 | c0001 | t0077 | g0159 | AFR | ACB | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG02451 | hp2 | a0001 | c0002 | t0120 | g0012 | AFR | ACB | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG02523 | hp1 | a0001 | c0001 | t0031 | g0340 | EAS | KHV | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG02523 | hp2 | a0001 | c0001 | t0004 | g0061 | EAS | KHV | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG02572 | hp1 | a0001 | c0001 | t0064 | g0155 | AFR | GWD | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG02572 | hp2 | a0001 | c0001 | t0073 | g0166 | AFR | GWD | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG02602 | hp1 | a0001 | c0001 | t0030 | g0182 | SAS | PJL | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG02602 | hp2 | a0001 | c0001 | t0034 | g0330 | SAS | PJL | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG02615 | hp1 | a0001 | c0001 | t0141 | g0301 | AFR | GWD | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG02615 | hp2 | a0001 | c0001 | t0104 | g0058 | AFR | GWD | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG02622 | hp1 | a0001 | c0002 | t0019 | g0092 | AFR | GWD | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG02622 | hp2 | a0001 | c0001 | t0008 | g0099 | AFR | GWD | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG02630 | hp1 | a0001 | c0003 | t0125 | g0309 | AFR | GWD | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG02630 | hp2 | a0001 | c0002 | t0026 | g0287 | AFR | GWD | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG02698 | hp1 | a0001 | c0001 | t0074 | g0162 | SAS | PJL | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG02698 | hp2 | a0001 | c0001 | t0007 | g0153 | SAS | PJL | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG02717 | hp1 | a0001 | c0002 | t0202 | g0318 | AFR | GWD | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG02717 | hp2 | a0001 | c0002 | t0019 | g0093 | AFR | GWD | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG02723 | hp1 | a0001 | c0002 | t0006 | g0291 | AFR | GWD | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG02723 | hp2 | a0001 | c0001 | t0094 | g0090 | AFR | GWD | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG02735 | hp1 | a0001 | c0001 | t0174 | g0331 | SAS | PJL | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0059 | SAS | PJL | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG02738 | hp1 | a0001 | c0001 | t0005 | g0218 | SAS | PJL | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG02738 | hp2 | a0001 | c0001 | t0002 | g0030 | SAS | PJL | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG02809 | hp1 | a0001 | c0002 | t0006 | g0320 | AFR | GWD | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG02809 | hp2 | a0001 | c0002 | t0025 | g0282 | AFR | GWD | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG02818 | hp1 | a0001 | c0003 | t0124 | g0308 | AFR | GWD | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG02818 | hp2 | a0001 | c0006 | t0143 | g0312 | AFR | GWD | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG02886 | hp1 | a0001 | c0001 | t0144 | g0298 | AFR | GWD | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG02886 | hp2 | a0001 | c0002 | t0203 | g0323 | AFR | GWD | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG02895 | hp1 | a0001 | c0001 | t0027 | g0306 | AFR | GWD | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG02895 | hp2 | a0002 | c0007 | t0039 | g0150 | AFR | GWD | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG02897 | hp1 | a0001 | c0001 | t0011 | g0304 | AFR | GWD | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG02897 | hp2 | a0001 | c0001 | t0027 | g0307 | AFR | GWD | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG02922 | hp1 | a0001 | c0001 | t0107 | g0056 | AFR | ESN | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG02922 | hp2 | a0001 | c0003 | t0098 | g0088 | AFR | ESN | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG02965 | hp1 | a0001 | c0001 | t0011 | g0305 | AFR | ESN | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG02965 | hp2 | a0001 | c0003 | t0099 | g0095 | AFR | ESN | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG02970 | hp1 | a0001 | c0001 | t0011 | g0299 | AFR | ESN | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG02970 | hp2 | a0001 | c0005 | t0100 | g0134 | AFR | ESN | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG03041 | hp1 | a0001 | c0003 | t0112 | g0087 | AFR | GWD | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG03041 | hp2 | a0001 | c0003 | t0119 | g0094 | AFR | GWD | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG03098 | hp1 | a0001 | c0002 | t0006 | g0314 | AFR | MSL | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG03098 | hp2 | a0001 | c0001 | t0023 | g0296 | AFR | MSL | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG03130 | hp1 | a0001 | c0001 | t0011 | g0319 | AFR | ESN | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG03130 | hp2 | a0001 | c0005 | t0156 | g0261 | AFR | ESN | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG03139 | hp1 | a0001 | c0003 | t0123 | g0364 | AFR | ESN | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG03139 | hp2 | a0001 | c0001 | t0022 | g0294 | AFR | ESN | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG03195 | hp1 | a0001 | c0001 | t0011 | g0303 | AFR | ESN | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG03195 | hp2 | a0001 | c0002 | t0026 | g0286 | AFR | ESN | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG03209 | hp1 | a0001 | c0001 | t0169 | g0352 | AFR | MSL | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG03209 | hp2 | a0001 | c0001 | t0044 | g0156 | AFR | MSL | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG03225 | hp1 | a0001 | c0002 | t0006 | g0316 | AFR | MSL | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG03225 | hp2 | a0001 | c0001 | t0093 | g0106 | AFR | MSL | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG03453 | hp1 | a0001 | c0003 | t0021 | g0354 | AFR | MSL | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG03453 | hp2 | a0001 | c0002 | t0024 | g0284 | AFR | MSL | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG03486 | hp1 | a0001 | c0001 | t0148 | g0302 | AFR | MSL | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG03486 | hp2 | a0001 | c0001 | t0146 | g0292 | AFR | MSL | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG03490 | hp1 | a0001 | c0001 | t0002 | g0036 | SAS | PJL | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG03490 | hp2 | a0001 | c0001 | t0007 | g0139 | SAS | PJL | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG03491 | hp1 | a0001 | c0001 | t0012 | g0180 | SAS | PJL | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG03491 | hp2 | a0001 | c0004 | t0014 | g0002 | SAS | PJL | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0038 | SAS | PJL | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG03492 | hp2 | a0001 | c0004 | t0014 | g0002 | SAS | PJL | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG03516 | hp1 | a0001 | c0001 | t0075 | g0165 | AFR | ESN | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG03516 | hp2 | a0001 | c0001 | t0106 | g0071 | AFR | ESN | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG03540 | hp1 | a0001 | c0001 | t0070 | g0157 | AFR | GWD | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG03540 | hp2 | a0002 | c0007 | t0081 | g0175 | AFR | GWD | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG03579 | hp1 | a0001 | c0003 | t0127 | g0356 | AFR | MSL | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG03579 | hp2 | a0001 | c0001 | t0076 | g0168 | AFR | MSL | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0205 | SAS | PJL | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0174 | SAS | PJL | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG03669 | hp1 | a0001 | c0001 | t0008 | g0176 | SAS | PJL | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG03669 | hp2 | a0001 | c0001 | t0005 | g0210 | SAS | PJL | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG03688 | hp1 | a0001 | c0001 | t0083 | g0141 | SAS | STU | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG03688 | hp2 | a0001 | c0001 | t0160 | g0212 | SAS | STU | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG03704 | hp1 | a0001 | c0001 | t0191 | g0347 | SAS | PJL | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG03704 | hp2 | a0001 | c0001 | t0086 | g0161 | SAS | PJL | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG03710 | hp1 | a0001 | c0001 | t0012 | g0181 | SAS | PJL | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0041 | SAS | PJL | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0008 | SAS | BEB | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG03834 | hp2 | a0001 | c0001 | t0159 | g0260 | SAS | BEB | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG03927 | hp1 | a0001 | c0001 | t0177 | g0362 | SAS | BEB | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG03927 | hp2 | a0001 | c0001 | t0002 | g0010 | SAS | BEB | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0048 | SAS | BEB | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG03942 | hp2 | a0001 | c0001 | t0005 | g0236 | SAS | BEB | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0242 | SAS | STU | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG04115 | hp2 | a0001 | c0002 | t0131 | g0272 | SAS | STU | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG04184 | hp1 | a0001 | c0001 | t0031 | g0334 | SAS | BEB | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0042 | SAS | BEB | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG04228 | hp1 | a0001 | c0001 | t0008 | g0152 | SAS | STU | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG04228 | hp2 | a0001 | c0001 | t0043 | g0007 | SAS | STU | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA18522 | hp1 | a0001 | c0002 | t0035 | g0324 | AFR | YRI | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA18522 | hp2 | a0001 | c0001 | t0071 | g0107 | AFR | YRI | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | CHB | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA18612 | hp2 | a0001 | c0001 | t0003 | g0019 | EAS | CHB | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA18747 | hp1 | a0001 | c0001 | t0004 | g0062 | EAS | CHB | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA18747 | hp2 | a0001 | c0002 | t0136 | g0268 | EAS | CHB | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA18906 | hp1 | a0001 | c0002 | t0206 | g0178 | AFR | YRI | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA18906 | hp2 | a0001 | c0001 | t0042 | g0102 | AFR | YRI | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA18940 | hp1 | a0004 | c0008 | t0005 | g0234 | EAS | JPT | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA18940 | hp2 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA18942 | hp1 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA18942 | hp2 | a0001 | c0001 | t0171 | g0342 | EAS | JPT | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA18944 | hp2 | a0001 | c0001 | t0004 | g0063 | EAS | JPT | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA18945 | hp1 | a0001 | c0001 | t0096 | g0076 | EAS | JPT | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA18945 | hp2 | a0001 | c0001 | t0010 | g0135 | EAS | JPT | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA18946 | hp1 | a0001 | c0001 | t0007 | g0144 | EAS | JPT | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA18951 | hp2 | a0001 | c0001 | t0003 | g0018 | EAS | JPT | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA18953 | hp1 | a0001 | c0001 | t0028 | g0258 | EAS | JPT | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA18953 | hp2 | a0001 | c0010 | t0189 | g0179 | EAS | JPT | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA18956 | hp1 | a0003 | c0009 | t0172 | g0217 | EAS | JPT | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA18956 | hp2 | a0001 | c0001 | t0015 | g0143 | EAS | JPT | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA18959 | hp1 | a0001 | c0001 | t0003 | g0078 | EAS | JPT | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA18959 | hp2 | a0001 | c0001 | t0164 | g0235 | EAS | JPT | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA18960 | hp1 | a0001 | c0001 | t0003 | g0027 | EAS | JPT | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA18960 | hp2 | a0001 | c0001 | t0092 | g0137 | EAS | JPT | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA18961 | hp1 | a0001 | c0001 | t0029 | g0254 | EAS | JPT | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA18961 | hp2 | a0001 | c0001 | t0060 | g0122 | EAS | JPT | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA18963 | hp1 | a0001 | c0001 | t0016 | g0332 | EAS | JPT | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA18963 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA18965 | hp1 | a0001 | c0001 | t0166 | g0345 | EAS | JPT | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA18966 | hp1 | a0001 | c0001 | t0008 | g0140 | EAS | JPT | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA18967 | hp1 | a0001 | c0001 | t0009 | g0077 | EAS | JPT | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA18967 | hp2 | a0001 | c0001 | t0010 | g0172 | EAS | JPT | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA18968 | hp2 | a0001 | c0001 | t0038 | g0115 | EAS | JPT | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA18969 | hp2 | a0001 | c0002 | t0150 | g0264 | EAS | JPT | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA18970 | hp1 | a0001 | c0001 | t0153 | g0244 | EAS | JPT | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA18970 | hp2 | a0001 | c0001 | t0121 | g0136 | EAS | JPT | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA18971 | hp1 | a0001 | c0002 | t0129 | g0275 | EAS | JPT | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA18971 | hp2 | a0001 | c0001 | t0049 | g0101 | EAS | JPT | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA18973 | hp1 | a0001 | c0001 | t0041 | g0128 | EAS | JPT | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA18973 | hp2 | a0001 | c0001 | t0009 | g0033 | EAS | JPT | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA18977 | hp1 | a0001 | c0001 | t0036 | g0065 | EAS | JPT | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA18978 | hp1 | a0001 | c0001 | t0007 | g0148 | EAS | JPT | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA18979 | hp1 | a0001 | c0001 | t0004 | g0066 | EAS | JPT | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA18979 | hp2 | a0001 | c0002 | t0128 | g0273 | EAS | JPT | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA18981 | hp2 | a0001 | c0001 | t0015 | g0145 | EAS | JPT | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA18982 | hp2 | a0001 | c0001 | t0015 | g0146 | EAS | JPT | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA18983 | hp1 | a0001 | c0001 | t0176 | g0199 | EAS | JPT | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA18983 | hp2 | a0001 | c0001 | t0018 | g0151 | EAS | JPT | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA18984 | hp1 | a0001 | c0001 | t0090 | g0104 | EAS | JPT | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA18984 | hp2 | a0001 | c0002 | t0135 | g0270 | EAS | JPT | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA18985 | hp2 | a0001 | c0001 | t0007 | g0169 | EAS | JPT | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA18986 | hp1 | a0001 | c0001 | t0009 | g0060 | EAS | JPT | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA18986 | hp2 | a0001 | c0001 | t0010 | g0103 | EAS | JPT | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA18988 | hp2 | a0001 | c0002 | t0130 | g0274 | EAS | JPT | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA18990 | hp1 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA18990 | hp2 | a0001 | c0001 | t0012 | g0227 | EAS | JPT | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA18992 | hp1 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA18992 | hp2 | a0001 | c0001 | t0047 | g0127 | EAS | JPT | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA18998 | hp1 | a0001 | c0001 | t0182 | g0225 | EAS | JPT | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA18999 | hp1 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA18999 | hp2 | a0001 | c0001 | t0051 | g0120 | EAS | JPT | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA19001 | hp1 | a0001 | c0001 | t0184 | g0200 | EAS | JPT | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA19002 | hp1 | a0001 | c0001 | t0181 | g0363 | EAS | JPT | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA19002 | hp2 | a0001 | c0001 | t0080 | g0147 | EAS | JPT | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA19005 | hp2 | a0001 | c0001 | t0009 | g0022 | EAS | JPT | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA19007 | hp1 | a0001 | c0001 | t0102 | g0170 | EAS | JPT | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA19007 | hp2 | a0001 | c0002 | t0137 | g0266 | EAS | JPT | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA19009 | hp2 | a0001 | c0001 | t0020 | g0023 | EAS | JPT | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA19010 | hp1 | a0001 | c0001 | t0054 | g0131 | EAS | JPT | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA19010 | hp2 | a0001 | c0001 | t0188 | g0201 | EAS | JPT | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA19011 | hp1 | a0001 | c0001 | t0187 | g0220 | EAS | JPT | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA19012 | hp1 | a0001 | c0001 | t0103 | g0100 | EAS | JPT | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA19012 | hp2 | a0001 | c0001 | t0004 | g0029 | EAS | JPT | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA19030 | hp1 | a0001 | c0001 | t0111 | g0052 | AFR | LWK | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA19030 | hp2 | a0001 | c0002 | t0147 | g0285 | AFR | LWK | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA19043 | hp1 | a0001 | c0001 | t0152 | g0243 | AFR | LWK | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA19043 | hp2 | a0001 | c0003 | t0097 | g0091 | AFR | LWK | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA19054 | hp1 | a0001 | c0001 | t0055 | g0126 | EAS | JPT | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA19055 | hp1 | a0001 | c0001 | t0168 | g0190 | EAS | JPT | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA19055 | hp2 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA19060 | hp1 | a0001 | c0001 | t0091 | g0149 | EAS | JPT | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA19060 | hp2 | a0001 | c0001 | t0197 | g0224 | EAS | JPT | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA19063 | hp1 | a0001 | c0001 | t0085 | g0173 | EAS | JPT | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA19063 | hp2 | a0001 | c0001 | t0016 | g0344 | EAS | JPT | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA19066 | hp1 | a0001 | c0001 | t0059 | g0125 | EAS | JPT | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA19066 | hp2 | a0001 | c0001 | t0012 | g0188 | EAS | JPT | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA19076 | hp2 | a0001 | c0001 | t0175 | g0219 | EAS | JPT | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA19078 | hp1 | a0001 | c0001 | t0004 | g0064 | EAS | JPT | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA19078 | hp2 | a0001 | c0001 | t0010 | g0167 | EAS | JPT | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA19080 | hp1 | a0001 | c0001 | t0005 | g0230 | EAS | JPT | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA19080 | hp2 | a0001 | c0001 | t0165 | g0339 | EAS | JPT | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA19081 | hp1 | a0001 | c0002 | t0138 | g0250 | EAS | JPT | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA19081 | hp2 | a0001 | c0001 | t0004 | g0028 | EAS | JPT | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA19083 | hp1 | a0001 | c0001 | t0009 | g0031 | EAS | JPT | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA19083 | hp2 | a0001 | c0001 | t0040 | g0113 | EAS | JPT | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA19085 | hp1 | a0001 | c0001 | t0087 | g0116 | EAS | JPT | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA19085 | hp2 | a0001 | c0001 | t0084 | g0117 | EAS | JPT | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA19088 | hp1 | a0001 | c0001 | t0008 | g0142 | EAS | JPT | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA19090 | hp1 | a0001 | c0001 | t0020 | g0080 | EAS | JPT | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA19091 | hp1 | a0001 | c0001 | t0029 | g0215 | EAS | JPT | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA19091 | hp2 | a0001 | c0001 | t0004 | g0075 | EAS | JPT | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA19240 | hp1 | a0001 | c0002 | t0006 | g0317 | AFR | YRI | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA19240 | hp2 | a0001 | c0001 | t0151 | g0353 | AFR | YRI | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA20129 | hp1 | a0001 | c0001 | t0072 | g0108 | AFR | ASW | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA20129 | hp2 | a0001 | c0001 | t0105 | g0057 | AFR | ASW | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0069 | EUR | TSI | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA20752 | hp2 | a0001 | c0001 | t0195 | g0337 | EUR | TSI | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA20805 | hp1 | a0001 | c0001 | t0109 | g0025 | EUR | TSI | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA20805 | hp2 | a0001 | c0001 | t0114 | g0160 | EUR | TSI | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG01123 | hp1 | a0001 | c0001 | t0095 | g0047 | AMR | CLM | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG01123 | hp2 | a0001 | c0001 | t0037 | g0163 | AMR | CLM | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG02109 | hp1 | a0001 | c0001 | t0078 | g0086 | AFR | ACB | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG02109 | hp2 | a0001 | c0002 | t0025 | g0283 | AFR | ACB | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG02486 | hp1 | a0001 | c0001 | t0002 | g0082 | AFR | ACB | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG02486 | hp2 | a0001 | c0002 | t0006 | g0321 | AFR | ACB | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG02559 | hp1 | a0001 | c0001 | t0023 | g0297 | AFR | ACB | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG02559 | hp2 | a0001 | c0006 | t0142 | g0310 | AFR | ACB | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG03471 | hp1 | a0001 | c0001 | t0067 | g0109 | AFR | MSL | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG03471 | hp2 | a0001 | c0003 | t0122 | g0357 | AFR | MSL | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG06807 | hp1 | a0001 | c0001 | t0002 | g0037 | AFR | USA | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
HG06807 | hp2 | a0001 | c0001 | t0022 | g0295 | AFR | USA | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA18955 | hp2 | a0001 | c0001 | t0116 | g0119 | EAS | JPT | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0325 | AFR | LWK | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
NA21309 | hp2 | a0001 | c0001 | t0045 | g0158 | AFR | LWK | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0026 | REF | REF | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0155 | g0311 | REF | REF | GNB5_chr15_52110100_52196392 | GNB5 | chr15 | 52110100 | 52196392 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr15:52133444
|
C | T | 1 | a0004 | 1 | NA18940.hp1 | stop_gained | HIGH | c.797G>A | p.Trp266* | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 9/13 | 886/8934 | 797/1188 | 266/395 | chr15 | 52133444 | ||
chr15:52133449
|
C | A | 1 | a0004 | 1 | NA18940.hp1 | missense_variant | MODERATE | c.792G>T | p.Met264Ile | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 9/13 | 881/8934 | 792/1188 | 264/395 | chr15 | 52133449 | ||
chr15:52133450
|
A | T | 1 | a0004 | 1 | NA18940.hp1 | missense_variant | MODERATE | c.791T>A | p.Met264Lys | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 9/13 | 880/8934 | 791/1188 | 264/395 | chr15 | 52133450 | ||
chr15:52133451
|
T | A | 1 | a0004 | 1 | NA18940.hp1 | missense_variant | MODERATE | c.790A>T | p.Met264Leu | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 9/13 | 879/8934 | 790/1188 | 264/395 | chr15 | 52133451 | ||
chr15:52133453
|
G | T | 1 | a0004 | 1 | NA18940.hp1 | missense_variant | MODERATE | c.788C>A | p.Ala263Asp | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 9/13 | 877/8934 | 788/1188 | 263/395 | chr15 | 52133453 | ||
chr15:52133454
|
C | G | 1 | a0004 | 1 | NA18940.hp1 | missense_variant | MODERATE | c.787G>C | p.Ala263Pro | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 9/13 | 876/8934 | 787/1188 | 263/395 | chr15 | 52133454 | ||
chr15:52133455
|
T | A | 1 | a0004 | 1 | NA18940.hp1 | missense_variant | MODERATE | c.786A>T | p.Lys262Asn | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 9/13 | 875/8934 | 786/1188 | 262/395 | chr15 | 52133455 | ||
chr15:52133457
|
T | G | 1 | a0004 | 1 | NA18940.hp1 | missense_variant | MODERATE | c.784A>C | p.Lys262Gln | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 9/13 | 873/8934 | 784/1188 | 262/395 | chr15 | 52133457 | ||
chr15:52135746
|
G | A | 1 | a0002 | 2 | HG02895.hp2 HG03540.hp2 |
missense_variant | MODERATE | c.638C>T | p.Ala213Val | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 8/13 | 727/8934 | 638/1188 | 213/395 | chr15 | 52135746 | ||
chr15:52141177
|
T | A | 1 | a0003 | 1 | NA18956.hp1 | missense_variant | MODERATE | c.590A>T | p.Tyr197Phe | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/13 | 679/8934 | 590/1188 | 197/395 | chr15 | 52141177 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr15:52124542
|
G | A | 1 | a0001c0006 | 2 | HG02559.hp2 HG02818.hp2 |
synonymous_variant | LOW | c.1107C>T | p.Arg369Arg | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 12/13 | 1196/8934 | 1107/1188 | 369/395 | chr15 | 52124542 | ||
chr15:52126021
|
T | C | 2 | a0001c0003a0001c0005 | 17 | HG01109.hp1 HG01884.hp1 HG01891.hp2 others(14): Show |
synonymous_variant | LOW | c.936A>G | p.Ala312Ala | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 11/13 | 1025/8934 | 936/1188 | 312/395 | chr15 | 52126021 | ||
chr15:52133446
|
C | T | 1 | a0004c0008 | 1 | NA18940.hp1 | synonymous_variant | LOW | c.795G>A | p.Val265Val | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 9/13 | 884/8934 | 795/1188 | 265/395 | chr15 | 52133446 | ||
chr15:52133458
|
C | T | 1 | a0004c0008 | 1 | NA18940.hp1 | synonymous_variant | LOW | c.783G>A | p.Lys261Lys | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 9/13 | 872/8934 | 783/1188 | 261/395 | chr15 | 52133458 | ||
chr15:52141200
|
C | T | 1 | a0001c0004 | 9 | HG00738.hp2 HG00741.hp1 HG01069.hp1 others(6): Show |
synonymous_variant | LOW | c.567G>A | p.Lys189Lys | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/13 | 656/8934 | 567/1188 | 189/395 | chr15 | 52141200 | ||
chr15:52147482
|
T | A | 1 | a0001c0010 | 1 | NA18953.hp2 | synonymous_variant | LOW | c.471A>T | p.Pro157Pro | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 6/13 | 560/8934 | 471/1188 | 157/395 | chr15 | 52147482 | ||
chr15:52154003
|
G | A | 3 | a0001c0002a0001c0003a0001c0004 | 60 | HG00738.hp2 HG00741.hp1 HG01069.hp1 others(57): Show |
synonymous_variant | LOW | c.312C>T | p.His104His | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 4/13 | 401/8934 | 312/1188 | 104/395 | chr15 | 52154003 | ||
chr15:52154063
|
C | T | 1 | a0001c0004 | 9 | HG00738.hp2 HG00741.hp1 HG01069.hp1 others(6): Show |
synonymous_variant | LOW | c.252G>A | p.Ala84Ala | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 4/13 | 341/8934 | 252/1188 | 84/395 | chr15 | 52154063 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr15:52115153
|
TAC | T | 13 | a0001c0002t0128a0001c0002t0129a0001c0002t0130others(10): Show | 13 | HG01934.hp2 HG01952.hp1 HG02004.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*7602_*7603delGT | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 7602 | chr15 | 52115153 | |||||
chr15:52115212
|
T | C | 47 | a0001c0001t0016a0001c0001t0031a0001c0001t0032others(44): Show | 53 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*7545A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 7545 | chr15 | 52115212 | |||||
chr15:52115405
|
C | T | 6 | a0001c0001t0032a0001c0001t0033a0001c0001t0192others(3): Show | 8 | HG01257.hp1 HG01943.hp2 HG01952.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*7352G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 7352 | chr15 | 52115405 | |||||
chr15:52115442
|
C | T | 7 | a0001c0003t0021a0001c0003t0122a0001c0003t0123others(4): Show | 8 | HG01891.hp2 HG02055.hp1 HG02630.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*7315G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 7315 | chr15 | 52115442 | |||||
chr15:52115642
|
T | C | 1 | a0001c0001t0107 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7115A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 7115 | chr15 | 52115642 | |||||
chr15:52115683
|
C | T | 1 | a0001c0001t0159 | 1 | HG03834.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7074G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 7074 | chr15 | 52115683 | |||||
chr15:52115803
|
C | T | 5 | a0001c0001t0005a0001c0001t0161a0001c0001t0163others(2): Show | 12 | HG00544.hp1 HG00558.hp2 HG01496.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*6954G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 6954 | chr15 | 52115803 | |||||
chr15:52115895
|
T | C | 1 | a0001c0001t0013 | 4 | HG00738.hp1 HG01081.hp1 HG01109.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*6862A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 6862 | chr15 | 52115895 | |||||
chr15:52115982
|
T | C | 1 | a0001c0001t0108 | 1 | HG02257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6775A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 6775 | chr15 | 52115982 | |||||
chr15:52116005
|
G | A | 1 | a0001c0001t0027 | 2 | HG02895.hp1 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6752C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 6752 | chr15 | 52116005 | |||||
chr15:52116006
|
C | A | 1 | a0001c0001t0065 | 1 | HG00323.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6751G>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 6751 | chr15 | 52116006 | |||||
chr15:52116241
|
T | C | 4 | a0001c0004t0014a0001c0004t0017a0001c0004t0204others(1): Show | 9 | HG00738.hp2 HG00741.hp1 HG01069.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*6516A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 6516 | chr15 | 52116241 | |||||
chr15:52116455
|
G | C | 65 | a0001c0001t0007a0001c0001t0008a0001c0001t0015others(62): Show | 77 | HG00323.hp2 HG00544.hp2 HG00597.hp1 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*6302C>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 6302 | chr15 | 52116455 | |||||
chr15:52116571
|
C | CATTT | 34 | a0001c0001t0011a0001c0001t0022a0001c0001t0023others(31): Show | 44 | HG01109.hp1 HG01496.hp1 HG01891.hp1 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*6182_*6185dupAAAT | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 6185 | chr15 | 52116571 | |||||
chr15:52116654
|
T | C | 2 | a0001c0001t0145a0001c0001t0146 | 2 | HG01891.hp1 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6103A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 6103 | chr15 | 52116654 | |||||
chr15:52116780
|
C | T | 4 | a0001c0004t0014a0001c0004t0017a0001c0004t0204others(1): Show | 9 | HG00738.hp2 HG00741.hp1 HG01069.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*5977G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5977 | chr15 | 52116780 | |||||
chr15:52116871
|
C | T | 7 | a0001c0002t0128a0001c0002t0129a0001c0002t0130others(4): Show | 7 | HG01934.hp2 HG01952.hp1 HG02132.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*5886G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5886 | chr15 | 52116871 | |||||
chr15:52116918
|
CT | C | 27 | a0001c0001t0046a0001c0001t0067a0001c0001t0068others(24): Show | 27 | HG01109.hp1 HG01256.hp2 HG01258.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*5838delA | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5838 | chr15 | 52116918 | |||||
chr15:52116918
|
CTT | C | 17 | a0001c0001t0011a0001c0001t0022a0001c0001t0023others(14): Show | 27 | HG01891.hp1 HG02109.hp2 HG02257.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*5837_*5838delAA | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5837 | chr15 | 52116918 | |||||
chr15:52116918
|
CTTTTTTT others(15): Show |
C | 2 | a0001c0002t0206a0001c0002t0207 | 2 | HG01496.hp1 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5817_*5838delAAAA others(18): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5817 | chr15 | 52116918 | |||||
chr15:52116994
|
G | A | 65 | a0001c0001t0007a0001c0001t0008a0001c0001t0015others(62): Show | 77 | HG00323.hp2 HG00544.hp2 HG00597.hp1 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*5763C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5763 | chr15 | 52116994 | |||||
chr15:52117049
|
G | A | 2 | a0001c0005t0156a0001c0005t0157 | 2 | HG01109.hp1 HG03130.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5708C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5708 | chr15 | 52117049 | |||||
chr15:52117081
|
G | T | 1 | a0001c0001t0185 | 1 | HG01099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5676C>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5676 | chr15 | 52117081 | |||||
chr15:52117089
|
A | AATATATA others(25): Show |
1 | a0001c0004t0205 | 1 | HG00741.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5667_*5668insATAT others(28): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5667 | chr15 | 52117089 | |||||
chr15:52117089
|
A | AATATATA others(31): Show |
1 | a0001c0001t0114 | 1 | NA20805.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5667_*5668insATAT others(34): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5667 | chr15 | 52117089 | |||||
chr15:52117092
|
A | T | 34 | a0001c0001t0011a0001c0001t0022a0001c0001t0023others(31): Show | 44 | HG01109.hp1 HG01496.hp1 HG01891.hp1 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*5665T>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5665 | chr15 | 52117092 | |||||
chr15:52117098
|
A | G | 1 | a0001c0002t0131 | 1 | HG04115.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5659T>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5659 | chr15 | 52117098 | |||||
chr15:52117102
|
A | ATATATAT others(64): Show |
1 | a0001c0001t0188 | 1 | NA19010.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5654_*5655insAAAA others(67): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5654 | chr15 | 52117102 | |||||
chr15:52117102
|
A | ATATATAT others(15): Show |
1 | a0001c0005t0156 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5654_*5655insATTA others(18): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5654 | chr15 | 52117102 | |||||
chr15:52117102
|
A | ATATATAT others(29): Show |
1 | a0001c0005t0157 | 1 | HG01109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5654_*5655insATTA others(32): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5654 | chr15 | 52117102 | |||||
chr15:52117102
|
A | ATATATAT others(87): Show |
1 | a0001c0001t0065 | 1 | HG00323.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5654_*5655insAAAA others(90): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5654 | chr15 | 52117102 | |||||
chr15:52117102
|
A | ATATATAT others(66): Show |
1 | a0001c0001t0037 | 1 | HG01123.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5654_*5655insAAAA others(69): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5654 | chr15 | 52117102 | |||||
chr15:52117102
|
A | ATATATAT others(41): Show |
1 | a0001c0001t0192 | 1 | HG01943.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5654_*5655insAAAA others(44): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5654 | chr15 | 52117102 | |||||
chr15:52117102
|
A | ATATATAT others(61): Show |
1 | a0001c0001t0055 | 1 | NA19054.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5654_*5655insAAAA others(64): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5654 | chr15 | 52117102 | |||||
chr15:52117102
|
A | ATATATAT others(65): Show |
2 | a0001c0001t0047a0001c0001t0067 | 2 | HG03471.hp1 NA18992.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5654_*5655insAAAA others(68): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5654 | chr15 | 52117102 | |||||
chr15:52117102
|
A | ATATATAT others(39): Show |
1 | a0001c0001t0032 | 2 | HG01257.hp1 HG01975.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5654_*5655insAAAA others(42): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5654 | chr15 | 52117102 | |||||
chr15:52117102
|
A | ATATATAT others(57): Show |
2 | a0001c0001t0041a0001c0001t0116 | 2 | NA18955.hp2 NA18973.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5654_*5655insAAAA others(60): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5654 | chr15 | 52117102 | |||||
chr15:52117102
|
A | ATATATAT others(60): Show |
1 | a0001c0001t0052 | 1 | HG00544.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5654_*5655insAAAA others(63): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5654 | chr15 | 52117102 | |||||
chr15:52117102
|
A | ATATATAT others(61): Show |
1 | a0001c0001t0071 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5654_*5655insAAAA others(64): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5654 | chr15 | 52117102 | |||||
chr15:52117102
|
A | ATATATAT others(37): Show |
2 | a0001c0001t0193a0001c0001t0199 | 2 | HG01981.hp1 HG02293.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5654_*5655insAAAA others(40): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5654 | chr15 | 52117102 | |||||
chr15:52117102
|
A | ATATATAT others(46): Show |
1 | a0001c0001t0063 | 1 | HG00673.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5654_*5655insAAAA others(49): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5654 | chr15 | 52117102 | |||||
chr15:52117102
|
A | ATATATAT others(52): Show |
1 | a0001c0001t0042 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5654_*5655insAAAA others(55): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5654 | chr15 | 52117102 | |||||
chr15:52117102
|
A | ATATATAT others(56): Show |
2 | a0001c0001t0056a0001c0001t0184 | 2 | HG02155.hp1 NA19001.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5654_*5655insAAAA others(59): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5654 | chr15 | 52117102 | |||||
chr15:52117102
|
A | ATATATAT others(58): Show |
1 | a0001c0001t0053 | 1 | HG00597.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5654_*5655insAAAA others(61): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5654 | chr15 | 52117102 | |||||
chr15:52117102
|
A | ATATATAT others(62): Show |
1 | a0003c0009t0172 | 1 | NA18956.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5654_*5655insAAAA others(65): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5654 | chr15 | 52117102 | |||||
chr15:52117102
|
A | ATATATAT others(35): Show |
1 | a0001c0001t0033 | 2 | HG01952.hp2 HG02273.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5654_*5655insAAAA others(38): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5654 | chr15 | 52117102 | |||||
chr15:52117102
|
A | ATATATAT others(48): Show |
1 | a0001c0001t0078 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5654_*5655insAAAA others(51): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5654 | chr15 | 52117102 | |||||
chr15:52117102
|
A | ATATATAT others(53): Show |
2 | a0001c0001t0040a0001c0001t0187 | 2 | NA19011.hp1 NA19083.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5654_*5655insAAAA others(56): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5654 | chr15 | 52117102 | |||||
chr15:52117102
|
A | ATATATAT others(56): Show |
2 | a0001c0001t0054a0001c0001t0164 | 2 | NA18959.hp2 NA19010.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5654_*5655insAAAA others(59): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5654 | chr15 | 52117102 | |||||
chr15:52117102
|
A | ATATATAT others(31): Show |
1 | a0001c0001t0170 | 1 | HG00735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5654_*5655insAATA others(34): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5654 | chr15 | 52117102 | |||||
chr15:52117102
|
A | ATATATAT others(49): Show |
1 | a0001c0001t0060 | 1 | NA18961.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5654_*5655insAAAA others(52): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5654 | chr15 | 52117102 | |||||
chr15:52117102
|
A | ATATATAT others(52): Show |
1 | a0001c0001t0057 | 1 | HG02056.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5654_*5655insAAAA others(55): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5654 | chr15 | 52117102 | |||||
chr15:52117102
|
A | ATATATAT others(54): Show |
1 | a0001c0001t0074 | 1 | HG02698.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5654_*5655insAAAA others(57): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5654 | chr15 | 52117102 | |||||
chr15:52117102
|
A | ATATATAT others(55): Show |
2 | a0001c0001t0018a0001c0001t0072 | 3 | HG02015.hp2 NA18983.hp2 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5654_*5655insAAAA others(58): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5654 | chr15 | 52117102 | |||||
chr15:52117102
|
A | ATATATAT others(56): Show |
1 | a0001c0001t0069 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5654_*5655insAAAA others(59): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5654 | chr15 | 52117102 | |||||
chr15:52117102
|
A | ATATATAT others(58): Show |
1 | a0001c0001t0093 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5654_*5655insAAAA others(61): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5654 | chr15 | 52117102 | |||||
chr15:52117102
|
A | ATATATAT others(31): Show |
1 | a0001c0001t0194 | 1 | HG01993.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5654_*5655insAAAA others(34): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5654 | chr15 | 52117102 | |||||
chr15:52117102
|
A | ATATATAT others(32): Show |
1 | a0001c0001t0191 | 1 | HG03704.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5654_*5655insAAAA others(35): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5654 | chr15 | 52117102 | |||||
chr15:52117102
|
A | ATATATAT others(44): Show |
1 | a0001c0001t0190 | 1 | HG02083.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5654_*5655insAAAA others(47): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5654 | chr15 | 52117102 | |||||
chr15:52117102
|
A | ATATATAT others(51): Show |
2 | a0001c0001t0175a0001c0001t0197 | 2 | NA19060.hp2 NA19076.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5654_*5655insAAAA others(54): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5654 | chr15 | 52117102 | |||||
chr15:52117102
|
A | ATATATAT others(52): Show |
1 | a0001c0001t0182 | 1 | NA18998.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5654_*5655insAAAA others(55): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5654 | chr15 | 52117102 | |||||
chr15:52117102
|
A | ATATATAT others(53): Show |
2 | a0001c0001t0051a0001c0001t0113 | 2 | HG00558.hp1 NA18999.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5654_*5655insAAAA others(56): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5654 | chr15 | 52117102 | |||||
chr15:52117102
|
A | ATATATAT others(54): Show |
1 | a0001c0001t0038 | 1 | NA18968.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5654_*5655insAAAA others(57): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5654 | chr15 | 52117102 | |||||
chr15:52117102
|
A | ATATATAT others(55): Show |
1 | a0001c0001t0048 | 1 | HG02080.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5654_*5655insAAAA others(58): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5654 | chr15 | 52117102 | |||||
chr15:52117102
|
A | ATATATAT others(46): Show |
1 | a0001c0001t0198 | 1 | HG00438.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5654_*5655insAAAA others(49): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5654 | chr15 | 52117102 | |||||
chr15:52117102
|
A | ATATATAT others(50): Show |
2 | a0001c0001t0183a0001c0002t0019 | 3 | HG02015.hp1 HG02622.hp1 HG02717.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5654_*5655insAAAA others(53): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5654 | chr15 | 52117102 | |||||
chr15:52117102
|
A | ATATATAT others(51): Show |
1 | a0001c0001t0179 | 1 | HG02129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5654_*5655insAAAA others(54): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5654 | chr15 | 52117102 | |||||
chr15:52117102
|
A | ATATATAT others(52): Show |
1 | a0001c0001t0046 | 1 | HG01256.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5654_*5655insAAAA others(55): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5654 | chr15 | 52117102 | |||||
chr15:52117102
|
A | ATATATAT others(53): Show |
1 | a0001c0001t0068 | 1 | HG01258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5654_*5655insAAAA others(56): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5654 | chr15 | 52117102 | |||||
