geneid | 2566 |
---|---|
ensemblid | ENSG00000113327.17 |
hgncid | 4087 |
symbol | GABRG2 |
name | gamma-aminobutyric acid type A receptor subunit gamma2 |
refseq_nuc | NM_198904.4 |
refseq_prot | NP_944494.1 |
ensembl_nuc | ENST00000639213.2 |
ensembl_prot | ENSP00000491909.2 |
mane_status | MANE Select |
chr | chr5 |
start | 162067773 |
end | 162155526 |
strand | + |
ver | v1.2 |
region | chr5:162067773-162155526 |
region5000 | chr5:162062773-162160526 |
regionname0 | GABRG2_chr5_162067773_162155526 |
regionname5000 | GABRG2_chr5_162062773_162160526 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 475 | 327 | 84 | 42 | 153 | 12 | 34 | 117 | GABRG2_chr5_162062773_162160526 | GABRG2 | copy fasta | chr5 | 162062773 | 162160526 |
a0002 | 0/0 | 475 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GABRG2_chr5_162062773_162160526 | GABRG2 | copy fasta | chr5 | 162062773 | 162160526 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 1428 | 145 | 34 | 12 | 88 | 5 | 6 | GABRG2_chr5_162062773_162160526 | GABRG2 | copy fasta | chr5 | 162062773 | 162160526 |
c0002 | 1/1 | 1428 | 109 | 38 | 19 | 27 | 5 | 18 | GABRG2_chr5_162062773_162160526 | GABRG2 | copy fasta | chr5 | 162062773 | 162160526 |
c0003 | 0/0 | 1428 | 52 | 0 | 5 | 37 | 2 | 8 | GABRG2_chr5_162062773_162160526 | GABRG2 | copy fasta | chr5 | 162062773 | 162160526 |
c0004 | 0/0 | 1428 | 10 | 8 | 2 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | copy fasta | chr5 | 162062773 | 162160526 |
c0005 | 0/0 | 1428 | 3 | 2 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | copy fasta | chr5 | 162062773 | 162160526 |
c0006 | 0/0 | 1428 | 2 | 0 | 2 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | copy fasta | chr5 | 162062773 | 162160526 |
c0007 | 0/0 | 1428 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | copy fasta | chr5 | 162062773 | 162160526 |
c0008 | 0/0 | 1428 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | copy fasta | chr5 | 162062773 | 162160526 |
c0009 | 0/0 | 1428 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | copy fasta | chr5 | 162062773 | 162160526 |
c0010 | 0/0 | 1428 | 1 | 0 | 0 | 0 | 0 | 1 | GABRG2_chr5_162062773_162160526 | GABRG2 | copy fasta | chr5 | 162062773 | 162160526 |
c0011 | 0/0 | 1428 | 1 | 0 | 0 | 0 | 0 | 1 | GABRG2_chr5_162062773_162160526 | GABRG2 | copy fasta | chr5 | 162062773 | 162160526 |
c0012 | 0/0 | 1428 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | copy fasta | chr5 | 162062773 | 162160526 |
c0013 | 0/0 | 1428 | 1 | 0 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | copy fasta | chr5 | 162062773 | 162160526 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/0 | 2386 | 112 | 25 | 21 | 41 | 6 | 18 | GABRG2_chr5_162062773_162160526 | GABRG2 | copy fasta | chr5 | 162062773 | 162160526 |
t0002 | 0/0 | 2384 | 100 | 18 | 9 | 64 | 3 | 6 | GABRG2_chr5_162062773_162160526 | GABRG2 | copy fasta | chr5 | 162062773 | 162160526 |
t0003 | 0/0 | 2386 | 56 | 3 | 6 | 37 | 1 | 9 | GABRG2_chr5_162062773_162160526 | GABRG2 | copy fasta | chr5 | 162062773 | 162160526 |
t0004 | 0/0 | 2386 | 16 | 15 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | copy fasta | chr5 | 162062773 | 162160526 |
t0005 | 0/0 | 2386 | 10 | 8 | 2 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | copy fasta | chr5 | 162062773 | 162160526 |
t0006 | 0/0 | 2386 | 6 | 6 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | copy fasta | chr5 | 162062773 | 162160526 |
t0007 | 0/1 | 2386 | 6 | 0 | 1 | 3 | 1 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | copy fasta | chr5 | 162062773 | 162160526 |
t0008 | 0/0 | 2384 | 3 | 0 | 0 | 3 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | copy fasta | chr5 | 162062773 | 162160526 |
t0009 | 0/0 | 2384 | 3 | 0 | 0 | 3 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | copy fasta | chr5 | 162062773 | 162160526 |
t0010 | 0/0 | 2386 | 3 | 3 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | copy fasta | chr5 | 162062773 | 162160526 |
t0011 | 0/0 | 2386 | 3 | 1 | 0 | 2 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | copy fasta | chr5 | 162062773 | 162160526 |
t0012 | 0/0 | 2386 | 2 | 0 | 2 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | copy fasta | chr5 | 162062773 | 162160526 |
t0013 | 0/0 | 2384 | 2 | 0 | 0 | 0 | 1 | 1 | GABRG2_chr5_162062773_162160526 | GABRG2 | copy fasta | chr5 | 162062773 | 162160526 |
t0014 | 0/0 | 2386 | 2 | 2 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | copy fasta | chr5 | 162062773 | 162160526 |
t0015 | 0/0 | 2386 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | copy fasta | chr5 | 162062773 | 162160526 |
t0016 | 0/0 | 2386 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | copy fasta | chr5 | 162062773 | 162160526 |
t0017 | 0/0 | 2386 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | copy fasta | chr5 | 162062773 | 162160526 |
t0018 | 0/0 | 2386 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | copy fasta | chr5 | 162062773 | 162160526 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0007 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0010 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0015 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0082 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0175 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 1428 | 145 | 34 | 12 | 88 | 5 | 6 | GABRG2_chr5_162062773_162160526 | GABRG2 | copy fasta | chr5 | 162062773 | 162160526 |
a0001c0002 | 1/1 | 1428 | 109 | 38 | 19 | 27 | 5 | 18 | GABRG2_chr5_162062773_162160526 | GABRG2 | copy fasta | chr5 | 162062773 | 162160526 |
a0001c0003 | 0/0 | 1428 | 52 | 0 | 5 | 37 | 2 | 8 | GABRG2_chr5_162062773_162160526 | GABRG2 | copy fasta | chr5 | 162062773 | 162160526 |
a0001c0004 | 0/0 | 1428 | 10 | 8 | 2 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | copy fasta | chr5 | 162062773 | 162160526 |
a0001c0005 | 0/0 | 1428 | 3 | 2 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | copy fasta | chr5 | 162062773 | 162160526 |
a0001c0006 | 0/0 | 1428 | 2 | 0 | 2 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | copy fasta | chr5 | 162062773 | 162160526 |
a0001c0008 | 0/0 | 1428 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | copy fasta | chr5 | 162062773 | 162160526 |
a0001c0009 | 0/0 | 1428 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | copy fasta | chr5 | 162062773 | 162160526 |
a0001c0010 | 0/0 | 1428 | 1 | 0 | 0 | 0 | 0 | 1 | GABRG2_chr5_162062773_162160526 | GABRG2 | copy fasta | chr5 | 162062773 | 162160526 |
a0001c0011 | 0/0 | 1428 | 1 | 0 | 0 | 0 | 0 | 1 | GABRG2_chr5_162062773_162160526 | GABRG2 | copy fasta | chr5 | 162062773 | 162160526 |
a0001c0012 | 0/0 | 1428 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | copy fasta | chr5 | 162062773 | 162160526 |
a0001c0013 | 0/0 | 1428 | 1 | 0 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | copy fasta | chr5 | 162062773 | 162160526 |
a0002c0007 | 0/0 | 1428 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | copy fasta | chr5 | 162062773 | 162160526 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 3813 | 14 | 4 | 2 | 6 | 1 | 1 | GABRG2_chr5_162062773_162160526 | GABRG2 | copy fasta | chr5 | 162062773 | 162160526 |
a0001c0001t0002 | 0/0 | 3811 | 78 | 11 | 7 | 53 | 3 | 4 | GABRG2_chr5_162062773_162160526 | GABRG2 | copy fasta | chr5 | 162062773 | 162160526 |
a0001c0001t0003 | 0/0 | 3813 | 27 | 2 | 2 | 22 | 0 | 1 | GABRG2_chr5_162062773_162160526 | GABRG2 | copy fasta | chr5 | 162062773 | 162160526 |
a0001c0001t0004 | 0/0 | 3813 | 14 | 13 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | copy fasta | chr5 | 162062773 | 162160526 |
a0001c0001t0008 | 0/0 | 3811 | 3 | 0 | 0 | 3 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | copy fasta | chr5 | 162062773 | 162160526 |
a0001c0001t0009 | 0/0 | 3811 | 3 | 0 | 0 | 3 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | copy fasta | chr5 | 162062773 | 162160526 |
a0001c0001t0010 | 0/0 | 3813 | 3 | 3 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | copy fasta | chr5 | 162062773 | 162160526 |
a0001c0001t0013 | 0/0 | 3811 | 1 | 0 | 0 | 0 | 1 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | copy fasta | chr5 | 162062773 | 162160526 |
a0001c0001t0016 | 0/0 | 3813 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | copy fasta | chr5 | 162062773 | 162160526 |
a0001c0001t0018 | 0/0 | 3813 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | copy fasta | chr5 | 162062773 | 162160526 |
a0001c0002t0001 | 1/0 | 3813 | 67 | 20 | 17 | 14 | 3 | 12 | GABRG2_chr5_162062773_162160526 | GABRG2 | copy fasta | chr5 | 162062773 | 162160526 |
a0001c0002t0002 | 0/0 | 3811 | 9 | 3 | 0 | 4 | 0 | 2 | GABRG2_chr5_162062773_162160526 | GABRG2 | copy fasta | chr5 | 162062773 | 162160526 |
a0001c0002t0003 | 0/0 | 3813 | 8 | 0 | 0 | 4 | 1 | 3 | GABRG2_chr5_162062773_162160526 | GABRG2 | copy fasta | chr5 | 162062773 | 162160526 |
a0001c0002t0004 | 0/0 | 3813 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | copy fasta | chr5 | 162062773 | 162160526 |
a0001c0002t0005 | 0/0 | 3813 | 6 | 5 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | copy fasta | chr5 | 162062773 | 162160526 |
a0001c0002t0006 | 0/0 | 3813 | 6 | 6 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | copy fasta | chr5 | 162062773 | 162160526 |
a0001c0002t0007 | 0/1 | 3813 | 6 | 0 | 1 | 3 | 1 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | copy fasta | chr5 | 162062773 | 162160526 |
a0001c0002t0011 | 0/0 | 3813 | 3 | 1 | 0 | 2 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | copy fasta | chr5 | 162062773 | 162160526 |
a0001c0002t0013 | 0/0 | 3811 | 1 | 0 | 0 | 0 | 0 | 1 | GABRG2_chr5_162062773_162160526 | GABRG2 | copy fasta | chr5 | 162062773 | 162160526 |
a0001c0002t0014 | 0/0 | 3813 | 2 | 2 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | copy fasta | chr5 | 162062773 | 162160526 |
a0001c0003t0001 | 0/0 | 3813 | 30 | 0 | 2 | 21 | 2 | 5 | GABRG2_chr5_162062773_162160526 | GABRG2 | copy fasta | chr5 | 162062773 | 162160526 |
a0001c0003t0002 | 0/0 | 3811 | 6 | 0 | 0 | 6 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | copy fasta | chr5 | 162062773 | 162160526 |
a0001c0003t0003 | 0/0 | 3813 | 16 | 0 | 3 | 10 | 0 | 3 | GABRG2_chr5_162062773_162160526 | GABRG2 | copy fasta | chr5 | 162062773 | 162160526 |
a0001c0004t0002 | 0/0 | 3811 | 5 | 4 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | copy fasta | chr5 | 162062773 | 162160526 |
a0001c0004t0005 | 0/0 | 3813 | 4 | 3 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | copy fasta | chr5 | 162062773 | 162160526 |
a0001c0004t0017 | 0/0 | 3813 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | copy fasta | chr5 | 162062773 | 162160526 |
a0001c0005t0003 | 0/0 | 3813 | 2 | 1 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | copy fasta | chr5 | 162062773 | 162160526 |
a0001c0005t0015 | 0/0 | 3813 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | copy fasta | chr5 | 162062773 | 162160526 |
a0001c0006t0012 | 0/0 | 3813 | 2 | 0 | 2 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | copy fasta | chr5 | 162062773 | 162160526 |
a0001c0008t0001 | 0/0 | 3813 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | copy fasta | chr5 | 162062773 | 162160526 |
a0001c0009t0004 | 0/0 | 3813 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | copy fasta | chr5 | 162062773 | 162160526 |
a0001c0010t0003 | 0/0 | 3813 | 1 | 0 | 0 | 0 | 0 | 1 | GABRG2_chr5_162062773_162160526 | GABRG2 | copy fasta | chr5 | 162062773 | 162160526 |
a0001c0011t0003 | 0/0 | 3813 | 1 | 0 | 0 | 0 | 0 | 1 | GABRG2_chr5_162062773_162160526 | GABRG2 | copy fasta | chr5 | 162062773 | 162160526 |
a0001c0012t0003 | 0/0 | 3813 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | copy fasta | chr5 | 162062773 | 162160526 |
a0001c0013t0002 | 0/0 | 3811 | 1 | 0 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | copy fasta | chr5 | 162062773 | 162160526 |
a0002c0007t0002 | 0/0 | 3811 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | copy fasta | chr5 | 162062773 | 162160526 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0002g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0002g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0002g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0002g0010 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0002g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0002g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0002g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0002g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0002g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0002g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0003g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0003g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0003g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0003g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0003g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0003g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0003g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0003g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0004g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0004g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0004g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0004g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0004g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0004g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0004g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0004g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0004g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0004g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0004g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0004g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0004g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0004g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0008g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0008g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0008g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0009g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0009g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0009g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0010g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0010g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0010g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0013g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0016g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0001t0018g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0002t0001g0001 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0002t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0002t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0002t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0002t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0002t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0002t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0002t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0002t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0002t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0002t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0002t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0002t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0002t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0002t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0002t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0002t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0002t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0002t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0002t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0002t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0002t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0002t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0002t0001g0175 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0002t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0002t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0002t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0002t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0002t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0002t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0002t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0002t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0002t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0002t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0002t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0002t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0002t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0002t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0002t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0002t0002g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0002t0002g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0002t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0002t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0002t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0002t0002g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0002t0002g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0002t0003g0007 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0002t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0002t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0002t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0002t0003g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0002t0003g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0002t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0002t0004g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0002t0005g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0002t0005g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0002t0005g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0002t0005g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0002t0005g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0002t0005g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0002t0006g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0002t0006g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0002t0006g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0002t0006g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0002t0006g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0002t0007g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0002t0007g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0002t0007g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0002t0007g0082 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0002t0007g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0002t0007g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0002t0011g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0002t0011g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0002t0011g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0002t0013g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0002t0014g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0002t0014g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0003t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0003t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0003t0001g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0003t0001g0015 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0003t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0003t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0003t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0003t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0003t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0003t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0003t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0003t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0003t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0003t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0003t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0003t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0003t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0003t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0003t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0003t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0003t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0003t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0003t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0003t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0003t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0003t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0003t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0003t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0003t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0003t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0003t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0003t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0003t0003g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0003t0003g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0003t0003g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0003t0003g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0003t0003g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0003t0003g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0003t0003g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0003t0003g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0003t0003g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0003t0003g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0003t0003g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0003t0003g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0003t0003g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0003t0003g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0003t0003g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0003t0003g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0004t0002g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0004t0002g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0004t0002g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0004t0002g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0004t0002g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0004t0005g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0004t0005g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0004t0005g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0004t0005g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0004t0017g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0005t0003g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0005t0003g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0005t0015g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0006t0012g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0008t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0009t0004g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0010t0003g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0011t0003g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0012t0003g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0001c0013t0002g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
a0002c0007t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0002 | t0001 | g0179 | EUR | GBR | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0072 | EUR | GBR | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG00140 | hp1 | a0001 | c0002 | t0003 | g0122 | EUR | GBR | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG00140 | hp2 | a0001 | c0002 | t0001 | g0001 | EUR | GBR | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG00423 | hp1 | a0001 | c0002 | t0001 | g0051 | EAS | CHS | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG00423 | hp2 | a0001 | c0001 | t0002 | g0200 | EAS | CHS | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG00438 | hp1 | a0001 | c0001 | t0003 | g0109 | EAS | CHS | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0065 | EAS | CHS | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG00558 | hp1 | a0001 | c0003 | t0001 | g0282 | EAS | CHS | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0184 | EAS | CHS | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG00597 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | CHS | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | CHS | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG00621 | hp1 | a0001 | c0001 | t0003 | g0203 | EAS | CHS | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG00621 | hp2 | a0001 | c0002 | t0001 | g0135 | EAS | CHS | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0163 | AMR | PUR | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG00639 | hp2 | a0001 | c0004 | t0005 | g0239 | AMR | PUR | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG00673 | hp1 | a0001 | c0002 | t0001 | g0150 | EAS | CHS | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG00673 | hp2 | a0001 | c0002 | t0002 | g0095 | EAS | CHS | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG00735 | hp1 | a0001 | c0002 | t0001 | g0234 | AMR | PUR | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG01069 | hp1 | a0001 | c0006 | t0012 | g0005 | AMR | PUR | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG01069 | hp2 | a0001 | c0002 | t0001 | g0087 | AMR | PUR | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG01071 | hp1 | a0001 | c0006 | t0012 | g0005 | AMR | PUR | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG01071 | hp2 | a0001 | c0002 | t0001 | g0177 | AMR | PUR | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG01074 | hp1 | a0001 | c0003 | t0003 | g0301 | AMR | PUR | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG01074 | hp2 | a0001 | c0002 | t0001 | g0174 | AMR | PUR | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG01081 | hp1 | a0001 | c0002 | t0001 | g0227 | AMR | PUR | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG01081 | hp2 | a0001 | c0002 | t0001 | g0157 | AMR | PUR | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG01106 | hp1 | a0001 | c0001 | t0002 | g0010 | AMR | PUR | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG01106 | hp2 | a0001 | c0002 | t0001 | g0188 | AMR | PUR | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0260 | AMR | PUR | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG01109 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG01169 | hp1 | a0001 | c0002 | t0001 | g0142 | AMR | PUR | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG01169 | hp2 | a0001 | c0002 | t0001 | g0236 | AMR | PUR | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG01175 | hp1 | a0001 | c0002 | t0001 | g0067 | AMR | PUR | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG01175 | hp2 | a0001 | c0002 | t0001 | g0232 | AMR | PUR | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG01192 | hp1 | a0001 | c0001 | t0004 | g0139 | AMR | PUR | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG01192 | hp2 | a0001 | c0002 | t0001 | g0235 | AMR | PUR | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG01243 | hp1 | a0001 | c0004 | t0002 | g0147 | AMR | PUR | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG01243 | hp2 | a0001 | c0005 | t0003 | g0028 | AMR | PUR | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG01258 | hp1 | a0001 | c0003 | t0001 | g0014 | AMR | CLM | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG01258 | hp2 | a0001 | c0002 | t0001 | g0156 | AMR | CLM | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG01261 | hp1 | a0001 | c0002 | t0001 | g0141 | AMR | CLM | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0023 | AMR | CLM | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG01346 | hp1 | a0001 | c0001 | t0002 | g0055 | AMR | CLM | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG01346 | hp2 | a0001 | c0001 | t0003 | g0126 | AMR | CLM | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG01433 | hp1 | a0001 | c0002 | t0007 | g0074 | AMR | CLM | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG01433 | hp2 | a0001 | c0001 | t0003 | g0105 | AMR | CLM | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG01496 | hp1 | a0001 | c0003 | t0003 | g0279 | AMR | CLM | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | CLM | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG01515 | hp1 | a0001 | c0001 | t0002 | g0010 | EUR | IBS | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG01515 | hp2 | a0001 | c0002 | t0007 | g0081 | EUR | IBS | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG01516 | hp1 | a0001 | c0003 | t0001 | g0015 | EUR | IBS | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0036 | EUR | IBS | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG01517 | hp1 | a0001 | c0001 | t0002 | g0202 | EUR | IBS | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG01517 | hp2 | a0001 | c0003 | t0001 | g0015 | EUR | IBS | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG01884 | hp1 | a0001 | c0005 | t0003 | g0075 | AFR | ACB | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG01884 | hp2 | a0001 | c0002 | t0006 | g0145 | AFR | ACB | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG01891 | hp1 | a0001 | c0002 | t0002 | g0016 | AFR | ACB | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG01891 | hp2 | a0001 | c0002 | t0001 | g0058 | AFR | ACB | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG01928 | hp1 | a0001 | c0003 | t0001 | g0014 | AMR | PEL | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG01928 | hp2 | a0001 | c0001 | t0002 | g0037 | AMR | PEL | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG01952 | hp1 | a0001 | c0013 | t0002 | g0274 | AMR | PEL | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG01952 | hp2 | a0001 | c0002 | t0001 | g0138 | AMR | PEL | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG01981 | hp1 | a0001 | c0001 | t0002 | g0056 | AMR | PEL | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG01981 | hp2 | a0001 | c0002 | t0005 | g0228 | AMR | PEL | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG02004 | hp1 | a0001 | c0002 | t0001 | g0120 | AMR | PEL | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG02004 | hp2 | a0001 | c0003 | t0003 | g0273 | AMR | PEL | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | KHV | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG02027 | hp2 | a0001 | c0001 | t0016 | g0121 | EAS | KHV | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | KHV | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG02040 | hp2 | a0001 | c0001 | t0002 | g0201 | EAS | KHV | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG02055 | hp1 | a0001 | c0002 | t0005 | g0224 | AFR | ACB | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG02055 | hp2 | a0001 | c0002 | t0001 | g0107 | AFR | ACB | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG02071 | hp1 | a0001 | c0003 | t0002 | g0281 | EAS | KHV | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG02071 | hp2 | a0001 | c0002 | t0001 | g0009 | EAS | KHV | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0209 | EAS | KHV | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG02074 | hp2 | a0001 | c0003 | t0001 | g0298 | EAS | KHV | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG02080 | hp1 | a0001 | c0001 | t0003 | g0169 | EAS | KHV | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0042 | EAS | KHV | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG02083 | hp1 | a0001 | c0001 | t0002 | g0245 | EAS | KHV | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG02083 | hp2 | a0001 | c0002 | t0003 | g0101 | EAS | KHV | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG02132 | hp1 | a0001 | c0001 | t0003 | g0071 | EAS | KHV | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | KHV | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG02135 | hp1 | a0001 | c0001 | t0002 | g0073 | EAS | KHV | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG02135 | hp2 | a0001 | c0002 | t0002 | g0092 | EAS | KHV | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG02145 | hp1 | a0001 | c0002 | t0006 | g0008 | AFR | ACB | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG02145 | hp2 | a0001 | c0001 | t0002 | g0217 | AFR | ACB | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0038 | EAS | CDX | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG02155 | hp2 | a0001 | c0002 | t0001 | g0154 | EAS | CDX | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0205 | EAS | CDX | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | CDX | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG02258 | hp1 | a0001 | c0004 | t0002 | g0149 | AFR | ACB | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG02258 | hp2 | a0001 | c0001 | t0004 | g0311 | AFR | ACB | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | ACB | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG02451 | hp2 | a0001 | c0002 | t0001 | g0229 | AFR | ACB | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG02572 | hp1 | a0001 | c0001 | t0004 | g0263 | AFR | GWD | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG02572 | hp2 | a0001 | c0002 | t0014 | g0076 | AFR | GWD | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0059 | SAS | PJL | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG02615 | hp1 | a0001 | c0002 | t0002 | g0006 | AFR | GWD | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG02615 | hp2 | a0001 | c0001 | t0004 | g0253 | AFR | GWD | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG02622 | hp1 | a0001 | c0001 | t0004 | g0256 | AFR | GWD | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG02622 | hp2 | a0001 | c0002 | t0001 | g0117 | AFR | GWD | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG02630 | hp1 | a0001 | c0001 | t0003 | g0130 | AFR | GWD | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG02630 | hp2 | a0001 | c0002 | t0001 | g0248 | AFR | GWD | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | GWD | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG02647 | hp2 | a0001 | c0004 | t0017 | g0246 | AFR | GWD | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG02683 | hp1 | a0001 | c0002 | t0001 | g0222 | SAS | PJL | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG02683 | hp2 | a0001 | c0003 | t0001 | g0275 | SAS | PJL | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG02698 | hp1 | a0001 | c0001 | t0003 | g0181 | SAS | PJL | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG02698 | hp2 | a0001 | c0011 | t0003 | g0272 | SAS | PJL | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG02717 | hp1 | a0001 | c0001 | t0002 | g0185 | AFR | GWD | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG02717 | hp2 | a0001 | c0001 | t0004 | g0254 | AFR | GWD | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG02723 | hp1 | a0001 | c0002 | t0001 | g0137 | AFR | GWD | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG02723 | hp2 | a0001 | c0001 | t0002 | g0160 | AFR | GWD | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG02735 | hp1 | a0001 | c0010 | t0003 | g0112 | SAS | PJL | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG02735 | hp2 | a0001 | c0002 | t0001 | g0192 | SAS | PJL | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG02738 | hp1 | a0001 | c0002 | t0001 | g0215 | SAS | PJL | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG02738 | hp2 | a0001 | c0002 | t0001 | g0180 | SAS | PJL | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG02809 | hp1 | a0001 | c0001 | t0002 | g0194 | AFR | GWD | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG02809 | hp2 | a0001 | c0002 | t0001 | g0191 | AFR | GWD | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG02818 | hp1 | a0001 | c0001 | t0004 | g0251 | AFR | GWD | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG02818 | hp2 | a0001 | c0004 | t0002 | g0018 | AFR | GWD | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG02886 | hp1 | a0001 | c0001 | t0004 | g0250 | AFR | GWD | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG02886 | hp2 | a0001 | c0002 | t0002 | g0006 | AFR | GWD | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG02897 | hp1 | a0001 | c0002 | t0001 | g0103 | AFR | GWD | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG02897 | hp2 | a0001 | c0004 | t0005 | g0240 | AFR | GWD | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG02922 | hp1 | a0001 | c0001 | t0002 | g0165 | AFR | ESN | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG02922 | hp2 | a0001 | c0002 | t0005 | g0223 | AFR | ESN | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG02965 | hp1 | a0001 | c0004 | t0002 | g0241 | AFR | ESN | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG02965 | hp2 | a0001 | c0001 | t0004 | g0310 | AFR | ESN | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0090 | SAS | PJL | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG03017 | hp2 | a0001 | c0002 | t0001 | g0168 | SAS | PJL | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG03041 | hp1 | a0001 | c0001 | t0002 | g0214 | AFR | GWD | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG03041 | hp2 | a0001 | c0001 | t0004 | g0309 | AFR | GWD | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG03130 | hp1 | a0001 | c0002 | t0001 | g0173 | AFR | ESN | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG03130 | hp2 | a0001 | c0002 | t0001 | g0116 | AFR | ESN | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG03139 | hp1 | a0001 | c0002 | t0006 | g0144 | AFR | ESN | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG03139 | hp2 | a0001 | c0002 | t0001 | g0230 | AFR | ESN | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG03195 | hp1 | a0001 | c0002 | t0001 | g0178 | AFR | ESN | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG03195 | hp2 | a0001 | c0001 | t0002 | g0204 | AFR | ESN | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG03209 | hp1 | a0001 | c0004 | t0005 | g0237 | AFR | MSL | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG03209 | hp2 | a0001 | c0001 | t0004 | g0252 | AFR | MSL | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG03225 | hp1 | a0001 | c0002 | t0001 | g0211 | AFR | MSL | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG03225 | hp2 | a0001 | c0005 | t0015 | g0243 | AFR | MSL | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG03453 | hp1 | a0001 | c0002 | t0006 | g0008 | AFR | MSL | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG03453 | hp2 | a0001 | c0001 | t0002 | g0164 | AFR | MSL | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG03491 | hp1 | a0001 | c0002 | t0001 | g0094 | SAS | PJL | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG03491 | hp2 | a0001 | c0002 | t0003 | g0007 | SAS | PJL | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG03492 | hp1 | a0001 | c0002 | t0003 | g0007 | SAS | PJL | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG03492 | hp2 | a0001 | c0003 | t0003 | g0280 | SAS | PJL | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG03516 | hp1 | a0001 | c0002 | t0011 | g0085 | AFR | ESN | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG03516 | hp2 | a0001 | c0001 | t0002 | g0029 | AFR | ESN | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG03540 | hp1 | a0001 | c0001 | t0004 | g0017 | AFR | GWD | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG03540 | hp2 | a0001 | c0002 | t0001 | g0132 | AFR | GWD | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG03579 | hp1 | a0001 | c0001 | t0003 | g0063 | AFR | MSL | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG03579 | hp2 | a0001 | c0002 | t0001 | g0118 | AFR | MSL | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG03654 | hp1 | a0001 | c0002 | t0013 | g0131 | SAS | PJL | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG03654 | hp2 | a0001 | c0002 | t0001 | g0070 | SAS | PJL | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG03669 | hp1 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG03669 | hp2 | a0001 | c0003 | t0003 | g0305 | SAS | PJL | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG03710 | hp1 | a0001 | c0002 | t0002 | g0218 | SAS | PJL | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG03710 | hp2 | a0001 | c0003 | t0001 | g0285 | SAS | PJL | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG03831 | hp1 | a0001 | c0002 | t0001 | g0212 | SAS | BEB | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG03831 | hp2 | a0001 | c0002 | t0001 | g0233 | SAS | BEB | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG03927 | hp1 | a0001 | c0002 | t0003 | g0128 | SAS | BEB | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG03927 | hp2 | a0001 | c0001 | t0002 | g0193 | SAS | BEB | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0064 | SAS | STU | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG04115 | hp2 | a0001 | c0003 | t0001 | g0271 | SAS | STU | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG04184 | hp1 | a0001 | c0003 | t0003 | g0267 | SAS | BEB | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG04184 | hp2 | a0001 | c0002 | t0001 | g0136 | SAS | BEB | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG04199 | hp1 | a0001 | c0003 | t0001 | g0287 | SAS | STU | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG04199 | hp2 | a0001 | c0002 | t0002 | g0186 | SAS | STU | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG04228 | hp1 | a0001 | c0003 | t0001 | g0019 | SAS | STU | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG04228 | hp2 | a0001 | c0002 | t0001 | g0129 | SAS | STU | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA18522 | hp1 | a0001 | c0008 | t0001 | g0247 | AFR | YRI | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA18522 | hp2 | a0001 | c0001 | t0004 | g0255 | AFR | YRI | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA18612 | hp1 | a0001 | c0001 | t0009 | g0216 | EAS | CHB | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | CHB | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0220 | EAS | CHB | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA18747 | hp2 | a0001 | c0002 | t0001 | g0089 | EAS | CHB | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA18906 | hp1 | a0001 | c0002 | t0006 | g0146 | AFR | YRI | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA18906 | hp2 | a0001 | c0001 | t0002 | g0161 | AFR | YRI | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA18941 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA18941 | hp2 | a0001 | c0002 | t0001 | g0199 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA18942 | hp1 | a0001 | c0001 | t0003 | g0170 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA18942 | hp2 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA18943 | hp1 | a0001 | c0003 | t0003 | g0289 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA18944 | hp1 | a0001 | c0001 | t0003 | g0061 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA18944 | hp2 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA18945 | hp2 | a0001 | c0003 | t0003 | g0114 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA18946 | hp1 | a0001 | c0001 | t0003 | g0111 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA18946 | hp2 | a0001 | c0002 | t0001 | g0155 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA18948 | hp1 | a0001 | c0001 | t0003 | g0167 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA18950 | hp1 | a0001 | c0001 | t0003 | g0123 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA18950 | hp2 | a0001 | c0002 | t0002 | g0100 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA18952 | hp2 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA18953 | hp1 | a0001 | c0001 | t0003 | g0182 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA18953 | hp2 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA18954 | hp1 | a0001 | c0012 | t0003 | g0266 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA18954 | hp2 | a0001 | c0001 | t0008 | g0044 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA18959 | hp1 | a0001 | c0003 | t0001 | g0284 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA18959 | hp2 | a0001 | c0002 | t0007 | g0084 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA18960 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA18960 | hp2 | a0001 | c0001 | t0009 | g0206 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA18962 | hp1 | a0001 | c0002 | t0001 | g0098 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA18962 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA18963 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA18963 | hp2 | a0001 | c0003 | t0003 | g0278 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA18964 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA18964 | hp2 | a0001 | c0003 | t0001 | g0300 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA18968 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA18968 | hp2 | a0001 | c0003 | t0003 | g0290 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA18969 | hp1 | a0001 | c0001 | t0008 | g0053 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA18969 | hp2 | a0001 | c0003 | t0001 | g0013 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA18971 | hp1 | a0001 | c0001 | t0003 | g0124 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA18971 | hp2 | a0001 | c0001 | t0002 | g0159 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA18977 | hp1 | a0001 | c0003 | t0001 | g0299 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA18977 | hp2 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA18978 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA18978 | hp2 | a0001 | c0001 | t0003 | g0134 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA18979 | hp1 | a0001 | c0003 | t0001 | g0295 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA18979 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA18980 | hp1 | a0001 | c0003 | t0001 | g0012 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA18980 | hp2 | a0001 | c0001 | t0008 | g0050 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA18984 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA18984 | hp2 | a0001 | c0003 | t0001 | g0303 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA18987 | hp1 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA18987 | hp2 | a0001 | c0003 | t0003 | g0277 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA18993 | hp1 | a0001 | c0001 | t0003 | g0171 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA18993 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA18994 | hp1 | a0001 | c0002 | t0007 | g0078 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA18994 | hp2 | a0001 | c0003 | t0003 | g0270 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA18995 | hp1 | a0001 | c0002 | t0003 | g0140 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA18995 | hp2 | a0001 | c0002 | t0002 | g0096 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA18997 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA18997 | hp2 | a0001 | c0003 | t0001 | g0283 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA18998 | hp1 | a0001 | c0002 | t0001 | g0153 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA18998 | hp2 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA18999 | hp1 | a0002 | c0007 | t0002 | g0033 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA18999 | hp2 | a0001 | c0003 | t0001 | g0013 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA19002 | hp1 | a0001 | c0002 | t0003 | g0091 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA19002 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA19003 | hp1 | a0001 | c0003 | t0001 | g0297 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA19003 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA19005 | hp1 | a0001 | c0003 | t0001 | g0293 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA19005 | hp2 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA19006 | hp1 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA19006 | hp2 | a0001 | c0003 | t0002 | g0268 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA19007 | hp1 | a0001 | c0002 | t0001 | g0097 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA19010 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA19010 | hp2 | a0001 | c0002 | t0001 | g0099 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA19011 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA19011 | hp2 | a0001 | c0003 | t0003 | g0264 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA19012 | hp1 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA19012 | hp2 | a0001 | c0003 | t0001 | g0288 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA19030 | hp1 | a0001 | c0002 | t0001 | g0020 | AFR | LWK | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA19030 | hp2 | a0001 | c0001 | t0010 | g0258 | AFR | LWK | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0244 | AFR | LWK | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA19043 | hp2 | a0001 | c0004 | t0005 | g0238 | AFR | LWK | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA19056 | hp1 | a0001 | c0002 | t0011 | g0079 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA19056 | hp2 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA19058 | hp1 | a0001 | c0001 | t0003 | g0125 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA19058 | hp2 | a0001 | c0003 | t0001 | g0308 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA19059 | hp1 | a0001 | c0001 | t0003 | g0242 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA19059 | hp2 | a0001 | c0001 | t0002 | g0312 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA19060 | hp2 | a0001 | c0003 | t0003 | g0265 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA19062 | hp1 | a0001 | c0003 | t0001 | g0304 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA19062 | hp2 | a0001 | c0001 | t0003 | g0024 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA19065 | hp1 | a0001 | c0003 | t0001 | g0294 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA19065 | hp2 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA19066 | hp1 | a0001 | c0002 | t0001 | g0088 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA19066 | hp2 | a0001 | c0003 | t0002 | g0286 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA19067 | hp1 | a0001 | c0003 | t0002 | g0269 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA19067 | hp2 | a0001 | c0002 | t0011 | g0077 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA19068 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA19068 | hp2 | a0001 | c0001 | t0009 | g0207 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA19072 | hp1 | a0001 | c0001 | t0003 | g0054 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA19072 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA19074 | hp1 | a0001 | c0003 | t0002 | g0291 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA19074 | hp2 | a0001 | c0002 | t0007 | g0083 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA19075 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA19075 | hp2 | a0001 | c0001 | t0003 | g0172 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA19076 | hp1 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA19076 | hp2 | a0001 | c0003 | t0003 | g0302 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA19079 | hp1 | a0001 | c0003 | t0001 | g0307 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA19079 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA19081 | hp1 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA19081 | hp2 | a0001 | c0002 | t0003 | g0093 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA19082 | hp1 | a0001 | c0003 | t0001 | g0012 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA19082 | hp2 | a0001 | c0001 | t0003 | g0110 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA19086 | hp1 | a0001 | c0003 | t0001 | g0292 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA19086 | hp2 | a0001 | c0001 | t0003 | g0106 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA19087 | hp1 | a0001 | c0001 | t0003 | g0108 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA19087 | hp2 | a0001 | c0003 | t0001 | g0306 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA19088 | hp1 | a0001 | c0003 | t0003 | g0276 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA19088 | hp2 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA19091 | hp1 | a0001 | c0003 | t0002 | g0296 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA19091 | hp2 | a0001 | c0001 | t0003 | g0060 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA19240 | hp1 | a0001 | c0001 | t0010 | g0261 | AFR | YRI | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA19240 | hp2 | a0001 | c0002 | t0014 | g0080 | AFR | YRI | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA20129 | hp1 | a0001 | c0002 | t0001 | g0102 | AFR | ASW | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA20129 | hp2 | a0001 | c0001 | t0004 | g0257 | AFR | ASW | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA20752 | hp1 | a0001 | c0001 | t0013 | g0210 | EUR | TSI | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA20752 | hp2 | a0001 | c0002 | t0001 | g0035 | EUR | TSI | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG02109 | hp1 | a0001 | c0001 | t0002 | g0166 | AFR | ACB | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG02109 | hp2 | a0001 | c0002 | t0005 | g0225 | AFR | ACB | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG02486 | hp1 | a0001 | c0002 | t0001 | g0231 | AFR | ACB | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG02486 | hp2 | a0001 | c0002 | t0001 | g0176 | AFR | ACB | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG02559 | hp1 | a0001 | c0002 | t0005 | g0226 | AFR | ACB | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG02559 | hp2 | a0001 | c0004 | t0002 | g0148 | AFR | ACB | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG03471 | hp1 | a0001 | c0001 | t0010 | g0259 | AFR | MSL | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG03471 | hp2 | a0001 | c0009 | t0004 | g0143 | AFR | MSL | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG06807 | hp1 | a0001 | c0002 | t0006 | g0249 | AFR | USA | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | USA | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA20300 | hp1 | a0001 | c0001 | t0018 | g0086 | AFR | USA | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA20300 | hp2 | a0001 | c0002 | t0001 | g0119 | AFR | USA | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA21309 | hp1 | a0001 | c0002 | t0004 | g0262 | AFR | LWK | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
NA21309 | hp2 | a0001 | c0002 | t0005 | g0221 | AFR | LWK | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0007 | g0082 | REF | REF | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
homoSapiens_grch38 | hp1 | a0001 | c0002 | t0001 | g0175 | REF | REF | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:162068051
|
G | C | 1 | a0002 | 1 | NA18999.hp1 | missense_variant | MODERATE | c.52G>C | p.Val18Leu | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/10 | 279/3813 | 52/1428 | 18/475 | chr5 | 162068051 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:162095550
|
C | T | 4 | a0001c0003a0001c0011a0001c0012others(1): Show | 55 | HG00558.hp1 HG01074.hp1 HG01258.hp1 others(52): Show |
synonymous_variant | LOW | c.315C>T | p.Asn105Asn | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 3/10 | 542/3813 | 315/1428 | 105/475 | chr5 | 162095550 | ||
chr5:162097664
|
G | A | 1 | a0001c0004 | 10 | HG00639.hp2 HG01243.hp1 HG02258.hp1 others(7): Show |
synonymous_variant | LOW | c.354G>A | p.Ala118Ala | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 4/10 | 581/3813 | 354/1428 | 118/475 | chr5 | 162097664 | ||
chr5:162097670
|
G | A | 2 | a0001c0006a0001c0008 | 3 | HG01069.hp1 HG01071.hp1 NA18522.hp1 |
synonymous_variant | LOW | c.360G>A | p.Thr120Thr | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 4/10 | 587/3813 | 360/1428 | 120/475 | chr5 | 162097670 | ||
chr5:162101274
|
C | T | 5 | a0001c0001a0001c0005a0001c0006others(2): Show | 152 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(149): Show |
synonymous_variant | LOW | c.588C>T | p.Asn196Asn | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 5/10 | 815/3813 | 588/1428 | 196/475 | chr5 | 162101274 | ||
chr5:162103974
|
A | G | 1 | a0001c0005 | 3 | HG01243.hp2 HG01884.hp1 HG03225.hp2 |
synonymous_variant | LOW | c.717A>G | p.Gln239Gln | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/10 | 944/3813 | 717/1428 | 239/475 | chr5 | 162103974 | ||
chr5:162104025
|
C | T | 1 | a0001c0010 | 1 | HG02735.hp1 | splice_region_variant&synonymous_variant | LOW | c.768C>T | p.Ser256Ser | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/10 | 995/3813 | 768/1428 | 256/475 | chr5 | 162104025 | ||
chr5:162142192
|
T | C | 1 | a0001c0009 | 1 | HG03471.hp2 | synonymous_variant | LOW | c.798T>C | p.Phe266Phe | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/10 | 1025/3813 | 798/1428 | 266/475 | chr5 | 162142192 | ||
chr5:162142234
|
T | C | 1 | a0001c0011 | 1 | HG02698.hp2 | synonymous_variant | LOW | c.840T>C | p.Tyr280Tyr | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/10 | 1067/3813 | 840/1428 | 280/475 | chr5 | 162142234 | ||
chr5:162153194
|
C | T | 1 | a0001c0012 | 1 | NA18954.hp1 | synonymous_variant | LOW | c.1254C>T | p.Asp418Asp | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 10/10 | 1481/3813 | 1254/1428 | 418/475 | chr5 | 162153194 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:162067846
|
C | T | 4 | a0001c0001t0018a0001c0002t0007a0001c0002t0011others(1): Show | 12 | HG01433.hp1 HG01515.hp2 HG02572.hp2 others(9): Show |
5_prime_UTR_variant | MODIFIER | c.-154C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/10 | 154 | chr5 | 162067846 | |||||
chr5:162153629
|
G | A | 1 | a0001c0001t0008 | 3 | NA18954.hp2 NA18969.hp1 NA18980.hp2 |
3_prime_UTR_variant | MODIFIER | c.*261G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 10/10 | 261 | chr5 | 162153629 | |||||
chr5:162153711
|
A | G | 2 | a0001c0001t0013a0001c0002t0013 | 2 | HG03654.hp1 NA20752.hp1 |
3_prime_UTR_variant | MODIFIER | c.*343A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 10/10 | 343 | chr5 | 162153711 | |||||
chr5:162153753
|
G | A | 1 | a0001c0006t0012 | 2 | HG01069.hp1 HG01071.hp1 |
3_prime_UTR_variant | MODIFIER | c.*385G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 10/10 | 385 | chr5 | 162153753 | |||||
chr5:162153977
|
C | T | 16 | a0001c0001t0002a0001c0001t0004a0001c0001t0008others(13): Show | 129 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(126): Show |
3_prime_UTR_variant | MODIFIER | c.*609C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 10/10 | 609 | chr5 | 162153977 | |||||
chr5:162154029
|
T | A | 26 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(23): Show | 190 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(187): Show |
3_prime_UTR_variant | MODIFIER | c.*661T>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 10/10 | 661 | chr5 | 162154029 | |||||
chr5:162154162
|
A | G | 1 | a0001c0001t0010 | 3 | HG03471.hp1 NA19030.hp2 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*794A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 10/10 | 794 | chr5 | 162154162 | |||||
chr5:162154865
|
C | T | 3 | a0001c0002t0005a0001c0002t0014a0001c0004t0005 | 12 | HG00639.hp2 HG01981.hp2 HG02055.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1497C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 10/10 | 1497 | chr5 | 162154865 | |||||
chr5:162154918
|
A | G | 1 | a0001c0001t0016 | 1 | HG02027.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1550A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 10/10 | 1550 | chr5 | 162154918 | |||||
chr5:162154925
|
A | C | 1 | a0001c0005t0015 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1557A>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 10/10 | 1557 | chr5 | 162154925 | |||||
chr5:162154928
|
C | G | 1 | a0001c0005t0015 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1560C>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 10/10 | 1560 | chr5 | 162154928 | |||||
chr5:162154929
|
A | T | 1 | a0001c0005t0015 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1561A>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 10/10 | 1561 | chr5 | 162154929 | |||||
chr5:162154930
|
T | A | 1 | a0001c0005t0015 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1562T>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 10/10 | 1562 | chr5 | 162154930 | |||||
chr5:162154933
|
T | A | 1 | a0001c0005t0015 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1565T>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 10/10 | 1565 | chr5 | 162154933 | |||||
chr5:162154934
|
G | A | 1 | a0001c0005t0015 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1566G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 10/10 | 1566 | chr5 | 162154934 | |||||
chr5:162154935
|
A | T | 1 | a0001c0005t0015 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1567A>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 10/10 | 1567 | chr5 | 162154935 | |||||
chr5:162154937
|
T | C | 1 | a0001c0005t0015 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1569T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 10/10 | 1569 | chr5 | 162154937 | |||||
chr5:162154940
|
A | T | 1 | a0001c0005t0015 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1572A>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 10/10 | 1572 | chr5 | 162154940 | |||||
chr5:162154941
|
G | T | 1 | a0001c0005t0015 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1573G>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 10/10 | 1573 | chr5 | 162154941 | |||||
chr5:162154945
|
T | G | 1 | a0001c0005t0015 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1577T>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 10/10 | 1577 | chr5 | 162154945 | |||||
chr5:162154948
|
C | T | 1 | a0001c0005t0015 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1580C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 10/10 | 1580 | chr5 | 162154948 | |||||
chr5:162154949
|
T | C | 1 | a0001c0005t0015 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1581T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 10/10 | 1581 | chr5 | 162154949 | |||||
chr5:162154953
|
T | A | 1 | a0001c0005t0015 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1585T>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 10/10 | 1585 | chr5 | 162154953 | |||||
chr5:162154954
|
G | C | 1 | a0001c0005t0015 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1586G>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 10/10 | 1586 | chr5 | 162154954 | |||||
chr5:162154956
|
A | G | 1 | a0001c0005t0015 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1588A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 10/10 | 1588 | chr5 | 162154956 | |||||
chr5:162154957
|
C | A | 1 | a0001c0005t0015 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1589C>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 10/10 | 1589 | chr5 | 162154957 | |||||
chr5:162154960
|
A | T | 1 | a0001c0005t0015 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1592A>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 10/10 | 1592 | chr5 | 162154960 | |||||
chr5:162154966
|
A | G | 1 | a0001c0005t0015 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1598A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 10/10 | 1598 | chr5 | 162154966 | |||||
chr5:162154967
|
A | T | 1 | a0001c0005t0015 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1599A>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 10/10 | 1599 | chr5 | 162154967 | |||||
chr5:162154968
|
T | A | 1 | a0001c0005t0015 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1600T>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 10/10 | 1600 | chr5 | 162154968 | |||||
chr5:162154969
|
C | T | 1 | a0001c0005t0015 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1601C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 10/10 | 1601 | chr5 | 162154969 | |||||
chr5:162154975
|
T | G | 1 | a0001c0005t0015 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1607T>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 10/10 | 1607 | chr5 | 162154975 | |||||
chr5:162154981
|
A | G | 1 | a0001c0005t0015 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1613A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 10/10 | 1613 | chr5 | 162154981 | |||||
chr5:162154987
|
G | T | 1 | a0001c0005t0015 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1619G>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 10/10 | 1619 | chr5 | 162154987 | |||||
chr5:162154988
|
C | T | 1 | a0001c0005t0015 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1620C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 10/10 | 1620 | chr5 | 162154988 | |||||
chr5:162155068
|
A | G | 1 | a0001c0005t0015 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1700A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 10/10 | 1700 | chr5 | 162155068 | |||||
chr5:162155129
|
C | A | 1 | a0001c0005t0015 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1761C>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 10/10 | 1761 | chr5 | 162155129 | |||||
chr5:162155336
|
T | G | 1 | a0001c0004t0017 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1968T>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 10/10 | 1968 | chr5 | 162155336 | |||||
chr5:162155342
|
G | A | 1 | a0001c0002t0006 | 6 | HG01884.hp2 HG02145.hp1 HG03139.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1974G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 10/10 | 1974 | chr5 | 162155342 | |||||
chr5:162155463
|
C | G | 1 | a0001c0001t0009 | 3 | NA18612.hp1 NA18960.hp2 NA19068.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2095C>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 10/10 | 2095 | chr5 | 162155463 | |||||
chr5:162155487
|
CAT | C | 10 | a0001c0001t0002a0001c0001t0008a0001c0001t0009others(7): Show | 108 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(105): Show |
3_prime_UTR_variant | MODIFIER | c.*2120_*2121delAT | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 10/10 | 2120 | chr5 | 162155487 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:162068198
|
A | G | 1 | a0001c0001t0002g0312 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.107+92A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162068198 | ||||||
chr5:162068217
|
G | A | 1 | a0001c0002t0002g0016 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.107+111G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162068217 | ||||||
chr5:162068296
|
A | G | 3 | a0001c0001t0004g0309a0001c0001t0004g0310a0001c0001t0004g0311 | 3 | HG02258.hp2 HG02965.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.107+190A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162068296 | ||||||
chr5:162068329
|
T | G | 5 | a0001c0001t0004g0017a0001c0001t0004g0309a0001c0001t0004g0310others(2): Show | 5 | HG02258.hp2 HG02818.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.107+223T>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162068329 | ||||||
chr5:162068410
|
G | T | 1 | a0001c0002t0002g0016 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.107+304G>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162068410 | ||||||
chr5:162068665
|
T | G | 1 | a0001c0003t0001g0019 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.107+559T>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162068665 | ||||||
chr5:162068754
|
T | C | 1 | a0001c0002t0001g0020 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.107+648T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162068754 | ||||||
chr5:162068846
|
C | T | 50 | a0001c0003t0001g0012a0001c0003t0001g0013a0001c0003t0001g0014others(47): Show | 54 | HG00558.hp1 HG01074.hp1 HG01258.hp1 others(51): Show |
intron_variant | MODIFIER | c.107+740C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162068846 | ||||||
chr5:162068949
|
G | A | 7 | a0001c0001t0002g0021a0001c0001t0002g0022a0001c0001t0002g0023others(4): Show | 7 | HG00597.hp1 HG01261.hp2 NA18952.hp1 others(4): Show |
intron_variant | MODIFIER | c.107+843G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162068949 | ||||||
chr5:162069264
|
C | G | 1 | a0001c0001t0004g0263 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.107+1158C>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162069264 | ||||||
chr5:162069387
|
C | T | 1 | a0001c0002t0004g0262 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.107+1281C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162069387 | ||||||
chr5:162069663
|
T | G | 1 | a0001c0005t0003g0028 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.107+1557T>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162069663 | ||||||
chr5:162069665
|
T | C | 1 | a0001c0001t0002g0029 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.107+1559T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162069665 | ||||||
chr5:162069830
|
T | C | 2 | a0001c0003t0003g0264a0001c0003t0003g0265 | 2 | NA19011.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.107+1724T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162069830 | ||||||
chr5:162069840
|
C | T | 1 | a0001c0002t0002g0016 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.107+1734C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162069840 | ||||||
chr5:162069926
|
C | G | 6 | a0001c0001t0002g0260a0001c0001t0004g0256a0001c0001t0004g0257others(3): Show | 6 | HG01109.hp1 HG02622.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.107+1820C>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162069926 | ||||||
chr5:162070012
|
T | G | 1 | a0001c0001t0001g0030 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.107+1906T>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162070012 | ||||||
chr5:162070044
|
T | C | 49 | a0001c0001t0001g0030a0001c0001t0001g0034a0001c0001t0001g0036others(46): Show | 54 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(51): Show |
intron_variant | MODIFIER | c.107+1938T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162070044 | ||||||
chr5:162070289
|
A | G | 50 | a0001c0003t0001g0012a0001c0003t0001g0013a0001c0003t0001g0014others(47): Show | 54 | HG00558.hp1 HG01074.hp1 HG01258.hp1 others(51): Show |
intron_variant | MODIFIER | c.107+2183A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162070289 | ||||||
chr5:162070367
|
G | A | 1 | a0001c0002t0007g0074 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.107+2261G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162070367 | ||||||
chr5:162070538
|
TA | T | 11 | a0001c0001t0004g0250a0001c0001t0004g0251a0001c0001t0004g0252others(8): Show | 13 | HG01258.hp1 HG01516.hp1 HG01517.hp2 others(10): Show |
intron_variant | MODIFIER | c.107+2442delA | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 162070538 | |||||
chr5:162070744
|
G | C | 6 | a0001c0001t0002g0260a0001c0001t0004g0256a0001c0001t0004g0257others(3): Show | 6 | HG01109.hp1 HG02622.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.107+2638G>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162070744 | ||||||
chr5:162070828
|
T | A | 6 | a0001c0001t0002g0260a0001c0001t0004g0256a0001c0001t0004g0257others(3): Show | 6 | HG01109.hp1 HG02622.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.107+2722T>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162070828 | ||||||
