geneid | 2767 |
---|---|
ensemblid | ENSG00000088256.9 |
hgncid | 4379 |
symbol | GNA11 |
name | G protein subunit alpha 11 |
refseq_nuc | NM_002067.5 |
refseq_prot | NP_002058.2 |
ensembl_nuc | ENST00000078429.9 |
ensembl_prot | ENSP00000078429.3 |
mane_status | MANE Select |
chr | chr19 |
start | 3094362 |
end | 3123999 |
strand | + |
ver | v1.2 |
region | chr19:3094362-3123999 |
region5000 | chr19:3089362-3128999 |
regionname0 | GNA11_chr19_3094362_3123999 |
regionname5000 | GNA11_chr19_3089362_3128999 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 359 | 419 | 95 | 74 | 185 | 18 | 46 | 139 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
a0002 | 0/0 | 359 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
a0003 | 0/0 | 359 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
a0004 | 0/0 | 359 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 1080 | 266 | 81 | 42 | 108 | 12 | 22 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
c0002 | 0/0 | 1080 | 149 | 12 | 32 | 77 | 5 | 23 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
c0003 | 0/0 | 1080 | 3 | 3 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
c0004 | 0/0 | 1080 | 2 | 0 | 2 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
c0005 | 0/0 | 1080 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
c0006 | 0/0 | 1080 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
c0007 | 0/0 | 1080 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
c0008 | 0/0 | 1080 | 1 | 0 | 0 | 0 | 0 | 1 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
c0009 | 0/0 | 1080 | 1 | 0 | 0 | 0 | 1 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/0 | 3111 | 65 | 18 | 11 | 25 | 2 | 8 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
t0002 | 0/0 | 3112 | 53 | 1 | 7 | 35 | 1 | 9 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
t0003 | 0/0 | 3110 | 42 | 6 | 9 | 21 | 3 | 3 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
t0004 | 0/0 | 3109 | 23 | 1 | 10 | 7 | 3 | 2 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
t0005 | 0/0 | 3114 | 22 | 0 | 6 | 11 | 0 | 5 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
t0006 | 0/0 | 3111 | 15 | 4 | 5 | 1 | 5 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
t0007 | 0/0 | 3112 | 13 | 1 | 2 | 8 | 0 | 2 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
t0008 | 0/0 | 3111 | 13 | 12 | 1 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
t0009 | 0/0 | 3115 | 12 | 0 | 2 | 10 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
t0010 | 0/0 | 3109 | 12 | 0 | 2 | 10 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
t0011 | 0/0 | 3111 | 11 | 11 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
t0012 | 0/0 | 3111 | 8 | 4 | 0 | 4 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
t0013 | 0/0 | 3112 | 8 | 4 | 0 | 1 | 0 | 3 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
t0014 | 0/0 | 3112 | 6 | 0 | 0 | 5 | 0 | 1 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
t0015 | 0/0 | 3110 | 5 | 5 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
t0016 | 0/0 | 3113 | 5 | 0 | 2 | 3 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
t0017 | 0/0 | 3113 | 5 | 0 | 0 | 5 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
t0018 | 0/0 | 3109 | 5 | 0 | 4 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
t0019 | 0/0 | 3110 | 5 | 1 | 0 | 4 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
t0020 | 0/0 | 3109 | 4 | 0 | 0 | 4 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
t0021 | 0/0 | 3111 | 4 | 1 | 2 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
t0022 | 0/0 | 3111 | 3 | 3 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
t0023 | 0/0 | 3111 | 3 | 0 | 0 | 0 | 0 | 3 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
t0024 | 0/0 | 3111 | 3 | 3 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
t0025 | 0/0 | 3109 | 3 | 0 | 0 | 0 | 0 | 3 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
t0026 | 0/0 | 3111 | 2 | 2 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
t0027 | 0/0 | 3114 | 2 | 2 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
t0028 | 0/0 | 3114 | 2 | 0 | 0 | 2 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
t0029 | 0/0 | 3114 | 2 | 0 | 0 | 2 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
t0030 | 0/0 | 3108 | 2 | 0 | 2 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
t0031 | 0/0 | 3111 | 2 | 0 | 2 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
t0032 | 0/0 | 3111 | 2 | 0 | 0 | 2 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
t0033 | 0/0 | 3111 | 2 | 0 | 0 | 1 | 0 | 1 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
t0034 | 0/0 | 3109 | 2 | 1 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
t0035 | 0/0 | 3112 | 2 | 0 | 1 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
t0036 | 0/0 | 3111 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
t0037 | 0/0 | 3112 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
t0038 | 0/0 | 3112 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
t0039 | 0/0 | 3112 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
t0040 | 0/0 | 3111 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
t0041 | 0/0 | 3110 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
t0042 | 0/0 | 3110 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
t0043 | 0/0 | 3114 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
t0044 | 0/0 | 3115 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
t0045 | 0/0 | 3112 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
t0046 | 0/0 | 3113 | 1 | 0 | 1 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
t0047 | 0/0 | 3112 | 1 | 0 | 0 | 0 | 0 | 1 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
t0048 | 0/0 | 3116 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
t0049 | 0/0 | 3111 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
t0050 | 0/0 | 3109 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
t0051 | 0/0 | 3109 | 1 | 0 | 1 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
t0052 | 0/0 | 3109 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
t0053 | 0/0 | 3109 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
t0054 | 0/0 | 3113 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
t0055 | 0/0 | 3113 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
t0056 | 0/0 | 3114 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
t0057 | 0/0 | 3111 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
t0058 | 0/0 | 3112 | 1 | 0 | 0 | 0 | 0 | 1 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
t0059 | 0/0 | 3112 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
t0060 | 0/0 | 3113 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
t0061 | 0/0 | 3112 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
t0062 | 0/0 | 3112 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
t0063 | 0/0 | 3112 | 1 | 0 | 0 | 0 | 0 | 1 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
t0064 | 0/0 | 3112 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
t0065 | 0/0 | 3112 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
t0066 | 0/0 | 3112 | 1 | 0 | 0 | 0 | 0 | 1 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
t0067 | 0/0 | 3112 | 1 | 0 | 1 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
t0068 | 0/0 | 3112 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
t0069 | 0/0 | 3111 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
t0070 | 0/0 | 3111 | 1 | 0 | 1 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
t0071 | 0/0 | 3111 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
t0072 | 0/0 | 3110 | 1 | 0 | 0 | 0 | 1 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
t0073 | 0/0 | 3110 | 1 | 0 | 1 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
t0074 | 0/0 | 3111 | 1 | 0 | 0 | 0 | 0 | 1 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
t0075 | 0/0 | 3111 | 1 | 0 | 1 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
t0076 | 0/0 | 3111 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
t0077 | 0/0 | 3111 | 1 | 0 | 0 | 0 | 0 | 1 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
t0078 | 0/0 | 3111 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
t0079 | 0/0 | 3111 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
t0080 | 0/0 | 3111 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
t0081 | 0/0 | 3111 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
t0082 | 0/0 | 3109 | 1 | 0 | 0 | 0 | 1 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
t0083 | 0/0 | 3110 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
t0084 | 0/0 | 3110 | 1 | 0 | 1 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
t0085 | 0/0 | 3110 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
t0086 | 0/0 | 3110 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
t0087 | 0/0 | 3109 | 1 | 0 | 0 | 0 | 1 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
t0088 | 0/0 | 3110 | 1 | 0 | 1 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
t0089 | 0/0 | 3109 | 1 | 0 | 0 | 0 | 1 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
t0090 | 0/0 | 3111 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
t0091 | 0/0 | 3110 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
t0092 | 0/0 | 3114 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 18 | 0 | 5 | 11 | 0 | 2 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0002 | 0/0 | 14 | 0 | 6 | 8 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0003 | 0/0 | 8 | 0 | 1 | 7 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0004 | 0/0 | 6 | 0 | 0 | 4 | 0 | 2 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0005 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0006 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0012 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0014 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0015 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0018 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0019 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0026 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0027 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0030 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0034 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0041 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0043 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0044 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0048 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0052 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0053 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0054 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0055 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0056 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0057 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0058 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0059 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0060 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0061 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0062 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0063 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0064 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0240 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0275 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 1080 | 266 | 81 | 42 | 108 | 12 | 22 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
a0001c0002 | 0/0 | 1080 | 149 | 12 | 32 | 77 | 5 | 23 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
a0001c0005 | 0/0 | 1080 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
a0001c0007 | 0/0 | 1080 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
a0001c0008 | 0/0 | 1080 | 1 | 0 | 0 | 0 | 0 | 1 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
a0001c0009 | 0/0 | 1080 | 1 | 0 | 0 | 0 | 1 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
a0002c0003 | 0/0 | 1080 | 3 | 3 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
a0003c0004 | 0/0 | 1080 | 2 | 0 | 2 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
a0004c0006 | 0/0 | 1080 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 4190 | 65 | 18 | 11 | 25 | 2 | 8 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
a0001c0001t0003 | 0/0 | 4189 | 38 | 5 | 7 | 21 | 2 | 3 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
a0001c0001t0005 | 0/0 | 4193 | 21 | 0 | 6 | 11 | 0 | 4 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
a0001c0001t0006 | 0/0 | 4190 | 15 | 4 | 5 | 1 | 5 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
a0001c0001t0008 | 0/0 | 4190 | 10 | 9 | 1 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
a0001c0001t0009 | 0/0 | 4194 | 12 | 0 | 2 | 10 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
a0001c0001t0011 | 0/0 | 4190 | 11 | 11 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
a0001c0001t0012 | 0/0 | 4190 | 8 | 4 | 0 | 4 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
a0001c0001t0014 | 0/0 | 4191 | 6 | 0 | 0 | 5 | 0 | 1 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
a0001c0001t0015 | 0/0 | 4189 | 5 | 5 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
a0001c0001t0016 | 0/0 | 4192 | 5 | 0 | 2 | 3 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
a0001c0001t0017 | 0/0 | 4192 | 5 | 0 | 0 | 5 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
a0001c0001t0019 | 0/0 | 4189 | 4 | 0 | 0 | 4 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
a0001c0001t0022 | 0/0 | 4190 | 3 | 3 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
a0001c0001t0023 | 0/0 | 4190 | 3 | 0 | 0 | 0 | 0 | 3 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
a0001c0001t0024 | 0/0 | 4190 | 3 | 3 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
a0001c0001t0026 | 0/0 | 4190 | 2 | 2 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
a0001c0001t0027 | 0/0 | 4193 | 2 | 2 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
a0001c0001t0028 | 0/0 | 4193 | 2 | 0 | 0 | 2 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
a0001c0001t0029 | 0/0 | 4193 | 2 | 0 | 0 | 2 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
a0001c0001t0031 | 0/0 | 4190 | 2 | 0 | 2 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
a0001c0001t0032 | 0/0 | 4190 | 2 | 0 | 0 | 2 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
a0001c0001t0034 | 0/0 | 4188 | 2 | 1 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
a0001c0001t0036 | 0/0 | 4190 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
a0001c0001t0037 | 0/0 | 4191 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
a0001c0001t0039 | 0/0 | 4191 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
a0001c0001t0040 | 0/0 | 4190 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
a0001c0001t0041 | 0/0 | 4189 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
a0001c0001t0042 | 0/0 | 4189 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
a0001c0001t0043 | 0/0 | 4193 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
a0001c0001t0044 | 0/0 | 4194 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
a0001c0001t0045 | 0/0 | 4191 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
a0001c0001t0046 | 0/0 | 4192 | 1 | 0 | 1 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
a0001c0001t0047 | 0/0 | 4191 | 1 | 0 | 0 | 0 | 0 | 1 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
a0001c0001t0048 | 0/0 | 4195 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
a0001c0001t0049 | 0/0 | 4190 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
a0001c0001t0056 | 0/0 | 4193 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
a0001c0001t0057 | 0/0 | 4190 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
a0001c0001t0061 | 0/0 | 4191 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
a0001c0001t0069 | 0/0 | 4190 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
a0001c0001t0070 | 0/0 | 4190 | 1 | 0 | 1 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
a0001c0001t0071 | 0/0 | 4190 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
a0001c0001t0072 | 0/0 | 4189 | 1 | 0 | 0 | 0 | 1 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
a0001c0001t0073 | 0/0 | 4189 | 1 | 0 | 1 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
a0001c0001t0074 | 0/0 | 4190 | 1 | 0 | 0 | 0 | 0 | 1 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
a0001c0001t0075 | 0/0 | 4190 | 1 | 0 | 1 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
a0001c0001t0076 | 0/0 | 4190 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
a0001c0001t0077 | 0/0 | 4190 | 1 | 0 | 0 | 0 | 0 | 1 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
a0001c0001t0078 | 0/0 | 4190 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
a0001c0001t0080 | 0/0 | 4190 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
a0001c0001t0081 | 0/0 | 4190 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
a0001c0001t0082 | 0/0 | 4188 | 1 | 0 | 0 | 0 | 1 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
a0001c0001t0083 | 0/0 | 4189 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
a0001c0001t0084 | 0/0 | 4189 | 1 | 0 | 1 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
a0001c0001t0085 | 0/0 | 4189 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
a0001c0001t0086 | 0/0 | 4189 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
a0001c0001t0087 | 0/0 | 4188 | 1 | 0 | 0 | 0 | 1 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
a0001c0001t0088 | 0/0 | 4189 | 1 | 0 | 1 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
a0001c0001t0090 | 0/0 | 4190 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
a0001c0001t0091 | 0/0 | 4189 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
a0001c0001t0092 | 0/0 | 4193 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
a0001c0002t0002 | 0/0 | 4191 | 52 | 1 | 7 | 34 | 1 | 9 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
a0001c0002t0004 | 0/0 | 4188 | 23 | 1 | 10 | 7 | 3 | 2 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
a0001c0002t0007 | 0/0 | 4191 | 13 | 1 | 2 | 8 | 0 | 2 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
a0001c0002t0010 | 0/0 | 4188 | 12 | 0 | 2 | 10 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
a0001c0002t0013 | 0/0 | 4191 | 8 | 4 | 0 | 1 | 0 | 3 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
a0001c0002t0018 | 0/0 | 4188 | 5 | 0 | 4 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
a0001c0002t0020 | 0/0 | 4188 | 4 | 0 | 0 | 4 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
a0001c0002t0021 | 0/0 | 4190 | 4 | 1 | 2 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
a0001c0002t0025 | 0/0 | 4188 | 3 | 0 | 0 | 0 | 0 | 3 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
a0001c0002t0030 | 0/0 | 4187 | 2 | 0 | 2 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
a0001c0002t0033 | 0/0 | 4190 | 2 | 0 | 0 | 1 | 0 | 1 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
a0001c0002t0035 | 0/0 | 4191 | 2 | 0 | 1 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
a0001c0002t0038 | 0/0 | 4191 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
a0001c0002t0050 | 0/0 | 4188 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
a0001c0002t0051 | 0/0 | 4188 | 1 | 0 | 1 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
a0001c0002t0052 | 0/0 | 4188 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
a0001c0002t0053 | 0/0 | 4188 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
a0001c0002t0054 | 0/0 | 4192 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
a0001c0002t0055 | 0/0 | 4192 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
a0001c0002t0058 | 0/0 | 4191 | 1 | 0 | 0 | 0 | 0 | 1 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
a0001c0002t0059 | 0/0 | 4191 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
a0001c0002t0060 | 0/0 | 4192 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
a0001c0002t0062 | 0/0 | 4191 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
a0001c0002t0063 | 0/0 | 4191 | 1 | 0 | 0 | 0 | 0 | 1 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
a0001c0002t0064 | 0/0 | 4191 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
a0001c0002t0065 | 0/0 | 4191 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
a0001c0002t0066 | 0/0 | 4191 | 1 | 0 | 0 | 0 | 0 | 1 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
a0001c0002t0067 | 0/0 | 4191 | 1 | 0 | 1 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
a0001c0002t0068 | 0/0 | 4191 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
a0001c0002t0079 | 0/0 | 4190 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
a0001c0002t0089 | 0/0 | 4188 | 1 | 0 | 0 | 0 | 1 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
a0001c0005t0019 | 0/0 | 4189 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
a0001c0007t0003 | 0/0 | 4189 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
a0001c0008t0005 | 0/0 | 4193 | 1 | 0 | 0 | 0 | 0 | 1 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
a0001c0009t0003 | 0/0 | 4189 | 1 | 0 | 0 | 0 | 1 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
a0002c0003t0008 | 0/0 | 4190 | 3 | 3 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
a0003c0004t0003 | 0/0 | 4189 | 2 | 0 | 2 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
a0004c0006t0002 | 0/0 | 4191 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | copy fasta | chr19 | 3089362 | 3128999 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0001g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0001g0014 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0001g0015 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0001g0052 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0001g0053 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0001g0055 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0001g0056 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0001g0240 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0003g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0003g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0003g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0003g0044 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0003g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0003g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0003g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0003g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0003g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0003g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0003g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0003g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0003g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0003g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0003g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0003g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0003g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0003g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0003g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0005g0001 | 0/0 | 10 | 0 | 4 | 4 | 0 | 2 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0005g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0005g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0005g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0005g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0005g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0005g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0005g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0005g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0005g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0005g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0005g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0006g0043 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0006g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0006g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0006g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0006g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0006g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0006g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0006g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0006g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0006g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0006g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0006g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0006g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0008g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0008g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0008g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0008g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0008g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0008g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0008g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0008g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0008g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0008g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0009g0001 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0009g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0009g0018 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0009g0063 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0009g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0009g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0011g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0011g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0011g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0011g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0011g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0011g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0011g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0011g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0011g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0011g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0011g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0012g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0012g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0012g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0012g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0012g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0014g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0014g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0014g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0014g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0015g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0015g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0015g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0015g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0016g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0016g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0016g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0016g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0017g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0017g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0017g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0017g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0017g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0019g0060 