chr15:52117102
|
A | ATATATAT others(25): Show |
2 | a0001c0004t0014a0001c0004t0017 | 7 | HG00738.hp2 HG01069.hp1 HG01071.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*5654_*5655insAATA others(28): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5654 | chr15 | 52117102 | |||||
chr15:52117102
|
A | ATATATAT others(27): Show |
1 | a0001c0004t0204 | 1 | HG01261.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5654_*5655insAAAA others(30): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5654 | chr15 | 52117102 | |||||
chr15:52117102
|
A | ATATATAT others(31): Show |
1 | a0001c0001t0084 | 1 | NA19085.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5654_*5655insAAAA others(34): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5654 | chr15 | 52117102 | |||||
chr15:52117102
|
A | ATATATAT others(44): Show |
2 | a0001c0001t0058a0001c0001t0168 | 2 | HG02148.hp1 NA19055.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5654_*5655insAAAA others(47): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5654 | chr15 | 52117102 | |||||
chr15:52117102
|
A | ATATATAT others(45): Show |
1 | a0001c0001t0173 | 1 | HG00609.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5654_*5655insAAAA others(48): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5654 | chr15 | 52117102 | |||||
chr15:52117102
|
A | ATATATAT others(46): Show |
2 | a0001c0001t0185a0001c0001t0186 | 2 | HG00741.hp2 HG01099.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5654_*5655insAAAA others(49): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5654 | chr15 | 52117102 | |||||
chr15:52117102
|
A | ATATATAT others(47): Show |
1 | a0001c0001t0196 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5654_*5655insAAAA others(50): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5654 | chr15 | 52117102 | |||||
chr15:52117102
|
A | ATATATAT others(49): Show |
1 | a0001c0001t0180 | 1 | HG02300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5654_*5655insAAAA others(52): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5654 | chr15 | 52117102 | |||||
chr15:52117102
|
A | ATATATAT others(51): Show |
1 | a0001c0001t0176 | 1 | NA18983.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5654_*5655insAAAA others(54): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5654 | chr15 | 52117102 | |||||
chr15:52117102
|
A | ATATATAT others(23): Show |
1 | a0001c0001t0034 | 2 | HG00099.hp2 HG02602.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5654_*5655insAATA others(26): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5654 | chr15 | 52117102 | |||||
chr15:52117102
|
A | ATATATAT others(30): Show |
1 | a0001c0001t0082 | 1 | HG02027.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5654_*5655insAAAA others(33): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5654 | chr15 | 52117102 | |||||
chr15:52117102
|
A | ATATATAT others(41): Show |
2 | a0001c0001t0169a0001c0003t0097 | 2 | HG03209.hp1 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5654_*5655insAAAA others(44): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5654 | chr15 | 52117102 | |||||
chr15:52117102
|
A | ATATATAT others(42): Show |
1 | a0001c0003t0112 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5654_*5655insAAAA others(45): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5654 | chr15 | 52117102 | |||||
chr15:52117102
|
A | ATATATAT others(43): Show |
1 | a0001c0001t0117 | 1 | HG01192.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5654_*5655insAAAA others(46): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5654 | chr15 | 52117102 | |||||
chr15:52117102
|
A | ATATATAT others(45): Show |
1 | a0001c0001t0016 | 3 | HG00408.hp2 NA18963.hp1 NA19063.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5654_*5655insAAAA others(48): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5654 | chr15 | 52117102 | |||||
chr15:52117102
|
A | ATATATAT others(46): Show |
1 | a0001c0001t0174 | 1 | HG02735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5654_*5655insAAAA others(49): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5654 | chr15 | 52117102 | |||||
chr15:52117102
|
A | ATATATAT others(48): Show |
3 | a0001c0001t0050a0001c0001t0088a0001c0001t0177 | 3 | HG01978.hp2 HG02135.hp1 HG03927.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5654_*5655insAAAA others(51): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5654 | chr15 | 52117102 | |||||
chr15:52117102
|
A | ATATATAT others(21): Show |
1 | a0001c0003t0124 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5654_*5655insAATA others(24): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5654 | chr15 | 52117102 | |||||
chr15:52117102
|
A | ATATATAT others(26): Show |
1 | a0001c0001t0091 | 1 | NA19060.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5654_*5655insAAAA others(29): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5654 | chr15 | 52117102 | |||||
chr15:52117102
|
A | ATATATAT others(30): Show |
1 | a0001c0001t0079 | 1 | HG00609.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5654_*5655insAAAA others(33): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5654 | chr15 | 52117102 | |||||
chr15:52117102
|
A | ATATATAT others(39): Show |
2 | a0001c0001t0061a0001c0001t0089 | 2 | HG01928.hp1 HG01943.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5654_*5655insAAAA others(42): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5654 | chr15 | 52117102 | |||||
chr15:52117102
|
A | ATATATAT others(43): Show |
1 | a0001c0001t0166 | 1 | NA18965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5654_*5655insAAAA others(46): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5654 | chr15 | 52117102 | |||||
chr15:52117102
|
A | ATATATAT others(44): Show |
1 | a0001c0001t0171 | 1 | NA18942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5654_*5655insAAAA others(47): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5654 | chr15 | 52117102 | |||||
chr15:52117102
|
A | ATATATAT others(45): Show |
1 | a0001c0001t0181 | 1 | NA19002.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5654_*5655insAAAA others(48): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5654 | chr15 | 52117102 | |||||
chr15:52117102
|
A | ATATATAT others(46): Show |
1 | a0001c0001t0178 | 1 | HG02074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5654_*5655insAAAA others(49): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5654 | chr15 | 52117102 | |||||
chr15:52117102
|
A | ATATATAT others(47): Show |
1 | a0001c0001t0165 | 1 | NA19080.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5654_*5655insAAAA others(50): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5654 | chr15 | 52117102 | |||||
chr15:52117102
|
A | ATATATAT others(22): Show |
2 | a0001c0001t0008a0001c0001t0153 | 6 | HG02622.hp2 HG03669.hp1 HG04228.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*5654_*5655insAAAA others(25): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5654 | chr15 | 52117102 | |||||
chr15:52117102
|
A | ATATATAT others(25): Show |
1 | a0001c0001t0085 | 1 | NA19063.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5654_*5655insAAAA others(28): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5654 | chr15 | 52117102 | |||||
chr15:52117102
|
A | ATATATAT others(26): Show |
2 | a0001c0001t0083a0001c0001t0090 | 2 | HG03688.hp1 NA18984.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5654_*5655insAAAA others(29): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5654 | chr15 | 52117102 | |||||
chr15:52117102
|
A | ATATATAT others(36): Show |
1 | a0001c0003t0119 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5654_*5655insAAAA others(39): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5654 | chr15 | 52117102 | |||||
chr15:52117102
|
A | ATATATAT others(46): Show |
1 | a0001c0001t0031 | 2 | HG02523.hp1 HG04184.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5654_*5655insAAAA others(49): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5654 | chr15 | 52117102 | |||||
chr15:52117102
|
A | ATATATAT others(17): Show |
1 | a0001c0003t0125 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5654_*5655insAATA others(20): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5654 | chr15 | 52117102 | |||||
chr15:52117102
|
A | ATATATAT others(22): Show |
2 | a0001c0001t0015a0001c0001t0092 | 4 | NA18956.hp2 NA18960.hp2 NA18981.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5654_*5655insAAAA others(25): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5654 | chr15 | 52117102 | |||||
chr15:52117102
|
A | ATATATAT others(24): Show |
1 | a0001c0005t0100 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5654_*5655insAAAA others(27): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5654 | chr15 | 52117102 | |||||
chr15:52117102
|
A | ATATATAT others(35): Show |
1 | a0001c0001t0062 | 1 | HG01106.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5654_*5655insAAAA others(38): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5654 | chr15 | 52117102 | |||||
chr15:52117102
|
A | ATATATAT others(38): Show |
1 | a0001c0001t0075 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5654_*5655insAAAA others(41): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5654 | chr15 | 52117102 | |||||
chr15:52117102
|
A | ATATATAT others(42): Show |
1 | a0001c0003t0099 | 1 | HG02965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5654_*5655insAAAA others(45): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5654 | chr15 | 52117102 | |||||
chr15:52117102
|
A | ATATATAT others(22): Show |
3 | a0001c0001t0007a0001c0001t0086a0001c0002t0150 | 7 | HG02698.hp2 HG03490.hp2 HG03704.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*5654_*5655insAAAA others(25): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5654 | chr15 | 52117102 | |||||
chr15:52117102
|
A | ATATATAT others(23): Show |
1 | a0002c0007t0081 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5654_*5655insAAAA others(26): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5654 | chr15 | 52117102 | |||||
chr15:52117102
|
A | ATATATAT others(24): Show |
1 | a0002c0007t0039 | 1 | HG02895.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5654_*5655insAAAA others(27): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5654 | chr15 | 52117102 | |||||
chr15:52117102
|
A | ATATATAT others(33): Show |
1 | a0001c0010t0189 | 1 | NA18953.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5654_*5655insAAAA others(36): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5654 | chr15 | 52117102 | |||||
chr15:52117102
|
A | ATATATAT others(39): Show |
1 | a0001c0001t0073 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5654_*5655insAAAA others(42): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5654 | chr15 | 52117102 | |||||
chr15:52117102
|
A | ATATATAT others(53): Show |
1 | a0001c0001t0043 | 1 | HG04228.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5654_*5655insAAAA others(56): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5654 | chr15 | 52117102 | |||||
chr15:52117102
|
A | ATATATAT others(16): Show |
3 | a0001c0003t0021a0001c0003t0122a0001c0003t0123 | 4 | HG01891.hp2 HG03139.hp1 HG03453.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5654_*5655insAAAA others(19): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5654 | chr15 | 52117102 | |||||
chr15:52117102
|
A | ATATATAT others(20): Show |
1 | a0001c0003t0127 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5654_*5655insAAAA others(23): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5654 | chr15 | 52117102 | |||||
chr15:52117102
|
A | ATATATAT others(22): Show |
1 | a0001c0001t0080 | 1 | NA19002.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5654_*5655insAAAA others(25): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5654 | chr15 | 52117102 | |||||
chr15:52117102
|
A | ATATATAT others(26): Show |
1 | a0001c0001t0045 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5654_*5655insAAAA others(29): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5654 | chr15 | 52117102 | |||||
chr15:52117102
|
A | ATATATAT others(27): Show |
1 | a0001c0001t0044 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5654_*5655insAAAA others(30): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5654 | chr15 | 52117102 | |||||
chr15:52117102
|
A | ATATATAT others(29): Show |
1 | a0001c0001t0152 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5654_*5655insAAAA others(32): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5654 | chr15 | 52117102 | |||||
chr15:52117102
|
A | ATATATAT others(32): Show |
1 | a0001c0001t0059 | 1 | NA19066.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5654_*5655insAAAA others(35): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5654 | chr15 | 52117102 | |||||
chr15:52117102
|
A | ATATATAT others(12): Show |
2 | a0001c0001t0195a0001c0001t0200 | 2 | HG01175.hp2 NA20752.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5654_*5655insAAAT others(15): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5654 | chr15 | 52117102 | |||||
chr15:52117102
|
A | ATATATAT others(18): Show |
1 | a0001c0003t0126 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5654_*5655insAAAA others(21): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5654 | chr15 | 52117102 | |||||
chr15:52117102
|
A | ATATATAT others(26): Show |
1 | a0001c0001t0064 | 1 | HG02572.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5654_*5655insAAAA others(29): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5654 | chr15 | 52117102 | |||||
chr15:52117102
|
A | ATATATAT others(21): Show |
1 | a0001c0003t0101 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5654_*5655insAAAA others(24): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5654 | chr15 | 52117102 | |||||
chr15:52117102
|
A | ATATATAT others(22): Show |
1 | a0001c0003t0098 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5654_*5655insAAAA others(25): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5654 | chr15 | 52117102 | |||||
chr15:52117102
|
A | ATATATAT others(25): Show |
2 | a0001c0001t0077a0001c0001t0151 | 2 | HG02451.hp1 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5654_*5655insAAAA others(28): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5654 | chr15 | 52117102 | |||||
chr15:52117102
|
A | ATATATAT others(26): Show |
1 | a0001c0001t0076 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5654_*5655insAAAA others(29): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5654 | chr15 | 52117102 | |||||
chr15:52117102
|
A | ATATATAT others(33): Show |
1 | a0001c0001t0049 | 1 | NA18971.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5654_*5655insAAAA others(36): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5654 | chr15 | 52117102 | |||||
chr15:52117102
|
A | ATATATAT others(13): Show |
1 | a0001c0002t0035 | 2 | HG01243.hp1 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5654_*5655insAAAA others(16): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5654 | chr15 | 52117102 | |||||
chr15:52117102
|
A | ATATATAT others(14): Show |
1 | a0001c0001t0144 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5654_*5655insAAAA others(17): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5654 | chr15 | 52117102 | |||||
chr15:52117102
|
A | ATATATAT others(5): Show |
3 | a0001c0002t0024a0001c0002t0026a0001c0002t0147 | 5 | HG02257.hp1 HG02630.hp2 HG03195.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*5654_*5655insAAAA others(8): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5654 | chr15 | 52117102 | |||||
chr15:52117102
|
A | ATATATAT others(8): Show |
2 | a0001c0002t0206a0001c0002t0207 | 2 | HG01496.hp1 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5654_*5655insAAAA others(11): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5654 | chr15 | 52117102 | |||||
chr15:52117102
|
A | ATATATAT others(13): Show |
4 | a0001c0001t0023a0001c0002t0006a0001c0002t0120others(1): Show | 10 | HG02055.hp2 HG02451.hp2 HG02486.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*5654_*5655insAAAA others(16): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5654 | chr15 | 52117102 | |||||
chr15:52117102
|
A | ATATATAT others(14): Show |
1 | a0001c0006t0143 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5654_*5655insAAAA others(17): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5654 | chr15 | 52117102 | |||||
chr15:52117102
|
A | ATATATAT others(5): Show |
1 | a0001c0002t0025 | 2 | HG02109.hp2 HG02809.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5654_*5655insAAAA others(8): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5654 | chr15 | 52117102 | |||||
chr15:52117102
|
A | ATATATAT others(11): Show |
1 | a0001c0002t0203 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5654_*5655insAAAA others(14): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5654 | chr15 | 52117102 | |||||
chr15:52117102
|
A | ATATATAT others(13): Show |
5 | a0001c0001t0011a0001c0001t0022a0001c0001t0027others(2): Show | 11 | HG02559.hp2 HG02717.hp1 HG02895.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*5654_*5655insAAAA others(16): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5654 | chr15 | 52117102 | |||||
chr15:52117102
|
A | ATATATAT others(14): Show |
2 | a0001c0001t0145a0001c0001t0146 | 2 | HG01891.hp1 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5654_*5655insAAAA others(17): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5654 | chr15 | 52117102 | |||||
chr15:52117102
|
A | ATATATTT others(13): Show |
3 | a0001c0001t0094a0001c0001t0141a0001c0001t0149 | 3 | HG02258.hp1 HG02615.hp1 HG02723.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5654_*5655insAAAA others(16): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5654 | chr15 | 52117102 | |||||
chr15:52117102
|
A | ATATATTT others(14): Show |
1 | a0001c0001t0148 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5654_*5655insAAAA others(17): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5654 | chr15 | 52117102 | |||||
chr15:52117102
|
A | ATATATTT others(24): Show |
1 | a0001c0001t0070 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5654_*5655insAAAA others(27): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5654 | chr15 | 52117102 | |||||
chr15:52117102
|
A | ATATATTT others(32): Show |
1 | a0001c0001t0066 | 1 | HG01192.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5654_*5655insAAAA others(35): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5654 | chr15 | 52117102 | |||||
chr15:52117102
|
A | ATTTTTTT others(15): Show |
1 | a0001c0001t0118 | 1 | HG01099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5654_*5655insAAAA others(18): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5654 | chr15 | 52117102 | |||||
chr15:52117102
|
A | ATTTTTTT others(17): Show |
1 | a0001c0001t0115 | 1 | HG01978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5654_*5655insAAAA others(20): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5654 | chr15 | 52117102 | |||||
chr15:52117102
|
A | T | 1 | a0001c0001t0003 | 11 | HG00408.hp1 NA18612.hp2 NA18940.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*5655T>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5655 | chr15 | 52117102 | |||||
chr15:52117103
|
T | TATATATA others(66): Show |
1 | a0001c0002t0138 | 1 | NA19081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5653_*5654insTATA others(69): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5653 | chr15 | 52117103 | |||||
chr15:52117103
|
T | TATATATA others(52): Show |
2 | a0001c0002t0131a0001c0002t0134 | 2 | HG02132.hp2 HG04115.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5653_*5654insTATA others(55): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5653 | chr15 | 52117103 | |||||
chr15:52117103
|
T | TATATATA others(50): Show |
2 | a0001c0002t0133a0001c0002t0140 | 2 | HG01934.hp2 HG02148.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5653_*5654insTATA others(53): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5653 | chr15 | 52117103 | |||||
chr15:52117103
|
T | TATATATA others(48): Show |
2 | a0001c0002t0132a0001c0002t0136 | 2 | HG01952.hp1 NA18747.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5653_*5654insTATA others(51): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5653 | chr15 | 52117103 | |||||
chr15:52117103
|
T | TATATATA others(44): Show |
1 | a0001c0002t0135 | 1 | NA18984.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5653_*5654insTATA others(47): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5653 | chr15 | 52117103 | |||||
chr15:52117103
|
T | TATATATA others(42): Show |
1 | a0001c0002t0137 | 1 | NA19007.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5653_*5654insTATA others(45): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5653 | chr15 | 52117103 | |||||
chr15:52117103
|
T | TATATATA others(38): Show |
1 | a0001c0002t0139 | 1 | HG02004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5653_*5654insTATA others(41): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5653 | chr15 | 52117103 | |||||
chr15:52117103
|
T | TATATATA others(34): Show |
1 | a0001c0002t0130 | 1 | NA18988.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5653_*5654insTATA others(37): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5653 | chr15 | 52117103 | |||||
chr15:52117103
|
T | TATATATA others(32): Show |
1 | a0001c0002t0129 | 1 | NA18971.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5653_*5654insTATA others(35): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5653 | chr15 | 52117103 | |||||
chr15:52117103
|
T | TATATATA others(30): Show |
1 | a0001c0002t0128 | 1 | NA18979.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5653_*5654insTATA others(33): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5653 | chr15 | 52117103 | |||||
chr15:52117104
|
T | A | 1 | a0001c0001t0102 | 1 | NA19007.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5653A>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5653 | chr15 | 52117104 | |||||
chr15:52117112
|
A | T | 65 | a0001c0001t0007a0001c0001t0008a0001c0001t0015others(62): Show | 77 | HG00323.hp2 HG00544.hp2 HG00597.hp1 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*5645T>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5645 | chr15 | 52117112 | |||||
chr15:52117114
|
T | G | 65 | a0001c0001t0007a0001c0001t0008a0001c0001t0015others(62): Show | 77 | HG00323.hp2 HG00544.hp2 HG00597.hp1 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*5643A>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5643 | chr15 | 52117114 | |||||
chr15:52117131
|
C | T | 17 | a0001c0001t0011a0001c0001t0022a0001c0001t0023others(14): Show | 27 | HG01891.hp1 HG02109.hp2 HG02257.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*5626G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5626 | chr15 | 52117131 | |||||
chr15:52117232
|
C | T | 6 | a0001c0002t0006a0001c0002t0035a0001c0002t0120others(3): Show | 12 | HG01243.hp1 HG02055.hp2 HG02451.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*5525G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5525 | chr15 | 52117232 | |||||
chr15:52117372
|
C | G | 3 | a0001c0001t0044a0001c0001t0045a0001c0001t0064 | 3 | HG02572.hp1 HG03209.hp2 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5385G>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5385 | chr15 | 52117372 | |||||
chr15:52117394
|
C | T | 5 | a0001c0003t0021a0001c0003t0122a0001c0003t0123others(2): Show | 6 | HG01891.hp2 HG02630.hp1 HG02818.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*5363G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5363 | chr15 | 52117394 | |||||
chr15:52117401
|
A | T | 3 | a0001c0001t0044a0001c0001t0045a0001c0001t0064 | 3 | HG02572.hp1 HG03209.hp2 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5356T>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5356 | chr15 | 52117401 | |||||
chr15:52117414
|
G | A | 21 | a0001c0001t0011a0001c0001t0022a0001c0001t0023others(18): Show | 31 | HG01109.hp1 HG01496.hp1 HG01891.hp1 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*5343C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5343 | chr15 | 52117414 | |||||
chr15:52117595
|
T | C | 1 | a0001c0001t0105 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5162A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5162 | chr15 | 52117595 | |||||
chr15:52117701
|
C | T | 3 | a0001c0002t0128a0001c0002t0129a0001c0002t0130 | 3 | NA18971.hp1 NA18979.hp2 NA18988.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5056G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5056 | chr15 | 52117701 | |||||
chr15:52117718
|
G | T | 3 | a0001c0001t0022a0001c0001t0023a0001c0001t0144 | 5 | HG02559.hp1 HG02886.hp1 HG03098.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*5039C>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5039 | chr15 | 52117718 | |||||
chr15:52117725
|
C | T | 19 | a0001c0001t0011a0001c0001t0022a0001c0001t0023others(16): Show | 29 | HG01496.hp1 HG01891.hp1 HG02109.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*5032G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5032 | chr15 | 52117725 | |||||
chr15:52117750
|
C | G | 1 | a0001c0001t0158 | 1 | HG01993.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5007G>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 5007 | chr15 | 52117750 | |||||
chr15:52117768
|
G | A | 1 | a0001c0003t0126 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4989C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 4989 | chr15 | 52117768 | |||||
chr15:52117790
|
G | A | 19 | a0001c0001t0011a0001c0001t0022a0001c0001t0023others(16): Show | 29 | HG01496.hp1 HG01891.hp1 HG02109.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*4967C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 4967 | chr15 | 52117790 | |||||
chr15:52117859
|
T | G | 1 | a0001c0001t0196 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4898A>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 4898 | chr15 | 52117859 | |||||
chr15:52117895
|
G | A | 1 | a0001c0001t0197 | 1 | NA19060.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4862C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 4862 | chr15 | 52117895 | |||||
chr15:52117957
|
G | A | 1 | a0001c0001t0086 | 1 | HG03704.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4800C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 4800 | chr15 | 52117957 | |||||
chr15:52118011
|
G | A | 4 | a0001c0004t0014a0001c0004t0017a0001c0004t0204others(1): Show | 9 | HG00738.hp2 HG00741.hp1 HG01069.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*4746C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 4746 | chr15 | 52118011 | |||||
chr15:52118104
|
C | T | 17 | a0001c0001t0011a0001c0001t0022a0001c0001t0023others(14): Show | 27 | HG01891.hp1 HG02109.hp2 HG02257.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*4653G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 4653 | chr15 | 52118104 | |||||
chr15:52118127
|
C | T | 3 | a0001c0001t0022a0001c0001t0023a0001c0001t0144 | 5 | HG02559.hp1 HG02886.hp1 HG03098.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4630G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 4630 | chr15 | 52118127 | |||||
chr15:52118258
|
C | G | 1 | a0001c0001t0164 | 1 | NA18959.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4499G>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 4499 | chr15 | 52118258 | |||||
chr15:52118288
|
G | A | 6 | a0001c0002t0135a0001c0002t0136a0001c0002t0137others(3): Show | 6 | HG02004.hp1 HG02148.hp2 NA18747.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4469C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 4469 | chr15 | 52118288 | |||||
chr15:52118328
|
C | A | 190 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(187): Show | 298 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(295): Show |
3_prime_UTR_variant | MODIFIER | c.*4429G>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 4429 | chr15 | 52118328 | |||||
chr15:52118344
|
C | T | 2 | a0001c0002t0206a0001c0002t0207 | 2 | HG01496.hp1 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4413G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 4413 | chr15 | 52118344 | |||||
chr15:52118360
|
CT | C | 62 | a0001c0001t0016a0001c0001t0031a0001c0001t0032others(59): Show | 79 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*4396delA | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 4396 | chr15 | 52118360 | |||||
chr15:52118433
|
G | C | 1 | a0001c0001t0160 | 1 | HG03688.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4324C>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 4324 | chr15 | 52118433 | |||||
chr15:52118470
|
T | G | 1 | a0001c0001t0175 | 1 | NA19076.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4287A>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 4287 | chr15 | 52118470 | |||||
chr15:52118609
|
C | T | 2 | a0001c0002t0206a0001c0002t0207 | 2 | HG01496.hp1 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4148G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 4148 | chr15 | 52118609 | |||||
chr15:52118639
|
T | C | 21 | a0001c0001t0011a0001c0001t0022a0001c0001t0023others(18): Show | 31 | HG01109.hp1 HG01496.hp1 HG01891.hp1 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*4118A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 4118 | chr15 | 52118639 | |||||
chr15:52118704
|
A | C | 13 | a0001c0002t0128a0001c0002t0129a0001c0002t0130others(10): Show | 13 | HG01934.hp2 HG01952.hp1 HG02004.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*4053T>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 4053 | chr15 | 52118704 | |||||
chr15:52118728
|
C | T | 3 | a0001c0001t0141a0001c0001t0148a0001c0001t0149 | 3 | HG02258.hp1 HG02615.hp1 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4029G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 4029 | chr15 | 52118728 | |||||
chr15:52118739
|
A | C | 26 | a0001c0001t0018a0001c0001t0038a0001c0001t0040others(23): Show | 28 | HG00544.hp2 HG00597.hp1 HG00673.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*4018T>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 4018 | chr15 | 52118739 | |||||
chr15:52118761
|
C | T | 65 | a0001c0001t0007a0001c0001t0008a0001c0001t0015others(62): Show | 77 | HG00323.hp2 HG00544.hp2 HG00597.hp1 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*3996G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 3996 | chr15 | 52118761 | |||||
chr15:52118819
|
G | A | 2 | a0001c0002t0206a0001c0002t0207 | 2 | HG01496.hp1 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3938C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 3938 | chr15 | 52118819 | |||||
chr15:52118824
|
C | T | 4 | a0001c0002t0024a0001c0002t0025a0001c0002t0026others(1): Show | 7 | HG02109.hp2 HG02257.hp1 HG02630.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3933G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 3933 | chr15 | 52118824 | |||||
chr15:52118831
|
C | T | 19 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(16): Show | 87 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*3926G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 3926 | chr15 | 52118831 | |||||
chr15:52118867
|
C | T | 100 | a0001c0001t0007a0001c0001t0008a0001c0001t0011others(97): Show | 122 | HG00323.hp2 HG00544.hp2 HG00597.hp1 others(119): Show |
3_prime_UTR_variant | MODIFIER | c.*3890G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 3890 | chr15 | 52118867 | |||||
chr15:52118869
|
T | TA | 32 | a0001c0001t0020a0001c0001t0022a0001c0001t0023others(29): Show | 39 | HG01109.hp1 HG01256.hp2 HG01496.hp2 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*3887dupT | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 3887 | chr15 | 52118869 | |||||
chr15:52118869
|
T | TAA | 133 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(130): Show | 225 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(222): Show |
3_prime_UTR_variant | MODIFIER | c.*3886_*3887dupTT | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 3887 | chr15 | 52118869 | |||||
chr15:52118869
|
T | TAAA | 22 | a0001c0001t0012a0001c0001t0038a0001c0001t0088others(19): Show | 27 | HG00438.hp1 HG00673.hp1 HG01175.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*3885_*3887dupTTT | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 3887 | chr15 | 52118869 | |||||
chr15:52118993
|
TGGATGGG others(37): Show |
T | 1 | a0003c0009t0172 | 1 | NA18956.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3720_*3763delCCCT others(40): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 3720 | chr15 | 52118993 | |||||
chr15:52118995
|
GATGGGGA others(37): Show |
G | 13 | a0001c0002t0006a0001c0002t0035a0001c0002t0120others(10): Show | 20 | HG01243.hp1 HG01891.hp2 HG02055.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*3718_*3761delTCCC others(40): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 3718 | chr15 | 52118995 | |||||
chr15:52119068
|
T | A | 36 | a0001c0001t0002a0001c0001t0011a0001c0001t0013others(33): Show | 83 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(80): Show |
3_prime_UTR_variant | MODIFIER | c.*3689A>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 3689 | chr15 | 52119068 | |||||
chr15:52119120
|
A | AG | 2 | a0001c0001t0011a0001c0001t0027 | 7 | HG02895.hp1 HG02897.hp1 HG02897.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3636dupC | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 3636 | chr15 | 52119120 | |||||
chr15:52119226
|
T | TGAGGAGA others(13): Show |
1 | a0001c0001t0163 | 1 | HG01496.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3511_*3530dupTGCC others(16): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 3530 | chr15 | 52119226 | |||||
chr15:52119287
|
T | C | 1 | a0001c0001t0030 | 2 | HG02155.hp2 HG02602.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3470A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 3470 | chr15 | 52119287 | |||||
chr15:52119302
|
AGGT | A | 46 | a0001c0001t0016a0001c0001t0031a0001c0001t0032others(43): Show | 52 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*3452_*3454delACC | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 3452 | chr15 | 52119302 | |||||
chr15:52119332
|
A | G | 171 | a0001c0001t0007a0001c0001t0008a0001c0001t0011others(168): Show | 211 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(208): Show |
3_prime_UTR_variant | MODIFIER | c.*3425T>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 3425 | chr15 | 52119332 | |||||
chr15:52119338
|
A | AAGGGAGG others(10): Show |
37 | a0001c0001t0018a0001c0001t0028a0001c0001t0038others(34): Show | 46 | HG00544.hp2 HG00597.hp1 HG00673.hp2 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*3402_*3418dupCCCA others(13): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 3418 | chr15 | 52119338 | |||||
chr15:52119338
|
A | AAGGGAGG others(27): Show |
65 | a0001c0001t0016a0001c0001t0031a0001c0001t0032others(62): Show | 71 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*3385_*3418dupCCCA others(30): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 3418 | chr15 | 52119338 | |||||
chr15:52119338
|
A | AAGGGAGG others(44): Show |
3 | a0001c0001t0170a0001c0003t0021a0001c0005t0156 | 4 | HG00735.hp2 HG01891.hp2 HG03130.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3368_*3418dupCCCA others(47): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 3418 | chr15 | 52119338 | |||||
chr15:52119338
|
AAGGGAGG others(10): Show |
A | 2 | a0001c0001t0110a0001c0001t0167 | 2 | HG00735.hp1 HG02273.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3402_*3418delCCCA others(13): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 3402 | chr15 | 52119338 | |||||
chr15:52119343
|
A | AGGAGGAG others(58): Show |
4 | a0001c0004t0014a0001c0004t0017a0001c0004t0204others(1): Show | 9 | HG00738.hp2 HG00741.hp1 HG01069.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3349_*3413dupCTCC others(61): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 3413 | chr15 | 52119343 | |||||
chr15:52119369
|
T | TGGGAGGG others(82): Show |
2 | a0001c0003t0119a0001c0005t0100 | 2 | HG02970.hp2 HG03041.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3387_*3388insTCCC others(85): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 3387 | chr15 | 52119369 | |||||
chr15:52119374
|
G | GGGAGGAG others(9): Show |
1 | a0001c0001t0040 | 1 | NA19083.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3367_*3382dupTCCC others(12): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 3382 | chr15 | 52119374 | |||||
chr15:52119394
|
AGGAGGAG others(7): Show |
A | 1 | a0001c0002t0207 | 1 | HG01496.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3349_*3362delCTCC others(10): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 3349 | chr15 | 52119394 | |||||
chr15:52119408
|
G | GGGAGGAG others(30): Show |
38 | a0001c0001t0007a0001c0001t0008a0001c0001t0015others(35): Show | 48 | HG00323.hp2 HG00609.hp1 HG01123.hp2 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*3348_*3349insTCCT others(33): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 3348 | chr15 | 52119408 | |||||
chr15:52119408
|
G | GGGAGGAG others(47): Show |
1 | a0001c0001t0043 | 1 | HG04228.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3348_*3349insTCCT others(50): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 3348 | chr15 | 52119408 | |||||
chr15:52119425
|
A | AG | 39 | a0001c0001t0007a0001c0001t0008a0001c0001t0015others(36): Show | 49 | HG00323.hp2 HG00609.hp1 HG01123.hp2 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*3331dupC | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 3331 | chr15 | 52119425 | |||||
chr15:52119425
|
A | AGGAGGAG others(14): Show |
25 | a0001c0001t0018a0001c0001t0038a0001c0001t0041others(22): Show | 27 | HG00544.hp2 HG00597.hp1 HG00673.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*3311_*3331dupCTCC others(17): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 3331 | chr15 | 52119425 | |||||
chr15:52119425
|
A | AGGGAGGA others(15): Show |
1 | a0001c0001t0040 | 1 | NA19083.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3331_*3332insCTCC others(18): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 3331 | chr15 | 52119425 | |||||
chr15:52119425
|
AGGAGGAG others(14): Show |
A | 1 | a0001c0001t0111 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3311_*3331delCTCC others(17): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 3311 | chr15 | 52119425 | |||||
chr15:52119446
|
G | GGGA | 34 | a0001c0001t0011a0001c0001t0022a0001c0001t0023others(31): Show | 44 | HG01109.hp1 HG01496.hp1 HG01891.hp1 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*3308_*3310dupTCC | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 3310 | chr15 | 52119446 | |||||
chr15:52119509
|
G | A | 17 | a0001c0001t0011a0001c0001t0022a0001c0001t0023others(14): Show | 27 | HG01891.hp1 HG02109.hp2 HG02257.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*3248C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 3248 | chr15 | 52119509 | |||||
chr15:52119554
|
G | T | 1 | a0001c0002t0024 | 2 | HG02257.hp1 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3203C>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 3203 | chr15 | 52119554 | |||||
chr15:52119718
|
T | C | 2 | a0001c0002t0206a0001c0002t0207 | 2 | HG01496.hp1 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3039A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 3039 | chr15 | 52119718 | |||||
chr15:52119811
|
C | T | 1 | a0001c0001t0114 | 1 | NA20805.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2946G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 2946 | chr15 | 52119811 | |||||
chr15:52119887
|
T | C | 7 | a0001c0002t0128a0001c0002t0129a0001c0002t0130others(4): Show | 7 | HG01934.hp2 HG01952.hp1 HG02132.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2870A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 2870 | chr15 | 52119887 | |||||
chr15:52119906
|
C | T | 71 | a0001c0001t0016a0001c0001t0031a0001c0001t0032others(68): Show | 83 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(80): Show |
3_prime_UTR_variant | MODIFIER | c.*2851G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 2851 | chr15 | 52119906 | |||||
chr15:52119977
|
C | T | 2 | a0001c0001t0040a0001c0001t0041 | 2 | NA18973.hp1 NA19083.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2780G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 2780 | chr15 | 52119977 | |||||
chr15:52120093
|
A | G | 1 | a0001c0005t0156 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2664T>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 2664 | chr15 | 52120093 | |||||
chr15:52120151
|
A | G | 1 | a0002c0007t0039 | 1 | HG02895.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2606T>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 2606 | chr15 | 52120151 | |||||
chr15:52120259
|
T | A | 1 | a0001c0003t0101 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2498A>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 2498 | chr15 | 52120259 | |||||
chr15:52120282
|
A | G | 1 | a0001c0001t0113 | 1 | HG00558.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2475T>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 2475 | chr15 | 52120282 | |||||
chr15:52120359
|
C | T | 7 | a0001c0001t0141a0001c0001t0148a0001c0001t0149others(4): Show | 10 | HG02109.hp2 HG02257.hp1 HG02258.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2398G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 2398 | chr15 | 52120359 | |||||
chr15:52120366
|
A | G | 134 | a0001c0001t0007a0001c0001t0008a0001c0001t0011others(131): Show | 167 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(164): Show |
3_prime_UTR_variant | MODIFIER | c.*2391T>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 2391 | chr15 | 52120366 | |||||
chr15:52120371
|
C | T | 1 | a0001c0001t0169 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2386G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 2386 | chr15 | 52120371 | |||||
chr15:52120431
|
T | G | 4 | a0001c0004t0014a0001c0004t0017a0001c0004t0204others(1): Show | 9 | HG00738.hp2 HG00741.hp1 HG01069.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2326A>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 2326 | chr15 | 52120431 | |||||
chr15:52120562
|
C | T | 2 | a0001c0001t0145a0001c0001t0146 | 2 | HG01891.hp1 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2195G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 2195 | chr15 | 52120562 | |||||
chr15:52120579
|
G | A | 7 | a0001c0003t0021a0001c0003t0122a0001c0003t0123others(4): Show | 8 | HG01891.hp2 HG02055.hp1 HG02630.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2178C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 2178 | chr15 | 52120579 | |||||
chr15:52120617
|
C | T | 1 | a0001c0001t0168 | 1 | NA19055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2140G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 2140 | chr15 | 52120617 | |||||
chr15:52120623
|
C | CA | 66 | a0001c0001t0016a0001c0001t0022a0001c0001t0023others(63): Show | 76 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(73): Show |
3_prime_UTR_variant | MODIFIER | c.*2133dupT | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 2133 | chr15 | 52120623 | |||||
chr15:52120623
|
C | CAA | 102 | a0001c0001t0007a0001c0001t0008a0001c0001t0011others(99): Show | 132 | HG00323.hp2 HG00544.hp2 HG00597.hp1 others(129): Show |
3_prime_UTR_variant | MODIFIER | c.*2132_*2133dupTT | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 2133 | chr15 | 52120623 | |||||
chr15:52120705
|
T | C | 1 | a0001c0001t0167 | 1 | HG02273.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2052A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 2052 | chr15 | 52120705 | |||||
chr15:52120853
|
A | C | 124 | a0001c0001t0007a0001c0001t0008a0001c0001t0011others(121): Show | 158 | HG00323.hp2 HG00544.hp2 HG00597.hp1 others(155): Show |
3_prime_UTR_variant | MODIFIER | c.*1904T>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 1904 | chr15 | 52120853 | |||||
chr15:52121119
|
G | C | 8 | a0001c0001t0002a0001c0001t0013a0001c0001t0095others(5): Show | 45 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*1638C>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 1638 | chr15 | 52121119 | |||||
chr15:52121518
|
T | TTTTC | 205 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(202): Show | 359 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(356): Show |
3_prime_UTR_variant | MODIFIER | c.*1235_*1238dupGAAA | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 1238 | chr15 | 52121518 | |||||
chr15:52121570
|
C | T | 2 | a0001c0006t0142a0001c0006t0143 | 2 | HG02559.hp2 HG02818.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1187G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 1187 | chr15 | 52121570 | |||||
chr15:52121610
|
A | AT | 98 | a0001c0001t0007a0001c0001t0008a0001c0001t0011others(95): Show | 125 | HG00323.hp2 HG00544.hp2 HG00597.hp1 others(122): Show |
3_prime_UTR_variant | MODIFIER | c.*1146dupA | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 1146 | chr15 | 52121610 | |||||
chr15:52121610
|