chr5:162071011
|
C | CAAT | 195 | a0001c0001t0001g0030a0001c0001t0001g0034a0001c0001t0001g0036others(192): Show | 207 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.107+2906_107+2908d others(5): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 162071011 | |||||
chr5:162071075
|
A | G | 1 | a0001c0002t0001g0142 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.107+2969A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162071075 | ||||||
chr5:162071092
|
A | G | 2 | a0001c0004t0017g0246a0001c0008t0001g0247 | 2 | HG02647.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.107+2986A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162071092 | ||||||
chr5:162071291
|
A | G | 1 | a0001c0002t0001g0141 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.107+3185A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162071291 | ||||||
chr5:162071539
|
T | C | 52 | a0001c0003t0001g0012a0001c0003t0001g0013a0001c0003t0001g0014others(49): Show | 56 | HG00558.hp1 HG01074.hp1 HG01243.hp2 others(53): Show |
intron_variant | MODIFIER | c.107+3433T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162071539 | ||||||
chr5:162071682
|
A | G | 1 | a0001c0002t0003g0140 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.107+3576A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162071682 | ||||||
chr5:162071731
|
T | C | 195 | a0001c0001t0001g0030a0001c0001t0001g0034a0001c0001t0001g0036others(192): Show | 207 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.107+3625T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162071731 | ||||||
chr5:162071791
|
A | G | 50 | a0001c0003t0001g0012a0001c0003t0001g0013a0001c0003t0001g0014others(47): Show | 54 | HG00558.hp1 HG01074.hp1 HG01258.hp1 others(51): Show |
intron_variant | MODIFIER | c.107+3685A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162071791 | ||||||
chr5:162071847
|
T | A | 1 | a0001c0003t0003g0264 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.107+3741T>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162071847 | ||||||
chr5:162071942
|
A | G | 1 | a0001c0001t0002g0245 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.107+3836A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162071942 | ||||||
chr5:162072085
|
T | G | 1 | a0001c0006t0012g0005 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.107+3979T>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162072085 | ||||||
chr5:162072102
|
A | G | 2 | a0001c0001t0001g0244a0001c0005t0015g0243 | 2 | HG03225.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.107+3996A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162072102 | ||||||
chr5:162072303
|
T | C | 2 | a0001c0004t0017g0246a0001c0008t0001g0247 | 2 | HG02647.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.107+4197T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162072303 | ||||||
chr5:162072404
|
A | T | 4 | a0001c0003t0001g0013a0001c0003t0001g0306a0001c0003t0001g0307others(1): Show | 5 | NA18969.hp2 NA18999.hp2 NA19058.hp2 others(2): Show |
intron_variant | MODIFIER | c.107+4298A>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162072404 | ||||||
chr5:162072416
|
T | C | 2 | a0001c0004t0017g0246a0001c0008t0001g0247 | 2 | HG02647.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.107+4310T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162072416 | ||||||
chr5:162072449
|
T | C | 50 | a0001c0003t0001g0012a0001c0003t0001g0013a0001c0003t0001g0014others(47): Show | 54 | HG00558.hp1 HG01074.hp1 HG01258.hp1 others(51): Show |
intron_variant | MODIFIER | c.107+4343T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162072449 | ||||||
chr5:162072522
|
A | G | 4 | a0001c0001t0004g0252a0001c0001t0004g0253a0001c0001t0004g0254others(1): Show | 4 | HG02615.hp2 HG02717.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.107+4416A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162072522 | ||||||
chr5:162072562
|
G | A | 5 | a0001c0002t0006g0008a0001c0002t0006g0144a0001c0002t0006g0145others(2): Show | 6 | HG01884.hp2 HG02145.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.107+4456G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162072562 | ||||||
chr5:162072731
|
G | T | 2 | a0001c0001t0002g0011a0001c0001t0003g0242 | 3 | NA18968.hp1 NA19059.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.107+4625G>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162072731 | ||||||
chr5:162072736
|
C | T | 1 | a0001c0002t0004g0262 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.107+4630C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162072736 | ||||||
chr5:162072769
|
A | T | 1 | a0001c0001t0002g0027 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.107+4663A>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162072769 | ||||||
chr5:162072820
|
G | GATA | 64 | a0001c0001t0002g0260a0001c0001t0004g0017a0001c0001t0004g0256others(61): Show | 68 | HG00558.hp1 HG01074.hp1 HG01109.hp1 others(65): Show |
intron_variant | MODIFIER | c.107+4716_107+4717i others(5): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 162072820 | |||||
chr5:162072831
|
A | G | 1 | a0001c0002t0002g0016 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.107+4725A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162072831 | ||||||
chr5:162072868
|
C | T | 5 | a0001c0001t0004g0017a0001c0001t0004g0309a0001c0001t0004g0310others(2): Show | 5 | HG02258.hp2 HG02818.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.107+4762C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162072868 | ||||||
chr5:162072995
|
G | A | 2 | a0001c0004t0017g0246a0001c0008t0001g0247 | 2 | HG02647.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.107+4889G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162072995 | ||||||
chr5:162073024
|
G | A | 12 | a0001c0001t0018g0086a0001c0002t0007g0074a0001c0002t0007g0078others(9): Show | 12 | HG01433.hp1 HG01515.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.107+4918G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162073024 | ||||||
chr5:162073191
|
C | A | 1 | a0001c0012t0003g0266 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.107+5085C>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162073191 | ||||||
chr5:162073233
|
T | C | 27 | a0001c0001t0002g0090a0001c0001t0018g0086a0001c0002t0001g0087others(24): Show | 28 | HG00673.hp2 HG01069.hp1 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.107+5127T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162073233 | ||||||
chr5:162073249
|
G | A | 1 | a0001c0002t0003g0101 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.107+5143G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162073249 | ||||||
chr5:162073267
|
GT | G | 20 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0002g0031others(17): Show | 22 | HG00673.hp1 HG01069.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.107+5171delT | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 162073267 | |||||
chr5:162073268
|
T | G | 3 | a0001c0004t0002g0147a0001c0004t0002g0148a0001c0004t0002g0149 | 3 | HG01243.hp1 HG02258.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.107+5162T>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162073268 | ||||||
chr5:162073645
|
A | T | 10 | a0001c0004t0002g0147a0001c0004t0002g0148a0001c0004t0002g0149others(7): Show | 10 | HG00639.hp2 HG01243.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.107+5539A>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162073645 | ||||||
chr5:162073781
|
C | A | 1 | a0001c0002t0004g0262 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.107+5675C>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162073781 | ||||||
chr5:162073960
|
C | T | 1 | a0001c0001t0002g0073 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.107+5854C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162073960 | ||||||
chr5:162074001
|
T | A | 1 | a0001c0003t0003g0267 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.107+5895T>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162074001 | ||||||
chr5:162074131
|
T | C | 9 | a0001c0001t0004g0250a0001c0001t0004g0251a0001c0001t0004g0252others(6): Show | 9 | HG02572.hp1 HG02615.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.107+6025T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162074131 | ||||||
chr5:162074203
|
C | T | 1 | a0001c0001t0001g0244 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.107+6097C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162074203 | ||||||
chr5:162074255
|
T | C | 1 | a0001c0002t0001g0087 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.107+6149T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162074255 | ||||||
chr5:162074379
|
G | A | 6 | a0001c0001t0004g0017a0001c0001t0004g0309a0001c0001t0004g0310others(3): Show | 6 | HG02258.hp2 HG02818.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.107+6273G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162074379 | ||||||
chr5:162074562
|
A | G | 1 | a0001c0001t0004g0139 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.107+6456A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162074562 | ||||||
chr5:162074605
|
A | G | 1 | a0001c0003t0003g0305 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.107+6499A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162074605 | ||||||
chr5:162074641
|
G | A | 2 | a0001c0002t0001g0156a0001c0002t0001g0157 | 2 | HG01081.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.107+6535G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162074641 | ||||||
chr5:162074786
|
G | C | 3 | a0001c0001t0004g0309a0001c0001t0004g0310a0001c0001t0004g0311 | 3 | HG02258.hp2 HG02965.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.107+6680G>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162074786 | ||||||
chr5:162074914
|
C | CTT | 64 | a0001c0001t0002g0260a0001c0001t0004g0017a0001c0001t0004g0256others(61): Show | 68 | HG00558.hp1 HG01074.hp1 HG01109.hp1 others(65): Show |
intron_variant | MODIFIER | c.107+6812_107+6813d others(4): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 162074914 | |||||
chr5:162074917
|
T | C | 1 | a0001c0001t0001g0030 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.107+6811T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162074917 | ||||||
chr5:162075183
|
A | G | 1 | a0001c0002t0001g0236 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.107+7077A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162075183 | ||||||
chr5:162075213
|
C | A | 1 | a0001c0002t0001g0236 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.107+7107C>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162075213 | ||||||
chr5:162075306
|
A | C | 16 | a0001c0002t0001g0222a0001c0002t0001g0227a0001c0002t0001g0229others(13): Show | 16 | HG00735.hp1 HG01081.hp1 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.107+7200A>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162075306 | ||||||
chr5:162075344
|
C | G | 2 | a0001c0005t0003g0028a0001c0005t0003g0075 | 2 | HG01243.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.107+7238C>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162075344 | ||||||
chr5:162075372
|
C | G | 2 | a0001c0003t0003g0264a0001c0003t0003g0265 | 2 | NA19011.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.107+7266C>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162075372 | ||||||
chr5:162075498
|
G | C | 1 | a0001c0002t0002g0006 | 2 | HG02615.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.107+7392G>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162075498 | ||||||
chr5:162075519
|
G | T | 8 | a0001c0001t0004g0017a0001c0001t0004g0309a0001c0001t0004g0310others(5): Show | 8 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.107+7413G>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162075519 | ||||||
chr5:162075551
|
C | T | 1 | a0001c0003t0001g0304 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.107+7445C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162075551 | ||||||
chr5:162075557
|
A | G | 1 | a0001c0002t0002g0016 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.107+7451A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162075557 | ||||||
chr5:162075583
|
C | T | 1 | a0001c0002t0004g0262 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.107+7477C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162075583 | ||||||
chr5:162075612
|
G | T | 1 | a0001c0002t0001g0087 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.107+7506G>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162075612 | ||||||
chr5:162075730
|
AG | A | 5 | a0001c0001t0004g0017a0001c0001t0004g0309a0001c0001t0004g0310others(2): Show | 5 | HG02258.hp2 HG02818.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.107+7625delG | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162075730 | ||||||
chr5:162075752
|
G | A | 1 | a0001c0001t0002g0032 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.107+7646G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162075752 | ||||||
chr5:162075850
|
G | A | 2 | a0001c0001t0002g0158a0001c0001t0002g0159 | 2 | NA18971.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.107+7744G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162075850 | ||||||
chr5:162075881
|
C | G | 1 | a0001c0001t0001g0244 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.107+7775C>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162075881 | ||||||
chr5:162075933
|
G | A | 2 | a0001c0002t0001g0088a0001c0002t0001g0089 | 2 | NA18747.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.107+7827G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162075933 | ||||||
chr5:162075972
|
G | T | 1 | a0001c0002t0001g0235 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.107+7866G>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162075972 | ||||||
chr5:162075989
|
G | GA | 57 | a0001c0001t0004g0017a0001c0001t0004g0309a0001c0001t0004g0310others(54): Show | 61 | HG00558.hp1 HG01074.hp1 HG01243.hp2 others(58): Show |
intron_variant | MODIFIER | c.107+7896dupA | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 162075989 | |||||
chr5:162076008
|
T | C | 1 | a0001c0001t0002g0312 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.107+7902T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162076008 | ||||||
chr5:162076107
|
G | A | 1 | a0001c0001t0002g0160 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.107+8001G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162076107 | ||||||
chr5:162076179
|
T | C | 2 | a0001c0003t0002g0268a0001c0003t0002g0269 | 2 | NA19006.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.107+8073T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162076179 | ||||||
chr5:162076335
|
C | T | 12 | a0001c0001t0018g0086a0001c0002t0007g0074a0001c0002t0007g0078others(9): Show | 12 | HG01433.hp1 HG01515.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.107+8229C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162076335 | ||||||
chr5:162076392
|
C | T | 1 | a0001c0001t0002g0220 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.107+8286C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162076392 | ||||||
chr5:162076399
|
T | C | 1 | a0001c0002t0001g0156 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.107+8293T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162076399 | ||||||
chr5:162076504
|
C | T | 1 | a0001c0002t0001g0234 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.107+8398C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162076504 | ||||||
chr5:162076736
|
G | T | 12 | a0001c0001t0018g0086a0001c0002t0007g0074a0001c0002t0007g0078others(9): Show | 12 | HG01433.hp1 HG01515.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.107+8630G>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162076736 | ||||||
chr5:162076810
|
C | G | 2 | a0001c0005t0003g0028a0001c0005t0003g0075 | 2 | HG01243.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.107+8704C>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162076810 | ||||||
chr5:162076915
|
GT | G | 6 | a0001c0001t0002g0260a0001c0001t0004g0256a0001c0001t0004g0257others(3): Show | 6 | HG01109.hp1 HG02622.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.107+8814delT | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 162076915 | |||||
chr5:162076989
|
T | A | 1 | a0001c0001t0002g0161 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.107+8883T>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162076989 | ||||||
chr5:162077073
|
C | CTG | 102 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0001g0244others(99): Show | 108 | HG00423.hp2 HG00558.hp1 HG00597.hp1 others(105): Show |
intron_variant | MODIFIER | c.107+9004_107+9005d others(4): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 162077073 | |||||
chr5:162077073
|
C | CTGTG | 26 | a0001c0001t0002g0159a0001c0001t0002g0160a0001c0001t0002g0217others(23): Show | 28 | HG01258.hp1 HG01516.hp1 HG01517.hp2 others(25): Show |
intron_variant | MODIFIER | c.107+9002_107+9005d others(6): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 162077073 | |||||
chr5:162077073
|
C | CTGTGTG | 8 | a0001c0001t0001g0219a0001c0003t0001g0300a0001c0003t0001g0303others(5): Show | 8 | HG00639.hp2 HG01074.hp1 HG02027.hp1 others(5): Show |
intron_variant | MODIFIER | c.107+9000_107+9005d others(8): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 162077073 | |||||
chr5:162077073
|
C | CTGTGTGT others(3): Show |
1 | a0001c0004t0002g0147 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.107+8996_107+9005d others(12): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 162077073 | |||||
chr5:162077073
|
C | CTGTGTGT others(5): Show |
2 | a0001c0004t0002g0148a0001c0004t0002g0149 | 2 | HG02258.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.107+8994_107+9005d others(14): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 162077073 | |||||
chr5:162077073
|
C | CTGTGTGT others(7): Show |
2 | a0001c0004t0017g0246a0001c0008t0001g0247 | 2 | HG02647.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.107+8992_107+9005d others(16): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 162077073 | |||||
chr5:162077073
|
CTG | C | 12 | a0001c0001t0003g0167a0001c0001t0003g0169a0001c0001t0003g0170others(9): Show | 12 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.107+9004_107+9005d others(4): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 162077073 | |||||
chr5:162077073
|
CTGTG | C | 13 | a0001c0001t0002g0072a0001c0001t0004g0250a0001c0001t0004g0251others(10): Show | 13 | HG00099.hp2 HG01952.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.107+9002_107+9005d others(6): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 162077073 | |||||
chr5:162077073
|
CTGTGTG | C | 100 | a0001c0001t0001g0030a0001c0001t0001g0045a0001c0001t0001g0113others(97): Show | 105 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.107+9000_107+9005d others(8): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 162077073 | |||||
chr5:162077073
|
CTGTGTGT others(1): Show |
C | 6 | a0001c0001t0001g0104a0001c0001t0002g0037a0001c0001t0003g0105others(3): Show | 6 | HG01169.hp1 HG01192.hp1 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.107+8998_107+9005d others(10): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 162077073 | |||||
chr5:162077073
|
CTGTGTGT others(3): Show |
C | 5 | a0001c0001t0001g0034a0001c0001t0001g0036a0001c0002t0001g0001others(2): Show | 7 | HG00140.hp2 HG00735.hp2 HG01109.hp2 others(4): Show |
intron_variant | MODIFIER | c.107+8996_107+9005d others(12): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 162077073 | |||||
chr5:162077103
|
GTGTGTGT others(2): Show |
G | 5 | a0001c0001t0004g0017a0001c0001t0004g0309a0001c0001t0004g0310others(2): Show | 5 | HG02258.hp2 HG02818.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.107+9001_107+9009d others(11): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 162077103 | |||||
chr5:162077109
|
GTGA | G | 3 | a0001c0001t0002g0260a0001c0001t0010g0259a0001c0001t0010g0261 | 3 | HG01109.hp1 HG03471.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.107+9006_107+9008d others(5): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 162077109 | |||||
chr5:162077159
|
T | G | 5 | a0001c0001t0004g0017a0001c0001t0004g0309a0001c0001t0004g0310others(2): Show | 5 | HG02258.hp2 HG02818.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.107+9053T>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162077159 | ||||||
chr5:162077161
|
ATTC | A | 10 | a0001c0004t0002g0147a0001c0004t0002g0148a0001c0004t0002g0149others(7): Show | 10 | HG00639.hp2 HG01243.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.107+9063_107+9065d others(5): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 162077161 | |||||
chr5:162077345
|
T | A | 1 | a0001c0002t0004g0262 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.107+9239T>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162077345 | ||||||
chr5:162077751
|
T | C | 1 | a0001c0001t0004g0139 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.107+9645T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162077751 | ||||||
chr5:162077955
|
G | A | 1 | a0001c0002t0003g0140 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.107+9849G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162077955 | ||||||
chr5:162077959
|
G | C | 5 | a0001c0001t0004g0017a0001c0001t0004g0309a0001c0001t0004g0310others(2): Show | 5 | HG02258.hp2 HG02818.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.107+9853G>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162077959 | ||||||
chr5:162078219
|
G | A | 14 | a0001c0001t0002g0260a0001c0001t0004g0017a0001c0001t0004g0256others(11): Show | 14 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.107+10113G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162078219 | ||||||
chr5:162078266
|
T | C | 1 | a0001c0004t0002g0241 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.107+10160T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162078266 | ||||||
chr5:162078369
|
C | CTA | 4 | a0001c0002t0007g0074a0001c0002t0011g0079a0001c0002t0014g0080others(1): Show | 4 | HG01433.hp1 NA19056.hp1 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.107+10291_107+1029 others(6): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 162078369 | |||||
chr5:162078369
|
C | CTATA | 7 | a0001c0002t0001g0097a0001c0002t0007g0078a0001c0002t0007g0082others(4): Show | 7 | HG02572.hp2 NA18994.hp1 NA18994.hp2 others(4): Show |
intron_variant | MODIFIER | c.107+10289_107+1029 others(8): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 162078369 | |||||
chr5:162078369
|
CTA | C | 39 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0002g0010others(36): Show | 41 | HG00099.hp1 HG00621.hp1 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.107+10291_107+1029 others(6): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 162078369 | |||||
chr5:162078369
|
CTATA | C | 28 | a0001c0001t0001g0030a0001c0001t0001g0133a0001c0001t0002g0004others(25): Show | 29 | HG00597.hp2 HG00621.hp2 HG01169.hp1 others(26): Show |
intron_variant | MODIFIER | c.107+10289_107+1029 others(8): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 162078369 | |||||
chr5:162078369
|
CTATATA | C | 16 | a0001c0001t0001g0045a0001c0001t0002g0003a0001c0001t0002g0046others(13): Show | 17 | HG00099.hp2 HG00423.hp1 HG02165.hp2 others(14): Show |
intron_variant | MODIFIER | c.107+10287_107+1029 others(10): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 162078369 | |||||
chr5:162078388
|
TATA | T | 5 | a0001c0001t0004g0253a0001c0001t0004g0254a0001c0001t0004g0255others(2): Show | 5 | HG02615.hp2 HG02717.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.107+10283_107+1028 others(7): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162078388 | ||||||
chr5:162078388
|
TATATA | T | 43 | a0001c0001t0001g0034a0001c0001t0001g0036a0001c0001t0001g0104others(40): Show | 46 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(43): Show |
intron_variant | MODIFIER | c.107+10283_107+1028 others(9): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162078388 | ||||||
chr5:162078388
|
TATATATA | T | 4 | a0001c0001t0002g0002a0001c0001t0002g0031a0001c0001t0002g0032others(1): Show | 5 | NA18979.hp2 NA18993.hp2 NA19003.hp2 others(2): Show |
intron_variant | MODIFIER | c.107+10283_107+1028 others(11): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162078388 | ||||||
chr5:162078390
|
TATA | T | 3 | a0001c0001t0002g0214a0001c0001t0003g0109a0001c0001t0003g0110 | 3 | HG00438.hp1 HG03041.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.107+10285_107+1028 others(7): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162078390 | ||||||
chr5:162078390
|
TATATA | T | 3 | a0001c0001t0003g0106a0001c0002t0001g0107a0001c0002t0003g0101 | 3 | HG02055.hp2 HG02083.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.107+10285_107+1028 others(9): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162078390 | ||||||
chr5:162078391
|
A | T | 3 | a0001c0001t0002g0042a0001c0001t0003g0071a0001c0001t0004g0263 | 3 | HG02080.hp2 HG02132.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.107+10285A>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162078391 | ||||||
chr5:162078392
|
TA | T | 5 | a0001c0001t0002g0026a0001c0001t0002g0029a0001c0002t0001g0233others(2): Show | 5 | HG02258.hp1 HG03516.hp2 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.107+10287delA | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162078392 | ||||||
chr5:162078392
|
TATA | T | 7 | a0001c0001t0002g0041a0001c0001t0002g0166a0001c0002t0001g0229others(4): Show | 7 | HG00639.hp2 HG02109.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.107+10287_107+1028 others(7): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162078392 | ||||||
chr5:162078393
|
A | AT | 3 | a0001c0001t0003g0172a0001c0002t0001g0211a0001c0002t0005g0228 | 3 | HG01981.hp2 HG03225.hp1 NA19075.hp2 |
intron_variant | MODIFIER | c.107+10288dupT | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 162078393 | |||||
chr5:162078393
|
A | T | 30 | a0001c0001t0001g0030a0001c0001t0001g0133a0001c0001t0001g0244others(27): Show | 32 | HG00597.hp2 HG00621.hp2 HG01175.hp1 others(29): Show |
intron_variant | MODIFIER | c.107+10287A>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162078393 | ||||||
chr5:162078394
|
TA | T | 16 | a0001c0001t0001g0219a0001c0001t0002g0011a0001c0001t0002g0023others(13): Show | 17 | HG00558.hp2 HG00597.hp1 HG01261.hp2 others(14): Show |
intron_variant | MODIFIER | c.107+10289delA | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162078394 | ||||||
chr5:162078394
|
TATA | T | 7 | a0001c0001t0001g0162a0001c0001t0002g0027a0001c0001t0002g0038others(4): Show | 7 | HG00639.hp1 HG01517.hp1 HG02155.hp1 others(4): Show |
intron_variant | MODIFIER | c.107+10289_107+1029 others(7): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162078394 | ||||||
chr5:162078395
|
A | AT | 4 | a0001c0001t0002g0021a0001c0001t0002g0200a0001c0001t0002g0201others(1): Show | 4 | HG00423.hp2 HG02040.hp2 NA18941.hp2 others(1): Show |
intron_variant | MODIFIER | c.107+10290dupT | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 162078395 | |||||
chr5:162078395
|
A | T | 136 | a0001c0001t0001g0030a0001c0001t0001g0034a0001c0001t0001g0036others(133): Show | 143 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.107+10289A>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162078395 | ||||||
chr5:162078397
|
A | ATATATAT others(6): Show |
1 | a0001c0001t0004g0256 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.107+10292_107+1029 others(17): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 162078397 | |||||
chr5:162078397
|
A | ATATATAT others(3): Show |
1 | a0001c0001t0004g0257 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.107+10292_107+1029 others(14): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 162078397 | |||||
chr5:162078397
|
A | ATATTTTT others(3): Show |
2 | a0001c0001t0010g0258a0001c0001t0010g0259 | 2 | HG03471.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.107+10292_107+1029 others(14): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 162078397 | |||||
chr5:162078397
|
A | T | 193 | a0001c0001t0001g0030a0001c0001t0001g0034a0001c0001t0001g0036others(190): Show | 203 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.107+10291A>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162078397 | ||||||
chr5:162078397
|
AT | A | 25 | a0001c0002t0001g0174a0001c0003t0001g0012a0001c0003t0001g0013others(22): Show | 27 | HG01074.hp1 HG01074.hp2 HG01952.hp1 others(24): Show |
intron_variant | MODIFIER | c.107+10318delT | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 162078397 | |||||
chr5:162078397
|
ATT | A | 6 | a0001c0002t0001g0173a0001c0002t0001g0236a0001c0003t0001g0271others(3): Show | 6 | HG00558.hp1 HG01169.hp2 HG02698.hp2 others(3): Show |
intron_variant | MODIFIER | c.107+10317_107+1031 others(6): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 162078397 | |||||
chr5:162078398
|
T | TA | 4 | a0001c0003t0001g0298a0001c0003t0002g0281a0001c0003t0003g0264others(1): Show | 4 | HG02071.hp1 HG02074.hp2 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.107+10292_107+1029 others(5): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162078398 | ||||||
chr5:162078398
|
T | TATA | 3 | a0001c0002t0007g0081a0001c0003t0001g0019a0001c0006t0012g0005 | 4 | HG01069.hp1 HG01071.hp1 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.107+10292_107+1029 others(7): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162078398 | ||||||
chr5:162078398
|
T | TATATATA others(12): Show |
1 | a0001c0001t0004g0017 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.107+10292_107+1029 others(23): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162078398 | ||||||
chr5:162078399
|
T | A | 24 | a0001c0002t0002g0016a0001c0002t0007g0078a0001c0002t0007g0083others(21): Show | 26 | HG01258.hp1 HG01496.hp1 HG01516.hp1 others(23): Show |
intron_variant | MODIFIER | c.107+10293T>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162078399 | ||||||
chr5:162078400
|
T | A | 32 | a0001c0001t0004g0017a0001c0002t0007g0084a0001c0003t0001g0012others(29): Show | 35 | HG01069.hp1 HG01071.hp1 HG01074.hp1 others(32): Show |
intron_variant | MODIFIER | c.107+10294T>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162078400 | ||||||
chr5:162078401
|
T | A | 24 | a0001c0002t0001g0173a0001c0002t0002g0016a0001c0002t0014g0076others(21): Show | 26 | HG00558.hp1 HG01258.hp1 HG01496.hp1 others(23): Show |
intron_variant | MODIFIER | c.107+10295T>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162078401 | ||||||
chr5:162078402
|
T | A | 29 | a0001c0001t0004g0017a0001c0003t0001g0012a0001c0003t0001g0013others(26): Show | 32 | HG01069.hp1 HG01071.hp1 HG01074.hp1 others(29): Show |
intron_variant | MODIFIER | c.107+10296T>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162078402 | ||||||
chr5:162078403
|
T | A | 20 | a0001c0002t0002g0016a0001c0003t0001g0014a0001c0003t0001g0015others(17): Show | 22 | HG00558.hp1 HG01258.hp1 HG01496.hp1 others(19): Show |
intron_variant | MODIFIER | c.107+10297T>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162078403 | ||||||
chr5:162078404
|
T | A | 16 | a0001c0003t0001g0013a0001c0003t0001g0019a0001c0003t0001g0275others(13): Show | 18 | HG01069.hp1 HG01071.hp1 HG01952.hp1 others(15): Show |
intron_variant | MODIFIER | c.107+10298T>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162078404 | ||||||
chr5:162078405
|
T | A | 5 | a0001c0002t0002g0016a0001c0003t0001g0271a0001c0003t0001g0303others(2): Show | 5 | HG01891.hp1 HG02698.hp2 HG04115.hp2 others(2): Show |
intron_variant | MODIFIER | c.107+10299T>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162078405 | ||||||
chr5:162078406
|
T | A | 5 | a0001c0003t0001g0013a0001c0003t0001g0306a0001c0003t0001g0307others(2): Show | 7 | HG01069.hp1 HG01071.hp1 NA18969.hp2 others(4): Show |
intron_variant | MODIFIER | c.107+10300T>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162078406 | ||||||
chr5:162078407
|
T | A | 1 | a0001c0003t0003g0302 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.107+10301T>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162078407 | ||||||
chr5:162078437
|
T | C | 234 | a0001c0001t0001g0030a0001c0001t0001g0034a0001c0001t0001g0036others(231): Show | 247 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.107+10331T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162078437 | ||||||
chr5:162078450
|
G | A | 7 | a0001c0001t0004g0017a0001c0001t0004g0309a0001c0001t0004g0310others(4): Show | 7 | HG01243.hp2 HG01884.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.107+10344G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162078450 | ||||||
chr5:162078480
|
C | A | 51 | a0001c0002t0002g0016a0001c0003t0001g0012a0001c0003t0001g0013others(48): Show | 55 | HG00558.hp1 HG01074.hp1 HG01258.hp1 others(52): Show |
intron_variant | MODIFIER | c.107+10374C>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162078480 | ||||||
chr5:162078492
|
C | T | 1 | a0001c0003t0001g0308 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.107+10386C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162078492 | ||||||
chr5:162078493
|
G | A | 1 | a0001c0002t0002g0016 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.107+10387G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162078493 | ||||||
chr5:162078518
|
A | T | 1 | a0001c0003t0001g0283 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.107+10412A>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162078518 | ||||||
chr5:162078576
|
T | C | 1 | a0001c0001t0002g0260 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.107+10470T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162078576 | ||||||
chr5:162078637
|
C | A | 2 | a0001c0001t0002g0187a0001c0001t0002g0193 | 2 | HG03927.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.107+10531C>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162078637 | ||||||
chr5:162078652
|
G | A | 1 | a0001c0001t0002g0026 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.107+10546G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162078652 | ||||||
chr5:162078754
|
A | G | 7 | a0001c0001t0004g0017a0001c0001t0004g0309a0001c0001t0004g0310others(4): Show | 7 | HG01243.hp2 HG01884.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.107+10648A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162078754 | ||||||
chr5:162078840
|
C | T | 1 | a0001c0002t0002g0006 | 2 | HG02615.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.107+10734C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162078840 | ||||||
chr5:162078935
|
T | A | 1 | a0001c0001t0002g0220 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.107+10829T>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162078935 | ||||||
chr5:162078952
|
A | C | 1 | a0001c0001t0002g0090 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.107+10846A>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162078952 | ||||||
chr5:162079015
|
T | A | 12 | a0001c0001t0018g0086a0001c0002t0007g0074a0001c0002t0007g0078others(9): Show | 12 | HG01433.hp1 HG01515.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.107+10909T>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162079015 | ||||||
chr5:162079016
|
T | C | 12 | a0001c0001t0018g0086a0001c0002t0007g0074a0001c0002t0007g0078others(9): Show | 12 | HG01433.hp1 HG01515.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.107+10910T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162079016 | ||||||
chr5:162079143
|
G | A | 1 | a0001c0002t0001g0215 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.107+11037G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162079143 | ||||||
chr5:162079177
|