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0019g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0019g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0022g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0022g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0022g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0023g0057 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0023g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0024g0059 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0024g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0026g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0026g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0027g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0027g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0028g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0029g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0029g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0031g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0031g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0032g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0032g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0034g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0034g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0036g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0037g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0039g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0040g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0041g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0042g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0043g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0044g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0045g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0046g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0047g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0048g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0049g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0056g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0057g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0061g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0069g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0070g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0071g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0072g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0073g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0074g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0075g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0076g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0077g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0078g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0080g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0081g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0082g0275 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0083g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0084g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0085g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0086g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0087g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0088g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0090g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0091g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0001t0092g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0002t0002g0004 | 0/0 | 4 | 0 | 0 | 2 | 0 | 2 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0002t0002g0005 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0002t0002g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0002t0002g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0002t0002g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0002t0002g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0002t0002g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0002t0002g0061 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0002t0002g0064 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0002t0002g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0002t0002g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0002t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0002t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0002t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0002t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0002t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0002t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0002t0002g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0002t0002g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0002t0002g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0002t0002g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0002t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0002t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0002t0002g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0002t0002g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0002t0002g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0002t0004g0002 | 0/0 | 6 | 0 | 4 | 2 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0002t0004g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0002t0004g0030 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0002t0004g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0002t0004g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0002t0004g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0002t0004g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0002t0004g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0002t0004g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0002t0004g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0002t0004g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0002t0004g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0002t0004g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0002t0004g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0002t0007g0006 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0002t0007g0027 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0002t0007g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0002t0007g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0002t0007g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0002t0007g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0002t0007g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0002t0007g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0002t0010g0002 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0002t0010g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0002t0010g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0002t0010g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0002t0010g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0002t0010g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0002t0013g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0002t0013g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0002t0013g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0002t0013g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0002t0013g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0002t0013g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0002t0013g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0002t0013g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0002t0018g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0002t0018g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0002t0018g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0002t0018g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0002t0020g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0002t0020g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0002t0020g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0002t0020g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0002t0021g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0002t0021g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0002t0021g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0002t0021g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0002t0025g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0002t0025g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0002t0025g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0002t0030g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0002t0030g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0002t0033g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0002t0033g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0002t0035g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0002t0035g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0002t0038g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0002t0050g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0002t0051g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0002t0052g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0002t0053g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0002t0054g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0002t0055g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0002t0058g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0002t0059g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0002t0060g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0002t0062g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0002t0063g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0002t0064g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0002t0065g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0002t0066g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0002t0067g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0002t0068g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0002t0079g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0002t0089g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0005t0019g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0007t0003g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0008t0005g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0001c0009t0003g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0002c0003t0008g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0002c0003t0008g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0003c0004t0003g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
a0004c0006t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0056 | EUR | GBR | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG00099 | hp2 | a0001 | c0009 | t0003 | g0179 | EUR | GBR | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG00140 | hp1 | a0001 | c0002 | t0004 | g0119 | EUR | GBR | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG00140 | hp2 | a0001 | c0002 | t0004 | g0150 | EUR | GBR | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG00280 | hp1 | a0001 | c0001 | t0006 | g0278 | EUR | FIN | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG00280 | hp2 | a0001 | c0001 | t0003 | g0044 | EUR | FIN | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG00323 | hp1 | a0001 | c0002 | t0002 | g0061 | EUR | FIN | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0014 | EUR | FIN | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG00408 | hp1 | a0001 | c0001 | t0009 | g0299 | EAS | CHS | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG00408 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | CHS | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG00423 | hp1 | a0001 | c0002 | t0020 | g0034 | EAS | CHS | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG00423 | hp2 | a0001 | c0001 | t0009 | g0001 | EAS | CHS | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG00438 | hp1 | a0001 | c0001 | t0005 | g0286 | EAS | CHS | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG00438 | hp2 | a0001 | c0001 | t0003 | g0176 | EAS | CHS | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | CHS | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG00544 | hp2 | a0001 | c0001 | t0003 | g0040 | EAS | CHS | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG00558 | hp1 | a0001 | c0001 | t0003 | g0172 | EAS | CHS | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG00558 | hp2 | a0001 | c0002 | t0068 | g0141 | EAS | CHS | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | CHS | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG00597 | hp2 | a0001 | c0002 | t0002 | g0094 | EAS | CHS | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG00609 | hp1 | a0001 | c0001 | t0076 | g0257 | EAS | CHS | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG00609 | hp2 | a0001 | c0002 | t0002 | g0008 | EAS | CHS | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | CHS | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG00621 | hp2 | a0001 | c0001 | t0003 | g0300 | EAS | CHS | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG00639 | hp1 | a0001 | c0002 | t0004 | g0033 | AMR | PUR | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG00639 | hp2 | a0001 | c0001 | t0031 | g0203 | AMR | PUR | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG00642 | hp1 | a0001 | c0002 | t0010 | g0031 | AMR | PUR | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0248 | AMR | PUR | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG00673 | hp1 | a0001 | c0001 | t0003 | g0192 | EAS | CHS | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG00673 | hp2 | a0001 | c0001 | t0005 | g0001 | EAS | CHS | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG00735 | hp2 | a0001 | c0002 | t0002 | g0270 | AMR | PUR | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG00738 | hp1 | a0001 | c0001 | t0005 | g0062 | AMR | PUR | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG00738 | hp2 | a0001 | c0002 | t0007 | g0027 | AMR | PUR | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG00741 | hp1 | a0001 | c0001 | t0003 | g0181 | AMR | PUR | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG00741 | hp2 | a0001 | c0002 | t0051 | g0117 | AMR | PUR | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG01069 | hp1 | a0001 | c0001 | t0046 | g0062 | AMR | PUR | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG01069 | hp2 | a0001 | c0001 | t0084 | g0048 | AMR | PUR | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG01070 | hp1 | a0003 | c0004 | t0003 | g0039 | AMR | PUR | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG01070 | hp2 | a0001 | c0002 | t0035 | g0031 | AMR | PUR | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG01071 | hp1 | a0003 | c0004 | t0003 | g0039 | AMR | PUR | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG01071 | hp2 | a0001 | c0001 | t0031 | g0048 | AMR | PUR | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0237 | AMR | PUR | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG01074 | hp2 | a0001 | c0002 | t0004 | g0002 | AMR | PUR | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG01099 | hp1 | a0001 | c0001 | t0003 | g0180 | AMR | PUR | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG01099 | hp2 | a0001 | c0002 | t0004 | g0030 | AMR | PUR | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG01106 | hp1 | a0001 | c0001 | t0006 | g0165 | AMR | PUR | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG01106 | hp2 | a0001 | c0001 | t0003 | g0042 | AMR | PUR | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG01109 | hp1 | a0001 | c0002 | t0004 | g0033 | AMR | PUR | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG01109 | hp2 | a0001 | c0001 | t0008 | g0229 | AMR | PUR | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG01167 | hp1 | a0001 | c0002 | t0030 | g0121 | AMR | PUR | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG01167 | hp2 | a0001 | c0002 | t0004 | g0002 | AMR | PUR | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG01168 | hp1 | a0001 | c0001 | t0006 | g0162 | AMR | PUR | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG01169 | hp2 | a0001 | c0002 | t0004 | g0034 | AMR | PUR | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG01175 | hp1 | a0001 | c0002 | t0007 | g0199 | AMR | PUR | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG01192 | hp1 | a0001 | c0002 | t0002 | g0131 | AMR | PUR | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG01192 | hp2 | a0001 | c0001 | t0073 | g0169 | AMR | PUR | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG01243 | hp1 | a0001 | c0001 | t0075 | g0219 | AMR | PUR | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG01243 | hp2 | a0001 | c0001 | t0006 | g0160 | AMR | PUR | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | CLM | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG01255 | hp2 | a0001 | c0002 | t0021 | g0184 | AMR | CLM | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG01256 | hp1 | a0001 | c0002 | t0018 | g0035 | AMR | CLM | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG01256 | hp2 | a0001 | c0002 | t0002 | g0012 | AMR | CLM | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG01257 | hp1 | a0001 | c0002 | t0002 | g0185 | AMR | CLM | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG01257 | hp2 | a0001 | c0001 | t0088 | g0158 | AMR | CLM | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG01258 | hp1 | a0001 | c0002 | t0021 | g0012 | AMR | CLM | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG01258 | hp2 | a0001 | c0001 | t0006 | g0161 | AMR | CLM | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG01261 | hp1 | a0001 | c0001 | t0003 | g0159 | AMR | CLM | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG01261 | hp2 | a0001 | c0001 | t0005 | g0001 | AMR | CLM | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG01358 | hp1 | a0001 | c0002 | t0004 | g0140 | AMR | CLM | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG01358 | hp2 | a0001 | c0001 | t0003 | g0041 | AMR | CLM | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG01361 | hp1 | a0001 | c0002 | t0002 | g0012 | AMR | CLM | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG01361 | hp2 | a0001 | c0001 | t0005 | g0001 | AMR | CLM | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG01433 | hp1 | a0001 | c0001 | t0070 | g0167 | AMR | CLM | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG01433 | hp2 | a0001 | c0002 | t0004 | g0002 | AMR | CLM | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG01496 | hp1 | a0001 | c0002 | t0002 | g0061 | AMR | CLM | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG01496 | hp2 | a0001 | c0002 | t0004 | g0002 | AMR | CLM | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG01515 | hp1 | a0001 | c0001 | t0087 | g0122 | EUR | IBS | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG01515 | hp2 | a0001 | c0001 | t0006 | g0043 | EUR | IBS | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG01516 | hp1 | a0001 | c0001 | t0006 | g0154 | EUR | IBS | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG01516 | hp2 | a0001 | c0001 | t0072 | g0274 | EUR | IBS | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG01517 | hp1 | a0001 | c0001 | t0006 | g0043 | EUR | IBS | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG01517 | hp2 | a0001 | c0001 | t0082 | g0275 | EUR | IBS | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG01884 | hp1 | a0001 | c0001 | t0037 | g0068 | AFR | ACB | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG01884 | hp2 | a0001 | c0001 | t0011 | g0050 | AFR | ACB | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG01891 | hp1 | a0001 | c0001 | t0056 | g0113 | AFR | ACB | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG01891 | hp2 | a0001 | c0001 | t0008 | g0268 | AFR | ACB | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG01928 | hp1 | a0001 | c0002 | t0018 | g0036 | AMR | PEL | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG01928 | hp2 | a0001 | c0002 | t0018 | g0035 | AMR | PEL | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG01934 | hp1 | a0001 | c0001 | t0009 | g0001 | AMR | PEL | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG01934 | hp2 | a0001 | c0001 | t0006 | g0157 | AMR | PEL | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG01975 | hp1 | a0001 | c0002 | t0030 | g0002 | AMR | PEL | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG01975 | hp2 | a0001 | c0002 | t0018 | g0137 | AMR | PEL | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0243 | AMR | PEL | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG01978 | hp2 | a0001 | c0001 | t0005 | g0001 | AMR | PEL | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG01993 | hp1 | a0001 | c0002 | t0010 | g0002 | AMR | PEL | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG01993 | hp2 | a0001 | c0001 | t0016 | g0019 | AMR | PEL | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG02004 | hp1 | a0001 | c0001 | t0005 | g0001 | AMR | PEL | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG02015 | hp1 | a0001 | c0001 | t0016 | g0291 | EAS | KHV | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG02015 | hp2 | a0001 | c0001 | t0003 | g0204 | EAS | KHV | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG02027 | hp1 | a0001 | c0001 | t0014 | g0003 | EAS | KHV | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG02027 | hp2 | a0001 | c0001 | t0003 | g0194 | EAS | KHV | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG02040 | hp1 | a0001 | c0002 | t0035 | g0002 | EAS | KHV | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG02040 | hp2 | a0001 | c0001 | t0043 | g0001 | EAS | KHV | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG02055 | hp1 | a0001 | c0002 | t0004 | g0120 | AFR | ACB | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG02055 | hp2 | a0001 | c0001 | t0015 | g0023 | AFR | ACB | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG02056 | hp1 | a0001 | c0002 | t0002 | g0097 | EAS | KHV | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG02056 | hp2 | a0001 | c0001 | t0005 | g0293 | EAS | KHV | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG02071 | hp1 | a0001 | c0002 | t0059 | g0108 | EAS | KHV | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG02071 | hp2 | a0001 | c0001 | t0003 | g0183 | EAS | KHV | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | KHV | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG02074 | hp2 | a0001 | c0001 | t0003 | g0173 | EAS | KHV | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG02080 | hp1 | a0001 | c0001 | t0019 | g0271 | EAS | KHV | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | KHV | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | KHV | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG02083 | hp2 | a0001 | c0002 | t0010 | g0002 | EAS | KHV | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG02129 | hp1 | a0001 | c0001 | t0005 | g0001 | EAS | KHV | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | KHV | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG02135 | hp1 | a0001 | c0001 | t0003 | g0207 | EAS | KHV | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG02135 | hp2 | a0001 | c0001 | t0081 | g0241 | EAS | KHV | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG02145 | hp1 | a0001 | c0005 | t0019 | g0273 | AFR | ACB | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG02145 | hp2 | a0001 | c0001 | t0061 | g0266 | AFR | ACB | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | PEL | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG02165 | hp1 | a0001 | c0002 | t0002 | g0005 | EAS | CDX | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG02165 | hp2 | a0001 | c0001 | t0028 | g0001 | EAS | CDX | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | ACB | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG02257 | hp2 | a0001 | c0001 | t0011 | g0269 | AFR | ACB | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG02258 | hp1 | a0001 | c0002 | t0007 | g0027 | AFR | ACB | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG02258 | hp2 | a0001 | c0001 | t0006 | g0164 | AFR | ACB | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG02273 | hp1 | a0001 | c0001 | t0005 | g0288 | AMR | PEL | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG02273 | hp2 | a0001 | c0002 | t0067 | g0036 | AMR | PEL | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG02280 | hp1 | a0001 | c0001 | t0011 | g0210 | AFR | ACB | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG02280 | hp2 | a0001 | c0001 | t0045 | g0283 | AFR | ACB | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG02293 | hp1 | a0001 | c0001 | t0009 | g0018 | AMR | PEL | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG02293 | hp2 | a0001 | c0001 | t0003 | g0178 | AMR | PEL | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG02300 | hp1 | a0001 | c0002 | t0002 | g0279 | AMR | PEL | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG02300 | hp2 | a0001 | c0001 | t0003 | g0042 | AMR | PEL | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG02451 | hp1 | a0002 | c0003 | t0008 | g0016 | AFR | ACB | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG02451 | hp2 | a0001 | c0002 | t0060 | g0079 | AFR | ACB | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG02523 | hp1 | a0001 | c0001 | t0034 | g0041 | EAS | KHV | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG02523 | hp2 | a0001 | c0001 | t0019 | g0272 | EAS | KHV | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG02572 | hp1 | a0001 | c0002 | t0002 | g0099 | AFR | GWD | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG02572 | hp2 | a0001 | c0001 | t0008 | g0260 | AFR | GWD | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG02615 | hp1 | a0001 | c0001 | t0049 | g0201 | AFR | GWD | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG02615 | hp2 | a0001 | c0001 | t0086 | g0263 | AFR | GWD | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG02622 | hp1 | a0001 | c0002 | t0013 | g0116 | AFR | GWD | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG02622 | hp2 | a0001 | c0001 | t0024 | g0264 | AFR | GWD | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG02630 | hp1 | a0001 | c0001 | t0039 | g0007 | AFR | GWD | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG02630 | hp2 | a0001 | c0001 | t0027 | g0304 | AFR | GWD | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG02647 | hp2 | a0001 | c0001 | t0008 | g0265 | AFR | GWD | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0100 | SAS | PJL | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG02683 | hp2 | a0001 | c0002 | t0004 | g0123 | SAS | PJL | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG02698 | hp1 | a0001 | c0002 | t0002 | g0102 | SAS | PJL | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0088 | SAS | PJL | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | GWD | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | GWD | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG02723 | hp1 | a0001 | c0001 | t0015 | g0023 | AFR | GWD | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | GWD | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG02735 | hp2 | a0001 | c0002 | t0058 | g0200 | SAS | PJL | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG02738 | hp1 | a0001 | c0002 | t0066 | g0155 | SAS | PJL | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG02738 | hp2 | a0001 | c0001 | t0023 | g0058 | SAS | PJL | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0230 | AFR | GWD | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG02809 | hp2 | a0001 | c0001 | t0003 | g0186 | AFR | GWD | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG02818 | hp1 | a0001 | c0001 | t0015 | g0082 | AFR | GWD | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0226 | AFR | GWD | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | GWD | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG02886 | hp2 | a0001 | c0001 | t0011 | g0146 | AFR | GWD | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG02895 | hp1 | a0001 | c0001 | t0090 | g0051 | AFR | GWD | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG02895 | hp2 | a0001 | c0001 | t0022 | g0215 | AFR | GWD | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG02896 | hp2 | a0001 | c0001 | t0012 | g0007 | AFR | GWD | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG02897 | hp1 | a0001 | c0001 | t0012 | g0007 | AFR | GWD | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG02897 | hp2 | a0001 | c0001 | t0091 | g0051 | AFR | GWD | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG02922 | hp1 | a0001 | c0001 | t0015 | g0083 | AFR | ESN | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG02922 | hp2 | a0001 | c0001 | t0012 | g0081 | AFR | ESN | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG02965 | hp1 | a0001 | c0001 | t0006 | g0047 | AFR | ESN | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG02965 | hp2 | a0001 | c0001 | t0034 | g0151 | AFR | ESN | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG02970 | hp1 | a0001 | c0002 | t0013 | g0029 | AFR | ESN | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | ESN | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG02976 | hp1 | a0001 | c0001 | t0006 | g0047 | AFR | ESN | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | ESN | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG03017 | hp1 | a0001 | c0001 | t0077 | g0058 | SAS | PJL | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG03017 | hp2 | a0001 | c0001 | t0047 | g0118 | SAS | PJL | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | GWD | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG03041 | hp2 | a0001 | c0002 | t0079 | g0029 | AFR | GWD | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG03098 | hp1 | a0001 | c0002 | t0052 | g0132 | AFR | MSL | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0242 | AFR | MSL | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG03130 | hp1 | a0002 | c0003 | t0008 | g0261 | AFR | ESN | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG03130 | hp2 | a0001 | c0002 | t0021 | g0104 | AFR | ESN | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG03195 | hp1 | a0002 | c0003 | t0008 | g0016 | AFR | ESN | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG03195 | hp2 | a0001 | c0001 | t0071 | g0197 | AFR | ESN | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG03209 | hp1 | a0001 | c0002 | t0013 | g0298 | AFR | MSL | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG03209 | hp2 | a0001 | c0001 | t0041 | g0020 | AFR | MSL | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | MSL | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG03225 | hp2 | a0001 | c0001 | t0008 | g0259 | AFR | MSL | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG03239 | hp1 | a0001 | c0002 | t0013 | g0218 | SAS | PJL | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG03239 | hp2 | a0001 | c0002 | t0033 | g0065 | SAS | PJL | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG03453 | hp1 | a0001 | c0001 | t0026 | g0221 | AFR | MSL | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG03453 | hp2 | a0001 | c0001 | t0026 | g0222 | AFR | MSL | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG03486 | hp1 | a0001 | c0001 | t0012 | g0080 | AFR | MSL | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG03486 | hp2 | a0001 | c0001 | t0008 | g0267 | AFR | MSL | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG03490 | hp1 | a0001 | c0002 | t0002 | g0004 | SAS | PJL | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG03490 | hp2 | a0001 | c0001 | t0005 | g0001 | SAS | PJL | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG03491 | hp1 | a0001 | c0001 | t0023 | g0057 | SAS | PJL | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG03491 | hp2 | a0001 | c0002 | t0025 | g0256 | SAS | PJL | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG03492 | hp1 | a0001 | c0001 | t0023 | g0057 | SAS | PJL | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG03492 | hp2 | a0001 | c0001 | t0005 | g0001 | SAS | PJL | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG03516 | hp1 | a0001 | c0001 | t0011 | g0126 | AFR | ESN | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG03516 | hp2 | a0001 | c0001 | t0027 | g0282 | AFR | ESN | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG03540 | hp1 | a0001 | c0001 | t0008 | g0016 | AFR | GWD | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG03540 | hp2 | a0001 | c0001 | t0006 | g0166 | AFR | GWD | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG03579 | hp1 | a0001 | c0007 | t0003 | g0187 | AFR | MSL | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG03579 | hp2 | a0001 | c0001 | t0024 | g0059 | AFR | MSL | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG03654 | hp1 | a0001 | c0002 | t0002 | g0136 | SAS | PJL | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG03654 | hp2 | a0001 | c0001 | t0074 | g0202 | SAS | PJL | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG03669 | hp1 | a0001 | c0002 | t0063 | g0103 | SAS | PJL | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG03669 | hp2 | a0001 | c0002 | t0013 | g0111 | SAS | PJL | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0238 | SAS | STU | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG03688 | hp2 | a0001 | c0001 | t0003 | g0156 | SAS | STU | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG03704 | hp1 | a0001 | c0001 | t0003 | g0044 | SAS | PJL | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG03704 | hp2 | a0001 | c0002 | t0002 | g0064 | SAS | PJL | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG03710 | hp1 | a0001 | c0001 | t0014 | g0250 | SAS | PJL | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0249 | SAS | PJL | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0239 | SAS | BEB | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG03831 | hp2 | a0001 | c0002 | t0002 | g0107 | SAS | BEB | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG03834 | hp1 | a0001 | c0002 | t0025 | g0255 | SAS | BEB | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG03834 | hp2 | a0001 | c0001 | t0003 | g0091 | SAS | BEB | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG03942 | hp1 | a0001 | c0002 | t0002 | g0092 | SAS | BEB | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG03942 | hp2 | a0001 | c0002 | t0002 | g0004 | SAS | BEB | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG04115 | hp1 | a0001 | c0002 | t0004 | g0030 | SAS | STU | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG04115 | hp2 | a0001 | c0001 | t0005 | g0292 | SAS | STU | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG04184 | hp1 | a0001 | c0002 | t0007 | g0208 | SAS | BEB | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG04184 | hp2 | a0001 | c0002 | t0007 | g0006 | SAS | BEB | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG04199 | hp1 | a0001 | c0001 | t0005 | g0294 | SAS | STU | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | STU | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0251 | SAS | STU | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG04204 | hp2 | a0001 | c0002 | t0002 | g0089 | SAS | STU | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG04228 | hp1 | a0001 | c0002 | t0025 | g0145 | SAS | STU | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG04228 | hp2 | a0001 | c0008 | t0005 | g0301 | SAS | STU | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0231 | AFR | YRI | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA18522 | hp2 | a0001 | c0001 | t0003 | g0174 | AFR | YRI | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA18612 | hp1 | a0001 | c0001 | t0009 | g0018 | EAS | CHB | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA18612 | hp2 | a0001 | c0001 | t0005 | g0001 | EAS | CHB | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA18747 | hp1 | a0001 | c0002 | t0010 | g0190 | EAS | CHB | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA18747 | hp2 | a0001 | c0002 | t0002 | g0021 | EAS | CHB | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA18906 | hp1 | a0001 | c0001 | t0022 | g0212 | AFR | YRI | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA18906 | hp2 | a0001 | c0001 | t0015 | g0020 | AFR | YRI | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA18939 | hp1 | a0001 | c0002 | t0020 | g0135 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA18939 | hp2 | a0001 | c0002 | t0007 | g0049 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA18941 | hp1 | a0001 | c0002 | t0002 | g0028 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA18941 | hp2 | a0001 | c0001 | t0036 | g0084 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA18942 | hp1 | a0001 | c0001 | t0003 | g0045 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA18942 | hp2 | a0001 | c0001 | t0042 | g0085 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA18943 | hp1 | a0001 | c0002 | t0002 | g0008 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA18943 | hp2 | a0001 | c0001 | t0009 | g0063 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA18945 | hp1 | a0001 | c0002 | t0053 | g0002 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA18945 | hp2 | a0001 | c0001 | t0009 | g0009 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA18947 | hp1 | a0001 | c0001 | t0017 | g0287 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA18948 | hp1 | a0001 | c0002 | t0021 | g0004 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA18950 | hp1 | a0001 | c0001 | t0005 | g0019 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA18950 | hp2 | a0001 | c0002 | t0002 | g0074 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA18951 | hp1 | a0001 | c0002 | t0002 | g0075 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA18952 | hp1 | a0001 | c0001 | t0003 | g0040 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA18952 | hp2 | a0001 | c0002 | t0004 | g0010 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA18953 | hp1 | a0001 | c0001 | t0003 | g0189 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA18953 | hp2 | a0001 | c0002 | t0020 | g0130 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA18954 | hp1 | a0001 | c0002 | t0002 | g0217 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA18954 | hp2 | a0001 | c0001 | t0028 | g0001 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA18956 | hp2 | a0001 | c0001 | t0019 | g0060 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA18957 | hp1 | a0001 | c0002 | t0007 | g0006 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA18959 | hp1 | a0001 | c0002 | t0002 | g0021 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA18959 | hp2 | a0001 | c0001 | t0005 | g0295 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA18961 | hp1 | a0001 | c0001 | t0083 | g0112 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA18961 | hp2 | a0001 | c0002 | t0055 | g0128 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA18962 | hp1 | a0001 | c0001 | t0009 | g0009 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA18963 | hp1 | a0004 | c0006 | t0002 | g0073 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA18963 | hp2 | a0001 | c0001 | t0032 | g0069 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA18964 | hp1 | a0001 | c0002 | t0020 | g0191 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA18964 | hp2 | a0001 | c0001 | t0009 | g0018 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA18966 | hp1 | a0001 | c0002 | t0050 | g0032 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA18966 | hp2 | a0001 | c0001 | t0085 | g0013 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA18967 | hp1 | a0001 | c0001 | t0014 | g0247 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA18967 | hp2 | a0001 | c0002 | t0010 | g0017 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA18969 | hp1 | a0001 | c0002 | t0010 | g0017 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA18969 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA18970 | hp1 | a0001 | c0001 | t0029 | g0037 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA18970 | hp2 | a0001 | c0002 | t0018 | g0138 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA18971 | hp2 | a0001 | c0002 | t0007 | g0049 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA18973 | hp1 | a0001 | c0001 | t0012 | g0024 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA18973 | hp2 | a0001 | c0002 | t0010 | g0002 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA18975 | hp1 | a0001 | c0001 | t0005 | g0297 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA18979 | hp1 | a0001 | c0002 | t0002 | g0077 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA18979 | hp2 | a0001 | c0002 | t0010 | g0002 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA18980 | hp1 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA18980 | hp2 | a0001 | c0002 | t0007 | g0066 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA18982 | hp2 | a0001 | c0002 | t0004 | g0134 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA18983 | hp1 | a0001 | c0002 | t0002 | g0022 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA18983 | hp2 | a0001 | c0001 | t0029 | g0127 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA18985 | hp1 | a0001 | c0001 | t0017 | g0001 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA18985 | hp2 | a0001 | c0002 | t0010 | g0133 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA18986 | hp1 | a0001 | c0002 | t0002 | g0076 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA18986 | hp2 | a0001 | c0001 | t0016 | g0289 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA18990 | hp2 | a0001 | c0002 | t0002 | g0008 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA18991 | hp1 | a0001 | c0002 | t0002 | g0105 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA18993 | hp1 | a0001 | c0001 | t0003 | g0045 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA18993 | hp2 | a0001 | c0001 | t0048 | g0296 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA18994 | hp1 | a0001 | c0001 | t0003 | g0046 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA18994 | hp2 | a0001 | c0002 | t0062 | g0004 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA18995 | hp1 | a0001 | c0001 | t0044 | g0001 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA18995 | hp2 | a0001 | c0001 | t0057 | g0170 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA19000 | hp1 | a0001 | c0002 | t0007 | g0006 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA19000 | hp2 | a0001 | c0002 | t0002 | g0106 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA19002 | hp1 | a0001 | c0002 | t0004 | g0010 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA19002 | hp2 | a0001 | c0002 | t0002 | g0098 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA19004 | hp1 | a0001 | c0002 | t0010 | g0002 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA19005 | hp1 | a0001 | c0001 | t0019 | g0060 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA19007 | hp1 | a0001 | c0002 | t0004 | g0129 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA19007 | hp2 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA19009 | hp1 | a0001 | c0001 | t0016 | g0001 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA19009 | hp2 | a0001 | c0002 | t0002 | g0090 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA19010 | hp2 | a0001 | c0002 | t0002 | g0193 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA19011 | hp1 | a0001 | c0001 | t0009 | g0009 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA19011 | hp2 | a0001 | c0001 | t0069 | g0003 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA19012 | hp1 | a0001 | c0002 | t0002 | g0093 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA19012 | hp2 | a0001 | c0001 | t0014 | g0003 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA19030 | hp1 | a0001 | c0001 | t0022 | g0050 | AFR | LWK | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA19030 | hp2 | a0001 | c0001 | t0078 | g0198 | AFR | LWK | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA19043 | hp1 | a0001 | c0001 | t0011 | g0213 | AFR | LWK | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | LWK | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA19054 | hp1 | a0001 | c0002 | t0004 | g0010 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA19054 | hp2 | a0001 | c0001 | t0012 | g0024 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA19056 | hp1 | a0001 | c0002 | t0002 | g0064 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA19056 | hp2 | a0001 | c0001 | t0003 | g0195 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA19057 | hp1 | a0001 | c0001 | t0009 | g0303 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA19057 | hp2 | a0001 | c0002 | t0007 | g0206 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA19060 | hp1 | a0001 | c0002 | t0002 | g0101 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA19060 | hp2 | a0001 | c0002 | t0013 | g0095 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA19064 | hp2 | a0001 | c0001 | t0003 | g0196 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA19065 | hp2 | a0001 | c0002 | t0007 | g0205 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA19066 | hp1 | a0001 | c0001 | t0017 | g0290 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA19066 | hp2 | a0001 | c0001 | t0003 | g0177 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA19067 | hp1 | a0001 | c0002 | t0004 | g0002 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA19067 | hp2 | a0001 | c0001 | t0009 | g0063 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA19070 | hp1 | a0001 | c0001 | t0003 | g0046 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA19070 | hp2 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA19074 | hp1 | a0001 | c0001 | t0012 | g0025 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA19074 | hp2 | a0001 | c0002 | t0033 | g0302 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA19078 | hp1 | a0001 | c0001 | t0006 | g0168 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA19078 | hp2 | a0001 | c0001 | t0017 | g0285 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA19079 | hp1 | a0001 | c0002 | t0054 | g0032 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA19079 | hp2 | a0001 | c0001 | t0014 | g0054 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA19080 | hp1 | a0001 | c0002 | t0010 | g0017 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA19080 | hp2 | a0001 | c0002 | t0002 | g0070 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA19081 | hp1 | a0001 | c0002 | t0007 | g0006 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA19081 | hp2 | a0001 | c0002 | t0002 | g0022 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA19082 | hp1 | a0001 | c0002 | t0002 | g0028 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA19082 | hp2 | a0001 | c0001 | t0017 | g0143 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA19083 | hp1 | a0001 | c0002 | t0065 | g0006 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA19084 | hp1 | a0001 | c0001 | t0005 | g0284 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA19084 | hp2 | a0001 | c0001 | t0012 | g0025 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA19085 | hp1 | a0001 | c0002 | t0064 | g0209 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA19085 | hp2 | a0001 | c0002 | t0002 | g0072 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA19086 | hp1 | a0001 | c0001 | t0032 | g0182 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA19086 | hp2 | a0001 | c0002 | t0010 | g0276 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA19087 | hp1 | a0001 | c0002 | t0004 | g0002 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA19087 | hp2 | a0001 | c0001 | t0003 | g0175 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA19088 | hp1 | a0001 | c0001 | t0092 | g0037 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA19088 | hp2 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA19090 | hp1 | a0001 | c0001 | t0014 | g0003 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA19090 | hp2 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA19091 | hp1 | a0001 | c0002 | t0002 | g0071 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA19091 | hp2 | a0001 | c0001 | t0003 | g0188 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA19240 | hp1 | a0001 | c0001 | t0080 | g0114 | AFR | YRI | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA19240 | hp2 | a0001 | c0001 | t0011 | g0216 | AFR | YRI | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA20129 | hp1 | a0001 | c0001 | t0008 | g0258 | AFR | ASW | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ASW | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA20752 | hp1 | a0001 | c0002 | t0004 | g0124 | EUR | TSI | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA20752 | hp2 | a0001 | c0001 | t0006 | g0163 | EUR | TSI | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA20805 | hp1 | a0001 | c0002 | t0089 | g0139 | EUR | TSI | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA20805 | hp2 | a0001 | c0001 | t0003 | g0067 | EUR | TSI | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA20905 | hp1 | a0001 | c0002 | t0002 | g0280 | SAS | GIH | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA20905 | hp2 | a0001 | c0002 | t0013 | g0096 | SAS | GIH | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG01123 | hp1 | a0001 | c0002 | t0004 | g0125 | AMR | CLM | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG01123 | hp2 | a0001 | c0001 | t0016 | g0019 | AMR | CLM | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG02109 | hp1 | a0001 | c0001 | t0003 | g0171 | AFR | ACB | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG02109 | hp2 | a0001 | c0001 | t0024 | g0059 | AFR | ACB | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG02486 | hp1 | a0001 | c0001 | t0011 | g0211 | AFR | ACB | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG02486 | hp2 | a0001 | c0002 | t0013 | g0115 | AFR | ACB | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG02559 | hp1 | a0001 | c0001 | t0003 | g0153 | AFR | ACB | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG02559 | hp2 | a0001 | c0001 | t0008 | g0262 | AFR | ACB | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG03471 | hp1 | a0001 | c0001 | t0008 | g0228 | AFR | MSL | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG03471 | hp2 | a0001 | c0001 | t0011 | g0144 | AFR | MSL | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | USA | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
HG06807 | hp2 | a0001 | c0001 | t0003 | g0152 | AFR | USA | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA18955 | hp2 | a0001 | c0001 | t0005 | g0281 | EAS | JPT | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA20300 | hp1 | a0001 | c0001 | t0011 | g0214 | AFR | USA | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA20300 | hp2 | a0001 | c0001 | t0040 | g0086 | AFR | USA | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA21309 | hp1 | a0001 | c0002 | t0038 | g0223 | AFR | LWK | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
NA21309 | hp2 | a0001 | c0001 | t0011 | g0277 | AFR | LWK | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0240 | REF | REF | GNA11_chr19_3089362_3128999 | GNA11 | chr19 | 3089362 | 3128999 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:3110205
|
G | A | 1 | a0002 | 3 | HG02451.hp1 HG03130.hp1 HG03195.hp1 |
missense_variant | MODERATE | c.193G>A | p.Ala65Thr | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 2/7 | 483/4190 | 193/1080 | 65/359 | chr19 | 3110205 | ||
chr19:3113370
|
T | G | 1 | a0004 | 1 | NA18963.hp1 | missense_variant | MODERATE | c.362T>G | p.Val121Gly | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 3/7 | 652/4190 | 362/1080 | 121/359 | chr19 | 3113370 | ||
chr19:3114975
|
T | A | 1 | a0003 | 2 | HG01070.hp1 HG01071.hp1 |
missense_variant | MODERATE | c.508T>A | p.Leu170Met | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 4/7 | 798/4190 | 508/1080 | 170/359 | chr19 | 3114975 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:3110153
|
G | A | 1 | a0001c0005 | 1 | HG02145.hp1 | synonymous_variant | LOW | c.141G>A | p.Thr47Thr | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 2/7 | 431/4190 | 141/1080 | 47/359 | chr19 | 3110153 | ||
chr19:3110201
|
C | T | 1 | a0001c0009 | 1 | HG00099.hp2 | synonymous_variant | LOW | c.189C>T | p.His63His | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 2/7 | 479/4190 | 189/1080 | 63/359 | chr19 | 3110201 | ||
chr19:3119044
|
G | A | 1 | a0001c0007 | 1 | HG03579.hp1 | synonymous_variant | LOW | c.726G>A | p.Ser242Ser | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 5/7 | 1016/4190 | 726/1080 | 242/359 | chr19 | 3119044 | ||
chr19:3119241
|
C | T | 2 | a0001c0002a0004c0006 | 150 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(147): Show |
synonymous_variant | LOW | c.771C>T | p.Thr257Thr | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 6/7 | 1061/4190 | 771/1080 | 257/359 | chr19 | 3119241 | ||
chr19:3119355
|
C | T | 1 | a0001c0008 | 1 | HG04228.hp2 | synonymous_variant | LOW | c.885C>T | p.Phe295Phe | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 6/7 | 1175/4190 | 885/1080 | 295/359 | chr19 | 3119355 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:3094373
|
C | T | 3 | a0001c0001t0092a0001c0002t0010a0001c0002t0035 | 15 | HG00642.hp1 HG01070.hp2 HG01993.hp1 others(12): Show |
5_prime_UTR_variant | MODIFIER | c.-279C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/7 | 279 | chr19 | 3094373 | |||||
chr19:3094452
|
C | T | 2 | a0001c0001t0090a0001c0001t0091 | 2 | HG02895.hp1 HG02897.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-200C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/7 | chr19 | 3094452 | ||||||
chr19:3094496
|
G | A | 1 | a0001c0001t0036 | 1 | NA18941.hp2 | 5_prime_UTR_variant | MODIFIER | c.-156G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/7 | 156 | chr19 | 3094496 | |||||
chr19:3094529
|
G | A | 12 | a0001c0001t0012a0001c0001t0015a0001c0001t0026others(9): Show | 24 | HG01884.hp1 HG02055.hp2 HG02630.hp1 others(21): Show |
5_prime_UTR_variant | MODIFIER | c.-123G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/7 | 123 | chr19 | 3094529 | |||||
chr19:3121249
|
C | T | 1 | a0001c0002t0089 | 1 | NA20805.hp1 | 3_prime_UTR_variant | MODIFIER | c.*70C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 7/7 | 70 | chr19 | 3121249 | |||||
chr19:3121291
|
G | A | 13 | a0001c0001t0005a0001c0001t0009a0001c0001t0016others(10): Show | 54 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*112G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 7/7 | 112 | chr19 | 3121291 | |||||
chr19:3121301
|
A | AT | 3 | a0001c0001t0006a0001c0001t0048a0001c0001t0088 | 17 | HG00280.hp1 HG01106.hp1 HG01168.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*133dupT | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 7/7 | 134 | INFO_REALIGN_3_PRIME | chr19 | 3121301 | ||||