A | ATT | 8 | a0001c0001t0141a0001c0002t0128a0001c0002t0129others(5): Show | 8 | HG01934.hp2 HG01952.hp1 HG02132.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1145_*1146dupAA | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 1146 | chr15 | 52121610 | |||||
chr15:52121610
|
AT | A | 45 | a0001c0001t0016a0001c0001t0031a0001c0001t0032others(42): Show | 51 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*1146delA | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 1146 | chr15 | 52121610 | |||||
chr15:52121728
|
C | T | 7 | a0001c0003t0021a0001c0003t0122a0001c0003t0123others(4): Show | 8 | HG01891.hp2 HG02055.hp1 HG02630.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1029G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 1029 | chr15 | 52121728 | |||||
chr15:52121760
|
C | T | 7 | a0001c0003t0021a0001c0003t0122a0001c0003t0123others(4): Show | 8 | HG01891.hp2 HG02055.hp1 HG02630.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*997G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 997 | chr15 | 52121760 | |||||
chr15:52121806
|
G | A | 1 | a0001c0003t0119 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*951C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 951 | chr15 | 52121806 | |||||
chr15:52121883
|
C | T | 13 | a0001c0002t0128a0001c0002t0129a0001c0002t0130others(10): Show | 13 | HG01934.hp2 HG01952.hp1 HG02004.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*874G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 874 | chr15 | 52121883 | |||||
chr15:52121984
|
T | A | 6 | a0001c0002t0006a0001c0002t0035a0001c0002t0120others(3): Show | 12 | HG01243.hp1 HG02055.hp2 HG02451.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*773A>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 773 | chr15 | 52121984 | |||||
chr15:52122038
|
T | C | 6 | a0001c0002t0206a0001c0002t0207a0001c0004t0014others(3): Show | 11 | HG00738.hp2 HG00741.hp1 HG01069.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*719A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 719 | chr15 | 52122038 | |||||
chr15:52122152
|
G | C | 1 | a0001c0001t0121 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*605C>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 605 | chr15 | 52122152 | |||||
chr15:52122355
|
C | G | 7 | a0001c0003t0021a0001c0003t0122a0001c0003t0123others(4): Show | 8 | HG01891.hp2 HG02055.hp1 HG02630.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*402G>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 402 | chr15 | 52122355 | |||||
chr15:52122373
|
A | G | 1 | a0001c0001t0036 | 1 | NA18977.hp1 | 3_prime_UTR_variant | MODIFIER | c.*384T>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 13/13 | 384 | chr15 | 52122373 | |||||
chr15:52191368
|
A | G | 98 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(95): Show | 174 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(171): Show |
5_prime_UTR_variant | MODIFIER | c.-65T>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 1/13 | 6692 | chr15 | 52191368 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr15:52122834
|
A | C | 12 | a0001c0002t0006g0291a0001c0002t0006g0314a0001c0002t0006g0316others(9): Show | 12 | HG01243.hp1 HG02055.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.1177-66T>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 12/12 | chr15 | 52122834 | ||||||
chr15:52122889
|
T | TAC | 12 | a0001c0002t0006g0291a0001c0002t0006g0314a0001c0002t0006g0316others(9): Show | 12 | HG01243.hp1 HG02055.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.1177-123_1177-122d others(4): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 12/12 | chr15 | 52122889 | ||||||
chr15:52122889
|
T | TACAC | 102 | a0001c0001t0007g0139a0001c0001t0007g0144a0001c0001t0007g0148others(99): Show | 102 | HG00323.hp2 HG00544.hp2 HG00597.hp1 others(99): Show |
intron_variant | MODIFIER | c.1177-125_1177-122d others(6): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 12/12 | chr15 | 52122889 | ||||||
chr15:52122889
|
T | TACACAC | 24 | a0001c0001t0037g0163a0001c0001t0145g0279a0001c0002t0128g0273others(21): Show | 26 | HG00738.hp2 HG00741.hp1 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.1177-127_1177-122d others(8): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 12/12 | chr15 | 52122889 | ||||||
chr15:52122907
|
A | C | 1 | a0001c0001t0144g0298 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1177-139T>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 12/12 | chr15 | 52122907 | ||||||
chr15:52122911
|
T | C | 6 | a0001c0003t0097g0091a0001c0003t0098g0088a0001c0003t0099g0095others(3): Show | 6 | HG01884.hp1 HG02922.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1177-143A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 12/12 | chr15 | 52122911 | ||||||
chr15:52122977
|
C | CA | 127 | a0001c0001t0007g0139a0001c0001t0007g0144a0001c0001t0007g0148others(124): Show | 129 | HG00323.hp2 HG00544.hp2 HG00597.hp1 others(126): Show |
intron_variant | MODIFIER | c.1177-210dupT | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 12/12 | chr15 | 52122977 | ||||||
chr15:52123049
|
C | CTA | 127 | a0001c0001t0007g0139a0001c0001t0007g0144a0001c0001t0007g0148others(124): Show | 129 | HG00323.hp2 HG00544.hp2 HG00597.hp1 others(126): Show |
intron_variant | MODIFIER | c.1177-282_1177-281i others(4): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 12/12 | chr15 | 52123049 | ||||||
chr15:52123061
|
C | A | 7 | a0001c0003t0097g0091a0001c0003t0098g0088a0001c0003t0099g0095others(4): Show | 7 | HG01884.hp1 HG02922.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1177-293G>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 12/12 | chr15 | 52123061 | ||||||
chr15:52123079
|
C | T | 12 | a0001c0002t0006g0291a0001c0002t0006g0314a0001c0002t0006g0316others(9): Show | 12 | HG01243.hp1 HG02055.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.1177-311G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 12/12 | chr15 | 52123079 | ||||||
chr15:52123114
|
A | G | 2 | a0001c0001t0145g0279a0001c0001t0146g0292 | 2 | HG01891.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1177-346T>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 12/12 | chr15 | 52123114 | ||||||
chr15:52123335
|
T | C | 1 | a0001c0001t0001g0326 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1177-567A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 12/12 | chr15 | 52123335 | ||||||
chr15:52123396
|
C | T | 1 | a0001c0005t0156g0261 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1177-628G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 12/12 | chr15 | 52123396 | ||||||
chr15:52123522
|
C | T | 8 | a0001c0001t0022g0294a0001c0001t0022g0295a0001c0001t0023g0296others(5): Show | 8 | HG01891.hp1 HG02559.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1177-754G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 12/12 | chr15 | 52123522 | ||||||
chr15:52123543
|
C | CT | 12 | a0001c0001t0001g0194a0001c0001t0009g0077a0001c0001t0016g0344others(9): Show | 12 | HG00438.hp2 HG01099.hp2 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1177-776dupA | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 12/12 | chr15 | 52123543 | ||||||
chr15:52123543
|
C | CTT | 8 | a0001c0002t0128g0273a0001c0002t0129g0275a0001c0002t0130g0274others(5): Show | 8 | HG01934.hp2 HG01952.hp1 HG02132.hp2 others(5): Show |
intron_variant | MODIFIER | c.1177-777_1177-776d others(4): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 12/12 | chr15 | 52123543 | ||||||
chr15:52123543
|
C | CTTT | 6 | a0001c0002t0135g0270a0001c0002t0136g0268a0001c0002t0137g0266others(3): Show | 6 | HG02004.hp1 HG02148.hp2 NA18747.hp2 others(3): Show |
intron_variant | MODIFIER | c.1177-778_1177-776d others(5): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 12/12 | chr15 | 52123543 | ||||||
chr15:52123543
|
CT | C | 89 | a0001c0001t0001g0246a0001c0001t0002g0051a0001c0001t0003g0013others(86): Show | 89 | HG00323.hp1 HG00323.hp2 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.1177-776delA | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 12/12 | chr15 | 52123543 | ||||||
chr15:52123676
|
G | A | 13 | a0001c0002t0128g0273a0001c0002t0129g0275a0001c0002t0130g0274others(10): Show | 13 | HG01934.hp2 HG01952.hp1 HG02004.hp1 others(10): Show |
intron_variant | MODIFIER | c.1176+797C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 12/12 | chr15 | 52123676 | ||||||
chr15:52123699
|
C | T | 113 | a0001c0001t0007g0139a0001c0001t0007g0144a0001c0001t0007g0148others(110): Show | 115 | HG00323.hp2 HG00544.hp2 HG00597.hp1 others(112): Show |
intron_variant | MODIFIER | c.1176+774G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 12/12 | chr15 | 52123699 | ||||||
chr15:52123889
|
AG | A | 5 | a0001c0001t0113g0021a0001c0001t0164g0235a0001c0001t0184g0200others(2): Show | 5 | HG00558.hp1 NA18956.hp1 NA18959.hp2 others(2): Show |
intron_variant | MODIFIER | c.1176+583delC | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 12/12 | chr15 | 52123889 | ||||||
chr15:52124005
|
C | CA | 57 | a0001c0001t0001g0204a0001c0001t0001g0216a0001c0001t0002g0042others(54): Show | 57 | HG00609.hp1 HG00735.hp1 HG01109.hp2 others(54): Show |
intron_variant | MODIFIER | c.1176+467dupT | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 12/12 | chr15 | 52124005 | ||||||
chr15:52124005
|
C | CAA | 7 | a0001c0001t0007g0169a0001c0001t0015g0143a0001c0001t0082g0154others(4): Show | 7 | HG02027.hp2 HG02630.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.1176+466_1176+467d others(4): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 12/12 | chr15 | 52124005 | ||||||
chr15:52124005
|
CA | C | 107 | a0001c0001t0001g0326a0001c0001t0002g0026a0001c0001t0002g0054others(104): Show | 107 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.1176+467delT | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 12/12 | chr15 | 52124005 | ||||||
chr15:52124005
|
CAAA | C | 7 | a0001c0004t0014g0002a0001c0004t0014g0280a0001c0004t0014g0290others(4): Show | 9 | HG00738.hp2 HG00741.hp1 HG01069.hp1 others(6): Show |
intron_variant | MODIFIER | c.1176+465_1176+467d others(5): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 12/12 | chr15 | 52124005 | ||||||
chr15:52124047
|
T | C | 12 | a0001c0002t0006g0291a0001c0002t0006g0314a0001c0002t0006g0316others(9): Show | 12 | HG01243.hp1 HG02055.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.1176+426A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 12/12 | chr15 | 52124047 | ||||||
chr15:52124135
|
G | C | 7 | a0001c0001t0011g0299a0001c0001t0011g0303a0001c0001t0011g0304others(4): Show | 7 | HG02895.hp1 HG02897.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.1176+338C>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 12/12 | chr15 | 52124135 | ||||||
chr15:52124207
|
G | A | 7 | a0001c0002t0128g0273a0001c0002t0129g0275a0001c0002t0130g0274others(4): Show | 7 | HG01934.hp2 HG01952.hp1 HG02132.hp2 others(4): Show |
intron_variant | MODIFIER | c.1176+266C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 12/12 | chr15 | 52124207 | ||||||
chr15:52124229
|
C | T | 1 | a0001c0001t0001g0241 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1176+244G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 12/12 | chr15 | 52124229 | ||||||
chr15:52124246
|
T | TA | 6 | a0001c0003t0097g0091a0001c0003t0098g0088a0001c0003t0099g0095others(3): Show | 6 | HG01884.hp1 HG02922.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1176+226dupT | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 12/12 | chr15 | 52124246 | ||||||
chr15:52124354
|
C | T | 1 | a0001c0001t0012g0227 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1176+119G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 12/12 | chr15 | 52124354 | ||||||
chr15:52124357
|
C | T | 6 | a0001c0001t0002g0039a0001c0001t0002g0040a0001c0001t0002g0054others(3): Show | 6 | HG01081.hp2 HG01123.hp1 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.1176+116G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 12/12 | chr15 | 52124357 | ||||||
chr15:52124394
|
C | G | 36 | a0001c0001t0011g0299a0001c0001t0011g0303a0001c0001t0011g0304others(33): Show | 38 | HG00738.hp2 HG00741.hp1 HG01069.hp1 others(35): Show |
intron_variant | MODIFIER | c.1176+79G>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 12/12 | chr15 | 52124394 | ||||||
chr15:52124738
|
G | T | 1 | a0001c0001t0105g0057 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1010-99C>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 11/12 | chr15 | 52124738 | ||||||
chr15:52124739
|
C | T | 27 | a0001c0001t0011g0299a0001c0001t0011g0303a0001c0001t0011g0304others(24): Show | 27 | HG01891.hp1 HG02109.hp2 HG02257.hp1 others(24): Show |
intron_variant | MODIFIER | c.1010-100G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 11/12 | chr15 | 52124739 | ||||||
chr15:52124803
|
T | C | 1 | a0001c0001t0002g0053 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1010-164A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 11/12 | chr15 | 52124803 | ||||||
chr15:52124928
|
G | C | 7 | a0001c0004t0014g0002a0001c0004t0014g0280a0001c0004t0014g0290others(4): Show | 9 | HG00738.hp2 HG00741.hp1 HG01069.hp1 others(6): Show |
intron_variant | MODIFIER | c.1010-289C>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 11/12 | chr15 | 52124928 | ||||||
chr15:52124940
|
A | G | 1 | a0001c0003t0126g0313 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1010-301T>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 11/12 | chr15 | 52124940 | ||||||
chr15:52124977
|
C | T | 7 | a0001c0001t0011g0299a0001c0001t0011g0303a0001c0001t0011g0304others(4): Show | 7 | HG02895.hp1 HG02897.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.1010-338G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 11/12 | chr15 | 52124977 | ||||||
chr15:52125034
|
G | A | 9 | a0001c0002t0206g0178a0001c0002t0207g0177a0001c0004t0014g0002others(6): Show | 11 | HG00738.hp2 HG00741.hp1 HG01069.hp1 others(8): Show |
intron_variant | MODIFIER | c.1010-395C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 11/12 | chr15 | 52125034 | ||||||
chr15:52125130
|
G | A | 1 | a0001c0001t0176g0199 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1010-491C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 11/12 | chr15 | 52125130 | ||||||
chr15:52125293
|
T | TC | 7 | a0001c0002t0128g0273a0001c0002t0129g0275a0001c0002t0130g0274others(4): Show | 7 | HG01934.hp2 HG01952.hp1 HG02132.hp2 others(4): Show |
intron_variant | MODIFIER | c.1009+654dupG | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 11/12 | chr15 | 52125293 | ||||||
chr15:52125389
|
C | T | 1 | a0001c0001t0032g0350 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1009+559G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 11/12 | chr15 | 52125389 | ||||||
chr15:52125410
|
T | A | 139 | a0001c0001t0007g0139a0001c0001t0007g0144a0001c0001t0007g0148others(136): Show | 141 | HG00323.hp2 HG00544.hp2 HG00597.hp1 others(138): Show |
intron_variant | MODIFIER | c.1009+538A>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 11/12 | chr15 | 52125410 | ||||||
chr15:52125431
|
G | A | 1 | a0001c0001t0118g0032 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1009+517C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 11/12 | chr15 | 52125431 | ||||||
chr15:52125499
|
T | C | 1 | a0001c0001t0070g0157 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1009+449A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 11/12 | chr15 | 52125499 | ||||||
chr15:52125550
|
G | A | 6 | a0001c0001t0022g0294a0001c0001t0022g0295a0001c0001t0023g0296others(3): Show | 6 | HG02559.hp1 HG02723.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1009+398C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 11/12 | chr15 | 52125550 | ||||||
chr15:52125576
|
C | T | 13 | a0001c0002t0128g0273a0001c0002t0129g0275a0001c0002t0130g0274others(10): Show | 13 | HG01934.hp2 HG01952.hp1 HG02004.hp1 others(10): Show |
intron_variant | MODIFIER | c.1009+372G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 11/12 | chr15 | 52125576 | ||||||
chr15:52125666
|
T | C | 13 | a0001c0002t0128g0273a0001c0002t0129g0275a0001c0002t0130g0274others(10): Show | 13 | HG01934.hp2 HG01952.hp1 HG02004.hp1 others(10): Show |
intron_variant | MODIFIER | c.1009+282A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 11/12 | chr15 | 52125666 | ||||||
chr15:52125730
|
C | T | 61 | a0001c0001t0011g0299a0001c0001t0011g0303a0001c0001t0011g0304others(58): Show | 63 | HG00738.hp2 HG00741.hp1 HG01069.hp1 others(60): Show |
intron_variant | MODIFIER | c.1009+218G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 11/12 | chr15 | 52125730 | ||||||
chr15:52125764
|
T | C | 1 | a0001c0001t0018g0133 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1009+184A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 11/12 | chr15 | 52125764 | ||||||
chr15:52125773
|
A | G | 3 | a0001c0001t0011g0299a0001c0001t0011g0303a0001c0001t0011g0304 | 3 | HG02897.hp1 HG02970.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1009+175T>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 11/12 | chr15 | 52125773 | ||||||
chr15:52125784
|
G | A | 2 | a0001c0001t0003g0005a0001c0001t0003g0015 | 2 | NA18940.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.1009+164C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 11/12 | chr15 | 52125784 | ||||||
chr15:52125830
|
C | T | 13 | a0001c0002t0128g0273a0001c0002t0129g0275a0001c0002t0130g0274others(10): Show | 13 | HG01934.hp2 HG01952.hp1 HG02004.hp1 others(10): Show |
intron_variant | MODIFIER | c.1009+118G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 11/12 | chr15 | 52125830 | ||||||
chr15:52125843
|
A | G | 21 | a0001c0002t0006g0291a0001c0002t0006g0314a0001c0002t0006g0316others(18): Show | 23 | HG00738.hp2 HG00741.hp1 HG01069.hp1 others(20): Show |
intron_variant | MODIFIER | c.1009+105T>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 11/12 | chr15 | 52125843 | ||||||
chr15:52125856
|
T | C | 7 | a0001c0001t0011g0299a0001c0001t0011g0303a0001c0001t0011g0304others(4): Show | 7 | HG02895.hp1 HG02897.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.1009+92A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 11/12 | chr15 | 52125856 | ||||||
chr15:52125858
|
G | A | 12 | a0001c0002t0006g0291a0001c0002t0006g0314a0001c0002t0006g0316others(9): Show | 12 | HG01243.hp1 HG02055.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.1009+90C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 11/12 | chr15 | 52125858 | ||||||
chr15:52125887
|
G | A | 13 | a0001c0002t0128g0273a0001c0002t0129g0275a0001c0002t0130g0274others(10): Show | 13 | HG01934.hp2 HG01952.hp1 HG02004.hp1 others(10): Show |
intron_variant | MODIFIER | c.1009+61C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 11/12 | chr15 | 52125887 | ||||||
chr15:52126071
|
C | G | 13 | a0001c0002t0128g0273a0001c0002t0129g0275a0001c0002t0130g0274others(10): Show | 13 | HG01934.hp2 HG01952.hp1 HG02004.hp1 others(10): Show |
intron_variant | MODIFIER | c.913-27G>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 10/12 | chr15 | 52126071 | ||||||
chr15:52126075
|
C | T | 2 | a0001c0006t0142g0310a0001c0006t0143g0312 | 2 | HG02559.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.913-31G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 10/12 | chr15 | 52126075 | ||||||
chr15:52126256
|
T | C | 13 | a0001c0002t0128g0273a0001c0002t0129g0275a0001c0002t0130g0274others(10): Show | 13 | HG01934.hp2 HG01952.hp1 HG02004.hp1 others(10): Show |
intron_variant | MODIFIER | c.913-212A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 10/12 | chr15 | 52126256 | ||||||
chr15:52126283
|
G | C | 13 | a0001c0002t0128g0273a0001c0002t0129g0275a0001c0002t0130g0274others(10): Show | 13 | HG01934.hp2 HG01952.hp1 HG02004.hp1 others(10): Show |
intron_variant | MODIFIER | c.913-239C>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 10/12 | chr15 | 52126283 | ||||||
chr15:52126286
|
A | T | 1 | a0001c0003t0112g0087 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.913-242T>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 10/12 | chr15 | 52126286 | ||||||
chr15:52126339
|
G | T | 53 | a0001c0001t0016g0332a0001c0001t0016g0343a0001c0001t0016g0344others(50): Show | 53 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.913-295C>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 10/12 | chr15 | 52126339 | ||||||
chr15:52126346
|
G | T | 1 | a0001c0005t0157g0278 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.913-302C>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 10/12 | chr15 | 52126346 | ||||||
chr15:52126469
|
G | A | 13 | a0001c0002t0128g0273a0001c0002t0129g0275a0001c0002t0130g0274others(10): Show | 13 | HG01934.hp2 HG01952.hp1 HG02004.hp1 others(10): Show |
intron_variant | MODIFIER | c.913-425C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 10/12 | chr15 | 52126469 | ||||||
chr15:52126541
|
T | A | 1 | a0001c0001t0016g0332 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.913-497A>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 10/12 | chr15 | 52126541 | ||||||
chr15:52126549
|
G | C | 13 | a0001c0002t0128g0273a0001c0002t0129g0275a0001c0002t0130g0274others(10): Show | 13 | HG01934.hp2 HG01952.hp1 HG02004.hp1 others(10): Show |
intron_variant | MODIFIER | c.913-505C>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 10/12 | chr15 | 52126549 | ||||||
chr15:52126639
|
T | C | 140 | a0001c0001t0001g0248a0001c0001t0007g0139a0001c0001t0007g0144others(137): Show | 142 | HG00323.hp2 HG00544.hp2 HG00597.hp1 others(139): Show |
intron_variant | MODIFIER | c.913-595A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 10/12 | chr15 | 52126639 | ||||||
chr15:52126855
|
C | T | 7 | a0001c0004t0014g0002a0001c0004t0014g0280a0001c0004t0014g0290others(4): Show | 9 | HG00738.hp2 HG00741.hp1 HG01069.hp1 others(6): Show |
intron_variant | MODIFIER | c.913-811G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 10/12 | chr15 | 52126855 | ||||||
chr15:52126856
|
G | A | 1 | a0001c0001t0007g0153 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.913-812C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 10/12 | chr15 | 52126856 | ||||||
chr15:52126925
|
T | C | 103 | a0001c0001t0001g0248a0001c0001t0007g0139a0001c0001t0007g0144others(100): Show | 103 | HG00323.hp2 HG00544.hp2 HG00597.hp1 others(100): Show |
intron_variant | MODIFIER | c.913-881A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 10/12 | chr15 | 52126925 | ||||||
chr15:52126957
|
T | C | 13 | a0001c0002t0128g0273a0001c0002t0129g0275a0001c0002t0130g0274others(10): Show | 13 | HG01934.hp2 HG01952.hp1 HG02004.hp1 others(10): Show |
intron_variant | MODIFIER | c.913-913A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 10/12 | chr15 | 52126957 | ||||||
chr15:52127090
|
C | G | 13 | a0001c0002t0128g0273a0001c0002t0129g0275a0001c0002t0130g0274others(10): Show | 13 | HG01934.hp2 HG01952.hp1 HG02004.hp1 others(10): Show |
intron_variant | MODIFIER | c.913-1046G>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 10/12 | chr15 | 52127090 | ||||||
chr15:52127288
|
A | G | 296 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0001g0187others(293): Show | 298 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(295): Show |
intron_variant | MODIFIER | c.912+908T>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 10/12 | chr15 | 52127288 | ||||||
chr15:52127365
|
C | G | 2 | a0001c0005t0156g0261a0001c0005t0157g0278 | 2 | HG01109.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.912+831G>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 10/12 | chr15 | 52127365 | ||||||
chr15:52127519
|
T | C | 65 | a0001c0001t0016g0332a0001c0001t0016g0343a0001c0001t0016g0344others(62): Show | 65 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.912+677A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 10/12 | chr15 | 52127519 | ||||||
chr15:52127559
|
A | C | 3 | a0001c0001t0141g0301a0001c0001t0148g0302a0001c0001t0149g0300 | 3 | HG02258.hp1 HG02615.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.912+637T>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 10/12 | chr15 | 52127559 | ||||||
chr15:52127814
|
GA | G | 191 | a0001c0001t0001g0248a0001c0001t0002g0003a0001c0001t0002g0011others(188): Show | 193 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(190): Show |
intron_variant | MODIFIER | c.912+381delT | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 10/12 | chr15 | 52127814 | ||||||
chr15:52127814
|
GAA | G | 25 | a0001c0002t0006g0291a0001c0002t0006g0314a0001c0002t0006g0316others(22): Show | 25 | HG01243.hp1 HG01934.hp2 HG01952.hp1 others(22): Show |
intron_variant | MODIFIER | c.912+380_912+381del others(2): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 10/12 | chr15 | 52127814 | ||||||
chr15:52127928
|
T | C | 7 | a0001c0004t0014g0002a0001c0004t0014g0280a0001c0004t0014g0290others(4): Show | 9 | HG00738.hp2 HG00741.hp1 HG01069.hp1 others(6): Show |
intron_variant | MODIFIER | c.912+268A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 10/12 | chr15 | 52127928 | ||||||
chr15:52128254
|
G | A | 1 | a0001c0001t0001g0203 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.864-10C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 9/12 | chr15 | 52128254 | ||||||
chr15:52128294
|
G | T | 53 | a0001c0001t0016g0332a0001c0001t0016g0343a0001c0001t0016g0344others(50): Show | 53 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.864-50C>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 9/12 | chr15 | 52128294 | ||||||
chr15:52128379
|
G | C | 1 | a0001c0001t0197g0224 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.864-135C>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 9/12 | chr15 | 52128379 | ||||||
chr15:52128721
|
A | T | 1 | a0001c0001t0110g0009 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.864-477T>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 9/12 | chr15 | 52128721 | ||||||
chr15:52128785
|
T | A | 61 | a0001c0001t0011g0299a0001c0001t0011g0303a0001c0001t0011g0304others(58): Show | 63 | HG00738.hp2 HG00741.hp1 HG01069.hp1 others(60): Show |
intron_variant | MODIFIER | c.864-541A>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 9/12 | chr15 | 52128785 | ||||||
chr15:52128803
|
A | G | 139 | a0001c0001t0001g0248a0001c0001t0007g0139a0001c0001t0007g0144others(136): Show | 141 | HG00323.hp2 HG00544.hp2 HG00597.hp1 others(138): Show |
intron_variant | MODIFIER | c.864-559T>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 9/12 | chr15 | 52128803 | ||||||
chr15:52128826
|
T | A | 3 | a0001c0001t0008g0140a0001c0001t0008g0142a0001c0001t0015g0143 | 3 | NA18956.hp2 NA18966.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.864-582A>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 9/12 | chr15 | 52128826 | ||||||
chr15:52128946
|
T | C | 1 | a0001c0001t0117g0006 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.864-702A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 9/12 | chr15 | 52128946 | ||||||
chr15:52128954
|
C | CT | 81 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0001g0187others(78): Show | 81 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.864-711dupA | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 9/12 | chr15 | 52128954 | ||||||
chr15:52128954
|
CTT | C | 127 | a0001c0001t0007g0139a0001c0001t0007g0144a0001c0001t0007g0153others(124): Show | 129 | HG00323.hp2 HG00544.hp2 HG00597.hp1 others(126): Show |
intron_variant | MODIFIER | c.864-712_864-711del others(2): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 9/12 | chr15 | 52128954 | ||||||
chr15:52128954
|
CTTT | C | 9 | a0001c0001t0001g0248a0001c0001t0022g0294a0001c0001t0027g0307others(6): Show | 9 | HG02109.hp1 HG02258.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.864-713_864-711del others(3): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 9/12 | chr15 | 52128954 | ||||||
chr15:52128955
|
T | C | 1 | a0001c0003t0097g0091 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.864-711A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 9/12 | chr15 | 52128955 | ||||||
chr15:52129039
|
T | G | 1 | a0001c0001t0162g0361 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.864-795A>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 9/12 | chr15 | 52129039 | ||||||
chr15:52129119
|
C | T | 1 | a0001c0001t0001g0213 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.864-875G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 9/12 | chr15 | 52129119 | ||||||
chr15:52129192
|
G | C | 7 | a0001c0003t0097g0091a0001c0003t0098g0088a0001c0003t0099g0095others(4): Show | 7 | HG01884.hp1 HG02922.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.864-948C>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 9/12 | chr15 | 52129192 | ||||||
chr15:52129235
|
C | T | 29 | a0001c0002t0006g0291a0001c0002t0006g0314a0001c0002t0006g0316others(26): Show | 29 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.864-991G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 9/12 | chr15 | 52129235 | ||||||
chr15:52129305
|
C | T | 1 | a0001c0001t0094g0090 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.864-1061G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 9/12 | chr15 | 52129305 | ||||||
chr15:52129382
|
G | A | 1 | a0001c0001t0176g0199 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.864-1138C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 9/12 | chr15 | 52129382 | ||||||
chr15:52129394
|
T | C | 7 | a0001c0002t0024g0281a0001c0002t0024g0284a0001c0002t0025g0282others(4): Show | 7 | HG02109.hp2 HG02257.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.864-1150A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 9/12 | chr15 | 52129394 | ||||||
chr15:52129505
|
T | C | 1 | a0001c0001t0092g0137 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.864-1261A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 9/12 | chr15 | 52129505 | ||||||
chr15:52129556
|
G | A | 2 | a0001c0001t0073g0166a0001c0001t0075g0165 | 2 | HG02572.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.864-1312C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 9/12 | chr15 | 52129556 | ||||||
chr15:52129822
|
G | A | 8 | a0001c0003t0021g0354a0001c0003t0021g0355a0001c0003t0122g0357others(5): Show | 8 | HG01891.hp2 HG02055.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.864-1578C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 9/12 | chr15 | 52129822 | ||||||
chr15:52129913
|
T | G | 1 | a0001c0001t0012g0180 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.864-1669A>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 9/12 | chr15 | 52129913 | ||||||
chr15:52129922
|
G | T | 1 | a0001c0001t0001g0326 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.864-1678C>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 9/12 | chr15 | 52129922 | ||||||
chr15:52129923
|
T | G | 1 | a0001c0001t0001g0326 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.864-1679A>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 9/12 | chr15 | 52129923 | ||||||
chr15:52129928
|
C | T | 1 | a0004c0008t0005g0234 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.864-1684G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 9/12 | chr15 | 52129928 | ||||||
chr15:52130008
|
TGGGATGC others(6): Show |
T | 1 | a0001c0001t0001g0208 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.864-1777_864-1765d others(15): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 9/12 | chr15 | 52130008 | ||||||
chr15:52130052
|
C | A | 7 | a0001c0003t0097g0091a0001c0003t0098g0088a0001c0003t0099g0095others(4): Show | 7 | HG01884.hp1 HG02922.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.864-1808G>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 9/12 | chr15 | 52130052 | ||||||
chr15:52130069
|
T | C | 4 | a0001c0001t0145g0279a0001c0001t0146g0292a0001c0002t0206g0178others(1): Show | 4 | HG01496.hp1 HG01891.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.864-1825A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 9/12 | chr15 | 52130069 | ||||||
chr15:52130092
|
G | A | 1 | a0001c0001t0001g0202 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.864-1848C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 9/12 | chr15 | 52130092 | ||||||
chr15:52130278
|
C | T | 13 | a0001c0002t0128g0273a0001c0002t0129g0275a0001c0002t0130g0274others(10): Show | 13 | HG01934.hp2 HG01952.hp1 HG02004.hp1 others(10): Show |
intron_variant | MODIFIER | c.864-2034G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 9/12 | chr15 | 52130278 | ||||||
chr15:52130324
|
G | A | 7 | a0001c0004t0014g0002a0001c0004t0014g0280a0001c0004t0014g0290others(4): Show | 9 | HG00738.hp2 HG00741.hp1 HG01069.hp1 others(6): Show |
intron_variant | MODIFIER | c.864-2080C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 9/12 | chr15 | 52130324 | ||||||
chr15:52130350
|
C | A | 7 | a0001c0004t0014g0002a0001c0004t0014g0280a0001c0004t0014g0290others(4): Show | 9 | HG00738.hp2 HG00741.hp1 HG01069.hp1 others(6): Show |
intron_variant | MODIFIER | c.864-2106G>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 9/12 | chr15 | 52130350 | ||||||
chr15:52130534
|
C | T | 1 | a0001c0001t0037g0163 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.864-2290G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 9/12 | chr15 | 52130534 | ||||||
chr15:52130769
|
G | A | 7 | a0001c0004t0014g0002a0001c0004t0014g0280a0001c0004t0014g0290others(4): Show | 9 | HG00738.hp2 HG00741.hp1 HG01069.hp1 others(6): Show |
intron_variant | MODIFIER | c.864-2525C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 9/12 | chr15 | 52130769 | ||||||
chr15:52130851
|
G | A | 117 | a0001c0001t0001g0248a0001c0001t0007g0139a0001c0001t0007g0144others(114): Show | 119 | HG00323.hp2 HG00544.hp2 HG00597.hp1 others(116): Show |
intron_variant | MODIFIER | c.863+2527C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 9/12 | chr15 | 52130851 | ||||||
chr15:52130888
|
C | T | 3 | a0001c0001t0058g0098a0001c0001t0061g0096a0001c0001t0089g0097 | 3 | HG01928.hp1 HG01943.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.863+2490G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 9/12 | chr15 | 52130888 | ||||||
chr15:52130916
|
G | C | 124 | a0001c0001t0001g0248a0001c0001t0007g0139a0001c0001t0007g0144others(121): Show | 126 | HG00323.hp2 HG00544.hp2 HG00597.hp1 others(123): Show |
intron_variant | MODIFIER | c.863+2462C>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 9/12 | chr15 | 52130916 | ||||||
chr15:52131006
|
G | A | 209 | a0001c0001t0001g0248a0001c0001t0007g0139a0001c0001t0007g0144others(206): Show | 211 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(208): Show |
intron_variant | MODIFIER | c.863+2372C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 9/12 | chr15 | 52131006 | ||||||
chr15:52131027
|
T | C | 9 | a0001c0001t0011g0299a0001c0001t0011g0303a0001c0001t0011g0304others(6): Show | 9 | HG02559.hp2 HG02818.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.863+2351A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 9/12 | chr15 | 52131027 | ||||||
chr15:52131474
|
G | T | 1 | a0001c0001t0001g0242 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.863+1904C>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 9/12 | chr15 | 52131474 | ||||||
chr15:52131514
|
C | T | 1 | a0001c0001t0034g0330 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.863+1864G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 9/12 | chr15 | 52131514 | ||||||
chr15:52131523
|
G | C | 8 | a0001c0003t0021g0354a0001c0003t0021g0355a0001c0003t0122g0357others(5): Show | 8 | HG01891.hp2 HG02055.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.863+1855C>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 9/12 | chr15 | 52131523 | ||||||
chr15:52131548
|
G | A | 7 | a0001c0002t0024g0281a0001c0002t0024g0284a0001c0002t0025g0282others(4): Show | 7 | HG02109.hp2 HG02257.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.863+1830C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 9/12 | chr15 | 52131548 | ||||||
chr15:52131699
|
T | G | 6 | a0001c0003t0097g0091a0001c0003t0098g0088a0001c0003t0099g0095others(3): Show | 6 | HG01884.hp1 HG02922.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.863+1679A>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 9/12 | chr15 | 52131699 | ||||||
chr15:52131745
|
T | C | 1 | a0001c0001t0001g0221 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.863+1633A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 9/12 | chr15 | 52131745 | ||||||
chr15:52131832
|
A | C | 1 | a0001c0001t0001g0208 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.863+1546T>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 9/12 | chr15 | 52131832 | ||||||
chr15:52131861
|
C | T | 1 | a0001c0001t0052g0121 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.863+1517G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 9/12 | chr15 | 52131861 | ||||||
chr15:52131874
|
G | A | 20 | a0001c0002t0024g0281a0001c0002t0024g0284a0001c0002t0025g0282others(17): Show | 20 | HG01934.hp2 HG01952.hp1 HG02004.hp1 others(17): Show |
intron_variant | MODIFIER | c.863+1504C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 9/12 | chr15 | 52131874 | ||||||
chr15:52132001
|
C | G | 87 | a0001c0001t0001g0248a0001c0001t0007g0139a0001c0001t0007g0144others(84): Show | 89 | HG00323.hp2 HG00544.hp2 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.863+1377G>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 9/12 | chr15 | 52132001 | ||||||
chr15:52132168
|
A | ACC | 295 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0001g0187others(292): Show | 297 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(294): Show |
intron_variant | MODIFIER | c.863+1209_863+1210i others(4): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 9/12 | chr15 | 52132168 | ||||||
chr15:52132169
|
T | A | 295 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0001g0187others(292): Show | 297 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(294): Show |
intron_variant | MODIFIER | c.863+1209A>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 9/12 | chr15 | 52132169 | ||||||
chr15:52132294
|
C | A | 12 | a0001c0002t0006g0291a0001c0002t0006g0314a0001c0002t0006g0316others(9): Show | 12 | HG01243.hp1 HG02055.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.863+1084G>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 9/12 | chr15 | 52132294 | ||||||
chr15:52132306
|
T | A | 2 | a0001c0005t0156g0261a0001c0005t0157g0278 | 2 | HG01109.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.863+1072A>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 9/12 | chr15 | 52132306 | ||||||
chr15:52132488
|
G | GT | 33 | a0001c0001t0001g0205a0001c0001t0001g0208a0001c0001t0001g0237others(30): Show | 35 | HG00544.hp1 HG00673.hp2 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.863+889dupA | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 9/12 | chr15 | 52132488 | ||||||
chr15:52132488
|
G | GTT | 13 | a0001c0002t0024g0284a0001c0002t0025g0282a0001c0002t0025g0283others(10): Show | 13 | HG01891.hp2 HG02004.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.863+888_863+889dup others(2): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 9/12 | chr15 | 52132488 | ||||||
chr15:52132488
|
G | GTTT | 7 | a0001c0002t0024g0281a0001c0002t0026g0287a0001c0002t0129g0275others(4): Show | 7 | HG01934.hp2 HG01952.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.863+887_863+889dup others(3): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 9/12 | chr15 | 52132488 | ||||||
chr15:52132613
|
C | G | 1 | a0001c0001t0160g0212 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.863+765G>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 9/12 | chr15 | 52132613 | ||||||
chr15:52132631
|
T | G | 115 | a0001c0001t0001g0248a0001c0001t0007g0139a0001c0001t0007g0144others(112): Show | 117 | HG00323.hp2 HG00544.hp2 HG00597.hp1 others(114): Show |
intron_variant | MODIFIER | c.863+747A>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 9/12 | chr15 | 52132631 | ||||||
chr15:52132636
|
A | AT | 23 | a0001c0001t0001g0237a0001c0001t0004g0066a0001c0001t0011g0299others(20): Show | 23 | HG01891.hp1 HG02258.hp1 HG02559.hp1 others(20): Show |
intron_variant | MODIFIER | c.863+741dupA | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 9/12 | chr15 | 52132636 | ||||||
chr15:52132636
|
A | ATTTTTTT others(1): Show |
9 | a0001c0001t0061g0096a0001c0002t0136g0268a0001c0003t0021g0354others(6): Show | 9 | HG01891.hp2 HG01943.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.863+734_863+741dup others(8): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 9/12 | chr15 | 52132636 | ||||||
chr15:52132636
|
A | ATTTTTTT others(2): Show |
13 | a0001c0002t0128g0273a0001c0002t0129g0275a0001c0002t0130g0274others(10): Show | 13 | HG01934.hp2 HG01952.hp1 HG02004.hp1 others(10): Show |
intron_variant | MODIFIER | c.863+733_863+741dup others(9): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 9/12 | chr15 | 52132636 | ||||||
chr15:52132636
|
A | ATTTTTTT others(3): Show |
37 | a0001c0001t0015g0146a0001c0001t0018g0133a0001c0001t0018g0151others(34): Show | 37 | HG00544.hp2 HG00597.hp1 HG00673.hp2 others(34): Show |
intron_variant | MODIFIER | c.863+732_863+741dup others(10): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 9/12 | chr15 | 52132636 | ||||||
chr15:52132636
|
A | ATTTTTTT others(4): Show |
41 | a0001c0001t0001g0248a0001c0001t0007g0139a0001c0001t0007g0144others(38): Show | 41 | HG00323.hp2 HG00609.hp1 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.863+731_863+741dup others(11): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 9/12 | chr15 | 52132636 | ||||||
chr15:52132636
|
A | ATTTTTTT others(5): Show |
12 | a0001c0001t0008g0099a0001c0001t0008g0176a0001c0001t0015g0145others(9): Show | 13 | HG00741.hp1 HG01123.hp2 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.863+730_863+741dup others(12): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 9/12 | chr15 | 52132636 | ||||||
chr15:52132636
|
A | ATTTTTTT others(6): Show |
2 | a0001c0004t0017g0001a0001c0004t0017g0293 | 3 | HG00738.hp2 HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.863+729_863+741dup others(13): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 9/12 | chr15 | 52132636 | ||||||
chr15:52132719
|
C | T | 28 | a0001c0001t0004g0064a0001c0001t0018g0133a0001c0001t0018g0151others(25): Show | 28 | HG00544.hp2 HG00597.hp1 HG00673.hp2 others(25): Show |
intron_variant | MODIFIER | c.863+659G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 9/12 | chr15 | 52132719 | ||||||
chr15:52132764
|
T | A | 1 | a0004c0008t0005g0234 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.863+614A>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 9/12 | chr15 | 52132764 | ||||||
chr15:52132791
|
A | T | 1 | a0004c0008t0005g0234 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.863+587T>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 9/12 | chr15 | 52132791 | ||||||
chr15:52132793
|
T | A | 1 | a0004c0008t0005g0234 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.863+585A>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 9/12 | chr15 | 52132793 | ||||||
chr15:52132836
|
A | T | 1 | a0004c0008t0005g0234 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.863+542T>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 9/12 | chr15 | 52132836 | ||||||
chr15:52132958
|
C | T | 1 | a0001c0001t0002g0046 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.863+420G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 9/12 | chr15 | 52132958 | ||||||
chr15:52132973
|
T | G | 2 | a0001c0001t0030g0182a0001c0001t0030g0206 | 2 | HG02155.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.863+405A>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 9/12 | chr15 | 52132973 | ||||||
chr15:52133065
|
T | C | 8 | a0001c0003t0021g0354a0001c0003t0021g0355a0001c0003t0122g0357others(5): Show | 8 | HG01891.hp2 HG02055.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.863+313A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 9/12 | chr15 | 52133065 | ||||||
chr15:52133101
|
T | C | 1 | a0001c0001t0074g0162 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.863+277A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 9/12 | chr15 | 52133101 | ||||||
chr15:52133170
|
G | A | 2 | a0001c0005t0156g0261a0001c0005t0157g0278 | 2 | HG01109.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.863+208C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 9/12 | chr15 | 52133170 | ||||||
chr15:52133263
|
G | C | 3 | a0001c0001t0141g0301a0001c0001t0148g0302a0001c0001t0149g0300 | 3 | HG02258.hp1 HG02615.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.863+115C>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 9/12 | chr15 | 52133263 | ||||||
chr15:52133542
|
T | C | 8 | a0001c0003t0021g0354a0001c0003t0021g0355a0001c0003t0122g0357others(5): Show | 8 | HG01891.hp2 HG02055.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.772-73A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 8/12 | chr15 | 52133542 | ||||||
chr15:52133543
|
A | G | 11 | a0001c0001t0003g0005a0001c0001t0003g0013a0001c0001t0003g0014others(8): Show | 11 | HG00408.hp1 NA18612.hp2 NA18940.hp2 others(8): Show |
intron_variant | MODIFIER | c.772-74T>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 8/12 | chr15 | 52133543 | ||||||
chr15:52133763