A | G | 6 | a0001c0001t0002g0260a0001c0001t0004g0256a0001c0001t0004g0257others(3): Show | 6 | HG01109.hp1 HG02622.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.107+11071A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162079177 | ||||||
chr5:162079216
|
G | C | 1 | a0001c0001t0004g0017 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.107+11110G>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162079216 | ||||||
chr5:162079228
|
C | A | 1 | a0001c0002t0002g0006 | 2 | HG02615.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.107+11122C>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162079228 | ||||||
chr5:162079397
|
G | A | 1 | a0001c0001t0008g0044 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.107+11291G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162079397 | ||||||
chr5:162079492
|
C | T | 1 | a0001c0004t0005g0240 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.107+11386C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162079492 | ||||||
chr5:162079617
|
A | T | 1 | a0001c0002t0001g0129 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.107+11511A>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162079617 | ||||||
chr5:162079822
|
G | A | 2 | a0001c0001t0001g0113a0001c0002t0001g0103 | 2 | HG02451.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.107+11716G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162079822 | ||||||
chr5:162079889
|
C | T | 1 | a0001c0001t0002g0213 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.107+11783C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162079889 | ||||||
chr5:162079917
|
T | C | 51 | a0001c0002t0002g0016a0001c0003t0001g0012a0001c0003t0001g0013others(48): Show | 55 | HG00558.hp1 HG01074.hp1 HG01258.hp1 others(52): Show |
intron_variant | MODIFIER | c.107+11811T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162079917 | ||||||
chr5:162079971
|
C | T | 1 | a0001c0001t0003g0181 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.107+11865C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162079971 | ||||||
chr5:162079972
|
G | A | 1 | a0001c0001t0004g0309 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.107+11866G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162079972 | ||||||
chr5:162080177
|
G | T | 51 | a0001c0002t0002g0016a0001c0003t0001g0012a0001c0003t0001g0013others(48): Show | 55 | HG00558.hp1 HG01074.hp1 HG01258.hp1 others(52): Show |
intron_variant | MODIFIER | c.107+12071G>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162080177 | ||||||
chr5:162080355
|
A | G | 1 | a0001c0003t0002g0281 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.107+12249A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162080355 | ||||||
chr5:162080502
|
T | C | 1 | a0001c0002t0001g0094 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.107+12396T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162080502 | ||||||
chr5:162080672
|
A | G | 1 | a0001c0012t0003g0266 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.107+12566A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162080672 | ||||||
chr5:162080769
|
G | T | 6 | a0001c0001t0002g0260a0001c0001t0004g0256a0001c0001t0004g0257others(3): Show | 6 | HG01109.hp1 HG02622.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.107+12663G>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162080769 | ||||||
chr5:162081093
|
T | G | 1 | a0001c0002t0001g0094 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.108-12735T>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162081093 | ||||||
chr5:162081119
|
C | T | 1 | a0001c0002t0003g0140 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.108-12709C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162081119 | ||||||
chr5:162081315
|
G | T | 1 | a0001c0006t0012g0005 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.108-12513G>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162081315 | ||||||
chr5:162081403
|
T | A | 1 | a0001c0002t0002g0016 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.108-12425T>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162081403 | ||||||
chr5:162081497
|
A | T | 64 | a0001c0001t0002g0260a0001c0001t0002g0312a0001c0001t0004g0017others(61): Show | 68 | HG00558.hp1 HG01074.hp1 HG01109.hp1 others(65): Show |
intron_variant | MODIFIER | c.108-12331A>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162081497 | ||||||
chr5:162081610
|
T | C | 13 | a0001c0001t0018g0086a0001c0002t0007g0074a0001c0002t0007g0078others(10): Show | 14 | HG01069.hp1 HG01071.hp1 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.108-12218T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162081610 | ||||||
chr5:162081722
|
C | T | 130 | a0001c0001t0001g0030a0001c0001t0001g0034a0001c0001t0001g0036others(127): Show | 138 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.108-12106C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162081722 | ||||||
chr5:162081727
|
A | G | 6 | a0001c0001t0002g0260a0001c0001t0004g0256a0001c0001t0004g0257others(3): Show | 6 | HG01109.hp1 HG02622.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.108-12101A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162081727 | ||||||
chr5:162082310
|
G | A | 3 | a0001c0004t0002g0147a0001c0004t0002g0148a0001c0004t0002g0149 | 3 | HG01243.hp1 HG02258.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.108-11518G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162082310 | ||||||
chr5:162082462
|
G | A | 1 | a0001c0002t0005g0223 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.108-11366G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162082462 | ||||||
chr5:162082559
|
T | C | 2 | a0001c0005t0003g0028a0001c0005t0003g0075 | 2 | HG01243.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.108-11269T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162082559 | ||||||
chr5:162082679
|
A | T | 1 | a0001c0001t0018g0086 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.108-11149A>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162082679 | ||||||
chr5:162082692
|
A | G | 2 | a0001c0002t0007g0083a0001c0002t0007g0084 | 2 | NA18959.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.108-11136A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162082692 | ||||||
chr5:162082756
|
T | C | 1 | a0001c0001t0002g0039 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.108-11072T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162082756 | ||||||
chr5:162082767
|
C | T | 1 | a0001c0003t0001g0287 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.108-11061C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162082767 | ||||||
chr5:162082801
|
TAAC | T | 15 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0002g0214others(12): Show | 16 | HG00673.hp1 HG01081.hp2 HG01258.hp2 others(13): Show |
intron_variant | MODIFIER | c.108-11021_108-1101 others(7): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 162082801 | |||||
chr5:162082896
|
C | T | 1 | a0001c0002t0004g0262 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.108-10932C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162082896 | ||||||
chr5:162082912
|
G | A | 1 | a0001c0001t0003g0203 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.108-10916G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162082912 | ||||||
chr5:162082969
|
A | G | 6 | a0001c0001t0002g0260a0001c0001t0004g0256a0001c0001t0004g0257others(3): Show | 6 | HG01109.hp1 HG02622.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.108-10859A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162082969 | ||||||
chr5:162083013
|
C | G | 1 | a0001c0001t0004g0139 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.108-10815C>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162083013 | ||||||
chr5:162083351
|
G | T | 1 | a0001c0002t0002g0016 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.108-10477G>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162083351 | ||||||
chr5:162083449
|
T | G | 25 | a0001c0002t0001g0222a0001c0002t0001g0227a0001c0002t0001g0229others(22): Show | 25 | HG00639.hp2 HG00735.hp1 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.108-10379T>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162083449 | ||||||
chr5:162083458
|
A | G | 1 | a0001c0003t0001g0287 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.108-10370A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162083458 | ||||||
chr5:162083601
|
A | C | 12 | a0001c0001t0018g0086a0001c0002t0007g0074a0001c0002t0007g0078others(9): Show | 12 | HG01433.hp1 HG01515.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.108-10227A>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162083601 | ||||||
chr5:162083685
|
A | T | 1 | a0001c0002t0001g0136 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.108-10143A>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162083685 | ||||||
chr5:162083693
|
G | T | 1 | a0001c0001t0008g0053 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.108-10135G>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162083693 | ||||||
chr5:162083790
|
T | C | 223 | a0001c0001t0001g0030a0001c0001t0001g0034a0001c0001t0001g0036others(220): Show | 236 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.108-10038T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162083790 | ||||||
chr5:162083899
|
A | G | 2 | a0001c0002t0014g0076a0001c0002t0014g0080 | 2 | HG02572.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.108-9929A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162083899 | ||||||
chr5:162083933
|
A | T | 1 | a0001c0006t0012g0005 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.108-9895A>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162083933 | ||||||
chr5:162084151
|
A | C | 1 | a0001c0002t0003g0128 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.108-9677A>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162084151 | ||||||
chr5:162084273
|
T | TA | 67 | a0001c0001t0001g0045a0001c0001t0002g0043a0001c0001t0002g0046others(64): Show | 71 | HG00423.hp1 HG00558.hp1 HG01074.hp1 others(68): Show |
intron_variant | MODIFIER | c.108-9554dupA | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 162084273 | |||||
chr5:162084274
|
A | G | 4 | a0001c0004t0005g0237a0001c0004t0005g0238a0001c0004t0005g0239others(1): Show | 4 | HG00639.hp2 HG02897.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.108-9554A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162084274 | ||||||
chr5:162084438
|
C | T | 1 | a0001c0002t0002g0016 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.108-9390C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162084438 | ||||||
chr5:162084560
|
T | C | 6 | a0001c0001t0002g0260a0001c0001t0004g0256a0001c0001t0004g0257others(3): Show | 6 | HG01109.hp1 HG02622.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.108-9268T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162084560 | ||||||
chr5:162084575
|
G | C | 5 | a0001c0001t0004g0017a0001c0001t0004g0309a0001c0001t0004g0310others(2): Show | 5 | HG02258.hp2 HG02818.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.108-9253G>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162084575 | ||||||
chr5:162084644
|
G | A | 5 | a0001c0001t0004g0017a0001c0001t0004g0309a0001c0001t0004g0310others(2): Show | 5 | HG02258.hp2 HG02818.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.108-9184G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162084644 | ||||||
chr5:162084848
|
A | C | 280 | a0001c0001t0001g0030a0001c0001t0001g0034a0001c0001t0001g0036others(277): Show | 295 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(292): Show |
intron_variant | MODIFIER | c.108-8980A>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162084848 | ||||||
chr5:162085015
|
G | A | 1 | a0001c0002t0007g0074 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.108-8813G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162085015 | ||||||
chr5:162085095
|
C | A | 2 | a0001c0001t0001g0244a0001c0005t0015g0243 | 2 | HG03225.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.108-8733C>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162085095 | ||||||
chr5:162085379
|
A | G | 4 | a0001c0001t0008g0044a0001c0001t0008g0050a0001c0001t0008g0053others(1): Show | 4 | HG00423.hp1 NA18954.hp2 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.108-8449A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162085379 | ||||||
chr5:162085558
|
C | CA | 7 | a0001c0002t0001g0156a0001c0002t0001g0157a0001c0002t0001g0192others(4): Show | 7 | HG01081.hp2 HG01258.hp2 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.108-8270_108-8269i others(3): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162085558 | ||||||
chr5:162085558
|
CT | C | 9 | a0001c0001t0001g0244a0001c0001t0004g0309a0001c0001t0004g0310others(6): Show | 9 | HG01243.hp2 HG01884.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.108-8259delT | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 162085558 | |||||
chr5:162085624
|
T | C | 2 | a0001c0005t0003g0028a0001c0005t0003g0075 | 2 | HG01243.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.108-8204T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162085624 | ||||||
chr5:162085655
|
G | C | 1 | a0001c0001t0003g0130 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.108-8173G>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162085655 | ||||||
chr5:162085712
|
G | C | 2 | a0001c0005t0003g0028a0001c0005t0003g0075 | 2 | HG01243.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.108-8116G>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162085712 | ||||||
chr5:162085714
|
TC | T | 2 | a0001c0006t0012g0005a0001c0008t0001g0247 | 3 | HG01069.hp1 HG01071.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.108-8112delC | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 162085714 | |||||
chr5:162085914
|
G | GT | 6 | a0001c0001t0002g0260a0001c0001t0004g0256a0001c0001t0004g0257others(3): Show | 6 | HG01109.hp1 HG02622.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.108-7907dupT | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 162085914 | |||||
chr5:162085951
|
G | A | 1 | a0001c0001t0002g0209 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.108-7877G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162085951 | ||||||
chr5:162085954
|
C | G | 109 | a0001c0001t0001g0030a0001c0001t0001g0034a0001c0001t0001g0036others(106): Show | 116 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(113): Show |
intron_variant | MODIFIER | c.108-7874C>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162085954 | ||||||
chr5:162085958
|
A | AT | 16 | a0001c0001t0001g0162a0001c0001t0002g0161a0001c0001t0002g0163others(13): Show | 17 | HG00639.hp1 HG01069.hp1 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.108-7859dupT | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 162085958 | |||||
chr5:162086045
|
C | A | 2 | a0001c0002t0001g0229a0001c0002t0001g0230 | 2 | HG02451.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.108-7783C>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162086045 | ||||||
chr5:162086339
|
A | G | 2 | a0001c0006t0012g0005a0001c0008t0001g0247 | 3 | HG01069.hp1 HG01071.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.108-7489A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162086339 | ||||||
chr5:162086514
|
A | G | 43 | a0001c0001t0001g0244a0001c0001t0002g0090a0001c0001t0002g0260others(40): Show | 44 | HG00099.hp1 HG00673.hp2 HG01069.hp2 others(41): Show |
intron_variant | MODIFIER | c.108-7314A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162086514 | ||||||
chr5:162086701
|
G | A | 43 | a0001c0001t0001g0244a0001c0001t0002g0090a0001c0001t0002g0260others(40): Show | 44 | HG00099.hp1 HG00673.hp2 HG01069.hp2 others(41): Show |
intron_variant | MODIFIER | c.108-7127G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162086701 | ||||||
chr5:162086725
|
T | C | 1 | a0001c0002t0013g0131 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.108-7103T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162086725 | ||||||
chr5:162086769
|
T | A | 1 | a0001c0009t0004g0143 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.108-7059T>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162086769 | ||||||
chr5:162086809
|
A | G | 1 | a0001c0002t0002g0016 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.108-7019A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162086809 | ||||||
chr5:162087273
|
T | G | 1 | a0001c0003t0001g0271 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.108-6555T>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162087273 | ||||||
chr5:162087298
|
T | C | 5 | a0001c0001t0002g0029a0001c0001t0002g0160a0001c0001t0002g0185others(2): Show | 5 | HG02145.hp2 HG02717.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.108-6530T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162087298 | ||||||
chr5:162087367
|
T | C | 2 | a0001c0003t0003g0273a0001c0013t0002g0274 | 2 | HG01952.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.108-6461T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162087367 | ||||||
chr5:162087508
|
A | G | 1 | a0001c0002t0002g0186 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.108-6320A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162087508 | ||||||
chr5:162087508
|
A | T | 1 | a0001c0002t0001g0107 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.108-6320A>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162087508 | ||||||
chr5:162087509
|
TC | T | 3 | a0001c0001t0004g0309a0001c0001t0004g0310a0001c0001t0004g0311 | 3 | HG02258.hp2 HG02965.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.108-6318delC | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162087509 | ||||||
chr5:162087605
|
A | G | 1 | a0001c0001t0004g0255 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.108-6223A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162087605 | ||||||
chr5:162087648
|
A | G | 1 | a0001c0002t0002g0016 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.108-6180A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162087648 | ||||||
chr5:162087685
|
C | T | 1 | a0001c0002t0002g0218 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.108-6143C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162087685 | ||||||
chr5:162087705
|
A | G | 1 | a0001c0002t0001g0087 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.108-6123A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162087705 | ||||||
chr5:162087757
|
A | G | 1 | a0001c0001t0002g0065 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.108-6071A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162087757 | ||||||
chr5:162087939
|
G | A | 5 | a0001c0004t0002g0018a0001c0004t0002g0147a0001c0004t0002g0148others(2): Show | 5 | HG01243.hp1 HG02258.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.108-5889G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162087939 | ||||||
chr5:162088014
|
C | T | 40 | a0001c0001t0001g0219a0001c0001t0002g0010a0001c0001t0002g0011others(37): Show | 42 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.108-5814C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162088014 | ||||||
chr5:162088043
|
C | T | 6 | a0001c0001t0002g0260a0001c0001t0004g0256a0001c0001t0004g0257others(3): Show | 6 | HG01109.hp1 HG02622.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.108-5785C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162088043 | ||||||
chr5:162088114
|
A | T | 35 | a0001c0001t0001g0219a0001c0001t0002g0010a0001c0001t0002g0011others(32): Show | 37 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(34): Show |
intron_variant | MODIFIER | c.108-5714A>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162088114 | ||||||
chr5:162088159
|
C | T | 1 | a0001c0002t0006g0249 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.108-5669C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162088159 | ||||||
chr5:162088209
|
C | T | 32 | a0001c0001t0001g0244a0001c0001t0002g0090a0001c0001t0003g0181others(29): Show | 33 | HG00099.hp1 HG00673.hp2 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.108-5619C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162088209 | ||||||
chr5:162088219
|
G | A | 1 | a0001c0001t0002g0023 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.108-5609G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162088219 | ||||||
chr5:162088225
|
T | C | 8 | a0001c0001t0001g0115a0001c0002t0001g0020a0001c0002t0001g0107others(5): Show | 8 | HG02055.hp2 HG02622.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.108-5603T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162088225 | ||||||
chr5:162088273
|
C | T | 4 | a0001c0003t0003g0276a0001c0003t0003g0277a0001c0003t0003g0278others(1): Show | 4 | NA18963.hp2 NA18968.hp2 NA18987.hp2 others(1): Show |
intron_variant | MODIFIER | c.108-5555C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162088273 | ||||||
chr5:162088362
|
A | G | 5 | a0001c0001t0004g0309a0001c0001t0004g0310a0001c0001t0004g0311others(2): Show | 5 | HG01243.hp2 HG01884.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.108-5466A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162088362 | ||||||
chr5:162088382
|
G | T | 4 | a0001c0001t0002g0043a0001c0001t0002g0047a0001c0001t0002g0048others(1): Show | 4 | NA18964.hp1 NA19003.hp2 NA19075.hp1 others(1): Show |
intron_variant | MODIFIER | c.108-5446G>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162088382 | ||||||
chr5:162088637
|
C | T | 1 | a0001c0003t0001g0283 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.108-5191C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162088637 | ||||||
chr5:162088638
|
A | C | 1 | a0001c0003t0001g0283 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.108-5190A>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162088638 | ||||||
chr5:162088639
|
T | A | 1 | a0001c0003t0001g0283 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.108-5189T>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162088639 | ||||||
chr5:162088659
|
T | C | 1 | a0001c0002t0004g0262 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.108-5169T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162088659 | ||||||
chr5:162088787
|
T | C | 1 | a0001c0003t0001g0306 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.108-5041T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162088787 | ||||||
chr5:162088847
|
A | T | 1 | a0001c0003t0003g0278 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.108-4981A>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162088847 | ||||||
chr5:162088860
|
A | G | 2 | a0001c0005t0003g0028a0001c0005t0003g0075 | 2 | HG01243.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.108-4968A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162088860 | ||||||
chr5:162088881
|
C | T | 1 | a0001c0002t0004g0262 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.108-4947C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162088881 | ||||||
chr5:162088900
|
G | A | 1 | a0001c0002t0001g0192 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.108-4928G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162088900 | ||||||
chr5:162088908
|
C | T | 1 | a0001c0002t0006g0249 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.108-4920C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162088908 | ||||||
chr5:162089037
|
G | T | 1 | a0001c0001t0002g0064 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.108-4791G>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162089037 | ||||||
chr5:162089173
|
G | A | 1 | a0001c0002t0004g0262 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.108-4655G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162089173 | ||||||
chr5:162089181
|
G | C | 1 | a0001c0001t0004g0139 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.108-4647G>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162089181 | ||||||
chr5:162089248
|
G | A | 1 | a0001c0001t0002g0158 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.108-4580G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162089248 | ||||||
chr5:162089267
|
G | A | 1 | a0001c0002t0004g0262 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.108-4561G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162089267 | ||||||
chr5:162089397
|
G | A | 38 | a0001c0001t0001g0244a0001c0001t0002g0090a0001c0001t0003g0181others(35): Show | 39 | HG00099.hp1 HG00673.hp2 HG01069.hp2 others(36): Show |
intron_variant | MODIFIER | c.108-4431G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162089397 | ||||||
chr5:162089497
|
T | C | 1 | a0001c0001t0002g0041 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.108-4331T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162089497 | ||||||
chr5:162089640
|
T | C | 1 | a0001c0002t0001g0107 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.108-4188T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162089640 | ||||||
chr5:162089837
|
C | T | 2 | a0001c0005t0003g0028a0001c0005t0003g0075 | 2 | HG01243.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.108-3991C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162089837 | ||||||
chr5:162090000
|
C | G | 1 | a0001c0003t0001g0015 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.108-3828C>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162090000 | ||||||
chr5:162090053
|
C | T | 156 | a0001c0001t0001g0030a0001c0001t0001g0034a0001c0001t0001g0036others(153): Show | 165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.108-3775C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162090053 | ||||||
chr5:162090064
|
A | C | 1 | a0001c0002t0001g0180 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.108-3764A>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162090064 | ||||||
chr5:162090239
|
C | T | 1 | a0001c0002t0002g0016 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.108-3589C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162090239 | ||||||
chr5:162090246
|
A | G | 2 | a0001c0003t0002g0268a0001c0003t0002g0269 | 2 | NA19006.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.108-3582A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162090246 | ||||||
chr5:162090251
|
T | C | 2 | a0001c0001t0002g0189a0001c0001t0002g0205 | 2 | HG02165.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.108-3577T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162090251 | ||||||
chr5:162090325
|
C | CCATACA | 105 | a0001c0001t0001g0030a0001c0001t0001g0036a0001c0001t0001g0104others(102): Show | 113 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(110): Show |
intron_variant | MODIFIER | c.108-3478_108-3473d others(8): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 162090325 | |||||
chr5:162090325
|
C | CCATACAC others(5): Show |
8 | a0001c0001t0001g0034a0001c0001t0004g0017a0001c0001t0004g0250others(5): Show | 8 | HG00735.hp2 HG02572.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.108-3484_108-3473d others(14): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 162090325 | |||||
chr5:162090325
|
CCATACA | C | 51 | a0001c0001t0001g0244a0001c0001t0002g0090a0001c0001t0002g0260others(48): Show | 52 | HG00099.hp1 HG00673.hp2 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.108-3478_108-3473d others(8): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 162090325 | |||||
chr5:162090343
|
A | ACATACAC others(5): Show |
1 | a0001c0001t0004g0252 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.108-3474_108-3473i others(14): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 162090343 | |||||
chr5:162090564
|
C | A | 120 | a0001c0001t0001g0030a0001c0001t0001g0034a0001c0001t0001g0036others(117): Show | 128 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.108-3264C>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162090564 | ||||||
chr5:162090768
|
A | G | 1 | a0001c0009t0004g0143 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.108-3060A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162090768 | ||||||
chr5:162091222
|
T | G | 1 | a0001c0002t0001g0222 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.108-2606T>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162091222 | ||||||
chr5:162091252
|
A | C | 1 | a0001c0001t0002g0031 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.108-2576A>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162091252 | ||||||
chr5:162091264
|
G | A | 114 | a0001c0001t0001g0030a0001c0001t0001g0034a0001c0001t0001g0036others(111): Show | 122 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(119): Show |
intron_variant | MODIFIER | c.108-2564G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162091264 | ||||||
chr5:162091287
|
T | C | 2 | a0001c0001t0002g0046a0001c0001t0003g0054 | 2 | NA18963.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.108-2541T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162091287 | ||||||
chr5:162091531
|
A | T | 1 | a0001c0001t0001g0244 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.108-2297A>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162091531 | ||||||
chr5:162091639
|
GA | G | 126 | a0001c0001t0001g0030a0001c0001t0001g0034a0001c0001t0001g0036others(123): Show | 134 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.108-2180delA | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 162091639 | |||||
chr5:162091878
|
A | T | 1 | a0001c0003t0001g0288 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.108-1950A>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162091878 | ||||||
chr5:162091940
|
A | G | 5 | a0001c0002t0006g0008a0001c0002t0006g0144a0001c0002t0006g0145others(2): Show | 6 | HG01884.hp2 HG02145.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.108-1888A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162091940 | ||||||
chr5:162091978
|
A | G | 126 | a0001c0001t0001g0030a0001c0001t0001g0034a0001c0001t0001g0036others(123): Show | 134 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.108-1850A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162091978 | ||||||
chr5:162092239
|
C | G | 177 | a0001c0001t0001g0030a0001c0001t0001g0034a0001c0001t0001g0036others(174): Show | 189 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(186): Show |
intron_variant | MODIFIER | c.108-1589C>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162092239 | ||||||
chr5:162092253
|
A | G | 1 | a0001c0002t0001g0236 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.108-1575A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162092253 | ||||||
chr5:162092367
|
G | A | 3 | a0001c0001t0004g0309a0001c0001t0004g0310a0001c0001t0004g0311 | 3 | HG02258.hp2 HG02965.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.108-1461G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162092367 | ||||||
chr5:162092533
|
A | C | 5 | a0001c0002t0006g0008a0001c0002t0006g0144a0001c0002t0006g0145others(2): Show | 6 | HG01884.hp2 HG02145.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.108-1295A>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162092533 | ||||||
chr5:162092641
|
G | A | 6 | a0001c0001t0002g0260a0001c0001t0004g0256a0001c0001t0004g0257others(3): Show | 6 | HG01109.hp1 HG02622.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.108-1187G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162092641 | ||||||
chr5:162092751
|
A | C | 9 | a0001c0001t0002g0260a0001c0001t0004g0256a0001c0001t0004g0257others(6): Show | 9 | HG01109.hp1 HG02258.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.108-1077A>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162092751 | ||||||
chr5:162092770
|
A | C | 1 | a0001c0003t0001g0283 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.108-1058A>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162092770 | ||||||
chr5:162092795
|
G | A | 1 | a0001c0002t0002g0186 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.108-1033G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162092795 | ||||||
chr5:162092873
|
T | C | 126 | a0001c0001t0001g0030a0001c0001t0001g0034a0001c0001t0001g0036others(123): Show | 134 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.108-955T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162092873 | ||||||
chr5:162092949
|
C | T | 3 | a0001c0001t0004g0309a0001c0001t0004g0310a0001c0001t0004g0311 | 3 | HG02258.hp2 HG02965.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.108-879C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162092949 | ||||||
chr5:162092961
|
G | A | 1 | a0001c0001t0002g0214 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.108-867G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162092961 | ||||||
chr5:162092974
|
G | A | 8 | a0001c0001t0004g0017a0001c0001t0004g0250a0001c0001t0004g0251others(5): Show | 8 | HG02572.hp1 HG02615.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.108-854G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162092974 | ||||||
chr5:162093070
|
G | T | 2 | a0001c0001t0002g0010a0001c0001t0002g0202 | 3 | HG01106.hp1 HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.108-758G>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162093070 | ||||||
chr5:162093147
|
G | A | 1 | a0001c0002t0001g0150 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.108-681G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162093147 | ||||||
chr5:162093262
|
G | A | 3 | a0001c0001t0004g0309a0001c0001t0004g0310a0001c0001t0004g0311 | 3 | HG02258.hp2 HG02965.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.108-566G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162093262 | ||||||
chr5:162093263
|
C | G | 3 | a0001c0001t0004g0309a0001c0001t0004g0310a0001c0001t0004g0311 | 3 | HG02258.hp2 HG02965.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.108-565C>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162093263 | ||||||
chr5:162093366
|
G | A | 1 | a0001c0001t0001g0244 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.108-462G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162093366 | ||||||
chr5:162093451
|
G | A | 3 | a0001c0001t0004g0309a0001c0001t0004g0310a0001c0001t0004g0311 | 3 | HG02258.hp2 HG02965.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.108-377G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162093451 | ||||||
chr5:162093497
|
T | G | 3 | a0001c0001t0004g0309a0001c0001t0004g0310a0001c0001t0004g0311 | 3 | HG02258.hp2 HG02965.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.108-331T>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162093497 | ||||||
chr5:162093536
|
G | C | 2 | a0001c0006t0012g0005a0001c0008t0001g0247 | 3 | HG01069.hp1 HG01071.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.108-292G>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162093536 | ||||||
chr5:162093646
|
G | A | 3 | a0001c0001t0004g0309a0001c0001t0004g0310a0001c0001t0004g0311 | 3 | HG02258.hp2 HG02965.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.108-182G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162093646 | ||||||
chr5:162093739
|
T | A | 2 | a0001c0003t0001g0304a0001c0003t0003g0302 | 2 | NA19062.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.108-89T>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162093739 | ||||||
chr5:162093795
|
T | G | 1 | a0001c0002t0001g0222 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.108-33T>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162093795 | ||||||
chr5:162094039
|
A | T | 3 | a0001c0001t0004g0309a0001c0001t0004g0310a0001c0001t0004g0311 | 3 | HG02258.hp2 HG02965.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.259+60A>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 2/9 | chr5 | 162094039 | ||||||
chr5:162094252
|
A | G | 3 | a0001c0001t0010g0258a0001c0001t0010g0259a0001c0001t0010g0261 | 3 | HG03471.hp1 NA19030.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.259+273A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 2/9 | chr5 | 162094252 | ||||||
chr5:162094274
|