chr19:3121301
|
AT | A | 2 | a0001c0001t0016a0001c0001t0036 | 6 | HG01123.hp2 HG01993.hp2 HG02015.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*133delT | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 7/7 | 133 | INFO_REALIGN_3_PRIME | chr19 | 3121301 | ||||
chr19:3121344
|
G | C | 1 | a0001c0001t0049 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*165G>C | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 7/7 | 165 | chr19 | 3121344 | |||||
chr19:3121368
|
C | T | 1 | a0001c0002t0025 | 3 | HG03491.hp2 HG03834.hp1 HG04228.hp1 |
3_prime_UTR_variant | MODIFIER | c.*189C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 7/7 | 189 | chr19 | 3121368 | |||||
chr19:3121419
|
C | G | 1 | a0001c0001t0087 | 1 | HG01515.hp1 | 3_prime_UTR_variant | MODIFIER | c.*240C>G | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 7/7 | 240 | chr19 | 3121419 | |||||
chr19:3121442
|
C | G | 1 | a0001c0001t0087 | 1 | HG01515.hp1 | 3_prime_UTR_variant | MODIFIER | c.*263C>G | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 7/7 | 263 | chr19 | 3121442 | |||||
chr19:3121454
|
T | TA | 22 | a0001c0001t0028a0001c0001t0036a0001c0001t0037others(19): Show | 93 | HG00323.hp1 HG00408.hp2 HG00597.hp2 others(90): Show |
3_prime_UTR_variant | MODIFIER | c.*291dupA | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 7/7 | 292 | INFO_REALIGN_3_PRIME | chr19 | 3121454 | ||||
chr19:3121454
|
T | TAA | 12 | a0001c0001t0005a0001c0001t0009a0001c0001t0016others(9): Show | 53 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*290_*291dupAA | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 7/7 | 292 | INFO_REALIGN_3_PRIME | chr19 | 3121454 | ||||
chr19:3121454
|
TA | T | 9 | a0001c0001t0034a0001c0001t0042a0001c0001t0082others(6): Show | 10 | HG01069.hp2 HG01257.hp2 HG01517.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*291delA | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 7/7 | 291 | INFO_REALIGN_3_PRIME | chr19 | 3121454 | ||||
chr19:3121468
|
AAAG | A | 12 | a0001c0001t0087a0001c0002t0004a0001c0002t0010others(9): Show | 55 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*292_*294delGAA | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 7/7 | 292 | INFO_REALIGN_3_PRIME | chr19 | 3121468 | ||||
chr19:3121512
|
G | GC | 16 | a0001c0001t0087a0001c0002t0004a0001c0002t0010others(13): Show | 59 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*337dupC | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 7/7 | 338 | INFO_REALIGN_3_PRIME | chr19 | 3121512 | ||||
chr19:3121551
|
C | T | 1 | a0001c0001t0041 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*372C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 7/7 | 372 | chr19 | 3121551 | |||||
chr19:3121552
|
G | A | 1 | a0001c0001t0069 | 1 | NA19011.hp2 | 3_prime_UTR_variant | MODIFIER | c.*373G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 7/7 | 373 | chr19 | 3121552 | |||||
chr19:3121573
|
C | T | 1 | a0001c0002t0053 | 1 | NA18945.hp1 | 3_prime_UTR_variant | MODIFIER | c.*394C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 7/7 | 394 | chr19 | 3121573 | |||||
chr19:3121577
|
G | A | 1 | a0001c0001t0043 | 1 | HG02040.hp2 | 3_prime_UTR_variant | MODIFIER | c.*398G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 7/7 | 398 | chr19 | 3121577 | |||||
chr19:3121611
|
C | T | 1 | a0001c0001t0081 | 1 | HG02135.hp2 | 3_prime_UTR_variant | MODIFIER | c.*432C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 7/7 | 432 | chr19 | 3121611 | |||||
chr19:3121701
|
G | A | 5 | a0001c0001t0015a0001c0001t0019a0001c0001t0041others(2): Show | 12 | HG01433.hp1 HG02055.hp2 HG02080.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*522G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 7/7 | 522 | chr19 | 3121701 | |||||
chr19:3121741
|
C | T | 1 | a0001c0001t0024 | 3 | HG02109.hp2 HG02622.hp2 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*562C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 7/7 | 562 | chr19 | 3121741 | |||||
chr19:3121758
|
A | T | 1 | a0001c0001t0080 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*579A>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 7/7 | 579 | chr19 | 3121758 | |||||
chr19:3121906
|
C | T | 1 | a0001c0001t0023 | 3 | HG02738.hp2 HG03491.hp1 HG03492.hp1 |
3_prime_UTR_variant | MODIFIER | c.*727C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 7/7 | 727 | chr19 | 3121906 | |||||
chr19:3121910
|
C | G | 34 | a0001c0001t0061a0001c0001t0078a0001c0001t0087others(31): Show | 152 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(149): Show |
3_prime_UTR_variant | MODIFIER | c.*731C>G | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 7/7 | 731 | chr19 | 3121910 | |||||
chr19:3121928
|
G | A | 1 | a0001c0001t0037 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*749G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 7/7 | 749 | chr19 | 3121928 | |||||
chr19:3121958
|
G | A | 1 | a0001c0001t0071 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*779G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 7/7 | 779 | chr19 | 3121958 | |||||
chr19:3121971
|
G | A | 1 | a0001c0002t0020 | 4 | HG00423.hp1 NA18939.hp1 NA18953.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*792G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 7/7 | 792 | chr19 | 3121971 | |||||
chr19:3122056
|
G | T | 1 | a0001c0002t0052 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*877G>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 7/7 | 877 | chr19 | 3122056 | |||||
chr19:3122098
|
G | A | 2 | a0001c0001t0072a0001c0001t0082 | 2 | HG01516.hp2 HG01517.hp2 |
3_prime_UTR_variant | MODIFIER | c.*919G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 7/7 | 919 | chr19 | 3122098 | |||||
chr19:3122147
|
A | G | 6 | a0001c0001t0008a0001c0001t0024a0001c0001t0026others(3): Show | 20 | HG01109.hp2 HG01891.hp2 HG02109.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*968A>G | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 7/7 | 968 | chr19 | 3122147 | |||||
chr19:3122200
|
C | T | 1 | a0001c0001t0047 | 1 | HG03017.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1021C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 7/7 | 1021 | chr19 | 3122200 | |||||
chr19:3122245
|
C | T | 6 | a0001c0002t0007a0001c0002t0033a0001c0002t0058others(3): Show | 19 | HG00738.hp2 HG01175.hp1 HG02258.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*1066C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 7/7 | 1066 | chr19 | 3122245 | |||||
chr19:3122367
|
G | A | 1 | a0001c0001t0073 | 1 | HG01192.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1188G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 7/7 | 1188 | chr19 | 3122367 | |||||
chr19:3122382
|
T | C | 28 | a0001c0001t0005a0001c0001t0008a0001c0001t0009others(25): Show | 91 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(88): Show |
3_prime_UTR_variant | MODIFIER | c.*1203T>C | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 7/7 | 1203 | chr19 | 3122382 | |||||
chr19:3122399
|
G | A | 1 | a0001c0001t0074 | 1 | HG03654.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1220G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 7/7 | 1220 | chr19 | 3122399 | |||||
chr19:3122430
|
C | T | 5 | a0001c0001t0012a0001c0001t0036a0001c0001t0039others(2): Show | 12 | HG02630.hp1 HG02896.hp2 HG02897.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1251C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 7/7 | 1251 | chr19 | 3122430 | |||||
chr19:3122460
|
C | T | 1 | a0001c0002t0063 | 1 | HG03669.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1281C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 7/7 | 1281 | chr19 | 3122460 | |||||
chr19:3122544
|
G | A | 6 | a0001c0001t0015a0001c0001t0019a0001c0001t0041others(3): Show | 13 | HG01243.hp1 HG01433.hp1 HG02055.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1365G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 7/7 | 1365 | chr19 | 3122544 | |||||
chr19:3122645
|
T | C | 1 | a0001c0002t0059 | 1 | HG02071.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1466T>C | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 7/7 | 1466 | chr19 | 3122645 | |||||
chr19:3122657
|
A | G | 18 | a0001c0001t0003a0001c0001t0006a0001c0001t0012others(15): Show | 79 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*1478A>G | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 7/7 | 1478 | chr19 | 3122657 | |||||
chr19:3122720
|
C | A | 15 | a0001c0001t0005a0001c0001t0009a0001c0001t0016others(12): Show | 57 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(54): Show |
3_prime_UTR_variant | MODIFIER | c.*1541C>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 7/7 | 1541 | chr19 | 3122720 | |||||
chr19:3122844
|
G | A | 1 | a0001c0001t0083 | 1 | NA18961.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1665G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 7/7 | 1665 | chr19 | 3122844 | |||||
chr19:3122845
|
C | G | 1 | a0001c0001t0083 | 1 | NA18961.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1666C>G | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 7/7 | 1666 | chr19 | 3122845 | |||||
chr19:3122886
|
G | A | 2 | a0001c0002t0050a0001c0002t0054 | 2 | NA18966.hp1 NA19079.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1707G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 7/7 | 1707 | chr19 | 3122886 | |||||
chr19:3122906
|
T | C | 1 | a0001c0002t0064 | 1 | NA19085.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1727T>C | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 7/7 | 1727 | chr19 | 3122906 | |||||
chr19:3122943
|
T | C | 34 | a0001c0001t0003a0001c0001t0005a0001c0001t0006others(31): Show | 137 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(134): Show |
3_prime_UTR_variant | MODIFIER | c.*1764T>C | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 7/7 | 1764 | chr19 | 3122943 | |||||
chr19:3122944
|
A | AC | 12 | a0001c0001t0005a0001c0001t0014a0001c0001t0016others(9): Show | 43 | HG00438.hp1 HG00673.hp2 HG00738.hp1 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*1775dupC | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 7/7 | 1776 | INFO_REALIGN_3_PRIME | chr19 | 3122944 | ||||
chr19:3122944
|
A | ACC | 5 | a0001c0001t0009a0001c0001t0028a0001c0001t0044others(2): Show | 17 | HG00408.hp1 HG00423.hp2 HG01891.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*1774_*1775dupCC | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 7/7 | 1776 | INFO_REALIGN_3_PRIME | chr19 | 3122944 | ||||
chr19:3122944
|
AC | A | 16 | a0001c0001t0003a0001c0001t0006a0001c0001t0015others(13): Show | 76 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(73): Show |
3_prime_UTR_variant | MODIFIER | c.*1775delC | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 7/7 | 1775 | INFO_REALIGN_3_PRIME | chr19 | 3122944 | ||||
chr19:3122947
|
C | G | 32 | a0001c0001t0087a0001c0002t0002a0001c0002t0004others(29): Show | 150 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(147): Show |
3_prime_UTR_variant | MODIFIER | c.*1768C>G | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 7/7 | 1768 | chr19 | 3122947 | |||||
chr19:3122949
|
C | G | 1 | a0001c0001t0077 | 1 | HG03017.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1770C>G | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 7/7 | 1770 | chr19 | 3122949 | |||||
chr19:3123107
|
G | A | 1 | a0001c0001t0056 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1928G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 7/7 | 1928 | chr19 | 3123107 | |||||
chr19:3123115
|
C | T | 33 | a0001c0001t0087a0001c0002t0002a0001c0002t0004others(30): Show | 151 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(148): Show |
3_prime_UTR_variant | MODIFIER | c.*1936C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 7/7 | 1936 | chr19 | 3123115 | |||||
chr19:3123171
|
T | C | 81 | a0001c0001t0003a0001c0001t0005a0001c0001t0006others(78): Show | 322 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(319): Show |
3_prime_UTR_variant | MODIFIER | c.*1992T>C | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 7/7 | 1992 | chr19 | 3123171 | |||||
chr19:3123209
|
G | A | 1 | a0001c0001t0037 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2030G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 7/7 | 2030 | chr19 | 3123209 | |||||
chr19:3123210
|
A | C | 1 | a0001c0001t0037 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2031A>C | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 7/7 | 2031 | chr19 | 3123210 | |||||
chr19:3123229
|
C | A | 2 | a0001c0002t0013a0001c0002t0079 | 9 | HG02486.hp2 HG02622.hp1 HG02970.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2050C>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 7/7 | 2050 | chr19 | 3123229 | |||||
chr19:3123240
|
G | C | 2 | a0001c0001t0090a0001c0001t0091 | 2 | HG02895.hp1 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2061G>C | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 7/7 | 2061 | chr19 | 3123240 | |||||
chr19:3123360
|
C | A | 1 | a0001c0002t0065 | 1 | NA19083.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2181C>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 7/7 | 2181 | chr19 | 3123360 | |||||
chr19:3123471
|
C | T | 3 | a0001c0001t0031a0001c0001t0074a0001c0001t0084 | 4 | HG00639.hp2 HG01069.hp2 HG01071.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2292C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 7/7 | 2292 | chr19 | 3123471 | |||||
chr19:3123495
|
C | T | 1 | a0001c0002t0066 | 1 | HG02738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2316C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 7/7 | 2316 | chr19 | 3123495 | |||||
chr19:3123543
|
A | G | 5 | a0001c0001t0012a0001c0001t0036a0001c0001t0039others(2): Show | 12 | HG02630.hp1 HG02896.hp2 HG02897.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2364A>G | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 7/7 | 2364 | chr19 | 3123543 | |||||
chr19:3123575
|
C | T | 1 | a0001c0002t0052 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2396C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 7/7 | 2396 | chr19 | 3123575 | |||||
chr19:3123576
|
G | A | 2 | a0001c0002t0018a0001c0002t0067 | 6 | HG01256.hp1 HG01928.hp1 HG01928.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2397G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 7/7 | 2397 | chr19 | 3123576 | |||||
chr19:3123637
|
C | T | 16 | a0001c0001t0003a0001c0001t0006a0001c0001t0012others(13): Show | 77 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*2458C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 7/7 | 2458 | chr19 | 3123637 | |||||
chr19:3123668
|
A | G | 1 | a0001c0001t0076 | 1 | HG00609.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2489A>G | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 7/7 | 2489 | chr19 | 3123668 | |||||
chr19:3123709
|
C | T | 1 | a0001c0002t0060 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2530C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 7/7 | 2530 | chr19 | 3123709 | |||||
chr19:3123864
|
G | A | 1 | a0001c0001t0022 | 3 | HG02895.hp2 NA18906.hp1 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2685G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 7/7 | 2685 | chr19 | 3123864 | |||||
chr19:3123873
|
C | T | 1 | a0001c0001t0044 | 1 | NA18995.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2694C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 7/7 | 2694 | chr19 | 3123873 | |||||
chr19:3123919
|
A | G | 13 | a0001c0001t0005a0001c0001t0009a0001c0001t0016others(10): Show | 54 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*2740A>G | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 7/7 | 2740 | chr19 | 3123919 | |||||
chr19:3123947
|
T | C | 13 | a0001c0001t0005a0001c0001t0009a0001c0001t0016others(10): Show | 54 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*2768T>C | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 7/7 | 2768 | chr19 | 3123947 | |||||
chr19:3123965
|
C | T | 1 | a0001c0002t0062 | 1 | NA18994.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2786C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 7/7 | 2786 | chr19 | 3123965 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:3094916
|
G | C | 1 | a0001c0002t0033g0065 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.136+129G>C | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3094916 | ||||||
chr19:3094925
|
C | T | 41 | a0001c0001t0003g0300a0001c0001t0005g0001a0001c0001t0005g0019others(38): Show | 58 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(55): Show |
intron_variant | MODIFIER | c.136+138C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3094925 | ||||||
chr19:3094941
|
T | A | 1 | a0001c0002t0007g0066 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.136+154T>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3094941 | ||||||
chr19:3095190
|
C | T | 1 | a0001c0001t0027g0304 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.136+403C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3095190 | ||||||
chr19:3095237
|
C | T | 38 | a0001c0001t0003g0300a0001c0001t0005g0001a0001c0001t0005g0019others(35): Show | 54 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.136+450C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3095237 | ||||||
chr19:3095264
|
C | G | 1 | a0001c0001t0006g0278 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.136+477C>G | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3095264 | ||||||
chr19:3095299
|
C | T | 1 | a0001c0001t0009g0303 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.136+512C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3095299 | ||||||
chr19:3095357
|
C | T | 1 | a0001c0001t0011g0277 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.136+570C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3095357 | ||||||
chr19:3095473
|
AGCCCTGT others(13): Show |
A | 3 | a0001c0002t0010g0017a0001c0002t0010g0276a0001c0002t0033g0302 | 5 | NA18967.hp2 NA18969.hp1 NA19074.hp2 others(2): Show |
intron_variant | MODIFIER | c.136+696_136+715del others(20): Show |
GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3095473 | |||||
chr19:3095483
|
ACTCCATG others(13): Show |
A | 1 | a0001c0001t0003g0067 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.136+716_136+735del others(20): Show |
GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3095483 | |||||
chr19:3095487
|
C | T | 2 | a0001c0001t0072g0274a0001c0001t0082g0275 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.136+700C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3095487 | ||||||
chr19:3095554
|
T | C | 1 | a0001c0001t0037g0068 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.136+767T>C | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3095554 | ||||||
chr19:3095669
|
C | T | 4 | a0001c0001t0019g0060a0001c0001t0019g0271a0001c0001t0019g0272others(1): Show | 5 | HG02080.hp1 HG02145.hp1 HG02523.hp2 others(2): Show |
intron_variant | MODIFIER | c.136+882C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3095669 | ||||||
chr19:3095839
|
G | T | 1 | a0001c0002t0002g0270 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.136+1052G>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3095839 | ||||||
chr19:3095928
|
C | T | 1 | a0001c0001t0011g0269 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.136+1141C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3095928 | ||||||
chr19:3095929
|
T | C | 195 | a0001c0001t0001g0011a0001c0001t0001g0026a0001c0001t0001g0038others(192): Show | 244 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.136+1142T>C | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3095929 | ||||||
chr19:3095935
|
T | C | 1 | a0001c0001t0071g0197 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.136+1148T>C | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3095935 | ||||||
chr19:3095971
|
T | G | 32 | a0001c0001t0003g0204a0001c0001t0003g0207a0001c0001t0006g0047others(29): Show | 37 | HG00639.hp2 HG01069.hp2 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.136+1184T>G | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3095971 | ||||||
chr19:3096126
|
T | A | 1 | a0001c0001t0075g0219 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.136+1339T>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3096126 | ||||||
chr19:3096221
|
T | A | 1 | a0001c0001t0078g0198 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.136+1434T>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3096221 | ||||||
chr19:3096257
|
G | T | 61 | a0001c0001t0003g0040a0001c0001t0003g0041a0001c0001t0003g0042others(58): Show | 69 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(66): Show |
intron_variant | MODIFIER | c.136+1470G>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3096257 | ||||||
chr19:3096281
|
AG | A | 213 | a0001c0001t0001g0026a0001c0001t0001g0078a0001c0001t0001g0087others(210): Show | 262 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(259): Show |
intron_variant | MODIFIER | c.136+1499delG | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3096281 | |||||
chr19:3096287
|
C | A | 213 | a0001c0001t0001g0026a0001c0001t0001g0078a0001c0001t0001g0087others(210): Show | 262 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(259): Show |
intron_variant | MODIFIER | c.136+1500C>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3096287 | ||||||
chr19:3096303
|
C | T | 5 | a0001c0001t0080g0114a0001c0002t0013g0029a0001c0002t0013g0115others(2): Show | 5 | HG02486.hp2 HG02622.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.136+1516C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3096303 | ||||||
chr19:3096352
|
C | T | 1 | a0001c0002t0004g0150 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.136+1565C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3096352 | ||||||
chr19:3096653
|
G | C | 1 | a0001c0001t0005g0281 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.136+1866G>C | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3096653 | ||||||
chr19:3096707
|
A | AC | 54 | a0001c0001t0001g0224a0001c0001t0003g0040a0001c0001t0003g0041others(51): Show | 61 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.136+1925dupC | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3096707 | |||||
chr19:3096711
|
C | CG | 9 | a0001c0001t0003g0045a0001c0001t0003g0046a0001c0001t0003g0192others(6): Show | 11 | HG00621.hp2 HG00673.hp1 HG02027.hp2 others(8): Show |
intron_variant | MODIFIER | c.136+1924_136+1925i others(3): Show |
GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3096711 | ||||||
chr19:3096790
|
T | G | 174 | a0001c0001t0001g0078a0001c0001t0001g0225a0001c0001t0001g0226others(171): Show | 214 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(211): Show |
intron_variant | MODIFIER | c.136+2003T>G | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3096790 | ||||||
chr19:3096924
|
C | T | 1 | a0001c0001t0026g0222 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.136+2137C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3096924 | ||||||
chr19:3096975
|
C | G | 14 | a0001c0001t0001g0011a0001c0001t0001g0038a0001c0001t0001g0148others(11): Show | 17 | HG01884.hp2 HG02486.hp1 HG02723.hp2 others(14): Show |
intron_variant | MODIFIER | c.136+2188C>G | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3096975 | ||||||
chr19:3097058
|
G | T | 21 | a0001c0001t0001g0147a0001c0001t0003g0186a0001c0001t0008g0016others(18): Show | 23 | HG01891.hp2 HG02109.hp2 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.136+2271G>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3097058 | ||||||
chr19:3097104
|
C | G | 1 | a0001c0001t0076g0257 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.136+2317C>G | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3097104 | ||||||
chr19:3097124
|
C | T | 1 | a0001c0002t0004g0150 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.136+2337C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3097124 | ||||||
chr19:3097183
|
C | A | 135 | a0001c0001t0001g0026a0001c0001t0001g0078a0001c0001t0001g0087others(132): Show | 183 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(180): Show |
intron_variant | MODIFIER | c.136+2396C>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3097183 | ||||||
chr19:3097184
|
G | A | 1 | a0001c0001t0037g0068 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.136+2397G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3097184 | ||||||
chr19:3097205
|
TGCA | T | 40 | a0001c0001t0003g0040a0001c0001t0003g0041a0001c0001t0003g0042others(37): Show | 47 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.136+2423_136+2425d others(5): Show |
GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3097205 | |||||
chr19:3097223
|
C | T | 14 | a0001c0001t0012g0007a0001c0001t0012g0024a0001c0001t0012g0025others(11): Show | 18 | HG02055.hp2 HG02630.hp1 HG02723.hp1 others(15): Show |
intron_variant | MODIFIER | c.136+2436C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3097223 | ||||||
chr19:3097276
|
C | T | 1 | a0001c0002t0060g0079 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.136+2489C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3097276 | ||||||
chr19:3097299
|
G | A | 44 | a0001c0001t0003g0040a0001c0001t0003g0041a0001c0001t0003g0042others(41): Show | 51 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.136+2512G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3097299 | ||||||
chr19:3097362
|
C | T | 1 | a0001c0002t0004g0150 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.136+2575C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3097362 | ||||||
chr19:3097383
|
G | A | 1 | a0001c0001t0001g0225 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.136+2596G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3097383 | ||||||
chr19:3097472
|
T | C | 1 | a0001c0002t0051g0117 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.136+2685T>C | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3097472 | ||||||
chr19:3097572
|
C | T | 1 | a0001c0001t0011g0126 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.136+2785C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3097572 | ||||||
chr19:3097587
|
A | T | 1 | a0001c0002t0004g0150 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.136+2800A>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3097587 | ||||||
chr19:3097650
|
G | A | 1 | a0001c0001t0003g0044 | 2 | HG00280.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.136+2863G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3097650 | ||||||
chr19:3097652
|
G | T | 1 | a0001c0002t0013g0111 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.136+2865G>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3097652 | ||||||
chr19:3097662
|
C | T | 3 | a0001c0001t0001g0078a0001c0001t0001g0109a0001c0001t0001g0110 | 3 | HG02074.hp1 NA18956.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.136+2875C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3097662 | ||||||
chr19:3097700
|
G | A | 1 | a0001c0001t0008g0258 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.136+2913G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3097700 | ||||||
chr19:3097725
|
T | A | 1 | a0001c0002t0010g0276 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.136+2938T>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3097725 | ||||||
chr19:3097753
|