|
G | A | 7 | a0001c0001t0011g0299a0001c0001t0011g0303a0001c0001t0011g0304others(4): Show | 7 | HG02895.hp1 HG02897.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.772-294C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 8/12 | chr15 | 52133763 | ||||||
chr15:52133787
|
T | C | 1 | a0001c0001t0037g0163 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.772-318A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 8/12 | chr15 | 52133787 | ||||||
chr15:52133833
|
G | A | 3 | a0001c0001t0141g0301a0001c0001t0148g0302a0001c0001t0149g0300 | 3 | HG02258.hp1 HG02615.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.772-364C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 8/12 | chr15 | 52133833 | ||||||
chr15:52134063
|
C | T | 2 | a0001c0001t0070g0157a0001c0001t0152g0243 | 2 | HG03540.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.772-594G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 8/12 | chr15 | 52134063 | ||||||
chr15:52134097
|
G | A | 84 | a0001c0001t0007g0139a0001c0001t0007g0144a0001c0001t0007g0148others(81): Show | 86 | HG00323.hp2 HG00544.hp2 HG00597.hp1 others(83): Show |
intron_variant | MODIFIER | c.772-628C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 8/12 | chr15 | 52134097 | ||||||
chr15:52134117
|
A | G | 8 | a0001c0003t0021g0354a0001c0003t0021g0355a0001c0003t0122g0357others(5): Show | 8 | HG01891.hp2 HG02055.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.772-648T>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 8/12 | chr15 | 52134117 | ||||||
chr15:52134135
|
G | T | 1 | a0001c0001t0063g0132 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.772-666C>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 8/12 | chr15 | 52134135 | ||||||
chr15:52134267
|
A | G | 1 | a0001c0001t0031g0340 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.772-798T>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 8/12 | chr15 | 52134267 | ||||||
chr15:52134394
|
G | A | 3 | a0001c0001t0141g0301a0001c0001t0148g0302a0001c0001t0149g0300 | 3 | HG02258.hp1 HG02615.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.772-925C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 8/12 | chr15 | 52134394 | ||||||
chr15:52134436
|
ATG | A | 8 | a0001c0001t0022g0294a0001c0001t0022g0295a0001c0001t0023g0296others(5): Show | 8 | HG01891.hp1 HG02559.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.772-969_772-968del others(2): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 8/12 | chr15 | 52134436 | ||||||
chr15:52134442
|
G | A | 8 | a0001c0003t0021g0354a0001c0003t0021g0355a0001c0003t0122g0357others(5): Show | 8 | HG01891.hp2 HG02055.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.772-973C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 8/12 | chr15 | 52134442 | ||||||
chr15:52134443
|
C | A | 8 | a0001c0003t0021g0354a0001c0003t0021g0355a0001c0003t0122g0357others(5): Show | 8 | HG01891.hp2 HG02055.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.772-974G>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 8/12 | chr15 | 52134443 | ||||||
chr15:52134454
|
G | C | 1 | a0001c0001t0065g0079 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.772-985C>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 8/12 | chr15 | 52134454 | ||||||
chr15:52134567
|
G | A | 1 | a0001c0001t0185g0228 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.771+1046C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 8/12 | chr15 | 52134567 | ||||||
chr15:52134577
|
A | G | 10 | a0001c0001t0037g0163a0001c0001t0043g0007a0001c0001t0065g0079others(7): Show | 10 | HG00323.hp2 HG01123.hp2 HG01192.hp1 others(7): Show |
intron_variant | MODIFIER | c.771+1036T>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 8/12 | chr15 | 52134577 | ||||||
chr15:52134594
|
C | T | 7 | a0001c0002t0024g0281a0001c0002t0024g0284a0001c0002t0025g0282others(4): Show | 7 | HG02109.hp2 HG02257.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.771+1019G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 8/12 | chr15 | 52134594 | ||||||
chr15:52134706
|
C | T | 2 | a0001c0001t0008g0152a0001c0001t0008g0176 | 2 | HG03669.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.771+907G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 8/12 | chr15 | 52134706 | ||||||
chr15:52134724
|
T | C | 54 | a0001c0001t0001g0192a0001c0001t0016g0332a0001c0001t0016g0343others(51): Show | 54 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.771+889A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 8/12 | chr15 | 52134724 | ||||||
chr15:52134769
|
G | A | 3 | a0001c0001t0046g0110a0001c0001t0068g0111a0001c0001t0069g0105 | 3 | HG01256.hp2 HG01258.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.771+844C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 8/12 | chr15 | 52134769 | ||||||
chr15:52134871
|
C | T | 8 | a0001c0003t0021g0354a0001c0003t0021g0355a0001c0003t0122g0357others(5): Show | 8 | HG01891.hp2 HG02055.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.771+742G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 8/12 | chr15 | 52134871 | ||||||
chr15:52134884
|
T | C | 54 | a0001c0001t0001g0192a0001c0001t0016g0332a0001c0001t0016g0343others(51): Show | 54 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.771+729A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 8/12 | chr15 | 52134884 | ||||||
chr15:52134944
|
G | A | 1 | a0001c0001t0146g0292 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.771+669C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 8/12 | chr15 | 52134944 | ||||||
chr15:52134982
|
T | A | 1 | a0001c0001t0002g0010 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.771+631A>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 8/12 | chr15 | 52134982 | ||||||
chr15:52135256
|
C | T | 86 | a0001c0001t0001g0248a0001c0001t0007g0139a0001c0001t0007g0144others(83): Show | 88 | HG00323.hp2 HG00544.hp2 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.771+357G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 8/12 | chr15 | 52135256 | ||||||
chr15:52135285
|
A | G | 2 | a0001c0005t0156g0261a0001c0005t0157g0278 | 2 | HG01109.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.771+328T>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 8/12 | chr15 | 52135285 | ||||||
chr15:52135344
|
C | T | 1 | a0001c0002t0202g0318 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.771+269G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 8/12 | chr15 | 52135344 | ||||||
chr15:52135407
|
C | T | 13 | a0001c0002t0128g0273a0001c0002t0129g0275a0001c0002t0130g0274others(10): Show | 13 | HG01934.hp2 HG01952.hp1 HG02004.hp1 others(10): Show |
intron_variant | MODIFIER | c.771+206G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 8/12 | chr15 | 52135407 | ||||||
chr15:52135453
|
G | A | 7 | a0001c0002t0024g0281a0001c0002t0024g0284a0001c0002t0025g0282others(4): Show | 7 | HG02109.hp2 HG02257.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.771+160C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 8/12 | chr15 | 52135453 | ||||||
chr15:52135763
|
G | A | 1 | a0001c0001t0069g0105 | 1 | HG02258.hp2 | splice_region_variant&intron_variant | LOW | c.628-7C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52135763 | ||||||
chr15:52135819
|
A | G | 1 | a0001c0001t0010g0103 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.628-63T>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52135819 | ||||||
chr15:52135852
|
A | AAC | 61 | a0001c0001t0001g0216a0001c0001t0001g0252a0001c0001t0001g0326others(58): Show | 61 | HG00099.hp1 HG00323.hp1 HG00733.hp1 others(58): Show |
intron_variant | MODIFIER | c.628-98_628-97dupGT | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52135852 | ||||||
chr15:52135852
|
A | AACAC | 34 | a0001c0001t0001g0205a0001c0001t0001g0223a0001c0001t0002g0011others(31): Show | 34 | HG00408.hp1 HG00639.hp2 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.628-100_628-97dupG others(3): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52135852 | ||||||
chr15:52135852
|
A | AACACAC | 50 | a0001c0001t0001g0248a0001c0001t0003g0005a0001c0001t0003g0015others(47): Show | 51 | HG00438.hp1 HG00673.hp2 HG01106.hp2 others(48): Show |
intron_variant | MODIFIER | c.628-102_628-97dupG others(5): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52135852 | ||||||
chr15:52135852
|
A | AACACACA others(1): Show |
17 | a0001c0001t0002g0030a0001c0001t0007g0139a0001c0001t0007g0148others(14): Show | 17 | HG00609.hp1 HG01934.hp2 HG02015.hp2 others(14): Show |
intron_variant | MODIFIER | c.628-104_628-97dupG others(7): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52135852 | ||||||
chr15:52135852
|
A | AACACACA others(3): Show |
16 | a0001c0001t0003g0016a0001c0001t0015g0145a0001c0001t0045g0158others(13): Show | 16 | HG01256.hp2 HG01258.hp1 HG01943.hp1 others(13): Show |
intron_variant | MODIFIER | c.628-106_628-97dupG others(9): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52135852 | ||||||
chr15:52135852
|
A | AACACACA others(5): Show |
16 | a0001c0001t0008g0176a0001c0001t0037g0163a0001c0001t0038g0115others(13): Show | 16 | HG01123.hp2 HG01168.hp1 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.628-108_628-97dupG others(11): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52135852 | ||||||
chr15:52135852
|
A | AACACACA others(7): Show |
16 | a0001c0001t0008g0152a0001c0001t0040g0113a0001c0001t0041g0128others(13): Show | 17 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(14): Show |
intron_variant | MODIFIER | c.628-110_628-97dupG others(13): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52135852 | ||||||
chr15:52135852
|
A | AACACACA others(9): Show |
4 | a0001c0001t0053g0171a0001c0002t0025g0283a0001c0002t0136g0268others(1): Show | 4 | HG00597.hp1 HG02004.hp1 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.628-112_628-97dupG others(15): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52135852 | ||||||
chr15:52135852
|
A | AACACACA others(11): Show |
1 | a0001c0001t0051g0120 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.628-114_628-97dupG others(17): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52135852 | ||||||
chr15:52135852
|
A | AACACACA others(13): Show |
1 | a0001c0002t0137g0266 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.628-116_628-97dupG others(19): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52135852 | ||||||
chr15:52135852
|
A | AACACACA others(15): Show |
2 | a0001c0001t0088g0114a0001c0003t0119g0094 | 2 | HG02135.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.628-118_628-97dupG others(21): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52135852 | ||||||
chr15:52135852
|
A | AACACACA others(17): Show |
1 | a0001c0002t0138g0250 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.628-120_628-97dupG others(23): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52135852 | ||||||
chr15:52135893
|
A | ACACACAC others(21): Show |
1 | a0001c0003t0127g0356 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.628-138_628-137ins others(28): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52135893 | ||||||
chr15:52135893
|
A | ACACACAC others(3): Show |
1 | a0001c0001t0048g0123 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.628-138_628-137ins others(10): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52135893 | ||||||
chr15:52135893
|
A | C | 3 | a0001c0001t0005g0231a0001c0001t0005g0232a0001c0001t0176g0199 | 3 | HG01934.hp1 HG01975.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.628-137T>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52135893 | ||||||
chr15:52135894
|
C | CA | 6 | a0001c0001t0001g0242a0001c0001t0029g0215a0001c0001t0103g0100others(3): Show | 6 | HG01099.hp1 HG01496.hp2 HG04115.hp1 others(3): Show |
intron_variant | MODIFIER | c.628-139_628-138ins others(1): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52135894 | ||||||
chr15:52135894
|
C | CACACACA others(6): Show |
3 | a0001c0002t0132g0276a0001c0002t0207g0177a0001c0003t0021g0355 | 3 | HG01496.hp1 HG01891.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.628-139_628-138ins others(13): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52135894 | ||||||
chr15:52135943
|
AAGAAGGA others(22): Show |
A | 1 | a0003c0009t0172g0217 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.628-216_628-188del others(29): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52135943 | ||||||
chr15:52135993
|
T | C | 1 | a0001c0001t0029g0215 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.628-237A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52135993 | ||||||
chr15:52136049
|
T | C | 15 | a0001c0002t0128g0273a0001c0002t0129g0275a0001c0002t0130g0274others(12): Show | 15 | HG01109.hp1 HG01934.hp2 HG01952.hp1 others(12): Show |
intron_variant | MODIFIER | c.628-293A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52136049 | ||||||
chr15:52136063
|
GAACACA | G | 14 | a0001c0001t0007g0144a0001c0001t0007g0148a0001c0001t0007g0169others(11): Show | 14 | NA18946.hp1 NA18956.hp2 NA18960.hp2 others(11): Show |
intron_variant | MODIFIER | c.628-313_628-308del others(6): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52136063 | ||||||
chr15:52136064
|
A | AAC | 27 | a0001c0001t0001g0203a0001c0001t0001g0213a0001c0001t0001g0223others(24): Show | 27 | HG00735.hp1 HG01069.hp2 HG01261.hp1 others(24): Show |
intron_variant | MODIFIER | c.628-310_628-309dup others(2): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52136064 | ||||||
chr15:52136064
|
A | AACAC | 23 | a0001c0001t0022g0294a0001c0001t0022g0295a0001c0001t0030g0182others(20): Show | 23 | HG01243.hp1 HG02055.hp2 HG02083.hp2 others(20): Show |
intron_variant | MODIFIER | c.628-312_628-309dup others(4): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52136064 | ||||||
chr15:52136064
|
A | AACACAC | 42 | a0001c0001t0016g0343a0001c0001t0016g0344a0001c0001t0031g0340others(39): Show | 42 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(39): Show |
intron_variant | MODIFIER | c.628-314_628-309dup others(6): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52136064 | ||||||
chr15:52136064
|
A | AACACACA others(1): Show |
7 | a0001c0001t0016g0332a0001c0001t0031g0334a0001c0001t0165g0339others(4): Show | 7 | HG01243.hp2 HG04184.hp1 NA18963.hp1 others(4): Show |
intron_variant | MODIFIER | c.628-316_628-309dup others(8): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52136064 | ||||||
chr15:52136064
|
A | AACACACA others(3): Show |
4 | a0001c0001t0117g0006a0001c0001t0166g0345a0001c0001t0168g0190others(1): Show | 4 | HG01192.hp2 HG03130.hp2 NA18965.hp1 others(1): Show |
intron_variant | MODIFIER | c.628-318_628-309dup others(10): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52136064 | ||||||
chr15:52136064
|
A | AACACACA others(5): Show |
5 | a0001c0002t0024g0281a0001c0002t0024g0284a0001c0002t0026g0286others(2): Show | 5 | HG02257.hp1 HG02630.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.628-320_628-309dup others(12): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52136064 | ||||||
chr15:52136064
|
AAC | A | 9 | a0001c0001t0002g0051a0001c0001t0002g0082a0001c0001t0004g0066others(6): Show | 9 | HG00323.hp1 HG01884.hp1 HG02129.hp2 others(6): Show |
intron_variant | MODIFIER | c.628-310_628-309del others(2): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52136064 | ||||||
chr15:52136064
|
AACAC | A | 6 | a0001c0001t0002g0030a0001c0001t0038g0115a0001c0001t0078g0086others(3): Show | 6 | HG01496.hp1 HG02109.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.628-312_628-309del others(4): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52136064 | ||||||
chr15:52136064
|
AACACAC | A | 60 | a0001c0001t0001g0248a0001c0001t0007g0139a0001c0001t0007g0153others(57): Show | 60 | HG00323.hp2 HG00544.hp2 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.628-314_628-309del others(6): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52136064 | ||||||
chr15:52136064
|
AACACACA others(3): Show |
A | 8 | a0001c0003t0021g0354a0001c0003t0021g0355a0001c0003t0122g0357others(5): Show | 8 | HG01891.hp2 HG02055.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.628-318_628-309del others(10): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52136064 | ||||||
chr15:52136098
|
CAGGGAAA others(6): Show |
C | 1 | a0001c0002t0137g0266 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.628-355_628-343del others(13): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52136098 | ||||||
chr15:52136098
|
CAGGGAAA others(8): Show |
C | 7 | a0001c0002t0128g0273a0001c0002t0129g0275a0001c0002t0130g0274others(4): Show | 7 | HG01934.hp2 HG01952.hp1 HG02132.hp2 others(4): Show |
intron_variant | MODIFIER | c.628-357_628-343del others(15): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52136098 | ||||||
chr15:52136113
|
A | AAC | 40 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0191others(37): Show | 40 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(37): Show |
intron_variant | MODIFIER | c.628-359_628-358dup others(2): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52136113 | ||||||
chr15:52136113
|
A | AACAC | 28 | a0001c0001t0001g0189a0001c0001t0001g0209a0001c0001t0001g0229others(25): Show | 29 | HG00544.hp2 HG00673.hp1 HG01099.hp1 others(26): Show |
intron_variant | MODIFIER | c.628-361_628-358dup others(4): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52136113 | ||||||
chr15:52136113
|
A | AACACAC | 36 | a0001c0001t0001g0185a0001c0001t0001g0193a0001c0001t0001g0195others(33): Show | 36 | HG00597.hp2 HG00621.hp1 HG00621.hp2 others(33): Show |
intron_variant | MODIFIER | c.628-363_628-358dup others(6): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52136113 | ||||||
chr15:52136113
|
A | AACACACA others(1): Show |
24 | a0001c0001t0001g0223a0001c0001t0001g0245a0001c0001t0001g0246others(21): Show | 24 | HG00408.hp2 HG00733.hp1 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.628-365_628-358dup others(8): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52136113 | ||||||
chr15:52136113
|
A | AACACACA others(3): Show |
14 | a0001c0001t0002g0034a0001c0001t0002g0069a0001c0001t0003g0027others(11): Show | 14 | HG00609.hp2 HG01081.hp1 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.628-367_628-358dup others(10): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52136113 | ||||||
chr15:52136113
|
A | AACACACA others(5): Show |
5 | a0001c0001t0001g0203a0001c0001t0002g0040a0001c0001t0005g0210others(2): Show | 5 | HG01981.hp2 HG03540.hp1 HG03669.hp2 others(2): Show |
intron_variant | MODIFIER | c.628-369_628-358dup others(12): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52136113 | ||||||
chr15:52136113
|
A | AACACACA others(7): Show |
6 | a0001c0001t0001g0252a0001c0001t0010g0112a0001c0001t0163g0222others(3): Show | 6 | HG01496.hp2 HG02055.hp2 HG02135.hp2 others(3): Show |
intron_variant | MODIFIER | c.628-371_628-358dup others(14): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52136113 | ||||||
chr15:52136113
|
A | AACACACA others(9): Show |
2 | a0001c0001t0153g0244a0001c0002t0203g0323 | 2 | HG02886.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.628-373_628-358dup others(16): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52136113 | ||||||
chr15:52136113
|
A | AACACACA others(74): Show |
1 | a0001c0001t0116g0119 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.628-358_628-357ins others(81): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52136113 | ||||||
chr15:52136113
|
A | ACACACAC others(4): Show |
1 | a0001c0003t0021g0355 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.628-358_628-357ins others(11): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52136113 | ||||||
chr15:52136113
|
A | ACACACAC others(6): Show |
1 | a0001c0001t0001g0251 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.628-358_628-357ins others(13): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52136113 | ||||||
chr15:52136113
|
A | C | 1 | a0001c0002t0137g0266 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.628-357T>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52136113 | ||||||
chr15:52136113
|
AAC | A | 13 | a0001c0001t0001g0240a0001c0001t0002g0011a0001c0001t0004g0029others(10): Show | 13 | HG00544.hp1 HG00639.hp2 HG00733.hp2 others(10): Show |
intron_variant | MODIFIER | c.628-359_628-358del others(2): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52136113 | ||||||
chr15:52136113
|
AACAC | A | 5 | a0001c0001t0001g0192a0001c0001t0001g0205a0001c0001t0002g0045others(2): Show | 5 | HG01071.hp2 HG02735.hp1 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.628-361_628-358del others(4): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52136113 | ||||||
chr15:52136113
|
AACACAC | A | 3 | a0001c0001t0003g0078a0001c0001t0004g0028a0001c0001t0194g0336 | 3 | HG01993.hp2 NA18959.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.628-363_628-358del others(6): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52136113 | ||||||
chr15:52136113
|
AACACACA others(3): Show |
A | 1 | a0001c0002t0206g0178 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.628-367_628-358del others(10): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52136113 | ||||||
chr15:52136113
|
AACACACA others(5): Show |
A | 1 | a0001c0001t0002g0085 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.628-369_628-358del others(12): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52136113 | ||||||
chr15:52136113
|
AACACACA others(7): Show |
A | 3 | a0001c0001t0141g0301a0001c0001t0148g0302a0001c0001t0149g0300 | 3 | HG02258.hp1 HG02615.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.628-371_628-358del others(14): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52136113 | ||||||
chr15:52136113
|
AACACACA others(9): Show |
A | 4 | a0001c0001t0002g0010a0001c0001t0005g0236a0001c0001t0036g0065others(1): Show | 4 | HG03927.hp2 HG03942.hp2 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.628-373_628-358del others(16): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52136113 | ||||||
chr15:52136113
|
AACACACA others(11): Show |
A | 11 | a0001c0001t0002g0004a0001c0001t0002g0008a0001c0001t0002g0036others(8): Show | 11 | HG00099.hp1 HG01168.hp2 HG02293.hp2 others(8): Show |
intron_variant | MODIFIER | c.628-375_628-358del others(18): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52136113 | ||||||
chr15:52136113
|
AACACACA others(17): Show |
A | 6 | a0001c0002t0135g0270a0001c0002t0136g0268a0001c0002t0138g0250others(3): Show | 6 | HG01109.hp1 HG02004.hp1 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.628-381_628-358del others(24): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52136113 | ||||||
chr15:52136123
|
C | G | 7 | a0001c0002t0128g0273a0001c0002t0129g0275a0001c0002t0130g0274others(4): Show | 7 | HG01934.hp2 HG01952.hp1 HG02132.hp2 others(4): Show |
intron_variant | MODIFIER | c.628-367G>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52136123 | ||||||
chr15:52136124
|
A | G | 7 | a0001c0002t0128g0273a0001c0002t0129g0275a0001c0002t0130g0274others(4): Show | 7 | HG01934.hp2 HG01952.hp1 HG02132.hp2 others(4): Show |
intron_variant | MODIFIER | c.628-368T>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52136124 | ||||||
chr15:52136125
|
C | G | 8 | a0001c0002t0128g0273a0001c0002t0129g0275a0001c0002t0130g0274others(5): Show | 8 | HG01934.hp2 HG01952.hp1 HG02132.hp2 others(5): Show |
intron_variant | MODIFIER | c.628-369G>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52136125 | ||||||
chr15:52136126
|
A | G | 1 | a0001c0002t0137g0266 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.628-370T>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52136126 | ||||||
chr15:52136127
|
C | A | 7 | a0001c0002t0128g0273a0001c0002t0129g0275a0001c0002t0130g0274others(4): Show | 7 | HG01934.hp2 HG01952.hp1 HG02132.hp2 others(4): Show |
intron_variant | MODIFIER | c.628-371G>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52136127 | ||||||
chr15:52136127
|
C | G | 1 | a0001c0002t0137g0266 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.628-371G>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52136127 | ||||||
chr15:52136129
|
C | A | 8 | a0001c0002t0128g0273a0001c0002t0129g0275a0001c0002t0130g0274others(5): Show | 8 | HG01934.hp2 HG01952.hp1 HG02132.hp2 others(5): Show |
intron_variant | MODIFIER | c.628-373G>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52136129 | ||||||
chr15:52136130
|
A | G | 7 | a0001c0002t0128g0273a0001c0002t0129g0275a0001c0002t0130g0274others(4): Show | 7 | HG01934.hp2 HG01952.hp1 HG02132.hp2 others(4): Show |
intron_variant | MODIFIER | c.628-374T>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52136130 | ||||||
chr15:52136131
|
C | A | 1 | a0001c0002t0137g0266 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.628-375G>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52136131 | ||||||
chr15:52136132
|
A | G | 1 | a0001c0002t0137g0266 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.628-376T>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52136132 | ||||||
chr15:52136133
|
C | G | 7 | a0001c0002t0128g0273a0001c0002t0129g0275a0001c0002t0130g0274others(4): Show | 7 | HG01934.hp2 HG01952.hp1 HG02132.hp2 others(4): Show |
intron_variant | MODIFIER | c.628-377G>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52136133 | ||||||
chr15:52136134
|
AC | A | 7 | a0001c0002t0128g0273a0001c0002t0129g0275a0001c0002t0130g0274others(4): Show | 7 | HG01934.hp2 HG01952.hp1 HG02132.hp2 others(4): Show |
intron_variant | MODIFIER | c.628-379delG | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52136134 | ||||||
chr15:52136135
|
C | A | 1 | a0001c0002t0137g0266 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.628-379G>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52136135 | ||||||
chr15:52136137
|
C | A | 1 | a0001c0002t0137g0266 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.628-381G>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52136137 | ||||||
chr15:52136169
|
CACA | C | 3 | a0001c0001t0015g0143a0001c0001t0066g0164a0001c0004t0017g0293 | 3 | HG01069.hp1 HG01192.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.628-416_628-414del others(3): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52136169 | ||||||
chr15:52136171
|
CA | C | 4 | a0001c0001t0072g0108a0001c0001t0088g0114a0001c0002t0025g0282others(1): Show | 4 | HG02135.hp1 HG02809.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.628-416delT | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52136171 | ||||||
chr15:52136172
|
A | AC | 7 | a0001c0001t0008g0140a0001c0001t0015g0146a0001c0001t0051g0120others(4): Show | 7 | HG01168.hp1 HG01169.hp1 NA18966.hp1 others(4): Show |
intron_variant | MODIFIER | c.628-417dupG | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52136172 | ||||||
chr15:52136172
|
A | ACAC | 11 | a0001c0001t0018g0151a0001c0001t0038g0115a0001c0001t0067g0109others(8): Show | 11 | HG00741.hp1 HG02109.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.628-417_628-416ins others(3): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52136172 | ||||||
chr15:52136172
|
A | ACACAC | 13 | a0001c0001t0007g0139a0001c0001t0008g0099a0001c0001t0023g0297others(10): Show | 13 | HG01261.hp2 HG01978.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.628-417_628-416ins others(5): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52136172 | ||||||
chr15:52136172
|
A | ACACACAC | 17 | a0001c0001t0007g0148a0001c0001t0007g0153a0001c0001t0007g0169others(14): Show | 17 | HG00609.hp1 HG00673.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.628-417_628-416ins others(7): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52136172 | ||||||
chr15:52136172
|
A | ACACACAC others(2): Show |
10 | a0001c0001t0008g0142a0001c0001t0040g0113a0001c0001t0041g0128others(7): Show | 10 | HG01256.hp2 HG01258.hp1 HG02056.hp2 others(7): Show |
intron_variant | MODIFIER | c.628-417_628-416ins others(9): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52136172 | ||||||
chr15:52136172
|
A | ACACACAC others(4): Show |
10 | a0001c0001t0007g0144a0001c0001t0008g0176a0001c0001t0018g0133others(7): Show | 10 | HG02015.hp2 HG02148.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.628-417_628-416ins others(11): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52136172 | ||||||
chr15:52136172
|
A | ACACACAC others(6): Show |
3 | a0001c0001t0053g0171a0001c0001t0075g0165a0001c0001t0082g0154 | 3 | HG00597.hp1 HG02027.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.628-417_628-416ins others(13): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52136172 | ||||||
chr15:52136172
|
A | ACACACAC others(8): Show |
4 | a0001c0001t0015g0145a0001c0001t0048g0123a0001c0001t0061g0096others(1): Show | 4 | HG01928.hp1 HG01943.hp1 HG02080.hp1 others(1): Show |
intron_variant | MODIFIER | c.628-417_628-416ins others(15): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52136172 | ||||||
chr15:52136172
|
A | ACACACAC others(10): Show |
2 | a0001c0001t0044g0156a0001c0001t0080g0147 | 2 | HG03209.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.628-417_628-416ins others(17): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52136172 | ||||||
chr15:52136172
|
A | ACACACAC others(12): Show |
2 | a0001c0001t0059g0125a0001c0002t0150g0264 | 2 | NA18969.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.628-417_628-416ins others(19): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52136172 | ||||||
chr15:52136172
|
A | ACACACAC others(24): Show |
1 | a0001c0001t0001g0248 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.628-417_628-416ins others(31): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52136172 | ||||||
chr15:52136172
|
A | ACACACAC others(13): Show |
1 | a0001c0002t0006g0316 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.628-417_628-416ins others(20): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52136172 | ||||||
chr15:52136172
|
A | ACACACAC others(7): Show |
2 | a0001c0001t0146g0292a0001c0003t0099g0095 | 2 | HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.628-417_628-416ins others(14): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52136172 | ||||||
chr15:52136172
|
A | ACACACAC others(5): Show |
3 | a0001c0001t0011g0304a0001c0001t0023g0296a0001c0003t0126g0313 | 3 | HG02055.hp1 HG02897.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.628-417_628-416ins others(12): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52136172 | ||||||
chr15:52136172
|
A | ACACACAC others(3): Show |
6 | a0001c0001t0011g0305a0001c0001t0011g0319a0001c0003t0021g0354others(3): Show | 6 | HG02630.hp1 HG02965.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.628-417_628-416ins others(10): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52136172 | ||||||
chr15:52136172
|
A | ACACACAC others(1): Show |
9 | a0001c0001t0002g0053a0001c0001t0011g0299a0001c0001t0022g0294others(6): Show | 9 | HG01175.hp1 HG02723.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.628-417_628-416ins others(8): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52136172 | ||||||
chr15:52136172
|
A | ACACC | 4 | a0001c0001t0011g0303a0001c0001t0033g0328a0001c0003t0122g0357others(1): Show | 4 | HG02273.hp1 HG02970.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.628-417_628-416ins others(4): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52136172 | ||||||
chr15:52136172
|
A | C | 23 | a0001c0001t0141g0301a0001c0001t0145g0279a0001c0001t0148g0302others(20): Show | 23 | HG01109.hp1 HG01884.hp1 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.628-416T>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52136172 | ||||||
chr15:52136176
|
T | C | 7 | a0001c0002t0024g0281a0001c0002t0024g0284a0001c0002t0025g0282others(4): Show | 7 | HG02109.hp2 HG02257.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.628-420A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52136176 | ||||||
chr15:52136219
|
A | G | 1 | a0001c0001t0005g0236 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.628-463T>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52136219 | ||||||
chr15:52136339
|
T | G | 1 | a0001c0001t0005g0236 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.628-583A>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52136339 | ||||||
chr15:52136379
|
T | C | 2 | a0002c0007t0039g0150a0002c0007t0081g0175 | 2 | HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.628-623A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52136379 | ||||||
chr15:52136442
|
A | G | 13 | a0001c0002t0128g0273a0001c0002t0129g0275a0001c0002t0130g0274others(10): Show | 13 | HG01934.hp2 HG01952.hp1 HG02004.hp1 others(10): Show |
intron_variant | MODIFIER | c.628-686T>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52136442 | ||||||
chr15:52136561
|
A | G | 1 | a0001c0001t0052g0121 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.628-805T>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52136561 | ||||||
chr15:52136672
|
G | A | 15 | a0001c0002t0024g0281a0001c0002t0024g0284a0001c0002t0025g0282others(12): Show | 15 | HG01891.hp2 HG02055.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.628-916C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52136672 | ||||||
chr15:52136836
|
C | T | 1 | a0001c0001t0192g0267 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.628-1080G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52136836 | ||||||
chr15:52136842
|
T | C | 1 | a0001c0001t0003g0015 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.628-1086A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52136842 | ||||||
chr15:52136866
|
C | T | 1 | a0001c0001t0151g0353 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.628-1110G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52136866 | ||||||
chr15:52136916
|
A | C | 2 | a0001c0001t0065g0079a0001c0001t0066g0164 | 2 | HG00323.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.628-1160T>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52136916 | ||||||
chr15:52136964
|
C | T | 1 | a0001c0001t0063g0132 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.628-1208G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52136964 | ||||||
chr15:52137020
|
G | A | 1 | a0001c0002t0140g0265 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.628-1264C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52137020 | ||||||
chr15:52137028
|
G | A | 13 | a0001c0002t0128g0273a0001c0002t0129g0275a0001c0002t0130g0274others(10): Show | 13 | HG01934.hp2 HG01952.hp1 HG02004.hp1 others(10): Show |
intron_variant | MODIFIER | c.628-1272C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52137028 | ||||||
chr15:52137066
|
C | A | 1 | a0001c0001t0113g0021 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.628-1310G>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52137066 | ||||||
chr15:52137086
|
T | C | 1 | a0001c0002t0136g0268 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.628-1330A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52137086 | ||||||
chr15:52137295
|
G | C | 2 | a0001c0001t0016g0332a0001c0001t0198g0351 | 2 | HG00438.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.628-1539C>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52137295 | ||||||
chr15:52137344
|
G | C | 12 | a0001c0002t0006g0291a0001c0002t0006g0314a0001c0002t0006g0316others(9): Show | 12 | HG01243.hp1 HG02055.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.628-1588C>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52137344 | ||||||
chr15:52137449
|
G | A | 6 | a0001c0002t0135g0270a0001c0002t0136g0268a0001c0002t0137g0266others(3): Show | 6 | HG02004.hp1 HG02148.hp2 NA18747.hp2 others(3): Show |
intron_variant | MODIFIER | c.628-1693C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52137449 | ||||||
chr15:52137576
|
C | T | 13 | a0001c0001t0001g0213a0001c0001t0001g0223a0001c0001t0001g0245others(10): Show | 13 | HG01069.hp2 HG01261.hp1 HG01358.hp1 others(10): Show |
intron_variant | MODIFIER | c.628-1820G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52137576 | ||||||
chr15:52137637
|
C | A | 2 | a0001c0003t0021g0354a0001c0003t0021g0355 | 2 | HG01891.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.628-1881G>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52137637 | ||||||
chr15:52137726
|
G | C | 76 | a0001c0001t0007g0139a0001c0001t0007g0144a0001c0001t0007g0148others(73): Show | 76 | HG00323.hp2 HG00544.hp2 HG00597.hp1 others(73): Show |
intron_variant | MODIFIER | c.628-1970C>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52137726 | ||||||
chr15:52137738
|
CG | C | 13 | a0001c0002t0128g0273a0001c0002t0129g0275a0001c0002t0130g0274others(10): Show | 13 | HG01934.hp2 HG01952.hp1 HG02004.hp1 others(10): Show |
intron_variant | MODIFIER | c.628-1983delC | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52137738 | ||||||
chr15:52137835
|
T | C | 24 | a0001c0002t0024g0281a0001c0002t0024g0284a0001c0002t0025g0282others(21): Show | 24 | HG01109.hp1 HG01496.hp1 HG01934.hp2 others(21): Show |
intron_variant | MODIFIER | c.628-2079A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52137835 | ||||||
chr15:52137889
|
T | C | 2 | a0001c0003t0098g0088a0001c0003t0101g0089 | 2 | HG01884.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.628-2133A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52137889 | ||||||
chr15:52137929
|
G | A | 4 | a0001c0001t0067g0109a0001c0001t0071g0107a0001c0001t0072g0108others(1): Show | 4 | HG03225.hp2 HG03471.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.628-2173C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52137929 | ||||||
chr15:52137981
|
G | A | 13 | a0001c0002t0128g0273a0001c0002t0129g0275a0001c0002t0130g0274others(10): Show | 13 | HG01934.hp2 HG01952.hp1 HG02004.hp1 others(10): Show |
intron_variant | MODIFIER | c.628-2225C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52137981 | ||||||
chr15:52137987
|
A | G | 1 | a0001c0001t0179g0198 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.628-2231T>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52137987 | ||||||
chr15:52138052
|
C | T | 2 | a0001c0001t0007g0169a0001c0002t0150g0264 | 2 | NA18969.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.628-2296G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52138052 | ||||||
chr15:52138212
|
A | T | 2 | a0001c0001t0007g0169a0001c0002t0150g0264 | 2 | NA18969.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.628-2456T>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52138212 | ||||||
chr15:52138263
|
G | A | 1 | a0001c0003t0112g0087 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.628-2507C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52138263 | ||||||
chr15:52138286
|
G | A | 1 | a0001c0005t0157g0278 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.628-2530C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52138286 | ||||||
chr15:52138314
|
C | T | 1 | a0001c0002t0206g0178 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.628-2558G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52138314 | ||||||
chr15:52138382
|
C | CA | 20 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0195others(17): Show | 20 | HG01106.hp1 HG01255.hp1 HG01255.hp2 others(17): Show |
intron_variant | MODIFIER | c.628-2627dupT | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52138382 | ||||||
chr15:52138382
|
CA | C | 11 | a0001c0001t0003g0016a0001c0001t0011g0299a0001c0001t0011g0303others(8): Show | 11 | HG02895.hp1 HG02897.hp1 HG02897.hp2 others(8): Show |
intron_variant | MODIFIER | c.628-2627delT | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52138382 | ||||||
chr15:52138386
|
A | C | 8 | a0001c0003t0021g0354a0001c0003t0021g0355a0001c0003t0122g0357others(5): Show | 8 | HG01891.hp2 HG02055.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.628-2630T>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52138386 | ||||||
chr15:52138390
|
A | C | 8 | a0001c0003t0021g0354a0001c0003t0021g0355a0001c0003t0122g0357others(5): Show | 8 | HG01891.hp2 HG02055.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.628-2634T>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52138390 | ||||||
chr15:52138401
|
A | AT | 25 | a0001c0001t0007g0148a0001c0001t0031g0334a0001c0001t0054g0131others(22): Show | 25 | HG00609.hp1 HG01192.hp2 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.628-2646_628-2645i others(3): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52138401 | ||||||
chr15:52138401
|
A | T | 174 | a0001c0001t0007g0139a0001c0001t0007g0144a0001c0001t0007g0153others(171): Show | 176 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(173): Show |
intron_variant | MODIFIER | c.628-2645T>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52138401 | ||||||
chr15:52138428
|
G | A | 2 | a0001c0002t0206g0178a0001c0002t0207g0177 | 2 | HG01496.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.628-2672C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52138428 | ||||||
chr15:52138491
|
A | T | 1 | a0001c0001t0005g0207 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.627+2649T>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52138491 | ||||||
chr15:52138939
|
G | A | 53 | a0001c0001t0016g0332a0001c0001t0016g0343a0001c0001t0016g0344others(50): Show | 53 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.627+2201C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52138939 | ||||||
chr15:52138953
|
C | T | 2 | a0001c0005t0156g0261a0001c0005t0157g0278 | 2 | HG01109.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.627+2187G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52138953 | ||||||
chr15:52139010
|
CAT | C | 13 | a0001c0002t0128g0273a0001c0002t0129g0275a0001c0002t0130g0274others(10): Show | 13 | HG01934.hp2 HG01952.hp1 HG02004.hp1 others(10): Show |
intron_variant | MODIFIER | c.627+2128_627+2129d others(4): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52139010 | ||||||
chr15:52139244
|
T | C | 12 | a0001c0002t0006g0291a0001c0002t0006g0314a0001c0002t0006g0316others(9): Show | 12 | HG01243.hp1 HG02055.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.627+1896A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52139244 | ||||||
chr15:52139310
|
C | T | 2 | a0001c0003t0021g0354a0001c0003t0021g0355 | 2 | HG01891.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.627+1830G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52139310 | ||||||
chr15:52139328
|
C | T | 12 | a0001c0002t0006g0291a0001c0002t0006g0314a0001c0002t0006g0316others(9): Show | 12 | HG01243.hp1 HG02055.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.627+1812G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52139328 | ||||||
chr15:52139447
|
C | A | 19 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0008others(16): Show | 19 | HG00099.hp1 HG00639.hp2 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.627+1693G>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52139447 | ||||||
chr15:52139458
|
A | AAAAC | 7 | a0001c0002t0024g0281a0001c0002t0024g0284a0001c0002t0025g0282others(4): Show | 7 | HG02109.hp2 HG02257.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.627+1678_627+1681d others(6): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52139458 | ||||||
chr15:52139577
|
T | C | 1 | a0001c0005t0100g0134 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.627+1563A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52139577 | ||||||
chr15:52139665
|
C | A | 1 | a0001c0005t0157g0278 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.627+1475G>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52139665 | ||||||
chr15:52139690
|
C | T | 1 | a0001c0003t0126g0313 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.627+1450G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52139690 | ||||||
chr15:52139775
|
G | A | 13 | a0001c0002t0128g0273a0001c0002t0129g0275a0001c0002t0130g0274others(10): Show | 13 | HG01934.hp2 HG01952.hp1 HG02004.hp1 others(10): Show |
intron_variant | MODIFIER | c.627+1365C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52139775 | ||||||
chr15:52139988
|
A | G | 14 | a0001c0002t0128g0273a0001c0002t0129g0275a0001c0002t0130g0274others(11): Show | 14 | HG01934.hp2 HG01952.hp1 HG02004.hp1 others(11): Show |
intron_variant | MODIFIER | c.627+1152T>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52139988 | ||||||
chr15:52140007
|
T | C | 14 | a0001c0002t0128g0273a0001c0002t0129g0275a0001c0002t0130g0274others(11): Show | 14 | HG01934.hp2 HG01952.hp1 HG02004.hp1 others(11): Show |
intron_variant | MODIFIER | c.627+1133A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52140007 | ||||||
chr15:52140073
|
G | A | 14 | a0001c0002t0128g0273a0001c0002t0129g0275a0001c0002t0130g0274others(11): Show | 14 | HG01934.hp2 HG01952.hp1 HG02004.hp1 others(11): Show |
intron_variant | MODIFIER | c.627+1067C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52140073 | ||||||
chr15:52140131
|
T | C | 14 | a0001c0002t0128g0273a0001c0002t0129g0275a0001c0002t0130g0274others(11): Show | 14 | HG01934.hp2 HG01952.hp1 HG02004.hp1 others(11): Show |
intron_variant | MODIFIER | c.627+1009A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52140131 | ||||||
chr15:52140255
|
A | G | 8 | a0001c0001t0022g0294a0001c0001t0022g0295a0001c0001t0023g0296others(5): Show | 8 | HG01891.hp1 HG02559.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.627+885T>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52140255 | ||||||