T | C | 2 | a0001c0006t0012g0005a0001c0008t0001g0247 | 3 | HG01069.hp1 HG01071.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.259+295T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 2/9 | chr5 | 162094274 | ||||||
chr5:162094335
|
T | C | 4 | a0001c0001t0008g0044a0001c0001t0008g0050a0001c0001t0008g0053others(1): Show | 4 | HG00423.hp1 NA18954.hp2 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.259+356T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 2/9 | chr5 | 162094335 | ||||||
chr5:162094418
|
A | G | 1 | a0001c0002t0004g0262 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.259+439A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 2/9 | chr5 | 162094418 | ||||||
chr5:162094469
|
C | T | 3 | a0001c0001t0004g0309a0001c0001t0004g0310a0001c0001t0004g0311 | 3 | HG02258.hp2 HG02965.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.259+490C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 2/9 | chr5 | 162094469 | ||||||
chr5:162094621
|
G | A | 3 | a0001c0001t0010g0258a0001c0001t0010g0259a0001c0001t0010g0261 | 3 | HG03471.hp1 NA19030.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.259+642G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 2/9 | chr5 | 162094621 | ||||||
chr5:162094685
|
C | T | 1 | a0001c0001t0002g0025 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.259+706C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 2/9 | chr5 | 162094685 | ||||||
chr5:162094688
|
G | C | 1 | a0001c0001t0009g0216 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.259+709G>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 2/9 | chr5 | 162094688 | ||||||
chr5:162094985
|
T | C | 2 | a0001c0001t0002g0158a0001c0001t0002g0159 | 2 | NA18971.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.260-510T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 2/9 | chr5 | 162094985 | ||||||
chr5:162095312
|
G | A | 311 | a0001c0001t0001g0030a0001c0001t0001g0034a0001c0001t0001g0036others(308): Show | 327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.260-183G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 2/9 | chr5 | 162095312 | ||||||
chr5:162095461
|
C | G | 1 | a0001c0001t0003g0071 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.260-34C>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 2/9 | chr5 | 162095461 | ||||||
chr5:162095623
|
G | A | 1 | a0001c0001t0002g0066 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.327+61G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 3/9 | chr5 | 162095623 | ||||||
chr5:162095628
|
G | A | 1 | a0001c0002t0002g0016 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.327+66G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 3/9 | chr5 | 162095628 | ||||||
chr5:162095748
|
G | A | 1 | a0001c0001t0002g0038 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.327+186G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 3/9 | chr5 | 162095748 | ||||||
chr5:162095870
|
A | G | 2 | a0001c0002t0001g0150a0001c0002t0001g0155 | 2 | HG00673.hp1 NA18946.hp2 |
intron_variant | MODIFIER | c.327+308A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 3/9 | chr5 | 162095870 | ||||||
chr5:162095949
|
G | A | 30 | a0001c0001t0001g0030a0001c0001t0001g0034a0001c0001t0001g0036others(27): Show | 33 | HG00099.hp2 HG00140.hp2 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.327+387G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 3/9 | chr5 | 162095949 | ||||||
chr5:162096015
|
A | G | 6 | a0001c0001t0002g0260a0001c0001t0004g0256a0001c0001t0004g0257others(3): Show | 6 | HG01109.hp1 HG02622.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.327+453A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 3/9 | chr5 | 162096015 | ||||||
chr5:162096081
|
A | G | 1 | a0001c0001t0001g0030 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.327+519A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 3/9 | chr5 | 162096081 | ||||||
chr5:162096195
|
A | G | 1 | a0001c0001t0001g0113 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.327+633A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 3/9 | chr5 | 162096195 | ||||||
chr5:162096544
|
G | A | 1 | a0001c0001t0001g0244 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.327+982G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 3/9 | chr5 | 162096544 | ||||||
chr5:162096553
|
G | T | 2 | a0001c0005t0003g0028a0001c0005t0003g0075 | 2 | HG01243.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.327+991G>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 3/9 | chr5 | 162096553 | ||||||
chr5:162096598
|
TGAACAAG | T | 3 | a0001c0001t0004g0309a0001c0001t0004g0310a0001c0001t0004g0311 | 3 | HG02258.hp2 HG02965.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.327+1038_328-1032d others(9): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 162096598 | |||||
chr5:162096717
|
A | G | 108 | a0001c0001t0001g0030a0001c0001t0001g0034a0001c0001t0001g0036others(105): Show | 115 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(112): Show |
intron_variant | MODIFIER | c.328-921A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 3/9 | chr5 | 162096717 | ||||||
chr5:162096742
|
G | A | 1 | a0001c0002t0001g0136 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.328-896G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 3/9 | chr5 | 162096742 | ||||||
chr5:162096769
|
G | A | 3 | a0001c0001t0004g0309a0001c0001t0004g0310a0001c0001t0004g0311 | 3 | HG02258.hp2 HG02965.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.328-869G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 3/9 | chr5 | 162096769 | ||||||
chr5:162096788
|
T | C | 3 | a0001c0001t0004g0309a0001c0001t0004g0310a0001c0001t0004g0311 | 3 | HG02258.hp2 HG02965.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.328-850T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 3/9 | chr5 | 162096788 | ||||||
chr5:162096864
|
G | A | 99 | a0001c0001t0001g0030a0001c0001t0001g0034a0001c0001t0001g0036others(96): Show | 106 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(103): Show |
intron_variant | MODIFIER | c.328-774G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 3/9 | chr5 | 162096864 | ||||||
chr5:162096894
|
T | C | 1 | a0001c0001t0004g0139 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.328-744T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 3/9 | chr5 | 162096894 | ||||||
chr5:162097095
|
G | C | 1 | a0001c0001t0002g0042 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.328-543G>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 3/9 | chr5 | 162097095 | ||||||
chr5:162097162
|
C | T | 1 | a0001c0003t0001g0297 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.328-476C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 3/9 | chr5 | 162097162 | ||||||
chr5:162097618
|
T | G | 6 | a0001c0002t0005g0221a0001c0002t0005g0223a0001c0002t0005g0224others(3): Show | 6 | HG01981.hp2 HG02055.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.328-20T>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 3/9 | chr5 | 162097618 | ||||||
chr5:162097984
|
A | G | 1 | a0001c0002t0002g0016 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.548+126A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 4/9 | chr5 | 162097984 | ||||||
chr5:162098047
|
T | G | 4 | a0001c0001t0002g0055a0001c0001t0002g0064a0001c0001t0002g0072others(1): Show | 4 | HG00099.hp2 HG01175.hp1 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.548+189T>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 4/9 | chr5 | 162098047 | ||||||
chr5:162098082
|
A | T | 6 | a0001c0001t0002g0260a0001c0001t0004g0256a0001c0001t0004g0257others(3): Show | 6 | HG01109.hp1 HG02622.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.548+224A>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 4/9 | chr5 | 162098082 | ||||||
chr5:162098088
|
G | T | 1 | a0001c0011t0003g0272 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.548+230G>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 4/9 | chr5 | 162098088 | ||||||
chr5:162098164
|
C | T | 1 | a0001c0002t0007g0074 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.548+306C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 4/9 | chr5 | 162098164 | ||||||
chr5:162098376
|
C | G | 1 | a0001c0002t0003g0007 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.548+518C>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 4/9 | chr5 | 162098376 | ||||||
chr5:162098462
|
TAATAA | T | 2 | a0001c0006t0012g0005a0001c0008t0001g0247 | 3 | HG01069.hp1 HG01071.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.548+610_548+614del others(5): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 162098462 | |||||
chr5:162098552
|
A | G | 3 | a0001c0004t0002g0147a0001c0004t0002g0148a0001c0004t0002g0149 | 3 | HG01243.hp1 HG02258.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.548+694A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 4/9 | chr5 | 162098552 | ||||||
chr5:162098591
|
C | G | 6 | a0001c0001t0002g0260a0001c0001t0004g0256a0001c0001t0004g0257others(3): Show | 6 | HG01109.hp1 HG02622.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.548+733C>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 4/9 | chr5 | 162098591 | ||||||
chr5:162098826
|
GCTGTCCC others(3): Show |
G | 4 | a0001c0004t0005g0237a0001c0004t0005g0238a0001c0004t0005g0239others(1): Show | 4 | HG00639.hp2 HG02897.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.548+973_548+982del others(10): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 162098826 | |||||
chr5:162099009
|
T | C | 3 | a0001c0001t0018g0086a0001c0005t0003g0028a0001c0005t0003g0075 | 3 | HG01243.hp2 HG01884.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.548+1151T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 4/9 | chr5 | 162099009 | ||||||
chr5:162099201
|
A | G | 5 | a0001c0002t0001g0135a0001c0002t0003g0007a0001c0002t0003g0101others(2): Show | 6 | HG00621.hp2 HG02083.hp2 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.548+1343A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 4/9 | chr5 | 162099201 | ||||||
chr5:162099256
|
G | A | 3 | a0001c0001t0004g0309a0001c0001t0004g0310a0001c0001t0004g0311 | 3 | HG02258.hp2 HG02965.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.548+1398G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 4/9 | chr5 | 162099256 | ||||||
chr5:162099513
|
C | A | 1 | a0001c0001t0002g0025 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.548+1655C>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 4/9 | chr5 | 162099513 | ||||||
chr5:162099515
|
T | G | 311 | a0001c0001t0001g0030a0001c0001t0001g0034a0001c0001t0001g0036others(308): Show | 327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.548+1657T>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 4/9 | chr5 | 162099515 | ||||||
chr5:162099561
|
C | A | 1 | a0001c0002t0001g0119 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.549-1674C>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 4/9 | chr5 | 162099561 | ||||||
chr5:162099568
|
C | T | 1 | a0001c0001t0002g0260 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.549-1667C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 4/9 | chr5 | 162099568 | ||||||
chr5:162099571
|
A | G | 1 | a0001c0003t0001g0307 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.549-1664A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 4/9 | chr5 | 162099571 | ||||||
chr5:162099720
|
T | G | 2 | a0001c0001t0003g0060a0001c0001t0003g0061 | 2 | NA18944.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.549-1515T>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 4/9 | chr5 | 162099720 | ||||||
chr5:162099786
|
G | C | 1 | a0001c0001t0002g0025 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.549-1449G>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 4/9 | chr5 | 162099786 | ||||||
chr5:162099928
|
T | C | 1 | a0001c0001t0004g0139 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.549-1307T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 4/9 | chr5 | 162099928 | ||||||
chr5:162099948
|
T | A | 1 | a0001c0002t0004g0262 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.549-1287T>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 4/9 | chr5 | 162099948 | ||||||
chr5:162100116
|
G | A | 2 | a0001c0006t0012g0005a0001c0008t0001g0247 | 3 | HG01069.hp1 HG01071.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.549-1119G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 4/9 | chr5 | 162100116 | ||||||
chr5:162100247
|
A | G | 32 | a0001c0001t0002g0090a0001c0001t0003g0181a0001c0002t0001g0087others(29): Show | 33 | HG00099.hp1 HG00673.hp2 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.549-988A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 4/9 | chr5 | 162100247 | ||||||
chr5:162100254
|
C | T | 1 | a0001c0001t0001g0244 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.549-981C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 4/9 | chr5 | 162100254 | ||||||
chr5:162100288
|
T | C | 1 | a0001c0011t0003g0272 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.549-947T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 4/9 | chr5 | 162100288 | ||||||
chr5:162100305
|
C | T | 1 | a0001c0002t0011g0079 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.549-930C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 4/9 | chr5 | 162100305 | ||||||
chr5:162100316
|
A | T | 1 | a0001c0009t0004g0143 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.549-919A>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 4/9 | chr5 | 162100316 | ||||||
chr5:162100332
|
T | G | 1 | a0001c0001t0002g0209 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.549-903T>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 4/9 | chr5 | 162100332 | ||||||
chr5:162100447
|
T | C | 7 | a0001c0001t0002g0260a0001c0001t0004g0256a0001c0001t0004g0257others(4): Show | 7 | HG01109.hp1 HG02622.hp1 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.549-788T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 4/9 | chr5 | 162100447 | ||||||
chr5:162100709
|
C | T | 1 | a0001c0001t0001g0045 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.549-526C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 4/9 | chr5 | 162100709 | ||||||
chr5:162100775
|
A | G | 6 | a0001c0001t0002g0260a0001c0001t0004g0256a0001c0001t0004g0257others(3): Show | 6 | HG01109.hp1 HG02622.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.549-460A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 4/9 | chr5 | 162100775 | ||||||
chr5:162100837
|
A | T | 1 | a0001c0001t0002g0059 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.549-398A>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 4/9 | chr5 | 162100837 | ||||||
chr5:162100927
|
C | T | 1 | a0001c0003t0003g0289 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.549-308C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 4/9 | chr5 | 162100927 | ||||||
chr5:162101022
|
G | C | 1 | a0001c0001t0004g0257 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.549-213G>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 4/9 | chr5 | 162101022 | ||||||
chr5:162101372
|
T | G | 2 | a0001c0003t0003g0301a0001c0003t0003g0305 | 2 | HG01074.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.631+55T>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 5/9 | chr5 | 162101372 | ||||||
chr5:162101580
|
CT | C | 15 | a0001c0001t0002g0047a0001c0001t0010g0258a0001c0001t0010g0259others(12): Show | 17 | HG00099.hp1 HG00140.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.631+275delT | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 162101580 | |||||
chr5:162101853
|
A | G | 1 | a0001c0002t0004g0262 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.631+536A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 5/9 | chr5 | 162101853 | ||||||
chr5:162101887
|
T | C | 9 | a0001c0001t0004g0309a0001c0001t0004g0310a0001c0001t0004g0311others(6): Show | 9 | HG00639.hp2 HG02258.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.631+570T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 5/9 | chr5 | 162101887 | ||||||
chr5:162102051
|
A | C | 3 | a0001c0005t0003g0028a0001c0005t0003g0075a0001c0005t0015g0243 | 3 | HG01243.hp2 HG01884.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.631+734A>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 5/9 | chr5 | 162102051 | ||||||
chr5:162102090
|
G | C | 16 | a0001c0001t0001g0115a0001c0001t0001g0162a0001c0001t0002g0260others(13): Show | 16 | HG01109.hp1 HG02572.hp1 HG02615.hp2 others(13): Show |
intron_variant | MODIFIER | c.631+773G>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 5/9 | chr5 | 162102090 | ||||||
chr5:162102241
|
T | C | 3 | a0001c0002t0001g0119a0001c0002t0001g0120a0001c0002t0001g0138 | 3 | HG01952.hp2 HG02004.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.631+924T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 5/9 | chr5 | 162102241 | ||||||
chr5:162102262
|
A | G | 1 | a0001c0002t0002g0006 | 2 | HG02615.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.631+945A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 5/9 | chr5 | 162102262 | ||||||
chr5:162102363
|
C | T | 63 | a0001c0001t0001g0045a0001c0001t0001g0152a0001c0002t0001g0001others(60): Show | 67 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(64): Show |
intron_variant | MODIFIER | c.631+1046C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 5/9 | chr5 | 162102363 | ||||||
chr5:162102422
|
A | G | 3 | a0001c0001t0004g0139a0001c0002t0001g0211a0001c0008t0001g0247 | 3 | HG01192.hp1 HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.631+1105A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 5/9 | chr5 | 162102422 | ||||||
chr5:162102565
|
A | G | 236 | a0001c0001t0001g0045a0001c0001t0001g0104a0001c0001t0001g0113others(233): Show | 247 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.631+1248A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 5/9 | chr5 | 162102565 | ||||||
chr5:162102625
|
G | T | 29 | a0001c0001t0001g0104a0001c0001t0001g0127a0001c0001t0001g0133others(26): Show | 30 | HG00140.hp1 HG00438.hp1 HG01346.hp2 others(27): Show |
intron_variant | MODIFIER | c.632-1264G>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 5/9 | chr5 | 162102625 | ||||||
chr5:162102627
|
C | A | 1 | a0001c0001t0004g0139 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.632-1262C>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 5/9 | chr5 | 162102627 | ||||||
chr5:162102714
|
A | G | 206 | a0001c0001t0001g0045a0001c0001t0001g0113a0001c0001t0001g0115others(203): Show | 216 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(213): Show |
intron_variant | MODIFIER | c.632-1175A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 5/9 | chr5 | 162102714 | ||||||
chr5:162102725
|
G | A | 23 | a0001c0002t0001g0001a0001c0002t0001g0035a0001c0002t0001g0051others(20): Show | 25 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(22): Show |
intron_variant | MODIFIER | c.632-1164G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 5/9 | chr5 | 162102725 | ||||||
chr5:162102802
|
C | T | 204 | a0001c0001t0001g0045a0001c0001t0001g0113a0001c0001t0001g0115others(201): Show | 214 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(211): Show |
intron_variant | MODIFIER | c.632-1087C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 5/9 | chr5 | 162102802 | ||||||
chr5:162102998
|
T | G | 1 | a0001c0002t0001g0192 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.632-891T>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 5/9 | chr5 | 162102998 | ||||||
chr5:162103147
|
C | T | 31 | a0001c0001t0001g0104a0001c0001t0001g0127a0001c0001t0001g0133others(28): Show | 32 | HG00140.hp1 HG00438.hp1 HG01346.hp2 others(29): Show |
intron_variant | MODIFIER | c.632-742C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 5/9 | chr5 | 162103147 | ||||||
chr5:162103262
|
A | G | 1 | a0001c0001t0003g0203 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.632-627A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 5/9 | chr5 | 162103262 | ||||||
chr5:162103300
|
A | G | 1 | a0001c0002t0001g0227 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.632-589A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 5/9 | chr5 | 162103300 | ||||||
chr5:162103379
|
T | C | 205 | a0001c0001t0001g0045a0001c0001t0001g0113a0001c0001t0001g0115others(202): Show | 215 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(212): Show |
intron_variant | MODIFIER | c.632-510T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 5/9 | chr5 | 162103379 | ||||||
chr5:162103411
|
C | T | 236 | a0001c0001t0001g0045a0001c0001t0001g0104a0001c0001t0001g0113others(233): Show | 247 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.632-478C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 5/9 | chr5 | 162103411 | ||||||
chr5:162103530
|
G | C | 1 | a0001c0002t0004g0262 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.632-359G>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 5/9 | chr5 | 162103530 | ||||||
chr5:162103532
|
G | A | 1 | a0001c0001t0004g0139 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.632-357G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 5/9 | chr5 | 162103532 | ||||||
chr5:162103597
|
G | C | 1 | a0001c0002t0001g0070 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.632-292G>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 5/9 | chr5 | 162103597 | ||||||
chr5:162103729
|
C | T | 205 | a0001c0001t0001g0045a0001c0001t0001g0113a0001c0001t0001g0115others(202): Show | 215 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(212): Show |
intron_variant | MODIFIER | c.632-160C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 5/9 | chr5 | 162103729 | ||||||
chr5:162103818
|
T | A | 1 | a0001c0002t0001g0035 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.632-71T>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 5/9 | chr5 | 162103818 | ||||||
chr5:162103834
|
C | T | 1 | a0001c0003t0002g0286 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.632-55C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 5/9 | chr5 | 162103834 | ||||||
chr5:162103879
|
C | A | 1 | a0001c0003t0001g0012 | 2 | NA18980.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.632-10C>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 5/9 | chr5 | 162103879 | ||||||
chr5:162104454
|
T | A | 239 | a0001c0001t0001g0045a0001c0001t0001g0104a0001c0001t0001g0113others(236): Show | 251 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(248): Show |
intron_variant | MODIFIER | c.769+428T>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162104454 | ||||||
chr5:162104675
|
C | T | 1 | a0001c0002t0001g0156 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.769+649C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162104675 | ||||||
chr5:162104762
|
A | ATTTAT | 142 | a0001c0001t0001g0045a0001c0001t0001g0113a0001c0001t0001g0115others(139): Show | 148 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(145): Show |
intron_variant | MODIFIER | c.769+740_769+741ins others(5): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162104762 | |||||
chr5:162104838
|
A | G | 7 | a0001c0001t0002g0158a0001c0001t0002g0159a0001c0001t0002g0183others(4): Show | 7 | NA18945.hp1 NA18953.hp2 NA18971.hp2 others(4): Show |
intron_variant | MODIFIER | c.769+812A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162104838 | ||||||
chr5:162104879
|
T | C | 1 | a0001c0002t0007g0081 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.769+853T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162104879 | ||||||
chr5:162104902
|
G | C | 3 | a0001c0002t0002g0006a0001c0002t0004g0262a0001c0009t0004g0143 | 4 | HG02615.hp1 HG02886.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.769+876G>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162104902 | ||||||
chr5:162104921
|
T | C | 1 | a0001c0002t0002g0100 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.769+895T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162104921 | ||||||
chr5:162105232
|
C | T | 3 | a0001c0005t0003g0028a0001c0005t0003g0075a0001c0005t0015g0243 | 3 | HG01243.hp2 HG01884.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.769+1206C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162105232 | ||||||
chr5:162105354
|
C | T | 3 | a0001c0005t0003g0028a0001c0005t0003g0075a0001c0005t0015g0243 | 3 | HG01243.hp2 HG01884.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.769+1328C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162105354 | ||||||
chr5:162105380
|
T | C | 6 | a0001c0002t0005g0221a0001c0002t0005g0223a0001c0002t0005g0224others(3): Show | 6 | HG01981.hp2 HG02055.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.769+1354T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162105380 | ||||||
chr5:162105397
|
C | A | 1 | a0001c0002t0011g0085 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.769+1371C>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162105397 | ||||||
chr5:162105423
|
T | C | 1 | a0001c0001t0013g0210 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.769+1397T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162105423 | ||||||
chr5:162105432
|
C | CTTTTTTT others(1): Show |
71 | a0001c0001t0001g0113a0001c0001t0001g0115a0001c0001t0001g0162others(68): Show | 73 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.769+1414_769+1421d others(10): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162105432 | |||||
chr5:162105432
|
C | CTTTTTTT others(2): Show |
63 | a0001c0001t0001g0045a0001c0001t0001g0152a0001c0001t0001g0219others(60): Show | 67 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(64): Show |
intron_variant | MODIFIER | c.769+1413_769+1421d others(11): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162105432 | |||||
chr5:162105432
|
C | CTTTTTTT others(3): Show |
33 | a0001c0001t0001g0104a0001c0001t0001g0127a0001c0001t0001g0133others(30): Show | 34 | HG00140.hp1 HG00438.hp1 HG00621.hp2 others(31): Show |
intron_variant | MODIFIER | c.769+1412_769+1421d others(12): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162105432 | |||||
chr5:162105432
|
C | CTTTTTTT others(4): Show |
7 | a0001c0002t0001g0020a0001c0002t0001g0098a0001c0002t0001g0116others(4): Show | 7 | HG01496.hp1 HG03130.hp2 NA18941.hp2 others(4): Show |
intron_variant | MODIFIER | c.769+1411_769+1421d others(13): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162105432 | |||||
chr5:162105432
|
C | CTTTTTTT others(5): Show |
55 | a0001c0001t0003g0071a0001c0002t0001g0097a0001c0002t0001g0099others(52): Show | 59 | HG00558.hp1 HG01074.hp1 HG01258.hp1 others(56): Show |
intron_variant | MODIFIER | c.769+1410_769+1421d others(14): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162105432 | |||||
chr5:162105432
|
C | CTTTTTTT others(6): Show |
2 | a0001c0003t0001g0288a0001c0003t0002g0268 | 2 | NA19006.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.769+1409_769+1421d others(15): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162105432 | |||||
chr5:162105432
|
C | CTTTTTTT others(8): Show |
1 | a0001c0003t0002g0269 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.769+1407_769+1421d others(17): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162105432 | |||||
chr5:162105490
|
C | T | 1 | a0001c0002t0001g0191 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.769+1464C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162105490 | ||||||
chr5:162105574
|
C | T | 1 | a0001c0001t0013g0210 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.769+1548C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162105574 | ||||||
chr5:162105587
|
G | A | 1 | a0001c0001t0004g0139 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.769+1561G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162105587 | ||||||
chr5:162105652
|
G | A | 4 | a0001c0002t0005g0223a0001c0002t0005g0224a0001c0002t0005g0225others(1): Show | 4 | HG01981.hp2 HG02055.hp1 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.769+1626G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162105652 | ||||||
chr5:162105705
|
C | T | 1 | a0001c0001t0003g0063 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.769+1679C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162105705 | ||||||
chr5:162105720
|
G | A | 6 | a0001c0002t0014g0076a0001c0002t0014g0080a0001c0004t0005g0237others(3): Show | 6 | HG00639.hp2 HG02572.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.769+1694G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162105720 | ||||||
chr5:162105796
|
T | C | 9 | a0001c0001t0004g0309a0001c0001t0004g0310a0001c0001t0004g0311others(6): Show | 9 | HG00639.hp2 HG02258.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.769+1770T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162105796 | ||||||
chr5:162105814
|
T | TAC | 3 | a0001c0001t0002g0047a0001c0001t0002g0048a0001c0001t0002g0059 | 3 | HG02602.hp2 NA18964.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.769+1817_769+1818d others(4): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162105814 | |||||
chr5:162105814
|
T | TACAC | 112 | a0001c0001t0001g0045a0001c0001t0001g0152a0001c0001t0018g0086others(109): Show | 118 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.769+1815_769+1818d others(6): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162105814 | |||||
chr5:162105814
|
T | TACACAC | 47 | a0001c0001t0001g0104a0001c0001t0001g0127a0001c0001t0001g0133others(44): Show | 49 | HG00438.hp1 HG01069.hp2 HG01258.hp1 others(46): Show |
intron_variant | MODIFIER | c.769+1813_769+1818d others(8): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162105814 | |||||
chr5:162105814
|
T | TACACACA others(1): Show |
6 | a0001c0001t0001g0244a0001c0001t0003g0063a0001c0001t0004g0256others(3): Show | 7 | HG00140.hp1 HG02622.hp1 HG02735.hp1 others(4): Show |
intron_variant | MODIFIER | c.769+1811_769+1818d others(10): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162105814 | |||||
chr5:162105814
|
T | TACACACA others(3): Show |
5 | a0001c0001t0004g0252a0001c0001t0004g0253a0001c0001t0004g0254others(2): Show | 5 | HG02615.hp2 HG02717.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.769+1809_769+1818d others(12): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162105814 | |||||
chr5:162105814
|
T | TACACACA others(5): Show |
6 | a0001c0001t0001g0115a0001c0001t0001g0162a0001c0001t0004g0017others(3): Show | 6 | HG02572.hp1 HG02647.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.769+1807_769+1818d others(14): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162105814 | |||||
chr5:162105814
|
T | TACACACA others(7): Show |
5 | a0001c0001t0002g0260a0001c0001t0004g0139a0001c0001t0010g0258others(2): Show | 5 | HG01109.hp1 HG01192.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.769+1805_769+1818d others(16): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162105814 | |||||
chr5:162105814
|
TACACAC | T | 47 | a0001c0001t0001g0113a0001c0001t0001g0219a0001c0001t0002g0011others(44): Show | 49 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.769+1813_769+1818d others(8): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162105814 | |||||
chr5:162105834
|
C | CACAT | 9 | a0001c0001t0004g0309a0001c0001t0004g0310a0001c0001t0004g0311others(6): Show | 9 | HG00639.hp2 HG02258.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.769+1811_769+1812i others(6): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162105834 | |||||
chr5:162105976
|
T | G | 3 | a0001c0001t0004g0309a0001c0001t0004g0310a0001c0001t0004g0311 | 3 | HG02258.hp2 HG02965.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.769+1950T>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162105976 | ||||||
chr5:162106060
|
C | T | 142 | a0001c0001t0001g0045a0001c0001t0001g0113a0001c0001t0001g0115others(139): Show | 148 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(145): Show |
intron_variant | MODIFIER | c.769+2034C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162106060 | ||||||
chr5:162106145
|
A | G | 1 | a0001c0002t0002g0186 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.769+2119A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162106145 | ||||||
chr5:162106379
|
T | C | 3 | a0001c0001t0004g0139a0001c0002t0001g0211a0001c0008t0001g0247 | 3 | HG01192.hp1 HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.769+2353T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162106379 | ||||||
chr5:162106397
|
C | T | 1 | a0001c0001t0018g0086 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.769+2371C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162106397 | ||||||
chr5:162106411
|
A | T | 1 | a0001c0003t0003g0305 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.769+2385A>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162106411 | ||||||
chr5:162106427
|
G | T | 31 | a0001c0001t0001g0104a0001c0001t0001g0127a0001c0001t0001g0133others(28): Show | 32 | HG00140.hp1 HG00438.hp1 HG01346.hp2 others(29): Show |
intron_variant | MODIFIER | c.769+2401G>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162106427 | ||||||
chr5:162106442
|
G | C | 236 | a0001c0001t0001g0045a0001c0001t0001g0104a0001c0001t0001g0113others(233): Show | 247 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.769+2416G>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162106442 | ||||||
chr5:162106490
|
C | T | 138 | a0001c0001t0001g0045a0001c0001t0001g0113a0001c0001t0001g0115others(135): Show | 144 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(141): Show |
intron_variant | MODIFIER | c.769+2464C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162106490 | ||||||
chr5:162106658
|
C | T | 1 | a0001c0004t0002g0149 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.769+2632C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162106658 | ||||||
chr5:162106706
|
C | G | 236 | a0001c0001t0001g0045a0001c0001t0001g0104a0001c0001t0001g0113others(233): Show | 247 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.769+2680C>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162106706 | ||||||
chr5:162106833
|
C | T | 1 | a0001c0003t0001g0013 | 2 | NA18969.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.769+2807C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162106833 | ||||||
chr5:162106871
|
A | T | 3 | a0001c0001t0004g0139a0001c0002t0001g0211a0001c0008t0001g0247 | 3 | HG01192.hp1 HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.769+2845A>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162106871 | ||||||
chr5:162106891
|
T | G | 1 | a0001c0002t0001g0179 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.769+2865T>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162106891 | ||||||
chr5:162106916
|
G | GGC | 233 | a0001c0001t0001g0045a0001c0001t0001g0104a0001c0001t0001g0113others(230): Show | 244 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.769+2891_769+2892i others(4): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162106916 | |||||
chr5:162106917
|
G | GC | 3 | a0001c0001t0004g0139a0001c0002t0001g0211a0001c0008t0001g0247 | 3 | HG01192.hp1 HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.769+2891_769+2892i others(3): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162106917 | ||||||
chr5:162106919
|
T | C | 233 | a0001c0001t0001g0045a0001c0001t0001g0104a0001c0001t0001g0113others(230): Show | 244 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.769+2893T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162106919 | ||||||
chr5:162106919
|
T | G | 6 | a0001c0001t0004g0139a0001c0002t0001g0211a0001c0002t0002g0006others(3): Show | 7 | HG01192.hp1 HG02615.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.769+2893T>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162106919 | ||||||
chr5:162106920
|