C | T | 1 | a0001c0002t0013g0111 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.136+2966C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3097753 | ||||||
chr19:3097772
|
C | T | 1 | a0001c0001t0056g0113 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.136+2985C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3097772 | ||||||
chr19:3097872
|
C | T | 89 | a0001c0001t0001g0078a0001c0001t0001g0100a0001c0001t0001g0109others(86): Show | 115 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.136+3085C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3097872 | ||||||
chr19:3097900
|
G | A | 1 | a0001c0008t0005g0301 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.136+3113G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3097900 | ||||||
chr19:3097925
|
G | C | 19 | a0001c0001t0008g0016a0001c0001t0008g0228a0001c0001t0008g0229others(16): Show | 21 | HG01109.hp2 HG01891.hp2 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.136+3138G>C | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3097925 | ||||||
chr19:3097945
|
A | G | 1 | a0001c0001t0005g0297 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.136+3158A>G | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3097945 | ||||||
chr19:3097954
|
TG | T | 38 | a0001c0001t0003g0040a0001c0001t0003g0041a0001c0001t0003g0042others(35): Show | 43 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(40): Show |
intron_variant | MODIFIER | c.136+3173delG | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3097954 | |||||
chr19:3098014
|
G | C | 14 | a0001c0001t0012g0007a0001c0001t0012g0024a0001c0001t0012g0025others(11): Show | 18 | HG02055.hp2 HG02630.hp1 HG02723.hp1 others(15): Show |
intron_variant | MODIFIER | c.136+3227G>C | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3098014 | ||||||
chr19:3098145
|
A | G | 107 | a0001c0001t0001g0078a0001c0001t0001g0100a0001c0001t0001g0109others(104): Show | 139 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.136+3358A>G | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3098145 | ||||||
chr19:3098247
|
A | G | 247 | a0001c0001t0001g0011a0001c0001t0001g0038a0001c0001t0001g0078others(244): Show | 313 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(310): Show |
intron_variant | MODIFIER | c.136+3460A>G | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3098247 | ||||||
chr19:3098283
|
C | T | 7 | a0001c0001t0011g0144a0001c0001t0019g0060a0001c0001t0019g0271others(4): Show | 8 | HG01243.hp1 HG01433.hp1 HG02080.hp1 others(5): Show |
intron_variant | MODIFIER | c.136+3496C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3098283 | ||||||
chr19:3098289
|
C | T | 2 | a0001c0001t0011g0144a0001c0002t0004g0030 | 3 | HG01099.hp2 HG03471.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.136+3502C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3098289 | ||||||
chr19:3098440
|
A | G | 2 | a0001c0002t0002g0022a0001c0002t0002g0077 | 3 | NA18979.hp1 NA18983.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.136+3653A>G | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3098440 | ||||||
chr19:3098614
|
C | T | 7 | a0001c0001t0001g0015a0001c0001t0001g0056a0001c0001t0001g0248others(4): Show | 11 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(8): Show |
intron_variant | MODIFIER | c.136+3827C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3098614 | ||||||
chr19:3098627
|
G | T | 5 | a0001c0001t0019g0060a0001c0001t0019g0271a0001c0001t0019g0272others(2): Show | 6 | HG01433.hp1 HG02080.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.136+3840G>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3098627 | ||||||
chr19:3098656
|
C | T | 1 | a0001c0002t0025g0145 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.136+3869C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3098656 | ||||||
chr19:3098762
|
T | G | 1 | a0001c0001t0019g0271 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.136+3975T>G | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3098762 | ||||||
chr19:3098766
|
G | A | 4 | a0001c0001t0001g0052a0001c0001t0001g0226a0001c0001t0001g0230others(1): Show | 5 | HG02257.hp1 HG02717.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.136+3979G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3098766 | ||||||
chr19:3098812
|
G | A | 1 | a0001c0001t0001g0232 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.136+4025G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3098812 | ||||||
chr19:3098944
|
C | T | 1 | a0001c0005t0019g0273 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.136+4157C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3098944 | ||||||
chr19:3098949
|
A | G | 2 | a0001c0002t0010g0017a0001c0002t0010g0276 | 4 | NA18967.hp2 NA18969.hp1 NA19080.hp1 others(1): Show |
intron_variant | MODIFIER | c.136+4162A>G | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3098949 | ||||||
chr19:3098986
|
G | A | 1 | a0001c0002t0007g0199 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.136+4199G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3098986 | ||||||
chr19:3099031
|
A | G | 253 | a0001c0001t0001g0011a0001c0001t0001g0038a0001c0001t0001g0078others(250): Show | 321 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(318): Show |
intron_variant | MODIFIER | c.136+4244A>G | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3099031 | ||||||
chr19:3099058
|
C | T | 1 | a0001c0001t0056g0113 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.136+4271C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3099058 | ||||||
chr19:3099105
|
C | T | 58 | a0001c0001t0005g0001a0001c0001t0005g0019a0001c0001t0005g0062others(55): Show | 79 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.136+4318C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3099105 | ||||||
chr19:3099125
|
G | C | 1 | a0001c0002t0021g0184 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.136+4338G>C | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3099125 | ||||||
chr19:3099150
|
G | T | 1 | a0001c0001t0011g0126 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.136+4363G>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3099150 | ||||||
chr19:3099242
|
C | CAG | 150 | a0001c0001t0001g0011a0001c0001t0001g0038a0001c0001t0001g0078others(147): Show | 190 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.136+4456_136+4457d others(4): Show |
GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3099242 | |||||
chr19:3099337
|
T | C | 1 | a0001c0002t0068g0141 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.136+4550T>C | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3099337 | ||||||
chr19:3099370
|
A | G | 1 | a0001c0001t0008g0265 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.136+4583A>G | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3099370 | ||||||
chr19:3099383
|
C | T | 1 | a0001c0001t0075g0219 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.136+4596C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3099383 | ||||||
chr19:3099455
|
G | A | 54 | a0001c0001t0005g0001a0001c0001t0005g0019a0001c0001t0005g0062others(51): Show | 75 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.136+4668G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3099455 | ||||||
chr19:3099456
|
G | T | 1 | a0001c0001t0003g0153 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.136+4669G>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3099456 | ||||||
chr19:3099537
|
C | T | 1 | a0001c0002t0059g0108 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.136+4750C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3099537 | ||||||
chr19:3099557
|
A | G | 257 | a0001c0001t0001g0011a0001c0001t0001g0038a0001c0001t0001g0100others(254): Show | 325 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(322): Show |
intron_variant | MODIFIER | c.136+4770A>G | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3099557 | ||||||
chr19:3099756
|
C | T | 104 | a0001c0001t0001g0100a0001c0001t0001g0252a0001c0001t0001g0253others(101): Show | 137 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.136+4969C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3099756 | ||||||
chr19:3099766
|
C | T | 7 | a0001c0001t0001g0011a0001c0001t0001g0038a0001c0001t0001g0142others(4): Show | 10 | HG02145.hp1 HG02647.hp1 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.136+4979C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3099766 | ||||||
chr19:3099890
|
C | A | 1 | a0001c0001t0075g0219 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.136+5103C>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3099890 | ||||||
chr19:3099984
|
T | C | 249 | a0001c0001t0001g0011a0001c0001t0001g0038a0001c0001t0001g0100others(246): Show | 316 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(313): Show |
intron_variant | MODIFIER | c.136+5197T>C | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3099984 | ||||||
chr19:3100001
|
C | T | 45 | a0001c0001t0003g0040a0001c0001t0003g0041a0001c0001t0003g0042others(42): Show | 51 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.136+5214C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3100001 | ||||||
chr19:3100004
|
G | A | 1 | a0001c0001t0011g0269 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.136+5217G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3100004 | ||||||
chr19:3100049
|
C | T | 1 | a0001c0002t0021g0184 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.136+5262C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3100049 | ||||||
chr19:3100050
|
G | A | 2 | a0001c0002t0007g0199a0001c0002t0058g0200 | 2 | HG01175.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.136+5263G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3100050 | ||||||
chr19:3100062
|
C | A | 1 | a0001c0002t0002g0089 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.136+5275C>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3100062 | ||||||
chr19:3100120
|
CCTGGGAT | C | 54 | a0001c0001t0001g0100a0001c0001t0003g0091a0001c0002t0002g0004others(51): Show | 70 | HG00323.hp1 HG00408.hp2 HG00597.hp2 others(67): Show |
intron_variant | MODIFIER | c.136+5351_136+5357d others(9): Show |
GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3100120 | |||||
chr19:3100191
|
G | A | 14 | a0001c0001t0012g0007a0001c0001t0012g0024a0001c0001t0012g0025others(11): Show | 18 | HG02055.hp2 HG02630.hp1 HG02723.hp1 others(15): Show |
intron_variant | MODIFIER | c.136+5404G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3100191 | ||||||
chr19:3100203
|
A | C | 1 | a0001c0001t0001g0249 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.136+5416A>C | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3100203 | ||||||
chr19:3100253
|
G | A | 41 | a0001c0001t0001g0011a0001c0001t0001g0038a0001c0001t0001g0142others(38): Show | 48 | HG00639.hp2 HG01069.hp2 HG01071.hp2 others(45): Show |
intron_variant | MODIFIER | c.136+5466G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3100253 | ||||||
chr19:3100472
|
G | T | 1 | a0001c0001t0037g0068 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.136+5685G>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3100472 | ||||||
chr19:3100481
|
A | G | 1 | a0001c0002t0004g0030 | 2 | HG01099.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.136+5694A>G | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3100481 | ||||||
chr19:3100504
|
C | G | 1 | a0001c0002t0002g0076 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.136+5717C>G | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3100504 | ||||||
chr19:3100540
|
C | G | 38 | a0001c0001t0001g0011a0001c0001t0001g0038a0001c0001t0001g0142others(35): Show | 45 | HG00639.hp2 HG01069.hp2 HG01071.hp2 others(42): Show |
intron_variant | MODIFIER | c.136+5753C>G | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3100540 | ||||||
chr19:3100777
|
G | A | 3 | a0001c0001t0006g0154a0001c0001t0006g0163a0001c0001t0006g0278 | 3 | HG00280.hp1 HG01516.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.136+5990G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3100777 | ||||||
chr19:3100815
|
C | T | 1 | a0001c0001t0011g0216 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.136+6028C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3100815 | ||||||
chr19:3100872
|
C | T | 4 | a0001c0001t0001g0052a0001c0001t0001g0226a0001c0001t0001g0230others(1): Show | 5 | HG02257.hp1 HG02717.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.136+6085C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3100872 | ||||||
chr19:3100928
|
C | T | 1 | a0001c0001t0070g0167 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.136+6141C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3100928 | ||||||
chr19:3101016
|
C | T | 1 | a0001c0001t0056g0113 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.136+6229C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3101016 | ||||||
chr19:3101073
|
G | A | 1 | a0001c0001t0011g0269 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.136+6286G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3101073 | ||||||
chr19:3101077
|
C | T | 101 | a0001c0001t0001g0100a0001c0001t0003g0091a0001c0001t0056g0113others(98): Show | 133 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.136+6290C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3101077 | ||||||
chr19:3101084
|
T | C | 160 | a0001c0001t0001g0100a0001c0001t0001g0252a0001c0001t0001g0253others(157): Show | 214 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.136+6297T>C | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3101084 | ||||||
chr19:3101095
|
C | T | 40 | a0001c0001t0003g0040a0001c0001t0003g0041a0001c0001t0003g0042others(37): Show | 45 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.136+6308C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3101095 | ||||||
chr19:3101165
|
G | A | 8 | a0001c0001t0001g0013a0001c0001t0001g0053a0001c0001t0001g0233others(5): Show | 10 | HG00544.hp1 HG00621.hp1 NA18961.hp1 others(7): Show |
intron_variant | MODIFIER | c.136+6378G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3101165 | ||||||
chr19:3101184
|
T | A | 1 | a0001c0002t0004g0129 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.136+6397T>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3101184 | ||||||
chr19:3101251
|
G | A | 39 | a0001c0001t0005g0001a0001c0001t0005g0019a0001c0001t0005g0062others(36): Show | 56 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(53): Show |
intron_variant | MODIFIER | c.136+6464G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3101251 | ||||||
chr19:3101362
|
C | G | 321 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0013others(318): Show | 401 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(398): Show |
intron_variant | MODIFIER | c.136+6575C>G | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3101362 | ||||||
chr19:3101407
|
C | T | 35 | a0001c0001t0005g0001a0001c0001t0005g0019a0001c0001t0005g0062others(32): Show | 52 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.136+6620C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3101407 | ||||||
chr19:3101423
|
C | CG | 4 | a0001c0001t0005g0284a0001c0001t0006g0168a0001c0001t0083g0112others(1): Show | 4 | NA18961.hp1 NA19078.hp1 NA19084.hp1 others(1): Show |
intron_variant | MODIFIER | c.136+6639dupG | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3101423 | |||||
chr19:3101516
|
G | A | 1 | a0001c0001t0071g0197 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.136+6729G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3101516 | ||||||
chr19:3101558
|
G | A | 1 | a0001c0002t0002g0090 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.136+6771G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3101558 | ||||||
chr19:3101566
|
G | GC | 337 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0013others(334): Show | 424 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(421): Show |
intron_variant | MODIFIER | c.136+6780dupC | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3101566 | |||||
chr19:3101791
|
G | T | 1 | a0001c0001t0011g0144 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.136+7004G>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3101791 | ||||||
chr19:3101891
|
C | T | 1 | a0001c0001t0056g0113 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.136+7104C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3101891 | ||||||
chr19:3101942
|
A | G | 1 | a0001c0001t0011g0277 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.136+7155A>G | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3101942 | ||||||
chr19:3101942
|
A | T | 1 | a0001c0001t0048g0296 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.136+7155A>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3101942 | ||||||
chr19:3102039
|
T | G | 1 | a0001c0001t0048g0296 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.136+7252T>G | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3102039 | ||||||
chr19:3102044
|
C | T | 1 | a0001c0001t0026g0222 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.136+7257C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3102044 | ||||||
chr19:3102125
|
C | T | 14 | a0001c0001t0012g0007a0001c0001t0012g0024a0001c0001t0012g0025others(11): Show | 18 | HG02055.hp2 HG02630.hp1 HG02723.hp1 others(15): Show |
intron_variant | MODIFIER | c.136+7338C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3102125 | ||||||
chr19:3102129
|
C | CA | 34 | a0001c0001t0001g0251a0001c0001t0003g0204a0001c0001t0003g0207others(31): Show | 38 | HG00639.hp2 HG01069.hp2 HG01071.hp2 others(35): Show |
intron_variant | MODIFIER | c.136+7352dupA | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3102129 | |||||
chr19:3102170
|
G | A | 101 | a0001c0001t0001g0100a0001c0001t0003g0091a0001c0001t0056g0113others(98): Show | 133 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.136+7383G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3102170 | ||||||
chr19:3102265
|
C | T | 35 | a0001c0001t0003g0040a0001c0001t0003g0041a0001c0001t0003g0042others(32): Show | 40 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(37): Show |
intron_variant | MODIFIER | c.136+7478C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3102265 | ||||||
chr19:3102326
|
G | T | 1 | a0001c0002t0004g0140 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.136+7539G>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3102326 | ||||||
chr19:3102370
|
G | A | 1 | a0001c0001t0003g0196 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.136+7583G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3102370 | ||||||
chr19:3102401
|
C | T | 1 | a0001c0002t0002g0107 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.136+7614C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3102401 | ||||||
chr19:3102440
|
C | T | 1 | a0001c0002t0038g0223 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.136+7653C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3102440 | ||||||
chr19:3102520
|
G | A | 1 | a0001c0001t0075g0219 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.137-7629G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3102520 | ||||||
chr19:3102537
|
G | A | 1 | a0001c0001t0075g0219 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.137-7612G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3102537 | ||||||
chr19:3102622
|
T | G | 1 | a0001c0002t0004g0119 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.137-7527T>G | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3102622 | ||||||
chr19:3102669
|
G | T | 5 | a0001c0001t0019g0060a0001c0001t0019g0271a0001c0001t0019g0272others(2): Show | 6 | HG01433.hp1 HG02080.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.137-7480G>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3102669 | ||||||
chr19:3102743
|
G | A | 4 | a0001c0001t0012g0007a0001c0001t0012g0080a0001c0001t0012g0081others(1): Show | 5 | HG02630.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.137-7406G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3102743 | ||||||
chr19:3102750
|
G | T | 45 | a0001c0001t0087g0122a0001c0002t0002g0131a0001c0002t0002g0136others(42): Show | 61 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(58): Show |
intron_variant | MODIFIER | c.137-7399G>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3102750 | ||||||
chr19:3102784
|
G | A | 55 | a0001c0001t0005g0001a0001c0001t0005g0019a0001c0001t0005g0062others(52): Show | 76 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.137-7365G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3102784 | ||||||
chr19:3102884
|
G | A | 1 | a0001c0001t0011g0269 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.137-7265G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3102884 | ||||||
chr19:3102896
|
G | C | 39 | a0001c0001t0005g0001a0001c0001t0005g0019a0001c0001t0005g0062others(36): Show | 56 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(53): Show |
intron_variant | MODIFIER | c.137-7253G>C | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3102896 | ||||||
chr19:3102985
|
C | T | 39 | a0001c0001t0005g0001a0001c0001t0005g0019a0001c0001t0005g0062others(36): Show | 56 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(53): Show |
intron_variant | MODIFIER | c.137-7164C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3102985 | ||||||
chr19:3102991
|
G | A | 1 | a0001c0001t0075g0219 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.137-7158G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3102991 | ||||||
chr19:3103018
|
T | G | 1 | a0001c0001t0011g0144 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.137-7131T>G | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3103018 | ||||||
chr19:3103047
|
C | T | 1 | a0001c0001t0075g0219 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.137-7102C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3103047 | ||||||
chr19:3103085
|
C | T | 5 | a0001c0001t0012g0024a0001c0001t0012g0025a0001c0001t0036g0084others(2): Show | 7 | NA18941.hp2 NA18942.hp2 NA18973.hp1 others(4): Show |
intron_variant | MODIFIER | c.137-7064C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3103085 | ||||||
chr19:3103125
|
C | T | 1 | a0001c0002t0025g0256 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.137-7024C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3103125 | ||||||
chr19:3103136
|
C | T | 1 | a0001c0002t0089g0139 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.137-7013C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3103136 | ||||||
chr19:3103203
|
G | GTTAT | 13 | a0001c0001t0012g0024a0001c0001t0012g0025a0001c0001t0019g0060others(10): Show | 16 | HG01433.hp1 HG02080.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.137-6923_137-6920d others(6): Show |
GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3103203 | |||||
chr19:3103252
|
T | C | 218 | a0001c0001t0001g0100a0001c0001t0001g0252a0001c0001t0001g0253others(215): Show | 279 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(276): Show |
intron_variant | MODIFIER | c.137-6897T>C | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3103252 | ||||||
chr19:3103502
|
T | C | 1 | a0001c0001t0075g0219 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.137-6647T>C | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3103502 | ||||||
chr19:3103505
|
G | A | 1 | a0001c0001t0011g0211 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.137-6644G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3103505 | ||||||
chr19:3103519
|
C | CG | 8 | a0001c0001t0001g0149a0001c0001t0003g0207a0001c0002t0007g0006others(5): Show | 11 | HG01175.hp1 HG02135.hp1 HG03041.hp1 others(8): Show |
intron_variant | MODIFIER | c.137-6630_137-6629i others(3): Show |
GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3103519 | ||||||
chr19:3103519
|
C | CT | 18 | a0001c0001t0001g0026a0001c0001t0001g0053a0001c0001t0001g0110others(15): Show | 20 | HG00544.hp1 HG00621.hp1 HG00642.hp2 others(17): Show |
intron_variant | MODIFIER | c.137-6599dupT | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3103519 | |||||
chr19:3103519
|
C | CTTTTTT | 15 | a0001c0001t0003g0040a0001c0001t0003g0041a0001c0001t0003g0045others(12): Show | 17 | HG00544.hp2 HG00558.hp1 HG00673.hp1 others(14): Show |
intron_variant | MODIFIER | c.137-6604_137-6599d others(8): Show |
GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3103519 | |||||
chr19:3103519
|
C | CTTTTTTT | 19 | a0001c0001t0003g0044a0001c0001t0003g0046a0001c0001t0003g0152others(16): Show | 21 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(18): Show |
intron_variant | MODIFIER | c.137-6605_137-6599d others(9): Show |
GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3103519 | |||||
chr19:3103519
|
C | CTTTTTTT others(1): Show |
12 | a0001c0001t0003g0042a0001c0001t0003g0067a0001c0001t0003g0159others(9): Show | 14 | HG01106.hp2 HG01168.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.137-6606_137-6599d others(10): Show |
GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3103519 | |||||
chr19:3103519
|
C | CTTTTTTT others(6): Show |
2 | a0001c0001t0006g0047a0001c0001t0006g0165 | 3 | HG01106.hp1 HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.137-6611_137-6599d others(15): Show |
GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3103519 | |||||
chr19:3103519
|
C | CTTTTTTT others(7): Show |
1 | a0001c0001t0006g0166 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.137-6612_137-6599d others(16): Show |
GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3103519 | |||||
chr19:3103519
|
CT | C | 25 | a0001c0001t0001g0011a0001c0001t0001g0054a0001c0001t0001g0056others(22): Show | 31 | HG00099.hp1 HG00558.hp2 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.137-6599delT | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3103519 | |||||
chr19:3103519
|
CTT | C | 16 | a0001c0001t0022g0215a0001c0002t0002g0021a0001c0002t0002g0028others(13): Show | 18 | HG00423.hp1 HG00735.hp2 HG01123.hp1 others(15): Show |
intron_variant | MODIFIER | c.137-6600_137-6599d others(4): Show |
GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3103519 | |||||
chr19:3103519
|
CTTT | C | 78 | a0001c0001t0001g0100a0001c0001t0003g0091a0001c0001t0003g0156others(75): Show | 105 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.137-6601_137-6599d others(5): Show |
GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3103519 | |||||
chr19:3103519
|
CTTTTT | C | 6 | a0001c0001t0012g0081a0001c0001t0019g0060a0001c0001t0019g0271others(3): Show | 7 | HG01433.hp1 HG02080.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.137-6603_137-6599d others(7): Show |
GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3103519 | |||||
chr19:3103519
|
CTTTTTT | C | 14 | a0001c0001t0012g0007a0001c0001t0012g0024a0001c0001t0012g0025others(11): Show | 18 | HG01192.hp2 HG02055.hp2 HG02630.hp1 others(15): Show |
intron_variant | MODIFIER | c.137-6604_137-6599d others(8): Show |
GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3103519 | |||||
chr19:3103519
|
CTTTTTTT | C | 8 | a0001c0001t0005g0019a0001c0001t0005g0281a0001c0001t0005g0284others(5): Show | 10 | HG01123.hp2 HG01993.hp2 HG03516.hp2 others(7): Show |
intron_variant | MODIFIER | c.137-6605_137-6599d others(9): Show |
GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3103519 | |||||
chr19:3103519
|
CTTTTTTT others(1): Show |
C | 30 | a0001c0001t0005g0001a0001c0001t0005g0062a0001c0001t0005g0286others(27): Show | 45 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(42): Show |
intron_variant | MODIFIER | c.137-6606_137-6599d others(10): Show |
GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3103519 | |||||
chr19:3103519
|
CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0056g0113 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.137-6610_137-6599d others(14): Show |
GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3103519 | |||||
chr19:3103520
|
T | G | 20 | a0001c0001t0001g0038a0001c0001t0001g0142a0001c0001t0001g0147others(17): Show | 22 | HG00639.hp2 HG01884.hp2 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.137-6629T>G | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3103520 | ||||||
chr19:3103521
|
T | G | 10 | a0001c0001t0001g0011a0001c0001t0001g0148a0001c0001t0011g0210others(7): Show | 12 | HG01069.hp2 HG01071.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.137-6628T>G | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3103521 | ||||||
chr19:3103522
|
T | G | 1 | a0001c0001t0022g0215 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.137-6627T>G | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3103522 | ||||||
chr19:3103619
|
G | T | 103 | a0001c0001t0001g0100a0001c0001t0003g0091a0001c0001t0056g0113others(100): Show | 135 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.137-6530G>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3103619 | ||||||
chr19:3103627
|
G | C | 1 | a0001c0001t0036g0084 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.137-6522G>C | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3103627 | ||||||
chr19:3103628
|
C | G | 1 | a0001c0001t0036g0084 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.137-6521C>G | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3103628 | ||||||
chr19:3103671
|
G | A | 5 | a0001c0001t0012g0024a0001c0001t0012g0025a0001c0001t0036g0084others(2): Show | 7 | NA18941.hp2 NA18942.hp2 NA18973.hp1 others(4): Show |
intron_variant | MODIFIER | c.137-6478G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3103671 | ||||||
chr19:3103812
|
C | G | 14 | a0001c0001t0012g0007a0001c0001t0012g0024a0001c0001t0012g0025others(11): Show | 18 | HG02055.hp2 HG02630.hp1 HG02723.hp1 others(15): Show |
intron_variant | MODIFIER | c.137-6337C>G | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3103812 | ||||||
chr19:3103847
|
G | A | 57 | a0001c0001t0003g0040a0001c0001t0003g0041a0001c0001t0003g0042others(54): Show | 65 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(62): Show |
intron_variant | MODIFIER | c.137-6302G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3103847 | ||||||
chr19:3103878
|
G | A | 1 | a0001c0001t0037g0068 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.137-6271G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3103878 | ||||||
chr19:3103892
|
A | G | 2 | a0001c0002t0013g0115a0001c0002t0013g0116 | 2 | HG02486.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.137-6257A>G | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3103892 | ||||||
chr19:3103950
|
G | T | 1 | a0001c0001t0011g0216 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.137-6199G>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3103950 | ||||||
chr19:3104011
|
G | A | 55 | a0001c0001t0001g0100a0001c0001t0003g0091a0001c0001t0061g0266others(52): Show | 71 | HG00323.hp1 HG00408.hp2 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.137-6138G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3104011 | ||||||
chr19:3104029
|
C | A | 1 | a0001c0001t0071g0197 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.137-6120C>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3104029 | ||||||
chr19:3104095
|
C | T | 60 | a0001c0001t0001g0011a0001c0001t0001g0038a0001c0001t0001g0142others(57): Show | 69 | HG00639.hp2 HG01069.hp2 HG01071.hp2 others(66): Show |
intron_variant | MODIFIER | c.137-6054C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3104095 | ||||||
chr19:3104109
|
C | T | 1 | a0001c0001t0056g0113 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.137-6040C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3104109 | ||||||
chr19:3104111
|
C | T | 39 | a0001c0001t0005g0001a0001c0001t0005g0019a0001c0001t0005g0062others(36): Show | 56 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(53): Show |
intron_variant | MODIFIER | c.137-6038C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3104111 | ||||||
chr19:3104112
|
G | A | 1 | a0001c0002t0002g0071 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.137-6037G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3104112 | ||||||
chr19:3104148
|
A | G | 60 | a0001c0001t0005g0001a0001c0001t0005g0019a0001c0001t0005g0062others(57): Show | 82 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.137-6001A>G | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3104148 | ||||||
chr19:3104158
|
G | C | 281 | a0001c0001t0001g0011a0001c0001t0001g0038a0001c0001t0001g0100others(278): Show | 352 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(349): Show |
intron_variant | MODIFIER | c.137-5991G>C | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3104158 | ||||||
chr19:3104169
|
G | A | 1 | a0001c0002t0007g0206 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.137-5980G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3104169 | ||||||
chr19:3104227
|
A | T | 60 | a0001c0001t0005g0001a0001c0001t0005g0019a0001c0001t0005g0062others(57): Show | 82 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.137-5922A>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3104227 | ||||||
chr19:3104242
|
G | T | 35 | a0001c0001t0003g0040a0001c0001t0003g0041a0001c0001t0003g0042others(32): Show | 40 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(37): Show |
intron_variant | MODIFIER | c.137-5907G>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3104242 | ||||||
chr19:3104355
|
C | A | 1 | a0001c0001t0045g0283 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.137-5794C>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3104355 | ||||||
chr19:3104429
|
T | A | 6 | a0001c0001t0001g0011a0001c0001t0001g0038a0001c0001t0001g0142others(3): Show | 9 | HG02647.hp1 HG02723.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.137-5720T>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3104429 | ||||||
chr19:3104497
|
G | C | 1 | a0001c0001t0037g0068 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.137-5652G>C | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3104497 | ||||||
chr19:3104498
|
T | G | 14 | a0001c0001t0012g0007a0001c0001t0012g0024a0001c0001t0012g0025others(11): Show | 18 | HG02055.hp2 HG02630.hp1 HG02723.hp1 others(15): Show |
intron_variant | MODIFIER | c.137-5651T>G | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3104498 | ||||||
chr19:3104595
|
G | T | 6 | a0001c0001t0019g0060a0001c0001t0019g0271a0001c0001t0019g0272others(3): Show | 7 | HG01433.hp1 HG01884.hp1 HG02080.hp1 others(4): Show |
intron_variant | MODIFIER | c.137-5554G>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3104595 | ||||||
chr19:3104631
|
T | C | 284 | a0001c0001t0001g0011a0001c0001t0001g0038a0001c0001t0001g0100others(281): Show | 355 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(352): Show |
intron_variant | MODIFIER | c.137-5518T>C | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3104631 | ||||||
chr19:3104632
|
G | A | 14 | a0001c0001t0012g0007a0001c0001t0012g0024a0001c0001t0012g0025others(11): Show | 18 | HG02055.hp2 HG02630.hp1 HG02723.hp1 others(15): Show |
intron_variant | MODIFIER | c.137-5517G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3104632 | ||||||
chr19:3104654
|
T | C | 178 | a0001c0001t0001g0011a0001c0001t0001g0038a0001c0001t0001g0142others(175): Show | 217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.137-5495T>C | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3104654 | ||||||
chr19:3104766
|
C | T | 102 | a0001c0001t0001g0100a0001c0001t0003g0091a0001c0001t0061g0266others(99): Show | 134 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.137-5383C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3104766 | ||||||
chr19:3104853
|
G | A | 14 | a0001c0001t0012g0007a0001c0001t0012g0024a0001c0001t0012g0025others(11): Show | 18 | HG02055.hp2 HG02630.hp1 HG02723.hp1 others(15): Show |
intron_variant | MODIFIER | c.137-5296G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3104853 | ||||||
chr19:3104888
|
G | A | 2 | a0001c0001t0026g0221a0001c0001t0026g0222 | 2 | HG03453.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.137-5261G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3104888 | ||||||
chr19:3104960
|
G | A | 19 | a0001c0001t0008g0016a0001c0001t0008g0228a0001c0001t0008g0229others(16): Show | 21 | HG01109.hp2 HG01891.hp2 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.137-5189G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3104960 | ||||||
chr19:3105053
|
C | T | 1 | a0001c0008t0005g0301 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.137-5096C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3105053 | ||||||
chr19:3105111
|
G | A | 39 | a0001c0001t0001g0011a0001c0001t0001g0038a0001c0001t0001g0142others(36): Show | 46 | HG00639.hp2 HG01069.hp2 HG01071.hp2 others(43): Show |
intron_variant | MODIFIER | c.137-5038G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3105111 | ||||||
chr19:3105211
|
ATGGCCGG others(5): Show |
A | 3 | a0001c0001t0006g0157a0001c0001t0015g0020a0001c0001t0041g0020 | 3 | HG01934.hp2 HG03209.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.137-4933_137-4922d others(14): Show |
GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3105211 | |||||
chr19:3105216
|
C | T | 112 | a0001c0001t0003g0040a0001c0001t0003g0041a0001c0001t0003g0042others(109): Show | 141 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.137-4933C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3105216 | ||||||
chr19:3105232
|
T | C | 2 | a0001c0001t0015g0020a0001c0001t0041g0020 | 2 | HG03209.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.137-4917T>C | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3105232 | ||||||
chr19:3105291
|
G | A | 3 | a0001c0002t0002g0070a0001c0002t0002g0072a0001c0002t0002g0074 | 3 | NA18950.hp2 NA19080.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.137-4858G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3105291 | ||||||
chr19:3105326
|
G | A | 2 | a0001c0001t0005g0062a0001c0001t0046g0062 | 2 | HG00738.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.137-4823G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3105326 | ||||||
chr19:3105337
|
G | A | 1 | a0001c0001t0056g0113 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.137-4812G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3105337 | ||||||
chr19:3105410
|
G | C | 2 | a0001c0002t0010g0031a0001c0002t0035g0031 | 2 | HG00642.hp1 HG01070.hp2 |
intron_variant | MODIFIER | c.137-4739G>C | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3105410 | ||||||
chr19:3105426
|
T | A | 3 | a0001c0002t0002g0012a0001c0002t0002g0185a0001c0002t0021g0012 | 4 | HG01256.hp2 HG01257.hp1 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.137-4723T>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3105426 | ||||||
chr19:3105524
|
G | A | 1 | a0001c0001t0005g0286 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.137-4625G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3105524 | ||||||
chr19:3105577
|
C | T | 1 | a0001c0001t0001g0220 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.137-4572C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3105577 | ||||||
chr19:3105579
|
T | C | 284 | a0001c0001t0001g0011a0001c0001t0001g0038a0001c0001t0001g0100others(281): Show | 355 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(352): Show |
intron_variant | MODIFIER | c.137-4570T>C | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3105579 | ||||||
chr19:3105582
|
C | T | 1 | a0001c0001t0037g0068 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.137-4567C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3105582 | ||||||
chr19:3105638
|
A | G | 55 | a0001c0001t0005g0001a0001c0001t0005g0019a0001c0001t0005g0062others(52): Show | 76 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.137-4511A>G | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3105638 | ||||||
chr19:3105708
|
G | A | 2 | a0001c0001t0011g0144a0001c0001t0011g0146 | 2 | HG02886.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.137-4441G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3105708 | ||||||
chr19:3105710
|
C | T | 3 | a0001c0001t0015g0020a0001c0001t0015g0083a0001c0001t0041g0020 | 3 | HG02922.hp1 HG03209.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.137-4439C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3105710 | ||||||
chr19:3105777
|
G | A | 1 | a0001c0001t0056g0113 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.137-4372G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3105777 | ||||||
chr19:3105810
|
T | C | 2 | a0001c0001t0090g0051a0001c0001t0091g0051 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.137-4339T>C | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3105810 | ||||||
chr19:3105933
|
C | G | 1 | a0001c0001t0056g0113 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.137-4216C>G | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3105933 | ||||||
chr19:3105957
|
G | A | 1 | a0001c0002t0020g0130 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.137-4192G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3105957 | ||||||
chr19:3105979
|
A | G | 1 | a0001c0001t0026g0221 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.137-4170A>G | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3105979 | ||||||
chr19:3105989
|
G | A | 102 | a0001c0001t0001g0100a0001c0001t0003g0091a0001c0001t0061g0266others(99): Show | 134 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.137-4160G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3105989 | ||||||
chr19:3106057
|
G | A | 3 | a0001c0001t0031g0048a0001c0001t0031g0203a0001c0001t0084g0048 | 3 | HG00639.hp2 HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.137-4092G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3106057 | ||||||
chr19:3106308
|
A | G | 187 | a0001c0001t0001g0100a0001c0001t0003g0040a0001c0001t0003g0041others(184): Show | 232 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.137-3841A>G | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3106308 | ||||||
chr19:3106359
|
C | A | 1 | a0001c0001t0006g0157 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.137-3790C>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3106359 | ||||||
chr19:3106534
|
G | A | 1 | a0001c0005t0019g0273 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.137-3615G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3106534 | ||||||
chr19:3106590
|
G | C | 103 | a0001c0001t0001g0100a0001c0001t0003g0091a0001c0001t0061g0266others(100): Show | 135 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.137-3559G>C | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3106590 | ||||||
chr19:3106638
|
C | T | 2 | a0001c0001t0012g0080a0001c0001t0012g0081 | 2 | HG02922.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.137-3511C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3106638 | ||||||
chr19:3106639
|
A | G | 25 | a0001c0001t0012g0007a0001c0001t0012g0024a0001c0001t0012g0025others(22): Show | 30 | HG01243.hp1 HG01433.hp1 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.137-3510A>G | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3106639 | ||||||
chr19:3106653
|
GC | G | 253 | a0001c0001t0001g0100a0001c0001t0003g0040a0001c0001t0003g0041others(250): Show | 319 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(316): Show |
intron_variant | MODIFIER | c.137-3494delC | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3106653 | |||||
chr19:3106710
|
C | T | 3 | a0001c0001t0015g0020a0001c0001t0015g0083a0001c0001t0041g0020 | 3 | HG02922.hp1 HG03209.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.137-3439C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3106710 | ||||||
chr19:3106751
|
C | CATGT | 20 | a0001c0001t0012g0007a0001c0001t0012g0024a0001c0001t0012g0025others(17): Show | 24 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.137-3393_137-3390d others(6): Show |
GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3106751 | |||||
chr19:3106785
|
G | A | 14 | a0001c0001t0012g0007a0001c0001t0012g0024a0001c0001t0012g0025others(11): Show | 18 | HG02055.hp2 HG02630.hp1 HG02723.hp1 others(15): Show |
intron_variant | MODIFIER | c.137-3364G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3106785 | ||||||
chr19:3106905
|
G | A | 1 | a0001c0001t0003g0153 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.137-3244G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3106905 | ||||||
chr19:3106947
|
G | A | 74 | a0001c0001t0001g0011a0001c0001t0001g0038a0001c0001t0001g0142others(71): Show | 98 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.137-3202G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3106947 | ||||||
chr19:3106967
|
T | C | 2 | a0001c0002t0002g0022a0001c0002t0002g0077 | 3 | NA18979.hp1 NA18983.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.137-3182T>C | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3106967 | ||||||
chr19:3106990
|
G | A | 1 | a0001c0001t0037g0068 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.137-3159G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3106990 | ||||||
chr19:3107143
|
G | GGA | 74 | a0001c0001t0001g0011a0001c0001t0001g0038a0001c0001t0001g0142others(71): Show | 98 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.137-3003_137-3002d others(4): Show |
GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3107143 | |||||
chr19:3107205
|
C | T | 105 | a0001c0001t0001g0100a0001c0001t0001g0252a0001c0001t0001g0253others(102): Show | 137 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.137-2944C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3107205 | ||||||
chr19:3107351
|
G | A | 1 | a0001c0001t0003g0153 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.137-2798G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3107351 | ||||||
chr19:3107437
|
G | A | 9 | a0001c0001t0012g0007a0001c0001t0012g0024a0001c0001t0012g0025others(6): Show | 12 | HG02630.hp1 HG02896.hp2 HG02897.hp1 others(9): Show |
intron_variant | MODIFIER | c.137-2712G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3107437 | ||||||
chr19:3107580
|
A | C | 281 | a0001c0001t0001g0011a0001c0001t0001g0038a0001c0001t0001g0100others(278): Show | 352 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(349): Show |
intron_variant | MODIFIER | c.137-2569A>C | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3107580 | ||||||
chr19:3107752
|
G | A | 5 | a0001c0001t0001g0230a0001c0001t0027g0282a0001c0001t0027g0304others(2): Show | 5 | HG02280.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.137-2397G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3107752 | ||||||
chr19:3107792
|
C | T | 1 | a0001c0001t0056g0113 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.137-2357C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3107792 | ||||||
chr19:3107808
|
G | A | 2 | a0001c0001t0012g0080a0001c0001t0012g0081 | 2 | HG02922.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.137-2341G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3107808 | ||||||
chr19:3107839
|
C | T | 1 | a0001c0001t0036g0084 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.137-2310C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3107839 | ||||||
chr19:3107884
|
C | T | 22 | a0001c0001t0003g0194a0001c0001t0003g0196a0001c0001t0008g0016others(19): Show | 24 | HG01109.hp2 HG01891.hp2 HG02027.hp2 others(21): Show |
intron_variant | MODIFIER | c.137-2265C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3107884 | ||||||
chr19:3107999
|
T | C | 253 | a0001c0001t0001g0100a0001c0001t0003g0040a0001c0001t0003g0041others(250): Show | 319 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(316): Show |
intron_variant | MODIFIER | c.137-2150T>C | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3107999 | ||||||
chr19:3108126
|
T | C | 3 | a0001c0002t0002g0070a0001c0002t0002g0072a0001c0002t0002g0074 | 3 | NA18950.hp2 NA19080.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.137-2023T>C | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3108126 | ||||||
chr19:3108341
|
T | G | 1 | a0001c0001t0006g0168 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.137-1808T>G | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3108341 | ||||||
chr19:3108458
|
G | A | 1 | a0001c0001t0008g0259 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.137-1691G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3108458 | ||||||
chr19:3108476
|
T | G | 1 | a0001c0001t0006g0168 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.137-1673T>G | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3108476 | ||||||
chr19:3108546
|
G | A | 51 | a0001c0001t0003g0040a0001c0001t0003g0041a0001c0001t0003g0042others(48): Show | 58 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(55): Show |
intron_variant | MODIFIER | c.137-1603G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3108546 | ||||||
chr19:3108585
|
G | A | 9 | a0001c0001t0012g0007a0001c0001t0012g0024a0001c0001t0012g0025others(6): Show | 12 | HG02630.hp1 HG02896.hp2 HG02897.hp1 others(9): Show |
intron_variant | MODIFIER | c.137-1564G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3108585 | ||||||
chr19:3108614
|
A | G | 18 | a0001c0001t0003g0204a0001c0001t0003g0207a0001c0001t0011g0211others(15): Show | 22 | HG01175.hp1 HG02015.hp2 HG02135.hp1 others(19): Show |
intron_variant | MODIFIER | c.137-1535A>G | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3108614 | ||||||
chr19:3108908
|
C | T | 1 | a0001c0001t0001g0226 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.137-1241C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3108908 | ||||||
chr19:3109107
|
G | T | 2 | a0001c0002t0002g0270a0001c0002t0063g0103 | 2 | HG00735.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.137-1042G>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3109107 | ||||||
chr19:3109227
|
C | G | 11 | a0001c0001t0003g0156a0001c0001t0003g0159a0001c0001t0003g0180others(8): Show | 13 | HG00639.hp1 HG00741.hp1 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.137-922C>G | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3109227 | ||||||
chr19:3109241
|
G | GTAA | 23 | a0001c0001t0001g0148a0001c0001t0003g0153a0001c0001t0008g0016others(20): Show | 25 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.137-907_137-906ins others(3): Show |
GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3109241 | |||||
chr19:3109331
|
G | A | 1 | a0001c0001t0011g0146 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.137-818G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3109331 | ||||||
chr19:3109360
|
A | G | 8 | a0001c0001t0001g0011a0001c0001t0001g0038a0001c0001t0001g0142others(5): Show | 11 | HG01891.hp1 HG02647.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.137-789A>G | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3109360 | ||||||
chr19:3109360
|
A | T | 27 | a0001c0001t0011g0213a0001c0001t0011g0216a0001c0001t0011g0269others(24): Show | 31 | HG00639.hp2 HG01069.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.137-789A>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3109360 | ||||||
chr19:3109523
|
G | A | 1 | a0001c0001t0006g0278 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.137-626G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3109523 | ||||||
chr19:3109547
|
C | T | 5 | a0001c0001t0001g0244a0001c0001t0001g0252a0001c0001t0001g0253others(2): Show | 5 | HG00597.hp1 HG02071.hp1 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.137-602C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3109547 | ||||||
chr19:3109620
|
G | A | 1 | a0001c0001t0056g0113 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.137-529G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3109620 | ||||||
chr19:3109667
|
C | T | 1 | a0002c0003t0008g0261 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.137-482C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3109667 | ||||||
chr19:3109689
|
G | C | 1 | a0001c0001t0011g0126 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.137-460G>C | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3109689 | ||||||
chr19:3109701
|
C | T | 1 | a0001c0002t0007g0027 | 2 | HG00738.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.137-448C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3109701 | ||||||
chr19:3109733
|
C | T | 8 | a0001c0001t0015g0020a0001c0001t0015g0023a0001c0001t0015g0082others(5): Show | 9 | HG02055.hp2 HG02280.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.137-416C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3109733 | ||||||
chr19:3109760
|
T | C | 282 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0038others(279): Show | 354 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(351): Show |
intron_variant | MODIFIER | c.137-389T>C | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3109760 | ||||||
chr19:3109761
|
G | A | 1 | a0001c0001t0045g0283 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.137-388G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3109761 | ||||||
chr19:3110022
|
G | A | 1 | a0001c0002t0002g0074 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.137-127G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3110022 | ||||||
chr19:3110023
|
G | C | 1 | a0001c0001t0017g0285 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.137-126G>C | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3110023 | ||||||
chr19:3110028
|
C | A | 1 | a0001c0001t0017g0285 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.137-121C>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3110028 | ||||||
chr19:3110100
|
G | A | 43 | a0001c0001t0003g0040a0001c0001t0003g0041a0001c0001t0003g0042others(40): Show | 48 | HG00099.hp2 HG00280.hp1 HG00438.hp2 others(45): Show |
intron_variant | MODIFIER | c.137-49G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3110100 | ||||||
chr19:3110125
|
G | A | 1 | a0001c0001t0011g0269 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.137-24G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 1/6 | chr19 | 3110125 | ||||||
chr19:3110351
|
T | G | 113 | a0001c0001t0061g0266a0001c0001t0078g0198a0001c0001t0087g0122others(110): Show | 149 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.321+18T>G | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 2/6 | chr19 | 3110351 | ||||||
chr19:3110363
|
C | T | 47 | a0001c0001t0061g0266a0001c0002t0002g0004a0001c0002t0002g0005others(44): Show | 64 | HG00323.hp1 HG00408.hp2 HG00735.hp2 others(61): Show |
intron_variant | MODIFIER | c.321+30C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 2/6 | chr19 | 3110363 | ||||||
chr19:3110424
|
G | A | 3 | a0001c0001t0031g0048a0001c0001t0031g0203a0001c0001t0084g0048 | 3 | HG00639.hp2 HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.321+91G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 2/6 | chr19 | 3110424 | ||||||
chr19:3110439
|
C | T | 1 | a0001c0001t0080g0114 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.321+106C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 2/6 | chr19 | 3110439 | ||||||
chr19:3110471
|
C | T | 1 | a0001c0002t0004g0124 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.321+138C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 2/6 | chr19 | 3110471 | ||||||