chr15:52140402
|
G | A | 1 | a0001c0001t0003g0013 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.627+738C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52140402 | ||||||
chr15:52140412
|
C | T | 8 | a0001c0001t0011g0299a0001c0001t0011g0303a0001c0001t0011g0304others(5): Show | 8 | HG02895.hp1 HG02897.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.627+728G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52140412 | ||||||
chr15:52140622
|
C | T | 16 | a0001c0002t0128g0273a0001c0002t0129g0275a0001c0002t0130g0274others(13): Show | 16 | HG01109.hp1 HG01934.hp2 HG01952.hp1 others(13): Show |
intron_variant | MODIFIER | c.627+518G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52140622 | ||||||
chr15:52140866
|
C | T | 8 | a0001c0001t0032g0333a0001c0001t0032g0350a0001c0001t0033g0328others(5): Show | 8 | HG01257.hp1 HG01943.hp2 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.627+274G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52140866 | ||||||
chr15:52140933
|
CTCAACAC others(2): Show |
C | 12 | a0001c0002t0006g0291a0001c0002t0006g0314a0001c0002t0006g0316others(9): Show | 12 | HG01243.hp1 HG02055.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.627+198_627+206del others(9): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52140933 | ||||||
chr15:52140937
|
A | T | 2 | a0001c0001t0145g0279a0001c0001t0146g0292 | 2 | HG01891.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.627+203T>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52140937 | ||||||
chr15:52141018
|
T | A | 1 | a0003c0009t0172g0217 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.627+122A>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52141018 | ||||||
chr15:52141052
|
C | T | 8 | a0001c0001t0002g0003a0001c0001t0002g0011a0001c0001t0002g0039others(5): Show | 8 | HG00639.hp2 HG00733.hp1 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.627+88G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 7/12 | chr15 | 52141052 | ||||||
chr15:52141329
|
T | C | 2 | a0001c0001t0145g0279a0001c0001t0146g0292 | 2 | HG01891.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.495-57A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 6/12 | chr15 | 52141329 | ||||||
chr15:52141403
|
T | C | 2 | a0001c0001t0046g0110a0001c0001t0068g0111 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.495-131A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 6/12 | chr15 | 52141403 | ||||||
chr15:52141502
|
G | A | 8 | a0001c0001t0022g0294a0001c0001t0022g0295a0001c0001t0023g0296others(5): Show | 8 | HG01891.hp1 HG02559.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.495-230C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 6/12 | chr15 | 52141502 | ||||||
chr15:52141611
|
G | GA | 8 | a0001c0003t0021g0354a0001c0003t0021g0355a0001c0003t0122g0357others(5): Show | 8 | HG01891.hp2 HG02055.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.495-340dupT | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 6/12 | chr15 | 52141611 | ||||||
chr15:52141789
|
C | T | 2 | a0001c0001t0022g0294a0001c0001t0022g0295 | 2 | HG03139.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.495-517G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 6/12 | chr15 | 52141789 | ||||||
chr15:52141907
|
C | A | 68 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0008others(65): Show | 68 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(65): Show |
intron_variant | MODIFIER | c.495-635G>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 6/12 | chr15 | 52141907 | ||||||
chr15:52141908
|
C | G | 68 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0008others(65): Show | 68 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(65): Show |
intron_variant | MODIFIER | c.495-636G>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 6/12 | chr15 | 52141908 | ||||||
chr15:52141915
|
C | T | 3 | a0001c0001t0141g0301a0001c0001t0148g0302a0001c0001t0149g0300 | 3 | HG02258.hp1 HG02615.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.495-643G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 6/12 | chr15 | 52141915 | ||||||
chr15:52141930
|
T | C | 1 | a0001c0001t0148g0302 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.495-658A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 6/12 | chr15 | 52141930 | ||||||
chr15:52142087
|
C | G | 70 | a0001c0001t0016g0332a0001c0001t0016g0343a0001c0001t0016g0344others(67): Show | 70 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.495-815G>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 6/12 | chr15 | 52142087 | ||||||
chr15:52142141
|
C | G | 70 | a0001c0001t0016g0332a0001c0001t0016g0343a0001c0001t0016g0344others(67): Show | 70 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.495-869G>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 6/12 | chr15 | 52142141 | ||||||
chr15:52142175
|
G | C | 1 | a0003c0009t0172g0217 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.495-903C>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 6/12 | chr15 | 52142175 | ||||||
chr15:52142228
|
G | A | 1 | a0001c0003t0097g0091 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.495-956C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 6/12 | chr15 | 52142228 | ||||||
chr15:52142395
|
G | A | 14 | a0001c0002t0128g0273a0001c0002t0129g0275a0001c0002t0130g0274others(11): Show | 14 | HG01934.hp2 HG01952.hp1 HG02004.hp1 others(11): Show |
intron_variant | MODIFIER | c.495-1123C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 6/12 | chr15 | 52142395 | ||||||
chr15:52142427
|
A | G | 176 | a0001c0001t0001g0248a0001c0001t0007g0139a0001c0001t0007g0144others(173): Show | 178 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(175): Show |
intron_variant | MODIFIER | c.495-1155T>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 6/12 | chr15 | 52142427 | ||||||
chr15:52142561
|
GT | G | 71 | a0001c0001t0002g0011a0001c0001t0003g0013a0001c0001t0003g0016others(68): Show | 71 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.495-1290delA | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 6/12 | chr15 | 52142561 | ||||||
chr15:52142563
|
T | G | 83 | a0001c0001t0001g0248a0001c0001t0007g0139a0001c0001t0007g0144others(80): Show | 85 | HG00323.hp2 HG00544.hp2 HG00597.hp1 others(82): Show |
intron_variant | MODIFIER | c.495-1291A>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 6/12 | chr15 | 52142563 | ||||||
chr15:52142564
|
T | G | 9 | a0001c0002t0024g0281a0001c0002t0024g0284a0001c0002t0025g0282others(6): Show | 9 | HG01109.hp1 HG02109.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.495-1292A>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 6/12 | chr15 | 52142564 | ||||||
chr15:52142572
|
T | A | 77 | a0001c0001t0001g0248a0001c0001t0007g0139a0001c0001t0007g0144others(74): Show | 77 | HG00323.hp2 HG00544.hp2 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.495-1300A>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 6/12 | chr15 | 52142572 | ||||||
chr15:52142800
|
C | A | 1 | a0001c0001t0001g0240 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.495-1528G>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 6/12 | chr15 | 52142800 | ||||||
chr15:52142883
|
G | A | 1 | a0001c0005t0100g0134 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.495-1611C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 6/12 | chr15 | 52142883 | ||||||
chr15:52142913
|
G | C | 3 | a0001c0001t0141g0301a0001c0001t0148g0302a0001c0001t0149g0300 | 3 | HG02258.hp1 HG02615.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.495-1641C>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 6/12 | chr15 | 52142913 | ||||||
chr15:52143117
|
C | T | 3 | a0001c0002t0006g0314a0001c0002t0006g0321a0001c0002t0201g0315 | 3 | HG02055.hp2 HG02486.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.495-1845G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 6/12 | chr15 | 52143117 | ||||||
chr15:52143118
|
G | A | 6 | a0001c0002t0135g0270a0001c0002t0136g0268a0001c0002t0137g0266others(3): Show | 6 | HG02004.hp1 HG02148.hp2 NA18747.hp2 others(3): Show |
intron_variant | MODIFIER | c.495-1846C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 6/12 | chr15 | 52143118 | ||||||
chr15:52143166
|
G | GA | 61 | a0001c0001t0002g0026a0001c0001t0002g0068a0001c0001t0002g0070others(58): Show | 61 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.495-1895dupT | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 6/12 | chr15 | 52143166 | ||||||
chr15:52143166
|
GA | G | 16 | a0001c0001t0003g0078a0001c0002t0128g0273a0001c0002t0129g0275others(13): Show | 16 | HG01934.hp2 HG01952.hp1 HG02004.hp1 others(13): Show |
intron_variant | MODIFIER | c.495-1895delT | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 6/12 | chr15 | 52143166 | ||||||
chr15:52143176
|
A | C | 1 | a0001c0001t0066g0164 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.495-1904T>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 6/12 | chr15 | 52143176 | ||||||
chr15:52143182
|
A | G | 5 | a0001c0002t0024g0281a0001c0002t0024g0284a0001c0002t0026g0286others(2): Show | 5 | HG02257.hp1 HG02630.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.495-1910T>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 6/12 | chr15 | 52143182 | ||||||
chr15:52143218
|
AG | A | 14 | a0001c0002t0128g0273a0001c0002t0129g0275a0001c0002t0130g0274others(11): Show | 14 | HG01934.hp2 HG01952.hp1 HG02004.hp1 others(11): Show |
intron_variant | MODIFIER | c.495-1947delC | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 6/12 | chr15 | 52143218 | ||||||
chr15:52143395
|
C | G | 6 | a0001c0002t0135g0270a0001c0002t0136g0268a0001c0002t0137g0266others(3): Show | 6 | HG02004.hp1 HG02148.hp2 NA18747.hp2 others(3): Show |
intron_variant | MODIFIER | c.495-2123G>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 6/12 | chr15 | 52143395 | ||||||
chr15:52143457
|
C | T | 2 | a0001c0005t0156g0261a0001c0005t0157g0278 | 2 | HG01109.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.495-2185G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 6/12 | chr15 | 52143457 | ||||||
chr15:52143499
|
T | C | 52 | a0001c0001t0016g0332a0001c0001t0016g0343a0001c0001t0016g0344others(49): Show | 52 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.495-2227A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 6/12 | chr15 | 52143499 | ||||||
chr15:52143504
|
G | C | 87 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0001g0187others(84): Show | 87 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.495-2232C>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 6/12 | chr15 | 52143504 | ||||||
chr15:52143623
|
G | T | 1 | a0001c0001t0071g0107 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.495-2351C>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 6/12 | chr15 | 52143623 | ||||||
chr15:52143706
|
A | C | 14 | a0001c0002t0128g0273a0001c0002t0129g0275a0001c0002t0130g0274others(11): Show | 14 | HG01934.hp2 HG01952.hp1 HG02004.hp1 others(11): Show |
intron_variant | MODIFIER | c.495-2434T>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 6/12 | chr15 | 52143706 | ||||||
chr15:52143729
|
T | C | 2 | a0001c0004t0014g0280a0001c0004t0014g0290 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.495-2457A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 6/12 | chr15 | 52143729 | ||||||
chr15:52143907
|
C | A | 4 | a0001c0001t0079g0138a0001c0001t0082g0154a0001c0001t0084g0117others(1): Show | 4 | HG00609.hp1 HG02027.hp2 NA19063.hp1 others(1): Show |
intron_variant | MODIFIER | c.495-2635G>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 6/12 | chr15 | 52143907 | ||||||
chr15:52143925
|
C | T | 2 | a0001c0005t0156g0261a0001c0005t0157g0278 | 2 | HG01109.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.495-2653G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 6/12 | chr15 | 52143925 | ||||||
chr15:52143968
|
A | C | 14 | a0001c0002t0128g0273a0001c0002t0129g0275a0001c0002t0130g0274others(11): Show | 14 | HG01934.hp2 HG01952.hp1 HG02004.hp1 others(11): Show |
intron_variant | MODIFIER | c.495-2696T>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 6/12 | chr15 | 52143968 | ||||||
chr15:52144110
|
C | T | 4 | a0001c0003t0021g0354a0001c0003t0021g0355a0001c0003t0126g0313others(1): Show | 4 | HG01891.hp2 HG02055.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.495-2838G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 6/12 | chr15 | 52144110 | ||||||
chr15:52144137
|
C | T | 100 | a0001c0001t0016g0332a0001c0001t0016g0343a0001c0001t0016g0344others(97): Show | 102 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.495-2865G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 6/12 | chr15 | 52144137 | ||||||
chr15:52144138
|
G | A | 1 | a0001c0001t0075g0165 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.495-2866C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 6/12 | chr15 | 52144138 | ||||||
chr15:52144166
|
C | T | 1 | a0001c0005t0100g0134 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.495-2894G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 6/12 | chr15 | 52144166 | ||||||
chr15:52144167
|
G | A | 14 | a0001c0002t0128g0273a0001c0002t0129g0275a0001c0002t0130g0274others(11): Show | 14 | HG01934.hp2 HG01952.hp1 HG02004.hp1 others(11): Show |
intron_variant | MODIFIER | c.495-2895C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 6/12 | chr15 | 52144167 | ||||||
chr15:52144171
|
C | T | 4 | a0001c0001t0002g0034a0001c0001t0002g0037a0001c0001t0002g0044others(1): Show | 4 | HG01169.hp2 HG01884.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.495-2899G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 6/12 | chr15 | 52144171 | ||||||
chr15:52144182
|
T | C | 2 | a0002c0007t0039g0150a0002c0007t0081g0175 | 2 | HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.495-2910A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 6/12 | chr15 | 52144182 | ||||||
chr15:52144194
|
C | T | 353 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0001g0187others(350): Show | 355 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(352): Show |
intron_variant | MODIFIER | c.495-2922G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 6/12 | chr15 | 52144194 | ||||||
chr15:52144367
|
T | C | 268 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0001g0187others(265): Show | 270 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(267): Show |
intron_variant | MODIFIER | c.494+3092A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 6/12 | chr15 | 52144367 | ||||||
chr15:52144393
|
G | A | 12 | a0001c0002t0006g0291a0001c0002t0006g0314a0001c0002t0006g0316others(9): Show | 12 | HG01243.hp1 HG02055.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.494+3066C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 6/12 | chr15 | 52144393 | ||||||
chr15:52144418
|
G | A | 8 | a0001c0002t0019g0092a0001c0002t0019g0093a0001c0003t0097g0091others(5): Show | 8 | HG01884.hp1 HG02622.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.494+3041C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 6/12 | chr15 | 52144418 | ||||||
chr15:52144423
|
A | G | 14 | a0001c0002t0128g0273a0001c0002t0129g0275a0001c0002t0130g0274others(11): Show | 14 | HG01934.hp2 HG01952.hp1 HG02004.hp1 others(11): Show |
intron_variant | MODIFIER | c.494+3036T>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 6/12 | chr15 | 52144423 | ||||||
chr15:52144486
|
T | A | 1 | a0001c0002t0137g0266 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.494+2973A>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 6/12 | chr15 | 52144486 | ||||||
chr15:52144729
|
G | A | 1 | a0001c0001t0107g0056 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.494+2730C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 6/12 | chr15 | 52144729 | ||||||
chr15:52144831
|
A | G | 1 | a0001c0001t0159g0260 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.494+2628T>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 6/12 | chr15 | 52144831 | ||||||
chr15:52144837
|
C | G | 1 | a0001c0001t0145g0279 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.494+2622G>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 6/12 | chr15 | 52144837 | ||||||
chr15:52144837
|
C | T | 6 | a0001c0001t0003g0005a0001c0001t0003g0014a0001c0001t0003g0015others(3): Show | 6 | HG00408.hp1 NA18940.hp2 NA18960.hp1 others(3): Show |
intron_variant | MODIFIER | c.494+2622G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 6/12 | chr15 | 52144837 | ||||||
chr15:52144856
|
C | T | 1 | a0001c0001t0160g0212 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.494+2603G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 6/12 | chr15 | 52144856 | ||||||
chr15:52144860
|
G | A | 14 | a0001c0002t0128g0273a0001c0002t0129g0275a0001c0002t0130g0274others(11): Show | 14 | HG01934.hp2 HG01952.hp1 HG02004.hp1 others(11): Show |
intron_variant | MODIFIER | c.494+2599C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 6/12 | chr15 | 52144860 | ||||||
chr15:52144910
|
C | T | 1 | a0001c0001t0060g0122 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.494+2549G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 6/12 | chr15 | 52144910 | ||||||
chr15:52144936
|
C | T | 1 | a0001c0001t0016g0332 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.494+2523G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 6/12 | chr15 | 52144936 | ||||||
chr15:52144940
|
C | T | 8 | a0001c0001t0022g0294a0001c0001t0022g0295a0001c0001t0023g0296others(5): Show | 8 | HG01891.hp1 HG02559.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.494+2519G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 6/12 | chr15 | 52144940 | ||||||
chr15:52144945
|
G | A | 5 | a0001c0001t0002g0081a0001c0001t0002g0082a0001c0001t0002g0084others(2): Show | 5 | HG01255.hp1 HG01358.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.494+2514C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 6/12 | chr15 | 52144945 | ||||||
chr15:52144982
|
T | C | 8 | a0001c0001t0022g0294a0001c0001t0022g0295a0001c0001t0023g0296others(5): Show | 8 | HG01891.hp1 HG02559.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.494+2477A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 6/12 | chr15 | 52144982 | ||||||
chr15:52145081
|
A | G | 52 | a0001c0001t0016g0332a0001c0001t0016g0343a0001c0001t0016g0344others(49): Show | 52 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.494+2378T>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 6/12 | chr15 | 52145081 | ||||||
chr15:52145476
|
C | CA | 14 | a0001c0002t0128g0273a0001c0002t0129g0275a0001c0002t0130g0274others(11): Show | 14 | HG01934.hp2 HG01952.hp1 HG02004.hp1 others(11): Show |
intron_variant | MODIFIER | c.494+1982dupT | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 6/12 | chr15 | 52145476 | ||||||
chr15:52145476
|
CA | C | 51 | a0001c0001t0016g0332a0001c0001t0016g0343a0001c0001t0016g0344others(48): Show | 51 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.494+1982delT | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 6/12 | chr15 | 52145476 | ||||||
chr15:52145518
|
G | A | 1 | a0001c0001t0104g0058 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.494+1941C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 6/12 | chr15 | 52145518 | ||||||
chr15:52145680
|
A | G | 1 | a0001c0001t0092g0137 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.494+1779T>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 6/12 | chr15 | 52145680 | ||||||
chr15:52145727
|
G | C | 6 | a0001c0002t0135g0270a0001c0002t0136g0268a0001c0002t0137g0266others(3): Show | 6 | HG02004.hp1 HG02148.hp2 NA18747.hp2 others(3): Show |
intron_variant | MODIFIER | c.494+1732C>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 6/12 | chr15 | 52145727 | ||||||
chr15:52145872
|
A | G | 14 | a0001c0002t0128g0273a0001c0002t0129g0275a0001c0002t0130g0274others(11): Show | 14 | HG01934.hp2 HG01952.hp1 HG02004.hp1 others(11): Show |
intron_variant | MODIFIER | c.494+1587T>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 6/12 | chr15 | 52145872 | ||||||
chr15:52145929
|
T | A | 4 | a0001c0002t0019g0092a0001c0002t0019g0093a0001c0003t0098g0088others(1): Show | 4 | HG01884.hp1 HG02622.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.494+1530A>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 6/12 | chr15 | 52145929 | ||||||
chr15:52145953
|
C | CT | 34 | a0001c0001t0002g0030a0001c0001t0004g0028a0001c0001t0004g0029others(31): Show | 34 | HG01109.hp1 HG01192.hp2 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.494+1505dupA | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 6/12 | chr15 | 52145953 | ||||||
chr15:52145953
|
CT | C | 75 | a0001c0001t0001g0186a0001c0001t0001g0189a0001c0001t0001g0191others(72): Show | 75 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.494+1505delA | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 6/12 | chr15 | 52145953 | ||||||
chr15:52145953
|
CTT | C | 10 | a0001c0001t0003g0016a0001c0001t0005g0207a0001c0001t0005g0230others(7): Show | 10 | HG00544.hp1 HG00558.hp2 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.494+1504_494+1505d others(4): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 6/12 | chr15 | 52145953 | ||||||
chr15:52145987
|
C | T | 8 | a0001c0002t0019g0092a0001c0002t0019g0093a0001c0003t0097g0091others(5): Show | 8 | HG01884.hp1 HG02622.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.494+1472G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 6/12 | chr15 | 52145987 | ||||||
chr15:52146042
|
C | T | 14 | a0001c0002t0128g0273a0001c0002t0129g0275a0001c0002t0130g0274others(11): Show | 14 | HG01934.hp2 HG01952.hp1 HG02004.hp1 others(11): Show |
intron_variant | MODIFIER | c.494+1417G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 6/12 | chr15 | 52146042 | ||||||
chr15:52146045
|
C | T | 8 | a0001c0003t0021g0354a0001c0003t0021g0355a0001c0003t0122g0357others(5): Show | 8 | HG01891.hp2 HG02055.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.494+1414G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 6/12 | chr15 | 52146045 | ||||||
chr15:52146140
|
G | T | 1 | a0001c0005t0156g0261 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.494+1319C>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 6/12 | chr15 | 52146140 | ||||||
chr15:52146292
|
A | T | 1 | a0001c0003t0126g0313 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.494+1167T>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 6/12 | chr15 | 52146292 | ||||||
chr15:52146503
|
C | T | 2 | a0001c0005t0156g0261a0001c0005t0157g0278 | 2 | HG01109.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.494+956G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 6/12 | chr15 | 52146503 | ||||||
chr15:52146674
|
C | G | 14 | a0001c0002t0128g0273a0001c0002t0129g0275a0001c0002t0130g0274others(11): Show | 14 | HG01934.hp2 HG01952.hp1 HG02004.hp1 others(11): Show |
intron_variant | MODIFIER | c.494+785G>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 6/12 | chr15 | 52146674 | ||||||
chr15:52146736
|
AT | A | 181 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0001g0189others(178): Show | 183 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(180): Show |
intron_variant | MODIFIER | c.494+722delA | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 6/12 | chr15 | 52146736 | ||||||
chr15:52146736
|
ATT | A | 63 | a0001c0001t0001g0211a0001c0001t0016g0332a0001c0001t0016g0343others(60): Show | 63 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(60): Show |
intron_variant | MODIFIER | c.494+721_494+722del others(2): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 6/12 | chr15 | 52146736 | ||||||
chr15:52146781
|
T | C | 70 | a0001c0001t0016g0332a0001c0001t0016g0343a0001c0001t0016g0344others(67): Show | 70 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.494+678A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 6/12 | chr15 | 52146781 | ||||||
chr15:52146868
|
T | C | 77 | a0001c0001t0016g0332a0001c0001t0016g0343a0001c0001t0016g0344others(74): Show | 77 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.494+591A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 6/12 | chr15 | 52146868 | ||||||
chr15:52146883
|
C | T | 112 | a0001c0001t0016g0332a0001c0001t0016g0343a0001c0001t0016g0344others(109): Show | 114 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.494+576G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 6/12 | chr15 | 52146883 | ||||||
chr15:52146899
|
T | A | 52 | a0001c0001t0016g0332a0001c0001t0016g0343a0001c0001t0016g0344others(49): Show | 52 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.494+560A>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 6/12 | chr15 | 52146899 | ||||||
chr15:52147069
|
T | C | 5 | a0001c0002t0006g0314a0001c0002t0006g0321a0001c0002t0035g0322others(2): Show | 5 | HG01243.hp1 HG02055.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.494+390A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 6/12 | chr15 | 52147069 | ||||||
chr15:52147166
|
G | GT | 15 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0008g0176others(12): Show | 15 | HG01243.hp1 HG02055.hp2 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.494+292dupA | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 6/12 | chr15 | 52147166 | ||||||
chr15:52147166
|
GT | G | 11 | a0001c0001t0001g0216a0001c0001t0028g0258a0001c0001t0055g0126others(8): Show | 11 | HG01109.hp1 HG01884.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.494+292delA | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 6/12 | chr15 | 52147166 | ||||||
chr15:52147170
|
T | TG | 7 | a0001c0004t0014g0002a0001c0004t0014g0280a0001c0004t0014g0290others(4): Show | 9 | HG00738.hp2 HG00741.hp1 HG01069.hp1 others(6): Show |
intron_variant | MODIFIER | c.494+288_494+289ins others(1): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 6/12 | chr15 | 52147170 | ||||||
chr15:52147171
|
T | G | 87 | a0001c0001t0016g0332a0001c0001t0016g0343a0001c0001t0016g0344others(84): Show | 87 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.494+288A>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 6/12 | chr15 | 52147171 | ||||||
chr15:52147172
|
T | G | 6 | a0001c0002t0019g0092a0001c0002t0019g0093a0001c0003t0098g0088others(3): Show | 6 | HG01109.hp1 HG01884.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.494+287A>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 6/12 | chr15 | 52147172 | ||||||
chr15:52147176
|
T | G | 1 | a0001c0001t0001g0189 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.494+283A>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 6/12 | chr15 | 52147176 | ||||||
chr15:52147251
|
C | T | 2 | a0001c0005t0156g0261a0001c0005t0157g0278 | 2 | HG01109.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.494+208G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 6/12 | chr15 | 52147251 | ||||||
chr15:52147364
|
C | T | 3 | a0001c0001t0076g0168a0001c0001t0077g0159a0001c0001t0151g0353 | 3 | HG02451.hp1 HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.494+95G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 6/12 | chr15 | 52147364 | ||||||
chr15:52147552
|
A | G | 1 | a0001c0003t0112g0087 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.418-17T>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 5/12 | chr15 | 52147552 | ||||||
chr15:52147577
|
A | T | 6 | a0001c0001t0018g0151a0001c0001t0047g0127a0001c0001t0049g0101others(3): Show | 6 | HG00673.hp2 HG01978.hp2 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.418-42T>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 5/12 | chr15 | 52147577 | ||||||
chr15:52147582
|
C | CT | 11 | a0001c0001t0003g0005a0001c0001t0003g0015a0001c0001t0003g0016others(8): Show | 11 | HG00673.hp2 HG01978.hp2 NA18940.hp2 others(8): Show |
intron_variant | MODIFIER | c.418-48dupA | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 5/12 | chr15 | 52147582 | ||||||
chr15:52147679
|
G | A | 1 | a0001c0001t0141g0301 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.418-144C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 5/12 | chr15 | 52147679 | ||||||
chr15:52147699
|
A | G | 1 | a0001c0001t0020g0080 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.418-164T>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 5/12 | chr15 | 52147699 | ||||||
chr15:52147738
|
A | G | 1 | a0001c0001t0002g0040 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.418-203T>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 5/12 | chr15 | 52147738 | ||||||
chr15:52147743
|
A | C | 75 | a0001c0001t0016g0332a0001c0001t0016g0343a0001c0001t0016g0344others(72): Show | 75 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.418-208T>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 5/12 | chr15 | 52147743 | ||||||
chr15:52147802
|
C | T | 3 | a0001c0001t0071g0107a0001c0005t0156g0261a0001c0005t0157g0278 | 3 | HG01109.hp1 HG03130.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.418-267G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 5/12 | chr15 | 52147802 | ||||||
chr15:52147978
|
T | C | 1 | a0001c0001t0067g0109 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.418-443A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 5/12 | chr15 | 52147978 | ||||||
chr15:52148060
|
C | CA | 15 | a0001c0001t0001g0187a0001c0002t0128g0273a0001c0002t0129g0275others(12): Show | 15 | HG01934.hp2 HG01952.hp1 HG02004.hp1 others(12): Show |
intron_variant | MODIFIER | c.418-526dupT | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 5/12 | chr15 | 52148060 | ||||||
chr15:52148060
|
C | CAA | 42 | a0001c0001t0016g0332a0001c0001t0016g0343a0001c0001t0031g0334others(39): Show | 42 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.418-527_418-526dup others(2): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 5/12 | chr15 | 52148060 | ||||||
chr15:52148060
|
C | CAAA | 12 | a0001c0001t0016g0344a0001c0001t0032g0333a0001c0001t0032g0350others(9): Show | 12 | HG00099.hp2 HG01257.hp1 HG01496.hp1 others(9): Show |
intron_variant | MODIFIER | c.418-528_418-526dup others(3): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 5/12 | chr15 | 52148060 | ||||||
chr15:52148060
|
CA | C | 6 | a0001c0002t0024g0281a0001c0002t0024g0284a0001c0002t0025g0282others(3): Show | 6 | HG02109.hp2 HG02257.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.418-526delT | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 5/12 | chr15 | 52148060 | ||||||
chr15:52148276
|
A | AGCCT | 8 | a0001c0003t0021g0354a0001c0003t0021g0355a0001c0003t0122g0357others(5): Show | 8 | HG01891.hp2 HG02055.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.418-745_418-742dup others(4): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 5/12 | chr15 | 52148276 | ||||||
chr15:52148361
|
A | G | 5 | a0001c0001t0002g0081a0001c0001t0002g0082a0001c0001t0002g0084others(2): Show | 5 | HG01255.hp1 HG01358.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.418-826T>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 5/12 | chr15 | 52148361 | ||||||
chr15:52148474
|
T | C | 15 | a0001c0001t0192g0267a0001c0002t0128g0273a0001c0002t0129g0275others(12): Show | 15 | HG01934.hp2 HG01943.hp2 HG01952.hp1 others(12): Show |
intron_variant | MODIFIER | c.418-939A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 5/12 | chr15 | 52148474 | ||||||
chr15:52148533
|
G | A | 8 | a0001c0001t0022g0294a0001c0001t0022g0295a0001c0001t0023g0296others(5): Show | 8 | HG01891.hp1 HG02559.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.418-998C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 5/12 | chr15 | 52148533 | ||||||
chr15:52148544
|
C | A | 6 | a0001c0001t0022g0294a0001c0001t0022g0295a0001c0001t0023g0296others(3): Show | 6 | HG02559.hp1 HG02723.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.418-1009G>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 5/12 | chr15 | 52148544 | ||||||
chr15:52148676
|
G | A | 1 | a0001c0001t0003g0013 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.418-1141C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 5/12 | chr15 | 52148676 | ||||||
chr15:52148841
|
A | G | 1 | a0001c0001t0169g0352 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.417+1043T>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 5/12 | chr15 | 52148841 | ||||||
chr15:52148891
|
C | T | 7 | a0001c0002t0024g0281a0001c0002t0024g0284a0001c0002t0025g0282others(4): Show | 7 | HG02109.hp2 HG02257.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.417+993G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 5/12 | chr15 | 52148891 | ||||||
chr15:52148974
|
C | A | 2 | a0002c0007t0039g0150a0002c0007t0081g0175 | 2 | HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.417+910G>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 5/12 | chr15 | 52148974 | ||||||
chr15:52149028
|
G | A | 1 | a0001c0002t0202g0318 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.417+856C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 5/12 | chr15 | 52149028 | ||||||
chr15:52149114
|
T | C | 176 | a0001c0001t0001g0248a0001c0001t0007g0139a0001c0001t0007g0144others(173): Show | 178 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(175): Show |
intron_variant | MODIFIER | c.417+770A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 5/12 | chr15 | 52149114 | ||||||
chr15:52149202
|
C | G | 1 | a0001c0001t0013g0035 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.417+682G>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 5/12 | chr15 | 52149202 | ||||||
chr15:52149278
|
T | C | 1 | a0001c0001t0002g0011 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.417+606A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 5/12 | chr15 | 52149278 | ||||||
chr15:52149317
|
T | G | 1 | a0001c0003t0112g0087 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.417+567A>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 5/12 | chr15 | 52149317 | ||||||
chr15:52149321
|
G | T | 156 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0001g0187others(153): Show | 156 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.417+563C>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 5/12 | chr15 | 52149321 | ||||||
chr15:52149327
|
C | T | 53 | a0001c0001t0016g0332a0001c0001t0016g0343a0001c0001t0016g0344others(50): Show | 53 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.417+557G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 5/12 | chr15 | 52149327 | ||||||
chr15:52149462
|
C | T | 7 | a0001c0002t0024g0281a0001c0002t0024g0284a0001c0002t0025g0282others(4): Show | 7 | HG02109.hp2 HG02257.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.417+422G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 5/12 | chr15 | 52149462 | ||||||
chr15:52149489
|
C | T | 75 | a0001c0001t0016g0332a0001c0001t0016g0343a0001c0001t0016g0344others(72): Show | 75 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.417+395G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 5/12 | chr15 | 52149489 | ||||||
chr15:52149604
|
T | A | 342 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0001g0187others(339): Show | 344 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(341): Show |
intron_variant | MODIFIER | c.417+280A>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 5/12 | chr15 | 52149604 | ||||||
chr15:52149790
|
G | A | 1 | a0001c0001t0160g0212 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.417+94C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 5/12 | chr15 | 52149790 | ||||||
chr15:52149807
|
G | A | 2 | a0001c0006t0142g0310a0001c0006t0143g0312 | 2 | HG02559.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.417+77C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 5/12 | chr15 | 52149807 | ||||||
chr15:52149970
|
C | A | 1 | a0001c0001t0167g0259 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.376-45G>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 4/12 | chr15 | 52149970 | ||||||
chr15:52150342
|
C | T | 2 | a0001c0001t0145g0279a0001c0001t0146g0292 | 2 | HG01891.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.376-417G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 4/12 | chr15 | 52150342 | ||||||
chr15:52150351
|
C | G | 1 | a0001c0001t0149g0300 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.376-426G>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 4/12 | chr15 | 52150351 | ||||||
chr15:52150377
|
C | T | 1 | a0001c0001t0002g0004 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.376-452G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 4/12 | chr15 | 52150377 | ||||||
chr15:52150415
|
C | G | 7 | a0001c0002t0024g0281a0001c0002t0024g0284a0001c0002t0025g0282others(4): Show | 7 | HG02109.hp2 HG02257.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.376-490G>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 4/12 | chr15 | 52150415 | ||||||
chr15:52150466
|
G | A | 2 | a0001c0001t0016g0332a0001c0001t0198g0351 | 2 | HG00438.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.376-541C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 4/12 | chr15 | 52150466 | ||||||
chr15:52150532
|
C | T | 1 | a0001c0002t0207g0177 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.376-607G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 4/12 | chr15 | 52150532 | ||||||
chr15:52150553
|
A | G | 1 | a0001c0005t0157g0278 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.376-628T>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 4/12 | chr15 | 52150553 | ||||||
chr15:52150637
|
C | T | 156 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0001g0187others(153): Show | 156 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.376-712G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 4/12 | chr15 | 52150637 | ||||||
chr15:52150699
|
C | G | 2 | a0001c0001t0030g0206a0001c0001t0160g0212 | 2 | HG02155.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.376-774G>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 4/12 | chr15 | 52150699 | ||||||
chr15:52150705
|
T | TG | 15 | a0001c0001t0192g0267a0001c0002t0128g0273a0001c0002t0129g0275others(12): Show | 15 | HG01934.hp2 HG01943.hp2 HG01952.hp1 others(12): Show |
intron_variant | MODIFIER | c.376-781dupC | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 4/12 | chr15 | 52150705 | ||||||
chr15:52150779
|
C | T | 2 | a0001c0001t0013g0049a0001c0001t0013g0050 | 2 | HG01109.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.376-854G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 4/12 | chr15 | 52150779 | ||||||
chr15:52150858
|
C | T | 2 | a0001c0002t0025g0282a0001c0002t0025g0283 | 2 | HG02109.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.376-933G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 4/12 | chr15 | 52150858 | ||||||
chr15:52150877
|
T | C | 87 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0001g0187others(84): Show | 87 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.376-952A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 4/12 | chr15 | 52150877 | ||||||
chr15:52150910
|
C | T | 73 | a0001c0001t0016g0332a0001c0001t0016g0343a0001c0001t0016g0344others(70): Show | 73 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.376-985G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 4/12 | chr15 | 52150910 | ||||||
chr15:52150912
|
G | A | 4 | a0001c0001t0011g0305a0001c0001t0011g0319a0001c0001t0027g0306others(1): Show | 4 | HG02895.hp1 HG02897.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.376-987C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 4/12 | chr15 | 52150912 | ||||||
chr15:52150921
|
CTTT | C | 8 | a0001c0002t0128g0273a0001c0002t0129g0275a0001c0002t0130g0274others(5): Show | 8 | HG01934.hp2 HG01952.hp1 HG02132.hp2 others(5): Show |
intron_variant | MODIFIER | c.376-999_376-997del others(3): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 4/12 | chr15 | 52150921 | ||||||
chr15:52150922
|
T | G | 7 | a0001c0001t0192g0267a0001c0002t0135g0270a0001c0002t0136g0268others(4): Show | 7 | HG01943.hp2 HG02004.hp1 HG02148.hp2 others(4): Show |
intron_variant | MODIFIER | c.376-997A>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 4/12 | chr15 | 52150922 | ||||||
chr15:52150937
|
G | A | 69 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0008others(66): Show | 69 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.376-1012C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 4/12 | chr15 | 52150937 | ||||||
chr15:52150960
|
T | C | 8 | a0001c0002t0019g0092a0001c0002t0019g0093a0001c0003t0097g0091others(5): Show | 8 | HG01884.hp1 HG02622.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.376-1035A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 4/12 | chr15 | 52150960 | ||||||
chr15:52150978
|
A | C | 15 | a0001c0001t0192g0267a0001c0002t0128g0273a0001c0002t0129g0275others(12): Show | 15 | HG01934.hp2 HG01943.hp2 HG01952.hp1 others(12): Show |
intron_variant | MODIFIER | c.376-1053T>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 4/12 | chr15 | 52150978 | ||||||
chr15:52151025
|
G | A | 85 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0001g0187others(82): Show | 85 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.376-1100C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 4/12 | chr15 | 52151025 | ||||||
chr15:52151036
|
G | A | 153 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0001g0187others(150): Show | 153 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(150): Show |
intron_variant | MODIFIER | c.376-1111C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 4/12 | chr15 | 52151036 | ||||||
chr15:52151183
|
C | A | 3 | a0001c0001t0046g0110a0001c0001t0068g0111a0001c0001t0069g0105 | 3 | HG01256.hp2 HG01258.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.376-1258G>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 4/12 | chr15 | 52151183 | ||||||
chr15:52151190
|
C | T | 5 | a0001c0001t0022g0294a0001c0001t0022g0295a0001c0001t0023g0296others(2): Show | 5 | HG02559.hp1 HG02886.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.376-1265G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 4/12 | chr15 | 52151190 | ||||||
chr15:52151277
|
T | C | 15 | a0001c0001t0192g0267a0001c0002t0128g0273a0001c0002t0129g0275others(12): Show | 15 | HG01934.hp2 HG01943.hp2 HG01952.hp1 others(12): Show |
intron_variant | MODIFIER | c.376-1352A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 4/12 | chr15 | 52151277 | ||||||
chr15:52151300
|
G | A | 4 | a0001c0001t0007g0144a0001c0001t0015g0145a0001c0001t0015g0146others(1): Show | 4 | NA18946.hp1 NA18970.hp1 NA18981.hp2 others(1): Show |
intron_variant | MODIFIER | c.376-1375C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 4/12 | chr15 | 52151300 | ||||||
chr15:52151383
|
G | A | 9 | a0001c0001t0064g0155a0001c0003t0021g0354a0001c0003t0021g0355others(6): Show | 9 | HG01891.hp2 HG02055.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.376-1458C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 4/12 | chr15 | 52151383 | ||||||
chr15:52151473
|
G | A | 7 | a0001c0004t0014g0002a0001c0004t0014g0280a0001c0004t0014g0290others(4): Show | 9 | HG00738.hp2 HG00741.hp1 HG01069.hp1 others(6): Show |
intron_variant | MODIFIER | c.376-1548C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 4/12 | chr15 | 52151473 | ||||||
chr15:52151746
|
T | A | 14 | a0001c0001t0001g0213a0001c0001t0001g0223a0001c0001t0001g0245others(11): Show | 14 | HG01069.hp2 HG01261.hp1 HG01358.hp1 others(11): Show |
intron_variant | MODIFIER | c.376-1821A>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 4/12 | chr15 | 52151746 | ||||||
chr15:52151865
|
A | G | 346 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0001g0187others(343): Show | 348 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(345): Show |
intron_variant | MODIFIER | c.376-1940T>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 4/12 | chr15 | 52151865 | ||||||
chr15:52152111
|
C | T | 7 | a0001c0002t0024g0281a0001c0002t0024g0284a0001c0002t0025g0282others(4): Show | 7 | HG02109.hp2 HG02257.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.375+1829G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 4/12 | chr15 | 52152111 | ||||||
chr15:52152183
|
G | A | 1 | a0001c0003t0119g0094 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.375+1757C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 4/12 | chr15 | 52152183 | ||||||
chr15:52152295
|
G | A | 1 | a0001c0001t0072g0108 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.375+1645C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 4/12 | chr15 | 52152295 | ||||||
chr15:52152357
|
C | T | 15 | a0001c0001t0192g0267a0001c0002t0128g0273a0001c0002t0129g0275others(12): Show | 15 | HG01934.hp2 HG01943.hp2 HG01952.hp1 others(12): Show |
intron_variant | MODIFIER | c.375+1583G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 4/12 | chr15 | 52152357 | ||||||
chr15:52152418
|
G | A | 1 | a0001c0001t0059g0125 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.375+1522C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 4/12 | chr15 | 52152418 | ||||||
chr15:52152474
|
C | G | 1 | a0001c0002t0207g0177 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.375+1466G>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 4/12 | chr15 | 52152474 | ||||||
chr15:52152569
|