G | A | 5 | a0001c0001t0002g0029a0001c0001t0002g0160a0001c0001t0002g0185others(2): Show | 5 | HG02145.hp2 HG02717.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.769+2894G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162106920 | ||||||
chr5:162106970
|
C | T | 236 | a0001c0001t0001g0045a0001c0001t0001g0104a0001c0001t0001g0113others(233): Show | 247 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.769+2944C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162106970 | ||||||
chr5:162107013
|
G | A | 31 | a0001c0001t0001g0104a0001c0001t0001g0127a0001c0001t0001g0133others(28): Show | 32 | HG00140.hp1 HG00438.hp1 HG01192.hp1 others(29): Show |
intron_variant | MODIFIER | c.769+2987G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162107013 | ||||||
chr5:162107079
|
C | T | 1 | a0001c0002t0001g0137 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.769+3053C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162107079 | ||||||
chr5:162107087
|
C | G | 1 | a0001c0001t0002g0037 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.769+3061C>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162107087 | ||||||
chr5:162107140
|
G | A | 236 | a0001c0001t0001g0045a0001c0001t0001g0104a0001c0001t0001g0113others(233): Show | 247 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.769+3114G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162107140 | ||||||
chr5:162107407
|
G | A | 4 | a0001c0001t0001g0244a0001c0001t0004g0139a0001c0002t0001g0211others(1): Show | 4 | HG01192.hp1 HG03225.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.769+3381G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162107407 | ||||||
chr5:162107496
|
A | G | 10 | a0001c0001t0001g0115a0001c0001t0001g0162a0001c0001t0004g0017others(7): Show | 10 | HG02572.hp1 HG02615.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.769+3470A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162107496 | ||||||
chr5:162107622
|
G | A | 1 | a0001c0003t0002g0268 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.769+3596G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162107622 | ||||||
chr5:162107630
|
G | A | 1 | a0001c0010t0003g0112 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.769+3604G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162107630 | ||||||
chr5:162107675
|
T | C | 4 | a0001c0002t0001g0117a0001c0002t0001g0118a0001c0002t0001g0132others(1): Show | 4 | HG02622.hp2 HG02723.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.769+3649T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162107675 | ||||||
chr5:162107787
|
C | A | 28 | a0001c0001t0001g0104a0001c0001t0001g0127a0001c0001t0001g0133others(25): Show | 29 | HG00140.hp1 HG00438.hp1 HG01346.hp2 others(26): Show |
intron_variant | MODIFIER | c.769+3761C>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162107787 | ||||||
chr5:162107819
|
C | T | 2 | a0001c0002t0001g0211a0001c0008t0001g0247 | 2 | HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.769+3793C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162107819 | ||||||
chr5:162107976
|
C | T | 30 | a0001c0001t0001g0104a0001c0001t0001g0127a0001c0001t0001g0133others(27): Show | 31 | HG00140.hp1 HG00438.hp1 HG01346.hp2 others(28): Show |
intron_variant | MODIFIER | c.769+3950C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162107976 | ||||||
chr5:162108024
|
G | A | 135 | a0001c0001t0001g0045a0001c0001t0001g0152a0001c0001t0003g0071others(132): Show | 143 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(140): Show |
intron_variant | MODIFIER | c.769+3998G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162108024 | ||||||
chr5:162108070
|
A | G | 1 | a0001c0001t0002g0090 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.769+4044A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162108070 | ||||||
chr5:162108113
|
G | A | 1 | a0001c0001t0002g0065 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.769+4087G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162108113 | ||||||
chr5:162108129
|
T | C | 239 | a0001c0001t0001g0045a0001c0001t0001g0104a0001c0001t0001g0113others(236): Show | 251 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(248): Show |
intron_variant | MODIFIER | c.769+4103T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162108129 | ||||||
chr5:162108387
|
G | A | 2 | a0001c0002t0001g0211a0001c0008t0001g0247 | 2 | HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.769+4361G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162108387 | ||||||
chr5:162108666
|
T | C | 1 | a0001c0002t0001g0236 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.769+4640T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162108666 | ||||||
chr5:162108749
|
C | T | 126 | a0001c0001t0001g0045a0001c0001t0001g0152a0001c0001t0003g0071others(123): Show | 134 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.769+4723C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162108749 | ||||||
chr5:162108926
|
C | T | 3 | a0001c0001t0002g0189a0001c0001t0002g0205a0001c0001t0002g0208 | 3 | HG02165.hp1 NA19012.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.769+4900C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162108926 | ||||||
chr5:162108956
|
C | T | 10 | a0001c0001t0001g0115a0001c0001t0001g0162a0001c0001t0004g0017others(7): Show | 10 | HG02572.hp1 HG02615.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.769+4930C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162108956 | ||||||
chr5:162109297
|
C | T | 1 | a0001c0001t0003g0024 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.769+5271C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162109297 | ||||||
chr5:162109330
|
T | A | 31 | a0001c0001t0001g0104a0001c0001t0001g0127a0001c0001t0001g0133others(28): Show | 32 | HG00140.hp1 HG00438.hp1 HG01192.hp1 others(29): Show |
intron_variant | MODIFIER | c.769+5304T>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162109330 | ||||||
chr5:162109356
|
C | T | 3 | a0001c0002t0002g0006a0001c0002t0004g0262a0001c0009t0004g0143 | 4 | HG02615.hp1 HG02886.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.769+5330C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162109356 | ||||||
chr5:162109382
|
A | G | 7 | a0001c0001t0001g0045a0001c0001t0001g0152a0001c0002t0001g0009others(4): Show | 8 | HG00673.hp1 HG02071.hp2 HG02132.hp2 others(5): Show |
intron_variant | MODIFIER | c.769+5356A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162109382 | ||||||
chr5:162109388
|
T | TTATATA | 4 | a0001c0001t0001g0115a0001c0001t0010g0258a0001c0001t0010g0259others(1): Show | 4 | HG03471.hp1 HG06807.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.769+5362_769+5363i others(8): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162109388 | ||||||
chr5:162109388
|
T | TTATATAT others(1): Show |
5 | a0001c0001t0002g0163a0001c0001t0002g0164a0001c0001t0002g0165others(2): Show | 5 | HG00639.hp1 HG02109.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.769+5362_769+5363i others(10): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162109388 | ||||||
chr5:162109388
|
T | TTATATAT others(3): Show |
4 | a0001c0001t0001g0113a0001c0001t0002g0194a0001c0001t0002g0214others(1): Show | 4 | HG02451.hp1 HG02622.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.769+5362_769+5363i others(12): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162109388 | ||||||
chr5:162109388
|
T | TTATATAT others(9): Show |
2 | a0001c0001t0002g0161a0001c0006t0012g0005 | 3 | HG01069.hp1 HG01071.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.769+5362_769+5363i others(18): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162109388 | ||||||
chr5:162109388
|
T | TTATATAT others(13): Show |
1 | a0001c0001t0004g0257 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.769+5362_769+5363i others(22): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162109388 | ||||||
chr5:162109388
|
TAATATAT others(1): Show |
T | 4 | a0001c0001t0004g0017a0001c0001t0004g0250a0001c0001t0004g0251others(1): Show | 4 | HG02572.hp1 HG02818.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.769+5363_769+5370d others(10): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162109388 | ||||||
chr5:162109389
|
A | AAT | 35 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(32): Show | 38 | HG00438.hp2 HG00735.hp1 HG01891.hp1 others(35): Show |
intron_variant | MODIFIER | c.769+5396_769+5397d others(4): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162109389 | |||||
chr5:162109389
|
A | AATAT | 18 | a0001c0001t0001g0030a0001c0001t0001g0034a0001c0001t0002g0010others(15): Show | 19 | HG00099.hp2 HG00735.hp2 HG01106.hp1 others(16): Show |
intron_variant | MODIFIER | c.769+5394_769+5397d others(6): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162109389 | |||||
chr5:162109389
|
A | AATATAT | 10 | a0001c0001t0001g0036a0001c0001t0002g0025a0001c0001t0002g0037others(7): Show | 10 | HG00597.hp1 HG01081.hp1 HG01516.hp2 others(7): Show |
intron_variant | MODIFIER | c.769+5392_769+5397d others(8): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162109389 | |||||
chr5:162109389
|
A | AATATATA others(1): Show |
9 | a0001c0001t0002g0064a0001c0001t0002g0208a0001c0001t0008g0044others(6): Show | 9 | HG01243.hp2 HG01884.hp1 HG01952.hp1 others(6): Show |
intron_variant | MODIFIER | c.769+5390_769+5397d others(10): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162109389 | |||||
chr5:162109389
|
A | AATATATA others(3): Show |
8 | a0001c0001t0001g0219a0001c0001t0002g0023a0001c0001t0002g0026others(5): Show | 8 | HG01261.hp2 HG02027.hp1 HG02083.hp1 others(5): Show |
intron_variant | MODIFIER | c.769+5388_769+5397d others(12): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162109389 | |||||
chr5:162109389
|
A | AATATATA others(5): Show |
14 | a0001c0001t0002g0184a0001c0001t0002g0190a0001c0001t0003g0170others(11): Show | 14 | HG00558.hp2 HG00621.hp1 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.769+5386_769+5397d others(14): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162109389 | |||||
chr5:162109389
|
A | AATATATA others(7): Show |
7 | a0001c0001t0002g0160a0001c0001t0002g0200a0001c0001t0002g0217others(4): Show | 7 | HG00423.hp2 HG02080.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.769+5384_769+5397d others(16): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162109389 | |||||
chr5:162109389
|
A | AATATATA others(9): Show |
6 | a0001c0001t0002g0022a0001c0001t0002g0027a0001c0001t0002g0185others(3): Show | 6 | HG00639.hp2 HG02717.hp1 NA18948.hp1 others(3): Show |
intron_variant | MODIFIER | c.769+5382_769+5397d others(18): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162109389 | |||||
chr5:162109389
|
A | AATATATA others(11): Show |
5 | a0001c0001t0002g0011a0001c0001t0002g0204a0001c0001t0002g0220others(2): Show | 6 | HG03195.hp2 NA18747.hp1 NA18953.hp1 others(3): Show |
intron_variant | MODIFIER | c.769+5380_769+5397d others(20): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162109389 | |||||
chr5:162109389
|
A | AATATATA others(13): Show |
2 | a0001c0001t0002g0029a0001c0004t0005g0237 | 2 | HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.769+5378_769+5397d others(22): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162109389 | |||||
chr5:162109389
|
A | AATATATA others(21): Show |
1 | a0001c0001t0002g0021 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.769+5370_769+5397d others(30): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162109389 | |||||
chr5:162109389
|
A | ATATATAT others(6): Show |
1 | a0001c0002t0004g0262 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.769+5363_769+5364i others(15): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162109389 | ||||||
chr5:162109389
|
A | T | 18 | a0001c0001t0001g0113a0001c0001t0001g0115a0001c0001t0001g0162others(15): Show | 19 | HG00639.hp1 HG01069.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.769+5363A>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162109389 | ||||||
chr5:162109389
|
AATAT | A | 8 | a0001c0002t0001g0094a0001c0002t0001g0176a0001c0002t0001g0231others(5): Show | 8 | HG02486.hp1 HG02486.hp2 HG03491.hp1 others(5): Show |
intron_variant | MODIFIER | c.769+5394_769+5397d others(6): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162109389 | |||||
chr5:162109389
|
AATATAT | A | 23 | a0001c0001t0001g0045a0001c0001t0001g0152a0001c0001t0004g0139others(20): Show | 24 | HG00673.hp1 HG01069.hp2 HG01192.hp1 others(21): Show |
intron_variant | MODIFIER | c.769+5392_769+5397d others(8): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162109389 | |||||
chr5:162109389
|
AATATATA others(1): Show |
A | 86 | a0001c0001t0003g0071a0001c0002t0001g0001a0001c0002t0001g0009others(83): Show | 92 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.769+5390_769+5397d others(10): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162109389 | |||||
chr5:162109389
|
AATATATA others(3): Show |
A | 12 | a0001c0002t0001g0067a0001c0002t0001g0236a0001c0002t0007g0078others(9): Show | 13 | HG01169.hp2 HG01175.hp1 HG01515.hp2 others(10): Show |
intron_variant | MODIFIER | c.769+5388_769+5397d others(12): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162109389 | |||||
chr5:162109412
|
A | T | 1 | a0001c0001t0001g0244 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.769+5386A>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162109412 | ||||||
chr5:162109416
|
A | ATATTTAT others(5): Show |
3 | a0001c0002t0001g0118a0001c0002t0001g0132a0001c0002t0001g0137 | 3 | HG02723.hp1 HG03540.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.769+5393_769+5394i others(14): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162109416 | |||||
chr5:162109416
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A | ATTTATTT others(3): Show |
1 | a0001c0002t0001g0107 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.769+5391_769+5392i others(12): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162109416 | |||||
chr5:162109416
|
A | T | 1 | a0001c0001t0001g0244 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.769+5390A>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162109416 | ||||||
chr5:162109420
|
A | ATATATAT others(7): Show |
1 | a0001c0009t0004g0143 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.769+5397_769+5398i others(16): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162109420 | |||||
chr5:162109420
|
A | ATATATAT others(5): Show |
3 | a0001c0001t0004g0310a0001c0001t0004g0311a0001c0001t0018g0086 | 3 | HG02258.hp2 HG02965.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.769+5397_769+5398i others(14): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162109420 | |||||
chr5:162109420
|
A | ATATATAT others(13): Show |
2 | a0001c0001t0001g0133a0001c0001t0003g0109 | 2 | HG00438.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.769+5397_769+5398i others(22): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162109420 | |||||
chr5:162109420
|
A | ATATATAT others(3): Show |
2 | a0001c0001t0004g0309a0001c0002t0002g0006 | 3 | HG02615.hp1 HG02886.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.769+5397_769+5398i others(12): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162109420 | |||||
chr5:162109420
|
A | ATATATAT others(7): Show |
1 | a0001c0001t0003g0063 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.769+5397_769+5398i others(16): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162109420 | |||||
chr5:162109420
|
A | ATATATAT others(11): Show |
3 | a0001c0001t0003g0108a0001c0001t0016g0121a0001c0002t0003g0122 | 3 | HG00140.hp1 HG02027.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.769+5397_769+5398i others(20): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162109420 | |||||
chr5:162109420
|
A | ATATATAT others(9): Show |
10 | a0001c0001t0001g0104a0001c0001t0001g0151a0001c0001t0003g0110others(7): Show | 11 | HG01496.hp2 HG02630.hp1 HG02698.hp1 others(8): Show |
intron_variant | MODIFIER | c.769+5397_769+5398i others(18): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162109420 | |||||
chr5:162109420
|
A | ATATATAT others(13): Show |
1 | a0001c0008t0001g0247 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.769+5397_769+5398i others(22): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162109420 | |||||
chr5:162109420
|
A | ATATATTT others(7): Show |
5 | a0001c0001t0001g0127a0001c0001t0003g0106a0001c0001t0003g0125others(2): Show | 5 | HG01346.hp2 HG02602.hp1 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.769+5397_769+5398i others(16): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162109420 | |||||
chr5:162109420
|
A | ATATATTT others(11): Show |
1 | a0001c0002t0001g0211 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.769+5397_769+5398i others(20): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162109420 | |||||
chr5:162109420
|
A | ATATTTAT others(5): Show |
2 | a0001c0001t0003g0105a0001c0002t0011g0085 | 2 | HG01433.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.769+5405_769+5406i others(14): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162109420 | |||||
chr5:162109420
|
A | ATTTATTT others(7): Show |
1 | a0001c0002t0001g0117 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.769+5395_769+5396i others(16): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162109420 | |||||
chr5:162109420
|
A | T | 8 | a0001c0001t0001g0244a0001c0001t0004g0139a0001c0002t0001g0107others(5): Show | 8 | HG01192.hp1 HG02055.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.769+5394A>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162109420 | ||||||
chr5:162109424
|
T | A | 2 | a0001c0002t0005g0224a0002c0007t0002g0033 | 2 | HG02055.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.769+5398T>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162109424 | ||||||
chr5:162109466
|
C | T | 31 | a0001c0001t0001g0104a0001c0001t0001g0127a0001c0001t0001g0133others(28): Show | 32 | HG00140.hp1 HG00438.hp1 HG01192.hp1 others(29): Show |
intron_variant | MODIFIER | c.769+5440C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162109466 | ||||||
chr5:162109542
|
A | G | 2 | a0001c0004t0002g0018a0001c0004t0017g0246 | 2 | HG02647.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.769+5516A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162109542 | ||||||
chr5:162109578
|
A | G | 233 | a0001c0001t0001g0045a0001c0001t0001g0104a0001c0001t0001g0113others(230): Show | 244 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.769+5552A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162109578 | ||||||
chr5:162109594
|
G | A | 8 | a0001c0002t0001g0097a0001c0002t0001g0098a0001c0002t0001g0099others(5): Show | 9 | NA18941.hp2 NA18962.hp1 NA18969.hp2 others(6): Show |
intron_variant | MODIFIER | c.769+5568G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162109594 | ||||||
chr5:162109775
|
G | T | 1 | a0001c0001t0001g0244 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.769+5749G>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162109775 | ||||||
chr5:162109922
|
A | G | 233 | a0001c0001t0001g0045a0001c0001t0001g0104a0001c0001t0001g0113others(230): Show | 244 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.769+5896A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162109922 | ||||||
chr5:162109923
|
G | T | 2 | a0001c0003t0003g0114a0001c0003t0003g0270 | 2 | NA18945.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.769+5897G>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162109923 | ||||||
chr5:162109953
|
A | G | 1 | a0001c0001t0002g0046 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.769+5927A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162109953 | ||||||
chr5:162110077
|
C | A | 49 | a0001c0001t0001g0113a0001c0001t0001g0219a0001c0001t0002g0011others(46): Show | 51 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.769+6051C>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162110077 | ||||||
chr5:162110124
|
G | T | 232 | a0001c0001t0001g0045a0001c0001t0001g0104a0001c0001t0001g0113others(229): Show | 243 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(240): Show |
intron_variant | MODIFIER | c.769+6098G>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162110124 | ||||||
chr5:162110202
|
G | T | 1 | a0001c0001t0001g0104 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.769+6176G>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162110202 | ||||||
chr5:162110416
|
T | C | 1 | a0001c0002t0001g0070 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.769+6390T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162110416 | ||||||
chr5:162110526
|
G | A | 2 | a0001c0002t0001g0067a0001c0002t0001g0236 | 2 | HG01169.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.769+6500G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162110526 | ||||||
chr5:162110630
|
AAAC | A | 32 | a0001c0001t0001g0104a0001c0001t0001g0127a0001c0001t0001g0133others(29): Show | 33 | HG00140.hp1 HG00438.hp1 HG01346.hp2 others(30): Show |
intron_variant | MODIFIER | c.769+6631_769+6633d others(5): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162110630 | |||||
chr5:162110642
|
C | T | 9 | a0001c0001t0004g0309a0001c0001t0004g0310a0001c0001t0004g0311others(6): Show | 9 | HG00639.hp2 HG02258.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.769+6616C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162110642 | ||||||
chr5:162111042
|
G | A | 1 | a0001c0002t0002g0095 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.769+7016G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162111042 | ||||||
chr5:162111303
|
C | T | 1 | a0001c0001t0001g0244 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.769+7277C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162111303 | ||||||
chr5:162111410
|
A | C | 1 | a0001c0001t0004g0139 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.769+7384A>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162111410 | ||||||
chr5:162111423
|
C | T | 1 | a0001c0002t0003g0101 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.769+7397C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162111423 | ||||||
chr5:162111433
|
T | G | 1 | a0001c0001t0003g0242 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.769+7407T>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162111433 | ||||||
chr5:162111489
|
A | G | 1 | a0001c0001t0002g0042 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.769+7463A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162111489 | ||||||
chr5:162111514
|
G | A | 2 | a0001c0002t0002g0016a0001c0004t0002g0241 | 2 | HG01891.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.769+7488G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162111514 | ||||||
chr5:162111515
|
G | T | 1 | a0001c0001t0002g0090 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.769+7489G>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162111515 | ||||||
chr5:162111811
|
T | C | 2 | a0001c0001t0004g0256a0001c0001t0004g0257 | 2 | HG02622.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.769+7785T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162111811 | ||||||
chr5:162111897
|
A | G | 3 | a0001c0005t0003g0028a0001c0005t0003g0075a0001c0005t0015g0243 | 3 | HG01243.hp2 HG01884.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.769+7871A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162111897 | ||||||
chr5:162111924
|
A | G | 1 | a0001c0002t0007g0082 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.769+7898A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162111924 | ||||||
chr5:162112021
|
G | C | 5 | a0001c0001t0002g0010a0001c0001t0002g0055a0001c0001t0002g0064others(2): Show | 6 | HG00099.hp2 HG01106.hp1 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.769+7995G>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162112021 | ||||||
chr5:162112128
|
G | C | 203 | a0001c0001t0001g0045a0001c0001t0001g0113a0001c0001t0001g0115others(200): Show | 213 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(210): Show |
intron_variant | MODIFIER | c.769+8102G>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162112128 | ||||||
chr5:162112260
|
AT | A | 197 | a0001c0001t0001g0045a0001c0001t0001g0113a0001c0001t0001g0115others(194): Show | 207 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(204): Show |
intron_variant | MODIFIER | c.769+8245delT | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162112260 | |||||
chr5:162112331
|
G | A | 1 | a0001c0002t0001g0097 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.769+8305G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162112331 | ||||||
chr5:162112351
|
T | A | 2 | a0001c0002t0007g0078a0001c0002t0011g0077 | 2 | NA18994.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.769+8325T>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162112351 | ||||||
chr5:162112352
|
G | A | 2 | a0001c0002t0007g0078a0001c0002t0011g0077 | 2 | NA18994.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.769+8326G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162112352 | ||||||
chr5:162112381
|
C | A | 1 | a0001c0003t0003g0289 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.769+8355C>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162112381 | ||||||
chr5:162112409
|
A | AT | 61 | a0001c0001t0003g0071a0001c0002t0001g0097a0001c0002t0001g0098others(58): Show | 65 | HG00558.hp1 HG01074.hp1 HG01258.hp1 others(62): Show |
intron_variant | MODIFIER | c.769+8393dupT | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162112409 | |||||
chr5:162112409
|
AT | A | 138 | a0001c0001t0001g0045a0001c0001t0001g0113a0001c0001t0001g0115others(135): Show | 144 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(141): Show |
intron_variant | MODIFIER | c.769+8393delT | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162112409 | |||||
chr5:162112427
|
C | T | 1 | a0001c0001t0018g0086 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.769+8401C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162112427 | ||||||
chr5:162112638
|
G | A | 1 | a0001c0003t0001g0275 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.769+8612G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162112638 | ||||||
chr5:162112876
|
G | A | 1 | a0001c0001t0001g0113 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.769+8850G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162112876 | ||||||
chr5:162113001
|
G | A | 94 | a0001c0001t0001g0104a0001c0001t0001g0127a0001c0001t0001g0133others(91): Show | 99 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.769+8975G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162113001 | ||||||
chr5:162113283
|
C | G | 138 | a0001c0001t0001g0045a0001c0001t0001g0113a0001c0001t0001g0115others(135): Show | 144 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(141): Show |
intron_variant | MODIFIER | c.769+9257C>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162113283 | ||||||
chr5:162113633
|
A | G | 1 | a0001c0003t0001g0013 | 2 | NA18969.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.769+9607A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162113633 | ||||||
chr5:162113794
|
G | A | 1 | a0001c0001t0003g0167 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.769+9768G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162113794 | ||||||
chr5:162114026
|
C | A | 6 | a0001c0001t0002g0260a0001c0001t0004g0256a0001c0001t0004g0257others(3): Show | 6 | HG01109.hp1 HG02622.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.769+10000C>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162114026 | ||||||
chr5:162114029
|
T | A | 140 | a0001c0001t0001g0045a0001c0001t0001g0113a0001c0001t0001g0115others(137): Show | 146 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(143): Show |
intron_variant | MODIFIER | c.769+10003T>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162114029 | ||||||
chr5:162114135
|
A | T | 140 | a0001c0001t0001g0045a0001c0001t0001g0113a0001c0001t0001g0115others(137): Show | 146 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(143): Show |
intron_variant | MODIFIER | c.769+10109A>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162114135 | ||||||
chr5:162114192
|
C | A | 1 | a0001c0001t0004g0139 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.769+10166C>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162114192 | ||||||
chr5:162114407
|
T | A | 1 | a0001c0003t0002g0291 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.769+10381T>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162114407 | ||||||
chr5:162114494
|
A | G | 311 | a0001c0001t0001g0030a0001c0001t0001g0034a0001c0001t0001g0036others(308): Show | 327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.769+10468A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162114494 | ||||||
chr5:162114502
|
C | T | 236 | a0001c0001t0001g0045a0001c0001t0001g0104a0001c0001t0001g0113others(233): Show | 247 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.769+10476C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162114502 | ||||||
chr5:162114645
|
C | T | 2 | a0001c0001t0002g0047a0001c0001t0002g0048 | 2 | NA18964.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.769+10619C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162114645 | ||||||
chr5:162114729
|
G | T | 140 | a0001c0001t0001g0045a0001c0001t0001g0113a0001c0001t0001g0115others(137): Show | 146 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(143): Show |
intron_variant | MODIFIER | c.769+10703G>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162114729 | ||||||
chr5:162114788
|
T | C | 5 | a0001c0002t0006g0008a0001c0002t0006g0144a0001c0002t0006g0145others(2): Show | 6 | HG01884.hp2 HG02145.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.769+10762T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162114788 | ||||||
chr5:162114925
|
C | T | 158 | a0001c0001t0001g0030a0001c0001t0001g0034a0001c0001t0001g0036others(155): Show | 168 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(165): Show |
intron_variant | MODIFIER | c.769+10899C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162114925 | ||||||
chr5:162114992
|
C | T | 2 | a0001c0001t0001g0244a0001c0001t0004g0139 | 2 | HG01192.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.769+10966C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162114992 | ||||||
chr5:162115222
|
A | G | 1 | a0001c0001t0018g0086 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.769+11196A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162115222 | ||||||
chr5:162115355
|
G | A | 1 | a0001c0001t0013g0210 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.769+11329G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162115355 | ||||||
chr5:162115403
|
T | A | 2 | a0001c0002t0001g0211a0001c0008t0001g0247 | 2 | HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.769+11377T>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162115403 | ||||||
chr5:162115603
|
A | G | 31 | a0001c0001t0001g0104a0001c0001t0001g0127a0001c0001t0001g0133others(28): Show | 32 | HG00140.hp1 HG00438.hp1 HG01346.hp2 others(29): Show |
intron_variant | MODIFIER | c.769+11577A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162115603 | ||||||
chr5:162115805
|
G | A | 139 | a0001c0001t0001g0045a0001c0001t0001g0113a0001c0001t0001g0115others(136): Show | 145 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(142): Show |
intron_variant | MODIFIER | c.769+11779G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162115805 | ||||||
chr5:162115844
|
A | G | 4 | a0001c0001t0004g0017a0001c0001t0004g0250a0001c0001t0004g0251others(1): Show | 4 | HG02572.hp1 HG02818.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.769+11818A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162115844 | ||||||
chr5:162115849
|
G | A | 158 | a0001c0001t0001g0030a0001c0001t0001g0034a0001c0001t0001g0036others(155): Show | 168 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(165): Show |
intron_variant | MODIFIER | c.769+11823G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162115849 | ||||||
chr5:162115905
|
G | A | 1 | a0001c0002t0007g0078 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.769+11879G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162115905 | ||||||
chr5:162115910
|
T | C | 3 | a0001c0005t0003g0028a0001c0005t0003g0075a0001c0005t0015g0243 | 3 | HG01243.hp2 HG01884.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.769+11884T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162115910 | ||||||
chr5:162116106
|
G | A | 1 | a0001c0001t0003g0130 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.769+12080G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162116106 | ||||||
chr5:162116109
|
CAT | C | 54 | a0001c0001t0001g0127a0001c0001t0003g0071a0001c0001t0003g0181others(51): Show | 57 | HG00558.hp1 HG01074.hp1 HG01258.hp1 others(54): Show |
intron_variant | MODIFIER | c.769+12084_769+1208 others(6): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162116109 | ||||||
chr5:162116109
|
CATGT | C | 3 | a0001c0003t0001g0303a0001c0003t0003g0278a0001c0012t0003g0266 | 3 | NA18954.hp1 NA18963.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.769+12084_769+1208 others(8): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162116109 | ||||||
chr5:162116109
|
CATGTGT | C | 3 | a0001c0002t0001g0136a0001c0003t0003g0280a0001c0003t0003g0289 | 3 | HG03492.hp2 HG04184.hp2 NA18943.hp1 |
intron_variant | MODIFIER | c.769+12084_769+1208 others(10): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162116109 | ||||||
chr5:162116110
|
A | ATG | 18 | a0001c0001t0001g0113a0001c0001t0002g0209a0001c0001t0003g0167others(15): Show | 20 | HG00423.hp1 HG01069.hp1 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.769+12120_769+1212 others(6): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162116110 | |||||
chr5:162116110
|
A | ATGTG | 47 | a0001c0001t0001g0115a0001c0001t0001g0162a0001c0001t0001g0219others(44): Show | 48 | HG00423.hp2 HG00558.hp2 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.769+12118_769+1212 others(8): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162116110 | |||||
chr5:162116110
|
A | ATGTGTG | 7 | a0001c0001t0002g0021a0001c0001t0002g0022a0001c0001t0002g0027others(4): Show | 7 | HG01952.hp1 HG03225.hp2 NA18952.hp1 others(4): Show |
intron_variant | MODIFIER | c.769+12116_769+1212 others(10): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162116110 | |||||
chr5:162116110
|
A | ATGTGTGT others(1): Show |
5 | a0001c0001t0002g0025a0001c0001t0002g0194a0001c0001t0004g0250others(2): Show | 5 | HG00597.hp1 HG02809.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.769+12114_769+1212 others(12): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162116110 | |||||
chr5:162116110
|
A | G | 36 | a0001c0001t0001g0104a0001c0001t0001g0133a0001c0001t0001g0151others(33): Show | 38 | HG00140.hp1 HG00438.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.769+12084A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162116110 | ||||||
chr5:162116110
|
ATG | A | 14 | a0001c0001t0001g0034a0001c0001t0004g0309a0001c0001t0004g0310others(11): Show | 16 | HG00140.hp2 HG00639.hp2 HG00673.hp1 others(13): Show |
intron_variant | MODIFIER | c.769+12120_769+1212 others(6): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162116110 | |||||
chr5:162116110
|
ATGTG | A | 65 | a0001c0001t0001g0030a0001c0001t0001g0036a0001c0001t0001g0045others(62): Show | 70 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(67): Show |
intron_variant | MODIFIER | c.769+12118_769+1212 others(8): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162116110 | |||||
chr5:162116120
|
G | A | 30 | a0001c0001t0001g0104a0001c0001t0001g0133a0001c0001t0001g0151others(27): Show | 31 | HG00140.hp1 HG00438.hp1 HG01346.hp2 others(28): Show |
intron_variant | MODIFIER | c.769+12094G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162116120 | ||||||
chr5:162116122
|