chr19:3110489
|
A | G | 60 | a0001c0001t0003g0040a0001c0001t0003g0041a0001c0001t0003g0042others(57): Show | 68 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.321+156A>G | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 2/6 | chr19 | 3110489 | ||||||
chr19:3110512
|
G | A | 1 | a0001c0001t0011g0269 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.321+179G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 2/6 | chr19 | 3110512 | ||||||
chr19:3110517
|
A | G | 113 | a0001c0001t0061g0266a0001c0001t0078g0198a0001c0001t0087g0122others(110): Show | 149 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.321+184A>G | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 2/6 | chr19 | 3110517 | ||||||
chr19:3110587
|
A | G | 287 | a0001c0001t0001g0011a0001c0001t0001g0038a0001c0001t0001g0052others(284): Show | 360 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(357): Show |
intron_variant | MODIFIER | c.321+254A>G | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 2/6 | chr19 | 3110587 | ||||||
chr19:3110609
|
G | C | 20 | a0001c0001t0011g0050a0001c0001t0011g0126a0001c0001t0011g0144others(17): Show | 20 | HG00639.hp2 HG01069.hp2 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.321+276G>C | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 2/6 | chr19 | 3110609 | ||||||
chr19:3110705
|
A | G | 191 | a0001c0001t0005g0001a0001c0001t0005g0019a0001c0001t0005g0062others(188): Show | 251 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(248): Show |
intron_variant | MODIFIER | c.321+372A>G | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 2/6 | chr19 | 3110705 | ||||||
chr19:3110707
|
G | A | 1 | a0001c0002t0004g0120 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.321+374G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 2/6 | chr19 | 3110707 | ||||||
chr19:3110731
|
G | A | 1 | a0001c0001t0001g0147 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.321+398G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 2/6 | chr19 | 3110731 | ||||||
chr19:3110786
|
T | TTTTTG | 66 | a0001c0001t0003g0040a0001c0001t0003g0041a0001c0001t0003g0042others(63): Show | 75 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(72): Show |
intron_variant | MODIFIER | c.321+479_321+483dup others(5): Show |
GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 3110786 | |||||
chr19:3110786
|
T | TTTTTGTT others(3): Show |
1 | a0001c0001t0006g0168 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.321+474_321+483dup others(10): Show |
GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 3110786 | |||||
chr19:3110786
|
T | TTTTTGTT others(8): Show |
1 | a0001c0001t0056g0113 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.321+469_321+483dup others(15): Show |
GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 3110786 | |||||
chr19:3110920
|
C | T | 2 | a0001c0001t0019g0060a0001c0001t0019g0271 | 3 | HG02080.hp1 NA18956.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.321+587C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 2/6 | chr19 | 3110920 | ||||||
chr19:3111096
|
C | T | 1 | a0001c0002t0013g0218 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.321+763C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 2/6 | chr19 | 3111096 | ||||||
chr19:3111112
|
C | CT | 18 | a0001c0001t0005g0293a0001c0001t0008g0016a0001c0001t0008g0228others(15): Show | 20 | HG01109.hp2 HG01891.hp2 HG02056.hp2 others(17): Show |
intron_variant | MODIFIER | c.321+789dupT | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 3111112 | |||||
chr19:3111120
|
T | C | 1 | a0001c0002t0013g0218 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.321+787T>C | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 2/6 | chr19 | 3111120 | ||||||
chr19:3111146
|
C | G | 1 | a0001c0001t0005g0292 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.321+813C>G | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 2/6 | chr19 | 3111146 | ||||||
chr19:3111146
|
C | T | 1 | a0001c0001t0003g0153 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.321+813C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 2/6 | chr19 | 3111146 | ||||||
chr19:3111147
|
CCT | C | 54 | a0001c0001t0005g0001a0001c0001t0005g0019a0001c0001t0005g0062others(51): Show | 70 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.321+815_321+816del others(2): Show |
GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 2/6 | chr19 | 3111147 | ||||||
chr19:3111162
|
C | T | 18 | a0001c0001t0008g0016a0001c0001t0008g0228a0001c0001t0008g0229others(15): Show | 20 | HG01109.hp2 HG01891.hp2 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.321+829C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 2/6 | chr19 | 3111162 | ||||||
chr19:3111233
|
ATATGTTT others(4): Show |
A | 1 | a0001c0001t0001g0234 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.321+901_321+911del others(11): Show |
GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 2/6 | chr19 | 3111233 | ||||||
chr19:3111342
|
C | T | 25 | a0001c0001t0001g0011a0001c0001t0001g0038a0001c0001t0001g0147others(22): Show | 28 | HG00639.hp2 HG01069.hp2 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.321+1009C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 2/6 | chr19 | 3111342 | ||||||
chr19:3111378
|
G | A | 1 | a0001c0001t0003g0172 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.321+1045G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 2/6 | chr19 | 3111378 | ||||||
chr19:3111436
|
G | A | 1 | a0001c0001t0019g0271 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.321+1103G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 2/6 | chr19 | 3111436 | ||||||
chr19:3111439
|
G | A | 1 | a0001c0001t0005g0294 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.321+1106G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 2/6 | chr19 | 3111439 | ||||||
chr19:3111565
|
CT | C | 13 | a0001c0001t0009g0018a0001c0001t0009g0063a0001c0001t0009g0303others(10): Show | 19 | HG02293.hp1 HG02630.hp1 HG02896.hp2 others(16): Show |
intron_variant | MODIFIER | c.321+1233delT | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 2/6 | chr19 | 3111565 | ||||||
chr19:3111622
|
C | T | 1 | a0001c0001t0075g0219 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.321+1289C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 2/6 | chr19 | 3111622 | ||||||
chr19:3111623
|
G | A | 13 | a0001c0001t0009g0018a0001c0001t0009g0063a0001c0001t0009g0303others(10): Show | 19 | HG02293.hp1 HG02630.hp1 HG02896.hp2 others(16): Show |
intron_variant | MODIFIER | c.321+1290G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 2/6 | chr19 | 3111623 | ||||||
chr19:3111776
|
G | C | 1 | a0001c0001t0056g0113 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.321+1443G>C | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 2/6 | chr19 | 3111776 | ||||||
chr19:3111847
|
C | T | 1 | a0001c0001t0006g0278 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.322-1483C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 2/6 | chr19 | 3111847 | ||||||
chr19:3111962
|
T | C | 280 | a0001c0001t0001g0011a0001c0001t0001g0038a0001c0001t0001g0142others(277): Show | 351 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(348): Show |
intron_variant | MODIFIER | c.322-1368T>C | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 2/6 | chr19 | 3111962 | ||||||
chr19:3112003
|
C | G | 1 | a0001c0002t0004g0010 | 3 | NA18952.hp2 NA19002.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.322-1327C>G | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 2/6 | chr19 | 3112003 | ||||||
chr19:3112005
|
C | T | 1 | a0001c0002t0064g0209 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.322-1325C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 2/6 | chr19 | 3112005 | ||||||
chr19:3112006
|
A | G | 290 | a0001c0001t0001g0011a0001c0001t0001g0038a0001c0001t0001g0052others(287): Show | 363 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(360): Show |
intron_variant | MODIFIER | c.322-1324A>G | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 2/6 | chr19 | 3112006 | ||||||
chr19:3112025
|
A | G | 117 | a0001c0001t0001g0252a0001c0001t0001g0253a0001c0001t0001g0254others(114): Show | 153 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.322-1305A>G | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 2/6 | chr19 | 3112025 | ||||||
chr19:3112084
|
T | TCAG | 30 | a0001c0001t0001g0011a0001c0001t0001g0038a0001c0001t0001g0142others(27): Show | 33 | HG00639.hp2 HG01069.hp2 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.322-1233_322-1231d others(5): Show |
GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 3112084 | |||||
chr19:3112369
|
G | A | 26 | a0001c0001t0001g0011a0001c0001t0001g0038a0001c0001t0001g0142others(23): Show | 29 | HG00639.hp2 HG01069.hp2 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.322-961G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 2/6 | chr19 | 3112369 | ||||||
chr19:3112459
|
C | G | 38 | a0001c0001t0003g0040a0001c0001t0003g0041a0001c0001t0003g0042others(35): Show | 43 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(40): Show |
intron_variant | MODIFIER | c.322-871C>G | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 2/6 | chr19 | 3112459 | ||||||
chr19:3112460
|
C | T | 38 | a0001c0001t0003g0040a0001c0001t0003g0041a0001c0001t0003g0042others(35): Show | 43 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(40): Show |
intron_variant | MODIFIER | c.322-870C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 2/6 | chr19 | 3112460 | ||||||
chr19:3112502
|
G | C | 38 | a0001c0002t0002g0004a0001c0002t0002g0005a0001c0002t0002g0008others(35): Show | 52 | HG00323.hp1 HG00408.hp2 HG00597.hp2 others(49): Show |
intron_variant | MODIFIER | c.322-828G>C | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 2/6 | chr19 | 3112502 | ||||||
chr19:3112508
|
G | A | 9 | a0001c0001t0012g0007a0001c0001t0012g0024a0001c0001t0012g0025others(6): Show | 12 | HG02630.hp1 HG02896.hp2 HG02897.hp1 others(9): Show |
intron_variant | MODIFIER | c.322-822G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 2/6 | chr19 | 3112508 | ||||||
chr19:3112647
|
A | C | 1 | a0004c0006t0002g0073 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.322-683A>C | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 2/6 | chr19 | 3112647 | ||||||
chr19:3112648
|
C | A | 1 | a0004c0006t0002g0073 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.322-682C>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 2/6 | chr19 | 3112648 | ||||||
chr19:3112679
|
G | A | 1 | a0001c0002t0007g0208 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.322-651G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 2/6 | chr19 | 3112679 | ||||||
chr19:3112723
|
G | A | 1 | a0001c0002t0002g0075 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.322-607G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 2/6 | chr19 | 3112723 | ||||||
chr19:3112734
|
G | A | 2 | a0001c0002t0004g0150a0001c0002t0030g0121 | 2 | HG00140.hp2 HG01167.hp1 |
intron_variant | MODIFIER | c.322-596G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 2/6 | chr19 | 3112734 | ||||||
chr19:3112749
|
G | A | 9 | a0001c0001t0012g0007a0001c0001t0012g0024a0001c0001t0012g0025others(6): Show | 12 | HG02630.hp1 HG02896.hp2 HG02897.hp1 others(9): Show |
intron_variant | MODIFIER | c.322-581G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 2/6 | chr19 | 3112749 | ||||||
chr19:3112795
|
C | T | 59 | a0001c0001t0003g0040a0001c0001t0003g0041a0001c0001t0003g0042others(56): Show | 66 | HG00099.hp2 HG00280.hp1 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.322-535C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 2/6 | chr19 | 3112795 | ||||||
chr19:3112796
|
G | A | 5 | a0001c0001t0019g0060a0001c0001t0019g0271a0001c0001t0019g0272others(2): Show | 6 | HG01433.hp1 HG02080.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.322-534G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 2/6 | chr19 | 3112796 | ||||||
chr19:3112809
|
C | G | 1 | a0001c0001t0001g0248 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.322-521C>G | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 2/6 | chr19 | 3112809 | ||||||
chr19:3112932
|
C | T | 1 | a0001c0002t0002g0098 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.322-398C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 2/6 | chr19 | 3112932 | ||||||
chr19:3112971
|
C | T | 7 | a0001c0001t0001g0242a0001c0001t0012g0024a0001c0001t0012g0025others(4): Show | 9 | HG01891.hp1 HG03098.hp2 NA18941.hp2 others(6): Show |
intron_variant | MODIFIER | c.322-359C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 2/6 | chr19 | 3112971 | ||||||
chr19:3112972
|
G | A | 1 | a0001c0001t0005g0293 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.322-358G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 2/6 | chr19 | 3112972 | ||||||
chr19:3113100
|
C | T | 1 | a0001c0002t0020g0135 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.322-230C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 2/6 | chr19 | 3113100 | ||||||
chr19:3113106
|
G | A | 1 | a0001c0001t0011g0214 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.322-224G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 2/6 | chr19 | 3113106 | ||||||
chr19:3113158
|
G | A | 7 | a0001c0002t0013g0029a0001c0002t0013g0095a0001c0002t0013g0115others(4): Show | 7 | HG02486.hp2 HG02622.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.322-172G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 2/6 | chr19 | 3113158 | ||||||
chr19:3113164
|
G | A | 17 | a0001c0001t0008g0016a0001c0001t0008g0228a0001c0001t0008g0229others(14): Show | 19 | HG01109.hp2 HG01891.hp2 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.322-166G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 2/6 | chr19 | 3113164 | ||||||
chr19:3113178
|
C | T | 203 | a0001c0001t0003g0040a0001c0001t0003g0041a0001c0001t0003g0042others(200): Show | 251 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(248): Show |
intron_variant | MODIFIER | c.322-152C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 2/6 | chr19 | 3113178 | ||||||
chr19:3113243
|
G | A | 2 | a0001c0001t0003g0156a0001c0001t0003g0159 | 2 | HG01261.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.322-87G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 2/6 | chr19 | 3113243 | ||||||
chr19:3113276
|
G | T | 1 | a0001c0002t0002g0107 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.322-54G>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 2/6 | chr19 | 3113276 | ||||||
chr19:3113307
|
G | C | 277 | a0001c0001t0001g0011a0001c0001t0001g0038a0001c0001t0001g0142others(274): Show | 348 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(345): Show |
intron_variant | MODIFIER | c.322-23G>C | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 2/6 | chr19 | 3113307 | ||||||
chr19:3113518
|
CGGCAGCT others(8): Show |
C | 27 | a0001c0001t0001g0011a0001c0001t0001g0038a0001c0001t0001g0142others(24): Show | 30 | HG00639.hp2 HG01069.hp2 HG01071.hp2 others(27): Show |
intron_variant | MODIFIER | c.476+36_476+50delGC others(13): Show |
GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 3113518 | |||||
chr19:3113520
|
G | A | 1 | a0001c0001t0001g0244 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.476+36G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 3/6 | chr19 | 3113520 | ||||||
chr19:3113561
|
C | T | 1 | a0001c0001t0061g0266 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.476+77C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 3/6 | chr19 | 3113561 | ||||||
chr19:3113579
|
C | T | 4 | a0001c0001t0011g0213a0001c0001t0011g0269a0001c0001t0049g0201others(1): Show | 4 | HG02257.hp2 HG02615.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.476+95C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 3/6 | chr19 | 3113579 | ||||||
chr19:3113608
|
G | A | 1 | a0001c0001t0037g0068 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.476+124G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 3/6 | chr19 | 3113608 | ||||||
chr19:3113629
|
C | T | 1 | a0001c0001t0001g0254 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.476+145C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 3/6 | chr19 | 3113629 | ||||||
chr19:3113682
|
G | A | 1 | a0001c0001t0075g0219 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.476+198G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 3/6 | chr19 | 3113682 | ||||||
chr19:3113739
|
C | T | 1 | a0001c0001t0056g0113 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.476+255C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 3/6 | chr19 | 3113739 | ||||||
chr19:3113772
|
T | C | 60 | a0001c0001t0003g0040a0001c0001t0003g0041a0001c0001t0003g0042others(57): Show | 67 | HG00099.hp2 HG00280.hp1 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.476+288T>C | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 3/6 | chr19 | 3113772 | ||||||
chr19:3113782
|
C | T | 57 | a0001c0001t0005g0001a0001c0001t0005g0019a0001c0001t0005g0062others(54): Show | 76 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.476+298C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 3/6 | chr19 | 3113782 | ||||||
chr19:3113819
|
G | GGAGGGCC others(17): Show |
1 | a0001c0001t0001g0234 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.476+336_476+359dup others(24): Show |
GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 3113819 | |||||
chr19:3113827
|
G | A | 1 | a0001c0001t0005g0288 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.476+343G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 3/6 | chr19 | 3113827 | ||||||
chr19:3113841
|
A | G | 39 | a0001c0001t0003g0040a0001c0001t0003g0041a0001c0001t0003g0042others(36): Show | 44 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.476+357A>G | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 3/6 | chr19 | 3113841 | ||||||
chr19:3113869
|
C | G | 4 | a0001c0001t0003g0174a0001c0001t0003g0180a0001c0001t0003g0181others(1): Show | 4 | HG00741.hp1 HG01099.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.476+385C>G | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 3/6 | chr19 | 3113869 | ||||||
chr19:3113890
|
C | G | 144 | a0001c0001t0003g0044a0001c0001t0011g0050a0001c0001t0011g0126others(141): Show | 183 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.476+406C>G | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 3/6 | chr19 | 3113890 | ||||||
chr19:3113905
|
G | T | 142 | a0001c0001t0003g0044a0001c0001t0011g0050a0001c0001t0011g0126others(139): Show | 181 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(178): Show |
intron_variant | MODIFIER | c.476+421G>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 3/6 | chr19 | 3113905 | ||||||
chr19:3114014
|
C | T | 1 | a0001c0002t0002g0131 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.476+530C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 3/6 | chr19 | 3114014 | ||||||
chr19:3114069
|
C | T | 2 | a0001c0001t0011g0144a0001c0001t0011g0146 | 2 | HG02886.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.476+585C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 3/6 | chr19 | 3114069 | ||||||
chr19:3114076
|
C | T | 1 | a0001c0001t0056g0113 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.476+592C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 3/6 | chr19 | 3114076 | ||||||
chr19:3114161
|
C | T | 9 | a0001c0001t0012g0007a0001c0001t0012g0024a0001c0001t0012g0025others(6): Show | 12 | HG02630.hp1 HG02896.hp2 HG02897.hp1 others(9): Show |
intron_variant | MODIFIER | c.476+677C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 3/6 | chr19 | 3114161 | ||||||
chr19:3114179
|
G | T | 4 | a0001c0001t0003g0174a0001c0001t0003g0180a0001c0001t0003g0181others(1): Show | 4 | HG00741.hp1 HG01099.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.476+695G>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 3/6 | chr19 | 3114179 | ||||||
chr19:3114231
|
G | A | 63 | a0001c0001t0003g0040a0001c0001t0003g0041a0001c0001t0003g0042others(60): Show | 71 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.477-713G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 3/6 | chr19 | 3114231 | ||||||
chr19:3114287
|
C | T | 55 | a0001c0001t0005g0001a0001c0001t0005g0019a0001c0001t0005g0062others(52): Show | 72 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.477-657C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 3/6 | chr19 | 3114287 | ||||||
chr19:3114375
|
G | A | 1 | a0001c0001t0016g0289 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.477-569G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 3/6 | chr19 | 3114375 | ||||||
chr19:3114381
|
A | C | 5 | a0001c0001t0015g0020a0001c0001t0015g0023a0001c0001t0015g0082others(2): Show | 6 | HG02055.hp2 HG02723.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.477-563A>C | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 3/6 | chr19 | 3114381 | ||||||
chr19:3114416
|
C | T | 9 | a0001c0001t0012g0007a0001c0001t0012g0024a0001c0001t0012g0025others(6): Show | 12 | HG02630.hp1 HG02896.hp2 HG02897.hp1 others(9): Show |
intron_variant | MODIFIER | c.477-528C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 3/6 | chr19 | 3114416 | ||||||
chr19:3114458
|
C | A | 1 | a0001c0001t0011g0277 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.477-486C>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 3/6 | chr19 | 3114458 | ||||||
chr19:3114547
|
T | C | 247 | a0001c0001t0001g0011a0001c0001t0001g0038a0001c0001t0001g0142others(244): Show | 313 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(310): Show |
intron_variant | MODIFIER | c.477-397T>C | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 3/6 | chr19 | 3114547 | ||||||
chr19:3114590
|
G | A | 6 | a0001c0001t0001g0011a0001c0001t0001g0038a0001c0001t0001g0142others(3): Show | 9 | HG02647.hp1 HG02723.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.477-354G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 3/6 | chr19 | 3114590 | ||||||
chr19:3114703
|
C | T | 18 | a0001c0001t0008g0016a0001c0001t0008g0228a0001c0001t0008g0229others(15): Show | 20 | HG01109.hp2 HG01891.hp2 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.477-241C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 3/6 | chr19 | 3114703 | ||||||
chr19:3114785
|
C | T | 1 | a0001c0001t0001g0149 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.477-159C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 3/6 | chr19 | 3114785 | ||||||
chr19:3114824
|
G | A | 1 | a0001c0001t0011g0277 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.477-120G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 3/6 | chr19 | 3114824 | ||||||
chr19:3114830
|
C | G | 1 | a0001c0002t0025g0255 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.477-114C>G | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 3/6 | chr19 | 3114830 | ||||||
chr19:3114843
|
C | A | 2 | a0001c0001t0012g0007a0001c0001t0039g0007 | 3 | HG02630.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.477-101C>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 3/6 | chr19 | 3114843 | ||||||
chr19:3114858
|
C | T | 1 | a0001c0001t0001g0235 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.477-86C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 3/6 | chr19 | 3114858 | ||||||
chr19:3114866
|
C | T | 59 | a0001c0002t0002g0004a0001c0002t0002g0005a0001c0002t0002g0008others(56): Show | 78 | HG00323.hp1 HG00408.hp2 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.477-78C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 3/6 | chr19 | 3114866 | ||||||
chr19:3114902
|
C | A | 5 | a0001c0001t0012g0024a0001c0001t0012g0025a0001c0001t0036g0084others(2): Show | 7 | NA18941.hp2 NA18942.hp2 NA18973.hp1 others(4): Show |
intron_variant | MODIFIER | c.477-42C>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 3/6 | chr19 | 3114902 | ||||||
chr19:3115078
|
G | C | 1 | a0001c0001t0036g0084 | 1 | NA18941.hp2 | splice_region_variant&intron_variant | LOW | c.605+6G>C | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 4/6 | chr19 | 3115078 | ||||||
chr19:3115126
|
C | T | 56 | a0001c0001t0003g0040a0001c0001t0003g0041a0001c0001t0003g0042others(53): Show | 63 | HG00099.hp2 HG00280.hp1 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.605+54C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 4/6 | chr19 | 3115126 | ||||||
chr19:3115174
|
C | T | 3 | a0001c0001t0001g0100a0001c0001t0001g0251a0001c0001t0014g0250 | 3 | HG02683.hp1 HG03710.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.605+102C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 4/6 | chr19 | 3115174 | ||||||
chr19:3115185
|
C | A | 1 | a0001c0001t0075g0219 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.605+113C>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 4/6 | chr19 | 3115185 | ||||||
chr19:3115384
|
G | A | 9 | a0001c0001t0012g0007a0001c0001t0012g0024a0001c0001t0012g0025others(6): Show | 12 | HG02630.hp1 HG02896.hp2 HG02897.hp1 others(9): Show |
intron_variant | MODIFIER | c.605+312G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 4/6 | chr19 | 3115384 | ||||||
chr19:3115404
|
C | T | 38 | a0001c0001t0003g0040a0001c0001t0003g0041a0001c0001t0003g0042others(35): Show | 43 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(40): Show |
intron_variant | MODIFIER | c.605+332C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 4/6 | chr19 | 3115404 | ||||||
chr19:3115528
|
G | C | 151 | a0001c0001t0001g0011a0001c0001t0001g0038a0001c0001t0001g0142others(148): Show | 194 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.605+456G>C | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 4/6 | chr19 | 3115528 | ||||||
chr19:3115550
|
C | A | 4 | a0001c0001t0003g0040a0001c0001t0003g0091a0001c0001t0003g0175others(1): Show | 5 | HG00438.hp2 HG00544.hp2 HG03834.hp2 others(2): Show |
intron_variant | MODIFIER | c.605+478C>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 4/6 | chr19 | 3115550 | ||||||
chr19:3115559
|
C | T | 1 | a0001c0001t0011g0216 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.605+487C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 4/6 | chr19 | 3115559 | ||||||
chr19:3115657
|
C | T | 2 | a0001c0002t0050g0032a0001c0002t0054g0032 | 2 | NA18966.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.605+585C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 4/6 | chr19 | 3115657 | ||||||
chr19:3115663
|
G | A | 9 | a0001c0001t0012g0007a0001c0001t0012g0024a0001c0001t0012g0025others(6): Show | 12 | HG02630.hp1 HG02896.hp2 HG02897.hp1 others(9): Show |
intron_variant | MODIFIER | c.605+591G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 4/6 | chr19 | 3115663 | ||||||
chr19:3115785
|
A | AG | 31 | a0001c0001t0001g0053a0001c0001t0001g0087a0001c0001t0001g0243others(28): Show | 34 | HG00438.hp1 HG00621.hp1 HG01099.hp1 others(31): Show |
intron_variant | MODIFIER | c.605+722dupG | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 3115785 | |||||
chr19:3115786
|
G | A | 6 | a0001c0001t0015g0020a0001c0001t0015g0023a0001c0001t0015g0082others(3): Show | 7 | HG02055.hp2 HG02723.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.605+714G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 4/6 | chr19 | 3115786 | ||||||
chr19:3115792
|
G | A | 120 | a0001c0001t0003g0044a0001c0001t0015g0020a0001c0001t0015g0023others(117): Show | 159 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.605+720G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 4/6 | chr19 | 3115792 | ||||||