T | A | 1 | a0001c0001t0001g0325 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.375+1371A>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 4/12 | chr15 | 52152569 | ||||||
chr15:52152592
|
T | G | 1 | a0001c0001t0169g0352 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.375+1348A>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 4/12 | chr15 | 52152592 | ||||||
chr15:52152629
|
A | C | 8 | a0001c0003t0021g0354a0001c0003t0021g0355a0001c0003t0122g0357others(5): Show | 8 | HG01891.hp2 HG02055.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.375+1311T>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 4/12 | chr15 | 52152629 | ||||||
chr15:52152635
|
C | CT | 52 | a0001c0001t0002g0003a0001c0001t0016g0332a0001c0001t0016g0343others(49): Show | 52 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.375+1304dupA | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 4/12 | chr15 | 52152635 | ||||||
chr15:52152676
|
G | C | 7 | a0001c0004t0014g0002a0001c0004t0014g0280a0001c0004t0014g0290others(4): Show | 9 | HG00738.hp2 HG00741.hp1 HG01069.hp1 others(6): Show |
intron_variant | MODIFIER | c.375+1264C>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 4/12 | chr15 | 52152676 | ||||||
chr15:52152750
|
C | T | 1 | a0001c0002t0120g0012 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.375+1190G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 4/12 | chr15 | 52152750 | ||||||
chr15:52152777
|
C | T | 7 | a0001c0002t0024g0281a0001c0002t0024g0284a0001c0002t0025g0282others(4): Show | 7 | HG02109.hp2 HG02257.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.375+1163G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 4/12 | chr15 | 52152777 | ||||||
chr15:52152845
|
G | A | 2 | a0001c0001t0016g0343a0001c0001t0183g0359 | 2 | HG00408.hp2 HG02015.hp1 |
intron_variant | MODIFIER | c.375+1095C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 4/12 | chr15 | 52152845 | ||||||
chr15:52152854
|
G | A | 1 | a0001c0001t0177g0362 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.375+1086C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 4/12 | chr15 | 52152854 | ||||||
chr15:52152885
|
A | T | 26 | a0001c0001t0018g0133a0001c0001t0018g0151a0001c0001t0038g0115others(23): Show | 26 | HG00544.hp2 HG00597.hp1 HG00673.hp2 others(23): Show |
intron_variant | MODIFIER | c.375+1055T>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 4/12 | chr15 | 52152885 | ||||||
chr15:52152893
|
A | G | 68 | a0001c0001t0016g0332a0001c0001t0016g0343a0001c0001t0016g0344others(65): Show | 68 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.375+1047T>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 4/12 | chr15 | 52152893 | ||||||
chr15:52152949
|
G | T | 1 | a0001c0001t0002g0039 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.375+991C>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 4/12 | chr15 | 52152949 | ||||||
chr15:52153036
|
A | G | 1 | a0001c0001t0002g0030 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.375+904T>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 4/12 | chr15 | 52153036 | ||||||
chr15:52153180
|
C | A | 14 | a0001c0002t0128g0273a0001c0002t0129g0275a0001c0002t0130g0274others(11): Show | 14 | HG01934.hp2 HG01952.hp1 HG02004.hp1 others(11): Show |
intron_variant | MODIFIER | c.375+760G>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 4/12 | chr15 | 52153180 | ||||||
chr15:52153280
|
C | T | 68 | a0001c0001t0016g0332a0001c0001t0016g0343a0001c0001t0016g0344others(65): Show | 68 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.375+660G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 4/12 | chr15 | 52153280 | ||||||
chr15:52153451
|
A | C | 1 | a0001c0001t0173g0183 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.375+489T>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 4/12 | chr15 | 52153451 | ||||||
chr15:52153471
|
G | A | 1 | a0001c0001t0030g0182 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.375+469C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 4/12 | chr15 | 52153471 | ||||||
chr15:52153671
|
CAT | C | 12 | a0001c0002t0006g0291a0001c0002t0006g0314a0001c0002t0006g0316others(9): Show | 12 | HG01243.hp1 HG02055.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.375+267_375+268del others(2): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 4/12 | chr15 | 52153671 | ||||||
chr15:52153785
|
A | G | 1 | a0001c0001t0002g0053 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.375+155T>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 4/12 | chr15 | 52153785 | ||||||
chr15:52153826
|
G | A | 1 | a0001c0001t0034g0330 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.375+114C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 4/12 | chr15 | 52153826 | ||||||
chr15:52153875
|
C | T | 7 | a0001c0002t0019g0092a0001c0002t0019g0093a0001c0003t0097g0091others(4): Show | 7 | HG01884.hp1 HG02622.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.375+65G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 4/12 | chr15 | 52153875 | ||||||
chr15:52153885
|
C | G | 1 | a0001c0001t0011g0319 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.375+55G>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 4/12 | chr15 | 52153885 | ||||||
chr15:52154094
|
T | G | 1 | a0001c0001t0146g0292 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.239-18A>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52154094 | ||||||
chr15:52154103
|
C | T | 16 | a0001c0002t0019g0092a0001c0002t0019g0093a0001c0003t0021g0354others(13): Show | 16 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.239-27G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52154103 | ||||||
chr15:52154159
|
C | T | 1 | a0001c0001t0059g0125 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.239-83G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52154159 | ||||||
chr15:52154246
|
C | T | 1 | a0001c0005t0157g0278 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.239-170G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52154246 | ||||||
chr15:52154267
|
G | C | 86 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0001g0187others(83): Show | 86 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.239-191C>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52154267 | ||||||
chr15:52154339
|
A | T | 1 | a0001c0001t0077g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.239-263T>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52154339 | ||||||
chr15:52154377
|
A | C | 6 | a0001c0001t0022g0294a0001c0001t0022g0295a0001c0001t0023g0296others(3): Show | 6 | HG02559.hp1 HG02723.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.239-301T>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52154377 | ||||||
chr15:52154377
|
A | T | 7 | a0001c0002t0024g0281a0001c0002t0024g0284a0001c0002t0025g0282others(4): Show | 7 | HG02109.hp2 HG02257.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.239-301T>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52154377 | ||||||
chr15:52154643
|
C | G | 3 | a0001c0001t0002g0030a0001c0001t0002g0051a0001c0001t0117g0006 | 3 | HG00323.hp1 HG01192.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.239-567G>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52154643 | ||||||
chr15:52154644
|
T | C | 1 | a0001c0001t0146g0292 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.239-568A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52154644 | ||||||
chr15:52154688
|
A | G | 2 | a0001c0001t0002g0036a0001c0001t0002g0038 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.239-612T>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52154688 | ||||||
chr15:52155078
|
T | G | 1 | a0001c0001t0102g0170 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.239-1002A>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52155078 | ||||||
chr15:52155102
|
A | G | 75 | a0001c0001t0016g0332a0001c0001t0016g0343a0001c0001t0016g0344others(72): Show | 75 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.239-1026T>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52155102 | ||||||
chr15:52155140
|
C | A | 2 | a0001c0002t0206g0178a0001c0002t0207g0177 | 2 | HG01496.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.239-1064G>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52155140 | ||||||
chr15:52155311
|
G | A | 52 | a0001c0001t0016g0332a0001c0001t0016g0343a0001c0001t0016g0344others(49): Show | 52 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.239-1235C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52155311 | ||||||
chr15:52155317
|
G | A | 52 | a0001c0001t0001g0248a0001c0001t0002g0081a0001c0001t0002g0084others(49): Show | 52 | HG00323.hp2 HG00609.hp1 HG01123.hp2 others(49): Show |
intron_variant | MODIFIER | c.239-1241C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52155317 | ||||||
chr15:52155350
|
C | T | 12 | a0001c0002t0006g0291a0001c0002t0006g0314a0001c0002t0006g0316others(9): Show | 12 | HG01243.hp1 HG02055.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.239-1274G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52155350 | ||||||
chr15:52155370
|
G | C | 14 | a0001c0002t0128g0273a0001c0002t0129g0275a0001c0002t0130g0274others(11): Show | 14 | HG01934.hp2 HG01952.hp1 HG02004.hp1 others(11): Show |
intron_variant | MODIFIER | c.239-1294C>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52155370 | ||||||
chr15:52155602
|
T | C | 8 | a0001c0003t0021g0354a0001c0003t0021g0355a0001c0003t0122g0357others(5): Show | 8 | HG01891.hp2 HG02055.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.239-1526A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52155602 | ||||||
chr15:52155642
|
T | C | 74 | a0001c0001t0001g0248a0001c0001t0007g0139a0001c0001t0007g0144others(71): Show | 74 | HG00323.hp2 HG00544.hp2 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.239-1566A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52155642 | ||||||
chr15:52155733
|
T | G | 1 | a0001c0002t0207g0177 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.239-1657A>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52155733 | ||||||
chr15:52155748
|
A | G | 1 | a0001c0002t0025g0283 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.239-1672T>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52155748 | ||||||
chr15:52155759
|
T | C | 1 | a0001c0005t0156g0261 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.239-1683A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52155759 | ||||||
chr15:52155839
|
A | G | 68 | a0001c0001t0016g0332a0001c0001t0016g0343a0001c0001t0016g0344others(65): Show | 68 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.239-1763T>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52155839 | ||||||
chr15:52155871
|
C | T | 3 | a0001c0001t0104g0058a0001c0001t0105g0057a0001c0001t0106g0071 | 3 | HG02615.hp2 HG03516.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.239-1795G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52155871 | ||||||
chr15:52155886
|
A | C | 5 | a0001c0002t0024g0281a0001c0002t0024g0284a0001c0002t0026g0286others(2): Show | 5 | HG02257.hp1 HG02630.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.239-1810T>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52155886 | ||||||
chr15:52156016
|
G | A | 1 | a0001c0001t0146g0292 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.239-1940C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52156016 | ||||||
chr15:52156032
|
CT | C | 7 | a0001c0002t0024g0281a0001c0002t0024g0284a0001c0002t0025g0282others(4): Show | 7 | HG02109.hp2 HG02257.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.239-1957delA | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52156032 | ||||||
chr15:52156236
|
C | T | 1 | a0001c0005t0156g0261 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.239-2160G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52156236 | ||||||
chr15:52156293
|
G | A | 1 | a0001c0001t0074g0162 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.239-2217C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52156293 | ||||||
chr15:52156459
|
C | T | 15 | a0001c0001t0192g0267a0001c0002t0128g0273a0001c0002t0129g0275others(12): Show | 15 | HG01934.hp2 HG01943.hp2 HG01952.hp1 others(12): Show |
intron_variant | MODIFIER | c.239-2383G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52156459 | ||||||
chr15:52156470
|
G | A | 5 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0216others(2): Show | 5 | NA18612.hp1 NA18982.hp1 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.239-2394C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52156470 | ||||||
chr15:52156660
|
G | A | 1 | a0001c0001t0002g0059 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.239-2584C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52156660 | ||||||
chr15:52156668
|
C | T | 69 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0008others(66): Show | 69 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.239-2592G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52156668 | ||||||
chr15:52156857
|
C | T | 16 | a0001c0002t0019g0092a0001c0002t0019g0093a0001c0003t0021g0354others(13): Show | 16 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.239-2781G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52156857 | ||||||
chr15:52156862
|
T | C | 1 | a0001c0001t0015g0145 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.239-2786A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52156862 | ||||||
chr15:52156901
|
G | A | 2 | a0001c0002t0206g0178a0001c0002t0207g0177 | 2 | HG01496.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.239-2825C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52156901 | ||||||
chr15:52156937
|
C | CT | 30 | a0001c0001t0001g0189a0001c0001t0001g0195a0001c0001t0001g0237others(27): Show | 30 | HG01884.hp1 HG01934.hp2 HG01943.hp2 others(27): Show |
intron_variant | MODIFIER | c.239-2862dupA | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52156937 | ||||||
chr15:52156958
|
C | T | 1 | a0001c0003t0112g0087 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.239-2882G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52156958 | ||||||
chr15:52156998
|
G | C | 53 | a0001c0001t0016g0332a0001c0001t0016g0343a0001c0001t0016g0344others(50): Show | 53 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.239-2922C>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52156998 | ||||||
chr15:52157029
|
G | A | 1 | a0001c0001t0007g0153 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.239-2953C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52157029 | ||||||
chr15:52157082
|
C | A | 4 | a0001c0002t0019g0092a0001c0002t0019g0093a0001c0003t0098g0088others(1): Show | 4 | HG01884.hp1 HG02622.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.239-3006G>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52157082 | ||||||
chr15:52157084
|
C | T | 4 | a0001c0001t0004g0028a0001c0001t0004g0029a0001c0001t0004g0075others(1): Show | 4 | NA18977.hp1 NA19012.hp2 NA19081.hp2 others(1): Show |
intron_variant | MODIFIER | c.239-3008G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52157084 | ||||||
chr15:52157096
|
T | C | 53 | a0001c0001t0016g0332a0001c0001t0016g0343a0001c0001t0016g0344others(50): Show | 53 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.239-3020A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52157096 | ||||||
chr15:52157163
|
T | C | 68 | a0001c0001t0016g0332a0001c0001t0016g0343a0001c0001t0016g0344others(65): Show | 68 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.239-3087A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52157163 | ||||||
chr15:52157178
|
C | T | 1 | a0001c0001t0002g0085 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.239-3102G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52157178 | ||||||
chr15:52157182
|
A | C | 53 | a0001c0001t0016g0332a0001c0001t0016g0343a0001c0001t0016g0344others(50): Show | 53 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.239-3106T>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52157182 | ||||||
chr15:52157188
|
G | A | 2 | a0001c0005t0156g0261a0001c0005t0157g0278 | 2 | HG01109.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.239-3112C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52157188 | ||||||
chr15:52157231
|
C | T | 6 | a0001c0001t0022g0294a0001c0001t0022g0295a0001c0001t0023g0296others(3): Show | 6 | HG02559.hp1 HG02723.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.239-3155G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52157231 | ||||||
chr15:52157250
|
C | A | 7 | a0001c0002t0024g0281a0001c0002t0024g0284a0001c0002t0025g0282others(4): Show | 7 | HG02109.hp2 HG02257.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.239-3174G>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52157250 | ||||||
chr15:52157250
|
C | CT | 80 | a0001c0001t0001g0248a0001c0001t0007g0139a0001c0001t0007g0144others(77): Show | 82 | HG00323.hp2 HG00544.hp2 HG00597.hp1 others(79): Show |
intron_variant | MODIFIER | c.239-3175dupA | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52157250 | ||||||
chr15:52157340
|
G | A | 8 | a0001c0002t0128g0273a0001c0002t0129g0275a0001c0002t0130g0274others(5): Show | 8 | HG01934.hp2 HG01952.hp1 HG02132.hp2 others(5): Show |
intron_variant | MODIFIER | c.239-3264C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52157340 | ||||||
chr15:52157404
|
G | A | 1 | a0001c0001t0146g0292 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.239-3328C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52157404 | ||||||
chr15:52157431
|
A | G | 184 | a0001c0001t0001g0248a0001c0001t0007g0139a0001c0001t0007g0144others(181): Show | 186 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(183): Show |
intron_variant | MODIFIER | c.239-3355T>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52157431 | ||||||
chr15:52157447
|
T | C | 1 | a0001c0005t0157g0278 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.239-3371A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52157447 | ||||||
chr15:52157536
|
G | A | 51 | a0001c0001t0016g0332a0001c0001t0016g0343a0001c0001t0016g0344others(48): Show | 51 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.239-3460C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52157536 | ||||||
chr15:52157569
|
A | G | 6 | a0001c0001t0010g0103a0001c0001t0010g0135a0001c0001t0010g0167others(3): Show | 6 | NA18945.hp2 NA18967.hp2 NA18970.hp2 others(3): Show |
intron_variant | MODIFIER | c.239-3493T>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52157569 | ||||||
chr15:52157614
|
A | G | 7 | a0001c0004t0014g0002a0001c0004t0014g0280a0001c0004t0014g0290others(4): Show | 9 | HG00738.hp2 HG00741.hp1 HG01069.hp1 others(6): Show |
intron_variant | MODIFIER | c.239-3538T>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52157614 | ||||||
chr15:52157783
|
T | C | 9 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0001g0194others(6): Show | 9 | HG00438.hp2 HG00621.hp1 HG02056.hp1 others(6): Show |
intron_variant | MODIFIER | c.239-3707A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52157783 | ||||||
chr15:52157898
|
T | TA | 77 | a0001c0001t0016g0332a0001c0001t0016g0343a0001c0001t0016g0344others(74): Show | 77 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(74): Show |
intron_variant | MODIFIER | c.239-3823dupT | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52157898 | ||||||
chr15:52158127
|
C | T | 1 | a0001c0005t0100g0134 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.239-4051G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52158127 | ||||||
chr15:52158193
|
T | G | 8 | a0001c0002t0019g0092a0001c0002t0019g0093a0001c0003t0097g0091others(5): Show | 8 | HG01884.hp1 HG02622.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.239-4117A>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52158193 | ||||||
chr15:52158226
|
A | G | 1 | a0001c0003t0112g0087 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.239-4150T>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52158226 | ||||||
chr15:52158317
|
T | A | 2 | a0001c0002t0206g0178a0001c0002t0207g0177 | 2 | HG01496.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.239-4241A>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52158317 | ||||||
chr15:52158399
|
A | G | 70 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0008others(67): Show | 70 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(67): Show |
intron_variant | MODIFIER | c.239-4323T>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52158399 | ||||||
chr15:52158420
|
G | T | 68 | a0001c0001t0016g0332a0001c0001t0016g0343a0001c0001t0016g0344others(65): Show | 68 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.239-4344C>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52158420 | ||||||
chr15:52158648
|
C | CT | 10 | a0001c0001t0046g0110a0001c0001t0068g0111a0001c0001t0069g0105others(7): Show | 10 | HG01256.hp2 HG01258.hp1 HG01943.hp2 others(7): Show |
intron_variant | MODIFIER | c.239-4573dupA | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52158648 | ||||||
chr15:52158737
|
G | A | 1 | a0001c0001t0002g0053 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.239-4661C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52158737 | ||||||
chr15:52158830
|
T | C | 1 | a0001c0001t0002g0085 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.239-4754A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52158830 | ||||||
chr15:52158917
|
C | G | 2 | a0001c0001t0023g0296a0001c0001t0023g0297 | 2 | HG02559.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.239-4841G>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52158917 | ||||||
chr15:52159145
|
C | G | 1 | a0001c0005t0157g0278 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.239-5069G>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52159145 | ||||||
chr15:52159200
|
C | G | 8 | a0001c0002t0019g0092a0001c0002t0019g0093a0001c0003t0097g0091others(5): Show | 8 | HG01884.hp1 HG02622.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.239-5124G>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52159200 | ||||||
chr15:52159306
|
C | T | 1 | a0001c0001t0052g0121 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.239-5230G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52159306 | ||||||
chr15:52159325
|
G | T | 1 | a0001c0003t0112g0087 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.239-5249C>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52159325 | ||||||
chr15:52159511
|
T | C | 1 | a0004c0008t0005g0234 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.239-5435A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52159511 | ||||||
chr15:52159573
|
C | G | 14 | a0001c0002t0128g0273a0001c0002t0129g0275a0001c0002t0130g0274others(11): Show | 14 | HG01934.hp2 HG01952.hp1 HG02004.hp1 others(11): Show |
intron_variant | MODIFIER | c.239-5497G>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52159573 | ||||||
chr15:52159586
|
T | A | 4 | a0001c0001t0067g0109a0001c0001t0071g0107a0001c0001t0072g0108others(1): Show | 4 | HG03225.hp2 HG03471.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.239-5510A>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52159586 | ||||||
chr15:52159601
|
G | A | 7 | a0001c0001t0002g0034a0001c0001t0002g0037a0001c0001t0002g0044others(4): Show | 7 | HG01071.hp2 HG01106.hp1 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.239-5525C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52159601 | ||||||
chr15:52159663
|
T | C | 2 | a0001c0004t0014g0280a0001c0004t0014g0290 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.239-5587A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52159663 | ||||||
chr15:52159687
|
G | A | 79 | a0001c0001t0007g0139a0001c0001t0007g0144a0001c0001t0007g0148others(76): Show | 81 | HG00323.hp2 HG00544.hp2 HG00597.hp1 others(78): Show |
intron_variant | MODIFIER | c.239-5611C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52159687 | ||||||
chr15:52159791
|
C | T | 7 | a0001c0002t0024g0281a0001c0002t0024g0284a0001c0002t0025g0282others(4): Show | 7 | HG02109.hp2 HG02257.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.239-5715G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52159791 | ||||||
chr15:52159827
|
G | A | 7 | a0001c0002t0019g0092a0001c0002t0019g0093a0001c0003t0097g0091others(4): Show | 7 | HG01884.hp1 HG02622.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.239-5751C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52159827 | ||||||
chr15:52159951
|
C | CT | 12 | a0001c0001t0016g0344a0001c0001t0107g0056a0001c0002t0019g0092others(9): Show | 12 | HG01496.hp1 HG01884.hp1 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.239-5876dupA | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52159951 | ||||||
chr15:52159951
|
CT | C | 8 | a0001c0001t0002g0068a0001c0001t0003g0013a0001c0001t0003g0078others(5): Show | 8 | HG01257.hp2 HG01943.hp2 NA18942.hp1 others(5): Show |
intron_variant | MODIFIER | c.239-5876delA | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52159951 | ||||||
chr15:52159975
|
T | A | 23 | a0001c0001t0007g0139a0001c0001t0007g0144a0001c0001t0007g0148others(20): Show | 23 | HG00609.hp1 HG02027.hp2 HG02698.hp2 others(20): Show |
intron_variant | MODIFIER | c.239-5899A>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52159975 | ||||||
chr15:52160064
|
C | T | 7 | a0001c0004t0014g0002a0001c0004t0014g0280a0001c0004t0014g0290others(4): Show | 9 | HG00738.hp2 HG00741.hp1 HG01069.hp1 others(6): Show |
intron_variant | MODIFIER | c.239-5988G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52160064 | ||||||
chr15:52160216
|
G | A | 14 | a0001c0002t0128g0273a0001c0002t0129g0275a0001c0002t0130g0274others(11): Show | 14 | HG01934.hp2 HG01952.hp1 HG02004.hp1 others(11): Show |
intron_variant | MODIFIER | c.239-6140C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52160216 | ||||||
chr15:52160237
|
T | C | 66 | a0001c0001t0016g0332a0001c0001t0016g0343a0001c0001t0016g0344others(63): Show | 66 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(63): Show |
intron_variant | MODIFIER | c.239-6161A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52160237 | ||||||
chr15:52160238
|
G | A | 8 | a0001c0002t0128g0273a0001c0002t0129g0275a0001c0002t0130g0274others(5): Show | 8 | HG01934.hp2 HG01952.hp1 HG02132.hp2 others(5): Show |
intron_variant | MODIFIER | c.239-6162C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52160238 | ||||||
chr15:52160313
|
A | T | 1 | a0001c0001t0196g0335 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.239-6237T>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52160313 | ||||||
chr15:52160433
|
T | A | 1 | a0001c0001t0002g0069 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.239-6357A>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52160433 | ||||||
chr15:52160437
|
A | C | 80 | a0001c0001t0007g0139a0001c0001t0007g0144a0001c0001t0007g0148others(77): Show | 82 | HG00323.hp2 HG00544.hp2 HG00597.hp1 others(79): Show |
intron_variant | MODIFIER | c.239-6361T>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52160437 | ||||||
chr15:52160453
|
G | A | 14 | a0001c0002t0128g0273a0001c0002t0129g0275a0001c0002t0130g0274others(11): Show | 14 | HG01934.hp2 HG01952.hp1 HG02004.hp1 others(11): Show |
intron_variant | MODIFIER | c.239-6377C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52160453 | ||||||
chr15:52160459
|
C | T | 1 | a0001c0001t0002g0010 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.239-6383G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52160459 | ||||||
chr15:52160500
|
T | A | 52 | a0001c0001t0016g0332a0001c0001t0016g0343a0001c0001t0016g0344others(49): Show | 52 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.239-6424A>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52160500 | ||||||
chr15:52160601
|
AT | A | 12 | a0001c0002t0006g0291a0001c0002t0006g0314a0001c0002t0006g0316others(9): Show | 12 | HG01243.hp1 HG02055.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.239-6526delA | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52160601 | ||||||
chr15:52160637
|
T | C | 52 | a0001c0001t0016g0332a0001c0001t0016g0343a0001c0001t0016g0344others(49): Show | 52 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.239-6561A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52160637 | ||||||
chr15:52160711
|
T | G | 8 | a0001c0002t0019g0092a0001c0002t0019g0093a0001c0003t0097g0091others(5): Show | 8 | HG01884.hp1 HG02622.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.239-6635A>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52160711 | ||||||
chr15:52160873
|
C | T | 3 | a0001c0001t0008g0140a0001c0001t0008g0142a0001c0001t0015g0143 | 3 | NA18956.hp2 NA18966.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.239-6797G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52160873 | ||||||
chr15:52160876
|
G | T | 1 | a0001c0003t0112g0087 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.239-6800C>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52160876 | ||||||
chr15:52161043
|
G | A | 1 | a0001c0001t0152g0243 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.239-6967C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52161043 | ||||||
chr15:52161273
|
G | A | 1 | a0001c0001t0054g0131 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.239-7197C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52161273 | ||||||
chr15:52161349
|
G | A | 1 | a0001c0001t0033g0328 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.239-7273C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52161349 | ||||||
chr15:52161359
|
G | A | 4 | a0001c0003t0122g0357a0001c0003t0123g0364a0001c0003t0124g0308others(1): Show | 4 | HG02630.hp1 HG02818.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.239-7283C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52161359 | ||||||
chr15:52161415
|
A | T | 1 | a0001c0003t0098g0088 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.239-7339T>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52161415 | ||||||
chr15:52161446
|
C | T | 1 | a0001c0001t0170g0338 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.239-7370G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52161446 | ||||||
chr15:52161447
|
G | A | 1 | a0001c0004t0014g0002 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.239-7371C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52161447 | ||||||
chr15:52161467
|
T | G | 4 | a0001c0001t0004g0061a0001c0001t0004g0062a0001c0001t0004g0063others(1): Show | 4 | HG02523.hp2 NA18747.hp1 NA18944.hp2 others(1): Show |
intron_variant | MODIFIER | c.239-7391A>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52161467 | ||||||
chr15:52161610
|
C | T | 1 | a0001c0003t0126g0313 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.239-7534G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52161610 | ||||||
chr15:52161831
|
G | T | 1 | a0001c0001t0175g0219 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.239-7755C>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52161831 | ||||||
chr15:52161841
|
T | C | 1 | a0001c0003t0127g0356 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.239-7765A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52161841 | ||||||
chr15:52161901
|
C | T | 52 | a0001c0001t0016g0332a0001c0001t0016g0343a0001c0001t0016g0344others(49): Show | 52 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.239-7825G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52161901 | ||||||
chr15:52161931
|
A | G | 1 | a0001c0001t0005g0207 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.239-7855T>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52161931 | ||||||
chr15:52162163
|
G | T | 1 | a0001c0001t0011g0304 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.239-8087C>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52162163 | ||||||
chr15:52162172
|
A | G | 1 | a0001c0001t0016g0332 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.239-8096T>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52162172 | ||||||
chr15:52162183
|
G | A | 14 | a0001c0002t0128g0273a0001c0002t0129g0275a0001c0002t0130g0274others(11): Show | 14 | HG01934.hp2 HG01952.hp1 HG02004.hp1 others(11): Show |
intron_variant | MODIFIER | c.239-8107C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52162183 | ||||||
chr15:52162186
|
C | T | 7 | a0001c0004t0014g0002a0001c0004t0014g0280a0001c0004t0014g0290others(4): Show | 9 | HG00738.hp2 HG00741.hp1 HG01069.hp1 others(6): Show |
intron_variant | MODIFIER | c.239-8110G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52162186 | ||||||
chr15:52162212
|
G | A | 7 | a0001c0004t0014g0002a0001c0004t0014g0280a0001c0004t0014g0290others(4): Show | 9 | HG00738.hp2 HG00741.hp1 HG01069.hp1 others(6): Show |
intron_variant | MODIFIER | c.239-8136C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52162212 | ||||||
chr15:52162228
|
C | T | 1 | a0001c0002t0206g0178 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.239-8152G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52162228 | ||||||
chr15:52162327
|
A | G | 2 | a0001c0002t0206g0178a0001c0002t0207g0177 | 2 | HG01496.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.239-8251T>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52162327 | ||||||
chr15:52162459
|
A | C | 1 | a0001c0001t0083g0141 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.239-8383T>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52162459 | ||||||
chr15:52162498
|
T | G | 1 | a0001c0001t0001g0262 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.239-8422A>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52162498 | ||||||
chr15:52162576
|
A | T | 12 | a0001c0002t0006g0291a0001c0002t0006g0314a0001c0002t0006g0316others(9): Show | 12 | HG01243.hp1 HG02055.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.239-8500T>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52162576 | ||||||
chr15:52162577
|
T | C | 1 | a0001c0002t0006g0317 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.239-8501A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52162577 | ||||||
chr15:52162690
|
C | G | 72 | a0001c0001t0001g0248a0001c0001t0007g0139a0001c0001t0007g0144others(69): Show | 72 | HG00323.hp2 HG00544.hp2 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.239-8614G>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52162690 | ||||||
chr15:52162716
|
A | G | 8 | a0001c0003t0021g0354a0001c0003t0021g0355a0001c0003t0122g0357others(5): Show | 8 | HG01891.hp2 HG02055.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.239-8640T>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52162716 | ||||||
chr15:52162784
|
T | C | 1 | a0001c0003t0099g0095 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.239-8708A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52162784 | ||||||
chr15:52162840
|
T | G | 5 | a0001c0001t0002g0081a0001c0001t0002g0082a0001c0001t0002g0084others(2): Show | 5 | HG01255.hp1 HG01358.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.239-8764A>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52162840 | ||||||
chr15:52162890
|
C | T | 2 | a0001c0001t0030g0206a0001c0001t0160g0212 | 2 | HG02155.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.239-8814G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52162890 | ||||||
chr15:52162943
|
C | T | 2 | a0001c0001t0002g0046a0001c0010t0189g0179 | 2 | HG01106.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.239-8867G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52162943 | ||||||
chr15:52163064
|
C | G | 5 | a0001c0001t0010g0135a0001c0001t0010g0167a0001c0001t0010g0172others(2): Show | 5 | NA18945.hp2 NA18967.hp2 NA18970.hp2 others(2): Show |
intron_variant | MODIFIER | c.239-8988G>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52163064 | ||||||
chr15:52163140
|
G | A | 1 | a0001c0001t0070g0157 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.239-9064C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52163140 | ||||||
chr15:52163212
|
G | A | 145 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0189others(142): Show | 145 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.239-9136C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52163212 | ||||||
chr15:52163283
|
G | A | 1 | a0001c0001t0177g0362 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.239-9207C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52163283 | ||||||
chr15:52163300
|
G | A | 1 | a0001c0001t0031g0334 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.239-9224C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52163300 | ||||||
chr15:52163359
|
T | C | 6 | a0001c0002t0019g0092a0001c0002t0019g0093a0001c0003t0097g0091others(3): Show | 6 | HG01884.hp1 HG02622.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.239-9283A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52163359 | ||||||
chr15:52163459
|
G | A | 6 | a0001c0002t0019g0092a0001c0002t0019g0093a0001c0003t0097g0091others(3): Show | 6 | HG01884.hp1 HG02622.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.239-9383C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52163459 | ||||||
chr15:52163468
|
G | A | 1 | a0001c0001t0106g0071 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.239-9392C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52163468 | ||||||
chr15:52163512
|
A | G | 82 | a0001c0001t0001g0248a0001c0001t0007g0139a0001c0001t0007g0144others(79): Show | 82 | HG00323.hp2 HG00544.hp2 HG00597.hp1 others(79): Show |
intron_variant | MODIFIER | c.239-9436T>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52163512 | ||||||
chr15:52163559
|
G | C | 1 | a0001c0001t0001g0326 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.239-9483C>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52163559 | ||||||
chr15:52163668
|
C | G | 6 | a0001c0002t0024g0281a0001c0002t0024g0284a0001c0002t0025g0282others(3): Show | 6 | HG02257.hp1 HG02630.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.239-9592G>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52163668 | ||||||
chr15:52163805
|
A | G | 2 | a0001c0001t0073g0166a0001c0001t0075g0165 | 2 | HG02572.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.239-9729T>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52163805 | ||||||
chr15:52163822
|
G | A | 1 | a0001c0002t0006g0320 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.239-9746C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52163822 | ||||||
chr15:52163829
|
C | T | 1 | a0001c0001t0037g0163 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.239-9753G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52163829 | ||||||
chr15:52163883
|
T | C | 1 | a0001c0001t0012g0257 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.239-9807A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52163883 | ||||||
chr15:52164085
|
C | T | 1 | a0001c0003t0112g0087 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.239-10009G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52164085 | ||||||
chr15:52164086
|
G | A | 5 | a0001c0001t0001g0192a0001c0001t0141g0301a0001c0001t0148g0302others(2): Show | 5 | HG02258.hp1 HG02615.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.239-10010C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52164086 | ||||||
chr15:52164119
|
T | C | 1 | a0001c0001t0078g0086 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.239-10043A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52164119 | ||||||
chr15:52164123
|
G | A | 8 | a0001c0001t0010g0112a0001c0001t0018g0133a0001c0001t0038g0115others(5): Show | 8 | HG00597.hp1 HG02015.hp2 HG02135.hp1 others(5): Show |
intron_variant | MODIFIER | c.239-10047C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52164123 | ||||||
chr15:52164181
|
G | A | 5 | a0001c0001t0022g0294a0001c0001t0022g0295a0001c0001t0023g0296others(2): Show | 5 | HG02559.hp1 HG02886.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.239-10105C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52164181 | ||||||
chr15:52164205
|
G | A | 1 | a0001c0001t0162g0361 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.239-10129C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52164205 | ||||||
chr15:52164222
|
C | A | 2 | a0001c0003t0021g0354a0001c0003t0021g0355 | 2 | HG01891.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.239-10146G>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52164222 | ||||||
chr15:52164308
|
T | TA | 6 | a0001c0001t0001g0262a0001c0001t0012g0181a0001c0001t0020g0023others(3): Show | 6 | HG03195.hp2 HG03710.hp1 NA19001.hp2 others(3): Show |
intron_variant | MODIFIER | c.239-10233dupT | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52164308 | ||||||
chr15:52164308
|
T | TAAA | 8 | a0001c0001t0011g0319a0001c0001t0148g0302a0001c0002t0006g0291others(5): Show | 8 | HG02717.hp1 HG02723.hp1 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.239-10235_239-1023 others(7): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52164308 | ||||||
chr15:52164308
|
T | TTA | 6 | a0001c0001t0022g0294a0001c0001t0022g0295a0001c0001t0023g0297others(3): Show | 6 | HG01168.hp1 HG02559.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.239-10233_239-1023 others(6): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52164308 | ||||||
chr15:52164308
|
T | TTAA | 4 | a0001c0001t0023g0296a0001c0004t0014g0002a0001c0004t0017g0001others(1): Show | 6 | HG00738.hp2 HG01069.hp1 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.239-10233_239-1023 others(7): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52164308 | ||||||
chr15:52164308
|
T | TTAAA | 3 | a0001c0004t0014g0290a0001c0004t0204g0288a0001c0004t0205g0289 | 3 | HG00741.hp1 HG01169.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.239-10233_239-1023 others(8): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52164308 | ||||||
chr15:52164308
|
TA | T | 192 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0189others(189): Show | 192 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(189): Show |
intron_variant | MODIFIER | c.239-10233delT | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52164308 | ||||||
chr15:52164308
|
TAA | T | 12 | a0001c0001t0001g0185a0001c0001t0001g0192a0001c0001t0001g0193others(9): Show | 12 | HG00438.hp2 HG00597.hp2 HG00621.hp1 others(9): Show |
intron_variant | MODIFIER | c.239-10234_239-1023 others(6): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52164308 | ||||||
chr15:52164308
|
TAAAAAA | T | 41 | a0001c0001t0016g0332a0001c0001t0016g0343a0001c0001t0031g0334others(38): Show | 41 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.239-10238_239-1023 others(10): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52164308 | ||||||
chr15:52164308
|
TAAAAAAA others(3): Show |
T | 16 | a0001c0001t0145g0279a0001c0001t0162g0361a0001c0002t0019g0092others(13): Show | 16 | HG01109.hp1 HG01255.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.239-10242_239-1023 others(14): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52164308 | ||||||
chr15:52164346
|
T | C | 4 | a0001c0001t0141g0301a0001c0001t0148g0302a0001c0001t0149g0300others(1): Show | 4 | HG02055.hp1 HG02258.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.239-10270A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52164346 | ||||||
chr15:52164389
|
C | T | 11 | a0001c0001t0011g0319a0001c0002t0006g0291a0001c0002t0006g0314others(8): Show | 11 | HG01243.hp1 HG02055.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.239-10313G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52164389 | ||||||
chr15:52164390
|
G | A | 2 | a0001c0003t0098g0088a0001c0003t0101g0089 | 2 | HG01884.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.239-10314C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52164390 | ||||||
chr15:52164584
|
C | T | 1 | a0001c0001t0149g0300 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.239-10508G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52164584 | ||||||
chr15:52164619
|
C | T | 3 | a0001c0001t0023g0296a0001c0001t0023g0297a0001c0001t0144g0298 | 3 | HG02559.hp1 HG02886.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.239-10543G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52164619 | ||||||
chr15:52164799
|
C | T | 4 | a0001c0003t0021g0354a0001c0003t0021g0355a0001c0003t0122g0357others(1): Show | 4 | HG01891.hp2 HG03139.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.239-10723G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52164799 | ||||||
chr15:52164853
|
A | G | 19 | a0001c0001t0011g0319a0001c0001t0162g0361a0001c0002t0006g0291others(16): Show | 19 | HG01243.hp1 HG01255.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.239-10777T>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52164853 | ||||||
chr15:52164897
|
G | C | 2 | a0001c0001t0015g0145a0001c0001t0015g0146 | 2 | NA18981.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.239-10821C>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52164897 | ||||||
chr15:52164962
|
T | C | 1 | a0001c0001t0013g0067 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.239-10886A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52164962 | ||||||
chr15:52165030
|
G | A | 96 | a0001c0001t0001g0202a0001c0001t0011g0319a0001c0001t0016g0332others(93): Show | 98 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.239-10954C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52165030 | ||||||