G | A | 2 | a0001c0001t0001g0127a0001c0001t0003g0181 | 2 | HG02602.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.769+12096G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162116122 | ||||||
chr5:162116238
|
CT | C | 59 | a0001c0001t0001g0030a0001c0001t0001g0034a0001c0001t0001g0036others(56): Show | 63 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.769+12213delT | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162116238 | ||||||
chr5:162116288
|
ATATAAGT others(570): Show |
A | 1 | a0001c0001t0004g0139 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.769+12265_769+1284 others(4): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162116288 | |||||
chr5:162116290
|
A | G | 1 | a0001c0002t0006g0146 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.769+12264A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162116290 | ||||||
chr5:162116348
|
C | A | 59 | a0001c0001t0001g0030a0001c0001t0001g0034a0001c0001t0001g0036others(56): Show | 63 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.769+12322C>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162116348 | ||||||
chr5:162116445
|
CAAAAGGG others(1): Show |
C | 59 | a0001c0001t0001g0030a0001c0001t0001g0034a0001c0001t0001g0036others(56): Show | 63 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.769+12423_769+1243 others(12): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162116445 | |||||
chr5:162116565
|
T | C | 159 | a0001c0001t0001g0030a0001c0001t0001g0034a0001c0001t0001g0036others(156): Show | 169 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(166): Show |
intron_variant | MODIFIER | c.769+12539T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162116565 | ||||||
chr5:162116705
|
A | G | 62 | a0001c0001t0001g0030a0001c0001t0001g0034a0001c0001t0001g0036others(59): Show | 67 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(64): Show |
intron_variant | MODIFIER | c.769+12679A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162116705 | ||||||
chr5:162116789
|
A | G | 2 | a0001c0002t0003g0091a0001c0002t0003g0093 | 2 | NA19002.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.769+12763A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162116789 | ||||||
chr5:162116846
|
G | A | 9 | a0001c0001t0004g0309a0001c0001t0004g0310a0001c0001t0004g0311others(6): Show | 9 | HG00639.hp2 HG02258.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.769+12820G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162116846 | ||||||
chr5:162116887
|
G | C | 1 | a0001c0001t0004g0139 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.769+12861G>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162116887 | ||||||
chr5:162116933
|
A | G | 1 | a0001c0001t0003g0108 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.769+12907A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162116933 | ||||||
chr5:162116968
|
T | C | 62 | a0001c0001t0001g0030a0001c0001t0001g0034a0001c0001t0001g0036others(59): Show | 67 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(64): Show |
intron_variant | MODIFIER | c.769+12942T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162116968 | ||||||
chr5:162117013
|
A | G | 160 | a0001c0001t0001g0030a0001c0001t0001g0034a0001c0001t0001g0036others(157): Show | 170 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(167): Show |
intron_variant | MODIFIER | c.769+12987A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162117013 | ||||||
chr5:162117015
|
A | C | 226 | a0001c0001t0001g0030a0001c0001t0001g0034a0001c0001t0001g0036others(223): Show | 238 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(235): Show |
intron_variant | MODIFIER | c.769+12989A>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162117015 | ||||||
chr5:162117325
|
G | A | 206 | a0001c0001t0001g0034a0001c0001t0001g0036a0001c0001t0001g0104others(203): Show | 218 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(215): Show |
intron_variant | MODIFIER | c.769+13299G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162117325 | ||||||
chr5:162117347
|
G | A | 1 | a0001c0003t0003g0276 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.769+13321G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162117347 | ||||||
chr5:162117355
|
G | A | 2 | a0001c0002t0001g0211a0001c0008t0001g0247 | 2 | HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.769+13329G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162117355 | ||||||
chr5:162117413
|
A | G | 1 | a0001c0001t0002g0194 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.769+13387A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162117413 | ||||||
chr5:162117423
|
T | C | 1 | a0001c0001t0003g0123 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.769+13397T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162117423 | ||||||
chr5:162117453
|
A | G | 2 | a0001c0003t0001g0297a0001c0003t0001g0300 | 2 | NA18964.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.769+13427A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162117453 | ||||||
chr5:162117492
|
A | C | 1 | a0001c0002t0004g0262 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.769+13466A>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162117492 | ||||||
chr5:162117496
|
T | A | 16 | a0001c0001t0001g0115a0001c0001t0001g0162a0001c0001t0002g0260others(13): Show | 16 | HG01109.hp1 HG02572.hp1 HG02615.hp2 others(13): Show |
intron_variant | MODIFIER | c.769+13470T>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162117496 | ||||||
chr5:162117540
|
T | C | 2 | a0001c0002t0002g0016a0001c0004t0002g0241 | 2 | HG01891.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.769+13514T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162117540 | ||||||
chr5:162117665
|
A | T | 1 | a0001c0001t0002g0064 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.769+13639A>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162117665 | ||||||
chr5:162117878
|
A | G | 4 | a0001c0001t0004g0017a0001c0001t0004g0250a0001c0001t0004g0251others(1): Show | 4 | HG02572.hp1 HG02818.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.769+13852A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162117878 | ||||||
chr5:162117958
|
G | A | 1 | a0001c0002t0002g0092 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.769+13932G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162117958 | ||||||
chr5:162117959
|
C | T | 1 | a0001c0001t0004g0255 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.769+13933C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162117959 | ||||||
chr5:162118204
|
G | GGT | 3 | a0001c0001t0003g0130a0001c0001t0016g0121a0001c0001t0018g0086 | 3 | HG02027.hp2 HG02630.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.769+14211_769+1421 others(6): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162118204 | |||||
chr5:162118204
|
G | GGTGT | 5 | a0001c0001t0001g0244a0001c0001t0002g0062a0001c0001t0004g0309others(2): Show | 5 | HG02258.hp2 HG02965.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.769+14209_769+1421 others(8): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162118204 | |||||
chr5:162118204
|
G | GGTGTGTG others(3): Show |
1 | a0001c0005t0015g0243 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.769+14203_769+1421 others(14): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162118204 | |||||
chr5:162118204
|
G | GGTGTGTG others(5): Show |
2 | a0001c0005t0003g0028a0001c0005t0003g0075 | 2 | HG01243.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.769+14201_769+1421 others(16): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162118204 | |||||
chr5:162118204
|
GGT | G | 152 | a0001c0001t0001g0034a0001c0001t0001g0045a0001c0001t0001g0104others(149): Show | 160 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(157): Show |
intron_variant | MODIFIER | c.769+14211_769+1421 others(6): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162118204 | |||||
chr5:162118204
|
GGTGT | G | 44 | a0001c0001t0001g0219a0001c0001t0002g0021a0001c0001t0002g0022others(41): Show | 46 | HG00597.hp1 HG00639.hp1 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.769+14209_769+1421 others(8): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162118204 | |||||
chr5:162118245
|
T | C | 6 | a0001c0002t0002g0006a0001c0002t0004g0262a0001c0005t0003g0028others(3): Show | 7 | HG01243.hp2 HG01884.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.769+14219T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162118245 | ||||||
chr5:162118755
|
G | A | 3 | a0001c0001t0010g0258a0001c0001t0010g0259a0001c0001t0010g0261 | 3 | HG03471.hp1 NA19030.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.769+14729G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162118755 | ||||||
chr5:162118789
|
A | G | 3 | a0001c0005t0003g0028a0001c0005t0003g0075a0001c0005t0015g0243 | 3 | HG01243.hp2 HG01884.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.769+14763A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162118789 | ||||||
chr5:162118965
|
C | T | 1 | a0001c0001t0001g0244 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.769+14939C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162118965 | ||||||
chr5:162118987
|
T | C | 1 | a0001c0001t0002g0208 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.769+14961T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162118987 | ||||||
chr5:162119189
|
C | T | 1 | a0001c0001t0003g0181 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.769+15163C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162119189 | ||||||
chr5:162119367
|
A | T | 1 | a0001c0001t0004g0139 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.769+15341A>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162119367 | ||||||
chr5:162119566
|
T | C | 25 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0031others(22): Show | 27 | HG00438.hp2 HG02135.hp1 HG02155.hp1 others(24): Show |
intron_variant | MODIFIER | c.769+15540T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162119566 | ||||||
chr5:162119815
|
T | C | 88 | a0001c0001t0001g0115a0001c0001t0001g0162a0001c0001t0001g0244others(85): Show | 89 | HG00140.hp1 HG00438.hp1 HG00621.hp1 others(86): Show |
intron_variant | MODIFIER | c.769+15789T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162119815 | ||||||
chr5:162119980
|
C | T | 1 | a0001c0001t0002g0184 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.769+15954C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162119980 | ||||||
chr5:162120046
|
G | A | 1 | a0001c0002t0004g0262 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.769+16020G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162120046 | ||||||
chr5:162120080
|
G | A | 1 | a0001c0002t0001g0192 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.769+16054G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162120080 | ||||||
chr5:162120234
|
A | T | 1 | a0001c0001t0004g0139 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.769+16208A>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162120234 | ||||||
chr5:162120376
|
C | T | 1 | a0001c0004t0002g0149 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.769+16350C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162120376 | ||||||
chr5:162120594
|
C | T | 1 | a0001c0009t0004g0143 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.769+16568C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162120594 | ||||||
chr5:162120598
|
A | G | 1 | a0001c0001t0003g0203 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.769+16572A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162120598 | ||||||
chr5:162120696
|
T | C | 1 | a0001c0001t0004g0139 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.769+16670T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162120696 | ||||||
chr5:162120704
|
C | A | 18 | a0001c0001t0001g0115a0001c0001t0001g0162a0001c0001t0001g0244others(15): Show | 19 | HG01069.hp1 HG01071.hp1 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.769+16678C>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162120704 | ||||||
chr5:162120917
|
T | C | 1 | a0001c0001t0008g0044 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.769+16891T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162120917 | ||||||
chr5:162121078
|
G | A | 3 | a0001c0005t0003g0028a0001c0005t0003g0075a0001c0005t0015g0243 | 3 | HG01243.hp2 HG01884.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.769+17052G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162121078 | ||||||
chr5:162121137
|
G | C | 2 | a0001c0001t0004g0139a0001c0002t0004g0262 | 2 | HG01192.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.769+17111G>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162121137 | ||||||
chr5:162121773
|
G | A | 1 | a0001c0002t0006g0145 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.769+17747G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162121773 | ||||||
chr5:162122279
|
A | G | 16 | a0001c0001t0001g0115a0001c0001t0001g0162a0001c0001t0002g0260others(13): Show | 16 | HG01109.hp1 HG02572.hp1 HG02615.hp2 others(13): Show |
intron_variant | MODIFIER | c.769+18253A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162122279 | ||||||
chr5:162122310
|
C | T | 1 | a0001c0001t0002g0011 | 2 | NA18968.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.769+18284C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162122310 | ||||||
chr5:162122464
|
T | C | 6 | a0001c0002t0001g0174a0001c0002t0001g0176a0001c0002t0001g0177others(3): Show | 7 | HG01071.hp2 HG01074.hp2 HG01106.hp2 others(4): Show |
intron_variant | MODIFIER | c.769+18438T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162122464 | ||||||
chr5:162122606
|
C | A | 1 | a0001c0002t0004g0262 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.769+18580C>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162122606 | ||||||
chr5:162122757
|
G | A | 1 | a0001c0002t0004g0262 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.769+18731G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162122757 | ||||||
chr5:162122888
|
A | T | 1 | a0001c0001t0018g0086 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.769+18862A>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162122888 | ||||||
chr5:162123177
|
A | G | 1 | a0001c0001t0009g0216 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.770-18987A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162123177 | ||||||
chr5:162123232
|
G | C | 22 | a0001c0001t0003g0063a0001c0001t0003g0105a0001c0001t0003g0126others(19): Show | 23 | HG00140.hp1 HG01074.hp1 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.770-18932G>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162123232 | ||||||
chr5:162123379
|
A | ATGATTAT others(3): Show |
70 | a0001c0001t0003g0024a0001c0001t0003g0054a0001c0001t0003g0060others(67): Show | 71 | HG00140.hp1 HG00438.hp1 HG00621.hp1 others(68): Show |
intron_variant | MODIFIER | c.770-18784_770-1878 others(14): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162123379 | |||||
chr5:162123397
|
C | T | 1 | a0001c0002t0001g0233 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.770-18767C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162123397 | ||||||
chr5:162123420
|
A | G | 22 | a0001c0001t0003g0063a0001c0001t0003g0105a0001c0001t0003g0126others(19): Show | 23 | HG00140.hp1 HG01074.hp1 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.770-18744A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162123420 | ||||||
chr5:162123551
|
G | C | 1 | a0001c0002t0004g0262 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.770-18613G>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162123551 | ||||||
chr5:162123674
|
G | A | 1 | a0001c0002t0007g0074 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.770-18490G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162123674 | ||||||
chr5:162124185
|
C | T | 3 | a0001c0001t0001g0113a0001c0002t0001g0103a0001c0002t0001g0142 | 3 | HG01169.hp1 HG02451.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.770-17979C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162124185 | ||||||
chr5:162124364
|
A | G | 1 | a0001c0006t0012g0005 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.770-17800A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162124364 | ||||||
chr5:162124496
|
GA | G | 3 | a0001c0002t0001g0051a0001c0002t0001g0088a0001c0002t0001g0089 | 3 | HG00423.hp1 NA18747.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.770-17663delA | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162124496 | |||||
chr5:162124764
|
G | A | 1 | a0001c0002t0004g0262 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.770-17400G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162124764 | ||||||
chr5:162124774
|
C | T | 1 | a0001c0001t0002g0165 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.770-17390C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162124774 | ||||||
chr5:162124958
|
A | ATG | 65 | a0001c0001t0001g0030a0001c0001t0001g0045a0001c0001t0001g0152others(62): Show | 68 | HG00639.hp2 HG00673.hp1 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.770-17170_770-1716 others(6): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162124958 | |||||
chr5:162124958
|
A | ATGTG | 17 | a0001c0001t0001g0133a0001c0001t0001g0151a0001c0001t0003g0181others(14): Show | 18 | HG01192.hp1 HG02055.hp2 HG02071.hp2 others(15): Show |
intron_variant | MODIFIER | c.770-17172_770-1716 others(8): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162124958 | |||||
chr5:162124958
|
A | ATGTGTG | 16 | a0001c0001t0001g0115a0001c0001t0001g0162a0001c0001t0003g0063others(13): Show | 17 | HG00140.hp1 HG01074.hp1 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.770-17174_770-1716 others(10): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162124958 | |||||
chr5:162124958
|
A | ATGTGTGT others(1): Show |
3 | a0001c0001t0004g0251a0001c0005t0003g0075a0001c0009t0004g0143 | 3 | HG01884.hp1 HG02818.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.770-17176_770-1716 others(12): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162124958 | |||||
chr5:162124958
|
A | ATGTGTGT others(3): Show |
5 | a0001c0001t0003g0130a0001c0002t0001g0157a0001c0002t0001g0227others(2): Show | 5 | HG01081.hp1 HG01081.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.770-17178_770-1716 others(14): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162124958 | |||||
chr5:162124958
|
ATG | A | 32 | a0001c0001t0002g0047a0001c0001t0002g0048a0001c0001t0002g0065others(29): Show | 35 | HG00423.hp1 HG00438.hp2 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.770-17170_770-1716 others(6): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162124958 | |||||
chr5:162124958
|
ATGTG | A | 71 | a0001c0001t0001g0113a0001c0001t0002g0002a0001c0001t0002g0003others(68): Show | 76 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.770-17172_770-1716 others(8): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162124958 | |||||
chr5:162125161
|
A | G | 16 | a0001c0001t0001g0115a0001c0001t0001g0162a0001c0001t0002g0260others(13): Show | 16 | HG01109.hp1 HG02572.hp1 HG02615.hp2 others(13): Show |
intron_variant | MODIFIER | c.770-17003A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162125161 | ||||||
chr5:162125207
|
T | A | 1 | a0001c0002t0005g0226 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.770-16957T>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162125207 | ||||||
chr5:162125219
|
C | T | 1 | a0001c0001t0002g0159 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.770-16945C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162125219 | ||||||
chr5:162125311
|
T | C | 2 | a0001c0002t0002g0016a0001c0004t0002g0241 | 2 | HG01891.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.770-16853T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162125311 | ||||||
chr5:162125362
|
C | T | 1 | a0001c0003t0003g0277 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.770-16802C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162125362 | ||||||
chr5:162125401
|
CTGGATTC others(130): Show |
C | 6 | a0001c0001t0002g0029a0001c0001t0002g0160a0001c0001t0002g0161others(3): Show | 6 | HG02145.hp2 HG02717.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.770-16761_770-1662 others(4): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162125401 | |||||
chr5:162125405
|
A | T | 12 | a0001c0001t0003g0063a0001c0001t0003g0105a0001c0001t0003g0126others(9): Show | 13 | HG00140.hp1 HG01074.hp1 HG01346.hp2 others(10): Show |
intron_variant | MODIFIER | c.770-16759A>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162125405 | ||||||
chr5:162125622
|
G | T | 1 | a0001c0001t0001g0244 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.770-16542G>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162125622 | ||||||
chr5:162125710
|
A | G | 4 | a0001c0001t0004g0139a0001c0005t0003g0028a0001c0005t0003g0075others(1): Show | 4 | HG01192.hp1 HG01243.hp2 HG01884.hp1 others(1): Show |
intron_variant | MODIFIER | c.770-16454A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162125710 | ||||||
chr5:162125833
|
G | T | 12 | a0001c0002t0005g0221a0001c0002t0005g0223a0001c0002t0005g0224others(9): Show | 12 | HG00639.hp2 HG01981.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.770-16331G>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162125833 | ||||||
chr5:162125941
|
T | C | 4 | a0001c0001t0004g0139a0001c0005t0003g0028a0001c0005t0003g0075others(1): Show | 4 | HG01192.hp1 HG01243.hp2 HG01884.hp1 others(1): Show |
intron_variant | MODIFIER | c.770-16223T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162125941 | ||||||
chr5:162126064
|
A | T | 1 | a0001c0001t0004g0254 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.770-16100A>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162126064 | ||||||
chr5:162126372
|
T | C | 3 | a0001c0001t0008g0044a0001c0001t0008g0050a0001c0001t0008g0053 | 3 | NA18954.hp2 NA18969.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.770-15792T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162126372 | ||||||
chr5:162126447
|
T | C | 3 | a0001c0005t0003g0028a0001c0005t0003g0075a0001c0005t0015g0243 | 3 | HG01243.hp2 HG01884.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.770-15717T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162126447 | ||||||
chr5:162126516
|
T | C | 3 | a0001c0005t0003g0028a0001c0005t0003g0075a0001c0005t0015g0243 | 3 | HG01243.hp2 HG01884.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.770-15648T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162126516 | ||||||
chr5:162127138
|
T | A | 6 | a0001c0001t0003g0167a0001c0001t0003g0169a0001c0001t0003g0170others(3): Show | 6 | HG02080.hp1 NA18942.hp1 NA18948.hp1 others(3): Show |
intron_variant | MODIFIER | c.770-15026T>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162127138 | ||||||
chr5:162127180
|
T | A | 1 | a0001c0003t0001g0304 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.770-14984T>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162127180 | ||||||
chr5:162127276
|
T | C | 3 | a0001c0005t0003g0028a0001c0005t0003g0075a0001c0005t0015g0243 | 3 | HG01243.hp2 HG01884.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.770-14888T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162127276 | ||||||
chr5:162127376
|
T | C | 12 | a0001c0001t0001g0127a0001c0002t0001g0001a0001c0002t0001g0035others(9): Show | 15 | HG00099.hp1 HG00140.hp2 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.770-14788T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162127376 | ||||||
chr5:162127394
|
A | T | 46 | a0001c0001t0003g0024a0001c0001t0003g0054a0001c0001t0003g0060others(43): Show | 46 | HG00438.hp1 HG00621.hp1 HG01496.hp1 others(43): Show |
intron_variant | MODIFIER | c.770-14770A>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162127394 | ||||||
chr5:162127399
|
T | C | 16 | a0001c0001t0003g0063a0001c0001t0003g0105a0001c0001t0003g0126others(13): Show | 17 | HG00140.hp1 HG01074.hp1 HG01346.hp2 others(14): Show |
intron_variant | MODIFIER | c.770-14765T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162127399 | ||||||
chr5:162127656
|
G | A | 2 | a0001c0003t0001g0284a0001c0003t0001g0299 | 2 | NA18959.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.770-14508G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162127656 | ||||||
chr5:162127657
|
T | C | 1 | a0001c0010t0003g0112 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.770-14507T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162127657 | ||||||
chr5:162127675
|
G | A | 1 | a0001c0001t0004g0139 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.770-14489G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162127675 | ||||||
chr5:162127749
|
T | C | 1 | a0001c0001t0002g0090 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.770-14415T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162127749 | ||||||
chr5:162127827
|
G | C | 4 | a0001c0001t0004g0139a0001c0005t0003g0028a0001c0005t0003g0075others(1): Show | 4 | HG01192.hp1 HG01243.hp2 HG01884.hp1 others(1): Show |
intron_variant | MODIFIER | c.770-14337G>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162127827 | ||||||
chr5:162127913
|
C | T | 3 | a0001c0005t0003g0028a0001c0005t0003g0075a0001c0005t0015g0243 | 3 | HG01243.hp2 HG01884.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.770-14251C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162127913 | ||||||
chr5:162127997
|
C | T | 2 | a0001c0002t0002g0095a0001c0002t0002g0096 | 2 | HG00673.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.770-14167C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162127997 | ||||||
chr5:162128007
|
A | G | 7 | a0001c0001t0001g0034a0001c0001t0001g0104a0001c0002t0001g0051others(4): Show | 7 | HG00423.hp1 HG00735.hp2 HG01069.hp2 others(4): Show |
intron_variant | MODIFIER | c.770-14157A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162128007 | ||||||
chr5:162128192
|
C | T | 19 | a0001c0001t0003g0063a0001c0001t0003g0105a0001c0001t0003g0126others(16): Show | 20 | HG00140.hp1 HG01074.hp1 HG01346.hp2 others(17): Show |
intron_variant | MODIFIER | c.770-13972C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162128192 | ||||||
chr5:162128285
|
C | A | 1 | a0001c0001t0002g0056 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.770-13879C>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162128285 | ||||||
chr5:162128436
|
A | G | 1 | a0001c0003t0003g0276 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.770-13728A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162128436 | ||||||
chr5:162128481
|
C | G | 1 | a0001c0002t0001g0236 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.770-13683C>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162128481 | ||||||
chr5:162128567
|
A | G | 1 | a0001c0002t0001g0211 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.770-13597A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162128567 | ||||||
chr5:162128617
|
C | G | 16 | a0001c0001t0003g0063a0001c0001t0003g0105a0001c0001t0003g0126others(13): Show | 17 | HG00140.hp1 HG01074.hp1 HG01346.hp2 others(14): Show |
intron_variant | MODIFIER | c.770-13547C>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162128617 | ||||||
chr5:162128668
|
C | A | 1 | a0001c0002t0004g0262 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.770-13496C>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162128668 | ||||||
chr5:162128833
|
A | G | 3 | a0001c0005t0003g0028a0001c0005t0003g0075a0001c0005t0015g0243 | 3 | HG01243.hp2 HG01884.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.770-13331A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162128833 | ||||||
chr5:162129052
|
G | A | 1 | a0001c0002t0004g0262 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.770-13112G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162129052 | ||||||
chr5:162129219
|
A | G | 16 | a0001c0001t0001g0115a0001c0001t0001g0162a0001c0001t0002g0260others(13): Show | 16 | HG01109.hp1 HG02572.hp1 HG02615.hp2 others(13): Show |
intron_variant | MODIFIER | c.770-12945A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162129219 | ||||||
chr5:162129611
|
T | C | 1 | a0001c0003t0002g0269 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.770-12553T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162129611 | ||||||
chr5:162129709
|
G | T | 1 | a0001c0002t0001g0094 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.770-12455G>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162129709 | ||||||
chr5:162129891
|
A | C | 2 | a0001c0001t0001g0244a0001c0006t0012g0005 | 3 | HG01069.hp1 HG01071.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.770-12273A>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162129891 | ||||||
chr5:162129988
|
G | T | 1 | a0001c0001t0002g0161 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.770-12176G>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162129988 | ||||||
chr5:162130232
|
G | A | 1 | a0001c0003t0002g0296 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.770-11932G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162130232 | ||||||
chr5:162130450
|
C | T | 1 | a0001c0003t0003g0276 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.770-11714C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162130450 | ||||||
chr5:162130471
|
A | G | 15 | a0001c0001t0003g0063a0001c0001t0003g0105a0001c0001t0003g0126others(12): Show | 16 | HG00140.hp1 HG01074.hp1 HG01346.hp2 others(13): Show |
intron_variant | MODIFIER | c.770-11693A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162130471 | ||||||
chr5:162130733
|
T | C | 4 | a0001c0001t0004g0139a0001c0005t0003g0028a0001c0005t0003g0075others(1): Show | 4 | HG01192.hp1 HG01243.hp2 HG01884.hp1 others(1): Show |
intron_variant | MODIFIER | c.770-11431T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162130733 | ||||||
chr5:162130734
|
G | A | 3 | a0001c0005t0003g0028a0001c0005t0003g0075a0001c0005t0015g0243 | 3 | HG01243.hp2 HG01884.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.770-11430G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162130734 | ||||||
chr5:162130882
|
C | T | 1 | a0001c0001t0004g0139 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.770-11282C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162130882 | ||||||
chr5:162130915
|
C | G | 3 | a0001c0001t0002g0010a0001c0001t0002g0055a0001c0001t0002g0202 | 4 | HG01106.hp1 HG01346.hp1 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.770-11249C>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162130915 | ||||||
chr5:162130947
|
A | C | 19 | a0001c0001t0003g0063a0001c0001t0003g0105a0001c0001t0003g0126others(16): Show | 20 | HG00140.hp1 HG01074.hp1 HG01346.hp2 others(17): Show |
intron_variant | MODIFIER | c.770-11217A>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162130947 | ||||||
chr5:162131058
|
A | G | 1 | a0001c0001t0004g0250 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.770-11106A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162131058 | ||||||
chr5:162131679
|
T | C | 2 | a0001c0002t0001g0020a0001c0002t0001g0116 | 2 | HG03130.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.770-10485T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162131679 | ||||||
chr5:162131841
|
CTTGGATT others(382): Show |
C | 2 | a0001c0001t0003g0105a0001c0001t0003g0126 | 2 | HG01346.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.770-10321_770-9933 others(3): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162131841 | |||||
chr5:162131904
|
A | G | 1 | a0001c0001t0004g0139 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.770-10260A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162131904 | ||||||
chr5:162132086
|
T | C | 3 | a0001c0002t0001g0051a0001c0002t0001g0088a0001c0002t0001g0089 | 3 | HG00423.hp1 NA18747.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.770-10078T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162132086 | ||||||
chr5:162132235
|
G | T | 2 | a0001c0001t0003g0105a0001c0001t0003g0126 | 2 | HG01346.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.770-9929G>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162132235 | ||||||
chr5:162132236
|
T | A | 2 | a0001c0001t0003g0105a0001c0001t0003g0126 | 2 | HG01346.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.770-9928T>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162132236 | ||||||
chr5:162132352
|
A | G | 2 | a0001c0003t0001g0292a0001c0003t0001g0295 | 2 | NA18979.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.770-9812A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162132352 | ||||||
chr5:162132396
|
C | T | 1 | a0001c0002t0001g0089 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.770-9768C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162132396 | ||||||
chr5:162132549
|
G | A | 6 | a0001c0001t0002g0163a0001c0001t0002g0164a0001c0001t0002g0165others(3): Show | 7 | HG00639.hp1 HG02109.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.770-9615G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162132549 | ||||||
chr5:162132869
|
C | T | 1 | a0001c0001t0003g0054 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.770-9295C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162132869 | ||||||
chr5:162132875
|
A | T | 1 | a0001c0011t0003g0272 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.770-9289A>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162132875 | ||||||
chr5:162133126
|
C | G | 42 | a0001c0001t0001g0115a0001c0001t0001g0162a0001c0001t0001g0244others(39): Show | 44 | HG00140.hp1 HG01069.hp1 HG01071.hp1 others(41): Show |
intron_variant | MODIFIER | c.770-9038C>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162133126 | ||||||
chr5:162133212
|
G | A | 1 | a0001c0002t0002g0006 | 2 | HG02615.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.770-8952G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162133212 | ||||||
chr5:162133218
|
C | A | 1 | a0001c0001t0002g0185 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.770-8946C>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162133218 | ||||||
chr5:162133256
|
T | C | 47 | a0001c0001t0003g0024a0001c0001t0003g0054a0001c0001t0003g0060others(44): Show | 47 | HG00438.hp1 HG00621.hp1 HG01496.hp1 others(44): Show |
intron_variant | MODIFIER | c.770-8908T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162133256 | ||||||
chr5:162133260
|
C | T | 16 | a0001c0001t0001g0115a0001c0001t0001g0162a0001c0001t0002g0260others(13): Show | 16 | HG01109.hp1 HG02572.hp1 HG02615.hp2 others(13): Show |
intron_variant | MODIFIER | c.770-8904C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162133260 | ||||||
chr5:162133261
|
G | A | 2 | a0001c0003t0003g0301a0001c0003t0003g0305 | 2 | HG01074.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.770-8903G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162133261 | ||||||
chr5:162133283
|
C | T | 13 | a0001c0001t0001g0127a0001c0002t0001g0001a0001c0002t0001g0035others(10): Show | 16 | HG00099.hp1 HG00140.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.770-8881C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162133283 | ||||||
chr5:162133451
|
A | T | 1 | a0001c0001t0001g0036 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.770-8713A>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162133451 | ||||||
chr5:162133463
|
T | C | 1 | a0001c0001t0002g0213 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.770-8701T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162133463 | ||||||
chr5:162133512
|
G | C | 22 | a0001c0001t0002g0021a0001c0001t0002g0022a0001c0001t0002g0023others(19): Show | 22 | HG00558.hp2 HG00597.hp1 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.770-8652G>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162133512 | ||||||
chr5:162133529
|