chr19:3115817
|
TGGAGGAG others(151): Show |
T | 8 | a0001c0001t0012g0007a0001c0001t0012g0024a0001c0001t0012g0025others(5): Show | 11 | HG02630.hp1 HG02896.hp2 HG02897.hp1 others(8): Show |
intron_variant | MODIFIER | c.605+782_605+939del | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 3115817 | |||||
chr19:3115824
|
GGGGTCAT others(150): Show |
G | 1 | a0001c0001t0036g0084 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.605+756_605+912del | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 3115824 | |||||
chr19:3115859
|
A | G | 59 | a0001c0001t0003g0040a0001c0001t0003g0041a0001c0001t0003g0042others(56): Show | 66 | HG00099.hp2 HG00280.hp1 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.605+787A>G | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 4/6 | chr19 | 3115859 | ||||||
chr19:3115865
|
T | C | 116 | a0001c0001t0003g0040a0001c0001t0003g0041a0001c0001t0003g0042others(113): Show | 142 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.605+793T>C | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 4/6 | chr19 | 3115865 | ||||||
chr19:3115865
|
T | TGAGGCTG others(58): Show |
37 | a0001c0001t0005g0001a0001c0001t0005g0019a0001c0001t0005g0062others(34): Show | 54 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.605+818_605+882dup others(65): Show |
GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 3115865 | |||||
chr19:3115865
|
T | TGAGTGGG others(150): Show |
18 | a0001c0001t0011g0050a0001c0001t0011g0126a0001c0001t0011g0210others(15): Show | 18 | HG00639.hp2 HG01069.hp2 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.605+796_605+797ins others(157): Show |
GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 3115865 | |||||
chr19:3115865
|
T | TGAGTGGG others(215): Show |
1 | a0001c0001t0080g0114 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.605+796_605+797ins others(222): Show |
GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 3115865 | |||||
chr19:3115865
|
T | TGAGTGGG others(150): Show |
2 | a0001c0001t0011g0144a0001c0001t0011g0146 | 2 | HG02886.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.605+796_605+797ins others(157): Show |
GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 3115865 | |||||
chr19:3115875
|
AG | A | 21 | a0001c0001t0011g0050a0001c0001t0011g0126a0001c0001t0011g0144others(18): Show | 21 | HG00639.hp2 HG01069.hp2 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.605+807delG | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 3115875 | |||||
chr19:3115878
|
G | A | 1 | a0001c0001t0006g0168 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.605+806G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 4/6 | chr19 | 3115878 | ||||||
chr19:3115881
|
G | A | 21 | a0001c0001t0011g0050a0001c0001t0011g0126a0001c0001t0011g0144others(18): Show | 21 | HG00639.hp2 HG01069.hp2 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.605+809G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 4/6 | chr19 | 3115881 | ||||||
chr19:3115899
|
G | A | 1 | a0001c0001t0011g0146 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.605+827G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 4/6 | chr19 | 3115899 | ||||||
chr19:3115900
|
A | AGGCTGTC others(60): Show |
1 | a0001c0001t0017g0285 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.605+855_605+856ins others(67): Show |
GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 3115900 | |||||
chr19:3115941
|
G | A | 1 | a0001c0002t0013g0115 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.605+869G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 4/6 | chr19 | 3115941 | ||||||
chr19:3115946
|
G | GGAGGGGT others(25): Show |
20 | a0001c0001t0008g0016a0001c0001t0008g0228a0001c0001t0008g0229others(17): Show | 22 | HG01109.hp2 HG01243.hp1 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.605+882_605+883ins others(32): Show |
GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 3115946 | |||||
chr19:3115955
|
G | A | 1 | a0001c0001t0001g0142 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.605+883G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 4/6 | chr19 | 3115955 | ||||||
chr19:3115972
|
G | A | 1 | a0001c0001t0045g0283 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.605+900G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 4/6 | chr19 | 3115972 | ||||||
chr19:3116068
|
C | T | 21 | a0001c0001t0011g0050a0001c0001t0011g0126a0001c0001t0011g0144others(18): Show | 21 | HG00639.hp2 HG01069.hp2 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.605+996C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 4/6 | chr19 | 3116068 | ||||||
chr19:3116075
|
T | C | 37 | a0001c0001t0005g0001a0001c0001t0005g0019a0001c0001t0005g0062others(34): Show | 54 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.605+1003T>C | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 4/6 | chr19 | 3116075 | ||||||
chr19:3116094
|
C | A | 1 | a0001c0002t0021g0104 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.605+1022C>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 4/6 | chr19 | 3116094 | ||||||
chr19:3116264
|
G | A | 4 | a0001c0001t0003g0152a0001c0001t0003g0153a0001c0001t0034g0151others(1): Show | 4 | HG02559.hp1 HG02965.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.605+1192G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 4/6 | chr19 | 3116264 | ||||||
chr19:3116282
|
T | G | 19 | a0001c0001t0011g0050a0001c0001t0011g0126a0001c0001t0011g0210others(16): Show | 19 | HG00639.hp2 HG01069.hp2 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.605+1210T>G | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 4/6 | chr19 | 3116282 | ||||||
chr19:3116289
|
C | T | 21 | a0001c0001t0011g0050a0001c0001t0011g0126a0001c0001t0011g0144others(18): Show | 21 | HG00639.hp2 HG01069.hp2 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.605+1217C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 4/6 | chr19 | 3116289 | ||||||
chr19:3116314
|
G | A | 2 | a0001c0001t0011g0213a0001c0001t0049g0201 | 2 | HG02615.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.605+1242G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 4/6 | chr19 | 3116314 | ||||||
chr19:3116342
|
C | T | 1 | a0001c0001t0011g0211 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.605+1270C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 4/6 | chr19 | 3116342 | ||||||
chr19:3116377
|
G | A | 1 | a0001c0001t0016g0291 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.605+1305G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 4/6 | chr19 | 3116377 | ||||||
chr19:3116448
|
C | CGCATCCT others(2): Show |
3 | a0001c0002t0002g0099a0001c0002t0004g0120a0001c0002t0051g0117 | 3 | HG00741.hp2 HG02055.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.605+1406_605+1414d others(11): Show |
GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 3116448 | |||||
chr19:3116448
|
CGCATCCT others(2): Show |
C | 30 | a0001c0001t0003g0045a0001c0001t0003g0046a0001c0001t0003g0067others(27): Show | 33 | HG00099.hp2 HG00621.hp2 HG00673.hp1 others(30): Show |
intron_variant | MODIFIER | c.605+1406_605+1414d others(11): Show |
GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 3116448 | |||||
chr19:3116448
|
CGCATCCT others(11): Show |
C | 9 | a0001c0001t0012g0007a0001c0001t0012g0024a0001c0001t0012g0025others(6): Show | 12 | HG02630.hp1 HG02896.hp2 HG02897.hp1 others(9): Show |
intron_variant | MODIFIER | c.605+1397_605+1414d others(20): Show |
GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 3116448 | |||||
chr19:3116449
|
G | A | 1 | a0001c0001t0011g0144 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.605+1377G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 4/6 | chr19 | 3116449 | ||||||
chr19:3116494
|
C | T | 1 | a0001c0001t0003g0176 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.605+1422C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 4/6 | chr19 | 3116494 | ||||||
chr19:3116529
|
C | T | 1 | a0001c0001t0006g0162 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.605+1457C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 4/6 | chr19 | 3116529 | ||||||
chr19:3116539
|
G | A | 4 | a0001c0001t0003g0152a0001c0001t0003g0153a0001c0001t0034g0151others(1): Show | 4 | HG02559.hp1 HG02965.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.605+1467G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 4/6 | chr19 | 3116539 | ||||||
chr19:3116696
|
G | A | 1 | a0001c0002t0013g0218 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.605+1624G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 4/6 | chr19 | 3116696 | ||||||
chr19:3116727
|
C | T | 46 | a0001c0001t0003g0044a0001c0001t0011g0146a0001c0001t0087g0122others(43): Show | 63 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(60): Show |
intron_variant | MODIFIER | c.605+1655C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 4/6 | chr19 | 3116727 | ||||||
chr19:3116760
|
C | T | 3 | a0001c0001t0056g0113a0001c0001t0090g0051a0001c0001t0091g0051 | 3 | HG01891.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.605+1688C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 4/6 | chr19 | 3116760 | ||||||
chr19:3116803
|
A | T | 1 | a0001c0001t0001g0234 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.605+1731A>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 4/6 | chr19 | 3116803 | ||||||
chr19:3116810
|
C | T | 1 | a0001c0002t0002g0094 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.605+1738C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 4/6 | chr19 | 3116810 | ||||||
chr19:3116859
|
T | C | 37 | a0001c0001t0005g0001a0001c0001t0005g0019a0001c0001t0005g0062others(34): Show | 54 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.605+1787T>C | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 4/6 | chr19 | 3116859 | ||||||
chr19:3117019
|
T | C | 237 | a0001c0001t0001g0231a0001c0001t0001g0252a0001c0001t0001g0253others(234): Show | 288 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(285): Show |
intron_variant | MODIFIER | c.606-1905T>C | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 4/6 | chr19 | 3117019 | ||||||
chr19:3117053
|
A | T | 1 | a0001c0002t0058g0200 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.606-1871A>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 4/6 | chr19 | 3117053 | ||||||
chr19:3117160
|
T | C | 21 | a0001c0001t0011g0050a0001c0001t0011g0126a0001c0001t0011g0144others(18): Show | 21 | HG00639.hp2 HG01069.hp2 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.606-1764T>C | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 4/6 | chr19 | 3117160 | ||||||
chr19:3117186
|
C | T | 1 | a0001c0002t0002g0136 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.606-1738C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 4/6 | chr19 | 3117186 | ||||||
chr19:3117343
|
C | A | 1 | a0001c0001t0037g0068 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.606-1581C>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 4/6 | chr19 | 3117343 | ||||||
chr19:3117344
|
C | T | 1 | a0001c0002t0064g0209 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.606-1580C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 4/6 | chr19 | 3117344 | ||||||
chr19:3117350
|
ACCATCTT others(11): Show |
A | 1 | a0001c0002t0038g0223 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.606-1570_606-1553d others(20): Show |
GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 3117350 | |||||
chr19:3117492
|
C | T | 37 | a0001c0001t0003g0040a0001c0001t0003g0041a0001c0001t0003g0042others(34): Show | 42 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(39): Show |
intron_variant | MODIFIER | c.606-1432C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 4/6 | chr19 | 3117492 | ||||||
chr19:3117494
|
GCCTCAGC others(33): Show |
G | 1 | a0001c0001t0001g0238 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.606-1427_606-1388d others(42): Show |
GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 3117494 | |||||
chr19:3117541
|
CT | C | 56 | a0001c0001t0003g0040a0001c0001t0003g0041a0001c0001t0003g0042others(53): Show | 64 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(61): Show |
intron_variant | MODIFIER | c.606-1382delT | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 4/6 | chr19 | 3117541 | ||||||
chr19:3117618
|
G | C | 1 | a0001c0001t0003g0040 | 2 | HG00544.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.606-1306G>C | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 4/6 | chr19 | 3117618 | ||||||
chr19:3117624
|
C | T | 2 | a0001c0001t0003g0171a0003c0004t0003g0039 | 3 | HG01070.hp1 HG01071.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.606-1300C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 4/6 | chr19 | 3117624 | ||||||
chr19:3117636
|
C | A | 69 | a0001c0001t0003g0040a0001c0001t0003g0041a0001c0001t0003g0042others(66): Show | 80 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(77): Show |
intron_variant | MODIFIER | c.606-1288C>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 4/6 | chr19 | 3117636 | ||||||
chr19:3117673
|
C | T | 1 | a0001c0001t0011g0146 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.606-1251C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 4/6 | chr19 | 3117673 | ||||||
chr19:3117700
|
C | T | 2 | a0001c0001t0037g0068a0001c0001t0056g0113 | 2 | HG01884.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.606-1224C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 4/6 | chr19 | 3117700 | ||||||
chr19:3117762
|
C | G | 4 | a0001c0001t0003g0152a0001c0001t0003g0153a0001c0001t0034g0151others(1): Show | 4 | HG02559.hp1 HG02965.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.606-1162C>G | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 4/6 | chr19 | 3117762 | ||||||
chr19:3117764
|
G | A | 1 | a0001c0001t0001g0252 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.606-1160G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 4/6 | chr19 | 3117764 | ||||||
chr19:3117837
|
C | T | 1 | a0001c0001t0037g0068 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.606-1087C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 4/6 | chr19 | 3117837 | ||||||
chr19:3117927
|
C | T | 1 | a0001c0001t0071g0197 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.606-997C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 4/6 | chr19 | 3117927 | ||||||
chr19:3117945
|
C | T | 1 | a0001c0001t0056g0113 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.606-979C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 4/6 | chr19 | 3117945 | ||||||
chr19:3118030
|
T | C | 16 | a0001c0001t0008g0016a0001c0001t0008g0228a0001c0001t0008g0229others(13): Show | 18 | HG01109.hp2 HG01891.hp2 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.606-894T>C | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 4/6 | chr19 | 3118030 | ||||||
chr19:3118049
|
C | T | 1 | a0001c0001t0040g0086 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.606-875C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 4/6 | chr19 | 3118049 | ||||||
chr19:3118066
|
C | T | 98 | a0001c0001t0005g0001a0001c0001t0005g0019a0001c0001t0005g0062others(95): Show | 134 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.606-858C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 4/6 | chr19 | 3118066 | ||||||
chr19:3118081
|
G | A | 1 | a0001c0001t0011g0146 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.606-843G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 4/6 | chr19 | 3118081 | ||||||
chr19:3118121
|
A | G | 174 | a0001c0001t0003g0040a0001c0001t0003g0041a0001c0001t0003g0042others(171): Show | 206 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(203): Show |
intron_variant | MODIFIER | c.606-803A>G | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 4/6 | chr19 | 3118121 | ||||||
chr19:3118209
|
G | C | 71 | a0001c0001t0011g0050a0001c0001t0011g0126a0001c0001t0011g0144others(68): Show | 88 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.606-715G>C | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 4/6 | chr19 | 3118209 | ||||||
chr19:3118248
|
C | G | 1 | a0001c0001t0012g0025 | 2 | NA19074.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.606-676C>G | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 4/6 | chr19 | 3118248 | ||||||
chr19:3118313
|
C | T | 5 | a0001c0001t0019g0060a0001c0001t0019g0271a0001c0001t0019g0272others(2): Show | 6 | HG01433.hp1 HG02080.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.606-611C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 4/6 | chr19 | 3118313 | ||||||
chr19:3118391
|
C | A | 115 | a0001c0001t0087g0122a0001c0002t0002g0004a0001c0002t0002g0005others(112): Show | 151 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.606-533C>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 4/6 | chr19 | 3118391 | ||||||
chr19:3118401
|
C | T | 1 | a0001c0002t0004g0134 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.606-523C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 4/6 | chr19 | 3118401 | ||||||
chr19:3118402
|
G | A | 1 | a0001c0008t0005g0301 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.606-522G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 4/6 | chr19 | 3118402 | ||||||
chr19:3118456
|
C | T | 1 | a0001c0001t0042g0085 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.606-468C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 4/6 | chr19 | 3118456 | ||||||
chr19:3118516
|
C | T | 1 | a0001c0002t0004g0030 | 2 | HG01099.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.606-408C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 4/6 | chr19 | 3118516 | ||||||
chr19:3118640
|
C | T | 37 | a0001c0001t0005g0001a0001c0001t0005g0019a0001c0001t0005g0062others(34): Show | 54 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.606-284C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 4/6 | chr19 | 3118640 | ||||||
chr19:3118718
|
G | A | 1 | a0001c0002t0025g0255 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.606-206G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 4/6 | chr19 | 3118718 | ||||||
chr19:3118783
|
C | A | 1 | a0001c0001t0037g0068 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.606-141C>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 4/6 | chr19 | 3118783 | ||||||
chr19:3119186
|
T | G | 253 | a0001c0001t0003g0040a0001c0001t0003g0041a0001c0001t0003g0042others(250): Show | 319 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(316): Show |
intron_variant | MODIFIER | c.736-20T>G | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 5/6 | chr19 | 3119186 | ||||||
chr19:3119367
|
G | A | 1 | a0001c0002t0002g0093 | 1 | NA19012.hp1 | splice_region_variant&intron_variant | LOW | c.889+8G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 6/6 | chr19 | 3119367 | ||||||
chr19:3119367
|
G | C | 21 | a0001c0001t0011g0050a0001c0001t0011g0126a0001c0001t0011g0144others(18): Show | 21 | HG00639.hp2 HG01069.hp2 HG01071.hp2 others(18): Show |
splice_region_variant&intron_variant | LOW | c.889+8G>C | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 6/6 | chr19 | 3119367 | ||||||
chr19:3119373
|
C | T | 1 | a0001c0001t0019g0271 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.889+14C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 6/6 | chr19 | 3119373 | ||||||
chr19:3119383
|
A | G | 1 | a0001c0001t0011g0269 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.889+24A>G | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 6/6 | chr19 | 3119383 | ||||||
chr19:3119407
|
T | G | 286 | a0001c0001t0001g0011a0001c0001t0001g0038a0001c0001t0001g0052others(283): Show | 359 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(356): Show |
intron_variant | MODIFIER | c.889+48T>G | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 6/6 | chr19 | 3119407 | ||||||
chr19:3119408
|
G | T | 114 | a0001c0001t0034g0151a0001c0002t0002g0004a0001c0002t0002g0005others(111): Show | 150 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.889+49G>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 6/6 | chr19 | 3119408 | ||||||
chr19:3119413
|
G | A | 1 | a0001c0002t0010g0133 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.889+54G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 6/6 | chr19 | 3119413 | ||||||
chr19:3119414
|
A | G | 1 | a0001c0002t0010g0133 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.889+55A>G | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 6/6 | chr19 | 3119414 | ||||||
chr19:3119542
|
G | A | 2 | a0001c0001t0011g0144a0001c0001t0011g0146 | 2 | HG02886.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.889+183G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 6/6 | chr19 | 3119542 | ||||||
chr19:3119555
|
G | A | 1 | a0001c0002t0002g0090 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.889+196G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 6/6 | chr19 | 3119555 | ||||||
chr19:3119560
|
G | C | 1 | a0001c0001t0056g0113 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.889+201G>C | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 6/6 | chr19 | 3119560 | ||||||
chr19:3119741
|
G | A | 2 | a0001c0001t0037g0068a0001c0001t0056g0113 | 2 | HG01884.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.889+382G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 6/6 | chr19 | 3119741 | ||||||
chr19:3119782
|
G | A | 1 | a0001c0002t0051g0117 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.889+423G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 6/6 | chr19 | 3119782 | ||||||
chr19:3119814
|
C | T | 1 | a0001c0002t0002g0280 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.889+455C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 6/6 | chr19 | 3119814 | ||||||
chr19:3119872
|
C | T | 1 | a0001c0001t0003g0091 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.889+513C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 6/6 | chr19 | 3119872 | ||||||
chr19:3119873
|
G | A | 13 | a0001c0001t0001g0015a0001c0001t0001g0056a0001c0001t0001g0248others(10): Show | 18 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.889+514G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 6/6 | chr19 | 3119873 | ||||||
chr19:3119875
|
A | G | 1 | a0001c0002t0060g0079 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.889+516A>G | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 6/6 | chr19 | 3119875 | ||||||
chr19:3119912
|
G | A | 114 | a0001c0002t0002g0004a0001c0002t0002g0005a0001c0002t0002g0008others(111): Show | 150 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.889+553G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 6/6 | chr19 | 3119912 | ||||||
chr19:3120002
|
C | G | 20 | a0001c0001t0011g0050a0001c0001t0011g0126a0001c0001t0011g0144others(17): Show | 20 | HG00639.hp2 HG01069.hp2 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.889+643C>G | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 6/6 | chr19 | 3120002 | ||||||
chr19:3120016
|
G | A | 2 | a0001c0001t0037g0068a0001c0001t0056g0113 | 2 | HG01884.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.889+657G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 6/6 | chr19 | 3120016 | ||||||
chr19:3120089
|
G | A | 1 | a0001c0001t0075g0219 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.889+730G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 6/6 | chr19 | 3120089 | ||||||
chr19:3120178
|
G | A | 1 | a0001c0002t0002g0093 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.890-811G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 6/6 | chr19 | 3120178 | ||||||
chr19:3120234
|
C | T | 34 | a0001c0001t0005g0001a0001c0001t0005g0019a0001c0001t0005g0062others(31): Show | 51 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.890-755C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 6/6 | chr19 | 3120234 | ||||||
chr19:3120275
|
C | T | 1 | a0001c0001t0075g0219 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.890-714C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 6/6 | chr19 | 3120275 | ||||||
chr19:3120293
|
C | T | 1 | a0001c0001t0056g0113 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.890-696C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 6/6 | chr19 | 3120293 | ||||||
chr19:3120344
|
T | C | 153 | a0001c0001t0005g0001a0001c0001t0005g0019a0001c0001t0005g0062others(150): Show | 206 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(203): Show |
intron_variant | MODIFIER | c.890-645T>C | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 6/6 | chr19 | 3120344 | ||||||
chr19:3120345
|
G | A | 1 | a0001c0002t0018g0138 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.890-644G>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 6/6 | chr19 | 3120345 | ||||||
chr19:3120345
|
G | C | 66 | a0001c0002t0002g0004a0001c0002t0002g0005a0001c0002t0002g0008others(63): Show | 85 | HG00323.hp1 HG00408.hp2 HG00597.hp2 others(82): Show |
intron_variant | MODIFIER | c.890-644G>C | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 6/6 | chr19 | 3120345 | ||||||
chr19:3120498
|
C | G | 59 | a0001c0001t0015g0020a0001c0001t0015g0023a0001c0001t0015g0082others(56): Show | 78 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.890-491C>G | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 6/6 | chr19 | 3120498 | ||||||
chr19:3120513
|
C | T | 91 | a0001c0001t0003g0040a0001c0001t0003g0041a0001c0001t0003g0042others(88): Show | 102 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.890-476C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 6/6 | chr19 | 3120513 | ||||||
chr19:3120612
|
G | GGGGGGGC others(17): Show |
1 | a0001c0001t0001g0238 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.890-377_890-376ins others(24): Show |
GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 6/6 | chr19 | 3120612 | ||||||
chr19:3120613
|
C | G | 1 | a0001c0001t0001g0238 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.890-376C>G | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 6/6 | chr19 | 3120613 | ||||||
chr19:3120644
|
T | A | 1 | a0001c0001t0001g0238 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.890-345T>A | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 6/6 | chr19 | 3120644 | ||||||
chr19:3120646
|
G | C | 1 | a0001c0001t0001g0238 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.890-343G>C | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 6/6 | chr19 | 3120646 | ||||||
chr19:3120648
|
A | T | 1 | a0001c0001t0001g0238 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.890-341A>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 6/6 | chr19 | 3120648 | ||||||
chr19:3120741
|
T | G | 184 | a0001c0001t0005g0001a0001c0001t0005g0019a0001c0001t0005g0062others(181): Show | 239 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.890-248T>G | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 6/6 | chr19 | 3120741 | ||||||
chr19:3120773
|
C | T | 1 | a0001c0002t0002g0102 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.890-216C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 6/6 | chr19 | 3120773 | ||||||
chr19:3120888
|
G | T | 1 | a0001c0001t0001g0100 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.890-101G>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 6/6 | chr19 | 3120888 | ||||||
chr19:3120900
|
C | T | 1 | a0001c0001t0037g0068 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.890-89C>T | GNA11 | ENSG00000088256.9 | transcript | ENST00000078429.9 | protein_coding | 6/6 | chr19 | 3120900 |