chr15:52165166
|
A | C | 15 | a0001c0001t0192g0267a0001c0002t0128g0273a0001c0002t0129g0275others(12): Show | 15 | HG01934.hp2 HG01943.hp2 HG01952.hp1 others(12): Show |
intron_variant | MODIFIER | c.239-11090T>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52165166 | ||||||
chr15:52165409
|
A | T | 3 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0028g0258 | 3 | HG00438.hp2 HG00621.hp1 NA18953.hp1 |
intron_variant | MODIFIER | c.239-11333T>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52165409 | ||||||
chr15:52165480
|
C | T | 1 | a0001c0002t0026g0287 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.239-11404G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52165480 | ||||||
chr15:52165524
|
G | A | 2 | a0001c0001t0162g0361a0001c0003t0126g0313 | 2 | HG01255.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.239-11448C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52165524 | ||||||
chr15:52165617
|
A | T | 3 | a0001c0001t0141g0301a0001c0001t0148g0302a0001c0001t0149g0300 | 3 | HG02258.hp1 HG02615.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.239-11541T>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52165617 | ||||||
chr15:52165739
|
C | CA | 61 | a0001c0001t0001g0202a0001c0001t0016g0332a0001c0001t0016g0343others(58): Show | 61 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.239-11664dupT | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52165739 | ||||||
chr15:52165776
|
C | T | 28 | a0001c0001t0008g0099a0001c0001t0010g0112a0001c0001t0018g0133others(25): Show | 28 | HG00544.hp2 HG00597.hp1 HG00673.hp2 others(25): Show |
intron_variant | MODIFIER | c.239-11700G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52165776 | ||||||
chr15:52165899
|
A | C | 8 | a0001c0002t0128g0273a0001c0002t0129g0275a0001c0002t0130g0274others(5): Show | 8 | HG01934.hp2 HG01952.hp1 HG02132.hp2 others(5): Show |
intron_variant | MODIFIER | c.239-11823T>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52165899 | ||||||
chr15:52166045
|
G | C | 2 | a0001c0001t0178g0226a0001c0001t0182g0225 | 2 | HG02074.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.239-11969C>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52166045 | ||||||
chr15:52166063
|
T | A | 3 | a0001c0001t0141g0301a0001c0001t0148g0302a0001c0001t0149g0300 | 3 | HG02258.hp1 HG02615.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.239-11987A>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52166063 | ||||||
chr15:52166092
|
A | G | 1 | a0001c0001t0146g0292 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.239-12016T>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52166092 | ||||||
chr15:52166608
|
T | C | 96 | a0001c0001t0001g0202a0001c0001t0011g0319a0001c0001t0016g0332others(93): Show | 98 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.239-12532A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52166608 | ||||||
chr15:52166650
|
C | A | 1 | a0001c0001t0177g0362 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.239-12574G>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52166650 | ||||||
chr15:52166680
|
A | C | 1 | a0001c0001t0049g0101 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.239-12604T>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52166680 | ||||||
chr15:52166813
|
G | A | 12 | a0001c0001t0145g0279a0001c0001t0146g0292a0001c0002t0019g0092others(9): Show | 12 | HG01496.hp1 HG01884.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.239-12737C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52166813 | ||||||
chr15:52166838
|
G | A | 2 | a0001c0001t0162g0361a0001c0003t0126g0313 | 2 | HG01255.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.239-12762C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52166838 | ||||||
chr15:52166991
|
G | A | 1 | a0001c0001t0002g0010 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.238+12777C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52166991 | ||||||
chr15:52167054
|
T | C | 1 | a0002c0007t0081g0175 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.238+12714A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52167054 | ||||||
chr15:52167083
|
T | C | 7 | a0001c0001t0046g0110a0001c0001t0067g0109a0001c0001t0068g0111others(4): Show | 7 | HG01256.hp2 HG01258.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.238+12685A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52167083 | ||||||
chr15:52167182
|
T | C | 59 | a0001c0001t0001g0202a0001c0001t0016g0332a0001c0001t0016g0343others(56): Show | 61 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.238+12586A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52167182 | ||||||
chr15:52167286
|
T | C | 96 | a0001c0001t0001g0202a0001c0001t0011g0319a0001c0001t0016g0332others(93): Show | 98 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.238+12482A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52167286 | ||||||
chr15:52167585
|
C | T | 1 | a0001c0001t0075g0165 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.238+12183G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52167585 | ||||||
chr15:52167594
|
G | T | 46 | a0001c0001t0001g0202a0001c0001t0016g0332a0001c0001t0016g0343others(43): Show | 46 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(43): Show |
intron_variant | MODIFIER | c.238+12174C>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52167594 | ||||||
chr15:52167671
|
CA | C | 94 | a0001c0001t0001g0202a0001c0001t0011g0319a0001c0001t0016g0332others(91): Show | 96 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.238+12096delT | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52167671 | ||||||
chr15:52167972
|
C | T | 9 | a0001c0001t0145g0279a0001c0002t0019g0092a0001c0002t0019g0093others(6): Show | 9 | HG01884.hp1 HG01891.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.238+11796G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52167972 | ||||||
chr15:52168019
|
C | T | 83 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0008others(80): Show | 83 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.238+11749G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52168019 | ||||||
chr15:52168114
|
C | T | 1 | a0001c0001t0145g0279 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.238+11654G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52168114 | ||||||
chr15:52168156
|
T | C | 1 | a0001c0002t0006g0321 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.238+11612A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52168156 | ||||||
chr15:52168178
|
C | T | 19 | a0001c0001t0011g0319a0001c0001t0162g0361a0001c0002t0006g0291others(16): Show | 19 | HG01243.hp1 HG01255.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.238+11590G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52168178 | ||||||
chr15:52168415
|
T | G | 96 | a0001c0001t0001g0202a0001c0001t0011g0319a0001c0001t0016g0332others(93): Show | 98 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.238+11353A>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52168415 | ||||||
chr15:52168567
|
G | A | 13 | a0001c0001t0115g0024a0001c0001t0145g0279a0001c0001t0146g0292others(10): Show | 13 | HG01496.hp1 HG01884.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.238+11201C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52168567 | ||||||
chr15:52168590
|
C | T | 1 | a0001c0001t0066g0164 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.238+11178G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52168590 | ||||||
chr15:52168604
|
T | C | 3 | a0001c0001t0141g0301a0001c0001t0148g0302a0001c0001t0149g0300 | 3 | HG02258.hp1 HG02615.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.238+11164A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52168604 | ||||||
chr15:52168607
|
G | A | 1 | a0001c0001t0016g0344 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.238+11161C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52168607 | ||||||
chr15:52168654
|
A | G | 3 | a0001c0001t0141g0301a0001c0001t0148g0302a0001c0001t0149g0300 | 3 | HG02258.hp1 HG02615.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.238+11114T>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52168654 | ||||||
chr15:52168818
|
C | T | 1 | a0001c0002t0006g0317 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.238+10950G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52168818 | ||||||
chr15:52168875
|
T | C | 1 | a0001c0001t0117g0006 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.238+10893A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52168875 | ||||||
chr15:52168890
|
A | G | 46 | a0001c0001t0001g0202a0001c0001t0016g0332a0001c0001t0016g0343others(43): Show | 46 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(43): Show |
intron_variant | MODIFIER | c.238+10878T>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52168890 | ||||||
chr15:52168916
|
T | C | 15 | a0001c0001t0192g0267a0001c0002t0128g0273a0001c0002t0129g0275others(12): Show | 15 | HG01934.hp2 HG01943.hp2 HG01952.hp1 others(12): Show |
intron_variant | MODIFIER | c.238+10852A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52168916 | ||||||
chr15:52168925
|
G | C | 3 | a0001c0001t0141g0301a0001c0001t0148g0302a0001c0001t0149g0300 | 3 | HG02258.hp1 HG02615.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.238+10843C>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52168925 | ||||||
chr15:52168929
|
G | T | 1 | a0001c0001t0146g0292 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.238+10839C>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52168929 | ||||||
chr15:52168995
|
A | T | 1 | a0001c0001t0145g0279 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.238+10773T>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52168995 | ||||||
chr15:52169073
|
C | T | 7 | a0001c0004t0014g0002a0001c0004t0014g0280a0001c0004t0014g0290others(4): Show | 9 | HG00738.hp2 HG00741.hp1 HG01069.hp1 others(6): Show |
intron_variant | MODIFIER | c.238+10695G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52169073 | ||||||
chr15:52169087
|
G | A | 19 | a0001c0001t0011g0319a0001c0001t0162g0361a0001c0002t0006g0291others(16): Show | 19 | HG01243.hp1 HG01255.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.238+10681C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52169087 | ||||||
chr15:52169102
|
T | C | 19 | a0001c0001t0011g0319a0001c0001t0162g0361a0001c0002t0006g0291others(16): Show | 19 | HG01243.hp1 HG01255.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.238+10666A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52169102 | ||||||
chr15:52169259
|
G | A | 53 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0008others(50): Show | 53 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(50): Show |
intron_variant | MODIFIER | c.238+10509C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52169259 | ||||||
chr15:52169263
|
T | C | 1 | a0001c0001t0044g0156 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.238+10505A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52169263 | ||||||
chr15:52169269
|
G | A | 1 | a0001c0002t0206g0178 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.238+10499C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52169269 | ||||||
chr15:52169307
|
C | A | 1 | a0001c0003t0112g0087 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.238+10461G>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52169307 | ||||||
chr15:52169400
|
T | A | 3 | a0001c0001t0141g0301a0001c0001t0148g0302a0001c0001t0149g0300 | 3 | HG02258.hp1 HG02615.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.238+10368A>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52169400 | ||||||
chr15:52169406
|
T | C | 3 | a0001c0001t0141g0301a0001c0001t0148g0302a0001c0001t0149g0300 | 3 | HG02258.hp1 HG02615.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.238+10362A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52169406 | ||||||
chr15:52169407
|
G | A | 3 | a0001c0001t0141g0301a0001c0001t0148g0302a0001c0001t0149g0300 | 3 | HG02258.hp1 HG02615.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.238+10361C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52169407 | ||||||
chr15:52169410
|
C | T | 49 | a0001c0001t0001g0202a0001c0001t0016g0332a0001c0001t0016g0343others(46): Show | 49 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(46): Show |
intron_variant | MODIFIER | c.238+10358G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52169410 | ||||||
chr15:52169411
|
A | G | 3 | a0001c0001t0141g0301a0001c0001t0148g0302a0001c0001t0149g0300 | 3 | HG02258.hp1 HG02615.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.238+10357T>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52169411 | ||||||
chr15:52169430
|
C | T | 2 | a0001c0002t0206g0178a0001c0002t0207g0177 | 2 | HG01496.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.238+10338G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52169430 | ||||||
chr15:52169456
|
T | G | 7 | a0001c0004t0014g0002a0001c0004t0014g0280a0001c0004t0014g0290others(4): Show | 9 | HG00738.hp2 HG00741.hp1 HG01069.hp1 others(6): Show |
intron_variant | MODIFIER | c.238+10312A>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52169456 | ||||||
chr15:52169522
|
G | A | 1 | a0004c0008t0005g0234 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.238+10246C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52169522 | ||||||
chr15:52169538
|
C | CA | 20 | a0001c0001t0001g0205a0001c0001t0007g0148a0001c0001t0007g0169others(17): Show | 20 | HG00609.hp1 HG00673.hp2 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.238+10229dupT | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52169538 | ||||||
chr15:52169538
|
C | CAA | 57 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0001g0187others(54): Show | 57 | HG00438.hp2 HG00544.hp1 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.238+10228_238+1022 others(6): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52169538 | ||||||
chr15:52169538
|
C | CAAA | 11 | a0001c0001t0001g0213a0001c0001t0001g0223a0001c0001t0001g0239others(8): Show | 11 | HG00639.hp1 HG00733.hp2 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.238+10227_238+1022 others(7): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52169538 | ||||||
chr15:52169538
|
CA | C | 95 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0008others(92): Show | 95 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.238+10229delT | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52169538 | ||||||
chr15:52169538
|
CAA | C | 65 | a0001c0001t0001g0202a0001c0001t0002g0037a0001c0001t0002g0054others(62): Show | 67 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.238+10228_238+1022 others(6): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52169538 | ||||||
chr15:52169538
|
CAAA | C | 6 | a0001c0001t0034g0346a0001c0001t0141g0301a0001c0001t0148g0302others(3): Show | 6 | HG00099.hp2 HG02258.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.238+10227_238+1022 others(7): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52169538 | ||||||
chr15:52169538
|
CAAAAA | C | 17 | a0001c0001t0011g0319a0001c0002t0006g0291a0001c0002t0006g0314others(14): Show | 17 | HG01243.hp1 HG01891.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.238+10225_238+1022 others(9): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52169538 | ||||||
chr15:52169555
|
A | G | 2 | a0001c0001t0022g0294a0001c0001t0022g0295 | 2 | HG03139.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.238+10213T>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52169555 | ||||||
chr15:52169559
|
A | G | 4 | a0001c0001t0146g0292a0001c0001t0193g0329a0001c0002t0206g0178others(1): Show | 4 | HG01496.hp1 HG01981.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.238+10209T>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52169559 | ||||||
chr15:52169677
|
A | C | 1 | a0001c0002t0206g0178 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.238+10091T>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52169677 | ||||||
chr15:52169682
|
T | C | 200 | a0001c0001t0001g0202a0001c0001t0002g0003a0001c0001t0002g0004others(197): Show | 202 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(199): Show |
intron_variant | MODIFIER | c.238+10086A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52169682 | ||||||
chr15:52169834
|
G | A | 3 | a0001c0001t0141g0301a0001c0001t0148g0302a0001c0001t0149g0300 | 3 | HG02258.hp1 HG02615.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.238+9934C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52169834 | ||||||
chr15:52169896
|
G | A | 1 | a0001c0001t0053g0171 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.238+9872C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52169896 | ||||||
chr15:52170016
|
A | T | 19 | a0001c0001t0011g0319a0001c0001t0162g0361a0001c0002t0006g0291others(16): Show | 19 | HG01243.hp1 HG01255.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.238+9752T>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52170016 | ||||||
chr15:52170264
|
A | C | 97 | a0001c0001t0001g0202a0001c0001t0011g0319a0001c0001t0016g0332others(94): Show | 99 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.238+9504T>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52170264 | ||||||
chr15:52170500
|
G | A | 19 | a0001c0001t0011g0319a0001c0001t0162g0361a0001c0002t0006g0291others(16): Show | 19 | HG01243.hp1 HG01255.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.238+9268C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52170500 | ||||||
chr15:52170712
|
G | GA | 18 | a0001c0001t0011g0319a0001c0001t0016g0344a0001c0001t0038g0115others(15): Show | 18 | HG01243.hp1 HG01891.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.238+9055dupT | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52170712 | ||||||
chr15:52170789
|
C | G | 1 | a0001c0001t0146g0292 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.238+8979G>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52170789 | ||||||
chr15:52170796
|
T | C | 2 | a0001c0002t0206g0178a0001c0002t0207g0177 | 2 | HG01496.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.238+8972A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52170796 | ||||||
chr15:52170821
|
T | C | 1 | a0001c0001t0050g0124 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.238+8947A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52170821 | ||||||
chr15:52170894
|
T | C | 2 | a0001c0002t0206g0178a0001c0002t0207g0177 | 2 | HG01496.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.238+8874A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52170894 | ||||||
chr15:52170934
|
T | TA | 53 | a0001c0001t0001g0202a0001c0001t0016g0332a0001c0001t0016g0343others(50): Show | 53 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.238+8833dupT | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52170934 | ||||||
chr15:52170956
|
T | C | 58 | a0001c0001t0001g0202a0001c0001t0016g0332a0001c0001t0016g0343others(55): Show | 60 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.238+8812A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52170956 | ||||||
chr15:52170985
|
T | C | 3 | a0001c0001t0141g0301a0001c0001t0148g0302a0001c0001t0149g0300 | 3 | HG02258.hp1 HG02615.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.238+8783A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52170985 | ||||||
chr15:52171086
|
C | T | 58 | a0001c0001t0001g0202a0001c0001t0016g0332a0001c0001t0016g0343others(55): Show | 60 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.238+8682G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52171086 | ||||||
chr15:52171093
|
C | CA | 28 | a0001c0001t0001g0189a0001c0001t0001g0256a0001c0001t0001g0262others(25): Show | 30 | HG00438.hp1 HG00738.hp2 HG00741.hp1 others(27): Show |
intron_variant | MODIFIER | c.238+8674dupT | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52171093 | ||||||
chr15:52171093
|
CA | C | 50 | a0001c0001t0001g0192a0001c0001t0001g0242a0001c0001t0002g0036others(47): Show | 50 | HG01099.hp1 HG01243.hp1 HG01255.hp2 others(47): Show |
intron_variant | MODIFIER | c.238+8674delT | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52171093 | ||||||
chr15:52171093
|
CAAAAAAA others(3): Show |
C | 5 | a0001c0001t0022g0294a0001c0001t0022g0295a0001c0001t0023g0296others(2): Show | 5 | HG02559.hp1 HG02886.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.238+8665_238+8674d others(12): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52171093 | ||||||
chr15:52171196
|
T | C | 2 | a0001c0001t0023g0296a0001c0001t0023g0297 | 2 | HG02559.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.238+8572A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52171196 | ||||||
chr15:52171288
|
A | C | 46 | a0001c0001t0001g0202a0001c0001t0016g0332a0001c0001t0016g0343others(43): Show | 46 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(43): Show |
intron_variant | MODIFIER | c.238+8480T>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52171288 | ||||||
chr15:52171296
|
A | G | 7 | a0001c0004t0014g0002a0001c0004t0014g0280a0001c0004t0014g0290others(4): Show | 9 | HG00738.hp2 HG00741.hp1 HG01069.hp1 others(6): Show |
intron_variant | MODIFIER | c.238+8472T>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52171296 | ||||||
chr15:52171435
|
T | G | 1 | a0001c0003t0099g0095 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.238+8333A>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52171435 | ||||||
chr15:52171727
|
T | C | 19 | a0001c0001t0011g0319a0001c0001t0162g0361a0001c0002t0006g0291others(16): Show | 19 | HG01243.hp1 HG01255.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.238+8041A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52171727 | ||||||
chr15:52171837
|
T | C | 15 | a0001c0001t0192g0267a0001c0002t0128g0273a0001c0002t0129g0275others(12): Show | 15 | HG01934.hp2 HG01943.hp2 HG01952.hp1 others(12): Show |
intron_variant | MODIFIER | c.238+7931A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52171837 | ||||||
chr15:52171944
|
G | A | 2 | a0001c0001t0013g0049a0001c0001t0013g0050 | 2 | HG01109.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.238+7824C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52171944 | ||||||
chr15:52171945
|
C | T | 15 | a0001c0001t0192g0267a0001c0002t0128g0273a0001c0002t0129g0275others(12): Show | 15 | HG01934.hp2 HG01943.hp2 HG01952.hp1 others(12): Show |
intron_variant | MODIFIER | c.238+7823G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52171945 | ||||||
chr15:52172176
|
C | T | 95 | a0001c0001t0001g0202a0001c0001t0011g0319a0001c0001t0016g0332others(92): Show | 97 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.238+7592G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52172176 | ||||||
chr15:52172306
|
A | G | 15 | a0001c0001t0192g0267a0001c0002t0128g0273a0001c0002t0129g0275others(12): Show | 15 | HG01934.hp2 HG01943.hp2 HG01952.hp1 others(12): Show |
intron_variant | MODIFIER | c.238+7462T>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52172306 | ||||||
chr15:52172358
|
C | G | 1 | a0001c0001t0102g0170 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.238+7410G>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52172358 | ||||||
chr15:52172393
|
G | A | 1 | a0001c0001t0059g0125 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.238+7375C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52172393 | ||||||
chr15:52172426
|
G | T | 1 | a0001c0001t0146g0292 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.238+7342C>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52172426 | ||||||
chr15:52172450
|
C | T | 30 | a0001c0001t0002g0174a0001c0001t0007g0139a0001c0001t0007g0144others(27): Show | 30 | HG00609.hp1 HG02027.hp2 HG02698.hp2 others(27): Show |
intron_variant | MODIFIER | c.238+7318G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52172450 | ||||||
chr15:52172487
|
A | C | 5 | a0001c0001t0094g0090a0001c0002t0019g0092a0001c0002t0019g0093others(2): Show | 5 | HG01884.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.238+7281T>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52172487 | ||||||
chr15:52172539
|
G | A | 12 | a0001c0001t0022g0294a0001c0001t0022g0295a0001c0001t0023g0296others(9): Show | 14 | HG00738.hp2 HG00741.hp1 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.238+7229C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52172539 | ||||||
chr15:52172593
|
G | A | 2 | a0001c0001t0002g0030a0001c0001t0002g0051 | 2 | HG00323.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.238+7175C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52172593 | ||||||
chr15:52172609
|
G | A | 3 | a0001c0001t0141g0301a0001c0001t0148g0302a0001c0001t0149g0300 | 3 | HG02258.hp1 HG02615.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.238+7159C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52172609 | ||||||
chr15:52172716
|
T | C | 1 | a0001c0001t0002g0004 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.238+7052A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52172716 | ||||||
chr15:52172798
|
G | A | 2 | a0001c0001t0195g0337a0001c0001t0200g0360 | 2 | HG01175.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.238+6970C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52172798 | ||||||
chr15:52172850
|
G | A | 7 | a0001c0004t0014g0002a0001c0004t0014g0280a0001c0004t0014g0290others(4): Show | 9 | HG00738.hp2 HG00741.hp1 HG01069.hp1 others(6): Show |
intron_variant | MODIFIER | c.238+6918C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52172850 | ||||||
chr15:52172981
|
G | T | 1 | a0001c0003t0126g0313 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.238+6787C>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52172981 | ||||||
chr15:52173287
|
C | A | 9 | a0001c0001t0094g0090a0001c0001t0145g0279a0001c0002t0019g0092others(6): Show | 9 | HG01884.hp1 HG01891.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.238+6481G>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52173287 | ||||||
chr15:52173376
|
A | G | 7 | a0001c0002t0024g0281a0001c0002t0024g0284a0001c0002t0025g0282others(4): Show | 7 | HG02109.hp2 HG02257.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.238+6392T>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52173376 | ||||||
chr15:52173390
|
A | G | 165 | a0001c0001t0001g0248a0001c0001t0002g0003a0001c0001t0002g0004others(162): Show | 165 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.238+6378T>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52173390 | ||||||
chr15:52173465
|
G | A | 1 | a0001c0001t0001g0216 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.238+6303C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52173465 | ||||||
chr15:52173617
|
G | A | 1 | a0001c0001t0002g0008 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.238+6151C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52173617 | ||||||
chr15:52173886
|
A | G | 96 | a0001c0001t0001g0202a0001c0001t0001g0326a0001c0001t0011g0319others(93): Show | 98 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.238+5882T>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52173886 | ||||||
chr15:52173917
|
A | AAAGGTAT others(77): Show |
1 | a0001c0001t0001g0223 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.238+5767_238+5850d others(86): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52173917 | ||||||
chr15:52173952
|
C | T | 12 | a0001c0001t0011g0319a0001c0002t0006g0291a0001c0002t0006g0314others(9): Show | 12 | HG01243.hp1 HG02055.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.238+5816G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52173952 | ||||||
chr15:52173984
|
G | C | 1 | a0001c0001t0146g0292 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.238+5784C>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52173984 | ||||||
chr15:52174323
|
A | G | 15 | a0001c0001t0192g0267a0001c0002t0128g0273a0001c0002t0129g0275others(12): Show | 15 | HG01934.hp2 HG01943.hp2 HG01952.hp1 others(12): Show |
intron_variant | MODIFIER | c.238+5445T>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52174323 | ||||||
chr15:52174380
|
T | G | 18 | a0001c0001t0141g0301a0001c0001t0148g0302a0001c0001t0149g0300others(15): Show | 18 | HG01934.hp2 HG01943.hp2 HG01952.hp1 others(15): Show |
intron_variant | MODIFIER | c.238+5388A>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52174380 | ||||||
chr15:52174458
|
G | A | 1 | a0001c0002t0026g0287 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.238+5310C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52174458 | ||||||
chr15:52174524
|
T | C | 1 | a0001c0001t0036g0065 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.238+5244A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52174524 | ||||||
chr15:52174559
|
C | A | 1 | a0001c0001t0002g0051 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.238+5209G>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52174559 | ||||||
chr15:52174672
|
GCCTTAAG others(2): Show |
G | 109 | a0001c0001t0001g0202a0001c0001t0001g0326a0001c0001t0011g0319others(106): Show | 111 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.238+5087_238+5095d others(11): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52174672 | ||||||
chr15:52174750
|
C | T | 3 | a0001c0001t0141g0301a0001c0001t0148g0302a0001c0001t0149g0300 | 3 | HG02258.hp1 HG02615.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.238+5018G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52174750 | ||||||
chr15:52174778
|
TC | T | 7 | a0001c0002t0024g0281a0001c0002t0024g0284a0001c0002t0025g0282others(4): Show | 7 | HG02109.hp2 HG02257.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.238+4989delG | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52174778 | ||||||
chr15:52174973
|
C | T | 1 | a0001c0003t0119g0094 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.238+4795G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52174973 | ||||||
chr15:52175074
|
AAAAC | A | 9 | a0001c0001t0010g0112a0001c0001t0018g0133a0001c0001t0030g0182others(6): Show | 9 | HG00597.hp1 HG02015.hp2 HG02056.hp2 others(6): Show |
intron_variant | MODIFIER | c.238+4690_238+4693d others(6): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52175074 | ||||||
chr15:52175324
|
C | T | 1 | a0001c0001t0007g0139 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.238+4444G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52175324 | ||||||
chr15:52175329
|
C | T | 12 | a0001c0001t0022g0294a0001c0001t0022g0295a0001c0001t0023g0296others(9): Show | 14 | HG00738.hp2 HG00741.hp1 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.238+4439G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52175329 | ||||||
chr15:52175349
|
C | G | 84 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0008others(81): Show | 84 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.238+4419G>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52175349 | ||||||
chr15:52175582
|
T | C | 1 | a0001c0001t0005g0236 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.238+4186A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52175582 | ||||||
chr15:52175711
|
C | T | 1 | a0001c0005t0156g0261 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.238+4057G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52175711 | ||||||
chr15:52175713
|
T | C | 1 | a0001c0001t0002g0004 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.238+4055A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52175713 | ||||||
chr15:52175722
|
G | A | 12 | a0001c0001t0022g0294a0001c0001t0022g0295a0001c0001t0023g0296others(9): Show | 14 | HG00738.hp2 HG00741.hp1 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.238+4046C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52175722 | ||||||
chr15:52175741
|
A | AAAAC | 280 | a0001c0001t0001g0202a0001c0001t0001g0248a0001c0001t0001g0326others(277): Show | 282 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(279): Show |
intron_variant | MODIFIER | c.238+4023_238+4026d others(6): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52175741 | ||||||
chr15:52175961
|
A | T | 31 | a0001c0001t0001g0248a0001c0001t0002g0174a0001c0001t0007g0139others(28): Show | 31 | HG00609.hp1 HG02027.hp2 HG02698.hp2 others(28): Show |
intron_variant | MODIFIER | c.238+3807T>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52175961 | ||||||
chr15:52176053
|
A | C | 6 | a0001c0001t0010g0112a0001c0001t0040g0113a0001c0001t0041g0128others(3): Show | 6 | HG00597.hp1 HG02056.hp2 HG02135.hp2 others(3): Show |
intron_variant | MODIFIER | c.238+3715T>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52176053 | ||||||
chr15:52176086
|
C | CAG | 92 | a0001c0001t0001g0202a0001c0001t0001g0326a0001c0001t0011g0319others(89): Show | 94 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.238+3681_238+3682i others(4): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52176086 | ||||||
chr15:52176086
|
C | G | 1 | a0001c0001t0016g0344 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.238+3682G>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52176086 | ||||||
chr15:52176176
|
T | C | 12 | a0001c0001t0011g0319a0001c0002t0006g0291a0001c0002t0006g0314others(9): Show | 12 | HG01243.hp1 HG02055.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.238+3592A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52176176 | ||||||
chr15:52176350
|
C | T | 12 | a0001c0001t0011g0319a0001c0002t0006g0291a0001c0002t0006g0314others(9): Show | 12 | HG01243.hp1 HG02055.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.238+3418G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52176350 | ||||||
chr15:52176351
|
G | A | 1 | a0001c0001t0115g0024 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.238+3417C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52176351 | ||||||
chr15:52176363
|
G | T | 12 | a0001c0001t0022g0294a0001c0001t0022g0295a0001c0001t0023g0296others(9): Show | 14 | HG00738.hp2 HG00741.hp1 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.238+3405C>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52176363 | ||||||
chr15:52176463
|
C | T | 8 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0001g0194others(5): Show | 8 | HG00438.hp2 HG00621.hp1 HG02056.hp1 others(5): Show |
intron_variant | MODIFIER | c.238+3305G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52176463 | ||||||
chr15:52176499
|
G | A | 1 | a0001c0001t0002g0051 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.238+3269C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52176499 | ||||||
chr15:52176523
|
C | T | 9 | a0001c0001t0094g0090a0001c0001t0145g0279a0001c0002t0019g0092others(6): Show | 9 | HG01884.hp1 HG01891.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.238+3245G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52176523 | ||||||
chr15:52176704
|
T | C | 2 | a0001c0003t0112g0087a0001c0003t0126g0313 | 2 | HG02055.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.238+3064A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52176704 | ||||||
chr15:52176759
|
C | T | 1 | a0001c0001t0146g0292 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.238+3009G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52176759 | ||||||
chr15:52176826
|
C | T | 14 | a0001c0001t0192g0267a0001c0002t0128g0273a0001c0002t0129g0275others(11): Show | 14 | HG01934.hp2 HG01943.hp2 HG01952.hp1 others(11): Show |
intron_variant | MODIFIER | c.238+2942G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52176826 | ||||||
chr15:52176832
|
A | G | 13 | a0001c0001t0094g0090a0001c0001t0145g0279a0001c0001t0146g0292others(10): Show | 13 | HG01496.hp1 HG01884.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.238+2936T>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52176832 | ||||||
chr15:52176984
|
A | C | 53 | a0001c0001t0001g0326a0001c0001t0016g0332a0001c0001t0016g0343others(50): Show | 53 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.238+2784T>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52176984 | ||||||
chr15:52176995
|
A | G | 40 | a0001c0001t0001g0326a0001c0001t0016g0332a0001c0001t0016g0343others(37): Show | 40 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(37): Show |
intron_variant | MODIFIER | c.238+2773T>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52176995 | ||||||
chr15:52177011
|
C | T | 1 | a0001c0001t0002g0074 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.238+2757G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52177011 | ||||||
chr15:52177019
|
T | A | 1 | a0001c0001t0086g0161 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.238+2749A>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52177019 | ||||||
chr15:52177020
|
A | G | 1 | a0001c0001t0086g0161 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.238+2748T>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52177020 | ||||||
chr15:52177028
|
C | CT | 39 | a0001c0001t0001g0191a0001c0001t0001g0249a0001c0001t0002g0053others(36): Show | 39 | HG00609.hp1 HG01109.hp1 HG01175.hp1 others(36): Show |
intron_variant | MODIFIER | c.238+2739dupA | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52177028 | ||||||
chr15:52177028
|
C | CTT | 46 | a0001c0001t0001g0326a0001c0001t0011g0319a0001c0001t0016g0332others(43): Show | 46 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(43): Show |
intron_variant | MODIFIER | c.238+2738_238+2739d others(4): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52177028 | ||||||
chr15:52177028
|
C | CTTT | 14 | a0001c0001t0022g0294a0001c0001t0022g0295a0001c0001t0023g0297others(11): Show | 14 | HG00735.hp2 HG00741.hp2 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.238+2737_238+2739d others(5): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52177028 | ||||||
chr15:52177028
|
C | CTTTT | 7 | a0001c0001t0023g0296a0001c0004t0014g0002a0001c0004t0014g0280others(4): Show | 9 | HG00738.hp2 HG00741.hp1 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.238+2736_238+2739d others(6): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52177028 | ||||||
chr15:52177028
|
CT | C | 84 | a0001c0001t0001g0262a0001c0001t0002g0003a0001c0001t0002g0004others(81): Show | 84 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.238+2739delA | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52177028 | ||||||
chr15:52177073
|
C | T | 1 | a0001c0001t0169g0352 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.238+2695G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52177073 | ||||||
chr15:52177104
|
G | C | 7 | a0001c0001t0037g0163a0001c0001t0066g0164a0001c0001t0070g0157others(4): Show | 7 | HG01123.hp2 HG01192.hp1 HG02698.hp1 others(4): Show |
intron_variant | MODIFIER | c.238+2664C>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52177104 | ||||||
chr15:52177279
|
C | T | 52 | a0001c0001t0001g0326a0001c0001t0011g0319a0001c0001t0016g0332others(49): Show | 52 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.238+2489G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52177279 | ||||||
chr15:52177330
|
T | G | 26 | a0001c0001t0022g0294a0001c0001t0022g0295a0001c0001t0023g0296others(23): Show | 28 | HG00738.hp2 HG00741.hp1 HG01069.hp1 others(25): Show |
intron_variant | MODIFIER | c.238+2438A>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52177330 | ||||||
chr15:52177397
|
C | T | 2 | a0001c0002t0206g0178a0001c0002t0207g0177 | 2 | HG01496.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.238+2371G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52177397 | ||||||
chr15:52177465
|
C | T | 2 | a0001c0001t0151g0353a0001c0003t0127g0356 | 2 | HG03579.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.238+2303G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52177465 | ||||||
chr15:52177607
|
T | C | 78 | a0001c0001t0001g0326a0001c0001t0011g0319a0001c0001t0016g0332others(75): Show | 80 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.238+2161A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52177607 | ||||||
chr15:52177650
|
C | CA | 35 | a0001c0001t0003g0005a0001c0001t0004g0066a0001c0001t0047g0127others(32): Show | 35 | HG00673.hp2 HG01109.hp1 HG01496.hp1 others(32): Show |
intron_variant | MODIFIER | c.238+2117dupT | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52177650 | ||||||
chr15:52177650
|
CA | C | 14 | a0001c0001t0001g0223a0001c0001t0022g0294a0001c0001t0022g0295others(11): Show | 16 | HG00609.hp1 HG00738.hp2 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.238+2117delT | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52177650 | ||||||
chr15:52177659
|
A | G | 52 | a0001c0001t0001g0326a0001c0001t0011g0319a0001c0001t0016g0332others(49): Show | 52 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.238+2109T>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52177659 | ||||||
chr15:52177781
|
TA | T | 14 | a0001c0001t0192g0267a0001c0002t0128g0273a0001c0002t0129g0275others(11): Show | 14 | HG01934.hp2 HG01943.hp2 HG01952.hp1 others(11): Show |
intron_variant | MODIFIER | c.238+1986delT | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52177781 | ||||||
chr15:52177892
|
C | T | 1 | a0001c0001t0005g0236 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.238+1876G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52177892 | ||||||
chr15:52178072
|
G | A | 12 | a0001c0001t0022g0294a0001c0001t0022g0295a0001c0001t0023g0296others(9): Show | 14 | HG00738.hp2 HG00741.hp1 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.238+1696C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52178072 | ||||||
chr15:52178089
|
A | G | 14 | a0001c0001t0192g0267a0001c0002t0128g0273a0001c0002t0129g0275others(11): Show | 14 | HG01934.hp2 HG01943.hp2 HG01952.hp1 others(11): Show |
intron_variant | MODIFIER | c.238+1679T>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52178089 | ||||||
chr15:52178425
|
T | C | 1 | a0001c0005t0156g0261 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.238+1343A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52178425 | ||||||
chr15:52178462
|
A | G | 12 | a0001c0001t0022g0294a0001c0001t0022g0295a0001c0001t0023g0296others(9): Show | 14 | HG00738.hp2 HG00741.hp1 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.238+1306T>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52178462 | ||||||
chr15:52178607
|
ACT | A | 12 | a0001c0001t0022g0294a0001c0001t0022g0295a0001c0001t0023g0296others(9): Show | 14 | HG00738.hp2 HG00741.hp1 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.238+1159_238+1160d others(4): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52178607 | ||||||
chr15:52178863
|
G | A | 14 | a0001c0001t0192g0267a0001c0002t0128g0273a0001c0002t0129g0275others(11): Show | 14 | HG01934.hp2 HG01943.hp2 HG01952.hp1 others(11): Show |
intron_variant | MODIFIER | c.238+905C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52178863 | ||||||
chr15:52178939
|
A | G | 352 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0001g0187others(349): Show | 354 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(351): Show |
intron_variant | MODIFIER | c.238+829T>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52178939 | ||||||
chr15:52179229
|
T | C | 264 | a0001c0001t0001g0248a0001c0001t0001g0326a0001c0001t0002g0003others(261): Show | 266 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(263): Show |
intron_variant | MODIFIER | c.238+539A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52179229 | ||||||
chr15:52179350
|
G | T | 66 | a0001c0001t0001g0326a0001c0001t0011g0319a0001c0001t0016g0332others(63): Show | 66 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(63): Show |
intron_variant | MODIFIER | c.238+418C>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52179350 | ||||||
chr15:52179409
|
C | A | 88 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0001g0187others(85): Show | 88 | HG00438.hp2 HG00544.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.238+359G>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52179409 | ||||||
chr15:52179498
|
GA | G | 5 | a0001c0001t0022g0294a0001c0001t0022g0295a0001c0001t0023g0296others(2): Show | 5 | HG02559.hp1 HG02886.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.238+269delT | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52179498 | ||||||
chr15:52179499
|
A | G | 259 | a0001c0001t0001g0248a0001c0001t0001g0326a0001c0001t0002g0003others(256): Show | 261 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(258): Show |
intron_variant | MODIFIER | c.238+269T>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52179499 | ||||||
chr15:52179503
|
C | A | 1 | a0001c0001t0146g0292 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.238+265G>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52179503 | ||||||
chr15:52179561
|
C | T | 1 | a0001c0001t0146g0292 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.238+207G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52179561 | ||||||
chr15:52179588
|
G | T | 1 | a0001c0001t0169g0352 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.238+180C>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52179588 | ||||||
chr15:52179653
|
G | A | 6 | a0001c0001t0192g0267a0001c0002t0135g0270a0001c0002t0136g0268others(3): Show | 6 | HG01943.hp2 HG02004.hp1 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.238+115C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52179653 | ||||||
chr15:52179731
|