C | T | 1 | a0001c0001t0004g0139 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.770-8635C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162133529 | ||||||
chr5:162133539
|
A | G | 1 | a0001c0001t0003g0203 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.770-8625A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162133539 | ||||||
chr5:162133784
|
G | T | 1 | a0001c0006t0012g0005 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.770-8380G>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162133784 | ||||||
chr5:162133972
|
A | G | 1 | a0001c0001t0003g0126 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.770-8192A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162133972 | ||||||
chr5:162134090
|
TTTTG | T | 7 | a0001c0001t0003g0060a0001c0001t0003g0061a0001c0002t0011g0077others(4): Show | 7 | NA18944.hp1 NA18963.hp2 NA18968.hp2 others(4): Show |
intron_variant | MODIFIER | c.770-8066_770-8063d others(6): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162134090 | |||||
chr5:162134109
|
A | T | 1 | a0001c0001t0003g0124 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.770-8055A>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162134109 | ||||||
chr5:162134161
|
CAGA | C | 22 | a0001c0001t0002g0021a0001c0001t0002g0022a0001c0001t0002g0023others(19): Show | 22 | HG00558.hp2 HG00597.hp1 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.770-8000_770-7998d others(5): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162134161 | |||||
chr5:162134166
|
G | A | 1 | a0001c0003t0001g0306 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.770-7998G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162134166 | ||||||
chr5:162134320
|
T | A | 1 | a0001c0001t0002g0164 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.770-7844T>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162134320 | ||||||
chr5:162134330
|
ATACT | A | 18 | a0001c0001t0003g0063a0001c0001t0003g0105a0001c0001t0003g0126others(15): Show | 19 | HG00140.hp1 HG01074.hp1 HG01346.hp2 others(16): Show |
intron_variant | MODIFIER | c.770-7831_770-7828d others(6): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162134330 | |||||
chr5:162134333
|
C | T | 122 | a0001c0001t0001g0115a0001c0001t0001g0162a0001c0001t0001g0244others(119): Show | 129 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(126): Show |
intron_variant | MODIFIER | c.770-7831C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162134333 | ||||||
chr5:162134365
|
C | G | 1 | a0001c0001t0004g0139 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.770-7799C>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162134365 | ||||||
chr5:162134673
|
A | T | 2 | a0001c0002t0001g0211a0001c0008t0001g0247 | 2 | HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.770-7491A>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162134673 | ||||||
chr5:162134797
|
G | T | 174 | a0001c0001t0001g0030a0001c0001t0001g0034a0001c0001t0001g0036others(171): Show | 184 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.770-7367G>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162134797 | ||||||
chr5:162134895
|
C | T | 4 | a0001c0001t0002g0029a0001c0001t0002g0185a0001c0001t0002g0204others(1): Show | 4 | HG02145.hp2 HG02717.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.770-7269C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162134895 | ||||||
chr5:162134998
|
C | T | 60 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(57): Show | 65 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.770-7166C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162134998 | ||||||
chr5:162135014
|
G | A | 1 | a0001c0002t0013g0131 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.770-7150G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162135014 | ||||||
chr5:162135025
|
A | G | 1 | a0001c0003t0001g0294 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.770-7139A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162135025 | ||||||
chr5:162135462
|
G | T | 1 | a0001c0001t0003g0167 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.770-6702G>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162135462 | ||||||
chr5:162135803
|
G | A | 3 | a0001c0005t0003g0028a0001c0005t0003g0075a0001c0005t0015g0243 | 3 | HG01243.hp2 HG01884.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.770-6361G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162135803 | ||||||
chr5:162135833
|
A | G | 6 | a0001c0001t0001g0030a0001c0001t0001g0036a0001c0002t0001g0067others(3): Show | 6 | HG01169.hp2 HG01175.hp1 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.770-6331A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162135833 | ||||||
chr5:162135854
|
A | T | 1 | a0001c0001t0018g0086 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.770-6310A>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162135854 | ||||||
chr5:162135881
|
A | AAAAAC | 14 | a0001c0001t0001g0115a0001c0001t0001g0162a0001c0001t0004g0017others(11): Show | 14 | HG02572.hp1 HG02615.hp2 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.770-6265_770-6261d others(7): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162135881 | |||||
chr5:162135974
|
G | T | 3 | a0001c0005t0003g0028a0001c0005t0003g0075a0001c0005t0015g0243 | 3 | HG01243.hp2 HG01884.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.770-6190G>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162135974 | ||||||
chr5:162136180
|
C | T | 2 | a0001c0002t0001g0107a0001c0002t0004g0262 | 2 | HG02055.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.770-5984C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162136180 | ||||||
chr5:162136275
|
A | G | 1 | a0001c0002t0004g0262 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.770-5889A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162136275 | ||||||
chr5:162136651
|
A | G | 2 | a0001c0001t0001g0115a0001c0001t0001g0162 | 2 | HG02647.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.770-5513A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162136651 | ||||||
chr5:162136743
|
G | A | 1 | a0001c0001t0002g0220 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.770-5421G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162136743 | ||||||
chr5:162136819
|
T | G | 1 | a0001c0002t0003g0128 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.770-5345T>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162136819 | ||||||
chr5:162136838
|
T | C | 1 | a0001c0001t0001g0030 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.770-5326T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162136838 | ||||||
chr5:162137178
|
G | A | 1 | a0001c0001t0002g0194 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.770-4986G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162137178 | ||||||
chr5:162137298
|
A | G | 1 | a0001c0001t0002g0245 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.770-4866A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162137298 | ||||||
chr5:162137440
|
A | C | 309 | a0001c0001t0001g0030a0001c0001t0001g0034a0001c0001t0001g0036others(306): Show | 325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.770-4724A>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162137440 | ||||||
chr5:162137462
|
T | C | 3 | a0001c0005t0003g0028a0001c0005t0003g0075a0001c0005t0015g0243 | 3 | HG01243.hp2 HG01884.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.770-4702T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162137462 | ||||||
chr5:162137475
|
A | G | 208 | a0001c0001t0001g0115a0001c0001t0001g0162a0001c0001t0001g0244others(205): Show | 216 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(213): Show |
intron_variant | MODIFIER | c.770-4689A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162137475 | ||||||
chr5:162137854
|
G | T | 1 | a0001c0002t0003g0007 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.770-4310G>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162137854 | ||||||
chr5:162137960
|
A | G | 1 | a0001c0001t0002g0041 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.770-4204A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162137960 | ||||||
chr5:162138049
|
C | T | 3 | a0001c0005t0003g0028a0001c0005t0003g0075a0001c0005t0015g0243 | 3 | HG01243.hp2 HG01884.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.770-4115C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162138049 | ||||||
chr5:162138134
|
A | T | 3 | a0001c0005t0003g0028a0001c0005t0003g0075a0001c0005t0015g0243 | 3 | HG01243.hp2 HG01884.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.770-4030A>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162138134 | ||||||
chr5:162138238
|
G | T | 1 | a0001c0001t0004g0139 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.770-3926G>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162138238 | ||||||
chr5:162138704
|
G | A | 15 | a0001c0001t0003g0063a0001c0001t0003g0105a0001c0001t0003g0126others(12): Show | 16 | HG00140.hp1 HG01074.hp1 HG01346.hp2 others(13): Show |
intron_variant | MODIFIER | c.770-3460G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162138704 | ||||||
chr5:162138723
|
G | C | 1 | a0001c0004t0017g0246 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.770-3441G>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162138723 | ||||||
chr5:162138804
|
C | T | 1 | a0001c0001t0018g0086 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.770-3360C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162138804 | ||||||
chr5:162138806
|
A | C | 1 | a0001c0001t0004g0139 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.770-3358A>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162138806 | ||||||
chr5:162138886
|
G | A | 1 | a0001c0003t0002g0286 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.770-3278G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162138886 | ||||||
chr5:162138986
|
C | T | 3 | a0001c0005t0003g0028a0001c0005t0003g0075a0001c0005t0015g0243 | 3 | HG01243.hp2 HG01884.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.770-3178C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162138986 | ||||||
chr5:162139009
|
C | T | 1 | a0001c0002t0002g0186 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.770-3155C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162139009 | ||||||
chr5:162139011
|
T | TA | 45 | a0001c0001t0003g0024a0001c0001t0003g0054a0001c0001t0003g0060others(42): Show | 45 | HG00438.hp1 HG00621.hp1 HG01496.hp1 others(42): Show |
intron_variant | MODIFIER | c.770-3142dupA | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162139011 | |||||
chr5:162139560
|
C | A | 4 | a0001c0001t0004g0139a0001c0005t0003g0028a0001c0005t0003g0075others(1): Show | 4 | HG01192.hp1 HG01243.hp2 HG01884.hp1 others(1): Show |
intron_variant | MODIFIER | c.770-2604C>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162139560 | ||||||
chr5:162140159
|
A | G | 1 | a0001c0002t0001g0211 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.770-2005A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162140159 | ||||||
chr5:162140161
|
C | T | 2 | a0001c0001t0002g0064a0001c0001t0002g0072 | 2 | HG00099.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.770-2003C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162140161 | ||||||
chr5:162140583
|
T | G | 1 | a0001c0002t0007g0084 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.770-1581T>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162140583 | ||||||
chr5:162140623
|
GAATTTAA others(1): Show |
G | 4 | a0001c0001t0002g0029a0001c0001t0002g0185a0001c0001t0002g0204others(1): Show | 4 | HG02145.hp2 HG02717.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.770-1540_770-1533d others(10): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162140623 | ||||||
chr5:162140898
|
G | A | 1 | a0001c0001t0004g0139 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.770-1266G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162140898 | ||||||
chr5:162141061
|
G | C | 2 | a0001c0003t0001g0297a0001c0003t0001g0300 | 2 | NA18964.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.770-1103G>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162141061 | ||||||
chr5:162141068
|
A | G | 4 | a0001c0001t0004g0139a0001c0005t0003g0028a0001c0005t0003g0075others(1): Show | 4 | HG01192.hp1 HG01243.hp2 HG01884.hp1 others(1): Show |
intron_variant | MODIFIER | c.770-1096A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162141068 | ||||||
chr5:162141105
|
C | T | 26 | a0001c0001t0002g0004a0001c0001t0002g0011a0001c0001t0002g0037others(23): Show | 28 | HG00423.hp2 HG00597.hp2 HG00673.hp2 others(25): Show |
intron_variant | MODIFIER | c.770-1059C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162141105 | ||||||
chr5:162141185
|
C | T | 2 | a0001c0004t0017g0246a0001c0009t0004g0143 | 2 | HG02647.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.770-979C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162141185 | ||||||
chr5:162141239
|
G | A | 3 | a0001c0005t0003g0028a0001c0005t0003g0075a0001c0005t0015g0243 | 3 | HG01243.hp2 HG01884.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.770-925G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162141239 | ||||||
chr5:162141279
|
C | T | 45 | a0001c0001t0003g0024a0001c0001t0003g0054a0001c0001t0003g0060others(42): Show | 45 | HG00438.hp1 HG00621.hp1 HG01496.hp1 others(42): Show |
intron_variant | MODIFIER | c.770-885C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162141279 | ||||||
chr5:162141284
|
T | G | 69 | a0001c0001t0003g0024a0001c0001t0003g0054a0001c0001t0003g0060others(66): Show | 70 | HG00140.hp1 HG00438.hp1 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.770-880T>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162141284 | ||||||
chr5:162141487
|
C | G | 2 | a0001c0001t0002g0039a0001c0001t0002g0040 | 2 | NA19010.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.770-677C>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162141487 | ||||||
chr5:162141637
|
T | C | 12 | a0001c0001t0001g0127a0001c0002t0001g0001a0001c0002t0001g0035others(9): Show | 15 | HG00099.hp1 HG00140.hp2 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.770-527T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162141637 | ||||||
chr5:162141806
|
C | T | 3 | a0001c0003t0001g0275a0001c0003t0001g0285a0001c0003t0001g0287 | 3 | HG02683.hp2 HG03710.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.770-358C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162141806 | ||||||
chr5:162141831
|
T | C | 1 | a0001c0002t0004g0262 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.770-333T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162141831 | ||||||
chr5:162141934
|
A | T | 40 | a0001c0002t0001g0070a0001c0002t0001g0097a0001c0002t0001g0098others(37): Show | 43 | HG00558.hp1 HG00621.hp2 HG01258.hp1 others(40): Show |
intron_variant | MODIFIER | c.770-230A>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162141934 | ||||||
chr5:162141941
|
C | A | 1 | a0001c0001t0002g0193 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.770-223C>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162141941 | ||||||
chr5:162142083
|
A | G | 23 | a0001c0001t0003g0063a0001c0001t0003g0105a0001c0001t0003g0126others(20): Show | 24 | HG00140.hp1 HG01074.hp1 HG01192.hp1 others(21): Show |
intron_variant | MODIFIER | c.770-81A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162142083 | ||||||
chr5:162142336
|
G | A | 1 | a0001c0001t0002g0052 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.922+20G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162142336 | ||||||
chr5:162142424
|
A | C | 12 | a0001c0001t0001g0127a0001c0002t0001g0001a0001c0002t0001g0035others(9): Show | 15 | HG00099.hp1 HG00140.hp2 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.922+108A>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162142424 | ||||||
chr5:162142430
|
A | G | 1 | a0001c0002t0005g0223 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.922+114A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162142430 | ||||||
chr5:162142506
|
C | T | 45 | a0001c0001t0003g0024a0001c0001t0003g0054a0001c0001t0003g0060others(42): Show | 45 | HG00438.hp1 HG00621.hp1 HG01496.hp1 others(42): Show |
intron_variant | MODIFIER | c.922+190C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162142506 | ||||||
chr5:162142642
|
C | T | 2 | a0001c0004t0017g0246a0001c0009t0004g0143 | 2 | HG02647.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.922+326C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162142642 | ||||||
chr5:162142655
|
A | T | 1 | a0001c0002t0011g0085 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.922+339A>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162142655 | ||||||
chr5:162142737
|
C | T | 1 | a0001c0002t0001g0235 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.922+421C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162142737 | ||||||
chr5:162142899
|
T | TA | 77 | a0001c0001t0001g0162a0001c0001t0001g0244a0001c0001t0002g0052others(74): Show | 79 | HG00140.hp1 HG00438.hp1 HG00621.hp1 others(76): Show |
intron_variant | MODIFIER | c.922+597dupA | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 162142899 | |||||
chr5:162142899
|
T | TAA | 122 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(119): Show | 128 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.922+596_922+597dup others(2): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 162142899 | |||||
chr5:162142946
|
A | T | 12 | a0001c0002t0005g0221a0001c0002t0005g0223a0001c0002t0005g0224others(9): Show | 12 | HG00639.hp2 HG01981.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.922+630A>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162142946 | ||||||
chr5:162143032
|
G | A | 1 | a0001c0002t0004g0262 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.922+716G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162143032 | ||||||
chr5:162143072
|
G | T | 7 | a0001c0001t0002g0163a0001c0001t0002g0164a0001c0001t0002g0165others(4): Show | 8 | HG00639.hp1 HG02109.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.922+756G>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162143072 | ||||||
chr5:162143175
|
A | G | 1 | a0001c0001t0008g0050 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.922+859A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162143175 | ||||||
chr5:162143182
|
C | T | 1 | a0001c0001t0004g0251 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.922+866C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162143182 | ||||||
chr5:162143227
|
C | G | 1 | a0001c0002t0001g0120 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.922+911C>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162143227 | ||||||
chr5:162143235
|
C | T | 45 | a0001c0001t0003g0024a0001c0001t0003g0054a0001c0001t0003g0060others(42): Show | 45 | HG00438.hp1 HG00621.hp1 HG01496.hp1 others(42): Show |
intron_variant | MODIFIER | c.922+919C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162143235 | ||||||
chr5:162143262
|
G | A | 3 | a0001c0005t0003g0028a0001c0005t0003g0075a0001c0005t0015g0243 | 3 | HG01243.hp2 HG01884.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.922+946G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162143262 | ||||||
chr5:162143322
|
A | G | 2 | a0001c0001t0002g0187a0001c0001t0002g0193 | 2 | HG03927.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.922+1006A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162143322 | ||||||
chr5:162143323
|
T | A | 1 | a0001c0001t0002g0056 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.922+1007T>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162143323 | ||||||
chr5:162143569
|
T | C | 4 | a0001c0001t0003g0111a0001c0001t0003g0123a0001c0001t0003g0125others(1): Show | 4 | NA18946.hp1 NA18950.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.922+1253T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162143569 | ||||||
chr5:162143597
|
A | G | 2 | a0001c0001t0004g0256a0001c0001t0004g0257 | 2 | HG02622.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.922+1281A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162143597 | ||||||
chr5:162143610
|
G | A | 3 | a0001c0005t0003g0028a0001c0005t0003g0075a0001c0005t0015g0243 | 3 | HG01243.hp2 HG01884.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.922+1294G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162143610 | ||||||
chr5:162143684
|
A | T | 13 | a0001c0001t0001g0045a0001c0001t0001g0133a0001c0001t0001g0151others(10): Show | 14 | HG00673.hp1 HG02027.hp1 HG02071.hp2 others(11): Show |
intron_variant | MODIFIER | c.922+1368A>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162143684 | ||||||
chr5:162143745
|
A | T | 1 | a0001c0001t0004g0139 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.922+1429A>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162143745 | ||||||
chr5:162143847
|
T | C | 1 | a0001c0003t0003g0302 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.922+1531T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162143847 | ||||||
chr5:162143949
|
A | G | 1 | a0001c0002t0003g0128 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.922+1633A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162143949 | ||||||
chr5:162144082
|
G | A | 1 | a0001c0001t0002g0023 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.922+1766G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162144082 | ||||||
chr5:162144207
|
G | C | 4 | a0001c0001t0002g0189a0001c0001t0002g0205a0001c0003t0002g0268others(1): Show | 4 | HG02165.hp1 NA19006.hp2 NA19067.hp1 others(1): Show |
intron_variant | MODIFIER | c.922+1891G>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162144207 | ||||||
chr5:162144222
|
G | A | 1 | a0001c0002t0001g0215 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.922+1906G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162144222 | ||||||
chr5:162144240
|
C | T | 1 | a0001c0001t0004g0139 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.922+1924C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162144240 | ||||||
chr5:162144421
|
G | C | 1 | a0001c0002t0001g0107 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.922+2105G>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162144421 | ||||||
chr5:162144431
|
A | T | 1 | a0001c0001t0004g0139 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.922+2115A>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162144431 | ||||||
chr5:162144638
|
G | A | 1 | a0001c0002t0001g0180 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.922+2322G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162144638 | ||||||
chr5:162144694
|
A | G | 15 | a0001c0001t0003g0063a0001c0001t0003g0105a0001c0001t0003g0126others(12): Show | 16 | HG00140.hp1 HG01074.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.922+2378A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162144694 | ||||||
chr5:162144725
|
G | T | 15 | a0001c0001t0003g0063a0001c0001t0003g0105a0001c0001t0003g0126others(12): Show | 16 | HG00140.hp1 HG01074.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.922+2409G>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162144725 | ||||||
chr5:162144907
|
C | A | 13 | a0001c0001t0001g0045a0001c0001t0001g0133a0001c0001t0001g0151others(10): Show | 14 | HG00673.hp1 HG02027.hp1 HG02071.hp2 others(11): Show |
intron_variant | MODIFIER | c.922+2591C>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162144907 | ||||||
chr5:162144941
|
A | G | 7 | a0001c0002t0001g0222a0001c0002t0001g0227a0001c0002t0001g0229others(4): Show | 7 | HG00735.hp1 HG01081.hp1 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.922+2625A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162144941 | ||||||
chr5:162145039
|
C | T | 3 | a0001c0001t0004g0309a0001c0001t0004g0310a0001c0001t0004g0311 | 3 | HG02258.hp2 HG02965.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.922+2723C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162145039 | ||||||
chr5:162145046
|
C | T | 1 | a0001c0001t0002g0260 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.922+2730C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162145046 | ||||||
chr5:162145612
|
T | G | 15 | a0001c0001t0003g0063a0001c0001t0003g0105a0001c0001t0003g0126others(12): Show | 16 | HG00140.hp1 HG01074.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.922+3296T>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162145612 | ||||||
chr5:162145618
|
A | T | 1 | a0001c0002t0001g0102 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.922+3302A>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162145618 | ||||||
chr5:162145674
|
A | G | 1 | a0001c0004t0002g0148 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.922+3358A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162145674 | ||||||
chr5:162145731
|
A | T | 1 | a0001c0006t0012g0005 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.923-3377A>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162145731 | ||||||
chr5:162145809
|
C | T | 1 | a0001c0002t0001g0070 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.923-3299C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162145809 | ||||||
chr5:162145946
|
ATAGAACT others(717): Show |
A | 2 | a0001c0002t0001g0211a0001c0008t0001g0247 | 2 | HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.923-3157_923-2434d others(2): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 162145946 | |||||
chr5:162146106
|
T | C | 4 | a0001c0002t0001g0173a0001c0002t0001g0178a0001c0002t0001g0191others(1): Show | 4 | HG02630.hp2 HG02809.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.923-3002T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162146106 | ||||||
chr5:162146486
|
C | G | 15 | a0001c0001t0003g0063a0001c0001t0003g0105a0001c0001t0003g0126others(12): Show | 16 | HG00140.hp1 HG01074.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.923-2622C>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162146486 | ||||||
chr5:162146511
|
C | A | 1 | a0001c0006t0012g0005 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.923-2597C>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162146511 | ||||||
chr5:162146595
|
C | T | 5 | a0001c0001t0004g0139a0001c0002t0004g0262a0001c0005t0003g0028others(2): Show | 5 | HG01192.hp1 HG01243.hp2 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.923-2513C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162146595 | ||||||
chr5:162147195
|
CTCTTTCT others(12): Show |
C | 2 | a0001c0004t0017g0246a0001c0009t0004g0143 | 2 | HG02647.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.923-1901_923-1883d others(21): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 162147195 | |||||
chr5:162147208
|
T | C | 1 | a0001c0002t0001g0231 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.923-1900T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162147208 | ||||||
chr5:162147247
|
CTTTA | C | 6 | a0001c0001t0002g0029a0001c0001t0002g0160a0001c0001t0002g0161others(3): Show | 6 | HG02145.hp2 HG02717.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.923-1857_923-1854d others(6): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 162147247 | |||||
chr5:162147290
|
CCTTT | C | 4 | a0001c0001t0002g0163a0001c0001t0002g0164a0001c0001t0002g0165others(1): Show | 4 | HG00639.hp1 HG02922.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.923-1805_923-1802d others(6): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 162147290 | |||||
chr5:162147306
|
TTTCC | T | 2 | a0001c0001t0001g0244a0001c0006t0012g0005 | 3 | HG01069.hp1 HG01071.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.923-1783_923-1780d others(6): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 162147306 | |||||
chr5:162147342
|
C | T | 1 | a0001c0001t0001g0034 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.923-1766C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162147342 | ||||||
chr5:162147428
|
G | T | 3 | a0001c0001t0004g0309a0001c0001t0004g0310a0001c0001t0004g0311 | 3 | HG02258.hp2 HG02965.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.923-1680G>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162147428 | ||||||
chr5:162147458
|
G | A | 8 | a0001c0001t0004g0139a0001c0001t0004g0309a0001c0001t0004g0310others(5): Show | 8 | HG01192.hp1 HG02258.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.923-1650G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162147458 | ||||||
chr5:162147518
|
C | T | 1 | a0001c0001t0001g0036 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.923-1590C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162147518 | ||||||
chr5:162147544
|
T | C | 2 | a0001c0001t0003g0105a0001c0001t0003g0126 | 2 | HG01346.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.923-1564T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162147544 | ||||||
chr5:162147552
|
G | A | 6 | a0001c0002t0001g0097a0001c0002t0001g0098a0001c0002t0001g0099others(3): Show | 6 | HG02074.hp2 NA18941.hp2 NA18962.hp1 others(3): Show |
intron_variant | MODIFIER | c.923-1556G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162147552 | ||||||
chr5:162147657
|
C | A | 12 | a0001c0002t0005g0221a0001c0002t0005g0223a0001c0002t0005g0224others(9): Show | 12 | HG00639.hp2 HG01981.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.923-1451C>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162147657 | ||||||
chr5:162147940
|
T | A | 1 | a0001c0001t0002g0042 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.923-1168T>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162147940 | ||||||
chr5:162148199
|
A | C | 1 | a0001c0002t0001g0102 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.923-909A>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162148199 | ||||||
chr5:162148219
|
T | A | 1 | a0001c0001t0001g0045 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.923-889T>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162148219 | ||||||
chr5:162148435
|
A | G | 1 | a0001c0001t0003g0063 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.923-673A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162148435 | ||||||
chr5:162148438
|
TA | T | 116 | a0001c0001t0001g0115a0001c0001t0001g0162a0001c0001t0002g0002others(113): Show | 122 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(119): Show |
intron_variant | MODIFIER | c.923-665delA | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 162148438 | |||||
chr5:162148447
|
T | G | 1 | a0001c0002t0004g0262 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.923-661T>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162148447 | ||||||
chr5:162148647
|
G | A | 141 | a0001c0001t0001g0115a0001c0001t0001g0162a0001c0001t0001g0244others(138): Show | 149 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(146): Show |
intron_variant | MODIFIER | c.923-461G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162148647 | ||||||
chr5:162149013
|
A | G | 3 | a0001c0005t0003g0028a0001c0005t0003g0075a0001c0005t0015g0243 | 3 | HG01243.hp2 HG01884.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.923-95A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162149013 | ||||||
chr5:162149395
|
A | C | 1 | a0001c0001t0003g0105 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1128+82A>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 8/9 | chr5 | 162149395 | ||||||
chr5:162149400
|
C | G | 1 | a0001c0003t0002g0296 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1128+87C>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 8/9 | chr5 | 162149400 | ||||||
chr5:162149412
|
C | A | 115 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(112): Show | 121 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(118): Show |
intron_variant | MODIFIER | c.1128+99C>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 8/9 | chr5 | 162149412 | ||||||
chr5:162149597
|
C | T | 1 | a0001c0002t0003g0093 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1128+284C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 8/9 | chr5 | 162149597 | ||||||
chr5:162149906
|
G | A | 3 | a0001c0005t0003g0028a0001c0005t0003g0075a0001c0005t0015g0243 | 3 | HG01243.hp2 HG01884.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1128+593G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 8/9 | chr5 | 162149906 | ||||||
chr5:162150069
|
G | A | 1 | a0001c0002t0001g0089 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1128+756G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 8/9 | chr5 | 162150069 | ||||||
chr5:162150094
|
G | A | 11 | a0001c0001t0004g0017a0001c0001t0004g0250a0001c0001t0004g0251others(8): Show | 11 | HG02572.hp1 HG02615.hp2 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.1128+781G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 8/9 | chr5 | 162150094 | ||||||
chr5:162150327
|
G | A | 1 | a0001c0001t0002g0068 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1128+1014G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 8/9 | chr5 | 162150327 | ||||||
chr5:162150639
|
C | T | 1 | a0001c0002t0011g0085 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1129-1091C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 8/9 | chr5 | 162150639 | ||||||
chr5:162150747
|
A | G | 1 | a0001c0002t0001g0058 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1129-983A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 8/9 | chr5 | 162150747 | ||||||
chr5:162150896
|
T | C | 1 | a0001c0001t0002g0166 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1129-834T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 8/9 | chr5 | 162150896 | ||||||
chr5:162151259
|
C | A | 3 | a0001c0005t0003g0028a0001c0005t0003g0075a0001c0005t0015g0243 | 3 | HG01243.hp2 HG01884.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1129-471C>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 8/9 | chr5 | 162151259 | ||||||
chr5:162151348
|
C | T | 2 | a0001c0004t0005g0237a0001c0004t0005g0238 | 2 | HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1129-382C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 8/9 | chr5 | 162151348 | ||||||
chr5:162151359
|
T | C | 1 | a0001c0002t0004g0262 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1129-371T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 8/9 | chr5 | 162151359 | ||||||
chr5:162151593
|
A | G | 2 | a0001c0003t0003g0264a0001c0003t0003g0265 | 2 | NA19011.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.1129-137A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 8/9 | chr5 | 162151593 | ||||||
chr5:162151779
|
C | T | 1 | a0001c0001t0010g0258 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1152+26C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 9/9 | chr5 | 162151779 | ||||||
chr5:162152143
|
TACTGTTT others(4): Show |
T | 1 | a0001c0002t0001g0168 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1152+394_1152+404d others(13): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr5 | 162152143 | |||||
chr5:162152144
|
A | G | 1 | a0001c0001t0002g0197 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1152+391A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 9/9 | chr5 | 162152144 | ||||||
chr5:162152435
|
A | G | 198 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(195): Show | 205 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(202): Show |
intron_variant | MODIFIER | c.1153-658A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 9/9 | chr5 | 162152435 | ||||||
chr5:162152766
|
A | G | 45 | a0001c0001t0003g0024a0001c0001t0003g0054a0001c0001t0003g0060others(42): Show | 45 | HG00438.hp1 HG00621.hp1 HG01496.hp1 others(42): Show |
intron_variant | MODIFIER | c.1153-327A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 9/9 | chr5 | 162152766 | ||||||
chr5:162152813
|
T | A | 1 | a0001c0002t0001g0138 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1153-280T>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 9/9 | chr5 | 162152813 |