T | G | 1 | a0001c0001t0002g0084 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.238+37A>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 3/12 | chr15 | 52179731 | ||||||
chr15:52179923
|
T | C | 12 | a0001c0001t0022g0294a0001c0001t0022g0295a0001c0001t0023g0296others(9): Show | 14 | HG00738.hp2 HG00741.hp1 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.127-44A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 2/12 | chr15 | 52179923 | ||||||
chr15:52179936
|
G | A | 1 | a0001c0001t0002g0004 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.127-57C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 2/12 | chr15 | 52179936 | ||||||
chr15:52179957
|
C | A | 1 | a0001c0001t0170g0338 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.127-78G>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 2/12 | chr15 | 52179957 | ||||||
chr15:52179957
|
C | G | 1 | a0001c0001t0001g0221 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.127-78G>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 2/12 | chr15 | 52179957 | ||||||
chr15:52180019
|
G | A | 1 | a0001c0001t0037g0163 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.127-140C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 2/12 | chr15 | 52180019 | ||||||
chr15:52180076
|
G | C | 51 | a0001c0001t0011g0319a0001c0001t0016g0332a0001c0001t0016g0343others(48): Show | 51 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.127-197C>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 2/12 | chr15 | 52180076 | ||||||
chr15:52180100
|
G | C | 2 | a0001c0001t0012g0180a0001c0001t0012g0181 | 2 | HG03491.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.127-221C>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 2/12 | chr15 | 52180100 | ||||||
chr15:52180165
|
A | G | 1 | a0001c0001t0034g0346 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.127-286T>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 2/12 | chr15 | 52180165 | ||||||
chr15:52180219
|
G | T | 35 | a0001c0001t0002g0174a0001c0001t0007g0139a0001c0001t0007g0144others(32): Show | 35 | HG00609.hp1 HG02027.hp2 HG02451.hp1 others(32): Show |
intron_variant | MODIFIER | c.127-340C>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 2/12 | chr15 | 52180219 | ||||||
chr15:52180305
|
T | C | 1 | a0001c0002t0134g0277 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.127-426A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 2/12 | chr15 | 52180305 | ||||||
chr15:52180348
|
T | C | 1 | a0001c0001t0049g0101 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.127-469A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 2/12 | chr15 | 52180348 | ||||||
chr15:52180454
|
T | G | 4 | a0001c0001t0002g0026a0001c0001t0002g0053a0001c0001t0065g0079others(1): Show | 4 | HG00323.hp2 HG01175.hp1 NA20805.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-575A>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 2/12 | chr15 | 52180454 | ||||||
chr15:52180486
|
G | T | 52 | a0001c0001t0001g0326a0001c0001t0011g0319a0001c0001t0016g0332others(49): Show | 52 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.127-607C>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 2/12 | chr15 | 52180486 | ||||||
chr15:52180516
|
A | G | 32 | a0001c0001t0001g0326a0001c0001t0016g0332a0001c0001t0016g0343others(29): Show | 32 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(29): Show |
intron_variant | MODIFIER | c.127-637T>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 2/12 | chr15 | 52180516 | ||||||
chr15:52180575
|
G | A | 7 | a0001c0002t0024g0281a0001c0002t0024g0284a0001c0002t0025g0282others(4): Show | 7 | HG02109.hp2 HG02257.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.127-696C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 2/12 | chr15 | 52180575 | ||||||
chr15:52180634
|
C | T | 2 | a0001c0006t0142g0310a0001c0006t0143g0312 | 2 | HG02559.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.127-755G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 2/12 | chr15 | 52180634 | ||||||
chr15:52180646
|
C | A | 14 | a0001c0001t0192g0267a0001c0002t0128g0273a0001c0002t0129g0275others(11): Show | 14 | HG01934.hp2 HG01943.hp2 HG01952.hp1 others(11): Show |
intron_variant | MODIFIER | c.127-767G>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 2/12 | chr15 | 52180646 | ||||||
chr15:52180758
|
T | G | 91 | a0001c0001t0001g0326a0001c0001t0011g0319a0001c0001t0016g0332others(88): Show | 93 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.127-879A>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 2/12 | chr15 | 52180758 | ||||||
chr15:52180843
|
G | A | 5 | a0001c0001t0022g0294a0001c0001t0022g0295a0001c0001t0023g0296others(2): Show | 5 | HG02559.hp1 HG02886.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.127-964C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 2/12 | chr15 | 52180843 | ||||||
chr15:52180941
|
T | C | 2 | a0001c0001t0002g0054a0001c0001t0002g0055 | 2 | HG01081.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.127-1062A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 2/12 | chr15 | 52180941 | ||||||
chr15:52180974
|
T | C | 1 | a0001c0001t0110g0009 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.127-1095A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 2/12 | chr15 | 52180974 | ||||||
chr15:52181129
|
T | C | 14 | a0001c0001t0192g0267a0001c0002t0128g0273a0001c0002t0129g0275others(11): Show | 14 | HG01934.hp2 HG01943.hp2 HG01952.hp1 others(11): Show |
intron_variant | MODIFIER | c.127-1250A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 2/12 | chr15 | 52181129 | ||||||
chr15:52181338
|
G | A | 51 | a0001c0001t0011g0319a0001c0001t0016g0332a0001c0001t0016g0343others(48): Show | 51 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.127-1459C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 2/12 | chr15 | 52181338 | ||||||
chr15:52181388
|
G | A | 5 | a0001c0002t0006g0314a0001c0002t0006g0321a0001c0002t0035g0322others(2): Show | 5 | HG01243.hp1 HG02055.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.127-1509C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 2/12 | chr15 | 52181388 | ||||||
chr15:52181506
|
C | T | 2 | a0001c0001t0013g0035a0001c0001t0013g0067 | 2 | HG00738.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.127-1627G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 2/12 | chr15 | 52181506 | ||||||
chr15:52181519
|
G | A | 51 | a0001c0001t0011g0319a0001c0001t0016g0332a0001c0001t0016g0343others(48): Show | 51 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.127-1640C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 2/12 | chr15 | 52181519 | ||||||
chr15:52181570
|
C | T | 12 | a0001c0001t0022g0294a0001c0001t0022g0295a0001c0001t0023g0296others(9): Show | 14 | HG00738.hp2 HG00741.hp1 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.127-1691G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 2/12 | chr15 | 52181570 | ||||||
chr15:52181609
|
CA | C | 14 | a0001c0001t0192g0267a0001c0002t0128g0273a0001c0002t0129g0275others(11): Show | 14 | HG01934.hp2 HG01943.hp2 HG01952.hp1 others(11): Show |
intron_variant | MODIFIER | c.127-1731delT | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 2/12 | chr15 | 52181609 | ||||||
chr15:52181617
|
AC | A | 7 | a0001c0004t0014g0002a0001c0004t0014g0280a0001c0004t0014g0290others(4): Show | 9 | HG00738.hp2 HG00741.hp1 HG01069.hp1 others(6): Show |
intron_variant | MODIFIER | c.127-1739delG | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 2/12 | chr15 | 52181617 | ||||||
chr15:52181618
|
C | A | 18 | a0001c0001t0022g0294a0001c0001t0022g0295a0001c0001t0023g0296others(15): Show | 18 | HG01496.hp1 HG01884.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.127-1739G>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 2/12 | chr15 | 52181618 | ||||||
chr15:52181650
|
G | A | 6 | a0001c0001t0192g0267a0001c0002t0135g0270a0001c0002t0136g0268others(3): Show | 6 | HG01943.hp2 HG02004.hp1 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.127-1771C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 2/12 | chr15 | 52181650 | ||||||
chr15:52181691
|
C | T | 6 | a0001c0001t0151g0353a0001c0003t0021g0354a0001c0003t0021g0355others(3): Show | 6 | HG01891.hp2 HG03139.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.127-1812G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 2/12 | chr15 | 52181691 | ||||||
chr15:52181835
|
A | C | 1 | a0001c0001t0001g0262 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.127-1956T>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 2/12 | chr15 | 52181835 | ||||||
chr15:52181880
|
A | G | 1 | a0001c0002t0207g0177 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.127-2001T>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 2/12 | chr15 | 52181880 | ||||||
chr15:52181896
|
CAT | C | 14 | a0001c0001t0192g0267a0001c0002t0128g0273a0001c0002t0129g0275others(11): Show | 14 | HG01934.hp2 HG01943.hp2 HG01952.hp1 others(11): Show |
intron_variant | MODIFIER | c.127-2019_127-2018d others(4): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 2/12 | chr15 | 52181896 | ||||||
chr15:52181907
|
C | T | 5 | a0001c0001t0022g0294a0001c0001t0022g0295a0001c0001t0023g0296others(2): Show | 5 | HG02559.hp1 HG02886.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.127-2028G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 2/12 | chr15 | 52181907 | ||||||
chr15:52182002
|
A | G | 14 | a0001c0001t0192g0267a0001c0002t0128g0273a0001c0002t0129g0275others(11): Show | 14 | HG01934.hp2 HG01943.hp2 HG01952.hp1 others(11): Show |
intron_variant | MODIFIER | c.127-2123T>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 2/12 | chr15 | 52182002 | ||||||
chr15:52182125
|
A | G | 2 | a0002c0007t0039g0150a0002c0007t0081g0175 | 2 | HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.127-2246T>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 2/12 | chr15 | 52182125 | ||||||
chr15:52182466
|
G | A | 9 | a0001c0001t0094g0090a0001c0001t0145g0279a0001c0002t0019g0092others(6): Show | 9 | HG01884.hp1 HG01891.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.126+2085C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 2/12 | chr15 | 52182466 | ||||||
chr15:52182599
|
T | G | 1 | a0001c0002t0207g0177 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.126+1952A>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 2/12 | chr15 | 52182599 | ||||||
chr15:52182686
|
C | T | 8 | a0001c0001t0151g0353a0001c0001t0162g0361a0001c0003t0021g0354others(5): Show | 8 | HG01255.hp2 HG01891.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.126+1865G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 2/12 | chr15 | 52182686 | ||||||
chr15:52182803
|
T | C | 1 | a0001c0003t0112g0087 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.126+1748A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 2/12 | chr15 | 52182803 | ||||||
chr15:52182946
|
G | A | 31 | a0001c0001t0016g0332a0001c0001t0016g0343a0001c0001t0016g0344others(28): Show | 31 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(28): Show |
intron_variant | MODIFIER | c.126+1605C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 2/12 | chr15 | 52182946 | ||||||
chr15:52182985
|
C | T | 7 | a0001c0004t0014g0002a0001c0004t0014g0280a0001c0004t0014g0290others(4): Show | 9 | HG00738.hp2 HG00741.hp1 HG01069.hp1 others(6): Show |
intron_variant | MODIFIER | c.126+1566G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 2/12 | chr15 | 52182985 | ||||||
chr15:52183094
|
G | A | 3 | a0001c0001t0141g0301a0001c0001t0148g0302a0001c0001t0149g0300 | 3 | HG02258.hp1 HG02615.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.126+1457C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 2/12 | chr15 | 52183094 | ||||||
chr15:52183103
|
G | A | 83 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0001g0187others(80): Show | 83 | HG00438.hp2 HG00544.hp1 HG00558.hp2 others(80): Show |
intron_variant | MODIFIER | c.126+1448C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 2/12 | chr15 | 52183103 | ||||||
chr15:52183247
|
A | C | 3 | a0001c0001t0023g0296a0001c0001t0023g0297a0001c0001t0144g0298 | 3 | HG02559.hp1 HG02886.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.126+1304T>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 2/12 | chr15 | 52183247 | ||||||
chr15:52183333
|
T | TG | 172 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(169): Show | 172 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(169): Show |
intron_variant | MODIFIER | c.126+1217dupC | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 2/12 | chr15 | 52183333 | ||||||
chr15:52183333
|
T | TGG | 55 | a0001c0001t0002g0003a0001c0001t0002g0010a0001c0001t0002g0011others(52): Show | 55 | HG00099.hp1 HG00323.hp1 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.126+1216_126+1217d others(4): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 2/12 | chr15 | 52183333 | ||||||
chr15:52183333
|
T | TGGG | 23 | a0001c0001t0002g0059a0001c0001t0002g0081a0001c0001t0002g0082others(20): Show | 23 | HG00597.hp1 HG01255.hp1 HG01358.hp2 others(20): Show |
intron_variant | MODIFIER | c.126+1215_126+1217d others(5): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 2/12 | chr15 | 52183333 | ||||||
chr15:52183335
|
G | GC | 12 | a0001c0001t0022g0294a0001c0001t0022g0295a0001c0001t0023g0296others(9): Show | 14 | HG00738.hp2 HG00741.hp1 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.126+1215_126+1216i others(3): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 2/12 | chr15 | 52183335 | ||||||
chr15:52183615
|
C | T | 7 | a0001c0004t0014g0002a0001c0004t0014g0280a0001c0004t0014g0290others(4): Show | 9 | HG00738.hp2 HG00741.hp1 HG01069.hp1 others(6): Show |
intron_variant | MODIFIER | c.126+936G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 2/12 | chr15 | 52183615 | ||||||
chr15:52183965
|
G | A | 1 | a0001c0001t0074g0162 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.126+586C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 2/12 | chr15 | 52183965 | ||||||
chr15:52184202
|
C | A | 1 | a0001c0001t0145g0279 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.126+349G>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 2/12 | chr15 | 52184202 | ||||||
chr15:52184283
|
C | A | 86 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0001g0187others(83): Show | 86 | HG00438.hp2 HG00544.hp1 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.126+268G>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 2/12 | chr15 | 52184283 | ||||||
chr15:52184419
|
C | T | 3 | a0001c0001t0007g0144a0001c0001t0015g0145a0001c0001t0015g0146 | 3 | NA18946.hp1 NA18981.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.126+132G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 2/12 | chr15 | 52184419 | ||||||
chr15:52184490
|
A | C | 14 | a0001c0001t0192g0267a0001c0002t0128g0273a0001c0002t0129g0275others(11): Show | 14 | HG01934.hp2 HG01943.hp2 HG01952.hp1 others(11): Show |
intron_variant | MODIFIER | c.126+61T>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 2/12 | chr15 | 52184490 | ||||||
chr15:52184964
|
T | C | 5 | a0001c0001t0022g0294a0001c0001t0022g0295a0001c0001t0023g0296others(2): Show | 5 | HG02559.hp1 HG02886.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.-18-270A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 1/12 | chr15 | 52184964 | ||||||
chr15:52185004
|
A | G | 1 | a0001c0001t0145g0279 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-18-310T>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 1/12 | chr15 | 52185004 | ||||||
chr15:52185005
|
A | G | 3 | a0001c0001t0022g0294a0001c0001t0022g0295a0001c0001t0145g0279 | 3 | HG01891.hp1 HG03139.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-18-311T>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 1/12 | chr15 | 52185005 | ||||||
chr15:52185013
|
C | T | 355 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0001g0187others(352): Show | 357 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(354): Show |
intron_variant | MODIFIER | c.-18-319G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 1/12 | chr15 | 52185013 | ||||||
chr15:52185146
|
G | C | 1 | a0001c0001t0086g0161 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-18-452C>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 1/12 | chr15 | 52185146 | ||||||
chr15:52185155
|
G | A | 1 | a0001c0001t0145g0279 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-18-461C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 1/12 | chr15 | 52185155 | ||||||
chr15:52185253
|
A | G | 9 | a0001c0001t0094g0090a0001c0001t0145g0279a0001c0002t0019g0092others(6): Show | 9 | HG01884.hp1 HG01891.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.-18-559T>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 1/12 | chr15 | 52185253 | ||||||
chr15:52185360
|
AATCTGTC others(8): Show |
A | 1 | a0001c0001t0002g0073 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-18-681_-18-667del others(15): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 1/12 | chr15 | 52185360 | ||||||
chr15:52185414
|
A | G | 1 | a0001c0001t0166g0345 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-18-720T>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 1/12 | chr15 | 52185414 | ||||||
chr15:52185505
|
G | A | 1 | a0001c0001t0001g0326 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.-18-811C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 1/12 | chr15 | 52185505 | ||||||
chr15:52185612
|
G | A | 31 | a0001c0001t0016g0332a0001c0001t0016g0343a0001c0001t0016g0344others(28): Show | 31 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(28): Show |
intron_variant | MODIFIER | c.-18-918C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 1/12 | chr15 | 52185612 | ||||||
chr15:52185750
|
CT | C | 20 | a0001c0001t0003g0027a0001c0001t0016g0332a0001c0001t0016g0343others(17): Show | 20 | HG00408.hp2 HG00735.hp2 HG01175.hp2 others(17): Show |
intron_variant | MODIFIER | c.-18-1057delA | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 1/12 | chr15 | 52185750 | ||||||
chr15:52185752
|
TTTTATTA others(3): Show |
T | 1 | a0001c0002t0006g0316 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-18-1068_-18-1059d others(12): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 1/12 | chr15 | 52185752 | ||||||
chr15:52185752
|
TTTTATTA others(18): Show |
T | 1 | a0001c0001t0169g0352 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-18-1083_-18-1059d others(27): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 1/12 | chr15 | 52185752 | ||||||
chr15:52185753
|
T | TTA | 15 | a0001c0001t0011g0319a0001c0001t0033g0348a0001c0001t0034g0346others(12): Show | 15 | HG00099.hp2 HG00741.hp2 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.-18-1060_-18-1059i others(4): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 1/12 | chr15 | 52185753 | ||||||
chr15:52185753
|
T | TTATTA | 3 | a0001c0001t0032g0350a0001c0001t0198g0351a0001c0002t0035g0324 | 3 | HG00438.hp1 HG01257.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-18-1060_-18-1059i others(7): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 1/12 | chr15 | 52185753 | ||||||
chr15:52185753
|
T | TTTA | 91 | a0001c0001t0001g0221a0001c0001t0001g0223a0001c0001t0001g0229others(88): Show | 91 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.-18-1062_-18-1060d others(5): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 1/12 | chr15 | 52185753 | ||||||
chr15:52185753
|
T | TTTATTA | 31 | a0001c0001t0001g0237a0001c0001t0001g0238a0001c0001t0001g0239others(28): Show | 31 | HG00639.hp1 HG00673.hp2 HG00733.hp2 others(28): Show |
intron_variant | MODIFIER | c.-18-1065_-18-1060d others(8): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 1/12 | chr15 | 52185753 | ||||||
chr15:52185753
|
T | TTTATTAT others(5): Show |
2 | a0001c0001t0001g0241a0001c0001t0018g0133 | 2 | HG02015.hp2 NA18965.hp2 |
intron_variant | MODIFIER | c.-18-1071_-18-1060d others(14): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 1/12 | chr15 | 52185753 | ||||||
chr15:52185753
|
T | TTTTTTA | 4 | a0001c0001t0004g0028a0001c0001t0004g0029a0001c0001t0004g0075others(1): Show | 4 | HG02965.hp2 NA19012.hp2 NA19081.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18-1060_-18-1059i others(8): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 1/12 | chr15 | 52185753 | ||||||
chr15:52185753
|
TTTA | T | 51 | a0001c0001t0001g0245a0001c0001t0001g0246a0001c0001t0001g0248others(48): Show | 51 | HG00639.hp2 HG00673.hp1 HG01069.hp2 others(48): Show |
intron_variant | MODIFIER | c.-18-1062_-18-1060d others(5): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 1/12 | chr15 | 52185753 | ||||||
chr15:52185753
|
TTTATTA | T | 21 | a0001c0001t0001g0242a0001c0001t0001g0262a0001c0001t0002g0008others(18): Show | 21 | HG00609.hp1 HG00735.hp1 HG01106.hp2 others(18): Show |
intron_variant | MODIFIER | c.-18-1065_-18-1060d others(8): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 1/12 | chr15 | 52185753 | ||||||
chr15:52185753
|
TTTATTAT others(2): Show |
T | 21 | a0001c0001t0022g0294a0001c0001t0022g0295a0001c0001t0023g0296others(18): Show | 23 | HG00738.hp2 HG00741.hp1 HG01069.hp1 others(20): Show |
intron_variant | MODIFIER | c.-18-1068_-18-1060d others(11): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 1/12 | chr15 | 52185753 | ||||||
chr15:52185753
|
TTTATTAT others(5): Show |
T | 8 | a0001c0002t0128g0273a0001c0002t0129g0275a0001c0002t0130g0274others(5): Show | 8 | HG01934.hp2 HG01952.hp1 HG02132.hp2 others(5): Show |
intron_variant | MODIFIER | c.-18-1071_-18-1060d others(14): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 1/12 | chr15 | 52185753 | ||||||
chr15:52185753
|
TTTATTAT others(8): Show |
T | 2 | a0001c0001t0092g0137a0001c0002t0206g0178 | 2 | NA18906.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.-18-1074_-18-1060d others(17): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 1/12 | chr15 | 52185753 | ||||||
chr15:52185753
|
TTTATTAT others(11): Show |
T | 1 | a0001c0002t0137g0266 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.-18-1077_-18-1060d others(20): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 1/12 | chr15 | 52185753 | ||||||
chr15:52185755
|
TA | T | 3 | a0001c0001t0151g0353a0001c0003t0021g0354a0001c0003t0021g0355 | 3 | HG01891.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-18-1062delT | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 1/12 | chr15 | 52185755 | ||||||
chr15:52185756
|
A | T | 1 | a0001c0001t0028g0184 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-18-1062T>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 1/12 | chr15 | 52185756 | ||||||
chr15:52185871
|
T | C | 14 | a0001c0001t0192g0267a0001c0002t0128g0273a0001c0002t0129g0275others(11): Show | 14 | HG01934.hp2 HG01943.hp2 HG01952.hp1 others(11): Show |
intron_variant | MODIFIER | c.-18-1177A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 1/12 | chr15 | 52185871 | ||||||
chr15:52185974
|
T | C | 85 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0008others(82): Show | 85 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.-18-1280A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 1/12 | chr15 | 52185974 | ||||||
chr15:52186012
|
C | G | 1 | a0001c0001t0037g0163 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-18-1318G>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 1/12 | chr15 | 52186012 | ||||||
chr15:52186100
|
C | T | 173 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0008others(170): Show | 175 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.-18-1406G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 1/12 | chr15 | 52186100 | ||||||
chr15:52186168
|
T | C | 12 | a0001c0001t0022g0294a0001c0001t0022g0295a0001c0001t0023g0296others(9): Show | 14 | HG00738.hp2 HG00741.hp1 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.-18-1474A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 1/12 | chr15 | 52186168 | ||||||
chr15:52186233
|
C | T | 6 | a0001c0001t0010g0103a0001c0001t0010g0135a0001c0001t0010g0167others(3): Show | 6 | NA18945.hp2 NA18967.hp2 NA18970.hp2 others(3): Show |
intron_variant | MODIFIER | c.-18-1539G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 1/12 | chr15 | 52186233 | ||||||
chr15:52186242
|
A | G | 7 | a0001c0004t0014g0002a0001c0004t0014g0280a0001c0004t0014g0290others(4): Show | 9 | HG00738.hp2 HG00741.hp1 HG01069.hp1 others(6): Show |
intron_variant | MODIFIER | c.-18-1548T>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 1/12 | chr15 | 52186242 | ||||||
chr15:52186275
|
A | T | 172 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0008others(169): Show | 174 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.-18-1581T>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 1/12 | chr15 | 52186275 | ||||||
chr15:52186342
|
A | G | 12 | a0001c0001t0022g0294a0001c0001t0022g0295a0001c0001t0023g0296others(9): Show | 14 | HG00738.hp2 HG00741.hp1 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.-18-1648T>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 1/12 | chr15 | 52186342 | ||||||
chr15:52186646
|
G | A | 13 | a0001c0001t0004g0075a0001c0001t0022g0294a0001c0001t0022g0295others(10): Show | 15 | HG00738.hp2 HG00741.hp1 HG01069.hp1 others(12): Show |
intron_variant | MODIFIER | c.-18-1952C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 1/12 | chr15 | 52186646 | ||||||
chr15:52186676
|
A | T | 1 | a0001c0001t0173g0183 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-18-1982T>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 1/12 | chr15 | 52186676 | ||||||
chr15:52186677
|
T | C | 52 | a0001c0001t0001g0326a0001c0001t0011g0319a0001c0001t0016g0332others(49): Show | 52 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.-18-1983A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 1/12 | chr15 | 52186677 | ||||||
chr15:52186692
|
G | T | 1 | a0001c0001t0008g0099 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-18-1998C>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 1/12 | chr15 | 52186692 | ||||||
chr15:52186821
|
G | C | 52 | a0001c0001t0001g0326a0001c0001t0011g0319a0001c0001t0016g0332others(49): Show | 52 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.-18-2127C>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 1/12 | chr15 | 52186821 | ||||||
chr15:52186876
|
G | A | 2 | a0001c0001t0046g0110a0001c0001t0068g0111 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.-18-2182C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 1/12 | chr15 | 52186876 | ||||||
chr15:52186947
|
A | G | 1 | a0001c0001t0030g0182 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-18-2253T>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 1/12 | chr15 | 52186947 | ||||||
chr15:52186962
|
C | G | 2 | a0001c0001t0012g0180a0001c0001t0012g0181 | 2 | HG03491.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.-18-2268G>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 1/12 | chr15 | 52186962 | ||||||
chr15:52187382
|
G | A | 1 | a0001c0001t0020g0080 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.-18-2688C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 1/12 | chr15 | 52187382 | ||||||
chr15:52187414
|
A | G | 1 | a0001c0010t0189g0179 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.-18-2720T>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 1/12 | chr15 | 52187414 | ||||||
chr15:52187449
|
G | A | 1 | a0001c0001t0145g0279 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-18-2755C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 1/12 | chr15 | 52187449 | ||||||
chr15:52187462
|
G | A | 1 | a0001c0001t0152g0243 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-18-2768C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 1/12 | chr15 | 52187462 | ||||||
chr15:52187658
|
T | A | 1 | a0001c0001t0001g0262 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.-18-2964A>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 1/12 | chr15 | 52187658 | ||||||
chr15:52187674
|
T | C | 78 | a0001c0001t0001g0326a0001c0001t0011g0319a0001c0001t0016g0332others(75): Show | 80 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.-18-2980A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 1/12 | chr15 | 52187674 | ||||||
chr15:52187720
|
G | A | 1 | a0001c0001t0001g0242 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-18-3026C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 1/12 | chr15 | 52187720 | ||||||
chr15:52187812
|
T | G | 1 | a0001c0001t0086g0161 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-18-3118A>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 1/12 | chr15 | 52187812 | ||||||
chr15:52187905
|
T | C | 78 | a0001c0001t0001g0326a0001c0001t0011g0319a0001c0001t0016g0332others(75): Show | 80 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.-18-3211A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 1/12 | chr15 | 52187905 | ||||||
chr15:52187907
|
C | CCA | 13 | a0001c0001t0022g0294a0001c0001t0022g0295a0001c0001t0023g0296others(10): Show | 15 | HG00738.hp2 HG00741.hp1 HG01069.hp1 others(12): Show |
intron_variant | MODIFIER | c.-18-3215_-18-3214d others(4): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 1/12 | chr15 | 52187907 | ||||||
chr15:52187934
|
G | A | 11 | a0001c0001t0011g0319a0001c0002t0006g0314a0001c0002t0006g0316others(8): Show | 11 | HG01243.hp1 HG02055.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.-18-3240C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 1/12 | chr15 | 52187934 | ||||||
chr15:52187958
|
T | A | 174 | a0001c0001t0001g0326a0001c0001t0002g0003a0001c0001t0002g0004others(171): Show | 176 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.-18-3264A>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 1/12 | chr15 | 52187958 | ||||||
chr15:52187965
|
T | TA | 78 | a0001c0001t0001g0326a0001c0001t0011g0319a0001c0001t0016g0332others(75): Show | 80 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.-18-3272dupT | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 1/12 | chr15 | 52187965 | ||||||
chr15:52187971
|
T | A | 180 | a0001c0001t0001g0326a0001c0001t0002g0003a0001c0001t0002g0008others(177): Show | 182 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.-18-3277A>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 1/12 | chr15 | 52187971 | ||||||
chr15:52187975
|
T | A | 85 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0008others(82): Show | 85 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.-18-3281A>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 1/12 | chr15 | 52187975 | ||||||
chr15:52188072
|
C | T | 2 | a0001c0002t0206g0178a0001c0002t0207g0177 | 2 | HG01496.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-19+3250G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 1/12 | chr15 | 52188072 | ||||||
chr15:52188161
|
C | T | 7 | a0001c0004t0014g0002a0001c0004t0014g0280a0001c0004t0014g0290others(4): Show | 9 | HG00738.hp2 HG00741.hp1 HG01069.hp1 others(6): Show |
intron_variant | MODIFIER | c.-19+3161G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 1/12 | chr15 | 52188161 | ||||||
chr15:52188202
|
C | T | 9 | a0001c0001t0094g0090a0001c0001t0145g0279a0001c0002t0019g0092others(6): Show | 9 | HG01884.hp1 HG01891.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.-19+3120G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 1/12 | chr15 | 52188202 | ||||||
chr15:52188239
|
C | T | 1 | a0001c0002t0140g0265 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.-19+3083G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 1/12 | chr15 | 52188239 | ||||||
chr15:52188240
|
G | A | 1 | a0001c0001t0074g0162 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-19+3082C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 1/12 | chr15 | 52188240 | ||||||
chr15:52188272
|
G | A | 2 | a0001c0001t0037g0163a0001c0001t0066g0164 | 2 | HG01123.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.-19+3050C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 1/12 | chr15 | 52188272 | ||||||
chr15:52188356
|
GA | G | 6 | a0001c0001t0003g0078a0001c0001t0022g0294a0001c0001t0022g0295others(3): Show | 6 | HG02559.hp1 HG02886.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.-19+2965delT | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 1/12 | chr15 | 52188356 | ||||||
chr15:52188479
|
T | C | 1 | a0001c0005t0100g0134 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-19+2843A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 1/12 | chr15 | 52188479 | ||||||
chr15:52188492
|
G | A | 77 | a0001c0001t0011g0319a0001c0001t0016g0332a0001c0001t0016g0343others(74): Show | 79 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.-19+2830C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 1/12 | chr15 | 52188492 | ||||||
chr15:52188554
|
T | C | 7 | a0001c0002t0024g0281a0001c0002t0024g0284a0001c0002t0025g0282others(4): Show | 7 | HG02109.hp2 HG02257.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.-19+2768A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 1/12 | chr15 | 52188554 | ||||||
chr15:52188609
|
G | A | 2 | a0001c0001t0009g0077a0001c0001t0096g0076 | 2 | NA18945.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.-19+2713C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 1/12 | chr15 | 52188609 | ||||||
chr15:52188789
|
G | A | 1 | a0001c0001t0145g0279 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-19+2533C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 1/12 | chr15 | 52188789 | ||||||
chr15:52188898
|
C | T | 1 | a0001c0001t0145g0279 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-19+2424G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 1/12 | chr15 | 52188898 | ||||||
chr15:52188909
|
C | T | 3 | a0001c0001t0141g0301a0001c0001t0148g0302a0001c0001t0149g0300 | 3 | HG02258.hp1 HG02615.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-19+2413G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 1/12 | chr15 | 52188909 | ||||||
chr15:52188915
|
C | T | 2 | a0001c0003t0098g0088a0001c0003t0101g0089 | 2 | HG01884.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.-19+2407G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 1/12 | chr15 | 52188915 | ||||||
chr15:52189176
|
G | A | 1 | a0001c0001t0152g0243 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-19+2146C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 1/12 | chr15 | 52189176 | ||||||
chr15:52189204
|
G | A | 4 | a0001c0001t0073g0166a0001c0001t0075g0165a0001c0003t0099g0095others(1): Show | 4 | HG02572.hp2 HG02965.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19+2118C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 1/12 | chr15 | 52189204 | ||||||
chr15:52189323
|
C | T | 13 | a0001c0001t0022g0294a0001c0001t0022g0295a0001c0001t0023g0296others(10): Show | 15 | HG00738.hp2 HG00741.hp1 HG01069.hp1 others(12): Show |
intron_variant | MODIFIER | c.-19+1999G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 1/12 | chr15 | 52189323 | ||||||
chr15:52189346
|
C | A | 5 | a0001c0001t0094g0090a0001c0002t0019g0092a0001c0002t0019g0093others(2): Show | 5 | HG01884.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-19+1976G>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 1/12 | chr15 | 52189346 | ||||||
chr15:52189369
|
G | A | 6 | a0001c0001t0022g0294a0001c0001t0022g0295a0001c0001t0023g0296others(3): Show | 6 | HG02559.hp1 HG02723.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19+1953C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 1/12 | chr15 | 52189369 | ||||||
chr15:52189440
|
C | T | 6 | a0001c0001t0192g0267a0001c0002t0135g0270a0001c0002t0136g0268others(3): Show | 6 | HG01943.hp2 HG02004.hp1 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.-19+1882G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 1/12 | chr15 | 52189440 | ||||||
chr15:52189534
|
C | T | 29 | a0001c0001t0016g0332a0001c0001t0016g0343a0001c0001t0016g0344others(26): Show | 29 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(26): Show |
intron_variant | MODIFIER | c.-19+1788G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 1/12 | chr15 | 52189534 | ||||||
chr15:52189575
|
G | A | 6 | a0001c0001t0022g0294a0001c0001t0022g0295a0001c0001t0023g0296others(3): Show | 6 | HG02559.hp1 HG02723.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19+1747C>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 1/12 | chr15 | 52189575 | ||||||
chr15:52189584
|
C | CA | 15 | a0001c0001t0010g0167a0001c0001t0192g0267a0001c0002t0128g0273others(12): Show | 15 | HG01934.hp2 HG01943.hp2 HG01952.hp1 others(12): Show |
intron_variant | MODIFIER | c.-19+1737dupT | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 1/12 | chr15 | 52189584 | ||||||
chr15:52189674
|
TCCA | T | 8 | a0001c0001t0094g0090a0001c0002t0019g0092a0001c0002t0019g0093others(5): Show | 8 | HG01884.hp1 HG02622.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.-19+1645_-19+1647d others(5): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 1/12 | chr15 | 52189674 | ||||||
chr15:52189951
|
C | A | 1 | a0001c0001t0183g0359 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-19+1371G>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 1/12 | chr15 | 52189951 | ||||||
chr15:52190104
|
C | T | 1 | a0001c0002t0024g0281 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-19+1218G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 1/12 | chr15 | 52190104 | ||||||
chr15:52190117
|
A | AT | 26 | a0001c0001t0007g0169a0001c0001t0008g0099a0001c0001t0018g0133others(23): Show | 26 | HG00544.hp2 HG00597.hp1 HG00673.hp2 others(23): Show |
intron_variant | MODIFIER | c.-19+1204dupA | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 1/12 | chr15 | 52190117 | ||||||
chr15:52190117
|
A | ATT | 7 | a0001c0001t0010g0112a0001c0001t0038g0115a0001c0001t0040g0113others(4): Show | 7 | HG01928.hp1 HG01943.hp1 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.-19+1203_-19+1204d others(4): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 1/12 | chr15 | 52190117 | ||||||
chr15:52190117
|
A | T | 3 | a0001c0001t0001g0245a0001c0001t0001g0246a0001c0001t0153g0244 | 3 | NA18946.hp2 NA18970.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.-19+1205T>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 1/12 | chr15 | 52190117 | ||||||
chr15:52190117
|
AT | A | 153 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0008others(150): Show | 153 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.-19+1204delA | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 1/12 | chr15 | 52190117 | ||||||
chr15:52190117
|
ATT | A | 18 | a0001c0001t0003g0078a0001c0001t0020g0080a0001c0001t0022g0294others(15): Show | 20 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(17): Show |
intron_variant | MODIFIER | c.-19+1203_-19+1204d others(4): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 1/12 | chr15 | 52190117 | ||||||
chr15:52190118
|
T | A | 2 | a0001c0002t0006g0314a0001c0002t0201g0315 | 2 | HG02055.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-19+1204A>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 1/12 | chr15 | 52190118 | ||||||
chr15:52190119
|
T | A | 62 | a0001c0001t0011g0319a0001c0001t0016g0332a0001c0001t0016g0343others(59): Show | 62 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(59): Show |
intron_variant | MODIFIER | c.-19+1203A>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 1/12 | chr15 | 52190119 | ||||||
chr15:52190120
|
T | A | 15 | a0001c0001t0022g0294a0001c0001t0022g0295a0001c0001t0023g0296others(12): Show | 17 | HG00738.hp2 HG00741.hp1 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.-19+1202A>T | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 1/12 | chr15 | 52190120 | ||||||
chr15:52190178
|
C | T | 6 | a0001c0001t0192g0267a0001c0002t0135g0270a0001c0002t0136g0268others(3): Show | 6 | HG01943.hp2 HG02004.hp1 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.-19+1144G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 1/12 | chr15 | 52190178 | ||||||
chr15:52190318
|
C | G | 4 | a0001c0001t0001g0245a0001c0001t0001g0246a0001c0001t0153g0244others(1): Show | 4 | HG01993.hp1 NA18946.hp2 NA18970.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19+1004G>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 1/12 | chr15 | 52190318 | ||||||
chr15:52190493
|
A | G | 11 | a0001c0001t0011g0319a0001c0002t0006g0314a0001c0002t0006g0316others(8): Show | 11 | HG01243.hp1 HG02055.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.-19+829T>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 1/12 | chr15 | 52190493 | ||||||
chr15:52190778
|
TAAAAAAA others(5): Show |
T | 1 | a0001c0001t0011g0299 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-19+532_-19+543del others(12): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 1/12 | chr15 | 52190778 | ||||||
chr15:52190778
|
TAAAAAAA others(6): Show |
T | 11 | a0001c0001t0022g0294a0001c0001t0022g0295a0001c0001t0023g0296others(8): Show | 13 | HG00738.hp2 HG01069.hp1 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.-19+531_-19+543del others(13): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 1/12 | chr15 | 52190778 | ||||||
chr15:52190778
|
TAAAAAAA others(7): Show |
T | 11 | a0001c0002t0006g0291a0001c0002t0024g0281a0001c0002t0024g0284others(8): Show | 11 | HG00741.hp1 HG01169.hp1 HG01261.hp2 others(8): Show |
intron_variant | MODIFIER | c.-19+530_-19+543del others(14): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 1/12 | chr15 | 52190778 | ||||||
chr15:52190778
|
TAAAAAAA others(8): Show |
T | 4 | a0001c0002t0019g0092a0001c0002t0019g0093a0001c0003t0097g0091others(1): Show | 4 | HG01168.hp1 HG02622.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19+529_-19+543del others(15): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 1/12 | chr15 | 52190778 | ||||||
chr15:52190778
|
TAAAAAAA others(9): Show |
T | 4 | a0001c0001t0078g0086a0001c0001t0094g0090a0001c0003t0098g0088others(1): Show | 4 | HG01884.hp1 HG02109.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19+528_-19+543del others(16): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 1/12 | chr15 | 52190778 | ||||||
chr15:52190778
|
TAAAAAAA others(10): Show |
T | 13 | a0001c0001t0002g0081a0001c0001t0002g0082a0001c0001t0002g0084others(10): Show | 13 | HG00597.hp1 HG01255.hp1 HG01358.hp2 others(10): Show |
intron_variant | MODIFIER | c.-19+527_-19+543del others(17): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 1/12 | chr15 | 52190778 | ||||||
chr15:52190778
|
TAAAAAAA others(11): Show |
T | 140 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0010others(137): Show | 140 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.-19+526_-19+543del others(18): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 1/12 | chr15 | 52190778 | ||||||
chr15:52190778
|
TAAAAAAA others(12): Show |
T | 67 | a0001c0001t0001g0325a0001c0001t0001g0326a0001c0001t0002g0004others(64): Show | 67 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.-19+525_-19+543del others(19): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 1/12 | chr15 | 52190778 | ||||||
chr15:52190778
|
TAAAAAAA others(13): Show |
T | 14 | a0001c0001t0192g0267a0001c0002t0128g0273a0001c0002t0129g0275others(11): Show | 14 | HG01934.hp2 HG01943.hp2 HG01952.hp1 others(11): Show |
intron_variant | MODIFIER | c.-19+524_-19+543del others(20): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 1/12 | chr15 | 52190778 | ||||||
chr15:52190778
|
TAAAAAAA others(14): Show |
T | 2 | a0001c0001t0001g0263a0001c0002t0150g0264 | 2 | HG02004.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.-19+523_-19+543del others(21): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 1/12 | chr15 | 52190778 | ||||||
chr15:52190778
|
TAAAAAAA others(15): Show |
T | 19 | a0001c0001t0001g0245a0001c0001t0001g0246a0001c0001t0001g0248others(16): Show | 19 | HG00673.hp1 HG01069.hp2 HG01261.hp1 others(16): Show |
intron_variant | MODIFIER | c.-19+522_-19+543del others(22): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 1/12 | chr15 | 52190778 | ||||||
chr15:52190778
|
TAAAAAAA others(16): Show |
T | 65 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0001g0187others(62): Show | 65 | HG00438.hp2 HG00544.hp1 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.-19+521_-19+543del others(23): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 1/12 | chr15 | 52190778 | ||||||
chr15:52190981
|
A | G | 1 | a0001c0001t0002g0003 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-19+341T>C | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 1/12 | chr15 | 52190981 | ||||||
chr15:52191153
|
T | C | 52 | a0001c0001t0001g0325a0001c0001t0001g0326a0001c0001t0011g0319others(49): Show | 52 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.-19+169A>G | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 1/12 | chr15 | 52191153 | ||||||
chr15:52191180
|
C | T | 95 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0008others(92): Show | 95 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.-19+142G>A | GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 1/12 | chr15 | 52191180 | ||||||
chr15:52191185
|
TAAC | T | 84 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0008others(81): Show | 84 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.-19+134_-19+136del others(3): Show |
GNB5 | ENSG00000069966.19 | transcript | ENST00000261837.12 | protein_coding | 1/12 | chr15 | 52191185 |